Metal-Oxide-Doped Silica Nanoparticles for the Catalytic Glycolysis of Polyethylene Terephthalate

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dc.contributor.authorImran, Muhammadko
dc.contributor.authorLee, Kyoung G.ko
dc.contributor.authorImtiaz, Qasimko
dc.contributor.authorKim, Bo-kyungko
dc.contributor.authorHan, Myungwanko
dc.contributor.authorCho, Bong Gyooko
dc.contributor.authorKim, DoHyunko
dc.date.accessioned2011-07-28T02:23:13Z-
dc.date.available2011-07-28T02:23:13Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-01-
dc.identifier.citationJOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, v.11, no.1, pp.824 - 828-
dc.identifier.issn1533-4880-
dc.identifier.urihttp://hdl.handle.net/10203/24716-
dc.description.abstractPolyethylene terephthalate (PET) was depolymerized to monomer bis(2-hydroxyethyl) terephthalate (BHET) using excess ethylene glycol (EG) in the presence of metal oxides that were impregnated on different forms of silica support [silica nanoparticles (SNPs) or silica microparticles (SMPs)] as glycolysis catalysts. The reactions were carried out at 300 degrees C and 1.1 MPa at an EG-to-PET molar ratio of 11:1 and a catalyst-to-PET-weight ratio of 1.0% for 40-80 min. Among the four prepared catalysts (Mn(3)O(4)/SNP5, ZnO/SNPs, Mn(3)O(4)/SMPs, and ZnO/SMPs), the Mn(3)O(4)/SNPs nanocomposite had the highest monomer yield (>90%). This high yield may be explained by the high surface area, amorphous and porous structure, and existence of numerous active sites on the nanocomposite catalyst. The BHET yield increased with time and reached the highest level where equilibrium was established between BHET and its dimer. The catalysts were characterized by their SEM, TEM, and BET surface areas, and via XRD, whereas the monomer BHET was characterized by HPLC and FT-IR. The glycolysis with the Mn(3)O(4)/SNPs nanocomposite as the glycolysis catalyst produced a maximum BHET in a short reaction time.-
dc.description.sponsorshipThe authors acknowledge the financial support of the Resource Recycling R&D Center sponsored by the 21C Frontier R&D Program and of the Center for Ultramicrochemical Process Systems sponsored by KOSEF.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherAMER SCIENTIFIC PUBLISHERS-
dc.subjectOXIDATION-
dc.subjectWASTE-
dc.subjectDEPOLYMERIZATION-
dc.subjectTEMPERATURE-
dc.subjectOZONE-
dc.titleMetal-Oxide-Doped Silica Nanoparticles for the Catalytic Glycolysis of Polyethylene Terephthalate-
dc.typeArticle-
dc.identifier.wosid000286344400154-
dc.identifier.scopusid2-s2.0-79955863714-
dc.type.rimsART-
dc.citation.volume11-
dc.citation.issue1-
dc.citation.beginningpage824-
dc.citation.endingpage828-
dc.citation.publicationnameJOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY-
dc.identifier.doi10.1166/jnn.2011.3201-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorKim, DoHyun-
dc.contributor.nonIdAuthorKim, Bo-kyung-
dc.contributor.nonIdAuthorHan, Myungwan-
dc.contributor.nonIdAuthorCho, Bong Gyoo-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorPET Recycling-
dc.subject.keywordAuthorBHET-
dc.subject.keywordAuthorDepolymerization-
dc.subject.keywordAuthorGlycolysis-
dc.subject.keywordAuthorNanocomposite-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusWASTE-
dc.subject.keywordPlusDEPOLYMERIZATION-
dc.subject.keywordPlusTEMPERATURE-
dc.subject.keywordPlusOZONE-
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