Abstract: Surface waters in the Pine Creek Geosyncline (located in Australia's “Top End”, defined as the area of Australia north of 15 degrees S) are characterized by their low carbonate buffering capacity. These waters are buffered by silicate weathering and hence are slightly acidic, ranging in pH from 4.0 to 6.0. The Pine Creek Geosyncline contains most of the Top Ends' economic mineral deposits and characteristically shows no correlation between carbonate minerals and sulfidic orebodies hosting gold deposits (unlike uranium deposits). Thus many gold mines do not have ready access to carbonate minerals for buffering acid mine drainage (AMD). It is possible that locally available fast-weathering silicate minerals may be used to buffer AMD seeps. The buffering intensity of silicate minerals exceeds that of carbonate minerals, but their slow dissolution kinetics has ensured that these materials have received little attention in treating AMD. In addition, carbonate mineral dissolution is retarded when contacted with intense AMD solutions due to the formation of surface coatings of iron minerals. The lower pH range of silicate mineral dissolution may prevent the formation of such coatings. The Pine Creek Geosyncline consists of a complex geochemistry, and a number of fast-weathering silicate minerals have been noted in various areas. The difficulty in assessing such minerals for use in buffering AMD is the lack of kinetic data available under conditions prevalent AMD (i.e., low pH solutions saturated with aluminium and silica). This study sets out to evaluate the applicability of using such minerals to treat AMD surface seeps.

Abstract: Processes affecting neutralization of acidic coal mine drainage were evaluated within 'anoxic' limestone drains (ALDs). Influents had pH less than or equal to 3.5 and dissolved oxygen < 2 mg/l. Even though effluents were near neutral (pH > 6 and alkalinity > acidity), two of the four ALDs were failing due to clogging. Mineral-saturation indices indicated the potential for dissolution of calcite and gypsum, and precipitation of Al3+ and Fe3+ compounds. Cleavage mounts of calcite and gypsum that were suspended within the ALDs and later examined microscopically showed dissolution features despite coatings by numerous bacteria, biofilms, and Fe-Al-Si precipitates. In the drain exhibiting the greatest flow reduction, Al-hydroxysulfates had accumulated onlimestone surfaces and calcite etch points, thus causing the decline in transmissivity and dissolution. Therefore, where Al loadings are high and flow rates are low, a pre-treatment step is indicated to promote Al removal before diverting acidic mine water into alkalinity-producing materials. Published by Elsevier Science Ltd.