物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2014年
5期
908-916
,共9页
曹绪龙%李静%杨勇%张继超%张磊%张路%赵濉
曹緒龍%李靜%楊勇%張繼超%張磊%張路%趙濉
조서룡%리정%양용%장계초%장뢰%장로%조수
部分水解聚丙烯酰胺%疏水改性聚丙烯酰胺%十二烷基苯磺酸钠%十六烷基三甲基溴化铵%界面剪切流变
部分水解聚丙烯酰胺%疏水改性聚丙烯酰胺%十二烷基苯磺痠鈉%十六烷基三甲基溴化銨%界麵剪切流變
부분수해취병희선알%소수개성취병희선알%십이완기분광산납%십륙완기삼갑기추화안%계면전절류변
Partial hydrolysis polyacrylamide%Hydrophobical y modified polyacrylamide%Sodium dodecyl benzene sulfonate%Hexadecyl trimethyl ammonium bromide%Interfacial shear rheology
利用双锥法研究了表面活性剂十二烷基苯磺酸钠(SDBS)和十六烷基三甲基溴化铵(CTAB)对油田现场用部分水解聚丙烯酰胺(PHPAM)和疏水改性聚丙烯酰胺(HMPAM)溶液的界面剪切流变性质的影响,实验结果表明: HMPAM分子通过疏水作用形成界面网络结构,界面剪切复合模量明显高于PHPAM. SDBS和CTAB通过疏水相互作用与HMPAM分子中的疏水嵌段形成聚集体,破坏界面网络结构,剪切模量随表面活性剂浓度增大明显降低.同时,界面膜从粘性膜向弹性膜转变.低SDBS浓度时,少量SDBS分子与PHPAM形成混合吸附膜,界面膜强度略有升高; SDBS浓度较高时,界面层中PHPAM分子被顶替,吸附膜强度开始减弱.阳离子表面活性剂CTAB通过静电相互作用中和PHPAM分子的负电性,造成聚合物链的部分卷曲,从而降低界面膜强度.弛豫实验结果证实了表面活性剂破坏HMPAM网络结构的机理.
利用雙錐法研究瞭錶麵活性劑十二烷基苯磺痠鈉(SDBS)和十六烷基三甲基溴化銨(CTAB)對油田現場用部分水解聚丙烯酰胺(PHPAM)和疏水改性聚丙烯酰胺(HMPAM)溶液的界麵剪切流變性質的影響,實驗結果錶明: HMPAM分子通過疏水作用形成界麵網絡結構,界麵剪切複閤模量明顯高于PHPAM. SDBS和CTAB通過疏水相互作用與HMPAM分子中的疏水嵌段形成聚集體,破壞界麵網絡結構,剪切模量隨錶麵活性劑濃度增大明顯降低.同時,界麵膜從粘性膜嚮彈性膜轉變.低SDBS濃度時,少量SDBS分子與PHPAM形成混閤吸附膜,界麵膜彊度略有升高; SDBS濃度較高時,界麵層中PHPAM分子被頂替,吸附膜彊度開始減弱.暘離子錶麵活性劑CTAB通過靜電相互作用中和PHPAM分子的負電性,造成聚閤物鏈的部分捲麯,從而降低界麵膜彊度.弛豫實驗結果證實瞭錶麵活性劑破壞HMPAM網絡結構的機理.
이용쌍추법연구료표면활성제십이완기분광산납(SDBS)화십륙완기삼갑기추화안(CTAB)대유전현장용부분수해취병희선알(PHPAM)화소수개성취병희선알(HMPAM)용액적계면전절류변성질적영향,실험결과표명: HMPAM분자통과소수작용형성계면망락결구,계면전절복합모량명현고우PHPAM. SDBS화CTAB통과소수상호작용여HMPAM분자중적소수감단형성취집체,파배계면망락결구,전절모량수표면활성제농도증대명현강저.동시,계면막종점성막향탄성막전변.저SDBS농도시,소량SDBS분자여PHPAM형성혼합흡부막,계면막강도략유승고; SDBS농도교고시,계면층중PHPAM분자피정체,흡부막강도개시감약.양리자표면활성제CTAB통과정전상호작용중화PHPAM분자적부전성,조성취합물련적부분권곡,종이강저계면막강도.이예실험결과증실료표면활성제파배HMPAM망락결구적궤리.
The effects of surfactants, namely sodium dodecylbenzenesulfonate (SDBS) and hexadecyltrimethylammonium bromide (CTAB), on the interfacial shear rheological properties of partial y hydrolyzed polyacrylamide (PHPAM) and hydrophobical y modified polyacrylamide (HMPAM) solutions, which are used in oilfields, were studied using a biconical method. The experimental results show that the interfacial shear complex modulus of HMPAM is significantly higher than that of PHPAM, because an interfacial net structure can be formed by HMPAM molecules through hydrophobic interactions. The SDBS and CTAB molecules can form interfacial aggregates with hydrophobic blocks of HMPAM and destroy the interfacial net structure, which results in a significant decrease in the shear modulus with increasing surfactant concentration. At the same time, the properties of the interfacial film change from viscous to elastic. At low SDBS concentrations, the mixed adsorption film formed by PHPAM and a few SDBS molecules has enhanced strength. However, SDBS molecules can displace PHPAM molecules at the interface and weaken the film at higher surfactant concentrations. The cationic surfactant CTAB neutralizes the negative charge on PHPAM, leading to partial curling of the polymer chain, which decreases the film strength. Relaxation measurements confirmed our mechanism involving destruction of the interfacial net structure of HMPAM by the surfactant.