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部分水解聚丙烯酰胺/乳酸铬在油田污水条件下的成胶特性研究
油田化学
2016年 33卷 第2期
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Title
Gelling Characteristic of Partially Hydrolyzed Polyacrylamide/Lactic Acid Chromium Gel in Oilfield Sewage
Authors
WANG Keliang, KONG Hui,FU Guoqiang,LI Weiliang
摘要
为了采用油田污水配制性能优良的聚合物弱凝胶调驱剂, 研究了油田污水中各组分对部分水解聚丙烯酰胺/乳酸铬成胶性能的影响, 优选出适合污水条件下的部分水解聚丙烯酰胺/乳酸铬凝胶体系, 考察了该凝胶体系对岩心的封堵作用。结果表明: 随着 Na+、 Mg2+、 Ca2+浓度及矿化度的增加, 部分水解聚丙烯酰胺/乳酸铬成胶时间缩短、 凝胶黏度增加; 随 S2-浓度增加, 成胶时间延长、 凝胶黏度降低, S2-加量大于 30 mg/L时, 体系难以成胶; 含油量对凝胶的成胶无影响; 凝胶最佳配方为: 三氯化铬与乳酸摩尔比 1∶8, 部分水解聚丙烯酰胺、 交联剂和硫脲的质量浓度分别为 2000、 200和 800 mg/L, 该凝胶体系的成胶时间为 25 h, 成胶后的黏度为 20 Pa·s, 对岩心的封堵率达 85%以上, 可用油田采出污水配制。表8参12
Abstract
In order to prepare polymer weak gel profile control agent with high performance using oilfield sewage,the influence of sewage component on the gelling property of partially hydrolyzed polyacrylamide/lactic acid chromium gel was studied. The optimum formula of partially hydrolyzed polyacrylamide/lactic acid chromium gel system that was suitable for sewage was selected,and the plugging effect was investigated. The results showed that the gelling time of partially hydrolyzed polyacrylamide/lactic acid chromium gel system decreased and gel viscosity increased with the increase of Na+,Mg2+ and Ca2+ concentration and salinity. The gelling time increased and gel viscosity decreased with increasing concentration of S2-. When the concentration of S2+ was more than 30 mg/L,it was hard to gel. The oil content had no effect on gel. The optimum formula of gel was obtained as follows: 1∶8 the molar ratio of chromium trichloride to lactic acid,2 g/L partially hydrolyzed polyacrylamide,200 mg/L crosslinking agent,800 mg/L thiourea. The gelling time was 25 hrs and the viscosity of gel was 20 Pa·s. The core plugging rate could reach more than 85% in three different permeability cores,indicating good compatibility between the gel and sewage.
关键词:
部分水解聚丙烯酰胺;
乳酸铬;
污水;
凝胶;
调剖剂;
成胶性能;
Keywords:
partially hydrolyzed polyacrylamide;
lactic acid chromium;
sewage;
gel;
profile control agent;
gelling characteristic;
DOI
10.19346/j.cnki.1000-4092.2016.06.011