Methane hydrate formation in confined nanospace can surpass nature

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dc.contributorMateriales Avanzadoses_ES
dc.contributor.authorCasco, Mirian Elizabeth-
dc.contributor.authorSilvestre-Albero, Joaquín-
dc.contributor.authorRamírez-Cuesta, Anibal J.-
dc.contributor.authorRey, Fernando-
dc.contributor.authorJordá, José L.-
dc.contributor.authorBansode, Atul-
dc.contributor.authorUrakawa, Atsushi-
dc.contributor.authorPeral, Inma-
dc.contributor.authorMartinez-Escandell, Manuel-
dc.contributor.authorKaneko, Katsumi-
dc.contributor.authorRodríguez Reinoso, Francisco-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Inorgánicaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Materialeses_ES
dc.date.accessioned2016-09-13T10:54:00Z-
dc.date.available2016-09-13T10:54:00Z-
dc.date.issued2015-03-02-
dc.identifier.citationNature Communications. 2015, 6: 6432. doi:10.1038/ncomms7432es_ES
dc.identifier.issn2041-1723-
dc.identifier.urihttp://hdl.handle.net/10045/57852-
dc.description.abstractNatural 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).es_ES
dc.description.sponsorshipWe acknowledge UK Science and Technlology Facilities Council for the provision of beam time on the TOSCA spectrometer (Projects RB1410624 and RB122099) and financial support from the European Commission under the 7th Framework Programme through the ‘Research Infrastructures’ action of the ‘Capacities’ Programme (NMI3-II Grant number 283883). J.S.-A. and F.R. acknowledges the financial support from MINECO: Strategic Japanese-Spanish Cooperation Program (PLE2009-0052), Concert Project-NASEMS (PCIN-2013-057) and Generalitat Valenciana (PROMETEO/2009/002). F.R. and J.L.J. thank the financial support from MINECO (MAT2012-38567-C02-01, Consolider Ingenio 2010-Multicat CSD-2009-00050 and SEV-2012-0267). K.K. thanks Grant-in-Aid for Scientific Research (A) (2424-1038), Japan. A.B. and A.U. thank the financial support from MINECO (SEV-2013-0319). J.L.J. and I.P. thank synchrotron ALBA for beamtime availability.es_ES
dc.languageenges_ES
dc.publisherMacmillan Publisherses_ES
dc.rightsThis work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/es_ES
dc.subjectMethane hydrate formationes_ES
dc.subjectConfined nanospacees_ES
dc.subject.otherQuímica Inorgánicaes_ES
dc.titleMethane hydrate formation in confined nanospace can surpass naturees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1038/ncomms7432-
dc.relation.publisherversionhttp://dx.doi.org/10.1038/ncomms7432es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/283883es_ES
Aparece en las colecciones:INV - LMA - Artículos de Revistas
Investigaciones financiadas por la UE

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