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5 results on '"Hakmé, Chady"'

2. Conductive polymer nanocomposites based on cyclic oligomers filled with multiwalled carbon nanotubes

Author

Bardash, Liubov, Boiteux, Gisèle, Rybak, Andrzej, Seytre, Gérard, Hakmé, Chady, Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Polymères et des Biomatériaux (IMP-LMPB), Centre National de la Recherche Scientifique (CNRS)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Institut de Chimie du CNRS (INC), and Institute of Macromolecular Chemistry of National Academy of Sciences of Ukraine

Subjects
[CHIM.POLY]Chemical Sciences/Polymers
Published
2008

3. In-situ monitoring of structure evolution by dielectric spectroscopy

Author

Boiteux, Gisèle, Hakmé, Chady, Stevenson, Isabelle, Maazouz, Abderrahim, Seytre, Gérard, Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Polymères et des Biomatériaux (IMP-LMPB), Centre National de la Recherche Scientifique (CNRS)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Institut de Chimie du CNRS (INC), Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Macromoléculaires (IMP-LMM), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), and Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet [Saint-Étienne] (UJM)-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.POLY]Chemical Sciences/Polymers, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2007

4. In-Situ monitoring of cyclic butylene terephtalate polymerization by dielectric sensing

Author

Hakmé, Chady, Stevenson, Isabelle, Maazouz, Abderrahim, Cassagnau, Philippe, Boiteux, Gisèle, Seytre, Gérard, Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Polymères et des Biomatériaux (IMP-LMPB), Centre National de la Recherche Scientifique (CNRS)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Institut de Chimie du CNRS (INC), Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Macromoléculaires (IMP-LMM), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon), and Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet [Saint-Étienne] (UJM)-Centre National de la Recherche Scientifique (CNRS)

Subjects
[CHIM.POLY]Chemical Sciences/Polymers, technology, industry, and agriculture
Abstract

International audience; The in situ monitoring of the polymerization of cyclic butylene terephtalate (CBT) oligomers by dielectric sensing has been investigated under isothermal conditions at different processing temperatures. The change in conductivity depends on the increase of molecular weight but is also influenced by crystallization of the obtained c-PBT during or after polymerization. Dielectric sensing investigations are in good agreement with SEC and DSC analysis which confirm the observation of polymerization and crystallization kinetics. Unfortunately, the conductivity signal could not distinguish between the polymerization and crystallization when they occur simultaneously at lower temperatures (

Published
2007

5. Thermo-mechanical behavior of uniaxially drawn and crystallized poly(ethylene naphthalene-2,6-dicarboxylate) (PEN) films

Author

Hakmé, Chady, Stevenson, Isabelle, David, Laurent, Seytre, Gérard, Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Polymères et des Biomatériaux (IMP-LMPB), Centre National de la Recherche Scientifique (CNRS)-Université Jean Monnet [Saint-Étienne] (UJM)-Institut National des Sciences Appliquées de Lyon (INSA Lyon), Institut National des Sciences Appliquées (INSA)-Université de Lyon-Institut National des Sciences Appliquées (INSA)-Université de Lyon-Université Claude Bernard Lyon 1 (UCBL), and Université de Lyon-Institut de Chimie du CNRS (INC)

Subjects
[CHIM.POLY]Chemical Sciences/Polymers
Abstract

International audience; Thermo-mechanical properties of poly(ethylene naphthalene-2,6-dicarboxylate) (PEN) films in the amorphous state, uniaxially stretched and thermally crystallized were compared and show different microstructure–property relationships. The glass transition temperature shifts to higher temperatures when films are stretched above Tg at 160 °C, in relation with a crystallinity increase and subsequent confinement effects of the amorphous phase, but films stretched below Tg at 100 °C show an opposite trend while drawing. This is discussed in relation with the highly mobile structural state arising from plastic deformation of the amorphous phase. The confinement effects were particularly assessed by the estimation of a ‘rigid amorphous fraction' (RAF). Crystallinities and RAF were estimated from DSC data for the uniaxially drawn and thermally crystallized films respectively. It was observed that the RAF was higher in thermally crystallized films than in uniaxially drawn samples in relation to a lamellar semi-crystalline morphology. In addition to this detailed thermo-mechanical characterizations, low stress creep measurements were carried out during heating scans. They can be related to the microstructure and thermal transitions of the films. In particular, for the uniaxially stretched films, the measured shrinkage decreases when the draw ratio increases because the crystalline entities developed during the draw process are locking the chain motions

Published
2007

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