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Evaluation of a Catalyst Durability in Absence and Presence of Toluene Impurity: Case of the Material Co(2)Ni(2)Mg(2)Al(2) Mixed Oxide Prepared by Hydrotalcite Route in Methane Dry Reforming to Produce Energy
Ni, Co, Mg, and Al mixed-oxide solids, synthesized via the hydrotalcite route, were investigated in previous works toward the dry reforming of methane for hydrogen production. The oxide Co(2)Ni(2)Mg(2)Al(2) calcined at 800 °C, Co(2)Ni(2)Mg(2)Al(2)800, showed the highest catalytic activity in the stu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540188/ https://www.ncbi.nlm.nih.gov/pubmed/31027355 http://dx.doi.org/10.3390/ma12091362 |
Sumario: | Ni, Co, Mg, and Al mixed-oxide solids, synthesized via the hydrotalcite route, were investigated in previous works toward the dry reforming of methane for hydrogen production. The oxide Co(2)Ni(2)Mg(2)Al(2) calcined at 800 °C, Co(2)Ni(2)Mg(2)Al(2)800, showed the highest catalytic activity in the studied series, which was ascribable to an interaction between Ni and Co, which is optimal for this Co/Ni ratio. In the present study, Co(2)Ni(2)Mg(2)Al(2)800 was compared to a commercial catalyst widely used in the industry, Ni(50%)/Al(2)O(3), and showed better activity despite its lower number of active sites, as well as lower amounts of carbon on its surface, i.e. less deactivation. In addition to this, Co(2)Ni(2)Mg(2)Al(2)800 showed stability for 20 h under stream during the dry reforming of methane. This good durability is attributed to a periodic cycle of carbon deposition and removal as well as to the strong interaction between Ni and Co, preventing the deactivation of the catalyst. The evaluation of the catalytic performances in the presence of toluene, which is an impurity that exists in biogas, is also a part of this work. In the presence of toluene, the catalytic activity of Co(2)Ni(2)Mg(2)Al(2)800 decreases, and higher carbon formation on the catalyst surface is detected. Toluene adsorption on catalytic sites, side reactions performed by toluene, and the competition between toluene and methane in the reaction with carbon dioxide are the main reasons for such results. |
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