Effect of competing anions on the adsorption of arsenate and arsenite by ferrihydrite

被引:356
作者
Jain, A [1 ]
Loeppert, RH [1 ]
机构
[1] Texas A&M Univ, Dept Soil & Crop Sci, College Stn, TX 77843 USA
关键词
D O I
10.2134/jeq2000.00472425002900050008x
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The competitive adsorption of arsenate and arsenite and the effect of phosphate and sulfate on adsorption of arsenate and arsenite by ferrihydrite were investigated in the pH range of 3 to 10 and at varying initial ligand concentrations. In dual anion systems, arsenate retention was greater at low pH compared with greater arsenite retention at high pH. In systems with arsenate and arsenite concentrations less than or equal to 2.08 mol(As) kg(fer)(-1) each, the effect of arsenate on arsenite sorption was more pronounced than vice versa, On the contrary, at arsenate and arsenite concentrations of 3.47 mol(As) kg(fer)(-1) each, arsenate did not influence arsenite sorption but arsenite substantially reduced arsenate adsorption, The different sorption behavior of arsenite at Low and high arsenite concentrations might be due to surface polymerization of adsorbed arsenite at high concentrations. The presence of phosphate resulted in a significant reduction in arsenate and arsenite adsorption by ferrihydrite, with strong dependence on pH and phosphate concentration. The effect of phosphate on arsenate adsorption was greater at high pH than at low pH, whereas the opposite trend was observed for arsenite. Results indicated that arsenate and phosphate compete for the same surface sites, with a moderate preference for arsenate adsorption. There was evidence of the presence of some surface sites that exhibited much higher affinity for arsenite than phosphate. The presence of sulfate did not influence arsenate adsorption but resulted in a considerable reduction in arsenite adsorption below pH 7.0, with the largest reduction at the lowest pH.
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页码:1422 / 1430
页数:9
相关论文
共 40 条
[1]   TESTING A MECHANISTIC MODEL .9. COMPETITION BETWEEN ANIONS FOR SORPTION BY SOIL [J].
BARROW, NJ .
JOURNAL OF SOIL SCIENCE, 1989, 40 (02) :415-425
[2]  
CRECELIUS EA, 1986, SPECIATION SELENIUM, V2
[3]   PHOSPHATE FERTILIZERS INFLUENCE LEACHING OF LEAD AND ARSENIC IN A SOIL CONTAMINATED WITH LEAD ARSENATE [J].
DAVENPORT, JR ;
PERYEA, FJ .
WATER AIR AND SOIL POLLUTION, 1991, 57-8 :101-110
[4]   ANION EXCHANGE IN SOILS .1. EXCHANGEABLE PHOSPHORUS AND THE ANION-EXCHANGE CAPACITY [J].
DEAN, LA ;
RUBINS, EJ .
SOIL SCIENCE, 1947, 63 (05) :377-387
[5]   ION-EXCHANGE STUDIES OF SOLUTIONS OF ARSENITES [J].
EVEREST, DA ;
POPIEL, WJ .
JOURNAL OF THE CHEMICAL SOCIETY, 1957, (JUN) :2433-2436
[6]   Arsenate and chromate retention mechanisms on goethite .1. Surface structure [J].
Fendorf, S ;
Eick, MJ ;
Grossl, P ;
Sparks, DL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (02) :315-320
[7]  
FERGUSON JF, 1974, CHEM WATER SUPPLY TR, P137
[8]  
Freeze R. H., 1979, GROUND WATER
[9]   SURFACE-CHEMISTRY OF FERRIHYDRITE .2. KINETICS OF ARSENATE ADSORPTION AND COPRECIPITATION [J].
FULLER, CC ;
DAVIS, JA ;
WAYCHUNAS, GA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1993, 57 (10) :2271-2282
[10]   The solubility of arsenious oxide in dilute solutions of hydrochloric acid and sodium hydroxide. The character of the ions of trivalent arsenic. Evidence for polymerization of arsenious acid [J].
Garrett, AB ;
Holmes, O ;
Laube, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1940, 62 :2024-2028