Palladium and Platinum Sorption on a Thiocarbamoyl-Derivative of Chitosan

被引:25
|
作者
Butewicz, A. [2 ]
Gavilan, K. Campos [1 ]
Pestov, A. V. [3 ]
Yatluk, Y. [3 ]
Trochimczuk, A. W. [2 ]
Guibal, E. [1 ]
机构
[1] Ecole Mines, Lab Genie Environm Ind, F-30319 Ales, France
[2] Wroclaw Univ Technol, Dept Chem, PL-50370 Wroclaw, Poland
[3] Russian Acad Sci, I Ya Postovsky Inst Organ Synth, Urals Div, Ekaterinenburg 620219, Russia
关键词
chitosan; thiocarbamoyl; palladium; platinum; sorption; isotherms; kinetics; desorption; CROSS-LINKED CHITOSAN; HYDROCHLORIC-ACID SOLUTION; BIOPOLYMER CAPSULES; SOLVENT-EXTRACTION; PRECIOUS METALS; CYPHOS IL-101; THIOPHOSPHORIC ACID; IMPREGNATED RESINS; CHLORIDE SOLUTIONS; ION-EXCHANGERS;
D O I
10.1002/app.31877
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Immobilizing thiourea onto chitosan allowed using the polymer for the recovery of platinum groups metals (PGMs) in acidic solutions (up to 1-2M HCl concentrations). At low HCl concentration protonated amine groups may sorb chloroanionic metal species (electrostatic attraction mechanism); however, most of sorption proceeds through chelation on sulfur containing groups (less sensitive to acidic conditions). The bi-site Langmuir equation was used for fitting sorption isotherms. The sorption of PGMs was weakly affected by the composition of the solution (presence of high concentration of anions and base metals). Maximum sorption capacities for Pd(II) and Pt(IV) ranged between 274 and 330 mg g(-1) in 0.25M HCl solutions and decreased to 150-198 mg g(-1) in 2M HCl solutions: Pd(II) sorption was systematically higher than Pt(IV) sorption. The pseudo-second rate equation was used for modeling the uptake kinetics. Agitation speed hardly affected uptake kinetics indicating that external diffusion resistance is not the rate controlling step. Desorption yield higher than 85% were obtained using thiourea in 0.1M HCI solution. The adsorbents could be reused for at least three cycles. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 116: 3318-3330, 2010
引用
收藏
页码:3318 / 3330
页数:13
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