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An intelligent CO2-responsive hydrogel for applications in enhanced oil recovery and CO2 geological storage
Separation and Purification Technology ( IF 8.1 ) Pub Date : 2024-11-20 , DOI: 10.1016/j.seppur.2024.130526
Pengwei Fang, Qun Zhang, Menqgi Wu, Can Zhou, Zhengming Yang, Hongwei Yu, Zemin Ji, Yina Yi, Wen Jiang, Xinliang Chen, Yuan Gao, Mengfei Zhou, Meiwen Cao

A novel CO2-responsive hydrogel for intelligent control of gas channeling in CO2– enhanced oil recovery (CO2-EOR) and geological CO2 storage has been developed. A monomeric long-chain tertiary amine surfactant (HXB-2) that has specific amide and carboxyl groups was synthesized. The surfactant can interact with CO2 in aqueous solution to increase the viscosity and induce gelation. The hydrogel is irreversible and does not revert to solution phase after N2 bubbling. It shows excellent structural stability and thermal resistance and the viscosity remains four times higher than that of the initial solution upon heating. For the mechanism, HXB-2 protonates in CO2 environment and self-assembles into worm-like micelles (WLMs) under synergistic forces of hydrophobic interaction, hydrogen bonding, and electrostatic interaction, which further crosslink to form a three-dimensional (3D) network to induce gelation. The hydrogel can be formed in-situ to control gas channeling intelligently and redirect the gas to unswept low-permeability channels. It can enhance the recovery rate by 23.53 % and the maximum seepage resistance reaches 29.45 MPa·min·cm−3 for water-alternatinggas flooding. Moreover, by having spontaneous association and shear-dissociation properties, the hydrogel in the rock pores causes minimal damage to the reservoir. This study provides valuable insights and empirical support for the development of irreversible CO2-responsive hydrogels for CO2 chemical sequestration and gas channeling control to help EOR and geological CO2 storage.

中文翻译:


一种智能 CO2 响应性水凝胶,适用于提高石油采收率和 CO2 地质封存



已经开发了一种新型的 CO2 响应水凝胶,用于智能控制 CO2 中的气体通道 - 提高石油采收率 (CO2-EOR) 和地质 CO2 封存。合成了具有特异性酰胺和羧基的单体长链叔胺表面活性剂 (HXB-2)。表面活性剂可与水溶液中的 CO2 相互作用,以增加粘度并诱导凝胶化。水凝胶是不可逆的,在 N2 鼓泡后不会恢复到溶液相。它表现出优异的结构稳定性和耐热性,加热后粘度仍比初始溶液高四倍。对于机制,HXB-2 在 CO2 环境中质子化,并在疏水相互作用、氢键和静电相互作用的协同作用下自组装成蠕虫状胶束 (WLM),进一步交联形成三维 (3D) 网络以诱导凝胶化。水凝胶可以在原位形成,以智能控制气体通道,并将气体重定向到未扫过的低渗透通道。它可以提高 23.53 % 的采收率,水交替驱的最大抗渗性达到 29.45 MPa·min·cm−3。此外,通过具有自发缔合和剪切解离特性,岩石孔隙中的水凝胶对储层造成的损害最小。本研究为开发用于 CO2 化学封存和气体通道控制的不可逆 CO2 响应性水凝胶提供了有价值的见解和实证支持,以帮助 EOR 和地质 CO2 封存。
更新日期:2024-11-21
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