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一种超支化聚合物的合成及其在提高采收率方面的性能

Syntheses of a Hyperbranched Polymer and Its Performance on Enhanced Oil Recovery.

作者信息

Qiao Sanyuan, Liu Qingwang, Zhang Xian, Che Hongchang

机构信息

Petroleum Engineering, Northeast Petroleum University, Daqing, China.

Wells and Operation Department, PetroChina International Middle East, Beijing, China.

出版信息

Front Chem. 2021 Nov 5;9:738717. doi: 10.3389/fchem.2021.738717. eCollection 2021.

Abstract

A hyperbranched carboxylate-type polymer was synthesized through esterification and carboxymethylation, and its performance on enhanced oil recovery was experimentally evaluated. The optimum condition for esterification was 8 h at 120°C, where 3% PTSA as the catalyst and 9:1 mol ratio of the AB intermediate and trimethylolpropane were used. The optimum condition for carboxymethylation was 4 h at 80°C. The critical micelle concentration of the hyperbranched polymer was 433.63 mg/L, the Krafft point was 5°C, and the surface tension was lowered to 28 mN/m. In the range of 400-500 mg/L concentration, the adsorption onto the oil sand surface achieved equilibrium, and micellar solubilization reached 600 ml/mol. The interfacial tension can be lowered to a level of 10mN/m by the single use of the hyperbranched polymer, and the value further decreased to a level of 10mN/m while being formulated with sodium dodecylsulfate or NaOH. Oil recovery of water flooding was further enhanced by the single use of a hyperbranched polymer or the combination of hyperbranched polymer/sodium dodecylsulfate. The latter exhibited more prosperous advantages in low-permeability reservoirs.

摘要

通过酯化和羧甲基化反应合成了一种超支化羧酸盐型聚合物,并对其提高采收率的性能进行了实验评估。酯化的最佳条件是在120℃下反应8小时,使用3%的对甲苯磺酸作为催化剂,AB中间体与三羟甲基丙烷的摩尔比为9:1。羧甲基化的最佳条件是在80℃下反应4小时。超支化聚合物的临界胶束浓度为433.63mg/L,克拉夫特点为5℃,表面张力降至28mN/m。在400-500mg/L浓度范围内,在油砂表面的吸附达到平衡,胶束增溶量达到600ml/mol。单独使用超支化聚合物可将界面张力降至10mN/m的水平,与十二烷基硫酸钠或氢氧化钠复配时,该值进一步降至10mN/m的水平。单独使用超支化聚合物或超支化聚合物/十二烷基硫酸钠组合均可进一步提高水驱采收率。后者在低渗透油藏中表现出更显著的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc83/8602859/e859726809cd/fchem-09-738717-g001.jpg

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