Methane hydrate formation in confined nanospace can surpass nature

dc.contributor.affiliationInstituto Universitario Mixto de Tecnología Química
dc.contributor.authorCasco, M.E.es_ES
dc.contributor.authorSilvestre Albero, Joaquines_ES
dc.contributor.authorRamirez-Cuesta, A.J.es_ES
dc.contributor.authorRey Garcia, Fernando
dc.contributor.authorJorda Moret, Jose Luis
dc.contributor.authorBansode, A.es_ES
dc.contributor.authorUrakawa, A.es_ES
dc.contributor.authorPeral, I.es_ES
dc.contributor.authorMartinez-Escandell, M.es_ES
dc.contributor.authorKaneko, K.es_ES
dc.contributor.authorRodríguez Reinoso, Franciscoes_ES
dc.contributor.funderEuropean Commission
dc.contributor.funderGeneralitat Valenciana
dc.contributor.funderMinisterio de Economía y Competitividad
dc.date.accessioned2016-05-17T09:42:51Z
dc.date.available2016-05-17T09:42:51Z
dc.date.issued2015-03
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 degrees 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.accrualMethodSes_ES
dc.description.bibliographicCitationCasco, M.; Silvestre Albero, J.; Ramirez-Cuesta, A.; Rey Garcia, F.; Jorda Moret, JL.; Bansode, A.; Urakawa, A.... (2015). Methane hydrate formation in confined nanospace can surpass nature. Nature Communications. 6(6432):1-8. https://doi.org/10.1038/ncomms7432es_ES
dc.description.issue6432es_ES
dc.description.referencesSloan, E. D. Jr., & Koh, C. A. Clathrate Hydrates of Natural Gases 3rd edn CRC Press (2007).es_ES
dc.description.referencesGutt, C. et al. The structure of deuterated methane-hydrate. J. Chem. Phys. 113, 4713–4721 (2000).es_ES
dc.description.referencesHolbrook, W. S., Hoskins, H., Wood, W. T., Stephen, R. A. & Lizarralde, D. Methane hydrate and free gas on the Blake Ridge from vertical seismic profiling. Science 273, 1840–1843 (1996).es_ES
dc.description.referencesSloan, E. D. Jr., Fundamental principles and applications of natural gas hydrates. Nature 426, 353–363 (2003).es_ES
dc.description.referencesRodríguez-Reinoso, F., Almansa, C. & Molina-Sabio, M. Contribution to the evaluation of density of methane adsorbed on activated carbon. J. Phys. Chem. B 109, 20227–20231 (2005).es_ES
dc.description.referencesKockrick, E. et al. Ordered mesoporous carbide derived carbons for high pressure gas storage. Carbon 48, 1707–1717 (2010).es_ES
dc.description.referencesKlein, N. et al. A mesoporous metal-organic framework. Angew. Chem. Int. Ed. 48, 9954–9957 (2009).es_ES
dc.description.referencesMakal, T. A., Li, J.-R., Lu, W. & Zhou, H.-C. Methane storage in advanced porous materials. Chem. Soc. Rev. 41, 7761–7779 (2012).es_ES
dc.description.referencesPeng, Y. et al. Methane storage in metal-organic frameworks: Current records, surprise findings, and challenges. J. Am.Chem. Soc. 135, 11887–11894 (2013).es_ES
dc.description.referencesCasco, M. E. et al. High-pressure methane storage in porous materials: are carbon materials in the pole position? Chem. Mater 27, 959–964 (2015).es_ES
dc.description.referencesRamos-Fernández, J. M., Martínez-Escandell, M. & Rodríguez-Reinoso, F. Production of binderless activated carbon monoliths by KOH activation of carbon mesophase materials. Carbon 46, 384–386 (2008).es_ES
dc.description.referencesMarsh, H. & Rodríguez-Reinoso, F. Activated Carbon Elsevier (2006).es_ES
dc.description.referencesKubo, T. et al. Diffusion-barrier-free porous carbon monoliths as a new form of activated carbon. ChemSusChem 5, 2271–2277 (2012).es_ES
dc.description.referencesKaneko, K., Itoh, T. & Fujimori, T. Collective interactions of molecules with an interfacial solid. Chem. Lett. 41, 466–475 (2012).es_ES
dc.description.referencesNakamura, M., Ohba, T., Branton, P., Kanoh, H. & Kaneko, K. Equilibrium-time and pore-width dependent hysteresis of water adsorption isotherm on hydrophobic microporous carbons. Carbon 48, 305–308 (2010).es_ES
dc.description.referencesVysniauskas, A. & Bishnoi, P. R. A kinetic study of methane hydrate formation. Chem. Eng. Sci. 38, 1061–1072 (1983).es_ES
dc.description.referencesJunhong, Q. & Tianmin, G. Kinetics of methane hydrate formation in pure water and inhibitor containing systems. Chin. J. Chem. Eng 10, 316–322 (2002).es_ES
dc.description.referencesLiu, J., Zhou, Y., Sun, Y., Su, W. & Zhou, L. Methane storage in wet carbon of tailored pore sizes. Carbon 49, 3731–3736 (2011).es_ES
dc.description.referencesPerrin, A., Celzard, A., Marêché, J. F. & Furdin, G. Methane storage within dry and wet activated carbons: a comparative study. Energy Fuels 17, 1283–1291 (2003).es_ES
dc.description.referencesZhou, L., Liu, L., Su, W., Sun, Y. & Zhou, Y. Progress in studies of natural gas storage with wet adsorbents. Energy Fuels 24, 3789–3795 (2010).es_ES
dc.description.referencesCelzard, A. & Marêché, J. F. Optimal wetting of activated carbons for methane hydrate formation. Fuel 85, 957–966 (2006).es_ES
dc.description.referencesWebb, E. B. et al. High pressure rheology of hydrate slurries formed from water-in-oil emulsions. Energy Fuels 26, 3504–3509 (2012).es_ES
dc.description.referencesUrita, K. et al. Confinement in carbon nanospace-induced production of KI nanocrystals of high-pressure phase. J. Am. Chem. Soc. 133, 10344–10347 (2011).es_ES
dc.description.referencesFujimori, T. et al. Conducting linear chains of sulphur inside carbon nanotubes. Nat. Commun. 4, 2162 (2013).es_ES
dc.description.referencesTse, J. S., Ratcliffe, C. L., Powell, B. M., Sears, V. F. & Handa, Y. P. Rotational and translational motions of trapped methane. Incoherent inelastic neutron scattering of methane hydrate. J. Phys. Chem. A 101, 4491–4495 (1997).es_ES
dc.description.referencesGutt, C. et al. Quantum rotations in natural methane-clathrates from the Pacific sea-floor. Europhys. Lett. 48, 269–275 (1999).es_ES
dc.description.referencesStern, L. A., Kirby, S. H. & Durham, W. B. Peculiarities of methane clathrate hydrate formation and solid-state deformation, including possible superheating of water ice. Science 273, 1843–1848 (1996).es_ES
dc.description.referencesGutt, C. et al. The structure of deuterated methane hydrate. J. Chem. Phys. 113, 4713–4721 (2000).es_ES
dc.description.referencesEverett, S. M. et al. Kinetics of methane hydrate decomposition studies via in situ low temperature X-ray powder diffraction. J. Phys. Chem. A 117, 3593–3598 (2013).es_ES
dc.description.referencesMiyawaki, J. et al. Macroscopic evidence of enhanced formation of methane nanohydrates in hydrophobic nanospaces. J. Phys. Chem. B 102, 2187–2192 (1998).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.en_EN
dc.description.upvformatpfin8es_ES
dc.description.upvformatpinicio1es_ES
dc.description.volume6es_ES
dc.identifier.doi10.1038/ncomms7432
dc.identifier.issn2041-1723
dc.identifier.urihttps://riunet.upv.es/handle/10251/64217
dc.languageIngléses_ES
dc.publisherNature Publishing Group: Nature Communicationses_ES
dc.relation.ispartofNature Communicationses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN//PLE2009-0052/ES/Monolitos nanoestructurados de carbón para almacenamiento y conversión de metano/
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/283883/EU/Neutron Scattering and Muon Spectroscopy Integrated Initiative/en_EN
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//PCIN-2013-057/ES/ADSORBENTES EQUIPADOS CON NANORADIADORES PARA ALMACENAMIENTO EFICIENTE Y SEGURO DE METANO/
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//MAT2012-38567-C02-01/ES/MATERIALES ZEOLITICOS COMO ESTRUCTURAS ANFITRIONAS DE NANOPARTICULAS. SINTESIS Y APLICACIONES NANOTECNOLOGICAS, CATALITICAS Y MEDIOAMBIENTALES/
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//SEV-2013-0319/ES/-/
dc.relation.projectIDinfo:eu-repo/grantAgreement/GVA//PROMETEO09%2F2009%2F002/ES/Desarrollo de nanomateriales para aplicaciones energéticas y medioambientales/
dc.relation.publisherversionhttp://dx.doi.org/10.1038/ncomms7432es_ES
dc.relation.references10.1201/9781420008494es_ES
dc.relation.references10.1063/1.1288789es_ES
dc.relation.references10.1126/science.273.5283.1840es_ES
dc.relation.references10.1038/nature02135es_ES
dc.relation.references10.1021/jp053840ees_ES
dc.relation.references10.1016/j.carbon.2010.01.004es_ES
dc.relation.references10.1002/anie.200904599es_ES
dc.relation.references10.1039/c2cs35251fes_ES
dc.relation.references10.1021/ja4045289es_ES
dc.relation.references10.1021/cm5042524es_ES
dc.relation.references10.1016/j.carbon.2007.11.042es_ES
dc.relation.references10.1002/cssc.201200234es_ES
dc.relation.references10.1246/cl.2012.466es_ES
dc.relation.references10.1016/j.carbon.2009.09.008es_ES
dc.relation.references10.1016/0009-2509(83)80027-Xes_ES
dc.relation.references10.1016/j.carbon.2011.05.005es_ES
dc.relation.references10.1021/ef030067ies_ES
dc.relation.references10.1021/ef100315tes_ES
dc.relation.references10.1016/j.fuel.2005.10.019es_ES
dc.relation.references10.1021/ef300163yes_ES
dc.relation.references10.1021/ja202565res_ES
dc.relation.references10.1038/ncomms3162es_ES
dc.relation.references10.1021/jp963006ces_ES
dc.relation.references10.1209/epl/i1999-00476-xes_ES
dc.relation.references10.1126/science.273.5283.1843es_ES
dc.relation.references10.1021/jp4020178es_ES
dc.relation.references10.1021/jp980034hes_ES
dc.relation.senia306410es_ES
dc.rightsReserva de todos los derechoses_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectMethane hydratees_ES
dc.subjectNanospacees_ES
dc.titleMethane hydrate formation in confined nanospace can surpass naturees_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dspace.entity.typePublication
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