Electro-Oxidation of Plastic Waste-Derived Ethylene Glycol for the Production of High Value Chemicals and Hydrogen
Helen Tyrrell a, Maria-Magdalena Titirici a, King Kuok (Mimi) Hii b, Klaus Hellgardt a
a Department of Chemical Engineering, Imperial College London, London, SW7 2AZ, UK
b Department of Chemistry, Molecular Sciences Research Hub, White City Campus, Imperial College London, London, W12 0BZ, U.K.
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Spring 2024 Conference (MATSUS24)
#MatInter - Materials and Interfaces for emerging electrocatalytic reactions
Barcelona, Spain, 2024 March 4th - 8th
Organizers: Marta Costa Figueiredo and María Escudero-Escribano
Poster, Helen Tyrrell, 524
Publication date: 18th December 2023

The global community is facing a devastating plastic pollution crisis. In 2018, the global production of plastic exceeded 359 million tonnes. However, to date, only 9% of all plastic has been recycled.[1] The lack of efficient chemical recycling processes continues to drive the production of petrochemical-derived plastic. As a result, the plastic industry is accountable for 4.5% of all global greenhouse gas emissions.[2]

Polyethylene terephthalate (PET) plastic, commonly used in clear food and drinks packaging, makes up a significant proportion of global plastic waste.[3] Recovering and upcycling the ethylene glycol monomer from used PET offers a solution to reduce plastic waste production. The ethylene glycol obtained from depolymerisation of waste PET can be upcycled using electrolysis to produce high-value chemicals and H2. The partial electrochemical oxidation of ethylene glycol can yield many organic aldehyde and acid species.[4] In particular, the conversion of ethylene glycol to glycolic acid is of interest because of its increasing popularity as an active skincare ingredient. Additionally, the electrolysis of ethylene glycol offers a lower-energy alternative to the sluggish water electrolysis process for green H2 production.[5]

In this work, the selective electrochemical oxidation of ethylene glycol to glycolic acid in alkaline conditions is investigated on commercial Pt/C and Au/C catalysts. The activity and pathway of ethylene glycol electro-oxidation on Pt/C and Au/C is examined in both 3-electrode and membrane electrode assembly cells coupled with high-performance liquid chromatography and gas chromatography for product analysis. The Au/C electrocatalyst was found to be more stable over time and showed higher faradaic efficiency towards glycolic acid production compared to Pt/C.

I would like to acknowledge and thank the EPSRC CDT in Next Generation Synthesis and Reaction Technology for funding this project. (Grant Ref: EP/S023232/1)

© FUNDACIO DE LA COMUNITAT VALENCIANA SCITO
We use our own and third party cookies for analysing and measuring usage of our website to improve our services. If you continue browsing, we consider accepting its use. You can check our Cookies Policy in which you will also find how to configure your web browser for the use of cookies. More info