Sae-Tang Nonthicha, Saconsint Supanida, Srifa Atthapon, Koo-Amornpattana Wanida, Assabumrungrat Suttichai, Fukuhara Choji, Ratchahat Sakhon
Department of Chemical Engineering, Faculty of Engineering, Mahidol University, Nakhon Pathom, 73170, Thailand.
Center of Excellence in Catalysis and Catalytic Reaction Engineering, Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok, 10330, Thailand.
Sci Rep. 2024 Jul 15;14(1):16282. doi: 10.1038/s41598-024-66938-6.
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 CH/CO 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 H/CO ratio of 1.1, and high biogas conversion (X = 86.44%, X = 95.62%) with stable performance over 3 h. The typical composition biogas (CH/CO = 1.5) is favorable for the integration process, while the CO rich biogas caused a larger grain size of catalyst and a formation of molybdenum oxide nanorods (MoO). 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.
通过甲烷干重整(DRM)和催化甲烷分解(CDM)的一体化过程将沼气直接转化,作为一种同时生产合成气和碳纳米管(CNT)的有前景的绿色催化过程,受到了广泛关注。在这项工作中,在固定床反应器中,在纯沼气的工业进料条件下,研究了700-1100℃的反应温度和沼气的CH/CO比在NiMo/MgO催化剂上的影响。700℃的反应在3小时内显示出催化剂迅速失活,这是由于催化剂表面形成了无定形碳。在800-900℃的较高温度下,该催化剂对合成气和碳纳米管的生产表现出优异的性能。有趣的是,在1000℃的高温下获得了最小直径和最高石墨化程度的碳纳米管,而将温度升高到1100℃会导致镍颗粒团聚,从而使碳纳米管尺寸更大。反应温度在800℃时表现出最佳值,可提供最高的碳纳米管产率,具有高石墨化程度,合成气纯度高达90.04%,H/CO比为1.1,并且在3小时内具有稳定性能的高沼气转化率(X = 86.44%,X = 95.62%)。典型组成的沼气(CH/CO = 1.5)有利于一体化过程,而富含CO的沼气会导致催化剂晶粒尺寸增大并形成氧化钼纳米棒(MoO)。NiMo/MgO催化剂在800℃的长期稳定性显示出稳定趋势(>20小时)。实验结果证实,NiMo/MgO在最佳条件下可表现出优异的活性和高稳定性,使该过程在实际应用中更具前景。