In-situ hydrogasification/regeneration of NiAl-hydrotalcite derived catalyst in the reaction of CO2 reforming of methane: A versatile approach to catalyst recycling. (June 2016)

• Record Type: Journal Article
• Authors: Abdelsadek, Z.; Sehailia, M.; Halliche, D.; Gonzalez-Delacruz, V.M.; Holgado, J.P.; Bachari, K.; Caballero, A.; Cherifi, O.
• Is Part Of: Journal of CO₂ utilization. Volume 14(2016)
• Page Start: 98
• Page End: 105
• Publication Date: 2016-06
• Subjects: Hydrotalcite -- Dry reforming of methane -- Hydrogasification -- Catalyst regeneration; Carbon dioxide -- Periodicals; Carbon dioxide -- Environmental aspects -- Periodicals; Carbon dioxide mitigation -- Periodicals; Carbon dioxide; Carbon dioxide -- Environmental aspects; Carbon dioxide mitigation; Periodicals; 628.53205
• DOI: 10.1016/j.jcou.2016.03.004
• Languages: English
• ISSNs: 2212-9820

Abstract

Graphical abstract: Highlights: NiAl hydrotalcite derived catalyst was successfully synthesized by co-precipitation. The catalyst was successfully utilized in the process of CO2 reforming of methane. Upon carbon deposition, the catalyst was regenerated using hydrogasification. The catalyst was successfully utilized in subsequent CO2 reforming of methane cycle. 14% increase in the amount of H2 /CO was attained after regeneration. Abstract: A novel approach describing the in-situ regeneration of NiAl hydroalcite derived catalyst between two cycle reaction systems of CO2 reforming of methane, also known as dry reforming of methane (DRM) is described herein. The catalyst was initially prepared by co-precipitation method at pH = 11 and calcined at 450 °C for 6 h. The obtained material was characterized using X-ray diffraction (XRD) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Brunauer-Emmett-Teller (BET), atomic absorption spectroscopy (AAS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetry (TG/ATD) and temperature programmed reduction (TPR-H2 ) techniques. Following treatment of our catalyst under DRM conditions, the catalyst was subjected to in-situ hydrogasification conditions to promote regeneration followed by a second DRM cycle. An increase of 15.7% in the conversion of CH4 and 17.3% in the conversion of CO2 was attained, while the ratio of resulting H2 /CO augmented by 14%. The ratio of H2 consumed over the course of two hours hydrogasification, to that generated over ten hours of DRM, was 9.6%. The small particle sizes of resulting Ni° species as well as their high stability were both key factors contributing to the increase in the amount of H2 /CO produced prior to and after regeneration.