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    • Alain Rousseau
    • Alain Rousseau

      Alain Rousseau

      INSA Lyon, Ingénierie des Matériaux Polymères, IMP, CNRS UMR5223, 17 Avenue Jean Capelle, 69621, Villeurbanne, France | Univ Lyon, INSA Lyon, CNRS, IMP UMR 5223, F-69621, ...

       

       

      KOL Resume for Alain Rousseau

      Year
      2020

      INSA Lyon, Ingénierie des Matériaux Polymères, IMP, CNRS UMR5223, 17 Avenue Jean Capelle, 69621, Villeurbanne, France

      2019

      Université de Lyon, F-69003, France

      2018

      Univ Lyon, INSA-Lyon, CNRS UMR 5223, Ingénierie des Matériaux Polymères, F- 69621, Villeurbanne Cedex, France

      2017

      Université‐Lyon, INSA‐Lyon, Ingénierie des Matériaux Polymères, IMP, UMR 5223 Villeurbanne France

      2016

      INSA-Lyon, Ingénierie des Matériaux Polymères, IMP, UMR5223, Unive Lyon, F-69621, Villeurbanne, France

      2015

      INSA-Lyon, Ingénierie des Matériaux Polymères, IMP, UMR5223, F-69621 Villeurbanne, France

      2014

      Ingénierie des Matériaux Polymères Université Lyon, INSA‐Lyon F‐69621 Villeurbanne France

      2011

      INSA‐Lyon, Ingénierie des Matériaux Polymères, IMP, CNRS UMR5223, F‐69621, Villeurbanne, France

      2010

      Université de Lyon, F-69003, Lyon, France

      2008

      Université Lyon 1‐IMP/LMM Laboratoire des Matériaux Macromoléculaires, Ingénierie des Matériaux Polymères, UMR CNRS 5223 INSA‐Lyon, 17 Avenue Jean Capelle, F‐69621 Villeurbanne Cedex, France

      2007

      Laboratoire des Matériaux Macromoléculaires, IMP/LMM CNRS, UMR #5627, INSA-Lyon, 17 Avenue Jean Capelle, 69621 Villeurbanne cedex, France; Groupe d'Etudes de Métallurgie Physique et de Physique des Matériaux, UMR-CNRS #5510, INSA-Lyon, 7 avenue Jean Capelle, 69621 Villeurbanne cedex, France; and Tergal Industries, Rue Jules Vercruysse, BP 1, 02430 Gauchy, France

      2006

      INSA de Lyon, UMR 5627, 20 av. A. Einstein, 69621 Villeurbanne Cedex, France

      2005

      Laboratoire de Chimie Macromoléculaire, Unité Mixte de Recherche ‐ Centre National de la Recherche Scientifique 5076, Ecole Nationale Supérieure de Chimie de Montpellier, 8 Rue de l'Ecole Normale, 34296 Montpellier Cedex 5, France

      2004

      Laboratoire de Chimie Macromoléculaire, UMR‐CNRS‐5076, Ecole Nationale de Chimie de Montpellier, 8 rue de l'Ecole Normale, 34 296 Montpellier Cedex 5, France

      2003

      Ecole Nationale Supérieure de Chimie, Laboratoire de Chimie Macromoléculaire, UMR5076, 8, rue de l’Ecole Normale 34296, Montpellier Cedex 5, France

      2002

      Laboratoire de Chimie Macromoléculaire, UMR‐CNRS 5076, Ecole Nationale Supérieure de Chimie de Montpellier, 8 Rue de l'Ecole Normale, 34296 Montpellier, France

      2001

      Laboratoire de Chimie Macromoléculaire, Unité Mixte de Recherche du Centre National de la Recherche Scientifique 5076, Ecole Nationale Supérieure de Chimie de Montpellier, 8 rue de l'Ecole Normale, 34296 Montpellier Cedex 5, France

      2000

      Laboratoire de Chimie Macromoléculaire–UMR CNRS 5076, Ecole Nationale Supérieure de Chimie de Montpellier, 8 Rue de l'Ecole Normale, 34296 Montpellier Cedex 5, France

      1999

      ESA 5076, Ecole Nationale Supérieure de Chimie, 8 Rue de l'Ecole Normale, 34296 Montpellier Cedex 5, France

      1998

      ENSCM-L.C.A.-UPRESA 5076-8, Rue de l'Ecole Normale, 34296 Montpellier, France

      1995

      Laboratoire de Chimie Appliquée, URA CNRS 1193, ENSCM, F-34053, Montpellier Cedex 1, France

      1992

      URA Dl1930, Ecole Nationale Supérieure de Chimie de Montpellier, 8, rue Ecole Normale, 34053 Montpellier-Cédex 1 France

      1988

      Laboratoire de Chimie Appliquée - Unité Associée 1193 au CNRS Ecole Nationale Supérieure de Chimie de Montpellier 8, rue Ecole Normale - 34075 Montpellier Cédex France

      1987

      Laboratoire de Chimie Appliquée - Unité Associée 1193 au CNRS Ecole Nationale Supérieure de Chimie de Montpellier 8, rue Ecole Normale - 34075 Montpellier Cedex France

      1986

      Laboratoire de Chimie Appliquée UA CNRS N∘ 1193, Ecole Nationale Supérieure de Chimie de Montpellier, 8, rue de l'Ecole Normale, F-34075, Montpellier Cédex, France

      1984

      Laboratoire de Chimie Appliquée Ecole Nationale Supérieure de Chimie de Montpellier 8, rue Ecole Normale - 34075 Montpellier Cedex France

       

       

      Alain Rousseau: Influence Statistics

      Sample of concepts for which Alain Rousseau is among the top experts in the world.
      Concept World rank
      α fluoroacrylate monomer #1
      activation disperse 1 #1
      114°c activation #1
      dep 114°c #1
      stability depolarization temperature #1
      nonlinear ellipsometry λ #1
      electrooptic response work #1
      depolarization temperature dep #1
      optic fluorinated #1
      benzoxazinones substituées #2
      polymères transparents #2
      α atfpi #2
      ° méthacrylates #2
      halogenated deuterated #2
      factor intrinsic absorption #2
      polyhybridsiloxanes htfphsx #2
      1550 nm stability #2
      tg polymères #2
      polyhybridsiloxane segments #2
      polyhybridsiloxanes #2
      mélange zinc #2
      aryl α chloroacrylates #2
      atfpi #2
      chclch2ccl3 #2
      comme polymères #2
      perhalogénés #2
      new halogenated monomers #2
      n20d13667 #2
      transparents partie #2
      c6f13ch2 polymers #2
      réfraction n20d #2
      cd3od dehalogenation #2
      cfci2cfci2 #2
      chclch2ccl3 cf2cfclncl #2
      bio‐based oligomers #2
      fpi α #2
      polyhybridsiloxane block #2
      fpi fphsx #2
      cfci3 moyen aici3 #2
      polymères létude #2
      c2f4nh #2
      groups −ch2n−rf #2
      series fpifphsx #2
      passive waveguide low #2
      dans laniline #2
      refractive acrylic monomers #2
      vis laniline study #2
      dindice réfraction n20d13667 #2
      fpi wiley periodicals #2
      celle tg situés #2

       

      Prominent publications by Alain Rousseau

      KOL-Index: 7266

      The radical copolymerization of tetrafluoroethylene (TFE) and trifluorovinyl ω-hydroxy comonomers [F2CCF(CH2)mOH with m = 1 (FA1) and m = 3 (FA3)] for the synthesis of fluorinated polymers bearing hydroxy side groups is presented. FA1 was prepared by dehydrofluorination of 2,2,3,3-tetrafluoropropanol, whereas FA3 was obtained in a three-step scheme starting from the radical addition of 1,2-dichloroiodotrifluoroethane to allyl alcohol. The copolymerization conditions (in bulk or in ...

      Known for Fluorinated Monomers | Tetrafluoroethylene Tfe | Fa3 Synthesis | Reaction Order | Radical Copolymerization
      KOL-Index: 7011

      The pilot scale synthesis of poly(butylene succinate) copolymers with rigid bio-based comonomers, namely isosorbide and 2,5-furandicarboxylic acid (FDCA) was investigated. The synthesis and properties of these copolymers were compared with aliphatic-aromatic polyesters containing the petrochemical terephthalic acid (PTA), such as poly(butylene succinate-co-terephthalate) (PBST) and commercial poly(butylene adipate-co-terephthalate) (PBAT). Compared to PBS, polycondensation was much ...

      Known for Polybutylene Succinate | Aromatic Polyesters | Fdca Synthesis | Thermal Properties | Low Reactivity
      KOL-Index: 5111

      The use of 1,4:3,6-dianhydrohexitols, isosorbide, isomannide and isoidide in polymers is reviewed. 1,4:3,6-Dianhydrohexitols are derived from renewable resources from cereal-based polysaccharides. In the field of polymeric materials, these diols are essentially employed to synthesize or modify polycondensates. Their attractive features as monomers are linked to their rigidity, chirality, non-toxicity, and the fact that they are not derived from petroleum. First, the synthesis of high ...

      Known for 1436dianhydrohexitols Isosorbide | Isomannide Isoidide | Polymer Synthesis | Renewable Resources | Industrial Scale
      KOL-Index: 4462

      This study concerns the synthesis of anhydride terminated oligoimides (ANTOI) and allyl terminated oligoimides (ALTOI), in acetic acid medium, which allows a very fast reaction and an easy working out. For the preparation of ALTOIs, two methods are compared: the first one consists of adding the monofunctional compound (allyl amine) to the ANTOI already formed during a first step by reaction of a dianhydride (excess) and a diamine. The second method consists of a “one pot” reaction ...

      Known for Thermal Properties | Transimidization Reaction | Thermogravimetric Analysis | Molecular Weights | Oligoimides Terminated
      KOL-Index: 4432

      The synthesis of perfectly alternating fluorinated polyimide–fluorinated polyhybridsiloxane block copolymers (FPI-FPHSX) was achieved through polyhydrosilylation of α,ω-diallylfluorinated polyimides (AT-FPI) and α,ω-dihydrosilane fluorinated–polyhybridsiloxanes (HT-FPHSX). A series of three FPI-FPHSX containing 15, 38, and 56 wt % of polyimide was synthesized and characterized by tuning the number-average molecular weight either of the hard polyimide segments or of the soft ...

      Known for Fluorinated Polyimide | Block Copolymers | Thermoplastic Elastomer | Synthesis Characterization | Thermal Stability
      KOL-Index: 4094

      The aim of this study is to investigate the synthesis of 2,5-furandicarboxylic acid (FDCA)-based copolyamides. Indeed, FDCA monomer may be a potential bio-based alternative to phthalic acids. A series of polyamides and copolyamides, PA 6-I(x)/6-F(y), are synthesized in a pilot scale reactor by melt polycondensation of salts based on FDCA, isophthalic acid (IPA), and 1,6-hexamethylenediamine. The chemical structure and composition of the resulting copolymers are extensively characterized ...

      Known for Thermal Properties | Molecular Dynamics | Furandicarboxylic Acid | Melt Polycondensation | Chemical Structure
      KOL-Index: 4045

      The insertion of soft polysiloxane segments into a polyimide backbone introduces changes in its properties (processability, low surface tension, gas permeability, and lower dielectric constant). Generally, these polyimide–polysiloxane copolymers are synthesized by the condensation of a dianhydride with an aromatic diamine and an amine telechelic polysiloxane, or by transimidization between an aminopyridine-terminated oligoimide and an amine end-capped oligosiloxane. This study ...

      Known for Block Copolymers | Physical Properties | Polyimide – | Aromatic Diamine | Polym Sci
      KOL-Index: 4002

      The efficiency of organometal- (Ti, Zr, Sn, Hf, and Bi) and metal oxide- (Ge and Sb) based catalysts was investigated during the transesterification step of the synthesis of poly(butylene succinate) (PBS). PBS was prepared from succinic acid and 1,4-butanediol via a two-stage melt polycondensation process. The catalytic efficiency of the organometal catalysts was as follows: Ti≫Zr∼ Sn>Hf>Sb>Bi. The germanium and antimony metal oxides displayed desirable catalytic efficiency when were ...

      Known for Polybutylene Succinate | Based Catalysts | Succinic Acid | Transesterification Reaction | Titanium Catalyst
      KOL-Index: 3985

      Deformation-induced modification of the dispersion state of silica nanoparticles in poly(ethylene terephthalate) (PET) has been characterized by means of transmission electron microscopy (TEM) and wide-angle X-ray diffraction (WAXD). We focused on the biaxial deformation applied at a temperature just above the glass transition temperature (110 °C), during the free stretch-blowing process of amorphous PET modified with submicron silica. The first nanocomposite studied contains 2.5 wt % of ...

      Known for Biaxial Deformation | Polyethylene Terephthalate | Glass Transition Temperature | Transmission Electron Microscopy | Silica Nanoparticles
      KOL-Index: 3943

      The synthesis and the nonlinear optical (NLO) properties of crosslinkable copolymers based on a novel NLO azo-dye chromophore bearing two functions: one used the free-radical copolymerization, that is, the methacrylate group, and the other one used for the crosslinking process, that is, the carboxylic acid function, are described. Copolymerization of this new monomer with glycidyl methacrylate leads to novel soluble crosslinkable NLO copolymers bearing free epoxy and carboxylic groups. ...

      Known for Poling Process | Glycidyl Methacrylate | Carboxylic Groups | Freeradical Copolymerization | Nlo Properties
      KOL-Index: 3544

      We report on the measurement of the electro-optic properties of poled polymers at λ=1.55 μm via the Teng and Man technique. Measurements of the electro-optic coefficient obtained for two different sandwich structures, using either indium tin oxide (ITO) or aluminum doped zinc oxide (ZnO:Al) semitransparent electrodes, are compared. The experimental results show that the use of ITO electrodes can lead to a largely wrong evaluation of the electro-optic coefficient r33, with respect to that ...

      Known for Poled Polymers | Sandwich Structures | Zinc Oxide | Optic Properties | Teng Technique
      KOL-Index: 3532

      In this paper, the synthesis and properties of poly(1,4-cyclohexanedimethylene-co-isosorbide terephthalate) (PCIT) with isosorbide (IS) content ranging from 16 to 61 mol% relative to the total diols amount were investigated. Amorphous polymers were successfully synthesized without isosorbide ring hydration. Glass transition temperature (Tg) linearly increased of 1.1 °C for each molar percent of isosorbide included in the polyester, meanwhile melting temperature (Tm) linearly decreased of ...

      Known for Synthesis Properties | Molar Percent | Amorphous Copolyesters | Glass Transition Temperature | Isosorbide Polyester
      KOL-Index: 3299

      Thermoplastic polyurethanes (TPUs) from fatty acids dimer-based polyester polyols, 4,4′-methylene bis(phenyl isocyanate) (MDI) and isosorbide (ISO) as chain extender were successfully synthesized by a two-stage synthesis. TPUs obtained from isosorbide were compared to the model 1,4-butanediol (BDO) −based materials. Differential scanning calorimetry revealed the phase-separated structure of these materials that displayed a typical thermoplastic elastomer behavior by dynamic mechanical ...

      Known for Chain Extender | Polyurethane Elastomers | Glass Transition | Slight Increase | Dynamic Mechanical Analysis
      KOL-Index: 3177

      The development of polymer waveguides leads to synthesis of fluorinated amorphous polymers with high transmission capacity, potential to tune their optical properties by tailoring the molecular structure, together with good processability, easy handling, good flexibility and low cost.In this work we have investigated new thermoplastic fluoroacrylated copolymers, synthesized by radical copolymerization of fluoroalkene(s) with five-membered cyclic carbonate and a third monomer or transfer ...

      Known for Radical Copolymerization | Thermal Stability | Molecular Structure | Optical Properties | Acrylating Agents
      KOL-Index: 3165

      Bulk radical telomerisation of chlorotrifluoroethylene (CTFE) with methanol was investigated for the synthesis of fluorinated alcohols. Improvements in the conversion of CTFE and of the selectivity of the reaction were sought by using different radical initiators (peroxides, percarbonates, peresters) and an excess of methanol. These reactions were compared in terms of CTFE conversion, yield of monoadduct and formation of higher molecular weight telomers. Under these conditions, radical ...

      Known for Fluorinated Telomers | Bistert Butylperoxy25 | Higher Molecular | Dimethylhexane Dhbp | Revealed Low

      Key People For Thermal Properties

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      Alain Rousseau:Expert Impact

      Concepts for whichAlain Rousseauhas direct influence:Thermal properties,  Biaxial deformation,  Radical polymerization,  Position 2,  Fluorinated polyimide,  Α ω,  Fluorinated monomers,  Sandwich structures.

      Alain Rousseau:KOL impact

      Concepts related to the work of other authors for whichfor which Alain Rousseau has influence:Thermal properties,  Renewable resources,  Molecular weight,  Polybutylene succinate,  Aliphatic polyesters,  Dimethyl carbonate,  Glass transition temperature.


       

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      INSA Lyon, Ingénierie des Matériaux Polymères, IMP, CNRS UMR5223, 17 Avenue Jean Capelle, 69621, Villeurbanne, France | Univ Lyon, INSA Lyon, CNRS, IMP UMR 5223, F-69621, Villeurbanne, France | Université de Lyon, Lyon, F-69003, France | Universi

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