Water-Soluble Polyelectrolytes with Ability to Remove Arsenic

被引:6
|
作者
Rivas, Bernabe L. [1 ]
Sanchez, Julio [1 ]
Amalia Pooley, S. [1 ,2 ]
Basaez, Luis [1 ]
Pereira, Eduardo [1 ]
Bucher, Christophe [2 ]
Royal, Guy [2 ]
Saint Aman, Eric [2 ]
Mouter, Jean-Claude [2 ]
机构
[1] Univ Concepcion, Fac Chem, Dept Polymer, Casilla 160-C, Concepcion, Chile
[2] San Jose State Univ, CNRS, Dept Chim Mol, UMR 5250, F-38041 Grenoble, France
来源
MODERN TRENDS IN POLYMER SCIENCE-EPF 09 | 2010年 / 296卷
关键词
membranes; metal-polymer complexes; water-soluble polymers; POLYMER-METAL COMPLEXES; ELECTROCATALYTIC OXIDATION; RETENTION PROPERTIES; PHASE; ULTRAFILTRATION; RESINS;
D O I
10.1002/masy.201051057
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Arsenic species can be removed from aqueous solutions using the liquid-phase polymer-based retention, LPR, technique. The LPR technique removes ionic species by functional groups of water-soluble polyelectrolytes (WSP) and then using a ultrafiltration membrane that does not let them pass through the membrane, thus separating them from the solution. The ability of WSP with groups (R)(4)N+X- to remove arsenate ions using LPR was studied. The interaction and arsenate anion retention capacity depended on: pH, the quaternary ammonium group's counter ion, and the ratio polymer: As(V), using different concentrations of As(V). Water-soluble polychelates were also used for one-step retention of As(III) in solution. The complex of poly(acrylic acid)-Sn, 10 and 20 wt-% of metal gave a high retention of As(III) species at pH 8, although the molar ratio polychelate: As(III) was 400:1. The enrichment method was used to determine the maximum retention capacity (C) for arsenate anions in aqueous solutions at pH 8. In similar conditions, the values of C were 142 mg g(-1) for P(ClAETA) and 75 mg g(-1) for P(SAETA). The combined treatment of arsenic aqueous solutions by electrocatalytic oxidation (EO) to convert the species of As(III) to As(V) with the LPR technique quantitatively removed arsenic.
引用
收藏
页码:416 / +
页数:3
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