Phongaksorn, M.

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  • Phongaksorn, M. (1)
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The Effect of Preparation Method on Ni/Ce/Al Catalyst for High Temperature Water-Gas Shift Reaction

Sangsong, S.; Srimala, K.; Radonjić, Mia; Tungkamani, S.; Sornchamni, T.; Phongaksorn, M.

(2017)

TY  - JOUR
AU  - Sangsong, S.
AU  - Srimala, K.
AU  - Radonjić, Mia
AU  - Tungkamani, S.
AU  - Sornchamni, T.
AU  - Phongaksorn, M.
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6346
AB  - High temperature water gas shift (HT-WGS) is an important catalytic process connected with reforming process in hydrogen production. Ni/CeO2-Al2O3 (or Al2O3) catalysts were studied in this work on the effect of catalyst preparation method toward the physicochemical properties and the HT-WGS activity. Ni/CeO2-Al2O3 were prepared by sol-gel and impregnation methods whereas Ni/Al2O3 was prepared by impregnation method. The catalyst samples were characterized by XRD, H2-TPR and H2-TPD techniques. The catalytic activities of HT-WGS catalysts was demonstrated at 550°C, GHSV of 2x105 mLh-1gcat-1and steam-to-CO ratio of 3. Nickel was detected as a nickel aluminate phase in the calcined catalyst. Ni strongly interacted with support in the calcined catalyst prepared by sol-gel method. The strong metal-support interaction can be resisted by preparing catalyst via impregnation and CeO2 can promote the H2O dissociation in HT-WGS mechanism. The highest metal dispersion, largest metal surface area and greatest HT-WGS activity were consequently achieved by Ni/CeO2-Al2O3 prepared from impregnation method.
T2  - Key Engineering Materials
T1  - The Effect of Preparation Method on Ni/Ce/Al Catalyst for High Temperature Water-Gas Shift Reaction
EP  - 175
SP  - 171
VL  - 757
DO  - 10.4028/www.scientific.net/KEM.757.171
ER  - 
@article{
author = "Sangsong, S. and Srimala, K. and Radonjić, Mia and Tungkamani, S. and Sornchamni, T. and Phongaksorn, M.",
year = "2017",
abstract = "High temperature water gas shift (HT-WGS) is an important catalytic process connected with reforming process in hydrogen production. Ni/CeO2-Al2O3 (or Al2O3) catalysts were studied in this work on the effect of catalyst preparation method toward the physicochemical properties and the HT-WGS activity. Ni/CeO2-Al2O3 were prepared by sol-gel and impregnation methods whereas Ni/Al2O3 was prepared by impregnation method. The catalyst samples were characterized by XRD, H2-TPR and H2-TPD techniques. The catalytic activities of HT-WGS catalysts was demonstrated at 550°C, GHSV of 2x105 mLh-1gcat-1and steam-to-CO ratio of 3. Nickel was detected as a nickel aluminate phase in the calcined catalyst. Ni strongly interacted with support in the calcined catalyst prepared by sol-gel method. The strong metal-support interaction can be resisted by preparing catalyst via impregnation and CeO2 can promote the H2O dissociation in HT-WGS mechanism. The highest metal dispersion, largest metal surface area and greatest HT-WGS activity were consequently achieved by Ni/CeO2-Al2O3 prepared from impregnation method.",
journal = "Key Engineering Materials",
title = "The Effect of Preparation Method on Ni/Ce/Al Catalyst for High Temperature Water-Gas Shift Reaction",
pages = "175-171",
volume = "757",
doi = "10.4028/www.scientific.net/KEM.757.171"
}
Sangsong, S., Srimala, K., Radonjić, M., Tungkamani, S., Sornchamni, T.,& Phongaksorn, M.. (2017). The Effect of Preparation Method on Ni/Ce/Al Catalyst for High Temperature Water-Gas Shift Reaction. in Key Engineering Materials, 757, 171-175.
https://doi.org/10.4028/www.scientific.net/KEM.757.171
Sangsong S, Srimala K, Radonjić M, Tungkamani S, Sornchamni T, Phongaksorn M. The Effect of Preparation Method on Ni/Ce/Al Catalyst for High Temperature Water-Gas Shift Reaction. in Key Engineering Materials. 2017;757:171-175.
doi:10.4028/www.scientific.net/KEM.757.171 .
Sangsong, S., Srimala, K., Radonjić, Mia, Tungkamani, S., Sornchamni, T., Phongaksorn, M., "The Effect of Preparation Method on Ni/Ce/Al Catalyst for High Temperature Water-Gas Shift Reaction" in Key Engineering Materials, 757 (2017):171-175,
https://doi.org/10.4028/www.scientific.net/KEM.757.171 . .