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dc.contributor.authorČarnogurská, Mária
dc.contributor.authorPříhoda, Miroslav
dc.contributor.authorLázár, Marián
dc.contributor.authorKurilla, Peter
dc.contributor.authorDobáková, Romana
dc.date.accessioned2018-07-02T11:19:47Z
dc.date.available2018-07-02T11:19:47Z
dc.date.issued2018
dc.identifier.citationMateriali in Tehnologije. 2018, vol. 52, no. 3, p. 335-340.cs
dc.identifier.issn1580-2949
dc.identifier.issn1580-3414
dc.identifier.urihttp://hdl.handle.net/10084/130385
dc.description.abstractThis paper presents the results from an experimental study of the thermal method applied for obtaining platinum-group metals (PGMs) by melting used autocatalysts in an 80 kVA plasma reactor, using suitable fluxes and a reducing agent. As the collector of noble metals, grey cast iron was used during the melting. The melt products were the alloy, inert vitrified slag, syngas and fly ash. In the alloy, when melting the catalyser based on cordierite. there was 99.27 % PGMs and 99.00 % in the case of Cr/Ni-strip catalysts. The loss of PGMs in the slag during the melting of cordierite catalysts was 0.34 % and for Cr/Ni catalysts, it was 0.26 %. A chemical analysis of the ash confirmed that in addition to the mechanically removed CaO, SiO2, MgO, Al2O3, it also contained condensed vapours of Fe+PGMs. During the melting of the cordierite catalyst, the ash contained 0.40 % of the refined metals, while 0.74 % was the figure for the Cr/Ni-strip catalyst. The synthesis gas from the process had a very low heating value (0.16 MJ m(-3) or 0.24 MJ m(-3)).cs
dc.format.extent1436820 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoencs
dc.publisherInštitut za kovinske materiale in tehnologijecs
dc.relation.ispartofseriesMateriali in Tehnologijecs
dc.relation.urihttps://doi.org/10.17222/mit.2017.174cs
dc.rights© MATERIALI IN TEHNOLOGIJEcs
dc.rightsThe journal MATERIALI IN TEHNOLOGIJE/MATERIALS AND TECHNOLOGY is an open access journal, this means its free availability on the public internet, permitting any users to read, download, copy, distribute, print, search, or link to the full texts of these articles, crawl them for indexing, pass them as data to software, or use them for any other non-commercial purposes, without financial, legal, or technical barriers other than those inseparable from gaining access to the internet itself. The only constraint is on reproduction, and the only role for copyright in this domain, should be to give authors control over the integrity of their work and the right to be properly acknowledged and cited.
dc.subjectwastecs
dc.subjectcatalysercs
dc.subjectplatinum-group metalscs
dc.subjectplasma technologycs
dc.titleHigh-temperature processing and recovery of autocatalystscs
dc.title.alternativeVisokotemperaturno procesiranje in reciklaža avtomobilskih katalizatorjevcs
dc.typearticlecs
dc.description.abstract-enV tem članku avtorji predstavljajo rezultate eksperimentalnih raziskav termičnega postopka pridobivanja kovin platinske skupine (PGM, angl.: Platinum Group Metals) s taljenjem izrabljenih avtomobilskih katalizatorjev v 80 kVA plazemskem reaktorju z uporabo primernih talil in redukcijskega sredstva. Kot zbiralnik plemenitih kovin je bila med taljenjem uporabljena siva litina. Produkti taljenja so zlitina, inertna steklasta žlindra, sintezni plin in pepel. V zlitini je bilo pri taljenju katalizatorja na osnovi kordierita koncentriranih 99,27 % PGM, pri katalizatorjih s Cr/Ni trakom pa 99,00%. Pri taljenju kordieritnih katalizatorjev se je v žlindri izgubilo 0,34 % PGM, pri Cr/Ni katalizatorjih pa 0,26 %. Kemijska analiza pepela je potrdila, da poleg mehansko pridobljenih oksidov CaO, SiO2, MgO, Al2O3, le-ta vsebuje tudi kondenzirane pare Fe in PGM. V pepelu se je pri taljenju katalizatorja na osnovi kordierita nahajalo 0,40 % plemenitih kovin, pri katalizatorju s Cr/Ni trakom pa 0,74 %. Sintezni plin iz procesa taljenja je imel zelo nizko kurilno (kalorično) vrednost (0,16 MJ m–3 oz. 0,24 MJ m–3).cs
dc.identifier.doi10.17222/mit.2017.174
dc.rights.accessopenAccesscs
dc.type.versionpublishedVersioncs
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume52cs
dc.description.issue3cs
dc.description.lastpage340cs
dc.description.firstpage335cs
dc.identifier.wos000435102200014


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