Process Optimization for Syngas Production from the Dry Reforming of Methane over 5Ni+3Sr/10Zr+Al Catalyst Using Multiple Response Surface Methodology

Author:

Al‐Fatesh Ahmed S.1,El‐Salamony Radwa A.2,Roushdy Mai H.3,Alwan Saba M.4,Osman Ahmed I.5ORCID,Alfatesh Sadeq A.1,Ahmed Hamid1,Fakeeha Anis H.1,Ibrahim Ahmed A.1

Affiliation:

1. Chemical Engineering Department College of Engineering King Saud University P.O. Box 800 Riyadh 11421 Saudi Arabia

2. Process Development Department Egyptian Petroleum Research Institute (EPRI) Cairo 11727 Egypt

3. Chemical Engineering Department Faculty of Engineering The British University in Egypt (BUE) El‐Sherouk City Cairo 11837 Egypt

4. College of Science King Saud University P.O. Box 800 Riyadh 11451 Saudi Arabia

5. School of Chemistry and Chemical Engineering Queen's University Belfast Belfast Northern Ireland BT9 5AG UK

Abstract

Abstract5Ni+3Sr/10Zr+Al catalyst is synthesized using the impregnation method, characterized, and tested for dry reforming of methane. The influence of reaction temperature, feed ratio (CO2/CH4), and gas hour space velocity are examined using multiple response surface methodology through three factors in, a four‐level central composite design. Second and higher‐order regression models are applied to evaluate the interaction between the process parameters and responses. The results indicate that the reaction temperature is the most influential followed by the space velocity, while the feed ratio has a weak effect. The optimum values that maximize each of the response variables are found to be the reaction temperature at 746 °C, the space velocity of 12 000 ccg−1h−1, and the feed ratio of 0.958. Under these conditions, the predicted CH4 and CO2 conversions are 86.83% and 92.27%, respectively. While the H2/CO ratio is 1.02. On the other hand, the experimental results match the predicted ones when the optimum predicted operating conditions are used for the process. A weight loss of <16% is obtained on the spent catalyst after 86 h on stream. This is attributed to the highly basic and oxidative nature of the ZrO2 co‐supported catalyst and indicates the suitability of the developed catalyst.

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials

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