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首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >Microwave intensified synthesis of Zeolite-Y from spent FCC catalyst after acid activation
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Microwave intensified synthesis of Zeolite-Y from spent FCC catalyst after acid activation

机译:微波从酸活化后从废FCC催化剂中加强沸石-Y的合成

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摘要

A novel microwave heating process for the synthesis of zeolite-Y from spent fluid catalytic cracking (SFCC) catalyst has been proposed in this work. The SFCC catalyst is firstly activated in microwave field by acid solution and then used as an aluminum source for the synthesis of zeolite-Y. The activation effect of hydrochloric acid and oxalic acid on the SFCC catalyst, and the synthesis effects of zeolite-Y production from the activated SFCC catalyst under microwave are studied by ICP, XRD, SEM, and N-2 sorption studies. The results show that microwave-assisted acid activation process can facilitate the formation of the active gamma-Al2O3 and as well enhance the crystallinity of zeolite-Y in the SFCC catalyst, which is beneficial for the synthesis of zeolite-Y. Compared with the inactivated SFCC catalyst, the activated SFCC catalyst has a larger specific surface area and a lower contaminated metal content. The specific surface areas of SFCC catalyst after activation by hydrochloric acid and oxalic acid are 197.1 and 113.6 m(2)/g, respectively, indicating better activation by hydrochloric acid compared to oxalic acid in the microwave field. The results demonstrate that increasing the synthesis temperature and prolonging the crystallization time favor the growth of zeolite-Y crystal particles, however, zeolite-Y partially transforms into zeolite-P. The priority of different aluminum sources in zeolite-Y synthesis is: hydrochloric acid activated SFCC catalyst oxalic acid activated SFCC catalyst inactivated SFCC catalyst. The zeolite-Y having a particle size range of 0.3-1 mu m is successfully synthesized from the activated SFCC catalyst at 100 degrees C for 2 h under microwave at 2 kg/cm(2) pressure and 1000 W power. (C) 2018 Elsevier B.V. All rights reserved.
机译:在这项工作中提出了一种用于合成废液催化裂化(SFCC)催化剂的沸石-Y的新微波加热过程。 SFCC催化剂首先通过酸溶液在微波场中活化,然后用作合成沸石-Y的铝源。通过ICP,XRD,SEM和N-2吸附研究,研究了盐酸和草酸对SFCC催化剂对SFCC催化剂的合成效果,以及沸石-Y在微波下生产的合成效应。结果表明,微波辅助酸活化方法可以促进活性γ-Al2O3的形成,同样增强SFCC催化剂中的沸石-Y的结晶度,这有利于沸石-Y的合成。与灭活的SFCC催化剂相比,活化的SFCC催化剂具有较大的比表面积和较低的污染金属含量。通过盐酸和草酸活化后SFCC催化剂的比表面积分别为197.1和113.6M(2)/ g,表明与微波田中的草酸相比,盐酸更好地激活。结果表明,增加合成温度和延长结晶时间赞成沸石-Y晶粒的生长,然而,沸石-Y部分地转化成沸石-P。沸石-Y合成中不同铝源的优先级是:盐酸活性SFCC催化剂>草酸活性SFCC催化剂>灭活的SFCC催化剂。粒径范围为0.3-1μm的沸石-y在微波下以2kg / cm(2)压力和1000W功率的微波以在100℃下从活化的SFCC催化剂中成功合成2小时。 (c)2018年elestvier b.v.保留所有权利。

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