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Fabrication polymer nanofiber networks with regulated microstructures via RAFT polymerization of supramolecular gels in different solvents

机译:通过不同溶剂中超分子凝胶筏聚合的制备聚合物纳米恐怖网络具有调节微观结构

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In this article, a new diurea type gelator synthesized from heptanediamine and 2-isocyanatoethyl methacrylate was found to gel dioxane effectively. During forming the gel, the gelator molecules assembled into nano-sized fibrillary network driving by hydrogen bonds of urea groups. In cyclohexane, toluene and their mixed solvents, polymer nanofiber networks were successfully fabricated via Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization of the xerogels as both templates and monomer source. The solvent polarity was found to affect both the polymerization rate and the microstructures of polymer fibers. As more toluene was used in the mixed solvents, larger-sized fibers with improved surface roughness were obtained, together with the increased product yields. The formation mechanism of the microstructures was discussed based on MALDI-TOF-MS and TEM analytical results. Furthermore, the adsorption to acid indigo blue of the resulting samples was investigated, which indicated that the maximum adsorption capacities were correlated well with the specific surface areas of the samples.
机译:在本文中,发现由庚烷二胺和2-异氰酸乙酯合成的新的DIUREA型凝胶剂,有效地凝胶二氧烷。在形成凝胶期间,胶凝胶分子组装成通过脲基团的氢键驱动的纳米纤维网。在环己烷,甲苯和它们的混合溶剂中,通过Xerogels作为模板和单体源的Xerogels的可逆添加 - 碎片链转移(筏)聚合成功地制造了聚合物纳米纤维网络。发现溶剂极性影响聚合物纤维的聚合速率和微观结构。随着在混合溶剂中使用更多甲苯,获得了具有改善的表面粗糙度的较大尺寸的纤维,以及增加的产物产率。基于MALDI-TOF-MS和TEM分析结果讨论了微观结构的形成机制。此外,研究了所得样品的酸性靛蓝蓝的吸附,表明最大吸附能力与样品的比表面积相比很好。

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