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dc.contributor.authorVivo Vílches, José Francisco
dc.contributor.authorBailón García, Esther 
dc.contributor.authorPérez Cadenas, Agustín Francisco 
dc.contributor.authorCarrasco Marín, Francisco 
dc.contributor.authorMaldonado Hodar, Francisco José 
dc.date.accessioned2025-01-28T10:36:38Z
dc.date.available2025-01-28T10:36:38Z
dc.date.issued2013-11-13
dc.identifier.citationCarbon 68, 2014, Pages 520-530es_ES
dc.identifier.urihttps://hdl.handle.net/10481/100708
dc.description.abstractAn activated carbon with developed porosity and surface area (SBET = 2387 m2 g−1) was prepared by chemical activation and then oxidized with ammonium peroxydisulfate. The oxidation treatment destroyed mesopore walls leading to a severe surface area reduction. Specific thermal treatments were carried out in different portions of the oxidized sample to selectively remove the oxygenated surface complexes. The combination of different techniques revealed that thermal treatment between 300 and 500 °C produces a strong reorganization of oxygenated groups on the chemical structure of carbons. CO2-evolving groups (around 75 wt.%) are selectively transformed into CO-evolving groups. These processes only occur inside the pores, and involve CO2 desorption and re-adsorption in this temperature range. At a higher treatment temperature (700 °C), re-oxidation is prevented and the surface chemistry becomes quite similar to the original activated carbon.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleTailoring the surface chemistry and porosity of activated carbons: evidence of reorganization and mobility of oxygenated surface groupses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsembargoed accesses_ES
dc.identifier.doihttps://doi.org/10.1016/j.carbon.2013.11.030
dc.type.hasVersionAMes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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