N,N,N',N'-tetraoctyl diglycolic amide

TODGA structure
PNG ChemDraw
General infos Separation factors Distribution coefficients Decontamination factors Stability Solubility References
Abbreviation(s)

TODGA, TOOPDA

Chemical group

diglycolamide

Formula

C36H72N2O3 CHON

Molecular mass

580.983 g/mol

Processes

Elements separated

An(III), Ln(III), An(IV)

Country of origin

Japan

Country that has performed tests

Japan, USA, Russia, Sweden, UK, Germany

Separation factors
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]
Distribution coefficients
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]
Decontamination factors
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]
Stability
Type of study Conditions Ref.
Radiolysis [22]
Hydrolysis 60days [22]
Radiolysis Gamma Radiolysis, 1MGy [22]
Solubility
Solvent Solubility Temperature Ref.
H2O 0.042 mM   [22]
References

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  16. doi:10.1080/07366299.2013.836422

  17. doi:10.1080/07366299.2014.952532

  18. doi:10.1080/07366290701784175

  19. doi:10.1080/07366290802544726

  20. doi:10.1080/07366290802672204

  21. doi:10.1080/07366299.2011.609392

  22. doi:10.1016/j.radphyschem.2006.05.008