不同类型增黏剂与褐煤共发酵降解的差异性分析

Comparative analysis of biodegradation differences in co-fermentation of various viscosifiers with lignite

  • 摘要: 针对生物成因煤层气储层改造中压裂液增黏剂与微生物代谢兼容性不足的难题,通过构建涵盖破胶效率、孔隙改造度及代谢激活度的多维度评价体系,系统对比了胍胶、黄原胶和改性纤维素3类增黏剂的生物协同增产机制。试验采用菌液和过硫酸铵溶液为破胶介质,测定0.4%质量分数下增黏剂黏度衰减动力学,筛选出黄原胶与胍胶,其60 h黏度分别降至3.5、2.3 mPa·s,降黏效率显著优于改性纤维素(4.8 mPa·s),而聚丙烯酰胺因生物降解惰性(残留黏度8.6 mPa·s)被排除。通过褐煤与增黏剂联合厌氧发酵试验发现,黄原胶体系累计产气量达321 mL,较胍胶和改性纤维素分别提高40.8%和205.7%,改进Gompertz模型拟合显示其最大产气潜能为对照组褐煤的4.7倍。孔隙结构表征表明,黄原胶使褐煤比表面积降低28.4%,介孔体积扩展至0.047 cm3/g,红外光谱分析证实其促进脂肪链和芳香结构裂解,释放可溶性有机质。三维荧光测试发现,黄原胶使发酵液可溶性有机质含量增加,为微生物代谢提供充足底物。宏基因组解析揭示,黄原胶特异性富集乙酸型产甲烷菌Methanothrix,显著激活乙酸脱羧代谢通路,其中K00925基因表达丰度达356.8,明显高于胍胶体系的259.9;同时,相关功能基因总丰度提升了20%以上。研究构建了涵盖破胶效率、孔隙改造度及代谢激活度的多维度评价体系,阐明增黏剂与生物协同效应的构效关系,证实黄原胶可同步实现储层物性优化与微生物代谢网络重构,为生物兼容型压裂液优选提供理论与技术支撑。

     

    Abstract: To address the challenge of poor compatibility between fracturing fluid thickeners and microbial metabolism in biogenic coalbed methane (CBM) reservoir stimulation, this study developed a multidimensional evaluation system encompassing gel-breaking efficiency, pore structure modification, and metabolic activation. Using this framework, the synergistic mechanisms of methane enhancement by three thickeners—guar gum, xanthan gum, and modified cellulose—were systematically compared. Gel-breaking agents comprising microbial consortia and ammonium persulfate were used to assess the viscosity degradation kinetics of the thickeners at 0.4% concentration. Xanthan gum and guar gum exhibited superior viscosity reduction, with final viscosities of 3.5 mPa·s and 2.3 mPa·s after 60 hours, significantly outperforming modified cellulose (4.8 mPa·s). Polyacrylamide was excluded due to its resistance to biodegradation, with a residual viscosity of 8.6 mPa·s. Anaerobic co-fermentation experiments with lignite and thickeners revealed that the xanthan gum system achieved a cumulative gas production of 321 mL, representing increases of 40.8% and 205.7% over guar gum and modified cellulose, respectively. Improved Gompertz model fitting indicated a maximum gas production potential 4.7 times that of the control lignite group. Pore structure characterization showed that xanthan gum reduced the specific surface area of lignite by 28.4% and expanded the mesopore volume to 0.047 cm3/g. Fourier transform infrared spectroscopy (FTIR) analysis confirmed its role in promoting the cleavage of aliphatic chains and aromatic structures, thereby releasing soluble organic matter. Three-dimensional fluorescence spectroscopy further revealed that xanthan gum increased the content of soluble organic matter in the fermentation broth, providing sufficient substrates for microbial metabolism. Metagenomic analysis demonstrated that xanthan gum specifically enriched the aceticlastic methanogen Methanothrix and significantly upregulated the acetate decarboxylation pathway. The expression level of the key gene K00925 reached 356.8, notably higher than that in the guar gum system (259.9). Moreover, the total abundance of related functional genes increased by more than 20%. This study established a multidimensional evaluation framework integrating gel-breaking performance, pore structure modification, and metabolic activation, elucidating the structure–function relationship of thickener–microbe synergy. The results demonstrate that xanthan gum enables simultaneous optimization of reservoir physical properties and reconstruction of microbial metabolic networks, offering theoretical and technical support for the development of bio-compatible fracturing fluids.

     

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