4.7 Article

Glycolysis of Poly(Ethylene Terephthalate) Using Biomass-Waste Derived Recyclable Heterogeneous Catalyst

期刊

POLYMERS
卷 13, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/polym13010037

关键词

biomass-waste; depolymerisation; glycolysis; heterogeneous catalyst; orange peel ash; PET waste

资金

  1. Science and Engineering Research Board (SERB), Department of Science and Technology, Govt. of India [EEQ/2017/000505]
  2. University Grants Commission, Govt. of India [43-210/2014(SR)]

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In this study, a biomass-waste-derived heterogeneous catalyst was prepared from waste orange peel for the depolymerisation of PET to its monomer, BHET. The catalyst showed excellent catalytic performance, depolymerising PET within 90 minutes and producing 79% recrystallised BHET. The ability to reuse the catalyst for multiple cycles without significant loss of activity and its environmentally-friendly nature make it a promising green route for PET recycling.
Plastic production has increased by almost 200-fold annually from 2 million metric tons per year in 1950s to 359 million metric tons in 2018. With this rapidly increasing production, plastic pollution has become one of the most demanding environmental issues and tremendous efforts have been initiated by the research community for its disposal. In this present study, we reported for the first time, a biomass-waste-derived heterogeneous catalyst prepared from waste orange peel for the depolymerisation of poly(ethylene terephthalate) (PET) to its monomer, bis(2-hydroxyethyl terephthalate) (BHET). The prepared orange peel ash (OPA) catalyst was well-characterised using techniques such as IR, inductively coupled plasma (ICP)-OES (Optical Emission Spectrometry), XRD, X-ray fluorescence (XRF), SEM, energy-dispersive X-ray spectroscopy (EDX), TEM, BET (Brunauer-Emmett-Teller) and TGA. The catalyst was found to be composed of basic sites, high surface area, and a notable type-IV N-2 adsorption-desorption isotherm indicating the mesoporous nature of the catalyst, which might have eventually enhanced the rate of the reaction as well as the yield of the product. The catalyst completely depolymerises PET within 90 min, producing 79% of recrystallised BHET. The ability of reusing the catalysts for 5 consecutive runs without significant depreciation in the catalytic activity and its eco- and environmental-friendliness endorses this protocol as a greener route for PET recycling.

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