Characterization of Competitive Adsorption of Multicomponent Gases Injected with CO(2) in a Coal Mine Goaf

煤矿采空区注入CO₂时多组分气体竞争吸附的特征分析

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Abstract

Injection of CO(2) into a coal mine goaf is the primary method for inhibiting coal spontaneous combustion and for driving outgas, and gases such as N(2), O(2), and CH(4) in coal are in competition with it, which in turn affects its adsorption effect in coal. In order to enhance the CO(2) suppression and expulsion effect, the competitive adsorption characteristics of multicomponent gases in the coal mine goaf were investigated. We carried out adsorption experiments with a specific surface area analyzer to clarify the adsorption law of coal on different gases, conducted CO(2) adsorption experiments with an in situ infrared device to reveal the role of functional groups, verified the single-component adsorption law with molecular dynamics simulation, elucidated the effect of temperature on the adsorption of multicomponent gases, and summarized the law of CO(2) competition under different pressures. The results showed that the degree of deterioration was negatively correlated with the adsorption capacity, which was N(2) < O(2) < CH(4) ≪ CO(2), and the functional group C=O promoted the adsorption of CO(2). N(2) and O(2) adsorption produced only van der Waals force, and CH(4) and CO(2) promoted electrostatic force, to which CO(2) had an obvious advantage of electrostatic potential. In the competition adsorption process, CO(2) produces the highest heat of adsorption, and the temperature increase affects the ability to positively correlate with the adsorption capacity of the adsorbate. The adsorption point of carbon dioxide is concentrated near the side branched chain, with better substitution of O(2) at P = 1 MPa, while CH(4) is mainly rejected at P = 2 MPa. The advantages of injecting CO(2) as an inert gas into the air-mining zone were elucidated in terms of functional groups, intermolecular forces, heat of adsorption, and adsorption sites, which provide theoretical support for the suppression of coal spontaneous combustion by replacing O(2) and the enhancement of extraction by replacing CH(4).

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