Voltage activation of poly (ethylene glycol) diacrylate

Free radical polymerization of acrylate resins may be initiated by light or heat, but a direct electronic mode of activation is missing. Voltage activated free-radical polymerization would address this limitation if suitable electronic initiators are available. Herein, a selection of initiators and...

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Main Authors: Ghosh, Animesh, Meyyappan, Priyavadana, Steele, Terry W. J.
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/156045
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1560452023-07-14T16:04:53Z Voltage activation of poly (ethylene glycol) diacrylate Ghosh, Animesh Meyyappan, Priyavadana Steele, Terry W. J. School of Materials Science and Engineering Engineering::Materials Poly (Ethylene Glycol) Diacrylate Electrocuring Free radical polymerization of acrylate resins may be initiated by light or heat, but a direct electronic mode of activation is missing. Voltage activated free-radical polymerization would address this limitation if suitable electronic initiators are available. Herein, a selection of initiators and electrolytes investigate electronic initiation of diacrylate resins. Electrochemistry and rheometry are combined in a custom electrorheometer towards the evaluation of relevant structure property relationships. Viscoelastic material properties are measured as a function of voltage, chemical initiator, cumulative charge, and electrolyte. Upon cathodic activation, liquid to solid transitions with a maximum shear modulus of 139 kPa is observed while anodic activation failed to initiate gelation. Storage modulus and adhesion strength measurements demonstrate that voltage activation of acrylate resins is feasible, but further improvements in increasing crosslinking kinetics are needed before industrial applicability. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Submitted/Accepted version The authors would like to acknowledge the financial support from the Agency for Science, Technology and Research (A*STAR) AME IRG grant (A1883c0001) - ‘Microprocessor based methods of composite curing’ and Ministry of Education – Singapore (RG47/21, 2021-T1-001- 077), ‘Electrocuring Resins for Advanced Manufacturing’. 2022-04-01T01:08:46Z 2022-04-01T01:08:46Z 2022 Journal Article Ghosh, A., Meyyappan, P. & Steele, T. W. J. (2022). Voltage activation of poly (ethylene glycol) diacrylate. Progress in Organic Coatings, 165, 106770-. https://dx.doi.org/10.1016/j.porgcoat.2022.106770 0300-9440 https://hdl.handle.net/10356/156045 10.1016/j.porgcoat.2022.106770 165 106770 en A1883c0001 RG47/21 2021-T1-001- 077 Progress in Organic Coatings © 2022 Elsevier B.V. All rights reserved. This paper was published in Progress in Organic Coatings and is made available with permission of Elsevier B.V. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials
Poly (Ethylene Glycol) Diacrylate
Electrocuring
spellingShingle Engineering::Materials
Poly (Ethylene Glycol) Diacrylate
Electrocuring
Ghosh, Animesh
Meyyappan, Priyavadana
Steele, Terry W. J.
Voltage activation of poly (ethylene glycol) diacrylate
description Free radical polymerization of acrylate resins may be initiated by light or heat, but a direct electronic mode of activation is missing. Voltage activated free-radical polymerization would address this limitation if suitable electronic initiators are available. Herein, a selection of initiators and electrolytes investigate electronic initiation of diacrylate resins. Electrochemistry and rheometry are combined in a custom electrorheometer towards the evaluation of relevant structure property relationships. Viscoelastic material properties are measured as a function of voltage, chemical initiator, cumulative charge, and electrolyte. Upon cathodic activation, liquid to solid transitions with a maximum shear modulus of 139 kPa is observed while anodic activation failed to initiate gelation. Storage modulus and adhesion strength measurements demonstrate that voltage activation of acrylate resins is feasible, but further improvements in increasing crosslinking kinetics are needed before industrial applicability.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Ghosh, Animesh
Meyyappan, Priyavadana
Steele, Terry W. J.
format Article
author Ghosh, Animesh
Meyyappan, Priyavadana
Steele, Terry W. J.
author_sort Ghosh, Animesh
title Voltage activation of poly (ethylene glycol) diacrylate
title_short Voltage activation of poly (ethylene glycol) diacrylate
title_full Voltage activation of poly (ethylene glycol) diacrylate
title_fullStr Voltage activation of poly (ethylene glycol) diacrylate
title_full_unstemmed Voltage activation of poly (ethylene glycol) diacrylate
title_sort voltage activation of poly (ethylene glycol) diacrylate
publishDate 2022
url https://hdl.handle.net/10356/156045
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