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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >A solid-state ~13C NMR study on phase heterogeneity in the miscible blend of amorphous poly(benzyl methacrylate) with semicrystalline poly(ethylene oxide)
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A solid-state ~13C NMR study on phase heterogeneity in the miscible blend of amorphous poly(benzyl methacrylate) with semicrystalline poly(ethylene oxide)

机译:固态〜13C NMR研究非晶态聚(甲基丙烯酸苄酯)与半结晶聚(环氧乙烷)混溶共混物中的相异质性

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摘要

Therotating-frame spin-I:lttice relaxation time for protons,T1P(IH), was measured indirectly from f3CcP/MAS/DD NMR to probe possible molecular scales of heterogeneity in the miscible poly(benzyl methacrylate) (PBzMA)/poly(ethylene oxide) (PEa) blend over the whole composition range. According to the NMR results, only one phase was observed for the blends in which the PEa component is less than 16% (w/w). This miscible amorphous phase withPBzMA andPEa chains was mixed at the molecular level. Three phases were detected for the blends with PEa component >16%,. containing one mjsGible homQgenous PBzMA-rich phase, one constrained PEa phase and one crystalline PEa phase. The PEa component asymptotically increases in the miscible homogenous PBzMA-richphase as the PEa composi- tion increases,. NMR analysis helped resolve the complex phase domains in the PBzMA/PEa blend that is composed of an amorphous roixture of PBzMA/PEa and crystalline PEa spherulite regions. The intra. and inter-lamellar domains in the PEa spherulites are influenced and complicated by the surrounding amorphous PBzMA/P£a mixture with varying composition.
机译:从f3CcP / MAS / DD NMR间接测量质子的旋转框架自旋I:质子弛豫时间T1P(IH),以探索可混溶的聚甲基丙烯酸苄酯(PBzMA)/聚乙烯中可能存在的异质性分子尺度氧化物(PEa)混合物在整个组成范围内。根据NMR结果,对于PEa组分小于16%(w / w)的共混物,仅观察到一个相。具有PBzMA和PEa链的这种可混溶的非晶相在分子水平上混合。检测到PEa组分> 16%的混合物的三相。包含一个易混合的富含PBzMA的均质相,一个受约束的PEa相和一个结晶性PEa相。随着PEa组成的增加,可混溶的均匀PBzMA富相中的PEa成分逐渐增加。 NMR分析有助于解决PBzMA / PEa混合物中的复杂相域,该混合物由PBzMA / PEa的非晶形混合物和结晶的PEa球晶区域组成。内。周围的无定形PBzMA / P £ a混合物具有不同的组成,从而影响和复杂化PEa球晶的层间和层间结构域。

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