n-octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide

CMPO structure
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General infos Separation factors Distribution coefficients Stability References
Abbreviation(s)

CMPO, OɸD(iB)CMPO

Chemical group

carbamylalkylphosphine oxide

Formula

C24H42NO2P not CHON

Molecular mass

407.569 g/mol

Processes

Elements separated

Pu, Am

Country of origin

USA

Country that has performed tests

USA

Separation factors
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]
Distribution coefficients
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]
Stability
Type of study Conditions Ref.
Radiolysis Gamma Radiolysis, 2MGy [11]
Radiolysis Gamma Radiolysis [12]
Radiolysis Alpha Radiolysis [13]
References

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  2. doi:10.1080/07366299.2012.670595

  3. doi:10.1007/s10967-011-1234-4

  4. doi:10.1080/01496398208060649

  5. doi:10.1080/07366298708918576

  6. doi:10.1080/07366298608917877

  7. doi:10.1080/07366298808917935

  8. doi:10.3327/jnst.29.1100

  9. doi:10.1080/07366298708918575

  10. doi:10.1080/07366299008917986

  11. doi:10.1080/18811248.2006.9711134

  12. doi:10.1080/07366299.2013.815491

  13. doi:10.1080/07366299.2013.850300