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复配碱–表面活性剂作用下含硫煤层煤尘与硫化氢协同治理

Synergistic control of coal dust and hydrogen sulfide in sulfur-bearing coal seams under the action of compound alkali–surfactant

  • 摘要: 为解决含硫煤层开采过程中煤尘与硫化氢复合污染问题,以内蒙古五虎山煤矿1008高硫综采工作面为工程背景,选取6种不同离子类型表面活性剂与质量分数为0.5%的碳酸钠构建复配碱−表面活性剂体系,通过界面性质测试、气载污染物吸附试验、MS分子模拟及现场工业试验,系统研究了复配体系对煤尘润湿与硫化氢吸附的协同作用规律,揭示了煤尘载体强化硫化氢吸附的耦合增效机制,验证了煤层注水配合工作面喷雾的协同治理方案应用效果。结果表明:阴离子型SDBS复配体系界面活性最优,质量分数为0.5%时煤样接触角降至25.31°,降幅达33.5%;硫化氢吸附能呈对称泊松分布,温度由273.15 K升至298.15 K时平均相互作用能由−35.77 kJ/mol偏移至−32.68 kJ/mol,288.15 K时吸附位点占据概率达峰值,呈现低温促进扩散择优吸附、高温脱附主导的双重调控效应,吸附过程随压力升高经历孤立吸附、微孔聚集、协同吸附至空间分层的动态演变。复配体系可显著提升煤基硫化氢吸附容量,吸附等温线符合Langmuir-Freundlich 模型(R2>0.98),SDBS复配体系吸附量较原煤提升174.76%。风载条件下煤尘作为吸收载体可使硫化氢吸附率提升3.75%~6.88%,最优复配体系降尘效率达95.23%、硫化氢吸收率达84.38%。现场实施复配碱−SDBS煤层注水配合全断面喷雾后,工作面硫化氢峰值浓度降幅达68.36%,全尘降尘效率达92%~97%。

     

    Abstract: To address the combined pollution of coal dust and hydrogen sulfide (H2S) during the mining of sulfur-bearing coal seams, this study takes the No.1008 high-sulfur fully mechanized mining face of Wuhushan Coal Mine in Inner Mongolia as the engineering background.Six surfactants with different ionic types were selected and compounded with sodium carbonate at a mass fraction of 0.5% to construct a compound alkali–surfactant system. Through interfacial property tests, airborne pollutant absorption experiments, MS molecular simulation, and on-site industrial tests, the synergistic law of the compound system governing coal dust wetting and H2S adsorption was systematically investigated, the coupling efficiency-enhancing mechanism by which coal dust carriers strengthen H2S absorption was revealed, and the application effect of the synergistic control scheme combining coal seam water infusion with working face spraying was verified. The results show that the anionic SDBS compound system exhibits the optimal interfacial activity. At a mass fraction of 0.5%, the contact angle of the coal sample decreases to 25.31°, with a reduction rate of 33.5%. The H2S adsorption energy follows a symmetric Poisson distribution; as the temperature rises from 273.15 K to 298.15 K, the mean interaction energy shifts from −35.77 kJ/mol to −32.68 kJ/mol, and the adsorption site occupancy probability peaks at 288.15 K, exhibiting a dual regulation effect of low-temperature-promoted diffusion and preferential adsorption versus high-temperature-dominated desorption. The adsorption process undergoes a dynamic evolution from isolated adsorption, micropore aggregation, and cooperative adsorption to spatial stratification with increasing pressure. The compound system can significantly enhance the coal-based H2S adsorption capacity, and the adsorption isotherm conforms well to the Langmuir-Freundlich model (R2>0.98); the adsorption capacity of the SDBS compound system is 174.76% higher than that of raw coal. Under wind-borne conditions, coal dust acting as an absorption carrier can increase the H2S absorption rate by 3.75%~6.88%; the optimal compound system achieves a dust suppression efficiency of 95.23% and an H2S absorption rate of 84.38%.After the on-site implementation of compound alkali-SDBS coal seam water infusion combined with full-section spraying, the peak H2S concentration in the working face decreases by 68.36%, and the total dust suppression efficiency reaches 92%~97%.

     

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