TY - JOUR
T1 - Oxidative Reforming of Methane over Rh-Containing Zeolites
T2 - Active Species and Role of Zeolite Framework
AU - Osuga, Ryota
AU - Yasuda, Shuhei
AU - Sawada, Masato
AU - Manabe, Ryo
AU - Shima, Hisashi
AU - Tsutsuminai, Susumu
AU - Fukuoka, Atsushi
AU - Kobayashi, Hirokazu
AU - Muramatsu, Atsushi
AU - Yokoi, Toshiyuki
N1 - Publisher Copyright:
© 2021 American Chemical Society
PY - 2021/6/23
Y1 - 2021/6/23
N2 - Rh ion-exchanged Y zeolite (Rh-Y) and amorphous silica-alumina (Rh-ASA) were prepared by the ion-exchange method. The Rh species were identified by UV-vis and IR spectroscopies, TEM, and H2-TPR measurements. Isolated Rh cations were preferentially formed on the Y zeolite, while Rh oxide mainly existed on ASA. The catalytic activities of the prepared samples for oxidative reforming of methane were evaluated. The Rh oxide on Rh-ASA exhibited slightly higher methane conversion and CO yield than those of the isolated Rh cation on Rh-Y. On the other hand, the catalytic lifetime over Rh-Y was longer than that over Rh-ASA because the isolated Rh cations were protected from aggregation by electrostatic interaction with the zeolite framework. In addition, Rh-Y exhibited a high catalytic activity even at low Rh contents owing to its high dispersibility. On the basis of the experimental facts, we have successfully clarified the active Rh species for this oxidative reforming of methane and demonstrated the effectiveness of the zeolite framework for the stabilization of the active species. This article provides the important concept for the design of highly active catalysts in this catalytic system.
AB - Rh ion-exchanged Y zeolite (Rh-Y) and amorphous silica-alumina (Rh-ASA) were prepared by the ion-exchange method. The Rh species were identified by UV-vis and IR spectroscopies, TEM, and H2-TPR measurements. Isolated Rh cations were preferentially formed on the Y zeolite, while Rh oxide mainly existed on ASA. The catalytic activities of the prepared samples for oxidative reforming of methane were evaluated. The Rh oxide on Rh-ASA exhibited slightly higher methane conversion and CO yield than those of the isolated Rh cation on Rh-Y. On the other hand, the catalytic lifetime over Rh-Y was longer than that over Rh-ASA because the isolated Rh cations were protected from aggregation by electrostatic interaction with the zeolite framework. In addition, Rh-Y exhibited a high catalytic activity even at low Rh contents owing to its high dispersibility. On the basis of the experimental facts, we have successfully clarified the active Rh species for this oxidative reforming of methane and demonstrated the effectiveness of the zeolite framework for the stabilization of the active species. This article provides the important concept for the design of highly active catalysts in this catalytic system.
UR - http://www.scopus.com/inward/record.url?scp=85108733423&partnerID=8YFLogxK
U2 - 10.1021/acs.iecr.1c01353
DO - 10.1021/acs.iecr.1c01353
M3 - 学術論文
AN - SCOPUS:85108733423
SN - 0888-5885
VL - 60
SP - 8696
EP - 8704
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 24
ER -