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Effect of NiO supported SiO2 in high concentration of CO.

Authors :
Dzakaria, Norliza
Lahuri, Azizul Hakim
Samidin, Salma
Sulhadi, Siti Sarahah
Saharuddin, Tengku Shafazila Tengku
Salleh, Fairous
Samsuri, Alinda
Yusop, Muhammad Rahimi
Yarmo, Ambar
Source :
AIP Conference Proceedings; 2024, Vol. 2925 Issue 1, p1-9, 9p
Publication Year :
2024

Abstract

The effect of a nickel oxide supported silica oxide (NiO/SiO<subscript>2</subscript>) catalyst on temperature programmed reduction (TPR) with 40% (v/v) carbon monoxide (CO) in nitrogen atmosphere as reductant agent was investigated. The conventional impregnation method was used to create the NiO/SiO<subscript>2</subscript> catalysts. The reduction characteristics of NiO to Ni were investigated up to 700 °C, followed by isothermal reduction. The TPR profile of 9% NiO/SiO<subscript>2</subscript> slightly shifted to lower temperature from 412 to 392 °C. Whereas the undoped NiO was reduced at a lower temperature of 387 °C. XRD diffractogram of the catalysts showed a complete reduction of NiO to Ni and have different intensities for each different loading of NiO catalyst on SiO<subscript>2</subscript> support. The TEM images indicated that the carbon nanotubes were deposited on the NiO surfaces indicating some chemical reactions occur on NiO. It was found that the addition of 3% of NiO on SiO<subscript>2</subscript> also exhibited a larger BET surface area (532.8 m<superscript>2</superscript>g<superscript>−1</superscript>) and insignificant pore diameter (5.9-6.0 nm). Based on these results, it is interesting to note that the addition of a small amount of NiO to SiO<subscript>2</subscript> has a remarkable influence by reducing the temperature in the reduction process. The 9% NiO/SiO<subscript>2</subscript> was found sufficient could enhance the reducibility of NiO at a lower temperature. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0094243X
Volume :
2925
Issue :
1
Database :
Complementary Index
Journal :
AIP Conference Proceedings
Publication Type :
Conference
Accession number :
174910696
Full Text :
https://doi.org/10.1063/5.0183364