Palladium and platinum sorption using chitosan-based hydrogels

被引:21
|
作者
Sicupira, Dalila [1 ,2 ]
Campos, Karol [2 ]
Vincent, Thierry [1 ]
Leao, Versiane [2 ]
Guibal, Eric [1 ]
机构
[1] Ecole Mines Ales, Lab Genie Environm Ind, F-30319 Ales, France
[2] Univ Fed Ouro Preto, Dept Met & Mat Engn, BR-35400000 Ouro Preto, MG, Brazil
关键词
Chitosan; Ionotropic gelation; Sodium polyphosphate; Hydrogels; Drying; Sorption isotherms; Intraparticle diffusion; Uptake kinetics; Desorption; CROSS-LINKED CHITOSAN; GEL BEADS; DIFFUSION PROPERTIES; BIOPOLYMER CAPSULES; CONTROLLED-RELEASE; CYPHOS IL-101; RECOVERY; TRIPOLYPHOSPHATE; ADSORPTION; SORBENTS;
D O I
10.1007/s10450-010-9210-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two chitosan hydrogels (prepared by NaOH neutralization and by polyphosphate ionotropic gelation) have been tested in the dry state for Pd(II) and Pt(IV) sorption at pH 2. Similar sorption isotherms with maximum sorption capacities close to 190 mg Pd g(-1) and 235 mg Pt g(-1) were achieved. The sorption mechanism involves electrostatic attraction of the chloro-an ionic species onto protonated amine groups; the drastic decrease of sorption capacity with the addition of chloride ions supports this hypothesis. SEM-EDAX analysis suggests that sorption proceeds, in kinetic terms, through a shrinking core mechanism. Metal ions can diffuse throughout all the sorbent volume. The main differences between the sorbents are revealed by kinetics. The hydrogels prepared by ionotropic gelation in polyphosphate (C-PPh) allows reaching equilibrium much faster than the hydrogels prepared by the neutralization process (C-NaOH). While for C-PPh sorbent the chemical reaction rate seems to control sorption profiles, in the case of C-NaOH a combination of mechanisms including intraparticle diffusion resistance controls uptake kinetics. Metal desorption from loaded sorbents is possible using thiourea alone or in association with HCl solutions. The recycling of the sorbents is possible but for a limited number of cycles.
引用
收藏
页码:127 / 139
页数:13
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