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Metatungstate and tungstoniobate-containing LDHs: Preparation, characterisation and activity in epoxidation of cyclooctene

机译:含钨酸钨酸和钨酸钨酸的LDH:环辛烯的制备,表征和环氧化活性

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Polyoxometalates (POMs) H2W12O406- and W4Nb2O194- have been intercalated between the brucite-like layers of Mg, Al and Zn, Al hydrotalcites by anion exchange, starting from the corresponding nitrate precursors. The solids have been characterised by Powder X-ray Diffraction (PXRD), Fourier Transform infrared (FT-IR) spectroscopy, N-2 adsorption-desorption at -196 degrees C and thermogravimetric (TG) and differential thermal analyses (DTA), and have been tested in the epoxidation of cyclooctene using H2O2 or t-BuOOH as oxidants. The results show that both anions are effectively located in the interlayer space maintaining their pristine structures without depolymerisation. Upon intercalation of such large anions microporosity is developed and subsequently an increase in the specific surface 06areas is also observed. In general, the prepared materials possess catalase and epoxidation activity, with ZnAl-intercalated H2W12O406- giving the best results in terms of epoxide yield (17% at 24 h). Product selectivity is different for the intercalated and free POMs, the latter yielding 1,2-cyclooctanediol as the only product, whereas the former produces only the epoxide. The epoxidation reaction seems to be catalysed in homogeneous phase by the POM. (c) 2007 Elsevier Ltd. All rights reserved.
机译:从相应的硝酸盐前体开始,通过阴离子交换,将多金属氧酸盐(POM)H2W12O406-和W4Nb2O194-插在镁铝镁合金的镁,铝和锌,铝水滑石类水镁石层之间。固体的特征在于粉末X射线衍射(PXRD),傅立叶变换红外(FT-IR)光谱,-196℃和热重(TG)和差热分析(​​DTA)的N-2吸附-脱附,以及已使用H2O2或t-BuOOH作为氧化剂在环辛烯的环氧化中进行了测试。结果表明,两种阴离子均有效地位于中间层空间中,保持其原始结构而不解聚。在插入如此大的阴离子后,形成了微孔,随后还观察到了比表面积06的增加。通常,所制备的材料具有过氧化氢酶和环氧化活性,其中嵌入ZnAl的H2W12O406-在环氧化物产率方面(24小时为17%)提供了最佳结果。插层和游离POM的产物选择性不同,后者仅产生1,2-环辛二醇作为唯一产物,而前者仅产生环氧化物。环氧化反应似乎是由POM在均相中催化的。 (c)2007 Elsevier Ltd.保留所有权利。

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