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具有柔软甲基丙烯酸酯中间链段和坚硬苯乙烯外支链的AxBAx型嵌段接枝聚合物:合成、形态及力学性能

AxBAx-type block-graft polymers with soft methacrylate middle segments and hard styrene outer grafts: synthesis, morphology, and mechanical properties.

作者信息

Miura Yu, Kaneko Takeshi, Satoh Kotaro, Kamigaito Masami, Jinnai Hiroshi, Okamoto Yoshio

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.

出版信息

Chem Asian J. 2007 May 4;2(5):662-72. doi: 10.1002/asia.200600403.

Abstract

Novel copolymers with controlled architectures can function as new building blocks for well-defined nanostructures on the basis of microphase separation, unlike conventional ABA triblock copolymers. A series of well-defined A(x)BA(x)-type block-graft copolymers consisting of soft middle segments (dodecyl methacrylate (DMA)) and hard outer graft chains (styrene (St)) were synthesized by ruthenium-catalyzed living radical block and graft polymerization. NMR spectroscopy and size-exclusion chromatography combined with multiangle laser light scattering confirmed the well-defined structure of the A(x)BA(x) block-graft copolymers with backbones and graft chains of controlled lengths. Transmission electron microscopy and transmission electron microtomography revealed a series of morphologies for the copolymers. Morphological changes were observed from PSt "honeycomb" cylinders to lamellae and poly(DMA) cylinders with increasing PSt-graft content, whereby the phase diagram was shifted significantly to lower volume fractions of the larger-number component (St) relative to those of the corresponding ABA triblock copolymers. More specifically, poly(DMA) cylinders were observed even before the St content reached 50 wt %. The A(x)BA(x) and ABA copolymers with 17-30 wt % of St exhibited characteristics of a thermoplastic elastomer with tensile strengths of 1-6 MPa and elongations at break of 70-300 %. These mechanical properties can be related well to the microphase structures of the A(x)BA(x) and ABA copolymers.

摘要

与传统的ABA三嵌段共聚物不同,具有可控结构的新型共聚物可作为基于微相分离的明确定义的纳米结构的新构建单元。通过钌催化的活性自由基嵌段和接枝聚合反应,合成了一系列由软质中间链段(甲基丙烯酸十二酯(DMA))和硬质外部接枝链(苯乙烯(St))组成的结构明确的A(x)BA(x)型嵌段接枝共聚物。核磁共振光谱以及尺寸排阻色谱结合多角度激光光散射证实了具有可控长度主链和接枝链的A(x)BA(x)嵌段接枝共聚物的明确结构。透射电子显微镜和透射电子显微断层扫描揭示了共聚物的一系列形态。随着PSt接枝含量的增加,观察到形态从PSt“蜂窝”圆柱体转变为片层和聚(DMA)圆柱体,由此相图相对于相应的ABA三嵌段共聚物显著向数量较多的组分(St)的较低体积分数偏移。更具体地说,甚至在St含量达到50 wt%之前就观察到了聚(DMA)圆柱体。含有17 - 30 wt% St的A(x)BA(x)和ABA共聚物表现出热塑性弹性体的特性,拉伸强度为1 - 6 MPa,断裂伸长率为70 - 300%。这些力学性能与A(x)BA(x)和ABA共聚物的微相结构密切相关。

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