N,N'-diethyl-N,N'-ditolyl-dipicolinamide (para)
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Abbreviation(s)
Et(p)TDPA
Chemical group
dipicolinamide
Formula
C25H27N3O2 CHON
Molecular mass
401.51 g/mol
Separation factors
| Factor | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
|---|---|---|---|---|---|---|---|---|---|
| Am/La | 4 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Ce | 4.4 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Pr | 3.5 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Nd | 4 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Sm | 4 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Eu | 4 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Gd | 5.8 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/La | 2.7 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Ce | 3.5 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Pr | 3.4 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Nd | 3.9 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Sm | 4.3 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Eu | 5.7 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Gd | 8.5 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/La | >1000 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Ce | 130 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Pm | 33 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Nd | 10 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Sm | 1.2 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Eu | 0.8 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Gd | 3.6 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/La | 115 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Ce | 80 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Pm | 24 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Nd | 10 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Sm | 2 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Eu | 1.7 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Gd | 2.5 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/La | 45 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Ce | 29 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Pm | 23 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Nd | 13 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Sm | 1.9 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Eu | 0.8 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Gd | 0.7 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] |
Distribution coefficients
| Element | Value | Conc. | Add. ligand | Aq. acid | Organic diluent | Temp. | Contact time | Additional | Ref. |
|---|---|---|---|---|---|---|---|---|---|
| Dy | ≈0.18 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈2.46 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈29.48 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈486.36 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈0.03 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈0.23 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈3.82 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈59.42 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈0.04 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈0.26 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈4.58 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈94.17 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈0.04 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈0.33 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈7.41 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈272.13 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈0.05 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈0.36 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈9.42 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈448.93 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈0.05 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈0.41 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈11.05 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈886.80 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Th | 0.25 | 0.001 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 3.4 | 0.001 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 15 | 0.001 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 30.6 | 0.001 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 35.6 | 0.001 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 29.3 | 0.001 M | HNO3 6 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| La | ≈1.95 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈2.02 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈3.74 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈2.92 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈4.01 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈4.95 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈5.04 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈14.46 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Dy | ≈27.72 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ho | ≈55.01 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Er | ≈88.42 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tm | ≈249.43 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Yb | ≈408.03 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Lu | ≈899.91 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈14.72 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈1.14 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈1.02 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈1.36 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈1.14 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈1.05 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈1.08 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈0.81 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈1.41 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Dy | ≈2.32 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ho | ≈3.68 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Er | ≈4.26 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tm | ≈6.85 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Yb | ≈8.54 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Lu | ≈10.25 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈4.87 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈0.45 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈0.35 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈0.36 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈0.31 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈0.29 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈0.22 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈0.14 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈0.16 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Dy | ≈0.18 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ho | ≈0.22 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Er | ≈0.25 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tm | ≈0.32 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Yb | ≈0.34 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Lu | ≈0.40 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈2.12 | 0.05 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈3.40 | 0.075 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈5.01 | 0.1 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈8.34 | 0.15 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈14.62 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈0.45 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈1.19 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈4.47 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈14.86 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈30.47 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Am | ≈49.38 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈0.17 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈0.46 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈1.20 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈2.02 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈2.37 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| La | ≈2.23 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈0.13 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈0.35 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈1.06 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈2.06 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈3.07 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Ce | ≈3.39 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈0.10 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈0.33 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈1.17 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈3.19 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈5.27 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Pr | ≈6.18 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈0.13 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈0.37 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈1.43 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈4.06 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈7.71 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Nd | ≈10.20 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈0.10 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈0.31 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈1.13 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈4.14 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈11.50 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Sm | ≈24.13 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈0.07 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈0.22 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈1.13 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈5.06 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈18.23 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Eu | ≈53.76 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈0.03 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈0.14 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈0.89 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈5.38 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈25.12 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Gd | ≈83.51 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈0.03 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈0.16 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈1.46 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈14.92 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Tb | ≈96.07 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] | ||
| Dy | ≈0.03 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [3] |