| Literature DB >> 25728378 |
Mirian E Casco1, Joaquín Silvestre-Albero1, Anibal J Ramírez-Cuesta2, Fernando Rey3, Jose L Jordá3, Atul Bansode4, Atsushi Urakawa4, Inma Peral5, Manuel Martínez-Escandell1, Katsumi Kaneko6, Francisco Rodríguez-Reinoso1.
Abstract
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).Entities:
Year: 2015 PMID: 25728378 DOI: 10.1038/ncomms7432
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919