石油化工
石油化工
석유화공
PETROCHEMICAL TECHNOLOGY
2015年
1期
83-88
,共6页
高媛萍%林蔚然%龙秋莲%张汝生%伊卓
高媛萍%林蔚然%龍鞦蓮%張汝生%伊卓
고원평%림위연%룡추련%장여생%이탁
可控延迟%压裂液%三元共聚物%复合交联剂
可控延遲%壓裂液%三元共聚物%複閤交聯劑
가공연지%압렬액%삼원공취물%복합교련제
delay-controllable%fracturing fluid%terpolymer%composite crosslinking agent
采用自由基水溶液共聚法,以丙烯酰胺(AM)、丙烯酸(AA)、2-丙烯酰胺-2-甲基丙磺酸(AMPS)等为功能单体合成了AM/AA/AMPS三元共聚物稠化剂(BHY9-6)。以BHY9-6为基液,加入一种中高温复合交联剂(QI-23)及其他添加剂得到了一种可控延迟的合成聚合物压裂液(简称B-Q压裂液)。研究了B-Q压裂液的交联性能、耐温耐剪切性能和破胶性能等。实验结果表明,通过控制交联剂静置时间、交联剂pH或基液pH中的一个或几个因素,可将B-Q压裂液的交联时间控制在合适的范围内(如40~120 s)。B-Q压裂液中各添加剂之间的配伍性好,对压裂液的交联时间及挑挂性能基本无影响,对耐温耐剪切性能的影响较小。B-Q压裂液经破胶后,破胶液黏度均小于3 mPa·s、破胶液表面张力均低于22 mN/m、无残渣、对地层伤害较小、破胶性能良好。B-Q压裂液与华北油田、东北油田、胜利油田等压裂用水配伍性好,性能优良,具有广泛的应用前景。
採用自由基水溶液共聚法,以丙烯酰胺(AM)、丙烯痠(AA)、2-丙烯酰胺-2-甲基丙磺痠(AMPS)等為功能單體閤成瞭AM/AA/AMPS三元共聚物稠化劑(BHY9-6)。以BHY9-6為基液,加入一種中高溫複閤交聯劑(QI-23)及其他添加劑得到瞭一種可控延遲的閤成聚閤物壓裂液(簡稱B-Q壓裂液)。研究瞭B-Q壓裂液的交聯性能、耐溫耐剪切性能和破膠性能等。實驗結果錶明,通過控製交聯劑靜置時間、交聯劑pH或基液pH中的一箇或幾箇因素,可將B-Q壓裂液的交聯時間控製在閤適的範圍內(如40~120 s)。B-Q壓裂液中各添加劑之間的配伍性好,對壓裂液的交聯時間及挑掛性能基本無影響,對耐溫耐剪切性能的影響較小。B-Q壓裂液經破膠後,破膠液黏度均小于3 mPa·s、破膠液錶麵張力均低于22 mN/m、無殘渣、對地層傷害較小、破膠性能良好。B-Q壓裂液與華北油田、東北油田、勝利油田等壓裂用水配伍性好,性能優良,具有廣汎的應用前景。
채용자유기수용액공취법,이병희선알(AM)、병희산(AA)、2-병희선알-2-갑기병광산(AMPS)등위공능단체합성료AM/AA/AMPS삼원공취물주화제(BHY9-6)。이BHY9-6위기액,가입일충중고온복합교련제(QI-23)급기타첨가제득도료일충가공연지적합성취합물압렬액(간칭B-Q압렬액)。연구료B-Q압렬액적교련성능、내온내전절성능화파효성능등。실험결과표명,통과공제교련제정치시간、교련제pH혹기액pH중적일개혹궤개인소,가장B-Q압렬액적교련시간공제재합괄적범위내(여40~120 s)。B-Q압렬액중각첨가제지간적배오성호,대압렬액적교련시간급도괘성능기본무영향,대내온내전절성능적영향교소。B-Q압렬액경파효후,파효액점도균소우3 mPa·s、파효액표면장력균저우22 mN/m、무잔사、대지층상해교소、파효성능량호。B-Q압렬액여화북유전、동북유전、성리유전등압렬용수배오성호,성능우량,구유엄범적응용전경。
A terpolymer(BHY9-6) was synthesized from acrylamide(AM),acrylic acid(AA) and 2-acrylamide-2-methyl propane sulfonic acid(AMPS) through aqueous solution copolymerization. By adding a medium/high temperature composite crosslinking agent(QI-23) and other additives to the BHY9-6 base fluid,a delay-controllable copolymer fracturing fluid (B-Q fracturing fluid)was prepared. The temperature resistance,shearing performance,crosslinking performance and gel breaking performance of the B-Q fracturing fluid were investigated. The results showed that the crosslinking time could be adjusted in a certain range(e.g. 40-120 s) by changing one or several factors,namely standing time of crosslinking agent,pH of crosslinking agent and pH of the base fluid. The additives barely affected the crosslinking performance of the B-Q fracturing fluid,and slightly influenced its temperature resistance and shearing performance. The B-Q fracturing fluid could be completely broken. The gel breaking fluid with viscosity of less than 3 mPa·s and surface tension of less than 22 mN/m has no residue and little formation damage. The B-Q fracturing fluid has good compatibility with the fracturing water of oilfields.