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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Wilén, Carl-Eric

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Åbo Akademi University

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2021Sulfenamides as Standalone Flame Retardants for Polystyrene19citations
  • 2018The Synthesis of Low-Viscosity Organotin-Free Moisture-Curable Silane-Terminated Poly(Urethane-Urea)s16citations
  • 2017Investigation on the Influence of Chain Extenders on the Performance of One-Component Moisture-Curable Polyurethane Adhesives33citations
  • 2016Structure–Property Studies on a New Family of Halogen Free Flame Retardants Based on Sulfenamide and Related Structures21citations
  • 2015The effect of core-shell particle morphology on adhesive properties of poly(styrene-co-butyl acrylate)21citations
  • 2014Template-induced fabrication of nanopatterned polymeric films by inkjet printing7citations
  • 2013Impact of functionalised dispersing agents on the mechanical and viscoelastic properties of pigment coating17citations
  • 2013Thermomechanical properties of CaCO₃-latex pigment coatings: impact of modified dispersing agents10citations

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Chart of shared publication
Sund, Pernilla
2 / 2 shared
Mountassir, Amira
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Tirri, Teija
5 / 10 shared
Luona, Viivi
1 / 1 shared
Tan, Chen
3 / 3 shared
Pawelec, Weronika
1 / 1 shared
Holappa, Anton
1 / 1 shared
Aubert, Melanie
1 / 1 shared
Ihalainen, Petri
1 / 17 shared
Smatt, Jan-Henrik
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Xu, Qian
1 / 1 shared
Maattanen, Anni
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Peltonen, Jouko
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Pahlevan, Mahdi
1 / 1 shared
Toivakka, Martti
2 / 54 shared
Touaiti, Farid
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Ansell, Mp
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Nilsson, R.
2 / 2 shared
Alam, Parvez
1 / 11 shared
Alam, P.
1 / 6 shared
Touaiti, F.
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Ansell, M. P.
1 / 1 shared
Pahlevan, M.
1 / 1 shared
Chart of publication period
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Co-Authors (by relevance)

  • Sund, Pernilla
  • Mountassir, Amira
  • Tirri, Teija
  • Luona, Viivi
  • Tan, Chen
  • Pawelec, Weronika
  • Holappa, Anton
  • Aubert, Melanie
  • Ihalainen, Petri
  • Smatt, Jan-Henrik
  • Xu, Qian
  • Maattanen, Anni
  • Peltonen, Jouko
  • Pahlevan, Mahdi
  • Toivakka, Martti
  • Touaiti, Farid
  • Ansell, Mp
  • Nilsson, R.
  • Alam, Parvez
  • Alam, P.
  • Touaiti, F.
  • Ansell, M. P.
  • Pahlevan, M.
OrganizationsLocationPeople

article

Structure–Property Studies on a New Family of Halogen Free Flame Retardants Based on Sulfenamide and Related Structures

  • Wilén, Carl-Eric
  • Pawelec, Weronika
  • Holappa, Anton
  • Aubert, Melanie
  • Tirri, Teija
Abstract

A wide variety of molecules containing S–N or S–N–S cores were synthesized, and their flame retardant properties in polypropylene (PP), low density polyethylene (LDPE) and polystyrene (PS) were investigated. In addition, polymers or oligomers bearing the sulfenamide functionality (SN) were also synthesized. It was shown that this radical generator family based on sulfenamides is very versatile in terms of structural modifications, and the thermal decomposition range can be easily adjusted by changing the R groups attached to the core. The thermal stabilities of the different sulfenamides were examined by thermogravimetric analysis (TGA). Radicals generated by the homolytic cleavage of the S–N or S–N–S bonds at an elevated temperature can effectively interact with the intermediate products of polymer thermolysis and provide excellent flame retardant properties. The choice of most suitable SN-structure varies depending on the polymer type. For polypropylene DIN 4102-1 B2 and UL94 VTM-2 classifications were achieved with only 0.5 to 1 wt % of sulfenamide, and, in some cases, no flaming dripping was observed. Also for LDPE thin films, sulfenamides offered the DIN 4102-1 B2 rating at low dosage. In the case of polystyrene, the very stringent UL94 V-0 classification was even achieved at a loading of 5 wt % of sulfenamide.

Topics
  • density
  • impedance spectroscopy
  • polymer
  • thin film
  • thermogravimetry
  • thermolysis