TY - JOUR
T1 - All Green Microwave Assisted 99% Depolymerisation of Polyethylene Terephthalate into Value Added Products via Glycerol Pre-treatment and Hydrolysis Reaction
AU - Azeem, Muhammad
AU - Attallah, Olivia A.
AU - Tas, Cuneyt Erdinc
AU - Fournet, Margaret Brennan
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2024/1
Y1 - 2024/1
N2 - Energy-efficient and fast depolymerisation technologies present as new sustainable and green recycling routes for achieving a circular economy for plastics. Herein, we present a highly efficient 2-step microwave-based (MW) degradation of polyethylene terephthalate (PET). Initially, a MW-assisted pre-treatment was evaluated using glycerol as a non-toxic reagent for the conversion of PET into a modified form that makes it easily depolymerised. Box Behnken Design was employed to determine the optimised pre-treatment conditions attaining maximum PET weight loss and favourable crystallinity and carbonyl indices for the pre-treated PET. Glycerol of 12 mL volume and 3 min of 182W MW irradiation resulted in 11% PET weight loss at onset temperature of degradation and gave rise to carbonyl index up to 4.22 and 33% crystallinity of pre-treated PET. MW assisted hydrolysis of the pre-treated PET was then performed in the presence of sodium bicarbonate and ethylene glycol as depolymerizing agents. Within 3 min, the proposed depolymerisation methodology provided 99.9% conversion of PET into 79.1% terephthalic acid (TPA), 17.6% monohydroxyethyl terephthalate (MHET), and 1.8% bis (2-hydroxyethyl) terephthalate (BHET). The obtained TPA was separated from the monomers mixtures and its purification was evaluated via different characterization techniques against a standard TPA. A purity of 95%, 82.4 APHA colour value, 645.3 mgKOH/g acid number and acceptable heavy metal content indicated that the purified TPA can be repolymerised as virgin PET. Graphical Abstract: [Figure not available: see fulltext.]
AB - Energy-efficient and fast depolymerisation technologies present as new sustainable and green recycling routes for achieving a circular economy for plastics. Herein, we present a highly efficient 2-step microwave-based (MW) degradation of polyethylene terephthalate (PET). Initially, a MW-assisted pre-treatment was evaluated using glycerol as a non-toxic reagent for the conversion of PET into a modified form that makes it easily depolymerised. Box Behnken Design was employed to determine the optimised pre-treatment conditions attaining maximum PET weight loss and favourable crystallinity and carbonyl indices for the pre-treated PET. Glycerol of 12 mL volume and 3 min of 182W MW irradiation resulted in 11% PET weight loss at onset temperature of degradation and gave rise to carbonyl index up to 4.22 and 33% crystallinity of pre-treated PET. MW assisted hydrolysis of the pre-treated PET was then performed in the presence of sodium bicarbonate and ethylene glycol as depolymerizing agents. Within 3 min, the proposed depolymerisation methodology provided 99.9% conversion of PET into 79.1% terephthalic acid (TPA), 17.6% monohydroxyethyl terephthalate (MHET), and 1.8% bis (2-hydroxyethyl) terephthalate (BHET). The obtained TPA was separated from the monomers mixtures and its purification was evaluated via different characterization techniques against a standard TPA. A purity of 95%, 82.4 APHA colour value, 645.3 mgKOH/g acid number and acceptable heavy metal content indicated that the purified TPA can be repolymerised as virgin PET. Graphical Abstract: [Figure not available: see fulltext.]
KW - Depolymerisation
KW - Glycerol pre-treatment
KW - Hydrolysis
KW - Microwave
KW - Monomers
KW - Polyethylene terephthalate
KW - Recycling
UR - http://www.scopus.com/inward/record.url?scp=85165902095&partnerID=8YFLogxK
U2 - 10.1007/s10924-023-02979-8
DO - 10.1007/s10924-023-02979-8
M3 - Article
AN - SCOPUS:85165902095
SN - 1566-2543
VL - 32
SP - 303
EP - 315
JO - Journal of Polymers and the Environment
JF - Journal of Polymers and the Environment
IS - 1
ER -