在镍基过氧化物上干法重整甲苯以生产合成气

Jie Ren, Zeeshan Abbasi, Inam Ullah, Feng Zeng
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引用次数: 0

摘要

开发高效的镍基催化剂和了解焦油脱除机理对于生物质气化技术的升级至关重要。文献指出,在蒸汽气氛下,镍基催化剂在重整焦油模型化合物(如甲苯)方面性能优越。在这项工作中,我们合成了 LaCeNiO 催化剂,并考察了它们与基准 ABO 型过氧化物在甲苯干重整(DRT)中的活性。催化实验表明,与 LaCeNiO 相比,LaCeNiO 催化剂在甲苯转化率(85.4%)方面表现出更高的活性和稳定性。通过各种技术进行的结构研究突出表明,镍更容易从 ABO 包晶晶格中还原,从而留下更多的氧空位,并且在 DRT 中对反应物的吸附具有更高的碱性。此外,DRIFTS 实验证实了 DRT 生成合成气的*CHO 参与途径。研究结果为设计催化剂提供了潜在的途径,以支持生物质气化,同时为全球碳减排做出贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dry reforming of toluene for syngas production over Ni-based perovskite-type oxides
Developing efficient Ni-based catalysts and understanding the mechanism of tar removal are crucial for upgrading biomass gasification technology. Literature has identified the superior performance of Ni-based catalysts in reforming tar model compounds like toluene under a steam atmosphere. In this work, we have synthesized LaCeNiO catalysts and examined their activity with benchmark ABO-type perovskites in dry reforming of toluene (DRT). Catalytic experiments revealed that LaCeNiO catalysts exhibited superior activity and stability regarding toluene conversion (85.4%) compared to LaCeNiO. The structural study, conducted through various techniques, highlighted the easier reducibility of Ni from the ABO perovskite lattice, leaving higher oxygen vacancies, and higher basicity for reactant adsorption in DRT. Besides, DRIFTS experiments confirmed the *CHO-participated pathway of syngas generation from DRT. The findings suggested potential pathways for designing catalysts to support biomass gasification while contributing to global carbon reduction.
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