Characterizing the geochemical reactions in overburden waste pile : Synerude Mine Site, Fort McMurray, Alberta, Canada
type: CreativeWork
description: Potential environmental risks of constructing waste piles from sulphide-bearing salinesodic overburden include acid-mine drainage and salinization of surface soils. Acid-mine drainage may result from the production of sulphuric acid during the oxidation of sulphide minerals. Acid production during the oxidation of sulphide minerals may also increase the concentrations of S0₄ (from sulphuric acid), Ca (from dissolution of carbonates), and Na (from cation exchange with saline-sodic overburden) in surface soils. To identify and quantify these potential environmental risks, in situ S0₄ and Ca production rates were calculated using two different methods. Sulphide mineral oxidation rates were calculated using simple one-dimensional analytical modelling (assuming diffusive gas transport) of in situ pore-gas 0₂ concentrations. Ca loading from carbonate mineral dissolution (resulting in C0₂ production) was also calculated using the simple one-dimensional modelling of measured pore-gas C0₂ concentrations. Mass balance calculations using solid sample chemistry (total S, soluble ion and TIC concentrations) were also used to quantify the rate of S0₄ and Ca production rates. Geochemical and geotechnical parameters controlling acid production and salt loadings were measured by installing gas probes to a depth of 25 m (n = 34) for in situ pore-gas 0₂, C0₂, CH₄ and N₂ concentrations, and δ¹³Cc₀₂ values), diviner tubes to depths of 1.6 m (n = 3; for shallow moisture contents), a neutron access tube to 25 m (for deep moisture contents), and a thermistor string to 20m (for temperatures). Pore-gas 0₂, C0₂, CH₄ and N₂ concentrations were measured using a field-portable gas chromatograph. Depth profiles of solid sulphur (samples stored in anaerobic chambers) and carbon concentrations and forms were measured and used for acid-base accounting. Pore-gas chemistry showed that 0₂ concentrations decreased from atmospheric to less than 13% at 5 m depth. C0₂ concentrations increased from atmosphe…
abstract: Potential environmental risks of constructing waste piles from sulphide-bearing salinesodic overburden include acid-mine drainage and salinization of surface soils. Acid-mine drainage may result from the production of sulphuric acid during the oxidation of sulphide minerals. Acid production during the oxidation of sulphide minerals may also increase the concentrations of S0₄ (from sulphuric acid), Ca (from dissolution of carbonates), and Na (from cation exchange with saline-sodic overburden) in surface soils. To identify and quantify these potential environmental risks, in situ S0₄ and Ca production rates were calculated using two different methods. Sulphide mineral oxidation rates were calculated using simple one-dimensional analytical modelling (assuming diffusive gas transport) of in situ pore-gas 0₂ concentrations. Ca loading from carbonate mineral dissolution (resulting in C0₂ production) was also calculated using the simple one-dimensional modelling of measured pore-gas C0₂ concentrations. Mass balance calculations using solid sample chemistry (total S, soluble ion and TIC concentrations) were also used to quantify the rate of S0₄ and Ca production rates. Geochemical and geotechnical parameters controlling acid production and salt loadings were measured by installing gas probes to a depth of 25 m (n = 34) for in situ pore-gas 0₂, C0₂, CH₄ and N₂ concentrations, and δ¹³Cc₀₂ values), diviner tubes to depths of 1.6 m (n = 3; for shallow moisture contents), a neutron access tube to 25 m (for deep moisture contents), and a thermistor string to 20m (for temperatures). Pore-gas 0₂, C0₂, CH₄ and N₂ concentrations were measured using a field-portable gas chromatograph. Depth profiles of solid sulphur (samples stored in anaerobic chambers) and carbon concentrations and forms were measured and used for acid-base accounting. Pore-gas chemistry showed that 0₂ concentrations decreased from atmospheric to less than 13% at 5 m depth. C0₂ concentrations increased from atmosphe…
author: Wall, Susan N.
language: en_US
date published: 2005
date modified: 2026-07-24T04:27:20Z
provider: University of Saskatchewan
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Saskatchewan

PropertyValue
property ID: Handle
value: https://hdl.handle.net/10388/etd-07112012-152130