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[Poly(ethylene terephthalate) ionomer]/silicate hybrid materials via polymer-in situ sol-gel reactions

机译:[聚(对苯二甲酸乙二酯)离聚物] /硅酸盐杂化材料通过聚合物原位溶胶-凝胶反应

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摘要

A scheme was developed for producing poly(ethylene terephthalate (PET) ionomer)/silicate hybrid materials via polymer-in situ sol-gel reactions for tetraethylorthosilicate (TEOS) using different solvents. Scanning electron microscopy/EDAX studies revealed that silicate structures existed deep within PET ionomer films that were melt pressed from silicate-incorporated resin pellets. Si-29 solid-state NMR spectroscopy revealed considerable Si-O-Si bond formation, but also a significant fraction of SiOH groups. Na-23 solid-state NMR spectra suggested the presence of ionic aggregates within the unfilled PET ionomer, and that these aggregates do not suffer major structural rearrangements by silicate incorporation. For an ionomer treated with TEOS using MeCl2, Na+ ions are less associated with each other than in the unfilled control, suggesting silicate intrusion between PET-SO3- Na+ ion pair associations. The ionomer treated with TEOS + tetrachloroethane had more poorly formed ionic aggregates, which illustrates the influence of solvent type on ionic aggregation. First-scan DSC thermograms for the ionomers demonstrate an increase in crystallinity after the incorporation of silicates, but solvent-induced crystallization also appears to be operative. Second-scan DSC thermograms also suggest that the addition of silicate particles is not the only factor implicated in recrystallization, and that solvent type is important even in second-scan behavior. Silicate incorporation does not profoundly affect the second scan T-g vs. solvent type, i.e., chain mobility in the amorphous regions is not severely restricted by silicate incorporation. Recrystallization and melting in these hybrids appears to be due to an interplay between a solvent-induced crystallization that strongly depends on solvent type and interactions between PET chains and in situ grown, sol-gel-derived silicate particles. (C) 2002 Wiley Periodicals, Inc. [References: 47]
机译:开发了一种通过使用不同溶剂的原硅酸四乙酯(TEOS)的聚合物原位溶胶-凝胶反应生产聚对苯二甲酸乙二酯(PET)离聚物/硅酸盐杂化材料的方案。扫描电子显微镜/ EDAX研究表明,在掺有硅酸盐的树脂粒料中熔融压制的PET离聚物薄膜中,硅酸盐结构深处存在。 Si-29固态NMR光谱显示大量的Si-O-Si键形成,但也有很大一部分的SiOH基团。 Na-23固态NMR光谱表明未填充的PET离聚物中存在离子聚集体,并且这些聚集体不会因掺入硅酸盐而遭受重大的结构重排。对于使用MeCl2用TEOS处理的离聚物,与未填充的对照相比,Na +离子之间的缔合较少,这表明PET-SO3- Na +离子对缔合之间的硅酸盐侵入。用TEOS +四氯乙烷处理的离聚物具有较差的离子聚集体,这说明了溶剂类型对离子聚集体的影响。离聚物的初次扫描DSC热谱图表明,掺入硅酸盐后结晶度增加,但溶剂诱导的结晶似乎也起作用。二次扫描DSC热谱图还表明,硅酸盐颗粒的添加不是重结晶的唯一因素,即使二次扫描行为,溶剂类型也很重要。与溶剂类型相比,硅酸盐的掺入不会对二次扫描T-g产生深远的影响,即无定形区域中的链迁移率不受硅酸盐掺入的严重限制。这些杂化物中的重结晶和熔融似乎是由于溶剂诱导的结晶之间的相互作用,该相互作用很大程度上取决于溶剂类型以及PET链与原位生长的溶胶-凝胶衍生的硅酸盐颗粒之间的相互作用。 (C)2002 Wiley Periodicals,Inc. [参考:47]

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