Effects of electrolyte composition on chromium desorption in soils contaminated by tannery waste

被引:21
作者
Avudainayagam, S
Naidu, R
Kookana, RS
Alston, AM
McClure, S
Smith, LH
机构
[1] CSIRO Land & Water, Glen Osmond, SA 5064, Australia
[2] Univ Adelaide, Dept Soil & Water, Glen Osmond, SA 5064, Australia
来源
AUSTRALIAN JOURNAL OF SOIL RESEARCH | 2001年 / 39卷 / 05期
关键词
hexavalent chromium; chromate; leaching; contaminated site;
D O I
10.1071/SR00085
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
We conducted batch studies to investigate the effect of phosphate and dominant cations present in tannery waste on desorption of chromium (Cr) from surface and subsurface soil horizons from a contaminated tannery waste site at Mount Barker, South Australia. The surface horizon (0-15 cm) of the soil profile was alkaline (pH 7.9) and the subsurface horizon (50-90 cm) was acidic (pH 3.9). Aqua-regia extractable Cr concentration ranged from 62 g/kg in the surface to 0.26 g/kg in the subsurface soils. X-ray diffraction and scanning electron microscopic studies revealed the predominance of carbonate and kaolin minerals in the surface soils, and highly weathered framboidal particles, with morphology similar to that of pyrites, in the subsurface soils. The amount of Cr desorbed from the contaminated soils varied considerably with both the electrolyte's cationic charge and soil properties. The effect of cations, Ca2+ and Na+ (CaCl2, NaCl), and phosphate on desorption of Cr was investigated. While the ionic strength of the solutions was standardised at approximately 0.03 mol/L, the concentration of phosphate (as KH2PO4) was varied from 0 to 3.2 mmol/L. On the basis of studies on solution to soil ratio and desorption kinetics we chose a 20:1 solution to soil ratio and 2 h equilibration time. In the surface alkaline soil, the amount of Cr released decreased in the order Na+ (286 mug/L) water (256 mug/L) > Ca2+ (156 mug/L). In contrast subsurface acidic soil showed a reverse trend, i.e. Ca2+ (52 mug/L) > Na+ (29 mug/L) > water (20 mug/L). Speciation of Cr in the extracts showed predominantly Cr(VI) in the alkaline surface soil and Cr(III) in the subsurface acidic soil. A strong effect of phosphate on the cumulative amount of chromate desorbed was observed. The study shows that the presence of high concentrations of Na+ (0.03 mol/L) and phosphate (3.2 mmol/L) in soil solution enhances Cr(VI) mobility. In contrast, Ca2+ may induce retention of Cr(VI) in Cr-contaminated alkaline soils.
引用
收藏
页码:1077 / 1089
页数:13
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