The nanometer-scaled pore systems of gas shale reservoirs were investigated from the Barnett, Marcellus, Woodford, and Haynesville gas shales in the United States and the Doig Formation of northeastern British Columbia, Canada. The purpose of this article is to provide awareness of the nature and variability in pore structures within gas shales and not to provide a representative evaluation on the previously mentioned North American reservoirs. To understand the pore system of these rocks, the total porosity, pore-size distribution, surface area, organic geochemistry, mineralogy, and image analyses by electron microscopy were performed. Total porosity from helium pycnometry ranges between 2.5 and 6.6%. Total organic carbon content ranges between 0.7 and 6.8 wt. %, and vitrinite reflectance measured between 1.45 and 2.37%. The gas shales in the United States are clay and quartz rich, with the Doig Formation samples being quartz and carbonate rich and clay poor. Higher porosity samples have higher values because of a greater abundance of mesopores compared with lower porosity samples. With decreasing total porosity, micropore volumes relatively increase whereas the sum of mesopores and macropore volumes decrease. Focused ion beam milling, field emission scanning electron microscopy, and transmission electron microscopy provide high-resolution (∼5 nm) images of pore distribution and geometries. Image analysis provides a visual appreciation of pore systems in gas shale reservoirs but is not a statistically valid method to evaluate gas shale reservoirs. Macropores and mesopores are observed as either intergranular porosity or are confined to kerogen-rich aggregates and show no preferred orientation or align parallel with the laminae of the shale. Networks of mesopores are observed to connect with the larger macropores within the kerogen-rich aggregates.

Carbon mineralization sequesters CO₂ by reaction of alkaline earth metal bearing silicate and hydroxide minerals with CO₂ to form stable carbonate minerals. Seifritz (1990) proposed harnessing this natural process as a method for sequestration of anthropogenic CO₂. It was first studied in detail as an industrial process by Lackner et al. (1995), which is often referred to as “mineral carbonation.” Much of this early research aimed to capitalize on the globally abundant natural deposits of ultramafic and mafic rocks, which are rich in alkaline earth metals, in addition to the long-term stability of the resultant...

Carbon dioxide (CO2) is sequestered through the weathering and subsequent mineralization of the chrysotile mine tailings at Clinton Creek, Yukon Territory, and Cassiar, British Columbia, Canada. Accelerated weathering is attributed to a dramatic increase in surface area, which occurs during the milling of ore. We provide a detailed account of the natural process of carbon trapping and storage as it occurs at Clinton Creek and Cassiar, including mineralogy, modes of occurrence, methods of formation for carbonate alteration, light stable isotope geochemistry, and radiocarbon analysis. Powder X-ray diffraction data were used to identify weathering products as the hydrated magnesium carbonate minerals nesquehonite [MgCO3·3H2O], dypingite [Mg5(CO3)4 (OH)2·5H2O], hydromagnesite [Mg5(CO3)4(OH)2·4H2O], and less commonly lansfordite [MgCO3·5H2O]. Textural relationships suggest that carbonate precipitates formed in situ after milling and deposition of tailings. Samples of efflorescent nesquehonite are characterized by δ13C values between 6.52 and 14.36 per mil, δ18O values between 20.93 and 26.62 per mil, and F14C values (fraction of modern carbon) between 1.072 and 1.114, values which are consistent with temperature-dependent fractionation of modern atmospheric CO2 during mineralization. Samples of dypingite ± hydromagnesite collected from within 0.2 m of the tailings surface give δ13C values between −1.51 and +10.02 per mil, δ18O values between +17.53 and +28.40 per mil, and F14C values between 1.026 and 1.146, which suggests precipitation from modern atmospheric CO2 in a soil-like environment. Field observations and isotopic data suggest that hydrated magnesium carbonate minerals formed in two environments. Nesquehonite formed in an evaporative environment on the surface of tailings piles, and dypingite and hydromagnesite formed in the subsurface environment with characteristics similar to soil carbonate. In both cases, these minerals have been trapping and storing the greenhouse gas, CO2, directly from the atmosphere. Combined use of δ13C, δ18O, and F14C data has been applied effectively as a tool for verifying and monitoring sequestration of atmospheric CO2 within mine tailings. A number of other deposit types produce tailings suitable for CO2 sequestration, including Cu-Ni-PGE deposits, diamondiferous kimberlite pipes, and podiform chromite deposits. Our results suggest that conversion of about 10 wt percent of tailings to carbonate minerals could offset the greenhouse gas emissions from many ultramafic-hosted mining operations.