Hydrogen production via sorption enhanced steam methane reforming process using Ni/CaO multifunctional catalyst

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Author listChanburanasiri N., Ribeiro A.M., Rodrigues A.E., Arpornwichanop A., Laosiripojana N., Praserthdam P., Assabumrungrat S.

Publication year2011

Volume number50

Issue number24

Start page13662

End page13671

Number of pages10

ISSN0888-5885

eISSN0888-5885

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-83655192555&doi=10.1021%2fie201226j&partnerID=40&md5=fd82c0045b6010d4ad2fb4d55c532948

LanguagesEnglish-Great Britain (EN-GB)


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Abstract

Sorption enhanced steam methane reforming (SESMR) is a promising concept for hydrogen production. The in situ removal of CO 2 shifts the reaction equilibrium toward increased H 2 production as well as H 2 concentration. Generally, most of the previous studies operated the SESMR system using separate materials of a CO 2 adsorbent and a reforming catalyst. In this study, a combined catalyst-adsorbent material (considered as multifunctional catalyst), whose functions are not only to catalyze the reaction but also to adsorb CO 2 simultaneously, was developed and utilized for the SESMR process. CaO and hydrotalcite (MK30-K), well-known adsorbents for CO 2 capture, were selected as supports to replace a conventional Al 2O 3 support for Ni catalyst. The material was prepared in the form of powder by incipient wetness technique, and the tests were carried out in the fixed bed reactor system. Experimental results indicated that the activity of Ni/CaO was less than Ni/Al 2O 3 but high hydrogen concentration in the product stream can be achieved. The effect of Ni loading was investigated, and it was found that at atmospheric pressure, steam to methane ratio of 3 and T = 873 K, 12.5 wt % Ni/CaO was the appropriate ratio, offering high hydrogen concentration (80%). The study also suggested that the use of the multifunctional catalyst eliminates the use of Al 2O 3 and thus requires a reactor with a smaller size. ฉ 2011 American Chemical Society.


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Last updated on 2023-04-10 at 07:35