CMPO, OɸD(iB)CMPO
carbamylalkylphosphine oxide
C24H42NO2P not CHON
407.569 g/mol
Pu, Am
USA
USA
Factor | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
---|---|---|---|---|---|---|---|---|---|
Am241/Ru106 | >110 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Sb125 | >700 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Cs137 | >22000 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Ce144 | >2600 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Eu154 | 1.9 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Cm244 | 0.83 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/La | >11 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Ce144 | >26 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Pr | >28 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Nd | >31 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Sm | 4.3 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Eu | 1.6 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Am241/Y | 1.3 | 0.2 M | TBP 1 M | HNO3 1.3 M | n-Dodecane | diluted PUREX raffinate; 0.01M H2C2O4 | [1] | ||
Sm/Am | 1.76 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
La/Am | 0.4 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
Eu/Am | 1.29 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
Ce/Am | 0.91 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
Gd/Am | 2.05 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
Pr/Am | 1.08 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
Y/Am | 22.6 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
Nd/Am | 1.11 | 0.1 M | HDEHP 1 M | HNO3 0.5 M | n-Dodecane | 2 min | simulate HLW | [2] | |
Am/Eu | 1.9 | 0.2 M | TBP 1.2 M | HNO3 1 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [3] | |
Am/Eu | 1.45 | 0.2 M | TBP 1.2 M | HNO3 2 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [3] | |
Am/Eu | 1.44 | 0.2 M | TBP 1.2 M | HNO3 3 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [3] | |
Am/Eu | 1.17 | 0.2 M | TBP 1.2 M | HNO3 4 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [3] | |
Am/Eu | 1.17 | 0.2 M | TBP 1.2 M | HNO3 5 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [3] | |
Am/Eu | 1.4 | 0.2 M | TBP 1.2 M | HNO3 1 M | n-Dodecane | 30°C | 180 min | [3] | |
Am/Eu | 1.2 | 0.2 M | TBP 1.2 M | HNO3 2 M | n-Dodecane | 30°C | 180 min | [3] | |
Am/Eu | 1.3 | 0.2 M | TBP 1.2 M | HNO3 3 M | n-Dodecane | 30°C | 180 min | [3] | |
Am/Eu | 1.3 | 0.2 M | TBP 1.2 M | HNO3 4 M | n-Dodecane | 30°C | 180 min | [3] | |
Am/Eu | 1.2 | 0.2 M | TBP 1.2 M | HNO3 5 M | n-Dodecane | 30°C | 180 min | [3] | |
Am(III)/Fe(III) | 110 | 0.5 M | HNO3 0.50 M | p-diisopropylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Fe(III) | 140 | 0.5 M | HNO3 1.00 M | p-diisopropylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Fe(III) | 76 | 0.5 M | HNO3 2.00 M | p-diisopropylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Fe(III) | 8.7 | 0.5 M | HNO3 4.00 M | p-diisopropylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Fe(III) | 1.2 | 0.5 M | HNO3 6.00 M | p-diisopropylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.73 | 0.02 M | HNO3 0.5 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.75 | 0.05 M | HNO3 0.5 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.78 | 0.1 M | HNO3 0.5 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.84 | 0.2 M | HNO3 0.5 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 1.07 | 0.5 M | HNO3 0.5 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.68 | 0.02 M | HNO3 3.0 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.75 | 0.05 M | HNO3 3.0 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.82 | 0.1 M | HNO3 3.0 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 0.99 | 0.2 M | HNO3 3.0 M | Diethylbenzene | 25°C | 1 min | [4] | ||
Am(III)/Eu(III) | 1.41 | 0.5 M | HNO3 3.0 M | Diethylbenzene | 25°C | 1 min | [4] | ||
U/Am | >100000 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | [5] | |||
Pu/Am | >100000 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | [5] | |||
U/Th | >100 | 0.5 M | HCl 0.5 M | Tetrachloroethylene | 25°C | [5] | |||
U/Np | >100 | 0.5 M | HCl 0.5 M | Tetrachloroethylene | 25°C | [5] | |||
Pu/Th | >100 | 0.5 M | HCl 0.5 M | Tetrachloroethylene | 25°C | [5] | |||
Am/Fe | 240 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Y | 5.4 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Zr | 19 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Mo | 9.2 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Tc | 8.6 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Ru | 100 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Rh | 2000 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Pd | 17 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/La | 2.1 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Ce | 1.3 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Pr | 1.2 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Nd | 1.2 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Sm | 1.2 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Eu | 1.2 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Fe | 91 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Y | 5.1 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Zr | 0.83 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Mo | 3.2 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Tc | 40 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Ru | 320 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Rh | 650 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Pd | 57 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/La | 2.9 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Ce | 1.5 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Pr | 1.2 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Nd | 1.2 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Sm | 1.1 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Eu | 1.3 | 0.25 M | TBP 0.75 M | HNO3 3.1 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Fe | 3.3 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Y | 3 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Zr | <0.1 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Mo | 0.66 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Tc | 84 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Ru | >600 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Rh | >600 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Pd | 140 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/La | 5.4 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Ce | 2.5 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Pr | 1.8 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Nd | 1.6 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Sm | 1.2 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Eu | 1.2 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [6] | |
Am/Fe | 72 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Y | 3.3 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Zr | 0.38 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Mo | 2.2 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Tc | 72 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Ru | >360 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Rh | 450 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Pd | 40 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/La | 4 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Ce | 2.1 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Pr | 1.6 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Nd | 1.5 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Sm | 1.2 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Am/Eu | 1.2 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [6] | ||
Sc/La | 3.6 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [6] |
Element | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
---|---|---|---|---|---|---|---|---|---|
Np(IV) | 16.6 | 0.2 M | TBP 1.2 M | HNO3 0.9 M | Dodecane | 23°C | 2 min | 0.07M HAN; 0.025M Fe(II) | [7] |
Np(IV) | 132 | 0.2 M | TBP 1.2 M | HNO3 0.9 M | Dodecane | 23°C | 10 min | 0.07M HAN; 0.025M Fe(II) | [7] |
Np(IV) | 1320 | 0.2 M | TBP 1.2 M | HNO3 0.9 M | Dodecane | 23°C | 20 min | 0.07M HAN; 0.025M Fe(II) | [7] |
Np(IV) | 8230 | 0.2 M | TBP 1.2 M | HNO3 0.9 M | Dodecane | 23°C | 40 min | 0.07M HAN; 0.025M Fe(II) | [7] |
Np(VI) | 0.203 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 0.5 min | 0.17M HAN; 0.010M Fe(II) | [7] |
Np(VI) | 0.25 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 1 min | 0.17M HAN; 0.010M Fe(II) | [7] |
Np(VI) | 0.394 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 2 min | 0.17M HAN; 0.010M Fe(II) | [7] |
Np(VI) | 2.58 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 20 min | 0.17M HAN; 0.010M Fe(II) | [7] |
Np(VI) | 21.9 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 60 min | 0.17M HAN; 0.010M Fe(II) | [7] |
Np(VI) | 3.1 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 0.5 min | 0.17M HAN | [7] |
Np(VI) | 1.3 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 1 min | 0.17M HAN | [7] |
Np(VI) | 0.59 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 2 min | 0.17M HAN | [7] |
Np(VI) | 0.173 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 20 min | 0.17M HAN | [7] |
Np(VI) | 0.142 | 0.2 M | TBP 1.2 M | HNO3 0.71 M | Dodecane | 23°C | 60 min | 0.17M HAN | [7] |
Np(VI) | 0.572 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 0.5 min | 0.47M H2O2 | [7] |
Np(VI) | 0.344 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 1 min | 0.47M H2O2 | [7] |
Np(VI) | 0.218 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 2 min | 0.47M H2O2 | [7] |
Np(VI) | 0.241 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 13 min | 0.47M H2O2 | [7] |
Np(VI) | 0.508 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 60 min | 0.47M H2O2 | [7] |
Np(VI) | 0.503 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 0.5 min | 0.47M H2O2; 4mM NaNO2 | [7] |
Np(VI) | 0.295 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 1 min | 0.47M H2O2; 4mM NaNO2 | [7] |
Np(VI) | 0.204 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 2 min | 0.47M H2O2; 4mM NaNO2 | [7] |
Np(VI) | 0.245 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 15 min | 0.47M H2O2; 4mM NaNO2 | [7] |
Np(VI) | 0.423 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 50 min | 0.47M H2O2; 4mM NaNO2 | [7] |
Np(VI) | 0.54 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 0.5 min | 0.47M H2O2; 4mM Fe(NO3)3 | [7] |
Np(VI) | 0.29 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 1 min | 0.47M H2O2; 4mM Fe(NO3)3 | [7] |
Np(VI) | 0.202 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 2 min | 0.47M H2O2; 4mM Fe(NO3)3 | [7] |
Np(VI) | 0.25 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 14 min | 0.47M H2O2; 4mM Fe(NO3)3 | [7] |
Np(VI) | 0.492 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 60 min | 0.47M H2O2; 4mM Fe(NO3)3 | [7] |
Np(VI) | 0.49 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 0.5 min | 0.47M H2O2; 0.10M Oxalic Acid | [7] |
Np(VI) | 0.296 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 1 min | 0.47M H2O2; 0.10M Oxalic Acid | [7] |
Np(VI) | 0.222 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 2 min | 0.47M H2O2; 0.10M Oxalic Acid | [7] |
Np(VI) | 0.58 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 21 min | 0.47M H2O2; 0.10M Oxalic Acid | [7] |
Np(VI) | 0.74 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 60 min | 0.47M H2O2; 0.10M Oxalic Acid | [7] |
Np(VI) | 0.31 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 0.5 min | 0.47M H2O2; 4mM NH4VO3 | [7] |
Np(VI) | 0.26 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 2 min | 0.47M H2O2; 4mM NH4VO3 | [7] |
Np(VI) | 1.07 | 0.2 M | TBP 1.2 M | HNO3 0.74 M | Dodecane | 23°C | 60 min | 0.47M H2O2; 4mM NH4VO3 | [7] |
Np(VI) | 0.267 | 0.2 M | TBP 1.2 M | HNO3 0.62 M | Dodecane | 23°C | 0.5 min | 0.098M Na2SO3 | [7] |
Np(VI) | 0.17 | 0.2 M | TBP 1.2 M | HNO3 0.62 M | Dodecane | 23°C | 1 min | 0.098M Na2SO3 | [7] |
Np(VI) | 0.126 | 0.2 M | TBP 1.2 M | HNO3 0.62 M | Dodecane | 23°C | 2 min | 0.098M Na2SO3 | [7] |
Np(VI) | 0.124 | 0.2 M | TBP 1.2 M | HNO3 0.62 M | Dodecane | 23°C | 20 min | 0.098M Na2SO3 | [7] |
Np(VI) | 0.122 | 0.2 M | TBP 1.2 M | HNO3 0.62 M | Dodecane | 23°C | 60 min | 0.098M Na2SO3 | [7] |
Np(VI) | 0.305 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 0.5 min | 0.098M Na2SO3; 0.02M H3NSO3 | [7] |
Np(VI) | 0.18 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 1 min | 0.098M Na2SO3; 0.02M H3NSO3 | [7] |
Np(VI) | 0.136 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 2 min | 0.098M Na2SO3; 0.02M H3NSO3 | [7] |
Np(VI) | 0.12 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 20 min | 0.098M Na2SO3; 0.02M H3NSO3 | [7] |
Np(VI) | 0.12 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 60 min | 0.098M Na2SO3; 0.02M H3NSO3 | [7] |
Np(VI) | 0.156 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 0.5 min | 0.096M Na2SO3; 0.01M H3NSO3 | [7] |
Np(VI) | 0.15 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 1 min | 0.096M Na2SO3; 0.01M H3NSO3 | [7] |
Np(VI) | 0.137 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 2 min | 0.096M Na2SO3; 0.01M H3NSO3 | [7] |
Np(VI) | 0.31 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 20 min | 0.096M Na2SO3; 0.01M H3NSO3 | [7] |
Np(VI) | 1.58 | 0.2 M | TBP 1.2 M | HNO3 0.64 M | Dodecane | 23°C | 60 min | 0.096M Na2SO3; 0.01M H3NSO3 | [7] |
Np(V) | ≈0.3 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | [8] | ||
Np(V) | ≈0.31 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 5mM U(VI) | [8] | |
Np(V) | ≈0.38 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 0.01M U(VI) | [8] | |
Np(V) | ≈0.38 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 0.02M U(VI) | [8] | |
Np(V) | ≈0.3 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 0.03M U(VI) | [8] | |
Np(V) | ≈0.29 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 5mM Nd(III) | [8] | |
Np(V) | ≈0.22 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 0.01M Nd(III) | [8] | |
Np(V) | ≈0.16 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 0.02M Nd(III) | [8] | |
Np(V) | ≈0.1 | 0.2 M | HNO3 2 M | Decalin | 25°C | 15 min | 0.03M Nd(III) | [8] | |
Np(V) | ≈0.41 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | [8] | |
Np(V) | ≈0.41 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 1mM U(VI) | [8] |
Np(V) | ≈0.46 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 5mM U(VI) | [8] |
Np(V) | ≈0.58 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 0.01M U(VI) | [8] |
Np(V) | ≈0.58 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 0.02M U(VI) | [8] |
Np(V) | ≈0.51 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 0.03M U(VI) | [8] |
Np(V) | ≈0.35 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 5mM Nd(III) | [8] |
Np(V) | ≈0.31 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 0.01M Nd(III) | [8] |
Np(V) | ≈0.26 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 0.02M Nd(III) | [8] |
Np(V) | ≈0.21 | 0.2 M | TBP 1.4 M | HNO3 2 M | n-Dodecane | 25°C | 15 min | 0.03M Nd(III) | [8] |
Am | 3.48 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Sm | 6.12 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
La | 1.39 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Eu | 4.49 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Ce | 3.16 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Gd | 7.12 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Pr | 3.75 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Y | 78.8 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Nd | 3.86 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Zr | 31000 | 0.1 M | HDEHP 1 M | HNO3 0.7 M | n-Dodecane | 2 min | simulate HLW | [8] | |
Am(III) | 0.09 | 0.5 M | HCl 3.15 M | tetrachloroethylene | 25°C | 1 min | [9] | ||
Am(III) | 0.7 | 0.5 M | HCl 4.25 M | tetrachloroethylene | 25°C | 1 min | [9] | ||
Am(III) | 0.17 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 3.38M LiCl | [9] | ||
Am(III) | 3.1 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 4.48M LiCl | [9] | ||
Am(III) | 0.73 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 4.83M NaCl | [9] | ||
Am(III) | 0.43 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 2.05M MgCl2 | [9] | ||
Am(III) | 4.9 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 2.55M MgCl2 | [9] | ||
Am(III) | 0.55 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 2.28M CaCl2 | [9] | ||
Am(III) | 4.4 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 2.8M CaCl2 | [9] | ||
Am(III) | 1.1 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 1.46M AlCl3 | [9] | ||
Am(III) | 7.6 | 0.5 M | tetrachloroethylene | 25°C | 1 min | 1.69M AlCl3 | [9] | ||
Am(III) | 0.15 | 0.25 M | tetrachloroethylene | 25°C | 1 min | 4M LiCl | [9] | ||
Am(III) | 1.4 | 0.25 M | tetrachloroethylene | 25°C | 1 min | 0.3M LiNO3 | [9] | ||
Eu(III) | 1040 | 0.2 M | TBP 1.2 M | HNO3 1 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Eu(III) | 560 | 0.2 M | TBP 1.2 M | HNO3 2 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Eu(III) | 408 | 0.2 M | TBP 1.2 M | HNO3 3 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Eu(III) | 240 | 0.2 M | TBP 1.2 M | HNO3 4 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Eu(III) | 160 | 0.2 M | TBP 1.2 M | HNO3 5 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Am(III) | 1975 | 0.2 M | TBP 1.2 M | HNO3 1 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Am(III) | 810 | 0.2 M | TBP 1.2 M | HNO3 2 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Am(III) | 520 | 0.2 M | TBP 1.2 M | HNO3 3 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Am(III) | 282 | 0.2 M | TBP 1.2 M | HNO3 4 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Am(III) | 188 | 0.2 M | TBP 1.2 M | HNO3 5 M | 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide | 30°C | 180 min | [9] | |
Eu(III) | 8.8 | 0.2 M | TBP 1.2 M | HNO3 1 M | n-Dodecane | 30°C | 180 min | [9] | |
Eu(III) | 11.7 | 0.2 M | TBP 1.2 M | HNO3 2 M | n-Dodecane | 30°C | 180 min | [9] | |
Eu(III) | 13 | 0.2 M | TBP 1.2 M | HNO3 3 M | n-Dodecane | 30°C | 180 min | [9] | |
Eu(III) | 11 | 0.2 M | TBP 1.2 M | HNO3 4 M | n-Dodecane | 30°C | 180 min | [9] | |
Eu(III) | 10.5 | 0.2 M | TBP 1.2 M | HNO3 5 M | n-Dodecane | 30°C | 180 min | [9] | |
Am(III) | 12.5 | 0.2 M | TBP 1.2 M | HNO3 1 M | n-Dodecane | 30°C | 180 min | [9] | |
Am(III) | 14 | 0.2 M | TBP 1.2 M | HNO3 2 M | n-Dodecane | 30°C | 180 min | [9] | |
Am(III) | 17 | 0.2 M | TBP 1.2 M | HNO3 3 M | n-Dodecane | 30°C | 180 min | [9] | |
Am(III) | 14.5 | 0.2 M | TBP 1.2 M | HNO3 4 M | n-Dodecane | 30°C | 180 min | [9] | |
Am(III) | 13 | 0.2 M | TBP 1.2 M | HNO3 5 M | n-Dodecane | 30°C | 180 min | [9] | |
Eu(III) | ≈12 | 0.25 M | HNO3 0.5 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈13 | 0.25 M | HNO3 1 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈9 | 0.25 M | HNO3 1.5 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈2 | 0.25 M | HNO3 2.5 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈0.7 | 0.25 M | HNO3 4 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈0.5 | 0.25 M | HNO3 5 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈2 | 0.1 M | HNO3 0.5 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈1.8 | 0.1 M | HNO3 1 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈1 | 0.1 M | HNO3 1.5 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈0.2 | 0.1 M | HNO3 2.5 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈0.04 | 0.1 M | HNO3 4 M | Mesitylene | 20°C | 10 min | [10] | ||
Eu(III) | ≈0.03 | 0.1 M | HNO3 5 M | Mesitylene | 20°C | 10 min | [10] | ||
U(VI) | ≈10 | 0.5 M | HCl 0.1 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈50 | 0.5 M | HCl 0.3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈150 | 0.5 M | HCl 0.5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈600 | 0.5 M | HCl 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈5000 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈60000 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈100000 | 0.5 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈1 | 0.5 M | HCl 0.2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈7 | 0.5 M | HCl 0.5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈70 | 0.5 M | HCl 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈2000 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈10000 | 0.5 M | HCl 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Np(IV) | ≈0.3 | 0.5 M | HCl 0.5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Np(IV) | ≈17 | 0.5 M | HCl 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Np(IV) | ≈170 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Np(IV) | ≈3000 | 0.5 M | HCl 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈0.01 | 0.5 M | HCl 0.3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈0.04 | 0.5 M | HCl 0.5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈0.4 | 0.5 M | HCl 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈17 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈350 | 0.5 M | HCl 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.1 | 0.5 M | HCl 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈3 | 0.5 M | HCl 5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈17 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈200 | 0.5 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈4 | 0.017 M | HCl 2.2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈10 | 0.25 M | HCl 2.2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈29 | 0.04 M | HCl 2.2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈110 | 0.07 M | HCl 2.2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈1000 | 0.2 M | HCl 2.2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
U(VI) | ≈6000 | 0.5 M | HCl 2.2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈1.1 | 0.05 M | HCl 3.0 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈17 | 0.1 M | HCl 3.0 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈110 | 0.25 M | HCl 3.0 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Th(IV) | ≈400 | 0.5 M | HCl 3.0 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈0.001 | 0.002 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈0.01 | 0.005 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈0.7 | 0.015 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈20 | 0.05 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈300 | 0.15 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈2000 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈16 | 0.005 M | HNO3 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈50 | 0.01 M | HNO3 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈200 | 0.025 M | HNO3 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈600 | 0.05 M | HNO3 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pu(IV) | ≈3000 | 0.1 M | HNO3 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Be | <0.003 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Be | <0.003 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Be | <0.06 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Be | <0.06 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Na | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Na | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Na | <0.01 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Na | <0.01 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Mg | <0.003 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Mg | <0.003 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Mg | <0.007 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Mg | <0.007 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Al(III) | <0.02 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Al(III) | <0.02 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Al(III) | <0.02 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Al(III) | <0.02 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
K | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
K | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
K | <0.01 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
K | <0.01 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Ca | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Ca | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Ca | 0.03 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Ca | 0.03 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
V(IV)+VO2(I) | 0.08 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
V(IV)+VO2(I) | 0.34 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
V(IV)+VO2(I) | 9.4 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
V(IV)+VO2(I) | 9.5 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Cr(III) | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Cr(III) | <0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Cr(III) | <0.01 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Cr(III) | <0.01 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Mn(II) | 0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Mn(II) | 0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Mn(II) | 0.31 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Mn(II) | 0.29 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Fe(III) | 27 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Fe(III) | 45 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Fe(III) | >100 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Fe(III) | >100 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Co(II) | 0.01 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Co(II) | 0.02 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Co(II) | 1.1 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Co(II) | 1.2 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Ni(II) | <0.006 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Ni(II) | <0.006 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Ni(II) | 0.016 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Ni(II) | 0.015 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Cu(II) | 0.09 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Cu(II) | 0.12 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Cu(II) | 1.1 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Cu(II) | 1.2 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Zn(II) | 34 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Zn(II) | 52 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Zn(II) | 16 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Zn(II) | 19 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Ga(III) | 6.2 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Ga(III) | 9 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Ga(III) | >100 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Ga(III) | >100 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Zr(IV) | 6.7 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Zr(IV) | 5.8 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Zr(IV) | >200 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Zr(IV) | >200 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
MoO2(II) | 100 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
MoO2(II) | 100 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
MoO2(II) | >150 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
MoO2(II) | >140 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Cd(II) | 3.3 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Cd(II) | 7.9 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Cd(II) | 13 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Cd(II) | 17 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Sn(II,IV) | >60 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Sn(II,IV) | >60 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Sn(II,IV) | >60 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Sn(II,IV) | >60 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Pb(II,IV) | 1.2 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Pb(II,IV) | 3.8 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Pb(II,IV) | 0.09 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.1M Hydroquinone | [10] | |
Pb(II,IV) | 0.54 | 0.5 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | 0.01M NaClO2 | [10] | |
Am(III) | ≈0.004 | 0.5 M | HCl 0.01 M | Tetrachloroethylene | 25°C | 1 min | 1M MgCl2 | [10] | |
Am(III) | ≈0.04 | 0.5 M | HCl 0.01 M | Tetrachloroethylene | 25°C | 1 min | 1.5M MgCl2 | [10] | |
Am(III) | ≈0.45 | 0.5 M | HCl 0.01 M | Tetrachloroethylene | 25°C | 1 min | 2M MgCl2 | [10] | |
Am(III) | ≈2 | 0.5 M | HCl 0.01 M | Tetrachloroethylene | 25°C | 1 min | 2.3M MgCl2 | [10] | |
Am(III) | ≈5 | 0.5 M | HCl 0.01 M | Tetrachloroethylene | 25°C | 1 min | 2.5M MgCl2 | [10] | |
Am(III) | ≈17 | 0.5 M | HCl 0.01 M | Tetrachloroethylene | 25°C | 1 min | 2.7M MgCl2 | [10] | |
Am(III) | ≈0.5 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 1M MgCl2 | [10] | |
Am(III) | ≈1.1 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 1.25M MgCl2 | [10] | |
Am(III) | ≈3 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 1.5M MgCl2 | [10] | |
Am(III) | ≈7 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 1.75M MgCl2 | [10] | |
Am(III) | ≈17 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 2M MgCl2 | [10] | |
Am(III) | ≈100 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 2.5M MgCl2 | [10] | |
Am(III) | ≈0.35 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 1M CaCl2 | [10] | |
Am(III) | ≈2 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 1.5M CaCl2 | [10] | |
Am(III) | ≈10 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 2M CaCl2 | [10] | |
Am(III) | ≈45 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 2.5M CaCl2 | [10] | |
Am(III) | ≈100 | 0.5 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | 3M CaCl2 | [10] | |
Am(III) | ≈0.003 | 1 M | HCl 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.05 | 1 M | HCl 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.5 | 1 M | HCl 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈4 | 1 M | HCl 4 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈30 | 1 M | HCl 5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈150 | 1 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈900 | 1 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.3 | 0.5 M | HCl 4 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.05 | 0.25 M | HCl 4 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.5 | 0.25 M | HCl 5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈4 | 0.25 M | HCl 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈10 | 0.25 M | HCl 7 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈30 | 0.25 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.04 | 0.5 M | HNO3 0.25 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.11 | 0.5 M | HNO3 0.5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.27 | 0.5 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.4 | 0.5 M | HNO3 2 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.5 | 0.5 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.6 | 0.5 M | HNO3 4 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.65 | 0.5 M | HNO3 5 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.9 | 0.5 M | HNO3 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.013 | 0.005 M | Tetrachloroethylene | 25°C | 1 min | 7.74M LiCl | [10] | ||
Am(III) | ≈0.4 | 0.015 M | Tetrachloroethylene | 25°C | 1 min | 7.74M LiCl | [10] | ||
Am(III) | ≈7 | 0.035 M | Tetrachloroethylene | 25°C | 1 min | 7.74M LiCl | [10] | ||
Am(III) | ≈50 | 0.06 M | Tetrachloroethylene | 25°C | 1 min | 7.74M LiCl | [10] | ||
Am(III) | ≈360 | 0.15 M | Tetrachloroethylene | 25°C | 1 min | 7.74M LiCl | [10] | ||
Am(III) | ≈0.03 | 0.015 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.25 | 0.035 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈1 | 0.06 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈5 | 0.15 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈30 | 0.2 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈250 | 0.5 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈900 | 1 M | HCl 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.1 | 0.06 M | HCl 6.3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈0.65 | 0.15 M | HCl 6.3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈4 | 0.2 M | HCl 6.3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈20 | 0.5 M | HCl 6.3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | ≈150 | 1 M | HCl 6.3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am(III) | 0.15 | 0.25 M | Tetrachloroethylene | 25°C | 1 min | 4.0M LiCl | [10] | ||
Am(III) | 1.4 | 0.25 M | Tetrachloroethylene | 25°C | 1 min | 0.3M LiNO3 | [10] | ||
Am | ≈3.6 | 0.25 M | TBP 0.75 M | HNO3 0.25 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | ≈8 | 0.25 M | TBP 0.75 M | HNO3 0.5 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | ≈11 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | ≈9 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | ≈6 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | ≈5.5 | 0.25 M | TBP 0.75 M | HNO3 8 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Fe | 0.049 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Y | 2.2 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Zr | 0.62 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Mo | 1.3 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Tc | 1.4 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Ru | 0.12 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Rh | 0.006 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Pd | 0.69 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
La | 5.6 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Ce | 9 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Pr | 9.8 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Nd | 9.8 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Sm | 9.8 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Eu | 9.8 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | 12 | 0.25 M | TBP 0.75 M | HNO3 1 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Fe | 0.1 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Y | 1.8 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Zr | 11 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Mo | 2.8 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Tc | 0.23 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Ru | 0.028 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Rh | 0.014 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Pd | 0.16 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
La | 3.1 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Ce | 6.1 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Pr | 7.6 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Nd | 7.6 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Sm | 8.3 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Eu | 7 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | 9.1 | 0.25 M | TBP 0.75 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Fe | 1.8 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Y | 2 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Zr | >59 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Mo | 9 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Tc | 0.07 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Ru | <0.01 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Rh | <0.01 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Pd | 0.042 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
La | 1.1 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Ce | 2.4 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Pr | 3.3 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Nd | 3.7 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Sm | 4.9 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Eu | 4.9 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Am | 5.9 | 0.25 M | TBP 0.75 M | HNO3 6 M | Tetrachloroethylene | 25°C | 1 min | [10] | |
Fe | 0.05 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Y | 1.1 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Zr | 9.5 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Mo | 1.6 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Tc | 0.05 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Ru | <0.01 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Rh | 0.008 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pd | 0.09 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
La | 0.9 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Ce | 1.7 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Pr | 2.3 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Nd | 2.4 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Sm | 2.9 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Eu | 2.9 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] | ||
Am | 3.6 | 0.25 M | HNO3 3 M | Tetrachloroethylene | 25°C | 1 min | [10] |
doi:10.1016/S0925-8388(98)00147-9
doi:10.1080/07366299.2012.670595
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doi:10.1080/07366298608917877
doi:10.1080/07366298808917935
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