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Synthesis and Characterization of Block Copolymer: Thermal and Morphological Properties of Sio2-Filled Block Copolymer Nanocomposites

dc.authorid Akinay, Yuksel/0000-0002-6171-6307
dc.authorscopusid 36090008900
dc.authorscopusid 57209101030
dc.authorscopusid 56401010700
dc.authorwosid Akinay, Yuksel/I-8092-2019
dc.contributor.author Goktas, Melahat
dc.contributor.author Aykac, Cengiz
dc.contributor.author Akinay, Yuksel
dc.date.accessioned 2025-05-10T17:20:40Z
dc.date.available 2025-05-10T17:20:40Z
dc.date.issued 2023
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Goktas, Melahat; Aykac, Cengiz] Yuzuncu Yil Univ, Dept Sci Educ, TR-65100 Van, Turkey; [Akinay, Yuksel] Yuzuncu Yil Univ, Dept Min Engn, TR-65100 Van, Turkey en_US
dc.description Akinay, Yuksel/0000-0002-6171-6307 en_US
dc.description.abstract With the development of nanotechnology, the production and use of the nanocomposites has been increased. Polymer nanocomposites are among the most widely used nanocomposites. In this study, block copolymer and block copolymer-based polymer nanocomposites were synthesized and evaluated. For this purpose; firstly, poly(beta-butyrolactone)-b-poly(methyl methacrylate) [P(BL-b-MMA)] block copolymers were prepared simultaneously in one-pot by recycling additive/fragmentation chain transfer (RAFT) and ring-opening (ROP) polymerizations using a novel bifunctional RAFT-ROP agent which synthesized by chemical reaction with 3-bromo-1-propanol and potassium ethyl xanthate. Secondly, for the preparation of polymer nanocomposite, SiO2 nanoparticles were added to the prepared block copolymer with a rate of 3 wt% both during the polymerization stage and after the polymerization stage. The synthesized RAFT-ROP agent, block copolymer, and polymer nanocomposites were characterized using spectroscopic methods. The effect of copolymerization reaction conditions on molecular weight and molecular weight distribution (dispersity) was investigated. In one-pot copolymerization processes, relatively high weight copolymers were obtained by changing the copolymerization conditions due to the active centers in the copolymerization environment. The thermal characterization showed that the glass transition temperature of the block copolymer decreases with the addition of SiO2 during the polymerization stage and increases with the addition of SiO2 after the polymerization stage. SEM surface morphologies showed that block copolymer and polymer nanocomposites morphology is different from each other. The difference can be explained by the good dispersion of the block copolymer and SiO2 nanoparticles within each other. en_US
dc.description.sponsorship Van Yuzunci Yil University Scientific Research Fund [FYL-2020-9254] en_US
dc.description.sponsorship This work was supported by the Van Yuzunci Yil University Scientific Research Fund (Grand Number: FYL-2020-9254). en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1007/s00289-022-04468-9
dc.identifier.endpage 8584 en_US
dc.identifier.issn 0170-0839
dc.identifier.issn 1436-2449
dc.identifier.issue 8 en_US
dc.identifier.scopus 2-s2.0-85138501705
dc.identifier.scopusquality Q2
dc.identifier.startpage 8565 en_US
dc.identifier.uri https://doi.org/10.1007/s00289-022-04468-9
dc.identifier.uri https://hdl.handle.net/20.500.14720/10176
dc.identifier.volume 80 en_US
dc.identifier.wos WOS:000858823900001
dc.identifier.wosquality Q2
dc.language.iso en en_US
dc.publisher Springer en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Recycling Additive/Fragmentation Chain Transfer (Raft) en_US
dc.subject Ring-Opening Polymerization (Rop) en_US
dc.subject Block Copolymer en_US
dc.subject Beta-Butyrolactone en_US
dc.subject Block Copolymerbased Nanocomposite en_US
dc.subject Sio2 Nanoparticle en_US
dc.title Synthesis and Characterization of Block Copolymer: Thermal and Morphological Properties of Sio2-Filled Block Copolymer Nanocomposites en_US
dc.type Article en_US

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