Physically cross-linked polyethylene via reactive extrusionElectronic supplementary information (ESI) available: NMR, DSC, TGA, rheology, DMTA, and stress-strain curves. See DOI: 10.1039/c9py00168a
Ureidopyrimidinone (UPy) is introduced into various polyethylenes (PEs) bearing hydroxyl groups by solution grafting, affording physically cross-linked PE via multiple H-bonding. Utilizing low melting UPy where the methyl group is substituted with isopropyl (isopropyl UPy, IPR-UPy), a reactive extru...
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02.04.2019
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Abstract | Ureidopyrimidinone (UPy) is introduced into various polyethylenes (PEs) bearing hydroxyl groups by solution grafting, affording physically cross-linked PE
via
multiple H-bonding. Utilizing low melting UPy where the methyl group is substituted with isopropyl (isopropyl UPy, IPR-UPy), a reactive extrusion process is developed that allows significant shortening of the reaction time and elimination of the use of solvents and catalysts. Chemical grafting is confirmed by Fourier Transform Infrared Spectroscopy (FT-IR) and proton Nuclear Magnetic Resonance (
1
H NMR). Differential Scanning Calorimetry (DSC), rheology and Dynamical Mechanical Thermal Analysis (DMTA) are employed to investigate the thermal stability of the obtained polymers and reveal that UPy functionalized PE can be safely processed
via
reactive extrusion below 150 °C. Introduction of UPy significantly improves the mechanical properties and alters the rheology, showing that quadruple hydrogen bonding interactions are present both in the solid state and in the PE melt.
Ureidopyrimidinone (UPy) is introduced into various polyethylenes (PEs) bearing hydroxyl groups by solution grafting, affording physically cross-linked PE
via
multiple H-bonding. |
---|---|
AbstractList | Ureidopyrimidinone (UPy) is introduced into various polyethylenes (PEs) bearing hydroxyl groups by solution grafting, affording physically cross-linked PE
via
multiple H-bonding. Utilizing low melting UPy where the methyl group is substituted with isopropyl (isopropyl UPy, IPR-UPy), a reactive extrusion process is developed that allows significant shortening of the reaction time and elimination of the use of solvents and catalysts. Chemical grafting is confirmed by Fourier Transform Infrared Spectroscopy (FT-IR) and proton Nuclear Magnetic Resonance (
1
H NMR). Differential Scanning Calorimetry (DSC), rheology and Dynamical Mechanical Thermal Analysis (DMTA) are employed to investigate the thermal stability of the obtained polymers and reveal that UPy functionalized PE can be safely processed
via
reactive extrusion below 150 °C. Introduction of UPy significantly improves the mechanical properties and alters the rheology, showing that quadruple hydrogen bonding interactions are present both in the solid state and in the PE melt.
Ureidopyrimidinone (UPy) is introduced into various polyethylenes (PEs) bearing hydroxyl groups by solution grafting, affording physically cross-linked PE
via
multiple H-bonding. |
Author | Soliman, Maria Vachon, Jérôme Pinalli, Roberta Zych, Arkadiusz Dalcanale, Enrico Verdelli, Alice |
AuthorAffiliation | Department of Chemistry University of Parma SABIC Technology & Innovation Urmonderbaan 22 STC Geleen Life Sciences and Environmental Sustainability |
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References_xml | – issn: 2016 publication-title: Supramolecular Polymer Networks and Gels doi: Seiffert Kumacheva Okay Anthamatten Chau Dankers Greenland Hayes Li Liu – issn: 2017 publication-title: Handbook of Industrial Polyethylene and Technology: Definitive Guide to Manufacturing, Properties, Processing, Applications and Markets doi: Kamykowski – issn: 2004 end-page: 2004052963 publication-title: WO doi: Bosman Janssen van Gemert Versteegen Meijer Sijbesma – issn: 2005 end-page: 2005042641A1 publication-title: WO doi: Janssen van Gemert Meijer Bosman – issn: 2012 publication-title: Szycher's handbook of polyurethanes doi: Szycher – issn: 1981 publication-title: Polymer melt rheology: a guide for industrial practice doi: Cogswell – issn: 2014 publication-title: Polymer Rheology: Fundamentals and Applications doi: Osswald Rudolph – issn: 1992 publication-title: Polyurethane elastomers doi: Hepburn – issn: 2015 end-page: 14057893 publication-title: US doi: van Gemert Janssen Meijer Bosman |
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