Recovery of rhodium-containing catalysts by silica-based chelating ion exchangers containing N and S donor atoms

被引:22
|
作者
Kramer, J [1 ]
Scholten, A [1 ]
Driessen, WL [1 ]
Reedijk, J [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
关键词
rhodium complexes; chelating ion exchange; azathia ligand complexes; kinetics;
D O I
10.1016/S0020-1693(01)00356-5
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two silica-based chelating ion exchangers have been synthesised for the recovery of the model catalysts RhCl . 3H(2)O and RhCl(PPh3)(3). The N,S-donor ligands 2-aminocyclopentene- l-dithiocarboxylic acid and 4-amino-3-methyl-1,2,4-triazole-5-thione have been attached to the bifunctional spacer (3-glycidoxypropyl)trimethoxysilane prior to immobilisation on silica. Both ion exchangers showed a high Rh(III)-uptake capacity and selectivity over Cu(II), even in the presence of an excess of the latter. The Rh(I) complex was adsorbed to a much smaller extent, probably due to the bulky triphenylphosphane groups. Aquation negatively influenced the Rh(III)-uptake kinetics, whereas experiments performed in ethanol significantly increased the kinetic-uptake behaviour. Stripping of the loaded polymers proved to be very difficult, probably due to the strong Rh-sulphur coordination. Only with thiourea a reasonable amount of Rh(III) could be stripped from the ion exchangers. (C) 2001 Elsevier Science B.V. All rights reserved.
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页码:183 / 190
页数:8
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