Makrlík Emanuel, Vaňura Petr, Selucký Pavel
Acta Chim Slov. 2010 Jun;57(2):485-90.
Solvent extraction of microamounts of calcium and strontium by a phenyltrifluoromethyl sulfone (FS 13) solution of hydrogen dicarbollylcobaltate (H+B-) in the presence of octyl-phenyl-N,N-diisobutylcarbamoylmethyl phosphine oxide ("classical" CMPO, L) has been investigated. The equilibrium data have been explained assuming that the species HL+, HL2+, ML2+, ML2+2 and ML2+3 (M2+ = Ca2+, Sr2+) are extracted into the organic phase. The values of extraction and stability constants of the cationic complex species in FS 13 saturated with water have been determined. In the considered FS 13 medium, it was found that the stability constants of the complex species CaL2+n, where n = 1, 2, 3 and L is "classical" CMPO, are higher than those of the corresponding complexes SrL2+n.
研究了在辛基苯基 - N,N - 二异丁基氨基甲酰甲基氧化膦(“经典”CMPO,L)存在下,用二碳酰钴氢化物(H + B - )的苯基三氟甲基砜(FS 13)溶液对微量钙和锶进行溶剂萃取。假设物种HL +、HL2 +、ML2 +、ML2 + 2和ML2 + 3(M2 + = Ca2 +,Sr2 +)被萃取到有机相中,对平衡数据进行了解释。已确定了在水饱和的FS 13中阳离子络合物物种的萃取常数和稳定常数。在所考虑的FS 13介质中,发现络合物物种CaL2 + n(其中n = 1、2、3且L为“经典”CMPO)的稳定常数高于相应络合物SrL2 + n的稳定常数。