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dc.contributor.authorParra Soto, José Bernardo-
dc.contributor.authorOvín Ania, María Concepción-
dc.contributor.authorArenillas de la Puente, Ana-
dc.contributor.authorRubiera González, Fernando-
dc.contributor.authorPalacios, José María-
dc.contributor.authorPis Martínez, José Juan-
dc.date.accessioned2009-02-24T13:02:08Z-
dc.date.available2009-02-24T13:02:08Z-
dc.date.issued2004-05-04-
dc.identifier.citationJournal of Alloys and Compounds 379(1-2): 280-289 (2004)en_US
dc.identifier.issn0925-8388-
dc.identifier.urihttp://hdl.handle.net/10261/10946-
dc.description10 pages, 7 figures.-- Printed version published on Oct 6, 2004.en_US
dc.description.abstractPolyethyleneterephthalate (PET) has become one of the major post-consumer plastic wastes. PET products present a problem of considerable concern due to the huge amount of solid waste produced. The disposal of this waste, together with its low bio- and photo−degradability represents a serious challenge for industrial countries all over the world. Pyrolysis could provide an alternative and economically viable route for processing PET waste due to the potential uses of different by-products: energy from the pyrolysis gases (58% yield in this work), recovery of terephthalic acid and other subproducts (20%), and a solid residue (22%), which has shown a high textural development after activation. The pyrolysis of PET waste was performed in a quartz reactor (i.d. 35 mm) under an inert atmosphere. Further activation was carried out at a temperature of 925°C, with a flow rate of 10 ml min−1 of CO2. A series of carbon materials with different burn-off degrees was obtained. Textural characterisation of the samples was carried out by performing N2 adsorption isotherms at −196°C. Changes in the morphological and structural properties of chars were studied by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The carbons obtained were isotropic and highly microporous materials with apparent BET surface areas of up to 2500 m2 g−1. The suitability of the samples for hydrogen storage was studied by performing H2 adsorption measurements in the 0–1 bar pressure range. Adsorption–desorption experiments showed that reversible physisorption takes place in all the samples. The hydrogen adsorption capacities of the activated PET waste compare favourably well with those attained with high-value carbon materials.en_US
dc.format.extent21442 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsopenAccessen_US
dc.subjectHydrogen storageen_US
dc.subjectCarbon materialsen_US
dc.subjectX-ray diffractionen_US
dc.titleTextural development and hydrogen adsorption of carbon materials from PET wasteen_US
dc.typeartículoen_US
dc.identifier.doi10.1016/j.jallcom.2004.02.044-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.jallcom.2004.02.044en_US
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