Sorption of arsenite and arsenate on ferrihydrite: Effect of organic and inorganic ligands

被引:111
|
作者
Zhu, Jun [1 ]
Pigna, Massimo [1 ]
Cozzolino, Vincenza [1 ]
Caporale, Antonio G. [1 ]
Violante, Antonio [1 ]
机构
[1] Univ Napoli Federico II, Dipartimento Sci Suolo Pianta Ambiente & Prod Ani, I-80055 Naples, Italy
关键词
Sorption; Ferrihydrite; As(III); As(V); Competition; Organic and inorganic ligands; COMPETITIVE ADSORPTION; OXIDE MINERALS; NATURAL-WATERS; CLAY-MINERALS; IRON-OXIDES; GOETHITE; MECHANISMS; PHOSPHATE; ARSENIC(III); HYDROXIDES;
D O I
10.1016/j.jhazmat.2011.02.071
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We studied the sorption of As(III) and As(V) onto ferrihydrite as affected by pH, nature and concentration of organic [oxalic (OX), malic (MAL), tartaric (TAR), and citric (CIT) acid] and inorganic [phosphate (PO(4)). sulphate (SO(4)), selenate (Seal) and selenite (SeO(3))] ligands, and the sequence of anion addition. The sorption capacity of As(III) was greater than that of As(V) in the range of pH 4.0-11.0. The capability of organic and inorganic ligands in preventing As sorption follows the sequence: SeO(4) approximate to SO(4) < OX < MAL approximate to TAR < CIT < SeO(3) << PO(4). The efficiency of most of the competing ligands in preventing As(III) and As(V) sorption increased by decreasing pH, but PO(4) whose efficiency increased by increasing pH. In acidic systems all the competing ligands inhibited the sorption of As(III) more than As(V), but in alkaline environments As(III) and As(V) seem to be retained with the same strength on the Fe-oxide. Finally, the competing anions prevented As(III) and As(V) sorption more when added before than together or after As(III) or As(V). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:564 / 571
页数:8
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