dc.contributor.author | Ozgumus, S | |
dc.contributor.author | Orbay, M | |
dc.contributor.author | Ozbudak, S | |
dc.contributor.author | Kasgoz, A | |
dc.contributor.author | Guclu, G | |
dc.date.accessioned | 2021-03-05T09:43:16Z | |
dc.date.available | 2021-03-05T09:43:16Z | |
dc.date.issued | 1998 | |
dc.identifier.citation | Guclu 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.issn | 0021-8995 | |
dc.identifier.other | av_9f3e9804-fce5-4766-8f44-761c0c049092 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/106907 | |
dc.description.abstract | To 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.iso | eng | |
dc.subject | Temel Bilimler (SCI) | |
dc.subject | Temel Bilimler | |
dc.subject | Fizikokimya | |
dc.subject | Polimer Karakterizasyonu | |
dc.subject | Kimya | |
dc.subject | POLİMER BİLİMİ | |
dc.title | Glycolysis of poly(ethylene terephthalate) wastes in xylene | |
dc.type | Makale | |
dc.relation.journal | JOURNAL OF APPLIED POLYMER SCIENCE | |
dc.contributor.department | , , | |
dc.identifier.volume | 69 | |
dc.identifier.issue | 12 | |
dc.identifier.startpage | 2311 | |
dc.identifier.endpage | 2319 | |
dc.contributor.firstauthorID | 121320 | |