Aqueous phase reforming of ethanol and acetic acid over TiO2 supported Ru catalysts

•Smaller Ru particles can prevent the undesirable methanation of CO2 during the EtOH·H2O aqueous reforming reaction.•Smaller Ru particles can participate in the complete reforming of AcOH to form 2:1 ratio of H2 and CO2.•Positively charged small Ru particles are responsible for the efficient activat...

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Published inApplied catalysis. B, Environmental Vol. 146; pp. 221 - 226
Main Authors Nozawa, Toshiaki, Mizukoshi, Yuichi, Yoshida, Akihiro, Naito, Shuichi
Format Journal Article Conference Proceeding
LanguageEnglish
Published Kidlington Elsevier B.V 01.03.2014
Elsevier
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Summary:•Smaller Ru particles can prevent the undesirable methanation of CO2 during the EtOH·H2O aqueous reforming reaction.•Smaller Ru particles can participate in the complete reforming of AcOH to form 2:1 ratio of H2 and CO2.•Positively charged small Ru particles are responsible for the efficient activation of acetic acid and water to form H2 and CO2 selectively.•In the presence of EtOH, AcOH·H2O reforming is suppressed seriously, which is the reason why complete EtOH reforming is difficult. This study examined the dependence of Ru particle sizes upon the activity and selectivity for aqueous phase reforming reactions of ethanol and acetic acid over Ru/TiO2 at 473K. For ethanol, irrespective of the Ru particle size, the 1:1 ratio of CH4 and CO2 was formed at the initial stage, indicating the absence of complete reforming with water. At the later stage, unfavorable methanation of CO2 by H2 was observed over larger Ru particle catalysts. That methanation was suppressed completely over smaller Ru particle catalysts. In the case of acetic acid reforming over smaller Ru particle catalysts, a 2:1 ratio of H2 and CO2 was formed constantly, indicating the operation of complete reforming reaction with water. Positively charged small Ru particles were responsible for the efficient activation of acetic acid and water to form H2 and CO2 selectively.
Bibliography:ObjectType-Article-2
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content type line 23
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2013.06.017