期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 47, 期 5, 页码 3237-3247出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.11.056
关键词
Carbon formation; Hydrogen production; Thermodynamic calculation; Water gas shift reaction
资金
- Qatar University Student Grant [QUST-2-CENG-2020-10]
- Graduate Teaching/Research Assistantship (GTRA) from Qatar University
Thermodynamic calculations were performed on water gas shift reaction with the addition of chemical additives such as ammonia, hydrazine, and urea. The results showed that urea has the highest potential for hydrogen enrichment but also increases carbon formation, while ammonia and hydrazine suppress carbon formation and assist in hydrogen production. Hydrazine was found to be the most effective in reducing carbon.
In the present study, thermodynamic calculations have been carried out on water gas shift reaction in presence of some selected chemical additives such as ammonia, hydrazine, and urea to understand their impact on the hydrogen generation and carbon suppression. The calculations were performed in a temperature range of 300-1300 K at constant pressure (1 bar) while varying the amount of additives from 0.5 to 2 mol. The results suggest that urea has the highest potential for hydrogen enrichment; however, it also increases carbon formation within the investigated conditions, as compared to other additives, ammonia and hydrazine, which suppress carbon formation along with assisting in hydrogen production. Hydrazine was found to be the most effective in reducing carbon and a molar ratio of N2H4:CH4:CO of 1.5:1:1 was sufficient for completely removing carbon throughout the temperature range of 300-1300 K, as compared to 2:1:1 M ratio for NH3:CH4:CO. Both, ammonia and hydrazine, being hydrogen storage materials release hydrogen along with suppressing carbon, which results in suitable conditions for sustained long term catalytic experiments where catalyst poisoning by coking can be eliminated. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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