N,N'-diethyl-N,N'-ditolyl-dipicolinamide (ortho)
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Abbreviation(s)
Et(o)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 | 16 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Ce | 6.8 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Pr | 4.8 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Nd | 3.4 | 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 | 4.4 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Gd | 6 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/La | 12.5 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Ce | 5.8 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Pr | 4.3 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Nd | 3.5 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Sm | 3.6 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Eu | 5 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/Gd | 8.3 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [1] | ||
| Am/La | 700 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Ce | 59 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Pm | 18 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Nd | 8.1 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Sm | 1.8 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Eu | 1.6 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Gd | 4.4 | 0.01 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/La | 530 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Ce | 120 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Pm | 19 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Nd | 8.6 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Sm | 2.8 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Eu | 2.3 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Gd | 3.4 | 0.01 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/La | 185 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Ce | 93 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Pm | 43 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Nd | 18 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Sm | 2 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Eu | 1 | 0.01 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | 0.02M hexachlorocobalt dicarbollide | [2] | |
| Am/Gd | 1.5 | 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. |
|---|---|---|---|---|---|---|---|---|---|
| La | ≈1.05 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈2.13 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈3.74 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈5.31 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈5.60 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈6.79 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈6.56 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈16.07 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈27.72 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈50.38 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈105.41 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈137.22 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈185.00 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈232.49 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈19.16 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈0.35 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈0.68 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈1.05 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈1.36 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈1.22 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈1.14 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈0.84 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈1.23 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈1.69 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈2.46 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈2.99 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈3.68 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈4.21 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈4.76 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈4.31 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈0.08 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈0.17 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈0.22 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈0.29 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈0.27 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈0.20 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈0.12 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈0.13 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈0.13 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈0.15 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈0.17 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈0.17 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈0.18 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈0.20 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈2.48 | 0.05 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈4.00 | 0.075 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈6.13 | 0.1 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈10.71 | 0.15 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈18.48 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈1.02 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈4.84 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈18.51 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈47.18 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Am | ≈126.36 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈0.02 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈0.08 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈0.35 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈1 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈1.93 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| La | ≈3.73 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈0.06 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈0.18 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈0.66 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈2.2 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈4.54 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ce | ≈9.1 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈0.075 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈0.23 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈1 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈3.76 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈8.81 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Pr | ≈18.2 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈0.09 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈0.29 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈1.37 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈5.49 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈13.7 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Nd | ≈32.13 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈0.094 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈0.28 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈1.17 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈5.67 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈22 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Sm | ≈91 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈0.064 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈0.2 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈1.1 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈6.64 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈34.2 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Eu | ≈1000 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈0.03 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈0.12 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈0.83 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈6.23 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈42.7 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Gd | ≈1208 | 0.2 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈0.03 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈0.13 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈1.21 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈16 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tb | ≈220 | 0.2 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈0.024 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈0.14 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈1.7 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Dy | ≈27.4 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈0.023 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈0.15 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈2.42 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Ho | ≈48.4 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈0.02 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈0.16 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈3.02 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Er | ≈100 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈0.023 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈0.176 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈3.76 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Tm | ≈137 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈0.02 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈0.18 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈4.13 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Yb | ≈176 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈0.024 | 0.2 M | HNO3 0.5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈0.2 | 0.2 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈4.84 | 0.2 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Lu | ≈220 | 0.2 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 3 min | [2] | ||
| Th | 0.06 | 0.001 M | HNO3 1 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 0.74 | 0.001 M | HNO3 2 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 3.8 | 0.001 M | HNO3 3 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 11 | 0.001 M | HNO3 4 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 18.8 | 0.001 M | HNO3 5 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] | ||
| Th | 18.6 | 0.001 M | HNO3 6 M | phenyl trifluoromethyl sulfone (FS-13) | 21°C | 4 min | [3] |