Materials Map

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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 (2/2 displayed)

  • 2004Synthesis of melt-stable and semi-crystalline poly(1,4-dioxan-2-one) by ring-opening (co)polymerisation of 1,4-dioxan-2-one with different lactones19citations
  • 2004Diblock copolymers based on 1,4-dioxan-2-one and ε-caprolactone10citations

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Chart of shared publication
Raquez, Jean Marie
2 / 47 shared
Degée, Philippe
2 / 39 shared
Dubois, Philippe
2 / 24 shared
Chart of publication period
2004

Co-Authors (by relevance)

  • Raquez, Jean Marie
  • Degée, Philippe
  • Dubois, Philippe
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article

Synthesis of melt-stable and semi-crystalline poly(1,4-dioxan-2-one) by ring-opening (co)polymerisation of 1,4-dioxan-2-one with different lactones

  • Narayan, Ramani
  • Raquez, Jean Marie
  • Degée, Philippe
  • Dubois, Philippe
Abstract

<p>High molecular weight poly(1,4-dioxan-2-one) (PPDX) can be readily synthesized by catalysed ring-opening polymerisation of 1,4-dioxan-2-one (PDX) using aluminium trialkoxide active species as initiator. Even though the resulting poly(ester-alt-ether) chains display good thermo-mechanical properties, they suffer from low thermal stability. PPDX is known to thermally degrade mainly through unzipping depolymerisation promoted from the hydroxyl end-groups and yielding PDX monomer. To overcome this drawback, chemical modification of the PPDX hydroxyl end-groups was first attempted with trichloroacetyl isocyanate; however, with limited success in terms of thermal stability. Interestingly, it has been shown that the copolymerisation of PDX with tiny amounts of lactones like ε-caprolactone (CL) and δ-valerolactone (VL), is an efficient way to enhance the thermal stability of the resulting polyester chains without significantly compromising the crystallinity and melting temperature of PPDX. The thermal stability of the resulting polyester chains was studied by isothermal TGA under inert atmosphere as well as under air. For instance, when PDX was copolymerised with a low amount of CL by initiation with Al(O<sup>i</sup>Pr)<sub>3</sub> at 100°C in bulk, a melt-stable copolymer was rapidly formed with a composition close to the starting feed and a multiblock-like structure as shown by <sup>1</sup>H and <sup>13</sup>C NMR spectroscopy. The incorporation of 3-15 wt% of CL into PPDX chains substantially increases the thermal stability of resulting PPDX-rich copolyesters, while preserving a high melting temperature ranging between 90 and 100°C. Furthermore, an interesting internal plasticising effect is also detected by DSC with the glass transition temperature decreasing from, e.g., -10 to -22°C in the presence of 14 wt% CL copolymerised in the PPDX chains.</p>

Topics
  • impedance spectroscopy
  • melt
  • aluminium
  • glass
  • glass
  • thermogravimetry
  • glass transition temperature
  • differential scanning calorimetry
  • molecular weight
  • copolymer
  • Nuclear Magnetic Resonance spectroscopy
  • ester
  • crystallinity
  • melting temperature