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991.
Gaëtan R. P. Henry Xavier Drooghaag Dimitri D. J. Rousseaux Michel Sclavons Jacques Devaux Jacqueline Marchand‐Brynaert Véronique Carlier 《Journal of polymer science. Part A, Polymer chemistry》2008,46(9):2936-2947
This study reports a reactive extrusion process leading to very high levels of anhydride grafting (2.5–3 wt %) along polypropylene backbone without recovering grafted PP waxes at the die exit. Such high graftings are attainable without excessive degradation of the PP chain by using a brominated reagent. Simultaneously, this brominated reagent allows the tuning of the grafted PP crystallinity via epimerization of the PP backbone. Indeed, the synthesis of a mainly isotactic/atactic stereoblock polymer containing high levels of grafted succinic anhydride moieties is demonstrated by NMR and melting enthalpies recorded by DSC are definitely observed depressed and broadened. Grafting levels of around 3 wt % have been achieved and ascertained by both chemical titration and NMR spectroscopy. In addition, FTIR spectroscopy reveals an unusual observation: for the first time, only one single pair of symmetric and asymmetric carbonyl stretching bands are observed on those grafted PP, while, in other processes of anhydride grafting, those symmetric and asymmetric bands were both split in at least two bands. This suggests, for the here reported process, the absence of interacting grafted anhydride rings, i.e., absence of closely grafted anhydride moieties and absence of poly(maleic anhydride). All those observations support that this “bromine route” brings a really new grafting process for PP. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2936–2947, 2008 相似文献
992.
Gaëtan R. P. Henry Xavier Drooghaag Mikhaël Vandeuren Michel Sclavons André Schanck Jacques Devaux Véronique Carlier Jacqueline Marchand‐Brynaert 《Journal of polymer science. Part A, Polymer chemistry》2009,47(18):4505-4518
Amorphous and low crystallinity polypropylenes were produced by reactive processing of commercial isotactic polypropylenes in the presence of a peroxide (2,5‐dimethyl‐2,5‐di(tert‐butylperoxy)hexane) and N‐bromosuccinimide. Characterization of the modified polypropylene microstructures using 13C NMR spectroscopy revealed that crystallinity loss is correlated with the epimerization of numerous methynes randomly along the polymer backbone, leading to decreasing isotacticities ([mmmm]) and average isotactic block lengths. Moreover, degradation usually induced by peroxide was shown to be comparatively limited in additional presence of N‐bromosuccinimide. This fast and easy process therefore allows the production of polypropylene plastomers and elastomers with controlled and homogeneous crystallinities and isotacticities, and relatively low molecular weight distributions. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4505–4518, 2009 相似文献
993.
Simon Clavaguera Olivier J. Dautel Lionel Hairault Christophe Méthivier Pierre Montméat Eric Pasquinet Claire‐Marie Pradier Françoise Serein‐Spirau Salem Wakim Florian Veignal Joël J. E. Moreau Jean‐Pierre Lère‐Porte 《Journal of polymer science. Part A, Polymer chemistry》2009,47(16):4141-4149
The detection of 2,4‐dinitrotoluene (DNT) by fluorescence quenching of a new class of polyimines consisting in π‐conjugated segments regularly alternated with chiral C2 symmetry units has been studied for solutions and thin films. Their photophysical properties and their sensitivity towards DNT detection has been compared to those of a small model molecule incorporating the same π‐conjugated segment. In solution, all the compounds exhibit the same photo‐physical properties and sensitivity towards DNT detection. In contrast, for thin films, better performances are observed in static conditions for this new class of polyimines compared to the small model molecule. It seems that C2 symmetry units prevent from the stacking of the π‐conjugated segments and provide in addition to high fluorescence signal an improved diffusion of the analyte inside the films. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4141–4149, 2009 相似文献
994.
995.
996.
Samuel P. Schofield Rao V. Garimella Marianne M. Francois Raphaël Loubère 《国际流体数值方法杂志》2008,56(6):643-659
We have developed a new, multi‐material, piecewise linear interface reconstruction method that correctly locates the position of each material in the mesh cell and matches the required volume fractions with no material ordering required. This is different from other volume tracking interface reconstruction methods in which an improper material ordering may result in materials being incorrectly located within the cell. The new method utilizes a type of weighted Voronoi diagram, known as a power diagram, to reconstruct the interface from approximate material locations derived either from a particle model or quadrature formula. It works on structured and general polygonal grids, for an arbitrary number of materials and can be naturally extended to three dimensions. Published in 2007 by John Wiley & Sons, Ltd. 相似文献
997.
Charlotte Dire Joël Belleney Julien Nicolas Denis Bertin Stéphanie Magnet Bernadette Charleux 《Journal of polymer science. Part A, Polymer chemistry》2008,46(18):6333-6345
Methyl methacrylate (MMA) was polymerized in bulk at 70 °C in the presence of an alkoxyamine initiator with low dissociation temperature (the so‐called BlocBuilder?) and increasing amounts of free N‐tert‐butyl‐N‐(1‐diethylphosphono‐2,2‐dimethylpropyl) nitroxide (SG1). Low final monomer conversions were reached, indicating a loss in radical activity due to side reactions such as irreversible homoterminations between the propagating radicals and β‐hydrogen transfer (also called disproportionation) from a propagating radical to a free‐SG1 nitroxide. Proton NMR and MALDI‐TOF mass spectrometry were used to analyze the polymer chain‐ends and to clearly identify the main mechanism of irreversible termination. In particular, it was shown that all polymer chains were terminated by an alkene function in the presence of a large excess of free SG1, meaning that β‐hydrogen transfer from PMMA propagating radicals to the nitroxide SG1 was the major chain‐stopping event. On the other hand, for a low excess of free SG1, the two termination modes coexisted. Kinetic modeling was then performed using the PREDICI software, and the rate constant of β‐hydrogen transfer, kβHtr, was estimated to be 1.69 × 103 L mol?1 s?1 at 70 °C. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6333–6345, 2008 相似文献
998.
999.
G. le Caër B. Malaman G. Venturini H. G. Wagner U. Gonser 《Hyperfine Interactions》1986,28(1-4):631-634
57Fe and119Sn Mössbauer spectra have been recorded at 100 K in applied fields of 32 and 64 kG on a FeSn2 sample obtained by arranging single crystal needles side by side. The present work confirms that the Sn fields are anisotropic above Tt=93 K. The field model has been used to determine the magnetic structure of FeSn2 below Tt. 相似文献
1000.
N. T. Vorob'ëv 《Siberian Mathematical Journal》1996,37(6):1137-1142