Scavenging of as from acid mine drainage by schwertmannite and ferrihydrite: A comparison with synthetic analogues

被引:366
作者
Carlson, L
Bigham, JM
Schwertmann, U
Kyek, A
Wagner, F
机构
[1] Ohio State Univ, Sch Nat Resources, Columbus, OH 43210 USA
[2] Univ Helsinki, FIN-00171 Helsinki, Finland
[3] Tech Univ Munich, Lehrstuhl Bodenkunde, D-85350 Freising Weihenstephan, Germany
[4] Tech Univ Munich, Phys Dept E15, D-85747 Garching, Germany
关键词
D O I
10.1021/es0110271
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ochreous precipitates containing 5.5-69.8 g/kg As were isolated from mine drainage in Finland and were composed of schwertmannite, ferrihydrite, and goethite. Schwert-mannite formation was favored at pH 3-4, but its structure was degraded at high As levels. A series of coprecipitates were therefore prepared from mixed iron arsenate/sulfate solutions to define the limits of schwertmannite stability. Schwertmannite was replaced as the dominant phase by a poorly crystalline iron(III) hydroxyarsenate (FeOHAs) when As/Fe mole ratios exceeded 0.15. The FeOHAs gave an X-ray diffraction pattern similar to that obtained from an "amorphous" iron(III) arsenate (As/Fe = 1.0) with broad peaks at 0.30 and 0.16 nm. The FeOHAs possessed a magnetic hyperfine field of 41.9 Tat 4.2 K that was intermediate to those of schwertmannite (46,1 T) and the iron(III) arsenate (24.8 T). These data indicate a strong disruptive effect of arsenate on magnetic ordering and structure development in schwertmannite. Equilibration of 0.01 M arsenate solutions with freshly prepared schwertmannite and 2-line ferrihydrite at pH 3.0 for up to 60 d gave sorbed As contents of 175 and 210 g/kg, respectively. Arsenate sorption degraded the host schwertmannite and ferrihydrite, perhaps due to the formation of an FeOHAs surface phase.
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页码:1712 / 1719
页数:8
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