Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification

This study aimed to further tune the capability of active metal exsolution onto the surface of the CO oxidative perovskite catalyst La0.7Ce0.1Co0.3Ni0.1Ti0.6O3 by tuning the reducing parameter. Under same calcination temperature of 800℃, XRD analysis shown that the precursors with calcination durati...

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Main Authors: G. L., Lew, N., Ibrahim, S., Abdullah, W. R., Wan Daud, W. K. W., Ramli
Format: Conference or Workshop Item
Language:English
Published: IOP Publishing Ltd 2021
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Online Access:http://umpir.ump.edu.my/id/eprint/35397/1/Exsolution%20enhancement%20of%20metal-support%20CO%20oxidation%20perovskite.pdf
http://umpir.ump.edu.my/id/eprint/35397/
https://doi.org/10.1088/1755-1315/765/1/012078
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Institution: Universiti Malaysia Pahang
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spelling my.ump.umpir.353972022-10-28T04:20:58Z http://umpir.ump.edu.my/id/eprint/35397/ Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification G. L., Lew N., Ibrahim S., Abdullah W. R., Wan Daud W. K. W., Ramli QD Chemistry T Technology (General) TA Engineering (General). Civil engineering (General) TP Chemical technology This study aimed to further tune the capability of active metal exsolution onto the surface of the CO oxidative perovskite catalyst La0.7Ce0.1Co0.3Ni0.1Ti0.6O3 by tuning the reducing parameter. Under same calcination temperature of 800℃, XRD analysis shown that the precursors with calcination duration of 6 hours (S2T8H6) was able to achieve similar crystalline structure to those with calcination duration of 12 hours (S2T8H12). In order for the active metal (CoNi) to be exsolved onto the perovskite surface, reducing parameter such as temperature and duration are deemed crucial to the reduction process. The exsolution of the active metals was observed when the samples were treated under reducing condition with varying temperatures of 550℃ and 700℃ and duration from 200 to 300 minutes. Through comparison with their EDX readings, S2T8H6 treated under 700℃ and 300 minutes (S2T8H6-R7H5) achieved the highest weight percentage of surface Cobalt and Nickel of 3.83 and 2.81. It was clear that by tuning the temperature and duration of reduction, the exsolution of the active metals onto the surface of the perovskite could be improved resulting in better exposure and dispersion of active metals onto the surface of catalyst. IOP Publishing Ltd 2021-05-24 Conference or Workshop Item PeerReviewed pdf en cc_by http://umpir.ump.edu.my/id/eprint/35397/1/Exsolution%20enhancement%20of%20metal-support%20CO%20oxidation%20perovskite.pdf G. L., Lew and N., Ibrahim and S., Abdullah and W. R., Wan Daud and W. K. W., Ramli (2021) Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification. In: IOP Conference Series: Earth and Environmental Science, 1st International Conference on Biomass Utilization and Sustainable Energy 2020, 15-16 December 2020 , Virtual Conference, Universiti Malaysia Perlis (UniMAP). pp. 1-8., 765 (012078). ISSN 1755-1307 https://doi.org/10.1088/1755-1315/765/1/012078
institution Universiti Malaysia Pahang
building UMP Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang
content_source UMP Institutional Repository
url_provider http://umpir.ump.edu.my/
language English
topic QD Chemistry
T Technology (General)
TA Engineering (General). Civil engineering (General)
TP Chemical technology
spellingShingle QD Chemistry
T Technology (General)
TA Engineering (General). Civil engineering (General)
TP Chemical technology
G. L., Lew
N., Ibrahim
S., Abdullah
W. R., Wan Daud
W. K. W., Ramli
Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification
description This study aimed to further tune the capability of active metal exsolution onto the surface of the CO oxidative perovskite catalyst La0.7Ce0.1Co0.3Ni0.1Ti0.6O3 by tuning the reducing parameter. Under same calcination temperature of 800℃, XRD analysis shown that the precursors with calcination duration of 6 hours (S2T8H6) was able to achieve similar crystalline structure to those with calcination duration of 12 hours (S2T8H12). In order for the active metal (CoNi) to be exsolved onto the perovskite surface, reducing parameter such as temperature and duration are deemed crucial to the reduction process. The exsolution of the active metals was observed when the samples were treated under reducing condition with varying temperatures of 550℃ and 700℃ and duration from 200 to 300 minutes. Through comparison with their EDX readings, S2T8H6 treated under 700℃ and 300 minutes (S2T8H6-R7H5) achieved the highest weight percentage of surface Cobalt and Nickel of 3.83 and 2.81. It was clear that by tuning the temperature and duration of reduction, the exsolution of the active metals onto the surface of the perovskite could be improved resulting in better exposure and dispersion of active metals onto the surface of catalyst.
format Conference or Workshop Item
author G. L., Lew
N., Ibrahim
S., Abdullah
W. R., Wan Daud
W. K. W., Ramli
author_facet G. L., Lew
N., Ibrahim
S., Abdullah
W. R., Wan Daud
W. K. W., Ramli
author_sort G. L., Lew
title Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification
title_short Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification
title_full Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification
title_fullStr Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification
title_full_unstemmed Exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification
title_sort exsolution enhancement of metal-support co oxidation perovskite catalyst with parameter modification
publisher IOP Publishing Ltd
publishDate 2021
url http://umpir.ump.edu.my/id/eprint/35397/1/Exsolution%20enhancement%20of%20metal-support%20CO%20oxidation%20perovskite.pdf
http://umpir.ump.edu.my/id/eprint/35397/
https://doi.org/10.1088/1755-1315/765/1/012078
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