4.7 Article

Development of stable MoO3/TiO2-Al2O3 catalyst for oxidative dehydrogenation of ethylbenzene to styrene using CO2 as soft oxidant

期刊

JOURNAL OF CO2 UTILIZATION
卷 18, 期 -, 页码 309-317

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jcou.2017.02.010

关键词

Dehydrogenation; Ethylbenzene S; tyrene; CO2 oxidant; MoO3; TiO2-Al2O3

资金

  1. SERB, Department of Science & Technology, Government of India [SB/FT/CS-044/2014, SR/NM/NS-20/2014]

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A novel MoO3/TiO2-Al2O3 (MTA) catalyst was employed for oxidative dehydrogenation of ethylbenzene to styrene using CO2 as a soft oxidant with CO2/ethylbenzene (molar ratio) = 9.8 and gas hourly space velocity (GHSV) was maintained at 0.08 molh (1)g (1)catalyst.Among different (2.5, 5.0, 7.5 and 10.0) wt.% loadings of MoO3, 7.5 wt.% loaded MoO3/TiO2-Al2O3 catalyst exhibited superior activity. The stability of the catalyst over time on stream was noteworthy where; the catalyst evinced notable activity up to 40 h with maximum ethylbenzene conversion of about 70% and styrene selectivity about 97%. The presence of titania greatly influenced the activity of the catalyst in terms of stability. The reaction with CO2 resulted in better activity compared to N-2 proving it to be an effective oxidant for the dehydrogenation reactions. The deactivation of the catalyst was due to excess coke formation which led to blocking of active sites. The coke was removed by regenerating the catalyst at 600 degrees C under air. Interestingly, the catalysts were found active even after 40 h as well as in between 10 h of regenerations. The catalysts were characterized by XRay Diffraction, X-ray Photoelectron Spectroscopy, Surface area and Pore Size Distribution, Scanning Electron Microscopy, Thermogravimetric Analysis, H-2-Temperature Programmed Reduction and Ammonia-Temperature Programmed Desorption. The results indicate that the surface area, interaction with the support, morphology of the catalyst and surface acidic sites exerted a significant influence on the activity. (C) 2017 Elsevier Ltd. All rights reserved.

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