Over a century of mining and smelting of the world-class porphyry lode ore deposit at Butte, Montana, has resulted in extensive environmental damage. In addition to its being the location of one of the world's largest and most acidic mining pit lakes, Butte is host to over 16,000 km of flooded underground mine workings. Of the more than 60 mine shafts that have historically operated in Butte, approximately one dozen are presently accessible for groundwater sampling. The geochemistry of the mine shaft waters is zoned and roughly coincides with a district-wide zonation in hydrothermal alteration and mineralization. Mine waters in the so-called "Central zone" of intense phyllic and advanced argillic alteration have lower pH and very high concentrations of As, Fe, Mn, and Zn, but very low concentrations of dissolved Cu. The scarcity of Cu is attributed to cementation onto scrap iron left in the mines, and/or to replacement of preexisting sulfide minerals below the water table in a manner analogous to supergene enrichment processes. At the other extreme, mine waters in the "Peripheral zone" of weakest alteration have near-neutral pH, low metal concentrations, and contain dissolved sulfide (H2S, HS -). These waters are close to equilibrium with calcite, siderite, crystalline or amorphous MnCO3, and mackinawite (poorly crystalline FeS). A suite of deep groundwater monitoring wells completed †
The mines of Butte, Montana include over 16,000 km of abandoned underground workings, most of which are now filled with water. The feasibility of using the flooded mine workings as a source of irrigation water was investigated. The geochemistry and stable isotopic composition of water produced during a 59 day pumping test of the flooded Belmont Mine workings are described. Although static water in the pumping well initially met proposed irrigation standards, the quality deteriorated during pumping as water from deeper in the mine complex was drawn into the well. Stable isotopes show that this lower-quality water was not sourced from the nearby Berkeley Pit lake, but most likely came from the mine shaft itself. At steady state, the water pumped to the surface had pH 5.5-6.0 with high concentrations (in mg/L) of dissolved SO 4 (1,600), Fe (160), Mn (19), Zn (15), and As (1.8). Despite substantial bicarbonate alkalinity (&150 mg/L as CaCO 3 ), the water became strongly acidic after equilibration with air due to oxidation and hydrolysis of Fe 2? . Benchtop experiments were performed to test different strategies for low-cost chemical treatment prior to irrigation. The most feasible alternative involved aeration (to remove large quantities of dissolved CO 2 ) prior to pH adjustment to [9 with lime or NaOH. Further work is needed to see if such treatment is economically viable compared to the cost of using municipal water. Another concern is whether irrigation of grass with high TDS, high sulfate water is sustainable. The mine water reached a steady-state temperature of 19°C during pumping, and therefore the possibility of using this water to help heat nearby buildings should also be explored.
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