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CO2响应型清洁压裂液性能及其转变机理分析*
油田化学
2021年 38卷 第4期
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Title
Performance and Transformation Mechanism of CO2 Responsive Clean Fracturing Fluid
Authors
WU Xuepeng
JIANG Shanhong
DAI Caili
摘要
为改善水力压裂返排液对储层的伤害和环境的污染,以硬脂酸与N,N-二甲氨基丙胺为原料、氟化钠为催 化剂,通过双分子亲核取代反应制备了具有CO2响应的表面活性剂(EA)。将其与反离子水杨酸钠复配制备具有 CO2响应增黏的水溶液体系,可作为清洁压裂液体系实现循环利用。利用流变仪研究了EA水溶液及其与反离 子复配体系的CO2响应性和循环可逆性,利用电子显微镜和分子动力学模拟从介观和微观层面揭示其响应及可逆 转变机理。结果表明,EA水溶液及复配体系均具有良好的CO2和pH响应增黏特性,通入N2或高温可实现体系降 黏。该溶液体系的CO2响应增黏率高、响应速度快、黏弹性模量高,可以实现多次可逆转变。分子动力学模拟及冷 冻电镜揭示了溶液体系中蠕虫状聚集体的形成及转变机理,为实现清洁压裂液循环利用提供理论基础。
Abstract
In order to improve the damage of hydraulic fracturing flow-back fluid to reservoir and the pollution to environment,the surfactant EA was synthesized by bimolecular nucleophilic substitution reaction with stearic acid and N,N-dimethylaminopropylamine as raw materials and sodium fluoride as catalyst. An CO2 responsive aqueous solution was constructed by mixing sodium salicylate and EA,which could be used as clean fracturing fluid and realize recycling. The reactivity and cyclic reversibility of EA aqueous solution and its compound system with counter ion were evaluated by rheometer. The responsive and reversible transformation mechanism were analyzed from mesoscopic and microscopic levels by electron microscope and molecular dynamics simulation. The results showed that EA aqueous solution and the compound system had good viscosity increasing characteristics to the response of CO2 and pH value,and the viscosity reduction of system could be realized by introducing N2 or high temperature. The solution system had high viscosity increasing rate to CO2 response,fast responsive speed and high viscoelastic modulus,and could realize multiple reversible transformations. Molecular dynamics simulation and freeze electron microscope revealed the formation and transformation mechanism of wormlike aggregates in solution system,which provided a theoretical basis for the recycling of clean fracturing fluid.
关键词:
CO2响应;
清洁压裂液;
循环利用;
自组装;
Keywords:
CO2 response;
clean fracturing fluid;
cyclic utilization;
self-assembly;
DOI
10.19346/j.cnki.1000-4092.2021.04.007