Demulsification mechanism of simulated liquid production in the polymer-surfactant flooding process

Mingxin Wang, Jin Huang, Xin Zhang, Jinling Li, Chunlin Xu, Lingzhi Sun, Chunhong Song, Yuexian Zhang
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Abstract

As a new type of oil displacement agent, the compound of polymer-surfactant has a strong ability of increasing viscosity, emulsifying, etc. Results of the field test showed that the polymer-surfactant flooding can enhance oil recovery by 18.8% above water flooding. Field test showed that compared with polymer flooding, the settling time of the produced liquid of polymer-surfactant flooding is longer, and dehydrated electricity is higher, so it is more difficult to handle the produced fluid which has a higher requirement for adaptability of dehydration system of water and polymer flooding. To improve the matching techniques of polymer-surfactant flooding and get a satisfied demulsification result to ensure the produced liquid of polymer-surfactant is separated effectively, the demulsification and demulsification mechanism is studied. The results showed that, the demulsification effect of the non-ion polyether demulsifier is better than the cation polyether demulsifier, and the demulsification effect of the HLX-2 demulsifier which is a non-ion polyether demulsifier is the best. When the concentration of the HLX-2 demulsifier is 50mg/L, the oil content in water is 257mg/L, the water cut in oil is 28%, and the demulsification ratio is 92.5%. Increasing the content of the polymer-surfactant, the oil-water interfacial shear viscosity is increased, the demulsification is more and more difficult, and the demulsification effect of the HLX-2 demulsifier is getting worse and worse. Results showed that, polymer-surfactant molecule in the oil-water interface was replaced by the demulsifier HLX-2, and the interfacial shear viscosity and interfacial elastic modulus was reduced, and the stability of the emulsion was declined. Increasing the concentration of the demulsifier HLX-2, the replacement role enhanced. So the demulsification mechanism of the nonionic polyether demulsifier is that interface membrane is replaced. After the molecule of the demulsifier replaced the emulsifier, the strength of interfacial film was reduced, and the molecular of the demulsifier can also “catch” a few emulsion droplets, resulting in more than one droplet was coalesced, and the purpose of fast-breaking was achieved.
聚合物-表面活性剂驱模拟产液破乳机理研究
聚合物-表面活性剂复配物是一种新型的驱油剂,具有较强的增粘、乳化等作用。现场试验结果表明,聚合物表面活性剂驱油比水驱油采收率提高18.8%。现场试验表明,与聚合物驱相比,聚合物-表面活性剂驱采出液沉淀时间更长,脱水电较高,采出液处理难度较大,对水-聚合物驱脱水体系的适应性提出了更高的要求。为改进聚合物-表面活性剂驱油配套技术,获得满意的破乳效果,保证聚合物-表面活性剂采出液的有效分离,对聚合物-表面活性剂的破乳及破乳机理进行了研究。结果表明,非离子聚醚破乳剂的破乳效果优于阳离子聚醚破乳剂,其中非离子聚醚破乳剂HLX-2破乳剂的破乳效果最好。当HLX-2破乳剂浓度为50mg/L时,水中含油量为257mg/L,油中含水率为28%,破乳率为92.5%。随着聚合物-表面活性剂含量的增加,油水界面剪切粘度增大,破乳难度越来越大,HLX-2型破乳剂的破乳效果越来越差。结果表明,破乳剂HLX-2取代了油水界面中的聚合物-表面活性剂分子,降低了界面剪切粘度和界面弹性模量,降低了乳液的稳定性。随着HLX-2破乳剂浓度的增加,其替代作用增强。因此,非离子聚醚破乳剂的破乳机理是界面膜的置换。破乳剂分子取代乳化剂后,界面膜强度降低,破乳剂分子还能“抓”几个乳滴,导致多个乳滴聚结,达到快破的目的。
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