Synthesis and Characterization of CaO-Zeolite Catalyst by Sonochemical Engineering Method

Widyarini Widyarini, M. D. Bustan, S. Haryati
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Abstract

Calcium Oxide (CaO) loaded on zeolite was categorized as a heterogeneous catalyst. The utilization of CaO catalyst could be implemented in catalytic pyrolysis enhance gaseous production. In this paper, CaSO4.2H2O is an active site embedded in natural zeolite, and the activity of the CaO-Zeolite catalyst is synthesized by a sonochemical impregnation-assisted drying process and calcination. The stirrer impregnation method was used as a control. CaO-Zeolite catalyst characterization and properties were identified via Scanning Electron Microscopy- Energy Dispersive X-Ray (SEM-EDX).The activation experiments were performed at an oven temperature of 120oC for 5 h and a calcination temperature of 300oC for 2 h. The synthesized catalysts of sonochemical were performed at 20 minutes, 20 kHz, and 1200 Watt, and the synthesized catalyst of stirrer were performed at 120 minutes, 1500 rpm, and 1000 watts. The experimental results revealed that the characterization of the catalysts prepared by the sonochemical method was better than that of the stirrer. Specifically, obtained CaO-Zeolite catalyst with Ca wt % increased from 0.86 wt% NZ (natural zeolite) to (11.3 wt%, 14.15 wt% and 23.48 wt%) of sonochemical and (11.82wt%, 13.95 wt% and 20.64wt%) of stirrer. The results demonstrated that Ca wt% by sonochemical in 20 minutes dispersed at support surface (zeolite) more effective than stirrer in 120 minutes. These results were impacted by acoustic cavitation and shockwave of ultrasonic on solid-liquid transport and distribution. On the other side, sonochemical assisted the activation technique to minimize particle size and allowed metal oxide (CaSO4.2H2O) to be dispersed uniformly into the pores structure of the zeolite. The utilization of sonochemical in CaO-Zeolite synthesizing enhanced catalyst activity.
用声化学工程方法合成曹石分子筛催化剂及表征
沸石负载氧化钙(CaO)是一种多相催化剂。利用CaO催化剂可以实现催化热解,提高产气率。本文将CaSO4.2H2O作为嵌入天然沸石中的活性位点,采用声化学浸渍辅助干燥和煅烧的方法合成cao -沸石催化剂的活性。以搅拌浸渍法为对照。通过扫描电子显微镜-能量色散x射线(SEM-EDX)对催化剂的表征和性能进行了鉴定。在120℃的烘箱温度下进行5 h的活化实验,在300℃的煅烧温度下进行2 h的活化实验。声化学合成催化剂在20分钟、20 kHz、1200瓦的条件下进行,搅拌器合成催化剂在120分钟、1500 rpm、1000瓦的条件下进行。实验结果表明,声化学法制备的催化剂性能优于搅拌法制备的催化剂。其中,Ca wt%由NZ(天然沸石)的0.86 wt%提高到声化学的(11.3 wt%, 14.15 wt%和23.48 wt%)和搅拌器的(11.82wt%, 13.95 wt%和20.64wt%)。结果表明,在载体表面(沸石)上,声化学法在20分钟内的Ca wt%的分散效果优于搅拌法在120分钟内的分散效果。这些结果与声空化和超声冲击波对固液输运和分布的影响有关。另一方面,声化学辅助活化技术使颗粒尺寸最小化,并使金属氧化物(CaSO4.2H2O)均匀分散到沸石的孔隙结构中。超声化学在高沸石合成中的应用提高了催化剂活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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