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Copper and ZnO dual-catalyzed photo-assisted depolymerization of poly(methyl methacrylate) without deoxygenation

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dc.title Copper and ZnO dual-catalyzed photo-assisted depolymerization of poly(methyl methacrylate) without deoxygenation en
dc.contributor.author Cvek, Martin
dc.contributor.author Moini Jazani, Arman
dc.contributor.author De Luca Bossa, Ferdinando
dc.contributor.author Bernat, Roksana
dc.contributor.author Kapil, Kriti
dc.contributor.author Matyjaszewski, Krzysztof
dc.relation.ispartof European Polymer Journal
dc.identifier.issn 0014-3057 Scopus Sources, Sherpa/RoMEO, JCR
dc.identifier.issn 1873-1945 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2024
utb.relation.volume 220
dc.type article
dc.language.iso en
dc.publisher Pergamon-Elsevier Science Ltd
dc.identifier.doi 10.1016/j.eurpolymj.2024.113429
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0014305724006906
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0014305724006906/pdfft?md5=6cceb12871ad80cce1f8965c15bd0d6e&pid=1-s2.0-S0014305724006906-main.pdf
dc.subject depolymerization en
dc.subject ATRP en
dc.subject polymers en
dc.subject oxygen en
dc.subject ligand complexes en
dc.subject catalyst en
dc.subject zinc oxide en
dc.description.abstract Despite significant advancements in thermal and photothermal depolymerizations, the success of these techniques relies on tedious deoxygenation procedures. Herein, we report the development of the depolymerization technique efficient without prior deoxygenation, which was enabled by copper/ligand complexes and the inclusion (0.25 wt% relative to solvent) of zinc oxide (ZnO) nanocrystals activated by UV light. This approach was tested for poly(methyl methacrylate) (PMMA) prepared by atom transfer radical polymerization (ATRP); the effects of solvent polarity and the activity of ligands were investigated. Unexpectedly, a low-activity Cu-complex with 2,2‘-bipyridine ligand, in combination with a low-polarity solvent, 1,2,4-trichlorobenzene, enabled relatively high depolymerization yields in less than 1 h at 150 °C. Higher activity ATRP complexes with tris(2-pyridylmethyl)amine (TPMA) and N,N,N‘,N‘‘,N‘‘-pentamethyldiethylenetriamine (PMDETA) ligands, were less efficient, which was associated with their thermal decomposition and/or the excessive formation of radicals and premature termination of the chain ends. The presented facile approach was designed to be used even in partially aerated reactors, opening new avenues for efficient depolymerization. en
utb.faculty University Institute
dc.identifier.uri http://hdl.handle.net/10563/1012130
utb.identifier.obdid 43885713
utb.identifier.scopus 2-s2.0-85203441679
utb.identifier.wok 001312208000001
utb.identifier.coden EUPJA
utb.source J-wok
dc.date.accessioned 2025-01-15T08:08:09Z
dc.date.available 2025-01-15T08:08:09Z
dc.description.sponsorship NSF [DMR 2202747, DMR 2324168]; J. W. Fulbright Commission in the Czech Republic [2022-21-1]; Ministry of Education, Youth and Sports of the Czech Republic [RP/CPS/2022/007, RP/CPS/2024-28/007]; Fonds de recherche du Quebec (FRQNT) [301734]; National Science Centre within the MINIATURA project [DEC-2023/07/X/ST5/01484]; Foundation for Polish Science (FNP)
dc.description.sponsorship Carnegie Mellon University, CMU; Fundacja na rzecz Nauki Polskiej, FNP; Ministerstvo Školství, Mládeže a Tělovýchovy, MŠMT; Fonds de recherche du Québec, FRQ; US-UK Fulbright Commission, (2022-21-1, RP/CPS/2024-28/007, RP/CPS/2022/007); Fonds de recherche du Québec – Nature et technologies, FRQNT, (301734); Narodowe Centrum Nauki, NCN, (DEC-2023/07/X/ST5/01484); National Science Foundation, NSF, (DMR 2202747, DMR 2324168)
dc.rights Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.access openAccess
utb.ou Centre of Polymer Systems
utb.contributor.internalauthor Cvek, Martin
utb.fulltext.sponsorship The financial support from NSF (DMR 2202747 and DMR 2324168) is acknowledged. M.C. is grateful to the J. W. Fulbright Commission in the Czech Republic for the financial support through a postdoctoral fellowship (grant number: 2022-21-1). M.C. further acknowledges the projects DKRVO (RP/CPS/2022/007) and (RP/CPS/2024-28/007) supported by the Ministry of Education, Youth and Sports of the Czech Republic. A.M.J greatly acknowledges the Fonds de recherche du Québec (FRQNT) for financial support (File#301734). R.B. acknowledges financial support from the National Science Centre within the MINIATURA project (DEC-2023/07/X/ST5/01484) and from the Foundation for Polish Science (FNP). The authors acknowledge Dr. Grzegorz Szczepaniak (University of Warsaw) and Dr. Gorkem Yilmaz (Carnegie Mellon University) for fruitful discussions.
utb.wos.affiliation [Cvek, Martin; Jazani, Arman Moini; Bossa, Ferdinando De Luca; Bernat, Roksana; Kapil, Kriti; Matyjaszewski, Krzysztof] Carnegie Mellon Univ, Dept Chem, 4400 Fifth Ave, Pittsburgh, PA 15213 USA; [Cvek, Martin] Tomas Bata Univ Zlin, Ctr Polymer Syst, Trida T Bati 5678, Zlin 76001, Czech Republic; [Bernat, Roksana] Univ Silesia, Inst Mat Engn, 75 Pulku Piechoty 1A, PL-41500 Chorzow, Poland
utb.scopus.affiliation Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, 152 13, PA, United States; Centre of Polymer Systems, Tomas Bata University in Zlin, Trida T. Bati 5678, Zlin, 760 01, Czech Republic; Institute of Materials Engineering, University of Silesia, 75 Pulku Piechoty 1A, Chorzow, 41-500, Poland
utb.fulltext.projects DMR 2202747
utb.fulltext.projects DMR 2324168
utb.fulltext.projects 2022-21-1
utb.fulltext.projects DKRVO (RP/CPS/2022/007)
utb.fulltext.projects (RP/CPS/2024-28/007)
utb.fulltext.projects FRQNT (File#301734)
utb.fulltext.projects MINIATURA (DEC-2023/07/X/ST5/01484)
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