Arsenic mobility in mildly alkaline drainage from an orogenic lode gold deposit, Bralorne mine, British Columbia
- 1. Geological Survey of Canada, Natural Resources Canada, 601 Booth St., Ottawa, ON K1A 0E8 (Canada)
- 2. Geological Survey of Canada (Atlantic), Natural Resources Canada, PO Box 1006, Dartmouth, NS B2Y 4A2 (Canada)
Description
Highlights: • As concentrations in flooded anoxic mine workings in range of 6000 μg/L. • Sorbed As released in workings by reductive dissolution of accumulated HFO. • As concentrations in portal effluent in range of 3000 μg/L. • Limited natural attenuation of As due to high pH and the lack of Fe sorbent. • Partitioning of As in effluent described by a field-scale distribution coefficient. - Abstract: The historical (1932–1971) Bralorne mine produced over 87 million grams of Au from an archetypal orogenic lode gold deposit in southwest British Columbia. High concentrations of As in mine drainage, however, represent an on-going environmental concern prompting a detailed study of effluent chemistry. The discharge rate at the mine portal was monitored continuously over a fourteen-month period during which effluent samples were collected on a quasi-weekly basis. Water samples were also collected on synoptic surveys of the adit between the portal and the main source of flow in the flooded workings. Total concentrations of As in the mildly alkaline (pH = 8.7) portal drainage average 3034 μg/L whereas at the source they average 5898 μg/L. As emergent waters from the flooded workings flow toward the portal, their dissolved oxygen content and pH increase from 0 to 10 mg/L and from 7.7 to 9, respectively. Near the emergence point, dissolved Fe precipitates rapidly, sorbing both As(III) and As(V). With increasing distance from the emergence point, dissolved As(III) concentrations drop to detection limits through sorption on hydrous ferric oxide and through oxidation to As(V). Concentrations of dissolved As(V), on the other hand, increase and stabilize, reflecting lower sorption at higher pH and the lack of available sorbent. Nonetheless, based on synoptic surveys, approximately 35% of the source As load is sequestered in the adit resulting in As sediment concentrations averaging 8.5 wt%. The remaining average As load of 1.34 kg/d is discharged from the portal. Partitioning of As(V) between dissolved and particulate phases in portal effluent is characterized by a sorption density of 0.37 mol As (mol Fe)−1 and by a distribution coefficient (Kd) of 130 L/g HFO. The relatively high sorption density may reflect co-precipitation of As with Fe oxyhydroxides rather than a purely adsorption-controlled process. Results of this study show that the As self-mitigating capacity of drainage from orogenic lode gold deposits may be poor in high-pH and Fe-limited settings
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apgeochem.2014.11.015Additional details
Identifiers
- DOI
- 10.1016/j.apgeochem.2014.11.015;
- PII
- S0883-2927(14)00286-8;
Publishing Information
- Journal Title
- Applied Geochemistry
- Journal Volume
- 57
- Journal Page Range
- p. 45-54
- ISSN
- 0883-2927
- CODEN
- APPGEY
Conference
- Title
- Joint Society of Economic Geologists and Geological Society of America short course on environmental geochemistry of modern mining
- Dates
- 31 Oct - 3 Nov 2010
- Place
- Denver, CO (United States)
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47043372
- Subject category
- S58: GEOSCIENCES;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ADSORPTION; ARSENIC; BRITISH COLUMBIA; CONCENTRATION RATIO; COPRECIPITATION; DEPOSITS; DISSOLUTION; DISSOLVED GASES; DRAINAGE; GEOCHEMICAL SURVEYS; GEOCHEMISTRY; GEOPHYSICAL SURVEYS; GOLD; MINES; NATURAL ATTENUATION; OXIDATION; OXYGEN; PH VALUE; WATER
- Descriptors DEC
- CANADA; CHEMICAL REACTIONS; CHEMISTRY; DEVELOPED COUNTRIES; DIMENSIONLESS NUMBERS; ELEMENTS; FLUIDS; GASES; GEOLOGIC SURVEYS; HYDROGEN COMPOUNDS; METALS; NONMETALS; NORTH AMERICA; OXYGEN COMPOUNDS; PRECIPITATION; SEMIMETALS; SEPARATION PROCESSES; SOLUTES; SORPTION; TRANSITION ELEMENTS; UNDERGROUND FACILITIES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.