共聚物
单体
高分子化学
甲基丙烯酸酯
叔胺
粘度
胺气处理
丙烯酰胺
材料科学
特性粘度
还原粘度
Zeta电位
阳离子聚合
聚合物
化学
化学工程
有机化学
纳米颗粒
复合材料
纳米技术
工程类
作者
Hongsheng Lu,Jifeng Jiang,Zhiyu Huang,Shanshan Dai
摘要
ABSTRACT A series of copolymers PDAMs were synthesized with varying monomer ratio of acrylamide (AM) and N , N ‐dimethylaminoethyl methacrylate (DMAEMA). The resulting copolymer solution shows an interesting property of viscosity‐response which is CO 2 ‐triggered and N 2 ‐enabled. Tertiary amine groups of PDAMs experience a reversible transition between hydrophobic and hydrophilic state upon CO 2 addition and its removal, which induced different rheological behavior. A combination of zeta‐potential, laser particle‐size analysis, and electrical conductivity analysis indicated that, when the monomer mole ratio of DMAEMA and AM is less than or equal to 3 : 7, the hydrophobic association structure between the copolymer molecules was destroyed by the leading of CO 2 and caused a viscosity decrease in its solution. On the contrary, when the monomer mole ratio of DMAEMA and AM is more than 3 : 7, a more extended conformation due to the protonated tertiary amine groups is formed and the enhanced repulsive interactions among the copolymer molecule results in a rise of its solution viscosity. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40872.
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