4.6 Article

Glycolytic Depolymerization of PET Waste in a Microwave Reactor

期刊

JOURNAL OF APPLIED POLYMER SCIENCE
卷 118, 期 5, 页码 3066-3073

出版社

JOHN WILEY & SONS INC
DOI: 10.1002/app.32737

关键词

recycling; plastics; glycolysis; microwave irradiation; poly(ethylene terephthalate)

资金

  1. King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia [AR-27-101]
  2. King Fahd University of Petroleum and Minerals
  3. Laboratory of Organic Chemical Technology, Department of Chemistry, Aristotle University of Thessaloniki

向作者/读者索取更多资源

Recycling of waste PET bottles was examined using glycolytic depolymerization with diethylene glycol, under microwave irradiation. The objective was to investigate if depolymerization using microwave energy could provide the same product distribution, while carried out in milder experimental conditions and/or shorter reaction times, resulting, thus besides to polymer recycling, in substantial energy saving. The reaction was carried out in a sealed microwave reactor in which the pressure and temperature were controlled. Experiments under constant temperature or microwave power were carried out at several time intervals. The main glycolysis product was analyzed and identified by FTIR measurements. The average molecular weight of the PET residues was found to decrease with the percentage of PET degradation. In the experiments carried out under constant microwave power, complete depolymerization was observed at irradiation powers greater than 150 W for 2 min, or 100 W for 5 min. In the constant temperature experiments, it was clear that at temperatures below 150 degrees C no degradation occurs, whereas complete depolymerization takes place at temperatures greater than or equal to 180 degrees C for 5 min. These results when compared to the conventional heating, where more than 4 h are needed for complete with PET degradation, confirm the importance of the microwave power technique and the substantial energy saving achieved. Finally, from a simple kinetic model the activation energy of the reaction was evaluated. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 118: 3066-3073, 2010

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