Aqueous phase reforming of xylitol over Pt-Re bimetallic catalyst: Effect of the Re addition

Alexey Kirilin; Anton Tokarev; Haresh Manyar; Chris Hardacre; Tapio Salmi; Jyri-Pekka Mikkola; Dmitry Murzin

doi:10.1016/j.cattod.2013.09.020

Aqueous phase reforming of xylitol over Pt-Re bimetallic catalyst: Effect of the Re addition

Alexey Kirilin
, Anton Tokarev
, Haresh Manyar
, Chris Hardacre
, Tapio Salmi
, Jyri-Pekka Mikkola
, Dmitry Murzin

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

57 Citeringar (Scopus)

Sammanfattning

The aqueous phase reforming (APR) of xylitol was studied in a continuous fixed bed reactor over three catalysts: Pt/Al₂O₃, Pt/TiO₂ and Pt-Re/TiO₂. The data obtained in the case of the monometallic Pt catalysts was compared to the bimetallic Pt-Re sample. The effect of Re addition on the catalyst stability, activity, product formation and selectivity toward hydrogen and alkanes was studied. The bimetallic catalyst demonstrated a higher selectivity to alkanes compared to the monometallic samples. The monometallic catalyst was more selective toward hydrogen formation. A plausible reaction scheme explaining differences in selectivity toward hydrogen and alkanes was proposed and discussed.

Originalspråk	Odefinierat/okänt
Sidor (från-till)	97–107
Tidskrift	Catalysis Today
Volym	223
DOI	https://doi.org/10.1016/j.cattod.2013.09.020
Status	Publicerad - 2014
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

Åtkomst av dokument

10.1016/j.cattod.2013.09.020

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title = "Aqueous phase reforming of xylitol over Pt-Re bimetallic catalyst: Effect of the Re addition",

abstract = "The aqueous phase reforming (APR) of xylitol was studied in a continuous fixed bed reactor over three catalysts: Pt/Al2O3, Pt/TiO2 and Pt-Re/TiO2. The data obtained in the case of the monometallic Pt catalysts was compared to the bimetallic Pt-Re sample. The effect of Re addition on the catalyst stability, activity, product formation and selectivity toward hydrogen and alkanes was studied. The bimetallic catalyst demonstrated a higher selectivity to alkanes compared to the monometallic samples. The monometallic catalyst was more selective toward hydrogen formation. A plausible reaction scheme explaining differences in selectivity toward hydrogen and alkanes was proposed and discussed.",

author = "Alexey Kirilin and Anton Tokarev and Haresh Manyar and Chris Hardacre and Tapio Salmi and Jyri-Pekka Mikkola and Dmitry Murzin",

year = "2014",

doi = "10.1016/j.cattod.2013.09.020",

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journal = "Catalysis Today",

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T1 - Aqueous phase reforming of xylitol over Pt-Re bimetallic catalyst: Effect of the Re addition

AU - Kirilin, Alexey

AU - Tokarev, Anton

AU - Manyar, Haresh

AU - Hardacre, Chris

AU - Salmi, Tapio

AU - Mikkola, Jyri-Pekka

AU - Murzin, Dmitry

PY - 2014

Y1 - 2014

N2 - The aqueous phase reforming (APR) of xylitol was studied in a continuous fixed bed reactor over three catalysts: Pt/Al2O3, Pt/TiO2 and Pt-Re/TiO2. The data obtained in the case of the monometallic Pt catalysts was compared to the bimetallic Pt-Re sample. The effect of Re addition on the catalyst stability, activity, product formation and selectivity toward hydrogen and alkanes was studied. The bimetallic catalyst demonstrated a higher selectivity to alkanes compared to the monometallic samples. The monometallic catalyst was more selective toward hydrogen formation. A plausible reaction scheme explaining differences in selectivity toward hydrogen and alkanes was proposed and discussed.

AB - The aqueous phase reforming (APR) of xylitol was studied in a continuous fixed bed reactor over three catalysts: Pt/Al2O3, Pt/TiO2 and Pt-Re/TiO2. The data obtained in the case of the monometallic Pt catalysts was compared to the bimetallic Pt-Re sample. The effect of Re addition on the catalyst stability, activity, product formation and selectivity toward hydrogen and alkanes was studied. The bimetallic catalyst demonstrated a higher selectivity to alkanes compared to the monometallic samples. The monometallic catalyst was more selective toward hydrogen formation. A plausible reaction scheme explaining differences in selectivity toward hydrogen and alkanes was proposed and discussed.

U2 - 10.1016/j.cattod.2013.09.020

DO - 10.1016/j.cattod.2013.09.020

M3 - Artikel

SN - 0920-5861

VL - 223

SP - 97

EP - 107

JO - Catalysis Today

JF - Catalysis Today

ER -