过硫酸铵
聚合物
高分子化学
单体
材料科学
甲基丙烯酰胺
化学工程
自愈水凝胶
水溶液
共聚物
凝点
化学
丙烯酰胺
复合材料
物理化学
工程类
作者
Hongbin Yang,Wanli Kang,Hairong Wu,Zhe Li,Yang Yu,Yao Lu,Liming Zhang,Man‐Ying Wang,Yuwei He
摘要
ABSTRACT One kind of polymer gel P(AM‐AA‐AMPS) was prepared by radical aqueous copolymerization, using acrylamide (AM), acrylic acid (AA) and 1‐acrylanmido‐2‐methylpropanesulfonic acid (AMPS) as monomers, N,N‐methacrylamide (MBA) as crosslinker and ammonium persulfate (APS) as initiator. The microstructure and molecular structure of the polymer gel were characterized by environmental scanning electron microscope (ESEM), infrared spectrometer (IR) and thermal gravity analysis (TGA). Main factors affecting the gelation behavior of P(AM‐AA‐AMPS) were qualitatively and quantitatively studied by multi‐speckle diffusion wave spectroscopy (MS‐DWS) technology, and the elasticity index (EI) and macroscopic viscosity index (MVI) were introduced to evaluate the elasticity and viscosity of the polymer gel. The results show that the synthesized P(AM‐AA‐AMPS) polymer gel has three‐dimensional network structure gel with thermally resistant and salts tolerant groups. The EI and MVI of solution increase abruptly during the gelation time and the two indexes tend to stabilize. Under certain conditions, with the increase of reaction temperature and concentration of monomers and initiator, the gelation time of polymer gel gets shorter and the gel strength increases; with the increase of concentration of crosslinker, the strength of polymer gels increases, while the gelation time remains almost unchanged. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133 , 43364.
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