Ainscow TA, Aldalur I, Beezer AE, Connor JA, Garbett NC, Mitchell JC, Page AL, Tindale N, Turner KA, Willson RJ
School of Physical Sciences, University of Kent, Canterbury, Kent, CT2 7NH, United Kingdom
J Colloid Interface Sci. 1999 May 1;213(1):87-91. doi: 10.1006/jcis.1999.6113.
Measurement of the kinetics of extraction of copper(II) by 19 different 5-alkyl-2-hydroxybenzaldoximes (alkyl is C7H15 and C9H19) from acidic (hydrogen sulfate buffer) aqueous solution in the range pH 3.4-2.0, into 20% v/v toluene in n-hexane is reported. The lowering of the interfacial tension has been measured in some cases. The solubility of the extractants in water has been measured spectrophotometrically. A modified Taylor-Aris dispersion technique has been used to measure the diffusion coefficients in n-hexane and Orfom SX7 of some of the extractants and of the copper(II) complexes which they form. At low initial bulk concentrations (<10 mol m-3) of the extractants, the rate of extraction is controlled by the rate of diffusion of the extractant from the bulk to the organic-aqueous interface. The diffusion coefficient is related to the steric bulk of the alkyl substituent. At higher initial bulk concentrations (200 mol m-3) of the extractants, when the interface is saturated, the rate of extraction is inversely related to the apparent steric bulk of the alkyl substituent. Copyright 1999 Academic Press.
本文报道了在pH值为3.4至2.0的酸性(硫酸氢盐缓冲液)水溶液中,用19种不同的5-烷基-2-羟基苯甲醛肟(烷基为C7H15和C9H19)从水相萃取铜(II)至正己烷中20%(v/v)甲苯有机相的动力学测定。在某些情况下还测量了界面张力的降低。通过分光光度法测定了萃取剂在水中的溶解度。采用改进的泰勒-阿里斯分散技术测量了部分萃取剂及其形成的铜(II)配合物在正己烷和Orfom SX7中的扩散系数。在萃取剂初始本体浓度较低(<10 mol m-3)时,萃取速率受萃取剂从本体扩散至有机-水界面的速率控制。扩散系数与烷基取代基的空间体积有关。在萃取剂初始本体浓度较高(200 mol m-3)时,当界面达到饱和,萃取速率与烷基取代基的表观空间体积成反比。版权所有1999年,学术出版社。