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Modeling and optimization of methane dry reforming over Ni–Cu/Al2O3 catalyst using Box–Behnken design

In this work the effects of the contents of nickel (5, 7.5, 10 wt%) and copper (0, 1, 2 wt%) and reaction temperature (650, 700, 750 °C) on the catalytic performance of Ni–Cu/Al2O3 catalyst in methane dry reforming were evaluated using Box–Behnken design in order to optimize methane conversion, H2/C...

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Bibliographic Details
Published in:Journal of energy chemistry 2018-09, Vol.27 (5), p.1475-1488
Main Authors: Nataj, Seyedeh Molood Masoom, Alavi, Seyed Mehdi, Mazloom, Golshan
Format: Article
Language:English
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Summary:In this work the effects of the contents of nickel (5, 7.5, 10 wt%) and copper (0, 1, 2 wt%) and reaction temperature (650, 700, 750 °C) on the catalytic performance of Ni–Cu/Al2O3 catalyst in methane dry reforming were evaluated using Box–Behnken design in order to optimize methane conversion, H2/CO ratio and the catalyst deactivation. Different catalysts were prepared by co-impregnation method and characterized by XRD, BET, H2-TPR, FESEM and TG/DTA analyses. The results revealed that copper addition improved the catalyst reducibility. Promoted catalyst with low amounts of Cu gave higher activity and stability with high resistance to coke deposition and agglomeration of active phase especially during the reaction. However catalysts with high amounts of Cu were less active and rather deactivated due to the active sites sintering as well as Ni covering by Cu-enriched phase. The optimal conditions were determined by desirability function approach as 10 wt% of Ni, 0.83 wt% of Cu at 750 °C. CH4 conversion of 95.1%, H2/CO ratio of 1 and deactivation of 1.4% were obtained experimentally under optimum conditions, which were in close agreement with the values predicted by the developed model. Ni/Al2O3 catalyst promoted with 0.83 wt% of Cu exhibited high activity and stability for the CO2 reforming of methane due to the alloy formation and restriction of sintering. Cu content was optimized using Box–Behnken design. [Display omitted]
ISSN:2095-4956
DOI:10.1016/j.jechem.2017.10.002