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791.
Jacqueline Marchand-Brynaert Nathalie Jongen Jean-Luc Dewez 《Journal of polymer science. Part A, Polymer chemistry》1997,35(7):1227-1235
The surface of PVDF film was selectively modified by wet chemistry. Treatment with aqueous LiOH produced HF-elimination and the emergence of an oxygen-containing functionality. The XPS analysis clearly indicated the presence of ketone-, ether(epoxide)-, and alcohol motifs. The percentage of alcohols could be significantly increased by reduction of the ketones with NaBH4 in 2-propanol, followed by reduction of the epoxides with DIBAL-H in hexane. Thus, the full treatment led to a PVDF surface displaying 7 to 16% of oxygen-containing units, of which about 60% consisted in alcohol motifs. The reactvity of the surface-displayed hydroxyl functions was assayed by radiolabeling with [3H]-Ac2O. © 1997 John Wiley & Sons, Inc. J. Polym Sci A: Polym Chem 35: 1227–1235, 1997 相似文献
792.
793.
794.
Jean-Luc Gardette Bndicte Mailhot Fabrice Posada Agns Rivaton Catherine Wilhelm 《Macromolecular Symposia》1999,143(1):95-109
The mechanisms of photooxidation of several polyether based polymers were compared in order to give general rules of orientation of the oxidative reactions. These polymers were a poly(ether-ester) and two poly(ether-urethane)s. The behavior of the polyether component as homopolymer was also studied. This study was extended to copolymers of fluorinated olefins and allyl or vinyl ethers, and the non fluorinated homologues. The elucidation of the photooxidation mechanisms was based on the identification of the photoproducts by analysis of both the solid polymeric matrix and the gaz phase formed on irradiation. It was shown that the photochemical sensitivity of the polyether component was responsible for the rapid oxidation of the copolymers. However, in the case of the fluorinated compounds, different behaviors were observed. It was shown that the presence of the fluorine atoms strongly influenced the orientation of the reaction and modified the oxidation kinetics. The reactivity of the methylene groups in α-position of the oxygen atom of the ether groups were not found to be equivalent regarding oxidation and the secondary was more oxidizable than the tertiary one. 相似文献
795.
Anna Calderone Roberto Lazzaroni Jean-Luc Brdas 《Macromolecular theory and simulations》1998,7(5):509-520
The interfaces between aluminium and poly(ethylene terephthalate), poly(ε-caprolactone), and polystyrene are investigated theoretically in order to assess the reactivity of aluminium towards the functional groups (i.e., ester functions and phenyl rings) present at the surface of the polymers. The theoretical approach consists in performing quantum-chemical calculations on small molecular model systems interacting with a few Al atoms. The geometric structures of the organometallic complexes are optimized and their stabilities and changes in charge densities due to Al bonding are evaluated. The results are compared to experimental X-ray photoelectron spectroscopy data collected during the early stages of interface formation following aluminium deposition on the polymer surfaces. In agreement with experimental data, it emerges from this study that aluminium interacts strongly wirth both polyesters by forming covalent bonds with the carbon and oxygen atoms of the ester functions. The attack of the poly(ethylene terephthalate) phenyl rings occurs only for high metal coverage and does not hamper the interaction with the ester sites. Furthermore, our theoretical investigation has confirmed, on one hand, that the aluminium/polystyrene interactions are weak, and on the other hand, the absence of strong reactions at the interfaces between aluminium and saturated hydrocarbon polymers. 相似文献
796.
François Constantin Françoise Fenouillot Jean-Luc Guillaume Raymond Koenig Jean-Pierre Pascault 《Macromolecular Symposia》2003,198(1):335-344
Properties of thermoplastic modified epoxy network have been studied. The particularity of this work is the use of new thermoplastic epoxies whose structure is close to the final matrix. Blends of thermoset epoxy (Diglycidyl Ether of Bisphenol A/4-4′ methylenebis [3-chloro 2,6-diethylaniline]) with a thermoplastic content from 5 to 40%w have been realised. Initial miscibility in the thermoset precursors shows an UCST behaviour with a maximal value near 130°C for a thermoplastic content of 10%. Due to the presence of tertiary amine and pendant hydroxyl groups on the thermoplastic backbone, epoxy amine reactions are faster than for the neat system but the thermoplastic seems not to have reacted with the thermoset network. The final blends are transparent but toughening increase is rather low. 相似文献
797.
Hélène Angellier Jean-Luc Putaux Sonia Molina-Boisseau Danielle Dupeyre Alain Dufresne 《Macromolecular Symposia》2005,221(1):95-104
Aqueous suspensions of nanocrystals can be obtained by acid hydrolysis of native waxy maize starch granules. The disruption of waxy maize starch granules by 2.2N HCl hydrolysis has been followed by scanning and transmission electron microscopy and laser granulometry. The mechanical properties of composite materials made of poly(styrene-co-butyl acrylate) filled with starch nanocrystals were characterized by dynamic mechanical analysis. These nanocrystals appeared to be an interesting reinforcing phase in a thermoplastic matrix. 相似文献
798.
Vincent Parent Jean-Luc Brdas Philippe Dubois Nathalie Ropson Robert Jrme 《Macromolecular theory and simulations》1996,5(3):525-546
We present a theoretical study on aluminium triisopropoxide (Al(OiPr)3) using both empirical (Molecular Mechanics, MM, with Dreiding II force field) and quantum-chemical (Austin Model 1, AM1, semiempirical Hartree-Fock) techniques. We determine the most stable geometries for both the tetramer and trimer of aluminium triisopropoxide as well as the thermodynamic characteristics of the equilibrium existing between these two aggregated structures. The theoretical results are compared to experimental data from X-ray diffraction and 27A1 NMR measurements. For the tetramer, it appears that the optimal equilibrium geometries are in good agreement with the experimental X-ray diffraction geometry; another geometry is also obtained with both theoretical approaches, which is slightly less stable but of higher symmetry. On the basis of the most stable configurations for the tetramer and trimer aggregates, the variation of free enthalpy (ΔG) between the two aggregated structures has been estimated. The evolution of the theoretical ΔG values indicates a displacement of equilibrium towards the trimer species with temperature, in good agreement with experimental 1H and 27A1 NMR data. Moreover, the AM1 heats of formation show a gain of 33.9 kcal/mol due to the aggregation of four A1(OiPr)3 instead of three, and thus a better stability of the tetramer. The molecular geometries being well described by the theoretical methods used in this study, we also present a model for the ring-opening polymerization complexes of ε-caprolactone and lactides. 相似文献
799.
Xavier Crispin Christophe Bureau Victor Geskin Roberto Lazzaroni Jean-Luc Bredas 《ChemInform》1999,30(13):no-no
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option. 相似文献
800.
: In an attempt to obtain a semiconducting poly(paraphenylene) PPP we have looked at the effect of ion implantion on this conjugated polymer (Ref. 1). The properties of the material may be varied according to the implantation parameters (Ref. 2) and the electrical conductivity after ion implantation of PPP remains almost constant for a long period of time. 相似文献