Superparamagnetic gamma -Fe sub(2)O sub(3) nanoparticles as an easily recoverable catalyst for the chemical recycling of PET

There have been numerous studies to develop catalysts for the chemical recycling of poly(ethylene terephthalate) (PET) viaglycolysis. However, in the field of PET glycolysis, only a few have attempted to recover and reuse the catalysts. This research utilized easily recoverable superparamagnetic gam...

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Published inGreen chemistry : an international journal and green chemistry resource : GC Vol. 16; no. 1; pp. 279 - 286
Main Authors Bartolome, Leian, Imran, Muhammad, Lee, Kyoung G, Sangalang, Arvin, Ahn, Jeong Keun, Kim, Do Hyun
Format Journal Article
LanguageEnglish
Published 01.12.2013
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Summary:There have been numerous studies to develop catalysts for the chemical recycling of poly(ethylene terephthalate) (PET) viaglycolysis. However, in the field of PET glycolysis, only a few have attempted to recover and reuse the catalysts. This research utilized easily recoverable superparamagnetic gamma -Fe sub(2)O sub(3) nanoparticles as a reusable catalyst for PET glycolysis. gamma -Fe sub(2)O sub(3) nanoparticles were produced by calcining Fe sub(3)O sub(4) nanoparticles prepared by the co-precipitation method. The produced gamma -Fe sub(2)O sub(3) nanoparticles had an average size of 10.5 plus or minus 1.4 nm, and a very high surface area reaching 147 m super(2) g super(-1). Its superparamagnetic property was also confirmed. Glycolysis reactions were carried out, and the gamma -Fe sub(2)O sub(3) catalysts were recovered after the reactions by simple magnetic decantation. The use of magnetic iron oxide allowed the easy recovery of the catalyst from the glycolysis products. At 300 degree C and a 0.05 catalyst/PET weight ratio, the maximum bis(2-hydroxyethlyl) terephthalate (BHET) monomer yield reached more than 90% in 60 min. At 255 degree C and a 0.10 catalyst/PET weight ratio, the BHET yield reached more than 80% in 80 min. The catalyst was reused 10 times, giving almost the same BHET yield each time.
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ISSN:1463-9262
1463-9270
DOI:10.1039/c3gc41834k