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Ultra-high molecular weight polyethylene nanocomposites for enhanced dielectric, thermal, and mechanical performance in polypropylene ‒ advancing towards a more sustainable high voltage power grid

Ultra-high molecular weight polyethylene nanocomposites for enhanced dielectric, thermal, and mechanical performance in polypropylene ‒ advancing towards a more sustainable high voltage power grid
Ultra-high molecular weight polyethylene nanocomposites for enhanced dielectric, thermal, and mechanical performance in polypropylene ‒ advancing towards a more sustainable high voltage power grid
This work reports on the effects of ultra-high molecular weight polyethylene (UHMWPE) nanocomposites, with the main objective of advancing the development of novel high voltage (HV) insulation cables using polypropylene (PP)-based materials for enhanced dielectric, thermal, and mechanical performance. Surface functionalisation of titanium dioxide (TiO2) and magnesium oxide (MgO) nanofillers with polar silane coupling agents (SCA) is implemented using the anhydrous technique. Nanocomposites are prepared using a solution blending method.Dielectric bulk properties, specifically the dielectric relaxation peak frequencies, are attributed to the water bonding states, which result from differences in the polarities of surface functional groups, rather than the bulk properties of the nanoparticles. Similar to charge transport, varying polarities of SCA result in different bonding states with water molecules. This, in turn, influences energy band levels at interfaces and affects the movement of charge carriers in the bulk materials. While the thermal conductivity in nanocomposites mainly results from the long molecular chains of UHMWPE rather than the high intrinsic thermal conductivity of nanofillers, the enhanced interfacial interaction between PP and UHMWPE, achieved by using nanoparticles as a compatibiliser, results in improved mechanical elasticity and elongation at break. Furthermore, this improved interfacial interaction is directly linked to enhanced dielectric performance in polymer blends and polymer nanocomposites, either through the heterogeneity of surface nucleation at the interfaces of PP/UHMWPE blends or by enhancing the interfacial interaction between two polymers using nanoparticles.
In addition, the presence of nanoparticles as a compatibiliser between two immiscible polymer blends delays thermo-oxidative reactions and structural changes during thermal ageing. This results in nanocomposites having a better ability to retain dielectric performance after thermal ageing than the unfilled blends. Overall, this study establishes the relationship between enhanced dielectric, thermal, and mechanical performance, and the physical and chemical characteristics in PP-based UHMWPE nanocomposites. The findings highlight the potential of these UHMWPE nanocomposites in a PP matrix as insulation materials for HV cables, contributing to a more sustainable HV power grid.
University of Southampton
Ketsamee, Phichet
320757bd-99cd-43d2-a8e8-b8100f15f461
Ketsamee, Phichet
320757bd-99cd-43d2-a8e8-b8100f15f461
Andritsch, Thomas
8681e640-e584-424e-a1f1-0d8b713de01c
Vaughan, Alun
6d813b66-17f9-4864-9763-25a6d659d8a3
Saeedi, Istebreq
6df4dfcf-9bb8-4edc-952e-ccc4841f7b54

Ketsamee, Phichet (2024) Ultra-high molecular weight polyethylene nanocomposites for enhanced dielectric, thermal, and mechanical performance in polypropylene ‒ advancing towards a more sustainable high voltage power grid. University of Southampton, Doctoral Thesis, 219pp.

Record type: Thesis (Doctoral)

Abstract

This work reports on the effects of ultra-high molecular weight polyethylene (UHMWPE) nanocomposites, with the main objective of advancing the development of novel high voltage (HV) insulation cables using polypropylene (PP)-based materials for enhanced dielectric, thermal, and mechanical performance. Surface functionalisation of titanium dioxide (TiO2) and magnesium oxide (MgO) nanofillers with polar silane coupling agents (SCA) is implemented using the anhydrous technique. Nanocomposites are prepared using a solution blending method.Dielectric bulk properties, specifically the dielectric relaxation peak frequencies, are attributed to the water bonding states, which result from differences in the polarities of surface functional groups, rather than the bulk properties of the nanoparticles. Similar to charge transport, varying polarities of SCA result in different bonding states with water molecules. This, in turn, influences energy band levels at interfaces and affects the movement of charge carriers in the bulk materials. While the thermal conductivity in nanocomposites mainly results from the long molecular chains of UHMWPE rather than the high intrinsic thermal conductivity of nanofillers, the enhanced interfacial interaction between PP and UHMWPE, achieved by using nanoparticles as a compatibiliser, results in improved mechanical elasticity and elongation at break. Furthermore, this improved interfacial interaction is directly linked to enhanced dielectric performance in polymer blends and polymer nanocomposites, either through the heterogeneity of surface nucleation at the interfaces of PP/UHMWPE blends or by enhancing the interfacial interaction between two polymers using nanoparticles.
In addition, the presence of nanoparticles as a compatibiliser between two immiscible polymer blends delays thermo-oxidative reactions and structural changes during thermal ageing. This results in nanocomposites having a better ability to retain dielectric performance after thermal ageing than the unfilled blends. Overall, this study establishes the relationship between enhanced dielectric, thermal, and mechanical performance, and the physical and chemical characteristics in PP-based UHMWPE nanocomposites. The findings highlight the potential of these UHMWPE nanocomposites in a PP matrix as insulation materials for HV cables, contributing to a more sustainable HV power grid.

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Published date: 2024

Identifiers

Local EPrints ID: 486485
URI: http://eprints.soton.ac.uk/id/eprint/486485
PURE UUID: b5628d73-eaab-4a37-932d-54e2a056b8a7
ORCID for Phichet Ketsamee: ORCID iD orcid.org/0000-0003-1733-6806
ORCID for Thomas Andritsch: ORCID iD orcid.org/0000-0002-3462-022X
ORCID for Alun Vaughan: ORCID iD orcid.org/0000-0002-0535-513X
ORCID for Istebreq Saeedi: ORCID iD orcid.org/0000-0002-1254-748X

Catalogue record

Date deposited: 24 Jan 2024 17:36
Last modified: 18 Mar 2024 04:01

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Contributors

Author: Phichet Ketsamee ORCID iD
Thesis advisor: Thomas Andritsch ORCID iD
Thesis advisor: Alun Vaughan ORCID iD
Thesis advisor: Istebreq Saeedi ORCID iD

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