Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/115378
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorResearch Institute for Smart Energyen_US
dc.creatorLiang, Nen_US
dc.creatorLi, Jen_US
dc.creatorChen, Yen_US
dc.creatorZhang, Men_US
dc.creatorXie, Ben_US
dc.creatorSun, Zen_US
dc.creatorZhong, Len_US
dc.creatorWang, Qen_US
dc.creatorWong, WYen_US
dc.date.accessioned2025-09-23T03:01:22Z-
dc.date.available2025-09-23T03:01:22Z-
dc.identifier.issn0272-8397en_US
dc.identifier.urihttp://hdl.handle.net/10397/115378-
dc.language.isoenen_US
dc.publisherJohn Wiley & Sonsen_US
dc.subjectNanosilicaen_US
dc.subjectNorbornenylen_US
dc.subjectPolydicyclopentadieneen_US
dc.subjectSilane coupling agenten_US
dc.titleNorbornenyl-modified nanosilica for reinforced polydicyclopentadiene compositesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1002/pc.70177en_US
dcterms.abstractPolydicyclopentadiene (PDCPD) is a type of rigid thermosetting engineering plastic that is polymerized from dicyclopentadiene (DCPD). In industry, it is often combined with various organic or inorganic fillers to produce composites. However, because DCPD is nonpolar, surface modification of the fillers is necessary to enhance composite performance. This study designed and synthesized four readily available norbornenyl-based silane coupling agents based on nadic anhydride and isocyanate siloxane to modify nanosilica. The modified nanosilicas were then stably dispersed in DCPD to prepare a series of norbornenyl-based nanosilica/PDCPD composites. The results showed that the nanosilica modified with additional phenyl groups can lead to better composite performance. The impact toughness of the composites can be increased by 100%, and the tensile and flexural strengths can be improved by approximately 10%. Moreover, these norbornenyl-based nanosilica/PDCPD composites demonstrated good thermal stability, with higher glass transition temperature (Tg) and maximum decomposition temperature (Tdmax) values.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationPolymer composites, First published: 17 July 2025, Early View, https://doi.org/10.1002/pc.70177en_US
dcterms.isPartOfPolymer compositesen_US
dcterms.issued2025-
dc.identifier.scopus2-s2.0-105010854433-
dc.description.validate202509 bcelen_US
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG000126/2025-08-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextFunding text 1: This work was supported by W.-Y.W. acknowledges the financial support from the Hong Kong Research Grants Council (PolyU 15307321), RGC Senior Research Fellowship Scheme (SRFS2021\u20105S01), Research Institute for Smart Energy (CDAQ), Research Centre for Nanoscience and Nanotechnology (CE2H), and Ms. Clarea Au for the Endowed Professorship in Energy (847S). Q.W. acknowledges the financial support of The National Key R&D Program of China (2023YFB3812400). M.Z. acknowledges the financial support from the National Natural Science Foundation of China (62205276) Research Centre for Organic Electronics (1\u2010CE32) and the Hong Kong Research Grants Council (PolyU 15308324). Funding: ; Funding text 2: W.-Y.W. acknowledges the financial support from the Hong Kong Research Grants Council (PolyU 15307321), RGC Senior Research Fellowship Scheme (SRFS2021\u20105S01), Research Institute for Smart Energy (CDAQ), Research Centre for Nanoscience and Nanotechnology (CE2H), and Ms. Clarea Au for the Endowed Professorship in Energy (847S). Q.W. acknowledges the financial support of the National Key R&D Program of China (2023YFB3812400). M.Z. acknowledges the financial support from the National Natural Science Foundation of China (62205276), Research Centre for Organic Electronics (1\u2010CE32) and the Hong Kong Research Grants Council (PolyU 15308324).en_US
dc.description.pubStatusEarly releaseen_US
dc.date.embargo0000-00-00 (to be updated)en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 0000-00-00 (to be updated)
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