Volume changes due to SO2-4, SeO2-4, and H2PO-4 adsorption on amorphous iron(III) hydroxide in an aqueous suspension

被引:26
作者
Yamaguchi, NU [1 ]
Okazaki, M
Hashitani, T
机构
[1] Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Tokyo 1848588, Japan
[2] Tokyo Univ Agr & Technol, Fac Agr, Tokyo 1838509, Japan
关键词
SO42-; SeO42-; H2PO4-; volume change; dilatometry; hydration; adsorption; amorphous iron(III) hydroxide;
D O I
10.1006/jcis.1998.5900
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
Volume changes due to SO42-, SeO42-, and H2PO4- adsorption on amorphous iron(III) hydroxide were determined by dilatometry in a mixture comprising an aqueous solution of Na2SO4, Na2SeO4, or NaH2PO4 and amorphous iron(III) hydroxide suspended in 0.1 mol dm(-3) NaClO4 at an initial pH ranged from 4.50 to 6.50. System volumes increased during SO42-, SeO42-, and H2PO4- adsorption on amorphous iron(III) hydroxide, suggesting that some hydrated water around aqueous SO42-, SeO42-, or H2PO4- ions and amorphous iron(III) hydroxide were released to the bulk. The volume changes due to SO42-, SeO42-, and H2PO4- adsorption at initial pH 4.50 were + 18, +18, and +14 cm(3) mol(-1), respectively. Phosphate, which adsorbed as an inner-sphere complex, released most of its hydration water to the bulk. The volume changes due to SO42- and SeO42- adsorption indicated that they were dehydrated at the water/amorphous iron(III) hydroxide interface. The smaller changes in volume for H2PO4- compared to SO42- and SeO42- may be explained by differences of charges and adsorption mechanisms of these oxoanions. (C) 1999 Academic Press.
引用
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页码:386 / 391
页数:6
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