Geochemical and mineralogical impacts of H2SO4 on clays between pH 5.0 and-3.0

被引:32
作者
Shaw, Sean A. [1 ]
Hendry, M. Jim [1 ]
机构
[1] Univ Saskatchewan, Dept Geol Sci, Saskatoon, SK S7N 5E2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
SULFIDE MINE TAILINGS; DISSOLUTION KINETICS; ACID ACTIVATION; WEATHERING RATES; ROOM-TEMPERATURE; INORGANIC ACIDS; MILL TAILINGS; SURFACE-AREAS; IRON MOUNTAIN; NEGATIVE PH;
D O I
10.1016/j.apgeochem.2008.10.011
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Natural and constructed clay liners are routinely used to contain waste and wastewater. The impact of acidic solutions on the geochemistry and mineralogy of clays has been widely investigated in relation to acid mine drainage systems at pH > 1.0. The impact of H2SO4 leachate characterized by pH < 1.0 and potentially negative pH values on the geochemistry and mineralogy of clays is, however, not clear, Thus, laboratory batch experiments were conducted on three natural clay samples with different mass ratios of smectite, illite and kaolinite to investigate the impact of H2SO4 on the geochemistry and mineralogy of aluminosilicates from pH 5.0 to -3.0. Batch testing was conducted at seven pH treatments (5.0, 3.0, 1.0, 0.0, -1.0, -2.0 and -3.0) using standardized H2SO4 solutions for four exposure periods (14, 90, 180, and 365 d). Aqueous geochemical and XRD analyses showed: increased dissolution of aluminosilicares with decreasing pH and increasing exposure period, that smectite was more susceptible to dissolution than illite and kaolinite, precipitation of an amorphous silica phase occurred at pH <= 0.0, and anhydrite precipitated in Ca-rich clays at pH <= -1.0. In addition, global dissolution rates were calculated for the clays and showed good agreement to literature smectite, illite and kaolinite dissolution rates. which suggests global dissolution rates for complex clays could be determined from monomineralic studies. A stepwise conceptual model of the impact of H2SO4 on aluminosilicate geochemistry and mineralogy between pH 5.0 and -3.0 is proposed. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:333 / 345
页数:13
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