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Synthesis, characterization and solution properties of hydrophobically modified polyelectrolyte poly(AA-co-TMSPMA)

机译:疏水改性聚电解质聚(AA-co-TMSPMA)的合成,表征和溶液性质

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The hydrophobically modified polyelectrolyte was synthesized using precipitation polymerization of acrylic acid and 3-[tris(trimethylsilyloxy)silyl]propyl methacrylate (TMSPMA) in various molar ratios in supercritical carbon dioxide. FT-IR, H-1 NMR, capillary viscometry, rotational viscometer, transmission electron microscopy and fluorescence spectroscopy were used to characterize this copolymer. The viscosity of the copolymers showed a strong dependence on pH with a maximum at pH=5.5. Associating morphologies of the copolymer were observed by TEM. Associating morphologies of poly(AA-co-TMSPMA) solution changed from a global structure to a shell-core structure with increasing hydrophobic levels. A solution of sample PAT4 with a shell-core structure had the largest viscosity value. In addition, the critical micelle concentration of copolymer solution, cmc, was determined from the relative viscosity. The critical micelle concentration was further confirmed by fluorescence spectroscopy using 1-pyrenemethylamine hydrochloride, PyMeA center dot HCl, as a cationic fluorescent probe. The cmc was determined from the intensity ratios, the first to the third emission peaks I (1)/I (3), and the excimer to monomer I (E)/I (M) ratio of the pyrene probe as a function of concentration.
机译:使用丙烯酸和甲基丙烯酸3- [三(三甲基硅烷氧基)硅烷基]丙基甲基丙烯酸酯(TMSPMA)的沉淀聚合反应,在超临界二氧化碳中合成疏水改性的聚电解质。 FT-IR,H-1 NMR,毛细管粘度法,旋转粘度计,透射电子显微镜和荧光光谱法表征了该共聚物。共聚物的粘度显示出对pH的强烈依赖性,在pH = 5.5时最大。通过TEM观察到共聚物的缔合形态。聚(AA-co-TMSPMA)溶液的相关形态从疏水性增加,从整体结构变为壳核结构。具有壳核结构的样品PAT4的溶液具有最大的粘度值。另外,由相对粘度确定共聚物溶液的临界胶束浓度cmc。通过使用1-methyl甲胺盐酸盐,PyMeA中心点HCl作为阳离子荧光探针的荧光光谱进一步确定了临界胶束浓度。根据强度比、,发射峰的第一至第三发射峰I(1)/ I(3)以及the探针的受激物与单体I(E)/ I(M)之比确定浓度,浓度。

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