RESUMEN
Direct conversion of biogas via the integrative process of dry reforming of methane (DRM) and catalytic methane decomposition (CDM) has received a great attention as a promising green catalytic process for simultaneous production of syngas and carbon nanotubes (CNTs). In this work, the effects of reaction temperature of 700-1100 °C and CH4/CO2 ratio of biogas were investigated over NiMo/MgO catalyst in a fixed bed reactor under industrial feed condition of pure biogas. The reaction at 700 °C showed a rapid catalyst deactivation within 3 h due to the formation of amorphous carbon on catalyst surface. At higher temperature of 800-900 °C, the catalyst can perform the excellent performance for producing syngas and carbon nanotubes. Interestingly, the smallest diameter and the highest graphitization of CNTs was obtained at high temperature of 1000 °C, while elevating temperature to 1100 °C leads to agglomeration of Ni particles, resulting in a larger size of CNTs. The reaction temperature exhibits optimum at 800 °C, providing the highest CNTs yield with high graphitization, high syngas purity up to 90.04% with H2/CO ratio of 1.1, and high biogas conversion (XCH4 = 86.44%, XCO2 = 95.62%) with stable performance over 3 h. The typical composition biogas (CH4/CO2 = 1.5) is favorable for the integration process, while the CO2 rich biogas caused a larger grain size of catalyst and a formation of molybdenum oxide nanorods (MoO3). The long-term stability of NiMo/MgO catalyst at 800 °C showed a stable trend (> 20 h). The experimental findings confirm that NiMo/MgO can perform the excellent activity and high stability at the optimum condition, allowing the process to be more promising for practical applications.
RESUMEN
Biogas has been widely regarded as a promising source of renewable energy. Recently, the direct conversion of biogas over heterogeneous catalysts for the simultaneous production of syngas and carbon nanotubes exhibits a high potential for full utilization of biogas with great benefits. Involving the combined dry reforming of methane and catalytic decomposition of methane, the efficiency of process is strongly depended on the catalyst activity/stability, mainly caused by carbon deposition. In this study, Ni-Mo catalyst is engineered to provide a life-long performance and perform high activity in the combined process. The surface modification of catalysts by a controlled carburization pretreatment is proposed for the first time to produce a carbide catalyst along with improving the catalyst stability as well as the reactivity for direct conversion of biogas. The performance of as-prepared carbide catalysts is investigated with comparison to the oxide and metallic ones. As a result, the Ni-Mo2C catalyst exhibited superior activity and stability over its counterparts, even though the condensed nanocarbon was largely grown and covered on the surface. In addition, up to 82% of CH4 conversion and 93% of CO2 conversion could remain almost constant at 800 °C throughout the entire test period of 3 h under a high flowrate inlet stream of pure biogas at 48,000 cm3 g-1 h-1. The XPS spectra of catalysts confirmed that the presence of Mo2C species on the catalyst surface could promote the stability and reactivity of the catalyst, resulting in higher productivity of carbon nanotubes over a longer time.
RESUMEN
Selecting a suitable catalyst for implementing the simultaneous production of hydrogen-rich syngas and multi-walled carbon nanotubes through the integration of dry reforming and methane decomposition reactions has recently gained great interests. In this study, a series of bimetallic (NiMo/MgO) and trimetallic (CoNiMo/MgO, FeNiMo/MgO, CoFeMo/MgO) catalysts was prepared and evaluated for a catalytic activity of CH4 and CO2 conversions of biogas in a fixed bed reactor at 800 °C and atmospheric pressure. Among the investigated catalysts, the bimetallic NiMo/MgO catalyst showed the outstanding catalytic performance with 86.4% CH4 conversion and 95.6% CO2 conversion as well as producing the highest syngas purity of 90.0% with H2/CO ratio = 1.1. Moreover, the characterization of the synthesized solid products proved that the well-aligned structured morphology, high purity, and excellent textural properties of CNTs were obtained by using NiMo/MgO catalyst. On the other hand, using trimetallic catalysts which have the composition of Co and Fe leads to the severe deactivation. This could be attributed the catalyst oxidation with CO2 in biogas, resulting in the transformation of metals into large metal oxides. The integrative process with NiMo/MgO catalyst is regarded as a promising pathway, which has a high potential for directly converting biogas into the high value-added products and providing a green approach for managing the enormous amounts of wastes.