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introduction <br />This paper deals primarily with the <br />acid mine drainage problem associated with <br />the bituminous coal fields of northern <br />Appalachia. Past research dealt with the <br />identification of the geologic factors <br />affecting the occurrence of acid mine drain- <br />age on a regional scale. More recently, <br />efforts are being directed toward the iden- <br />tification of potentially acid or alkaline <br />producing material. This latter effort, <br />when coached in a multifactored conceptual <br />model that predicts mine drainage quality, <br />has Led to the formulation of a field <br />analytical technique that rapidly and ac- <br />curatelp identifies acid prod uci ny strata <br />(which are to be selectively handled and <br />isolated from the surface environment to <br />minimize the environmental impact), alkaline <br />producing strata (which are ideally suited <br />for soil-vegetational substrate) and <br />chemically inert material (which lends it- <br />self to stable backfill material). <br />Because of the interrelationship of <br />the regional and site specific facets of <br />mine drainage characterization, this paper <br />is presented in two parts; the first is <br />an overview of the acid mine drainage prob- <br />lem and the geologic factors responsible for <br />its occurrence, while the second part is a <br />discussion of a study that led to the iden- <br />tification of two parameters that can be <br />used to assess the rock's potential to pro- <br />duce alkaline oz acid leachates. <br />Background of the Acid Mine Drainage Problem <br />During earth moving operations, such <br />as in strip mining of coal, large volumes <br />of rock overlying the coal (the overburden) <br />are removed to expose the seam. This land <br />disturbance may impact the environment with <br />mine drainages that are laden with suspended <br />sediment, dissolved solids, heavy and minor <br />metals and, in certain cases, acidic mine <br />waters. Within a particular strip mine, <br />numerous strata of varying mine ra logics are <br />disrupted by the mining process and the <br />quality of the drainage emanating from the <br />mine site is a blend of water chemistries <br />produced by each rock type, In some mines <br />the combination of water chemistries yields <br />acidic drainages. <br />Acid mine drainage, as the name im- <br />plies, is an extremely acidic, iron and <br />sulfate rich drainage that forms under <br />natural conditions when certain coal seams <br />are mined and the strata are exposed to <br />accelerated oxidizing environments. During <br />this process, a variety of iron sulfides <br />(Fe52), occurring commonly as marcasite and <br />pyrite, oxidize in the presence of oxygen <br />and water to form soluble hydrous iron sul- <br />fates. These compounds appear as the white <br />and yellow-green salt crusts on the surface <br />of weathered rock faces. Natural waters <br />flwinq over the weathered surfaces readily <br />dissolve these compounds which hydroli ze <br />and form acidic high-sulfate, high-iron <br />drainages. The first step of the race [ion <br />releases ferrous iron, which can be oxidized <br />to the ferric state, and forms oxyhydroxides <br />that impart the red and yellow color that <br />is characteristic of acid mine drainage. <br />These iron hydroxide precipitates are the <br />'yellow boy that is often observed in the <br />streams and drainages of some coal mine <br />areas. <br />The oxidation of ferrous iron to Eerric <br />iron usually proceeds slowly under normal <br />conditions. Hoveve r, certain iron bacteria <br />act as catalysts and accele r.a to the chemical <br />reaction rate with an increase in acidity. <br />These iron oxidizing bacteria are indigenous <br />to aqueous environments with pH values that <br />range from 2.8 io },2 and are generally <br />absent or inactive in hydcogrologic ragimes <br />wi t5 pH values greater than around 5.5. <br />Factors Affecting Mine Drainage Quality <br />Aciaitr. It is generally recognized that <br />the oxidation of the iron disulfides (here- <br />after called pyrite) and the subsequent <br />hydrolysis of the oxidation products is the <br />cause of acidity. Because of this relation- <br />ship, it is often assumed that the amount of <br />acidity produced is related +ro the amount of <br />pyrite present, i.e., the hiyher the pyrite <br />(or sulfur) content the greater the poten- <br />tial of the sample to produces acid. How- <br />ever, Caruccio showed that rcpcks with a <br />paucity of carbonate produced acidities <br />that varied more directly with the particle <br />size of the pyrite than with the amount of <br />pyrite present. 2,} It was shown that small <br />particles of pyrite (less than 0.25 microns) <br />rapidly decomposed when exposed to the atmo- <br />sphere while coarse grained (pyrite particles <br />(greater than 50 microns) remained relative- <br />ly stable. In terms of a sample's poten- <br />tial to produce acidity, all other things <br />being equal, the samples with a preponder- <br />ance of fine grained (framboi~dal) pyrite <br />generate orders of magnitude more acid than <br />samples having coarse grained (secondary, <br />plant replacement, cleat coats, etc.) <br />pyrite. <br />Alkalinity. Previous work by Caruccio2 and <br />Caruccio and reide l4 has shown that the de- <br />gree of acidity is also a function of the <br />calcareous material content crf the strata, <br />which has the potential to produce alka- <br />linity and a highly buffered and potentially <br />neutralizing drainage. In addition, the <br />calcareous material maintains the pH of the <br />ground water regime in the alkaline range <br />which effectively surpresses the iron bac- <br />teria and reduces the catalye+is of the oxi- <br />dation of ferrous iron. <br />However, unlike the ac icl-formi nq reac- <br />tions (which have feu rate limiting steps <br />due to the high solubility of the oxidation <br />products) the geochemistry of alkaline pro- <br />duction from calcareous material is con- <br />strained by the low solubility of the spe- <br />cific carbonate mineral in water (sideri to <br />excluded).5 As a result, alkalinity con- <br />centrations are fixed by [he partial pres- <br />sure of carbon dioxide, the tt ime of water <br />contact and the solubility of the specific <br />mineral or rock, e.q., calcine, dolomite, <br />limestone. <br />438 <br />