甲烷
水合物
纳米孔
笼状水合物
永久冻土
材料科学
化学物理
同步加速器
化学计量学
中子衍射
天然气
化学工程
中子散射
散射
化学
纳米技术
晶体结构
地质学
物理化学
结晶学
物理
有机化学
光学
工程类
海洋学
作者
Mirian Elizabeth Casco,Joaquín Silvestre-Albero,Anibal J. Ramírez-Cuesta,Fernando Rey,José L. Jordá,Atul Bansode,Atsushi Urakawa,Inma Peral,Manuel Martínez Escandell,Katsumi Kaneko,F. Rodrı́guez-Reinoso
摘要
Natural methane hydrates are believed to be the largest source of hydrocarbons on Earth. These structures are formed in specific locations such as deep-sea sediments and the permafrost based on demanding conditions of high pressure and low temperature. Here we report that, by taking advantage of the confinement effects on nanopore space, synthetic methane hydrates grow under mild conditions (3.5 MPa and 2 °C), with faster kinetics (within minutes) than nature, fully reversibly and with a nominal stoichiometry that mimics nature. The formation of the hydrate structures in nanospace and their similarity to natural hydrates is confirmed using inelastic neutron scattering experiments and synchrotron X-ray powder diffraction. These findings may be a step towards the application of a smart synthesis of methane hydrates in energy-demanding applications (for example, transportation).
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