Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2018Synthesis of Bioacrylic Polymers from Dihydro-5-hydroxyl furan-2-one (2H-HBO) by Free and Controlled Radical Polymerization27citations

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Saito, Kei
1 / 5 shared
Hughes, Timothy
1 / 1 shared
Smith, Craig
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2018

Co-Authors (by relevance)

  • Saito, Kei
  • Hughes, Timothy
  • Smith, Craig
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article

Synthesis of Bioacrylic Polymers from Dihydro-5-hydroxyl furan-2-one (2H-HBO) by Free and Controlled Radical Polymerization

  • Saito, Kei
  • Ray, Parijat
  • Hughes, Timothy
  • Smith, Craig
Abstract

<p>In this work, dihydro-5-hydroxyl furan-2-one (2H-HBO), a renewable-sourced chemical containing the hydroxyl functionality, is converted into its acrylic counterpart for the first time through a green chemical procedure using methacrylic anhydride. This newly synthesized acrylic monomer is able to be polymerized using different techniques such as bulk, solution, and emulsion polymerization. The ability of this monomer to copolymerize with other commercially available acrylates is studied using emulsion polymerization techniques. The pendent lactone ring remains unopened during polymerization and the new monomer is able to copolymerize with other acrylates such as methyl methacrylate and styrene. Reversible addition-fragmentation chain transfer reaction emulsion polymerization is also studied with the same monomer, leading to a steady conversion (∼60%) with a low polydispersity of 1.06. The homopolymer produced from such an emulsion polymerization shows a higher molecular weight than that produced from other methods, with a glass transition temperature of around 105 °C. This demonstrates the potential of this monomer as an interesting, green replacement for methyl methacrylate in certain fields of application.</p>

Topics
  • impedance spectroscopy
  • glass
  • glass
  • glass transition temperature
  • molecular weight
  • homopolymer
  • polydispersity