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Effect of commonly used EOR polymers on low concentration surfactant phase behaviors

机译:常用EOR聚合物对低浓度表面活性剂相行为的影响

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High molecular weight polymers are required for the purpose of mobility and conformance control during surfactant chemical flooding. However, they are usually not incorporated in the process of phase behavior tests to screen surfactant formulations. Literature review shows some particular polymers have a boosting effect on surfactant solubilization efficiency. To gain more insight into this subject, we performed phase behavior tests in the presence of four commonly used EOR polymers for low concentration surfactant systems (0.3%). They were two partially hydrolyzed polyacrylamides (HPAM) with different molecular weights, one xanthan gum, and one hydrophobically associating polymer (HAP). Their influence on the optimal salinity, solubilization ratio, quickness of phase equilibration, and middle phase rheological behavior was assessed. The results showed: (1) a decrease of surfactant solubilization efficiency and the optimal salinity was observed with HPAM polymers. This trend became more pronounced as increase of polymer concentration and molecular weight; (2) xanthan seemed to slightly increase the optimal salinity without significantly affecting middle phase volume; (3) both HPAM and xanthan did not delay or quicken the equilibration of various phases compared to the zero polymer case. The analysis of the oil/water solubilization ratios showed HPAM tended to drag water out of the middle phase, while the presence of xanthan increased the water solubilization in the middle phase; (4) the viscosity and rheology of the middle phase microemulsions were very similar for systems containing HPAM, xanthan, and zero polymer. This confirmed the partitioning of polymer molecules in the middle phase was negligible; (5) the association of HAP with surfactants thickened the surfactant-rich phase, which made the phase separation dramatically slow. These phenomena could be explained well by the nature of their molecular structures. For both water-soluble HPAM and xanthan gum, unlike the reported diblock copolymers, they lack the amphiphilic features, which prevents them from adsorbing in the surfactant film. Conversely, the introduction of hydrophobic group into the backbone renders associating polymers some surfactant-like attributes, enabling them to associate with surfactant molecules and affect the surfactant-rich phase behaviors.
机译:在表面活性剂化学洪水期间,需要高分子量聚合物来迁移率和一致性控制。然而,它们通常不掺入筛选表面活性剂配方的相行为试验中。文献综述表明一些特定的聚合物对表面活性剂溶解效率具有促进效果。为了获得更多洞察力,我们在4种常用的EOR聚合物存在下进行阶段行为试验,用于低浓度表面活性剂系统(0.3%)。它们是两种部分水解的聚丙烯酰胺(HPAM),具有不同的分子量,一个黄原胶和一种疏水性缔合聚合物(HAP)。评估它们对最佳盐度,溶解比,相平衡的速度和中间流变行为的影响。结果表明:(1)用HPAM聚合物观察表面活性剂溶解效率的降低,并用HPAM聚合物观察到最佳盐度。这种趋势变得更加明显,随着聚合物浓度和分子量的增加; (2)黄原似乎略微增加了最佳盐度,而不会显着影响中相体积; (3)与零聚合物箱相比,HPAM和黄原均未延迟或加快各个阶段的平衡。油/水溶性比的分析显示HPAM倾向于将水拖出中间阶段,而黄原的存在增加了中期的水溶性; (4)中相微乳液的粘度和流变学非常相似,对于含有HPAM,黄原烷和零聚合物的系统非常相似。这证实了中间阶段中聚合物分子的分配可忽略不计; (5)HAP与表面活性剂的关联加厚了富含表面活性剂的相,这使得相分离显着慢。可以通过其分子结构的性质来解释这些现象。对于水溶性HPAM和黄原胶,与报道的二嵌段共聚物不同,它们缺乏两亲性特征,这防止了它们在表面活性剂膜中吸附。相反,将疏水基团引入骨干呈伴者将聚合物呈一些表面活性剂样的属性,使它们能够与表面活性剂分子相关,并影响富含表面活性剂的相行为。

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