Cue Gonzalez Alejandra, Weiss-Hortala Elsa, Pham Quoc Nghi, Pham Minh Doan
Centre RAPSODEE, IMT Mines Albi, UMR CNRS 5302, Université de Toulouse, Campus Jarlard, CEDEX 09, 81013 Albi, France.
ICMMO (Institute of Molecular Chemistry and Materials), Université Paris-Saclay, CNRS, 91400 Orsay, France.
Molecules. 2025 May 9;30(10):2110. doi: 10.3390/molecules30102110.
The catalytic methanation reaction allows for the attainment of methane from carbon dioxide and hydrogen. This reaction is particularly interesting for the direct upgrading of biogas, which mainly contains methane and carbon dioxide, into biomethane. This work focused on the synthesis and evaluation of natural clay-supported nickel catalysts in the catalytic methanation reaction. Natural clay could be directly used as a low-cost catalyst support for the deposition of small nickel nanoparticles (1-15 nm) by the standard incipient wetness impregnation method. These catalysts showed high activity and excellent selectivity into methane and excellent catalytic stability (80% carbon dioxide conversion, nearly 100% methane selectivity at 500 °C, 1 bar, and WHSV = 17,940 mL·g·h for 48 h on stream) and outperformed their counterparts prepared with an industrial alumina support as reference.
催化甲烷化反应可实现由二氧化碳和氢气制取甲烷。该反应对于将主要含有甲烷和二氧化碳的沼气直接升级为生物甲烷尤为重要。这项工作聚焦于天然粘土负载型镍催化剂在催化甲烷化反应中的合成与评价。天然粘土可直接用作低成本催化剂载体,通过标准的初湿浸渍法沉积小尺寸镍纳米颗粒(1 - 15纳米)。这些催化剂表现出高活性、对甲烷的优异选择性以及出色的催化稳定性(在500℃、1巴和空速为17,940 mL·g·h的条件下连续运行48小时,二氧化碳转化率达80%,甲烷选择性近100%),且性能优于以工业氧化铝载体为参比制备的同类催化剂。