共聚物
纳米孔
材料科学
小角X射线散射
聚苯乙烯
化学工程
高分子化学
透射电子显微镜
相(物质)
散射
复合材料
纳米技术
化学
聚合物
有机化学
光学
工程类
物理
作者
Di Zeng,Alexander E. Ribbe,Ryan C. Hayward
出处
期刊:Macromolecules
[American Chemical Society]
日期:2017-06-06
卷期号:50 (12): 4668-4676
被引量:32
标识
DOI:10.1021/acs.macromol.7b00007
摘要
Microphase separation within randomly end-linked copolymer networks (RECNs) provides access to disordered bicontinuous morphologies over a wide composition range of the constituent network strands. Here, we rely on end-linking of telechelic hydroxyl-terminated polystyrene (PS) and poly(D,Llactide) (PLA) chains of equal molecular weight, with a tetrafunctional isocyanate cross-linker in a good solvent for both strands, followed by solvent removal to induce microphase separation, and finally etching of the PLA phase to yield nanoporous materials. Transmission electron microscopy (TEM) tomographic reconstructed 3D images along with gravimetric measurements and small-angle X-ray scattering (SAXS) indicate the formation of highly interconnected structures over a range of ~40-70 vol % of PLA, while N2 adsorption measurements indicate narrowly distributed pore sizes that can be tuned by varying the strand molecular weights. Stretching of the PS/PLA copolymer networks above the glass transition temperatures of both components prior to etching the PLA phase provides a straightforward means to introduce controlled anisotropy into the 3D interconnected porous materials.
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