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      Isocyanate- and solvent-free synthesis of melt processible polyurea elastomers derived from urea as a monomer†

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      RSC Advances
      The Royal Society of Chemistry

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          Abstract

          Polyurea elastomers are utilized for a myriad of applications ranging from coatings and foams to dielectric materials for capacitors and actuators. However, current synthetic methods for polyureas rely on highly reactive isocyanates, solvents, and catalysts, which collectively pose serious safety considerations. This report details the synthesis and characterization of melt processible, poly(tetramethylene oxide) (PTMO)-based segmented polyurea elastomers utilizing an isocyanate-, solvent-, and catalyst-free approach. Dynamic mechanical analysis and differential scanning calorimetry suggested microphase separation between the hard and soft segments. Tensile analysis revealed high strain at break for all segmented copolymers between 340 and 770%, and tunable modulus between 0.76 and 29.5 MPa. Dielectric spectroscopy revealed that the composition containing 20 wt% hard segment offered the highest permittivity at 10.6 (1 kHz, 300 K) of the segmented copolymers, indicating potential as a dielectric elastomer.

          Abstract

          Polyurea elastomers derived in part from a bio-sourced feedstock and synthesized using an isocyanate-, solvent-, and catalyst-free approach exhibit elastomeric properties while maintaining melt-processibility.

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          Most cited references1

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          Handbook of low and high dielectric constant materials and their applications, two-volume set

          H. Nalwa, Nalwa (1999)
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            Author and article information

            Journal
            RSC Adv
            RSC Adv
            RA
            RSCACL
            RSC Advances
            The Royal Society of Chemistry
            2046-2069
            18 May 2020
            14 May 2020
            18 May 2020
            : 10
            : 32
            : 18760-18768
            Affiliations
            [a] Department of Chemistry, Macromolecules Innovation Institute (MII), Virginia Tech Blacksburg VA 24061 USA telong@ 123456vt.edu +1 540 231 8517 +1 540 231 2480
            [b] Department of Chemistry, Bethel University St. Paul MN 55112 USA
            [c] Department of Chemical and Biomolecular Engineering, University of Tennessee Knoxville TN 37996 USA
            Author information
            https://orcid.org/0000-0002-0266-1238
            https://orcid.org/0000-0001-9515-5491
            Article
            d0ra02369h
            10.1039/d0ra02369h
            9054001
            35518320
            4fea10bb-9df8-4473-93db-29343e1cbdfd
            This journal is © The Royal Society of Chemistry
            History
            : 13 March 2020
            : 1 May 2020
            Page count
            Pages: 9
            Funding
            Funded by: Division of Materials Research, doi 10.13039/100000078;
            Award ID: DMR-1905597
            Categories
            Chemistry
            Custom metadata
            Paginated Article

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