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The influence of CO, CO2 and H2O on selective CO methanation over Ni(Cl)/CeO2 catalyst : On the way to formic acid derived CO-free hydrogen. / Konishcheva, M. V.; Potemkin, D. I.; Snytnikov, P. V. и др.

в: International Journal of Hydrogen Energy, Том 44, № 20, 19.04.2019, стр. 9978-9986.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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APA

Vancouver

Konishcheva MV, Potemkin DI, Snytnikov PV, Sobyanin VA. The influence of CO, CO2 and H2O on selective CO methanation over Ni(Cl)/CeO2 catalyst: On the way to formic acid derived CO-free hydrogen. International Journal of Hydrogen Energy. 2019 апр. 19;44(20):9978-9986. doi: 10.1016/j.ijhydene.2018.12.192

Author

Konishcheva, M. V. ; Potemkin, D. I. ; Snytnikov, P. V. и др. / The influence of CO, CO2 and H2O on selective CO methanation over Ni(Cl)/CeO2 catalyst : On the way to formic acid derived CO-free hydrogen. в: International Journal of Hydrogen Energy. 2019 ; Том 44, № 20. стр. 9978-9986.

BibTeX

@article{fc41d96eef78440e8866cfea266ca96a,
title = "The influence of CO, CO2 and H2O on selective CO methanation over Ni(Cl)/CeO2 catalyst: On the way to formic acid derived CO-free hydrogen",
abstract = "For the first time the influence of CO, CO2 and H2O content on the performance of chlorinated Ni–CeO2 catalyst in selective or preferential CO methanation was studied systematically. It was shown that the rate of CO methanation over Ni(Cl)/CeO2 increases with the increasing H2 concentration, is independent of CO2 concentration and decreases with increasing CO and H2O concentrations; the rate of CO2 methanation is weakly sensitive to H2 and CO2 concentrations and decreases with increasing CO and H2O concentrations. High catalyst selectivity was attributed to Ni surface blockage by strongly adsorbed CO molecules and ceria surface blockage by Cl, which both inhibit CO2 hydrogenation. For the first time, selective CO methanation over Ni(Cl)/CeO2 was studied for deep CO removal from formic acid derived hydrogen-rich gases characterized by high CO2 (40–50 vol%), low CO (30–1000 ppm) content and trace amounts of water. Composite Ni(Cl)/CeO2-η-Al2O3/FeCrAl wire mesh catalyst was demonstrated to be effective for this process at temperatures of 180–220°С selectivity 30–70%, WHSV up to 200 L (STP)/(g∙h). The catalyst provides high process productivity, low pressure drop, uniform temperature distribution, and appears highly promising for the development of a compact CO cleanup reactor. Selective CO methanation was concluded to be a convenient way to CO-free hydrogen produced by formic acid decomposition.",
keywords = "CO cleanup, CO methanation, Formic acid, Nickel-ceria catalysts, Preferential CO methanation, Selective CO methanation, NI/TIO2 CATALYST, PERFORMANCE, STEAM, PREFERENTIAL OXIDATION, SUPPORTED NICKEL-CATALYSTS, REMOVAL, CARBON-MONOXIDE, WATER-VAPOR, GAS, TRACE CHLORINE",
author = "Konishcheva, {M. V.} and Potemkin, {D. I.} and Snytnikov, {P. V.} and Sobyanin, {V. A.}",
note = "Publisher Copyright: {\textcopyright} 2019 Hydrogen Energy Publications LLC",
year = "2019",
month = apr,
day = "19",
doi = "10.1016/j.ijhydene.2018.12.192",
language = "English",
volume = "44",
pages = "9978--9986",
journal = "International Journal of Hydrogen Energy",
issn = "0360-3199",
publisher = "Elsevier Ltd",
number = "20",

}

RIS

TY - JOUR

T1 - The influence of CO, CO2 and H2O on selective CO methanation over Ni(Cl)/CeO2 catalyst

T2 - On the way to formic acid derived CO-free hydrogen

AU - Konishcheva, M. V.

AU - Potemkin, D. I.

AU - Snytnikov, P. V.

AU - Sobyanin, V. A.

N1 - Publisher Copyright: © 2019 Hydrogen Energy Publications LLC

PY - 2019/4/19

Y1 - 2019/4/19

N2 - For the first time the influence of CO, CO2 and H2O content on the performance of chlorinated Ni–CeO2 catalyst in selective or preferential CO methanation was studied systematically. It was shown that the rate of CO methanation over Ni(Cl)/CeO2 increases with the increasing H2 concentration, is independent of CO2 concentration and decreases with increasing CO and H2O concentrations; the rate of CO2 methanation is weakly sensitive to H2 and CO2 concentrations and decreases with increasing CO and H2O concentrations. High catalyst selectivity was attributed to Ni surface blockage by strongly adsorbed CO molecules and ceria surface blockage by Cl, which both inhibit CO2 hydrogenation. For the first time, selective CO methanation over Ni(Cl)/CeO2 was studied for deep CO removal from formic acid derived hydrogen-rich gases characterized by high CO2 (40–50 vol%), low CO (30–1000 ppm) content and trace amounts of water. Composite Ni(Cl)/CeO2-η-Al2O3/FeCrAl wire mesh catalyst was demonstrated to be effective for this process at temperatures of 180–220°С selectivity 30–70%, WHSV up to 200 L (STP)/(g∙h). The catalyst provides high process productivity, low pressure drop, uniform temperature distribution, and appears highly promising for the development of a compact CO cleanup reactor. Selective CO methanation was concluded to be a convenient way to CO-free hydrogen produced by formic acid decomposition.

AB - For the first time the influence of CO, CO2 and H2O content on the performance of chlorinated Ni–CeO2 catalyst in selective or preferential CO methanation was studied systematically. It was shown that the rate of CO methanation over Ni(Cl)/CeO2 increases with the increasing H2 concentration, is independent of CO2 concentration and decreases with increasing CO and H2O concentrations; the rate of CO2 methanation is weakly sensitive to H2 and CO2 concentrations and decreases with increasing CO and H2O concentrations. High catalyst selectivity was attributed to Ni surface blockage by strongly adsorbed CO molecules and ceria surface blockage by Cl, which both inhibit CO2 hydrogenation. For the first time, selective CO methanation over Ni(Cl)/CeO2 was studied for deep CO removal from formic acid derived hydrogen-rich gases characterized by high CO2 (40–50 vol%), low CO (30–1000 ppm) content and trace amounts of water. Composite Ni(Cl)/CeO2-η-Al2O3/FeCrAl wire mesh catalyst was demonstrated to be effective for this process at temperatures of 180–220°С selectivity 30–70%, WHSV up to 200 L (STP)/(g∙h). The catalyst provides high process productivity, low pressure drop, uniform temperature distribution, and appears highly promising for the development of a compact CO cleanup reactor. Selective CO methanation was concluded to be a convenient way to CO-free hydrogen produced by formic acid decomposition.

KW - CO cleanup

KW - CO methanation

KW - Formic acid

KW - Nickel-ceria catalysts

KW - Preferential CO methanation

KW - Selective CO methanation

KW - NI/TIO2 CATALYST

KW - PERFORMANCE

KW - STEAM

KW - PREFERENTIAL OXIDATION

KW - SUPPORTED NICKEL-CATALYSTS

KW - REMOVAL

KW - CARBON-MONOXIDE

KW - WATER-VAPOR

KW - GAS

KW - TRACE CHLORINE

UR - http://www.scopus.com/inward/record.url?scp=85060146924&partnerID=8YFLogxK

U2 - 10.1016/j.ijhydene.2018.12.192

DO - 10.1016/j.ijhydene.2018.12.192

M3 - Article

AN - SCOPUS:85060146924

VL - 44

SP - 9978

EP - 9986

JO - International Journal of Hydrogen Energy

JF - International Journal of Hydrogen Energy

SN - 0360-3199

IS - 20

ER -

ID: 18290523