油页岩
干酪根
介孔材料
化学工程
聚结(物理)
体积热力学
材料科学
多孔性
吸附
化学
惰性气体
矿物学
孔隙水压力
比表面积
地质学
复合材料
有机化学
烃源岩
热力学
工程类
天体生物学
古生物学
催化作用
岩土工程
物理
构造盆地
作者
Debanjan Chandra,Tuli Bakshi,Vikram Vishal
标识
DOI:10.1016/j.micromeso.2021.110969
摘要
Abstract Kerogens are the primary hosts of micropores and mesopores which determine the gas storage capacity in shale. The prime focus of this study is to assess the mode of organic pore development in shale under different heating environments. The clay-rich shales display a reduction in the aliphaticity index from 100 °C to 300 °C, indicating structural changes in kerogen at the higher temperature. Scanning electron microscopic images reveal an increasing interconnectivity of organic pores with increasing temperature. Low pressure gas adsorption analysis confirms appearance of newer micropores and coalescence of micropores into mesopores at 300 °C. Nevertheless, the changes in pore characteristics occur differently when the heating modes are different. Oxic heating causes a noticeable increase in the surface area, and pore volume. Along with that, the pore size distribution peaks become sharper and of higher magnitude. Upon anoxic heating, the presence of bitumen in pores results in pore-blockage, leading to a reduction in surface area and pore volume. The surface roughness does not change in newly formed coarser mesopores upon combustion, whereas, with increasing temperature, the fractal dimensions of both finer and coarser pores suggest new pore formation during inert heating.
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