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Photopolymerizable Nanogels as Macromolecular Precursors to Covalently Crosslinked Water-Based Networks

机译:可光聚合的纳米凝胶作为共价交联的水基网络的高分子前体

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摘要

We present a strategy for directly and efficiently polymerizing aqueous dispersions of reactive nanogels into covalently crosslinked polymer networks with properties that are determined by the initial chemical and physical nanogel structure. This technique can extend the range of achievable properties and architectures for networks formed in solution, particularly in water where monomer selection for direct polymerization and the final network properties are quite limited. Nanogels were initially obtained from a solution polymerization of a hydrophilic monomethacrylate and either a hydrophilic PEG-based dimethacrylate or a more hydrophobic urethane dimethacrylate, which produced globular particles with diameters of 10–15 nm with remarkably low polydispersity in some cases. Networks derived from a single type of nanogel or a blend of nanogels with different chemistries when dispersed in water gelled within minutes when exposed to low intensity UV light. Modifying the nanogel structure changes both covalent and non-covalent secondary interactions in the crosslinked networks and reveals critical design criteria for the development of networks from highly internally branched, nanoscale prepolymer precursors.
机译:我们提出了一种策略,可以直接有效地将反应性纳米凝胶的水分散体聚合成具有由初始化学和物理纳米凝胶结构决定的性能的共价交联的聚合物网络。该技术可以扩展溶液中形成的网络可达到的性能和结构的范围,尤其是在水中,直接聚合的单体选择和最终网络性能受到很大限制的水中。纳米凝胶最初是由亲水性单甲基丙烯酸酯与亲水性基于PEG的二甲基丙烯酸酯或更具疏水性的氨基甲酸酯二甲基丙烯酸酯的溶液聚合而获得的,在某些情况下,它们产生的球形颗粒直径为10-15 nm,且多分散性非常低。当暴露于低强度紫外线下时,分散在水中的凝胶会在数分钟内形成凝胶,而这些网络是由具有不同化学性质的单一类型的纳米凝胶或纳米凝胶的混合物形成的。修饰纳米凝胶的结构会改变交联网络中的共价和非共价二级相互作用,并揭示了从高度内部分支的纳米级预聚物前体开发网络的关键设计标准。

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