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dc.contributor.authorOzgumus, S
dc.contributor.authorOrbay, M
dc.contributor.authorOzbudak, S
dc.contributor.authorKasgoz, A
dc.contributor.authorGuclu, G
dc.date.accessioned2021-03-05T09:43:16Z
dc.date.available2021-03-05T09:43:16Z
dc.date.issued1998
dc.identifier.citationGuclu G., Kasgoz A., Ozbudak S., Ozgumus S., Orbay M., "Glycolysis of poly(ethylene terephthalate) wastes in xylene", JOURNAL OF APPLIED POLYMER SCIENCE, cilt.69, ss.2311-2319, 1998
dc.identifier.issn0021-8995
dc.identifier.otherav_9f3e9804-fce5-4766-8f44-761c0c049092
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/106907
dc.description.abstractTo reclaim the monomers or prepare intermediates suitable for other polymers zinc acetate catalayzed glycolysis of waste poly(ethylene terephthalate) (PET) was carried out with ethylene or propylene glycol, with PET/glycol molar ratios of 1 : 0.5-1 : 3, in xylene at 170-245 degrees C. During the multiphase reaction, depolymerization products transferred to the xylene medium from the dispersed PET/glycol droplets, shifting the equilibrium to glycolysis. Best results were obtained from the ethylene glycol (EG) reaction at 220 degrees C, which yielded 80 mol % bis-2-hydroxyethyl terephthalate monomer and 20 mol % dimer fractions in quite pure crystalline form. Other advantages of employment of xylene in glycolysis of PET were improvement of mixing at high PET/EG ratios and recycling possibility of excess glycol, which separates from the xylene phase at low temperatures. (C) 1998 John Wiley & Sons, Inc.
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectTemel Bilimler
dc.subjectFizikokimya
dc.subjectPolimer Karakterizasyonu
dc.subjectKimya
dc.subjectPOLİMER BİLİMİ
dc.titleGlycolysis of poly(ethylene terephthalate) wastes in xylene
dc.typeMakale
dc.relation.journalJOURNAL OF APPLIED POLYMER SCIENCE
dc.contributor.department, ,
dc.identifier.volume69
dc.identifier.issue12
dc.identifier.startpage2311
dc.identifier.endpage2319
dc.contributor.firstauthorID121320


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