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首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >Synthesis of large-pore face-centered-cubic periodic mesoporous organosilicas with unsaturated bridging groups
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Synthesis of large-pore face-centered-cubic periodic mesoporous organosilicas with unsaturated bridging groups

机译:具有不饱和桥基的大孔面心立方周期性介孔有机硅的合成

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Periodic mesoporous organosilicas (PMOs) with ethenylene ( -CH = CH-) bridging groups in the framework and large spherical mesopores of tunable size arranged in face-centered-cubic structures (Fm3m symmetry) were synthesized using Pluronic F127 (EO106PO70EO106) as a surfactant and xylene (isomer mixture) as a swelling agent at low temperature (7 degrees C) under moderately acidic conditions (0.1 M HCl). The resulting PMOs were characterized by small-angle X-ray scattering, nitrogen adsorption, transmission electron microscopy and solid-state Si-29 NMR. The unit-cell parameters were enlarged from 31 to 42 nm and the pore diameters increased from 14 nm to as much as 22 nm while increasing the amount of the swelling agent in the reaction mixture, until these two structural parameters reached a plateau. The enlargement was not accompanied by a loss of structural ordering, which is exceptional for not only PMOs, but also other surfactant-templated materials. While the extraction of the surfactant was ineffective in generating readily accessible mesopores for samples prepared with low relative quantities of the swelling agent, extracted samples prepared with higher proportions of the swelling agent exhibited good mesopore accessibility. On the other hand, the calcination under argon at 350 degrees C afforded well accessible mesopores in all cases, even though the unit-cell shrinkage was significant and a substantial fraction of Si-C bonds was cleaved. (C) 2015 Elsevier Inc. All rights reserved.
机译:使用Pluronic F127(EO106PO70EO106)作为表面活性剂合成了周期性的介孔有机硅(PMO),该骨架在骨架中带有亚乙基(-CH = CH-)桥接基团,并以面心立方结构(Fm3m对称性)排列大小可调的大球形介孔。在适度的酸性条件下(0.1 M HCl)在低温(7摄氏度)下作为膨胀剂的二甲苯(异构体混合物)。所得的PMO通过小角度X射线散射,氮吸附,透射电子显微镜和固态Si-29 NMR进行表征。在增加反应混合物中溶胀剂的量的同时,晶胞参数从31nm增加到42nm,并且孔径从14nm增加到多达22nm,直到这两个结构参数达到稳定。扩大并没有伴随着结构有序性的丧失,这不仅对于PMOs,而且对于其他表面活性剂模板的材料都是例外。尽管表面活性剂的提取不能有效地产生相对较低的膨胀剂含量的样品,但使用较高比例的膨胀剂制备的样品却具有良好的中孔可及性。另一方面,在氩气中350℃下的煅烧在所有情况下都提供了易于接近的中孔,即使晶胞收缩显着并且大部分Si-C键被裂解也是如此。 (C)2015 Elsevier Inc.保留所有权利。

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