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Kinetic modelling of the hydrothermal carbonization of compost derived from municipal solid waste

dc.contributor.authorRoman, Fernanda
dc.contributor.authorDíaz de Tuesta, Jose Luis
dc.contributor.authorPraça, Paulo
dc.contributor.authorSilva, Adrián
dc.contributor.authorFaria, Joaquim
dc.contributor.authorGomes, Helder
dc.date.accessioned2020-01-14T15:09:37Z
dc.date.available2020-01-14T15:09:37Z
dc.date.issued2019
dc.description.abstractNowadays, municipal solid waste (MSW) management commonly includes a mechanical and biological treatment process (MBT). The solid stream from the anaerobic digestion of the organic fraction can be processed to obtain a compost, which can be used as fertilizer. However, compost production is higher than the existing demand, and the expected developments on up-coming directives ruling “End-of-waste” criteria are leading to barriers on the use of MSW-derived fertilizers [1]. Thus, the development of new alternatives for the treatment of organic wastes and compost valorization are necessary. This work deals with the valorization of compost from MBT, through the production of catalysts by Hydrothermal Carbonization (HTC) [2]. HTC of the compost was carried out in a Teflon vessel inserted in a stainless-steel body at different operating conditions (150-230 ºC,1-5 h, 1-4 g of compost, 30 mL). A Doehlert Matrix was considered to plan the experiments. The carbon balance and the kinetic equations were evaluated from experimental data reporting the carbon content in the liquid (estimated by TOC analysis) and solid phases (estimated by elemental analysis). A lumped kinetic model based on the elemental carbon content is proposed (Fig. 1), anticipating that the compost (C) undergoes reactions that originate liquid intermediates (L), reaction 1, and sequentially results in hydrochar (HC) and gases (G), reactions 2 and 3, respectively. In addition, it was assumed that HC and G were also produced from the compost directly, reactions 4 and 5, respectively. The highest kinetic constant at 190 ºC (8.3·10-4 min-1) was found for the formation of the liquid soluble intermediates from compost (reaction 1), whereas the production of hydrochar from the liquid intermediates (reaction 2) shows the lowest kinetic constant (3.1·10-4 min-1). The lowest activation energy was estimated for reaction 1 (23 kJ·mol-1), while reactions 2 and 4, related to the formation of hydrochar, resulted in the highest values (85 and 195 kJ·mol-1, respectively), meaning that the production of hydrochar strongly depends on the temperature.pt_PT
dc.description.sponsorshipThis work was financially supported by project “VALORCOMP - Valorización de compost y otros desechos procedentes de la fracción orgánica de los residuos municipales”, 0119_VALORCOMP_2_P, and project “AIProcMat@N2020 - Advanced Industrial Processes and Materials for a Sustainable Northern Region of Portugal 2020”, reference NORTE-01-0145-FEDER-000006, supported by NORTE 2020, under the Portugal 2020 Partnership Agreement, through FEDER; the Associate Laboratory LSRELCM - UID/EQU/50020/2019 - funded by national funds through FCT/MCTES (PIDDAC); and CIMO UID/AGR/00690/2019 through FEDER under Program PT2020.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRoman, Fernanda Fontana; Díaz de Tuesta, Jose Luis; Praça, Paulo; Silva, Adrián; Faria, Joaquim; Gomes, Helder (2019). Kinetic modelling of the hydrothermal carbonization of compost derived from municipal solid waste. In XXV Encontro Galego-Português de Química. Santiago de Compostela. ISBN 978-84-09-16320-5pt_PT
dc.identifier.issn978-84-09-16320-5
dc.identifier.urihttp://hdl.handle.net/10198/20360
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.titleKinetic modelling of the hydrothermal carbonization of compost derived from municipal solid wastept_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceSantiago de Compostela, Espanhapt_PT
oaire.citation.startPage235pt_PT
oaire.citation.titleXXV Encontro Galego-Portugues de Quimicapt_PT
person.familyNameRoman
person.familyNameDíaz de Tuesta
person.familyNameGomes
person.givenNameFernanda F.
person.givenNameJose Luis
person.givenNameHelder T.
person.identifier.ciencia-idEE1B-DAA7-D0BD
person.identifier.ciencia-id7A1F-022B-7DBF
person.identifier.ciencia-id6218-1E19-13EE
person.identifier.orcid0000-0001-5360-5298
person.identifier.orcid0000-0003-2408-087X
person.identifier.orcid0000-0001-6898-2408
person.identifier.ridD-9785-2017
person.identifier.scopus-author-id55755821600
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublicationc145030b-c811-4be4-b6af-1926e364cb33
relation.isAuthorOfPublication2ad0465f-5f8a-4b14-90f5-bf85996f9ce1
relation.isAuthorOfPublication0eb96337-224a-4339-9918-334436fbbb99
relation.isAuthorOfPublication.latestForDiscovery0eb96337-224a-4339-9918-334436fbbb99

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