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Self-assembly networks of wormlike micelles and hydrophobically modified polyacrylamide with high performance in fracturing fluid application

机译:蠕虫状胶束和疏水改性聚丙烯酰胺的自组装网络在压裂液应用中具有高性能

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摘要

Dynamic rheology and steady shear viscosity of an aqueous salt solution of 2 wt% viscoelastic gemini surfactant 1,2-N,N'-bis (dimethyloctadecyl) ethene ammonium bromide and its mixture with low molecular weight hydrophobically modified polyacrylamide (HMPAM) were investigated. The solution of surfactant in the presence of potassium chloride exhibited typical Maxwellian fluid behavior with a single stress relaxation time, indicating the formation of transient networks of entangled wormlike micelles (WLMs). Polymer profoundly affected the rheological properties of WLMs. The WLMs/HMPAM system demonstrated higher plateau modulus and zero-shear viscosity than the single WLMs system by self-assembling into common networks which was identified by scanning electron microscopy morphology. In contrast to the WLMs system, the WLMs/HMPAM system exhibited better temperature and shear resistance while retaining complete responsiveness to hydrocarbons. Based on the fracturing fluid application evaluation, the WLMs/HMPAM system had an applicable temperature, which was 30 degrees C higher than the WLMs system, and the core damage rate showed that the WLMs/HMPAM system was very promising in clean fracturing fluid application.
机译:研究了2 wt%粘弹性双子表面活性剂1,2-N,N'-双(二甲基十八烷基)乙烯溴化铵及其与低分子量疏水改性聚丙烯酰胺(HMPAM)的混合物的动态流变学和稳态剪切粘度。在氯化钾存在下的表面活性剂溶液表现出典型的麦克斯韦流体行为,具有单个应力松弛时间,表明缠结的蠕虫状胶束(WLM)形成了瞬态网络。聚合物深刻影响了WLM的流变性。 WLMs / HMPAM系统通过自组装成共同的网络而表现出比单个WLMs系统更高的平稳模量和零剪切粘度,这是通过扫描电子显微镜形态学确定的。与WLMs系统相比,WLMs / HMPAM系统表现出更好的温度和抗剪切性,同时保留了对烃类的完全响应性。根据压裂液应用评估,WLMs / HMPAM系统的适用温度比WLMs系统高30摄氏度,岩心损坏率表明WLMs / HMPAM系统在清洁压裂液应用中非常有前途。

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