dc.contributor.author | Jung, Youn Seo | |
dc.contributor.author | Canlier, Ali | |
dc.contributor.author | Hwang, Taek Sung | |
dc.date.accessioned | 2021-05-18T08:51:35Z | |
dc.date.available | 2021-05-18T08:51:35Z | |
dc.date.issued | 2018 | en_US |
dc.identifier.issn | 0032-3861 | |
dc.identifier.issn | 1873-2291 | |
dc.identifier.uri | https://doi.org/10.1016/j.polymer.2018.03.007 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12573/717 | |
dc.description | This work was supported by the Commercializations Promotion Agency for R&D Outcomes Grant funded by the Korean Government (MSIP)" (2017, 2017K000215, Joint Research Corporations Support Program). This work was also supported by the Human Resource Training Program for Regional Innovation and Creativity through the Ministry of Education and National Research Foundation of Korea (NRF-2015H1C1A1035652). | en_US |
dc.description.abstract | Polyketone is a thermoplastic polymer known for its strong mechanical properties and chemical resistance. Such superiorities make it difficult to process and chemically modify for further functionalizations and applications. In this work, we introduce a novel method for functionalizing the alpha carbon of polyketone. We succeeded to attach allyl groups to the backbone of polyketone by a heterogeneous reaction between polyketone enolate and allyl bromide. Allylated polyketone is not soluble in common solvents. Since we started with a membrane of polyketone, there is no need to cast again. Further functionalization is possible through pending allyl groups via alkene addition reactions and ionic or radicalic polymerization. FTIR, elemental analysis, solid NMR, FT-Raman, SEM and XPS methods were employed to confirm the elemental composition, molecular structure and morphology. In addition, X-ray diffractometer (XRD), UVeVisible spectroscopy and thermal analysis were used to investigate the crystal structure, physical and electronic properties. (c) 2018 Elsevier Ltd. All rights reserved. | en_US |
dc.description.sponsorship | Commercializations Promotion Agency for R&D Outcomes Grant - Korean Government (MSIP)
2017K000215
Human Resource Training Program for Regional Innovation and Creativity through the Ministry of Education and National Research Foundation of Korea | en_US |
dc.language.iso | eng | en_US |
dc.publisher | ELSEVIER SCI LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND | en_US |
dc.relation.isversionof | 10.1016/j.polymer.2018.03.007 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Grafting | en_US |
dc.subject | Allyl bromide | en_US |
dc.subject | Enolization | en_US |
dc.subject | Potassium tert-butoxide | en_US |
dc.subject | Polyketone | en_US |
dc.title | An efficient and facile method of grafting Allyl groups to chemically resistant polyketone membranes | en_US |
dc.type | article | en_US |
dc.contributor.department | AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü | en_US |
dc.contributor.authorID | 0000-0002-5462-6039 | en_US |
dc.identifier.volume | Volume: 141 Pages: 102-108 | en_US |
dc.relation.journal | POLYMER | en_US |
dc.relation.publicationcategory | Makale - Uluslararası - Editör Denetimli Dergi | en_US |