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Polymerization of Nonionic Surfactants: Poly(ethylene oxide) Macromonomers

机译:非离子表面活性剂的聚合:聚环氧乙烷大分子单体

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摘要

A series of polymerizable macromonomers of co-methoxy poly(ethylene oxide)_n undecyl-a-methacrylate (PEO-R-MA-n, where n = 10, 15, 40) were synthesized. The critical micelle concentration of the PEO-macromonomer with n = 40 is 6.6 × 10~(-5) mol/L at 25℃. The kinetics of its polymerization in aqueous solution follows conventional solution polymerization, i.e., first and half order with respect to the concentrations of the PEO-macromonomer and K_2S_2O_8, respectively. The rate of its polymerization in water was extremely rapid as compared to its solution polymerization in benzene. The activation energies for the polymerization were 57 kJ/mol in water but 179 kJ/mol in benzene. The aqueous system produced polymers with a number-average degree of polymerization (DP_n) ranging from about 130 to 160, but it was around 7 for the benzene system, the results suggested that organized structures and compact cores of macromonomer micelles are responsible for the unusually rapid polymerization in aqueous solution.
机译:合成了一系列可共聚的甲氧基聚(环氧乙烷)_n-甲基丙烯酸十一烷基酯(PEO-R-MA-n,其中n = 10、15、40)的大分子单体。 25℃下n = 40的PEO-大分子单体的临界胶束浓度为6.6×10〜(-5)mol / L。其在水溶液中的聚合动力学遵循常规的溶液聚合,即分别相对于PEO-大分子单体和K_2S_2O_8的浓度为一阶和半阶。与其在苯中的溶液聚合相比,其在水中的聚合速率非常快。聚合反应的活化能在水中为57 kJ / mol,在苯中为179 kJ / mol。水性体系产生的聚合物的数均聚合度(DP_n)为约130-160,但苯体系为约7,结果表明大分子胶束的组织结构和紧密核是异常的原因。在水溶液中快速聚合。

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