Nasreddine Kébir

ORCID: 0000-0002-5390-157X
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About
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Research Areas
  • biodegradable polymer synthesis and properties
  • Polymer composites and self-healing
  • Carbon dioxide utilization in catalysis
  • Antimicrobial agents and applications
  • Synthetic Organic Chemistry Methods
  • Polymer Surface Interaction Studies
  • Polymer Nanocomposites and Properties
  • Bacterial biofilms and quorum sensing
  • Nanofabrication and Lithography Techniques
  • Synthesis and properties of polymers
  • Analytical Chemistry and Chromatography
  • Mass Spectrometry Techniques and Applications
  • Antimicrobial Peptides and Activities
  • Chemistry and Chemical Engineering
  • Microfluidic and Capillary Electrophoresis Applications
  • Asymmetric Synthesis and Catalysis
  • Plant-Derived Bioactive Compounds
  • Silicone and Siloxane Chemistry
  • Analytical chemistry methods development
  • Nanocomposite Films for Food Packaging
  • Polymer crystallization and properties
  • Biodiesel Production and Applications
  • Microplastics and Plastic Pollution
  • Material Properties and Applications
  • 3D Printing in Biomedical Research

Normandie Université
2014-2024

Polymères, Biopolymères, Surfaces
2015-2024

Université de Rouen Normandie
2014-2024

Institut National des Sciences Appliquées Rouen Normandie
2014-2024

Centre National de la Recherche Scientifique
2013-2024

Institut Curie
2008-2015

Physique des Cellules et Cancers
2011-2015

Sorbonne Université
2015

Université Toulouse III - Paul Sabatier
2012

Délégation Normandie
2012

ABSTRACT Novel fully renewable AA‐BB type nonisocyanate polyurethanes (NIPUs) were synthesized using the transurethanization approach. Dicarbamate monomers prepared by reaction of a diamine with an excess dimethylcarbonate (DMC), in presence 1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene (TBD) as catalyst. Then, dicarbamate was reacted diol to afford polymer, TBD or K 2 CO 3 Several diamines and diols tested. The two steps conducted under neat conditions. obtained materials exhibited T g values varying...

10.1002/pola.27568 article EN Journal of Polymer Science Part A Polymer Chemistry 2015-03-03

ABSTRACT Novel fully renewable AA‐BB type non‐isocyanate polyhydroxyurethanes were synthesized by the classical reaction between a diamine and dicyclocarbonate. Sebacic acid was first reacted with an excess of glycerol carbonate, in presence DCC DMPA, leading to dicyclocarbonate monomer. Then, this monomer several diamines, 1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene (TBD), as organocatalyst, afford linear branched polymers. The obtained materials exhibited T g values varied from −27 −8 °C, m...

10.1002/pola.27908 article EN Journal of Polymer Science Part A Polymer Chemistry 2015-09-28

ABSTRACT Nonisocyanate thermoplastic polyurethane elastomers (NIPUs) were synthesized with the transurethanization approach. Dimethyl dicarbamates (DCs) prepared by reaction of a diamine an excess dimethyl carbonate in presence 1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene (TBD) as catalyst. Then, polymers obtained under neat conditions through DC polyethyleneglycol average molecular weight 1500 g/mol (PEG1500) at variable temperatures different amounts 1,4‐butanediol. TBD, dibutyltin dilaurate...

10.1002/app.44991 article EN Journal of Applied Polymer Science 2017-03-01

A heterogeneous catalyst for producing epoxidized vegetable oils, an important intermediate in the production of non-isocyanate polyurethanes, is essential product separation and decreasing side-reaction, i.e., ring-opening reaction, via Prileschajew method. The development reliable kinetic models considering key variables both phases mass transfer phenomena missing literature. reaction pathway also under debate. Therefore, we studied kinetics epoxidation cottonseed oil by perpropionic acid...

10.3390/catal13020274 article EN Catalysts 2023-01-26

An antiadhesive nanofilm has been designed and prepared in one step water onto commercial poly(dimethylsiloxane) (PDMS) by mimicking the external region of cell membranes. The resulting biomimetic surfaces are effective suppressing protein adsorption as well bacterial mammalian adhesion.

10.1002/anie.201101029 article EN Angewandte Chemie International Edition 2011-09-21

Abstract New hydroxytelechelic cis ‐1,4‐oligoisoprenes exhibiting variable values and distributions of the hydroxyl functionality were successfully prepared. The synthesis reactions involved chemical modifications carbonyl telechelic ‐1,4‐polyisoprene, which was obtained by controlled degradation synthetic or natural rubber. These new oligomers reacted with toluene diisocyanate to elaborate crosslinked polyurethane elastomers. thermomechanical properties prepared polyurethanes investigated....

10.1002/app.34013 article EN Journal of Applied Polymer Science 2011-06-01
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