Partial oxidation of methane over CeO2 loaded hydrotalcite (MgNiAl) catalyst for the production of hydrogen rich syngas (H2, CO)

Author(s):  
Muhammad Anees Ul Hasnain ◽  
Asif Hussain Khoja ◽  
Faaz Ahmed Butt ◽  
Mariam Ayesha ◽  
Faisal Saleem ◽  
...  
1993 ◽  
Vol 115 (4) ◽  
pp. 307-313 ◽  
Author(s):  
G. A. Karim ◽  
G. Zhou

The combustion of rich mixtures of methane representing natural gas in air or oxygenated air involving the uncatalyzed partial oxidation of methane is examined analytically with the view of hydrogen and/or synthesis gas (carbon monoxide and hydrogen) production from natural gas. This is carried out in turn for isothermal, constant pressure and constant volume combustion processes over the feed temperature range of 800–2000K and equivalence ratio of up to 3.5. The role of various operating parameters in establishing the yield of hydrogen is presented and discussed. The effectiveness of the controlled recirculation of combustion gases to the feed for enhancing the reaction and conversion rates of methane into hydrogen is examined. It is shown that there are some conditions that can be employed for such recirculation to yield significant increases in the conversion rate.


2010 ◽  
Vol 489 (1) ◽  
pp. 316-323 ◽  
Author(s):  
Ana C. Ferreira ◽  
A.M. Ferraria ◽  
A.M. Botelho do Rego ◽  
António P. Gonçalves ◽  
M. Rosário Correia ◽  
...  

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2495
Author(s):  
Daniela Pietrogiacomi ◽  
Maria Cristina Campa ◽  
Ida Pettiti ◽  
Simonetta Tuti ◽  
Giulia Luccisano ◽  
...  

Ni/ZrO2 catalysts, active and selective for the catalytic partial oxidation of methane to syngas (CH4-CPO), were prepared by the dry impregnation of zirconium oxyhydroxide (Zhy) or monoclinic ZrO2 (Zm), calcination at 1173 K and activation by different procedures: oxidation-reduction (ox-red) or direct reduction (red). The characterization included XRD, FESEM, in situ FTIR and Raman spectroscopies, TPR, and specific surface area measurements. Catalytic activity experiments were carried out in a flow apparatus with a mixture of CH4:O2 = 2:1 in a short contact time. Compared to Zm, Zhy favoured the formation of smaller NiO particles, implying a higher number of Ni sites strongly interacting with the support. In all the activated Ni/ZrO2 catalysts, the Ni–ZrO2 interaction was strong enough to limit Ni aggregation during the catalytic runs. The catalytic activity depended on the activation procedures; the ox-red treatment yielded very active and stable catalysts, whereas the red treatment yielded catalysts with oscillating activity, ascribed to the formation of Niδ+ carbide-like species. The results suggested that Ni dispersion was not the main factor affecting the activity, and that active sites for CH4-CPO could be Ni species at the boundary of the metal particles in a specific configuration and nuclearity.


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