TODGA, TOOPDA
diglycolamide
C36H72N2O3 CHON
580.983 g/mol
An(III), Ln(III), An(IV)
Japan
Japan,
USA,
Russia,
Sweden,
UK,
Germany
Factor | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
---|---|---|---|---|---|---|---|---|---|
La/Am | ≈0.94 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Ce/Am | ≈1.30 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Pr/Am | ≈1.80 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Nd/Am | ≈2.14 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Sm/Am | ≈3.91 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Eu/Am | ≈5.10 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Gd/Am | ≈8.64 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
La/Am | ≈2.22 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Ce/Am | ≈3.72 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Pr/Am | ≈3.96 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Nd/Am | ≈4.12 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Sm/Am | ≈4.07 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Eu/Am | ≈5.16 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Gd/Am | ≈8.11 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
La/Am | ≈5.16 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Ce/Am | ≈10.30 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Pr/Am | ≈7.06 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Nd/Am | ≈5.36 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Sm/Am | ≈4.38 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Eu/Am | ≈5.43 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Gd/Am | ≈7.15 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
La/Am | ≈12.43 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Ce/Am | ≈14.10 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Pr/Am | ≈9.20 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Nd/Am | ≈7.06 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Sm/Am | ≈4.55 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Eu/Am | ≈5.56 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Gd/Am | ≈7.06 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
La/Am | ≈27.43 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Ce/Am | ≈22.72 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Pr/Am | ≈11.53 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Nd/Am | ≈9.20 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Sm/Am | ≈4.79 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Eu/Am | ≈5.78 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Gd/Am | ≈6.23 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
La/Am | ≈62.05 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Ce/Am | ≈40.48 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Pr/Am | ≈15.98 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Nd/Am | ≈12.43 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Sm/Am | ≈5.03 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Eu/Am | ≈6.08 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Gd/Am | ≈5.78 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
La/Cm | ≈0.85 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Ce/Cm | ≈1.16 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Pr/Cm | ≈1.63 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Nd/Cm | ≈1.92 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Sm/Cm | ≈8.71 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Eu/Cm | ≈11.33 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
Gd/Cm | ≈19.66 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.3 pH | [1] | |
La/Cm | ≈1.89 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Ce/Cm | ≈3.05 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Pr/Cm | ≈3.32 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Nd/Cm | ≈3.41 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Sm/Cm | ≈10.00 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Eu/Cm | ≈12.68 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
Gd/Cm | ≈19.66 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.4 pH | [1] | |
La/Cm | ≈4.22 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Ce/Cm | ≈8.50 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Pr/Cm | ≈5.77 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Nd/Cm | ≈4.55 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Sm/Cm | ≈11.19 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Eu/Cm | ≈14.02 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
Gd/Cm | ≈18.93 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.5 pH | [1] | |
La/Cm | ≈9.63 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Ce/Cm | ≈10.92 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Pr/Cm | ≈7.22 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Nd/Cm | ≈5.48 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Sm/Cm | ≈13.01 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Eu/Cm | ≈15.50 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
Gd/Cm | ≈19.66 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.6 pH | [1] | |
La/Cm | ≈20.15 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Ce/Cm | ≈16.91 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Pr/Cm | ≈8.29 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Nd/Cm | ≈6.70 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Sm/Cm | ≈14.74 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Eu/Cm | ≈17.78 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
Gd/Cm | ≈19.90 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [1] | |
La/Cm | ≈44.89 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Ce/Cm | ≈30.08 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Pr/Cm | ≈11.77 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Nd/Cm | ≈9.28 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Sm/Cm | ≈17.13 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Eu/Cm | ≈19.66 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Gd/Cm | ≈19.17 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [1] | |
Ca/Sr | 15 | HNO3 2.9 M | n-Dodecane | 25°C | 120 min | average SF; 0.005-0.1M TODGA | [2] | ||
Sr/Ba | 78 | HNO3 2.9 M | n-Dodecane | 25°C | 120 min | average SF; 0.02-0.5M TODGA | [2] | ||
Ca/Sr | 39 | 0.1 M | HNO3 4.65 M | n-Dodecane | 25°C | 120 min | [2] | ||
Sr/Ba | 197 | 0.1 M | HNO3 4.65 M | n-Dodecane | 25°C | 120 min | [2] | ||
Am/La | 4.8 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 20 min | [3] | ||
Nd/Am | 1.47 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 20 min | [3] | ||
Cm/Am | 1.89 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 20 min | [3] | ||
Gd/La | 33.2 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 20 min | [3] | ||
Eu/Am | 0.01 | 0.2 M | HNO3 0.09 M | hydrogenated tetrapropene/1-Octanol, 5% | 20°C | 15 min | [4] | ||
Eu/Am | ≈0.01 | 0.2 M | HNO3 0.19 M | hydrogenated tetrapropene/1-Octanol, 5% | 20°C | 15 min | [4] | ||
Eu/Am | ≈0.005 | 0.2 M | HNO3 0.45 M | hydrogenated tetrapropene/1-Octanol, 5% | 20°C | 15 min | [4] | ||
Cm(III)/Am(III) | ≈1.6 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-Octanol, 5% | 20°C | 15 min | [4] | ||
Eu(III)/Am(III) | ≈7.5 | 0.2 M | HEDTA 0.02 M | HNO3 4.2 M | hydrogenated tetrapropene/1-Octanol, 5% | 20°C | 15 min | 0.2M Oxalic Acid | [4] |
La(III)/Am(III) | 0.18 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Eu(III)/Am(III) | 8.8 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Lu(III)/Am(III) | 21 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Th(IV)/Am(III) | 4.9 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
U(VI)/Am(III) | 0.027 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Np(V)/Am(III) | 0.0002 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Am(III)/Am(III) | 1 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Cm(III)/Am(III) | 2.6 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Cf(III)/Am(III) | 5.2 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [5] | ||
Eu(III)/Am(III) | 1.9 | 0.1 M | HNO3 3 M | HPT/1-Octanol, 1:1 | 22°C | 10 min | [6] |
Element | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
---|---|---|---|---|---|---|---|---|---|
Ce | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [7] | |
Cs | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [7] | |
Rh | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [7] | |
Te | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [7] | |
Al | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [7] | |
Na | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [7] | |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | 0.025M CDTA; 0.0004M Zr | [7] |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | 0.025M CDTA; 0.001M Zr | [7] |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | 0.025M CDTA; 0.00015M Zr | [7] |
Zr | 0.002 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | 0.025M CDTA; 0.003M Zr | [7] |
Zr | 0.004 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | 0.025M CDTA; 0.006M Zr | [7] |
Zr | 0.011 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | 0.025M CDTA; 0.012M Zr | [7] |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | 0.05M CDTA; 0.0004M Zr | [7] |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | 0.05M CDTA; 0.001M Zr | [7] |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | 0.05M CDTA; 0.00015M Zr | [7] |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | 0.05M CDTA; 0.003M Zr | [7] |
Zr | ≤0.001 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | 0.05M CDTA; 0.006M Zr | [7] |
Zr | 0.005 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | 0.05M CDTA; 0.012M Zr | [7] |
Zr(IV) | 350 | 0.1 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | [8] | ||
Pd(II) | 20 | 0.1 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | [8] | ||
Sr(II) | 3.2 | 0.1 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | [8] | ||
Mo(IV) | 0.23 | 0.1 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | [8] | ||
Zr(IV) | 1.43 | 0.1 M | HEDTA 0.05 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | 0.2M oxalic acid | [8] |
Pd(II) | 0.4 | 0.1 M | HEDTA 0.05 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | 0.2M oxalic acid | [8] |
Sr(II) | 2.88 | 0.1 M | HEDTA 0.05 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | 0.2M oxalic acid | [8] |
Mo(IV) | 0.07 | 0.1 M | HEDTA 0.05 M | HNO3 3 M | hydrogenated tetrapropene/octanol, 95:5 | 22°C | 15 min | 0.2M oxalic acid | [8] |
Am(III) | 24 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am(III) | 0.3 | 0.1 M | HNO3 1 M | toluene | 25°C | 45 min | SHLW | [9] | |
Am(III) | 68 | 0.1 M | HNO3 1 M | 1-octanol | 25°C | 45 min | SHLW | [9] | |
Am(III) | 12 | 0.1 M | HNO3 1 M | 1,2-dichloroethane | 25°C | 45 min | SHLW | [9] | |
Am(III) | 202 | 0.1 M | HNO3 1 M | nitrobenzene | 25°C | 45 min | SHLW | [9] | |
Am | 0.001 | 0.1 M | HNO3 0.01 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 0.013 | 0.1 M | HNO3 0.1 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 0.78 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 24 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 171 | 0.1 M | HNO3 2 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 297 | 0.1 M | HNO3 3 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 349 | 0.1 M | HNO3 4 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 336 | 0.1 M | HNO3 5 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 341 | 0.1 M | HNO3 6 M | n-Dodecane | 25°C | 45 min | SHLW | [9] | |
Am | 0.001 | 0.1 M | DHOA 0.5 M | HNO3 0.01 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 0.006 | 0.1 M | DHOA 0.5 M | HNO3 0.1 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 0.24 | 0.1 M | DHOA 0.5 M | HNO3 0.5 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 9.8 | 0.1 M | DHOA 0.5 M | HNO3 1 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 176 | 0.1 M | DHOA 0.5 M | HNO3 2 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 274 | 0.1 M | DHOA 0.5 M | HNO3 3 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 289 | 0.1 M | DHOA 0.5 M | HNO3 4 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 284 | 0.1 M | DHOA 0.5 M | HNO3 5 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Am | 319 | 0.1 M | DHOA 0.5 M | HNO3 6 M | n-Dodecane | 25°C | 45 min | SHLW | [9] |
Y | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Ce | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Pr | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Nd | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Sm | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
La | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Eu | 68 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Gd | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Mo | 1.7 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Sr | 2 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Pd | 0.22 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Se | 0.18 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Cd | 0.16 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Ru | 0.41 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Ba | 0.14 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Cs | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Zr | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Ag | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Ni | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Rb | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Rh | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Sn | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Sb | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Te | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Cu | <0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3.2 M | Exxsol-D80 | 22°C | 15 min | simulated HAR; 0.05M CDTA | [10] |
Eu(III) | ≈300 | 0.2 M | HNO3 | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | 0.5M NH4NO3 | [10] | |
Am(III) | ≈60 | 0.2 M | HNO3 | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | 0.5M NH4NO3 | [10] | |
Eu(III) | 950 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [10] | ||
Am(III) | 120 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [10] | ||
Y(III) | ≈200 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [10] | ||
Y(III) | ≈500 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [10] | ||
Y(III) | ≈900 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [10] | ||
La | ≈0.47 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Ce | ≈0.71 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Pr | ≈0.75 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Nd | ≈0.84 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Sm | ≈3.15 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Eu | ≈5.93 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Gd | ≈8.48 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Tb | ≈17.99 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Dy | ≈28.46 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Ho | ≈38.52 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Er | ≈44.61 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Tm | ≈46.27 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Yb | ≈50.26 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
Lu | ≈52.62 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 0.97 pH | [10] | ||
La | ≈0.36 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Ce | ≈1.00 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Pr | ≈0.58 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Nd | ≈0.76 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Sm | ≈1.95 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Eu | ≈3.68 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Gd | ≈5.17 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Tb | ≈11.48 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Dy | ≈17.82 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Ho | ≈25.73 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Er | ≈31.19 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Tm | ≈31.77 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Yb | ≈35.14 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
Lu | ≈37.13 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.55 pH | [10] | ||
La | ≈0.35 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Ce | ≈1.26 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Pr | ≈0.56 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Nd | ≈0.79 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Sm | ≈1.83 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Eu | ≈3.33 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Gd | ≈4.71 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Tb | ≈10.09 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Dy | ≈16.72 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Ho | ≈23.04 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Er | ≈27.68 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Tm | ≈29.79 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Yb | ≈32.06 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
Lu | ≈34.82 | 0.1 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 2.03 pH | [10] | ||
La | ≈0.59 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Ce | ≈0.94 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Pr | ≈1.22 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Nd | ≈1.32 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Sm | ≈6.11 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Eu | ≈14.07 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Gd | ≈29.45 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Tb | ≈34.93 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Dy | ≈59.38 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Ho | ≈97.20 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Er | ≈97.20 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Tm | ≈115.27 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Yb | ≈119.73 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
Lu | ≈122.02 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.25 pH | [10] | |
La | ≈0.47 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Ce | ≈0.77 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Pr | ≈0.85 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Nd | ≈0.88 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Sm | ≈1.56 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Eu | ≈2.24 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Gd | ≈3.40 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Tb | ≈5.15 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Dy | ≈8.12 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Ho | ≈14.89 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Er | ≈73.15 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Tm | ≈93.58 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Yb | ≈97.20 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
Lu | ≈100.95 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.42 pH | [10] | |
La | ≈0.41 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Ce | ≈0.45 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Pr | ≈0.27 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Nd | ≈0.25 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Sm | ≈0.13 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Eu | ≈0.15 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Gd | ≈0.21 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Tb | ≈0.24 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Dy | ≈0.31 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Ho | ≈0.46 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Er | ≈0.65 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Tm | ≈0.80 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Yb | ≈1.03 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
Lu | ≈1.59 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.7 pH | [10] | |
La | ≈0.24 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Ce | ≈0.10 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Pr | ≈0.04 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Nd | ≈0.03 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Sm | ≈0.01 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Eu | ≈0.01 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Gd | ≈0.02 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Tb | ≈0.02 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Dy | ≈0.02 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Ho | ≈0.04 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Er | ≈0.05 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Tm | ≈0.06 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Yb | ≈0.08 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
Lu | ≈0.11 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.9 pH | [10] | |
La | ≈0.28 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Ce | ≈0.21 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Pr | ≈0.10 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Nd | ≈0.05 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Sm | ≈0.04 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Gd | ≈0.05 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
La | ≈0.18 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Ce | ≈0.11 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Pr | ≈0.05 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Eu | ≈0.01 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
La | ≈0.11 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Ce | ≈0.06 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Pr | ≈0.02 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Nd | ≈0.02 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Sm | ≈0.01 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Eu | ≈0.01 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Gd | ≈0.01 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Tb | ≈0.06 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Er | ≈0.13 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Tm | ≈0.16 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Yb | ≈0.23 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Lu | ≈0.32 | 0.1 M | DTPA 0.01 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Tb | ≈0.02 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Dy | ≈0.03 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Ho | ≈0.04 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Er | ≈0.06 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Tm | ≈0.07 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Yb | ≈0.09 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Lu | ≈0.13 | 0.1 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Tb | ≈0.01 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Dy | ≈0.02 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Ho | ≈0.03 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Er | ≈0.04 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Tm | ≈0.05 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Yb | ≈0.06 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
Lu | ≈0.09 | 0.1 M | DTPA 0.05 M | n-Dodecane | 25°C | 60 min | 1M NaNO3; 1.8 pH | [10] | |
La | ≈1.07 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Ce | ≈1.26 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Pr | ≈0.91 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Nd | ≈0.78 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Sm | ≈0.43 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Eu | ≈0.48 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Gd | ≈0.70 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
La | ≈4.56 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Ce | ≈3.10 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Nd | ≈2.81 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Eu | ≈0.97 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Gd | ≈1.46 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
La | ≈31.17 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Ce | ≈25.56 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Pr | ≈10.60 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Nd | ≈10.08 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Sm | ≈3.98 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Eu | ≈4.13 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Gd | ≈5.77 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
La | ≈0.02 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.15M NaNO3; 1.8 pH | [10] | |
Ce | ≈6.45 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.15M NaNO3; 1.8 pH | [10] | |
Pr | ≈5.23 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.15M NaNO3; 1.8 pH | [10] | |
Nd | ≈3.79 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.15M NaNO3; 1.8 pH | [10] | |
Eu | ≈1.84 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.15M NaNO3; 1.8 pH | [10] | |
Gd | ≈2.64 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.15M NaNO3; 1.8 pH | [10] | |
Tb | ≈0.80 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Dy | ≈1.07 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Ho | ≈1.55 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Er | ≈2.14 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Tm | ≈2.46 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Yb | ≈2.90 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Lu | ≈4.38 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.54M NaNO3; 1.8 pH | [10] | |
Tb | ≈2.82 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Dy | ≈3.87 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Ho | ≈4.97 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Er | ≈5.78 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Tm | ≈6.39 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Yb | ≈7.71 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Lu | ≈8.97 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 0.88M NaNO3; 1.8 pH | [10] | |
Tb | ≈5.93 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Dy | ≈7.24 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Ho | ≈8.64 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Er | ≈9.67 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Tm | ≈10.56 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Yb | ≈10.96 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Lu | ≈12.91 | 0.2 M | DTPA 0.02 M | n-Dodecane | 25°C | 60 min | 1.73M NaNO3; 1.8 pH | [10] | |
Ln | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Zr | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Pd | 4.2 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Mo | 1.93 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Sr | 1.43 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Se | 0.77 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Fe | 0.25 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Cd | 0.25 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Ru | 0.23 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Ba | 0.13 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Cr | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Ni | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Rb | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Rh | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Sn | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Sb | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Te | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Cs | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Ln | >100 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Zr | ≤0.01 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Pd | 0.07 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Mo | 2.1 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Sr | 2.25 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Se | 0.74 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Fe | 0.25 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Cd | 0.17 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Ru | 0.32 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Ba | 0.2 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Cr | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Ni | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Rb | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Rh | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Sn | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Sb | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Te | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Cs | ≤0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Zr | 30 | 0.2 M | DMDOHEMA 0.5 M | HNO3 1 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Zr | ≤0.01 | 0.2 M | DMDOHEMA 0.5 M | HNO3 1 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Mo | 1.21 | 0.2 M | DMDOHEMA 0.5 M | HNO3 1 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Mo | 1.43 | 0.2 M | DMDOHEMA 0.5 M | HNO3 1 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Zr | 86 | 0.2 M | DMDOHEMA 0.5 M | HNO3 2 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Zr | ≤0.01 | 0.2 M | DMDOHEMA 0.5 M | HNO3 2 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Mo | 1.36 | 0.2 M | DMDOHEMA 0.5 M | HNO3 2 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Mo | 1.08 | 0.2 M | DMDOHEMA 0.5 M | HNO3 2 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Zr | 142 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Zr | ≤0.01 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Mo | 1.93 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Mo | 2.1 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Zr | 376 | 0.2 M | DMDOHEMA 0.5 M | HNO3 4 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Zr | 0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 4 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Mo | 3.62 | 0.2 M | DMDOHEMA 0.5 M | HNO3 4 M | Exxsol D80 | 22°C | org/aq=1 | [11] | |
Mo | 4.12 | 0.2 M | DMDOHEMA 0.5 M | HNO3 4 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA | [11] | |
Am(III)241 | 65 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.01M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Pu(IV)239 | 60 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.01M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Zr(IV) | 7.7 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.01M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Pd(II) | 0.5 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.01M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Am(III)241 | 42 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Pu(IV)239 | 35 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Zr(IV) | 1.2 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Pd(II) | 0.05 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.05M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Am(III)241 | 40 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.1M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Pu(IV)239 | 32 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.1M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Zr(IV) | 0.2 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.1M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Pd(II) | 0.02 | 0.2 M | DMDOHEMA 0.5 M | HNO3 3 M | Exxsol D80 | 22°C | org/aq=1; 0.1M CDTA; 17 g/L Pu239 + 0.1 g/L Am241 | [11] | |
Am241 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Pu239 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Y | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
La | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Ce(IV) | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Pr | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Nd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Sm | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Eu | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Eu152 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Gd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Zr | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Pd | 9.31 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Ag | 0.69 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Ba | 0.13 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Cd | 0.14 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Mo | 0.26 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Ni | 0.05 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Sr | 1.5 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Rb | 0.1 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Ru | 0.34 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Cr | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Cu | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Sb | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Sn | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Se | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Ce | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Cs | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Rh | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Te | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Al | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Na | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR | [11] |
Am241 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Pu239 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Y | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
La | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Ce(IV) | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Pr | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Nd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Sm | 99.2 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Eu | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Eu152 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Gd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Zr | 0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Pd | 0.07 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Ag | 0.06 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Ba | 0.08 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Cd | 0.08 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Mo | 0.12 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Ni | 0.02 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Sr | 2.84 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Rb | 0.03 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Ru | 0.32 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Cr | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Cu | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Sb | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Sn | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Se | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Ce | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Cs | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Rh | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Te | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Al | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Na | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M EDTA | [11] |
Am241 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Pu239 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Y | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
La | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Ce(IV) | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Pr | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Nd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Sm | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Eu | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Eu152 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Gd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Zr | 0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Pd | 0.07 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Ag | 0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Ba | 0.03 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Cd | 0.08 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Mo | 0.19 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Ni | 0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Sr | 3.31 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Rb | 0.14 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Ru | 0.32 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Cr | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Cu | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Sb | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Sn | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Se | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Ce | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Cs | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Rh | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Te | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Al | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Na | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M CDTA | [11] |
Am241 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Y | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
La | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Ce(IV) | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Pr | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Nd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Sm | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Eu | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Eu152 | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Gd | >100 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Zr | 32.8 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Pd | 0.07 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Ag | 0.59 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Ba | 0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Cd | 0.14 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Mo | 0.23 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Ni | 0.08 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Sr | 1.54 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Rb | 0.09 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Ru | 0.23 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Cr | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Cu | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Sb | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Sn | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Se | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Ce | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Cs | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Rh | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Te | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Al | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Na | <0.01 | 0.2 M | TBP 0.5 M | HNO3 3.1 M | hydrogenated tetrapropene | 22°C | 15 min | HAR; 0.05M HEDTA | [11] |
Am241 | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Y | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
La | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Ce(IV) | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Pr | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Nd | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Sm | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Eu | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Eu152 | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Gd | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Zr | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Pd | 4.75 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Ba | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Cd | 0.07 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Mo | 0.24 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Ni | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Sr | 1.23 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Rb | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Ru | 0.21 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Cr | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Cu | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Sb | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Sn | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Se | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Ce | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Cs | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Rh | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Te | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Al | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Na | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR | [11] | |
Am241 | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Y | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
La | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Ce(IV) | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Pr | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Nd | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Sm | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Eu | 70 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Eu152 | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Gd | >100 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Zr | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Pd | 0.05 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Ba | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Cd | 0.11 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Mo | 0.19 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Ni | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Sr | 3.14 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Rb | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Ru | 0.13 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Cr | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Cu | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Sb | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Sn | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Se | <0.01 | 0.2 M | HNO3 3.1 M | hydrogenated tetrapropene/1-octanol, 5% | 22°C | 15 min | HAR; 0.05M CDTA | [11] | |
Eu(III) | 0.097 | 0.1 M | HNO3 1 M | Chloroform | 25°C | 120 min | [11] | ||
Eu(III) | 300 | 0.1 M | HNO3 1 M | Diethylether | 25°C | 120 min | [11] | ||
Eu(III) | 0.83 | 0.1 M | HNO3 1 M | Benzene | 25°C | 120 min | [11] | ||
Eu(III) | 0.79 | 0.1 M | HNO3 1 M | Toluene | 25°C | 120 min | [11] | ||
Eu(III) | 0.39 | 0.1 M | HNO3 1 M | Tetrachloromethane | 25°C | 120 min | [11] | ||
Eu(III) | 265 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Eu(III) | >500 | 0.1 M | HNO3 1 M | n-Hexane | 25°C | 120 min | [11] | ||
Th(IV) | ≈0.158 | 0.1 M | HNO3 0.03 M | n-Dodecane | 25°C | 120 min | [11] | ||
Th(IV) | ≈0.251 | 0.1 M | HNO3 0.1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Th(IV) | ≈158.5 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
U(VI) | ≈0.003 | 0.1 M | HNO3 0.01 M | n-Dodecane | 25°C | 120 min | [11] | ||
U(VI) | ≈0.008 | 0.1 M | HNO3 0.1 M | n-Dodecane | 25°C | 120 min | [11] | ||
U(VI) | ≈0.794 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
U(VI) | ≈6.31 | 0.1 M | HNO3 3 M | n-Dodecane | 25°C | 120 min | [11] | ||
Np(V) | ≈0.005 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Np(V) | ≈0.126 | 0.1 M | HNO3 3 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈0.316 | 0.1 M | HNO3 0.35 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈1.259 | 0.1 M | HNO3 0.12 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈7.943 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈0.005 | 0.1 M | HNO3 0.05 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈0.016 | 0.1 M | HNO3 0.1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈0.05 | 0.1 M | HNO3 0.2 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈0.501 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈31.6 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | ≈0.006 | 0.1 M | HNO3 0.01 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | ≈0.04 | 0.1 M | HNO3 0.1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | ≈1.995 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | ≈63.1 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Th(IV) | ≈0.0316 | 0.008 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Th(IV) | ≈0.398 | 0.018 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Th(IV) | ≈7.94 | 0.045 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
U(VI) | ≈0.00316 | 0.018 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
U(VI) | ≈0.0398 | 0.045 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈0.158 | 0.018 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈0.501 | 0.045 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈15.8 | 0.079 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈63.1 | 0.158 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pu(IV) | ≈100 | 0.2 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈0.00631 | 0.01 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈0.0631 | 0.02 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | ≈3.16 | 0.05 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | ≈0.00251 | 0.008 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | ≈0.0316 | 0.018 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | ≈1.58 | 0.045 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [11] | ||
La | ≈0.501 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Ce | ≈0.794 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pr | ≈1 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Nd | ≈1.78 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Sm | ≈10 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Eu | ≈0.0398 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Gd | ≈20 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Tb | ≈17.8 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Dy | ≈63.1 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Ho | ≈79.4 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Er | ≈141 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Tm | ≈158 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Yb | ≈178 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Lu | ≈178 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am | ≈200 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm | ≈0.562 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cf | ≈1.58 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 120 min | [11] | ||
La(III) | 5.3 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Ce | ≈5.01 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Pr | ≈10 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Nd | ≈15.8 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Sm | ≈39.8 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Eu(III) | 265 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Gd | ≈251 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Tb | ≈501 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Dy | ≈501 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Ho | ≈562 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Er | ≈631 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Tm | ≈631 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Yb | ≈631 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Lu(III) | 631 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Th(IV) | 147 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
U(VI) | 0.8 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Np(V) | 0.0056 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | 30 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cm(III) | 78 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Cf(III) | 156 | 0.1 M | HNO3 1.0 M | n-Dodecane | 25°C | 120 min | [11] | ||
Am(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Cm(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Cf(III) | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Eu | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Gd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Nd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Pr | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Sm | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Y | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
La | 32 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Ce | 98 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Mo | 0.081 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Pd | 0.16 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Sr | 1.1 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Zr | 0.68 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Ru | 0.17 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [12] |
Eu(III)152 | ≈1000.00 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Cm(III)244 | ≈0.25 | 0.2 M | TBP 0.5 M | HNO3 0.1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Cm(III)244 | ≈1.15 | 0.2 M | TBP 0.5 M | HNO3 0.2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Cm(III)244 | ≈12.53 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Cm(III)244 | ≈157.06 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Cm(III)244 | ≈1435.04 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Cm(III)244 | ≈2253.93 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Am(III)241 | ≈0.16 | 0.2 M | TBP 0.5 M | HNO3 0.1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Am(III)241 | ≈0.96 | 0.2 M | TBP 0.5 M | HNO3 0.2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Am(III)241 | ≈8.73 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Am(III)241 | ≈95.59 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Am(III)241 | ≈834.77 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Am(III)241 | ≈1968.42 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
U(VI) | ≈0.15 | 0.2 M | TBP 0.5 M | HNO3 0.1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
U(VI) | ≈0.42 | 0.2 M | TBP 0.5 M | HNO3 0.2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
U(VI) | ≈1.64 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
U(VI) | ≈4.24 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
U(VI) | ≈11.98 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
U(VI) | ≈21.54 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Th(IV) | ≈0.73 | 0.2 M | TBP 0.5 M | HNO3 0.16 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Th(IV) | ≈3.09 | 0.2 M | TBP 0.5 M | HNO3 0.245 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Th(IV) | ≈29.55 | 0.2 M | TBP 0.5 M | HNO3 0.56 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Th(IV) | ≈157.06 | 0.2 M | TBP 0.5 M | HNO3 1.06 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Th(IV) | ≈1000.00 | 0.2 M | TBP 0.5 M | HNO3 2.13 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Th(IV) | ≈2059.33 | 0.2 M | TBP 0.5 M | HNO3 3.12 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Zr | ≈0.01 | 0.2 M | TBP 0.5 M | HNO3 0.09 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Zr | ≈0.08 | 0.2 M | TBP 0.5 M | HNO3 0.18 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Zr | ≈15.51 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Zr | ≈124.52 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Zr | ≈84.83 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Zr | ≈182.77 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Pd | ≈2.83 | 0.2 M | TBP 0.5 M | HNO3 0.09 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Pd | ≈2.04 | 0.2 M | TBP 0.5 M | HNO3 0.18 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Pd | ≈1.73 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Pd | ≈1.64 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Pd | ≈1.93 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Pd | ≈1.83 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Sr | ≈0.01 | 0.2 M | TBP 0.5 M | HNO3 0.09 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Sr | ≈0.01 | 0.2 M | TBP 0.5 M | HNO3 0.18 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Sr | ≈0.06 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Sr | ≈0.39 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Sr | ≈1.12 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Sr | ≈1.25 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Ru | ≈0.01 | 0.2 M | TBP 0.5 M | HNO3 0.09 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Ru | ≈0.02 | 0.2 M | TBP 0.5 M | HNO3 0.18 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Ru | ≈0.08 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Ru | ≈0.12 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Ru | ≈0.15 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Ru | ≈0.17 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Mo | ≈18.28 | 0.2 M | TBP 0.5 M | HNO3 0.09 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Mo | ≈6.45 | 0.2 M | TBP 0.5 M | HNO3 0.18 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Mo | ≈0.24 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Mo | ≈0.03 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Mo | ≈0.04 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Mo | ≈0.06 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [12] | |
Am(III) | ≈0.03 | 0.1 M | HNO3 0.01 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Am(III) | ≈0.09 | 0.1 M | HNO3 0.1 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Am(III) | ≈20 | 0.1 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Am(III) | ≈190 | 0.1 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Am(III) | ≈310 | 0.1 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Am(III) | ≈500 | 0.1 M | HNO3 4 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Eu(III) | ≈0.08 | 0.1 M | HNO3 0.01 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Eu(III) | ≈0.4 | 0.1 M | HNO3 0.1 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Eu(III) | ≈90 | 0.1 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Eu(III) | ≈200 | 0.1 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Eu(III) | ≈310 | 0.1 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Eu(III) | ≈500 | 0.1 M | HNO3 4 M | hydrogenated tetrapropene | 22°C | 15 min | [13] | ||
Am(III) | 6 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | 8 MBq/L Am; 8 MBq/L Eu | [14] | |
Eu(III) | 57 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | 8 MBq/L Am; 8 MBq/L Eu | [14] | |
Am(III) | ≈4.5 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | 8 MBq/L Am; 8 MBq/L Eu; Multiple Ln | [14] | |
Eu(III) | ≈40 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | 8 MBq/L Am; 8 MBq/L Eu; Multiple Ln | [14] | |
La(III) | ≈52 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | Multiple Ln | [14] | |
Ce(III) | ≈72 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | Multiple Ln | [14] | |
Pr(III) | ≈70 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | Multiple Ln | [14] | |
Nd(III) | ≈42 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | Multiple Ln | [14] | |
Sm(III) | ≈114 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | Multiple Ln | [14] | |
Eu(III) | ≈39 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | Multiple Ln | [14] | |
Gd(III) | ≈80 | 0.05 M | HNO3 1 M | hydrogenated tetrapropene | 21°C | 60 min | Multiple Ln | [14] | |
Y(III) | ≈0.0017 | 0.1 M | n-Dodecane | 25°C | 60 min | [15] | |||
Y(III) | ≈0.21 | 0.1 M | HNO3 0.1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈110 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈250 | 0.1 M | HNO3 2 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈280 | 0.1 M | HNO3 3 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈190 | 0.1 M | HNO3 4 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈55 | 0.1 M | HNO3 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.00075 | 0.1 M | HNO3 0.1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Ag | 0.62 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Cd | 0.039 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Ba | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Cr | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Cs | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Cu | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Fe | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Na | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Ni | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Rb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Rh | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Sb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Se | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Sn | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Te | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid | [15] |
Am(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Cm(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Cf(III) | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Eu | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Gd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Nd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Pr | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Sm | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Y | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
La | 31 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Ce | 108 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Mo | 0.071 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Pd | 0.091 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Sr | 0.84 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Zr | 0.26 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Ru | 0.22 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Ag | 0.28 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Cd | 0.039 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Ba | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Cr | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Cs | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Cu | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Fe | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Na | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Ni | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Rb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Rh | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Sb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Se | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Sn | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Te | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.2M Oxalic Acid | [15] |
Am(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Cm(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Cf(III) | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Eu | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Gd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Nd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Pr | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Sm | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Y | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
La | 44 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Ce | 170 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Mo | 0.087 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Pd | 0.048 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Sr | 1.5 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Zr | 0.1 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Ru | 0.2 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Ag | 0.12 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Cd | 0.05 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Ba | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Cr | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Cs | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Cu | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Fe | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Na | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Ni | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Rb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Rh | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Sb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Se | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Sn | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Te | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.25M Oxalic Acid | [15] |
Am(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Cm(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Cf(III) | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Eu | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Gd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Nd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Pr | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Sm | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Y | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
La | 43 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Ce | 164 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Mo | 0.11 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Pd | 0.055 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Sr | 1.6 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Zr | 0.097 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Ru | 0.19 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Ag | 0.11 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Cd | 0.052 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Ba | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Cr | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Cs | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Cu | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Fe | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Na | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Ni | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Rb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Rh | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Sb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Se | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Sn | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Te | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.3M Oxalic Acid | [15] |
Am(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Cm(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Cf(III) | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Eu | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Gd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Nd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Pr | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Sm | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Y | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
La | 43 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Ce | 164 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Mo | 0.12 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Pd | 0.046 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Sr | 1.8 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Zr | 0.056 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Ru | 0.16 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Ag | 0.066 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Cd | 0.059 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Ba | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Cr | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Cs | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Cu | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Fe | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Na | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Ni | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Rb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Rh | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Sb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Se | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Sn | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Te | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.35M Oxalic Acid | [15] |
Am(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Cm(III) | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Cf(III) | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Eu | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Gd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Nd | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Pr | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Sm | >200 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Y | >1000 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
La | 51 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Ce | 197 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Mo | 0.14 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Pd | 0.038 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Sr | 1.9 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Zr | 0.042 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Ru | 0.18 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Ag | 0.056 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Cd | 0.062 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Ba | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Cr | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Cs | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Cu | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Fe | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Na | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Ni | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Rb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Rh | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Sb | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Se | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Sn | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Te | <0.01 | 0.2 M | HEDTA 0.05 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.4M Oxalic Acid | [15] |
Am(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.06 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.3 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.23 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.4 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 5.9 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Am(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.08 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.36 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.22 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.59 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 5.8 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.05M Oxalic Acid; 0.05M HEDTA | [15] |
Am(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.05 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.16 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.22 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.54 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 0.82 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Am(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.06 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.18 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.19 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.73 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 1.1 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.10M Oxalic Acid; 0.05M HEDTA | [15] |
Am(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.04 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.07 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.25 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.44 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 0.18 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Am(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.05 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.07 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.2 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.77 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 0.19 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.15M Oxalic Acid; 0.05M HEDTA | [15] |
Am(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.04 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.03 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.25 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.42 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 0.06 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.5 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Am(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Cm(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Ln(III) | >200 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Mo | 0.05 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Pd | 0.04 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Ru | 0.21 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Sr | 0.64 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Zr | 0.09 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
F.P. | <0.03 | 0.2 M | TBP 0.25 M | HNO3 3.2 M | hydrogenated tetrapropene | 22°C | 15 min | Synthetic Highly Active Raffinate; 0.20M Oxalic Acid; 0.05M HEDTA | [15] |
Cf(III)252 | ≈2.25 | 0.2 M | TBP 0.5 M | HNO3 0.1 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Cf(III)252 | ≈13.11 | 0.2 M | TBP 0.5 M | HNO3 0.2 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Cf(III)252 | ≈188.15 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Cf(III)252 | ≈1371.69 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Cf(III)252 | ≈5080.22 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Cf(III)252 | ≈3540.13 | 0.2 M | TBP 0.5 M | HNO3 3 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Eu(III)152 | ≈1.00 | 0.2 M | TBP 0.5 M | HNO3 0.1 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Eu(III)152 | ≈5.08 | 0.2 M | TBP 0.5 M | HNO3 0.2 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Eu(III)152 | ≈55.60 | 0.2 M | TBP 0.5 M | HNO3 0.5 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Eu(III)152 | ≈424.08 | 0.2 M | TBP 0.5 M | HNO3 1 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Eu(III)152 | ≈1000.00 | 0.2 M | TBP 0.5 M | HNO3 2 M | hydrogenated tetrapropene | 22°C | 15 min | [15] | |
Y(III) | ≈2500 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Y(III) | ≈5000 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Y(III) | ≈17000 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Dy(III) | ≈280 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Dy(III) | ≈700 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Dy(III) | ≈1500 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Dy(III) | ≈4800 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Dy(III) | ≈7000 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Tb(III) | ≈200 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Tb(III) | ≈500 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Tb(III) | ≈900 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Tb(III) | ≈2200 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Tb(III) | ≈7000 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Tb(III) | ≈13000 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Gd(III) | ≈80 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Gd(III) | ≈200 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Gd(III) | ≈400 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Gd(III) | ≈600 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Gd(III) | ≈2800 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Gd(III) | ≈4800 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Eu(III) | ≈80 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Eu(III) | ≈200 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Eu(III) | ≈400 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Eu(III) | ≈1000 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Eu(III) | ≈2800 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Eu(III) | ≈8500 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Sm(III) | ≈40 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Sm(III) | ≈100 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Sm(III) | ≈270 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Sm(III) | ≈470 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Sm(III) | ≈1200 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Sm(III) | ≈2800 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Cm(III) | ≈18 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Cm(III) | ≈40 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Cm(III) | ≈75 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Cm(III) | ≈170 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Am(III) | ≈11 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Am(III) | ≈25 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Am(III) | ≈50 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Am(III) | ≈100 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Am(III) | ≈300 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Am(III) | ≈600 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Nd(III) | ≈6 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Nd(III) | ≈17 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Nd(III) | ≈30 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Nd(III) | ≈70 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Nd(III) | ≈210 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Nd(III) | ≈450 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Pr(III) | ≈3 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Pr(III) | ≈8 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Pr(III) | ≈12 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Pr(III) | ≈30 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Pr(III) | ≈90 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Pr(III) | ≈190 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Ce(III) | ≈1.9 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Ce(III) | ≈4.2 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Ce(III) | ≈7.5 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Ce(III) | ≈17 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Ce(III) | ≈45 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Ce(III) | ≈85 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
La(III) | ≈1 | 0.2 M | HNO3 0.15 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
La(III) | ≈2.5 | 0.2 M | HNO3 0.25 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
La(III) | ≈4 | 0.2 M | HNO3 0.35 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
La(III) | ≈9 | 0.2 M | HNO3 0.5 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
La(III) | ≈21 | 0.2 M | HNO3 0.75 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
La(III) | ≈38 | 0.2 M | HNO3 1 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | [15] | ||
Am(III) | 23 | 0.2 M | HEDTA 0.02 M | HNO3 4.2 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | 0.2M Oxalic Acid | [15] |
Eu(III) | 180 | 0.2 M | HEDTA 0.02 M | HNO3 4.2 M | hydrogenated tetrapropene/1-octanol, 5% | 20°C | 15 min | 0.2M Oxalic Acid | [15] |
Am(III) | 220 | 0.1 M | HNO3 1 M | Nitrobenzene | 25°C | 120 min | [15] | ||
Am(III) | 9.9 | 0.1 M | HNO3 1 M | 1,2-Dichloroethane | 25°C | 120 min | [15] | ||
Am(III) | 81 | 0.1 M | HNO3 1 M | 1-Octanol | 25°C | 120 min | [15] | ||
Am(III) | >500 | 0.1 M | HNO3 1 M | Ethyl Acetate | 25°C | 120 min | [15] | ||
Am(III) | 0.12 | 0.1 M | HNO3 1 M | Chloroform | 25°C | 120 min | [15] | ||
Am(III) | 100 | 0.1 M | HNO3 1 M | Diethylether | 25°C | 120 min | [15] | ||
Am(III) | 0.39 | 0.1 M | HNO3 1 M | Benzene | 25°C | 120 min | [15] | ||
Am(III) | 0.3 | 0.1 M | HNO3 1 M | Toluene | 25°C | 120 min | [15] | ||
Am(III) | 0.095 | 0.1 M | HNO3 1 M | Tetrachloromethane | 25°C | 120 min | [15] | ||
Am(III) | 30 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 120 min | [15] | ||
Am(III) | 33 | 0.1 M | HNO3 1 M | n-Hexane | 25°C | 120 min | [15] | ||
Eu(III) | >500 | 0.1 M | HNO3 1 M | Nitrobenzene | 25°C | 120 min | [15] | ||
Eu(III) | 34 | 0.1 M | HNO3 1 M | 1,2-Dichloroethane | 25°C | 120 min | [15] | ||
Eu(III) | >500 | 0.1 M | HNO3 1 M | 1-Octanol | 25°C | 120 min | [15] | ||
Eu(III) | >500 | 0.1 M | HNO3 1 M | Ethyl Acetate | 25°C | 120 min | [15] | ||
Sr(II) | ≈0.11 | 0.1 M | HNO3 1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.6 | 0.1 M | HNO3 2 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈1.1 | 0.1 M | HNO3 3 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈1.2 | 0.1 M | HNO3 4 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.05 | 0.1 M | HNO3 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈0.0003 | 0.1 M | n-Dodecane | 25°C | 60 min | [15] | |||
Y(III) | ≈0.00035 | 0.1 M | HCl 0.1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈0.0012 | 0.1 M | HCl 1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈0.025 | 0.1 M | HCl 2 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈0.45 | 0.1 M | HCl 3 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈140 | 0.1 M | HCl 4 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈900 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.0008 | 0.1 M | n-Dodecane | 25°C | 60 min | [15] | |||
Sr(II) | ≈0.0005 | 0.1 M | HCl 0.1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.0048 | 0.1 M | HCl 1 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.0048 | 0.1 M | HCl 2 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.0034 | 0.1 M | HCl 3 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.0055 | 0.1 M | HCl 4 M | n-Dodecane | 25°C | 60 min | [15] | ||
Sr(II) | ≈0.017 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈0.191 | 0.001 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈1 | 0.002 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈4.22 | 0.003 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈10.7 | 0.004 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈24 | 0.005 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈0 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 0 min | [15] | ||
Y(III) | ≈71 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 5 min | [15] | ||
Y(III) | ≈72 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 10 min | [15] | ||
Y(III) | ≈82 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 30 min | [15] | ||
Y(III) | ≈66 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 60 min | [15] | ||
Y(III) | ≈72 | 0.1 M | HCl 6 M | n-Dodecane | 25°C | 120 min | [15] | ||
Y(III) | ≈7 | 0.005 M | HNO3 6 M | n-Dodecane | 10°C | 60 min | [15] | ||
Y(III) | ≈12 | 0.005 M | HNO3 6 M | n-Dodecane | 20°C | 60 min | [15] | ||
Y(III) | ≈20 | 0.005 M | HNO3 6 M | n-Dodecane | 30°C | 0 min | [15] | ||
Y(III) | ≈55 | 0.005 M | HNO3 6 M | n-Dodecane | 40°C | 5 min | [15] | ||
Y(III) | ≈0.015 | 0.001 M | HCl 6 M | n-Dodecane | 10°C | 10 min | [15] | ||
Y(III) | ≈0.05 | 0.001 M | HCl 6 M | n-Dodecane | 20°C | 30 min | [15] | ||
Y(III) | ≈0.1 | 0.001 M | HCl 6 M | n-Dodecane | 30°C | 60 min | [15] | ||
Y(III) | ≈0.17 | 0.001 M | HCl 6 M | n-Dodecane | 40°C | 120 min | [15] | ||
Am(III) | 170 | 0.1 M | HNO3 3 M | HPT/1-Octanol, 1:1 | 22°C | 10 min | [15] | ||
Eu(III) | 330 | 0.1 M | HNO3 3 M | HPT/1-Octanol, 1:1 | 22°C | 10 min | [15] | ||
La | ≈0.50 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Ce | ≈0.80 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Pr | ≈1.12 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Nd | ≈1.86 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Sm | ≈9.62 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Eu | ≈18.94 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Gd | ≈18.04 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Tb | ≈59.02 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Dy | ≈78.90 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Ho | ≈144.43 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Er | ≈155.30 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Tm | ≈179.56 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Yb | ≈183.95 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] | ||
Lu | ≈207.60 | 0.1 M | HNO3 0.5 M | n-Dodecane | 25°C | 30 min | [16] |
Element | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Additional | Stages | Ref. |
---|---|---|---|---|---|---|---|---|---|
Na | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [17] | ||
Rb | 1.01 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Cs | 0.99 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Sr | 0.96 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Ba | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Zr | 0.86 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Mo | 0.98 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Ru | 1.12 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Rh | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Pd | 1.05 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Ag | 0.97 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Cd | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Te | 0.94 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Y | 4042 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
La | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Ce | 7336 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Pr | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Nd | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Sm | 699 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Eu | 175 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Gd | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
U | 69 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate | 16 | [18] | |
Am241 | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate; DFs according to gamma-decay | 16 | [18] | |
Eu152 | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate; DFs according to gamma-decay | 16 | [18] | |
Cs134 | 0.95 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate; DFs according to gamma-decay | 16 | [18] | |
Cm244 | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate; DFs according to alpha-decay | 16 | [18] | |
Cf252 | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate; DFs according to alpha-decay | 16 | [18] | |
Am241 | >10000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; Simulated PUREX Feed; raffinate; DFs according to alpha-decay | 16 | [18] | |
Rb | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Sr | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Y | 1600 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Zr | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Mo | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Ru | 1.2 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Rh | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Ag | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Pd | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Te | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Cs | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Ba | 1 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
La | >1000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Ce | 5400 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Pr | 12000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Nd | 15000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Sm | 1600 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Eu | >1000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Am | 41000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Cm | 40000 | 0.2 M | TBP 0.5 M | HNO3 4.4 M | hydrogenated tetrapropene | 0.2M Oxalic Acid; 0.05M HEDTA; 60 GWd/tM UO2 fuel | 16 | [19] | |
Y | 1 | 0.015 M | DMDOHEMA 0.25 M | HNO3 2 M | n-Octanol | TODGA Process Product | 16 | [20] | |
La | 1 | 0.015 M | DMDOHEMA 0.25 M | HNO3 2 M | n-Octanol | TODGA Process Product | 16 | [20] | |
Ce | 1 | 0.015 M | DMDOHEMA 0.25 M | HNO3 2 M | n-Octanol | TODGA Process Product | 16 | [20] | |
Eu152 | 0.98 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Sr85+Sr89 | 2990 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Fe59 | 1997 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Cs137 | 3918 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Ru106 | 1407 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Mo99 | 3250 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Pd109 | 1185 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Zr95 | 1150 | 0.05 M | HNO3 3 M | n-dodecane/iso-decanol, 5% | SHLW of PHWR; 0.1M oxalic acid; 0.05M HEDTA | 12 | [21] | ||
Am241 | 2600 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Cm244 | 750 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Eu152 | 1100 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
La | 23000 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Ce | 570000 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Pr | 220000 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Nd | 39000 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Sm | 3400 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Eu | 380 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Gd | 49000 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Y | 47000 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Ru | 1.2 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Pd | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Zr | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Mo | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Sr | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Rh | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Rb | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Ba | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Cs | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Te | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Cd | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Sn | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Sb | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Cu | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Ni | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Cr | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] | ||
Fe | 1 | 0.2 M | HNO3 4.45 M | hydrogenated tetrapropene/ 1-octanol, 5% | 0.05M CDTA | 16 | [21] |
Solvent | Solubility | Temperature | Ref. |
---|---|---|---|
H2O | 0.042 mM | [22] |
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