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首页> 外文期刊>Bulletin of the American Physical Society >APS -APS March Meeting 2017 - Event - Disordered bicontinuous nanostructures from randomly end-linked copolymer networks
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APS -APS March Meeting 2017 - Event - Disordered bicontinuous nanostructures from randomly end-linked copolymer networks

机译:APS -APS 2017年3月会议-事件-来自随机末端连接的共聚物网络的无序双连续纳米结构

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Self-assembly within randomly cross-linked copolymer networks can provide co-continuous nanometer-scale structures in a wide variety of material systems. Copolymer networks prepared by end-linking pairs of telechelic polymers in a common solvent are particularly attractive in this regard as systems with well-defined and easily tuned network parameters. For sufficiently high levels of immiscibility between the constituent polymers, removal of solvent leads to microphase separation into disordered nanoscale structures. Using copolymer networks with a glassy strand and an ion-conducting strand, we have found that disordered morphologies with well-percolated domains of both phases persist across a wide range of compositions of the two materials. Similarly, by including a degradable component, we have found that interpenetrating porous structures are formed over a wide range of loading. These materials show a narrow distribution of pore sizes that can be tuned by adjusting the molecular weight of the starting polymers.
机译:随机交联的共聚物网络中的自组装可在多种材料系统中提供连续的纳米级结构。在这方面,通过将遥测聚合物对在一种普通溶剂中进行末端连接而制备的共聚物网络,在具有明确定义且易于调整的网络参数的系统方面特别有吸引力。对于组成聚合物之间足够高的不溶混性,溶剂的去除导致微相分离成无序的纳米级结构。使用具有玻璃状链和离子导电链的共聚物网络,我们发现两种相都具有良好渗透区的无序形态在两种材料的广泛组成范围内仍然存在。类似地,通过包含可降解组分,我们发现互穿的多孔结构是在较宽的载荷范围内形成的。这些材料显示出狭窄的孔径分布,可以通过调节起始聚合物的分子量来调节。

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