Current estimates suggest that there will be more plastic than fish in the oceans by 2050 if the
mounting plastic waste problem that society is facing remains unaddressed. New technologies will be
required in order to shift society towards a circular economy which will support a more sustainable
future. Hydrothermal liquefaction (HTL) shows promise to be a major part of the solution for dealing
with the rapidly growing quantities of plastic waste generated each year. Yet, there are still many
unknowns pertaining to the reaction pathways occurring during the HTL of plastic wastes. The work
within this thesis will explore the role that water plays during the decomposition of plastic waste in
sub- and supercritical water. Water’s role as a solvent and a reactant will be investigated and
clarified.
Chapter 2 focuses on the reactivity of water with a hydrocarbon substrate. Contradictory claims in the
literature about whether water or oxygen are responsible for the formation of oxygenated compounds
have been clarified. Adventitious oxygen was found to be responsible for formation of oxygenated
species, which is consistent with mechanisms proposed for SCWO.
Chapter 3 examines the behaviour of scrap tyres in HTL. The particle size of a tyre granulate sample
was varied to examine effects on the product distribution. Fundamental reaction pathways
responsible for the decomposition of the polyisoprene chain are identified.
Chapter 4 is a studies the HTL conversion of limonene to aromatics. The behaviour in supercritical
water has been identified to diverge from previously published pyrolysis of limonene and the role of
water was identified as promoting isomerisation of the double bonds within limonene.
Chapter 5 focuses on the hydrothermal decomposition of polyamides. Whilst the behaviour in
subcritical water is well known, the same cannot be said about the behaviour in supercritical water. A
hydrolysis mechanism accounts for the observed behaviour at all conditions examined
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