...
首页> 外文期刊>Journal of Macromolecular Science. Pure and Applied Chemistry >Synthesis and characterization of a novel hydrophobically associating relative permeability modifier
【24h】

Synthesis and characterization of a novel hydrophobically associating relative permeability modifier

机译:新型疏水缔合相对磁导率调节剂的合成与表征

获取原文
获取原文并翻译 | 示例
           

摘要

A novel hydrophobically associating copolymer P (MPEGA-DMAEMA) has been synthesized by inverse emulsion polymerization, using N,N-dimethylaminoethyl methacrylate (DMAEMA) and methoxy polyethylene glycol acrylate (MPEGA) as comonomers. The synthesized copolymer has been characterized by FT-IR spectroscopy, 1H-NMR spectroscopy, scanning electron microscopy (SEM), thermal analysis (TA) and intrinsic viscosity measurement. The results reveal that P (MPEGA-DMAEMA) copolymer has been synthesized successfully. The copolymer has a smooth surface with many irregular caves, and has thermal stability above 170C in an atmosphere of air. Reactivity ratios of DMAEMA and MPEGA are determined by Fineman-Ross method and are shown to be equal to r(DMAEMA)=0.29 and r(MPEGA)=2.66. Intrinsic viscosity of the hydrophobically associating copolymer reaches 282.84mL/g at 30C. In temperature, salt and shear resistant experiments, the copolymer aqueous solution exhibits efficient anti-heat and salt resistance characteristics, and has unique rheological behavior. Coreflood experiment results show that the copolymer reduces permeability to water above 90%, while to oil under 40%, which indicates that the copolymer has obvious selectivity to water and oil.
机译:通过使用N,N-甲基丙烯酸二甲基氨基乙酯(DMAEMA)和甲氧基聚乙二醇丙烯酸酯(MPEGA)作为共聚单体,通过反相乳液聚合合成了新型疏水缔合共聚物P(MPEGA-DMAEMA)。通过FT-IR光谱,1H-NMR光谱,扫描电子显微镜(SEM),热分析(TA)和特性粘度测量来表征合成的共聚物。结果表明,已成功合成了P(MPEGA-DMAEMA)共聚物。该共聚物具有光滑的表面和许多不规则的凹坑,并且在空气中在170℃以上具有热稳定性。 DMAEMA和MPEGA的反应率是通过Fineman-Ross方法确定的,显示为等于r(DMAEMA)= 0.29和r(MPEGA)= 2.66。疏水缔合共聚物的特性粘度在30℃下达到282.84mL / g。在耐温度,耐盐和抗剪切的实验中,共聚物水溶液显示出有效的抗热和耐盐特性,并具有独特的流变行为。 Coreflood实验结果表明,该共聚物对90%以上的水的渗透性降低,而对40%以下的油的渗透率降低,这表明该共聚物对水和油具有明显的选择性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号