Design, synthesis, and characterization of novel copolymer gel particles for water-plugging applications

吸水率 共聚物 离子强度 材料科学 化学工程 滴定法 化学 复合材料 聚合物 水溶液 有机化学 工程类
作者
Dingjun Zhang,M. Zhang,Z. Luo,Shengxiang Zhang
出处
期刊:E-polymers [De Gruyter]
卷期号:24 (1) 被引量:1
标识
DOI:10.1515/epoly-2024-0016
摘要

Abstract Multi-stage plugging represents a promising strategy for enhancing production and injection rates in medium-and low-permeability oilfields. Despite its potential, the efficacy of current plugging agents, particularly hydrophobically bonded water-soluble polyacrylamide-based gel microspheres, is hindered by notable drawbacks such as low stability and inadequate compressive strength. Therefore, a comprehensive understanding of water plugging mechanisms coupled with the optimization of gel microsphere properties is essential for advancing the development of gel-based plugging agents with superior characteristics or intelligent regulatory capabilities. The P(AA-AM-[PrSO 3 ]Vim) ionic liquid copolymerized gel particles were designed and synthesized by using microfluidic technique and titration gel method with AM, acrylic acid (AA), 1-vinylimidazole (Vim) and 1,3-propylsulfonyl lactone (PrSO 3 ) as the raw materials. The morphology and structure of the copolymer gel particles were characterized, and the effects of [PrSO 3 ]Vim and cross-linker content on the water-absorbing properties and strength of the gel particles were investigated. When the amount of [PrSO 3 ]Vim was 12%, the concentration of crosslinker was 1.5%, and the temperature was 40°C, the water absorption capacity reached the maximum value of 163 g·g −1 . The strength of the P(AA–AM–[PrSO 3 ]Vim) spherical gel particles was maximized at a [PrSO 3 ]Vim content of 4%. Furthermore, the chemical and physical roles of the P(AA–AM–[PrSO 3 ]Vim) spherical gel particles were studied in a typical water-plugging environment. This study provides experimental data and a theoretical basis for the application of functional spherical gel-plugging particles in current oilfield environments.
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