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New Macroporous Crosslinked Polymer Gels Prepared via Living Radical Polymerization

机译:通过活性自由基聚合制备新的大孔交联聚合物凝胶

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Macroporous crosslinked polymer gels have been prepared via TEMPO-mediated living radical polymerization of divinylbenzene (DVB) in a solvent with a counter polymer. Incorporating a counter polymer, poly(dimethylsiloxane) (PDMS), induced macroscopic spinodal-type phase separation during the course of polymerization of DVB while suppressing the segregation of DVB-derived particles from the solution by living polymerization. Well-defined macroporous morphologies comprising continuous DVB-derived skeletons have thus obtained. Macropore volume and diameter were independently controlled by altering the concentrations of PDMS and the solvent. Since the present polymer gels are prepared using only the multifunctional "crosslinker", mechanical durability against bending and compression was found to be as high as inorganic ceramics with similar morphologies and porosities.
机译:通过在用反应聚合物的溶剂中通过蒸馏果介导的二乙烯基苯(DVB)的活性自由基聚合制备大孔交联聚合物凝胶。掺入反应聚合物,聚(二甲基硅氧烷)(PDMS),在DVB的聚合过程中诱导宏观旋光膜型相分离,同时通过生物聚合抑制DVB衍生的颗粒的偏析。由此获得了包含连续DVB衍生骨架的明确定义的大孔形态。通过改变PDMS和溶剂的浓度来独立地控制大孔体积和直径。由于仅使用多功能的“交联剂”制备本发明的聚合物凝胶,因此发现针对弯曲和压缩的机械耐久性与具有相似形态和孔隙的无机陶瓷一样高。

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