Casco Mirian E, Jordá José L, Rey Fernando, Fauth François, Martinez-Escandell Manuel, Rodríguez-Reinoso Francisco, Ramos-Fernández Enrique V, Silvestre-Albero Joaquín
Laboratorio de Materiales Avanzados, Instituto Universitario de Materiales-, Departamento de Química Inorgánica, Universidad de Alicante, Ctra. San Vicente-Alicante s/n, 03690, San Vicente del Raspeig, Spain.
Instituto de Tecnología Química, Universidad Politécnica de Valencia-CSIC, Avda. de los Naranjos s/n, 46022, Valencia, Spain.
Chemistry. 2016 Jul 11;22(29):10028-35. doi: 10.1002/chem.201600958. Epub 2016 Jun 6.
The molecular exchange of CH4 for CO2 in gas hydrates grown in confined nanospace has been evaluated for the first time using activated carbons as a host structure. The nano-confinement effects taking place inside the carbon cavities and the exceptional physicochemical properties of the carbon structure allows us to accelerate the formation and decomposition process of the gas hydrates from the conventional timescale of hours/days in artificial bulk systems to minutes in confined nanospace. The CH4 /CO2 exchange process is fully reversible with high efficiency at practical temperature and pressure conditions. Furthermore, these activated carbons can be envisaged as promising materials for long-distance natural gas and CO2 transportation because of the combination of a high storage capacity, a high reversibility, and most important, with extremely fast kinetics for gas hydrate formation and release.
首次使用活性炭作为主体结构,对在受限纳米空间中生长的气体水合物中CH4与CO2的分子交换进行了评估。碳孔内部发生的纳米限域效应以及碳结构特殊的物理化学性质,使我们能够将气体水合物的形成和分解过程从人工本体系统中数小时/数天的传统时间尺度加速至受限纳米空间中的数分钟。在实际温度和压力条件下,CH4/CO2交换过程完全可逆且效率很高。此外,由于具有高储存容量、高可逆性,最重要的是具有极快的气体水合物形成和释放动力学,这些活性炭有望成为长距离天然气和CO2运输的材料。