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11.
Frdric Tronc Warner Chen Mitchell A. Winnik Sarah T. Eckersley Gene D. Rose J. M. Weishuhn D. M. Meunier 《Journal of polymer science. Part A, Polymer chemistry》2002,40(22):4098-4116
This article describes the results of experiments examining the competition between the polymer diffusion rate and the crosslinking rate in low‐glass‐transition‐temperature, epoxy‐containing latex films in the presence of a diamine. We examined films formed from donor‐ and acceptor‐labeled poly(butyl acrylate‐co‐methyl methacrylate‐co‐glycidyl methacrylate) copolymer latex and studied the influence of several parameters on the growth rate of gel content and the rate of polymer diffusion. These factors include the molecular weight of the latex polymer, the presence or absence of a diamine crosslinking agent, and the cure protocol. The results were compared to the predictions of a recent theory of the competition between crosslinking and polymer diffusion across interfaces. In the initially formed films, polymer diffusion occurs more rapidly than the chemical reaction rate. Therefore, these films fall into the fast‐diffusion category of this model. In our system (unlike in the model), the latex polymer has a broad distribution of molecular weights and a distribution of diffusivities. The shortest chains contribute to the early time diffusion that we measure. At later stages of our experiment, slower diffusing species contribute to the signal that we measure. The diffusion time decreases substantially, and we observe a crossover to a regime in which the chemical reaction dominates. The increases in chain branching and gel formation bring polymer diffusion to a halt. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 4098–4116, 2002 相似文献
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Kujawa P Moraille P Sanchez J Badia A Winnik FM 《Journal of the American Chemical Society》2005,127(25):9224-9234
The layer-by-layer growth of multilayer assemblies of two polysaccharides, the polyanion hyaluronan (HA) and the polycation chitosan (CH), was investigated using atomic force microscopy (AFM) and surface plasmon resonance (SPR) spectroscopy, with primary emphasis on the effect of the polysaccharide molecular weights on the film thickness and surface morphology. The HA/CH multilayers exhibit an exponential increase of the optical film thickness with the number of deposited bilayers. We show that the multilayer thickness at a given stage depends on the size of both CH, the diffusing polyelectrolyte, and HA, the non-diffusing species. Assemblies (12 bilayers) of high molecular weight polysaccharides (HA, 360,000; CH, 160,000) were twice as thick (approximately 900 nm vs approximately 450 nm) as those obtained with low molecular weight polymers (HA, 30,000; CH, 31,000), as assessed by AFM scratch tests. The exponential growth rate is the same for the high and low molecular weight pairs; the larger film thicknesses observed by SPR and by AFM arising from an earlier onset of the steep exponential growth phase in the case of the high molecular weight pair. In all cases, isolated islets form during the deposition of the first CH layer onto the underlying HA. Upon further film growth, individual islets coalesce into larger vermiculate features. The transition from distinct islands to vermiculate structures depends on the molecular weights of the polysaccharides and the lower molecular weight construct presents larger worm-like surface domains than the high molecular weight pair. 相似文献
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A number of fundamental studies on the interactions between lipid bilayers and (ethylene oxide)-b-(propylene oxide)-b-(ethylene oxide) copolymers (PEO-PPO-PEO, Pluronics) have been carried out recently as model systems for the complex behavior of cell membranes with this class of polymers often employed in pharmaceutical formulations. We report here a study by differential scanning calorimetry (DSC) of the interactions in water between Pluronic F127 (F127), and the cationic vesicles of di-n-octadecyldimethylammonium bromide (DODAB), as a function of concentration of the two components (DODAB 0.1 and 1.0 mM; F127 0.1 to 5.0 mM) and of the sample preparation protocol. The DSC studies follow the critical micellization temperature (cmt ≈ 27 °C at 1.0 mM) of F127 and the gel-liquid crystal transition (T(m) ≈ 45 °C) of the DODAB bilayer and of F127/DODAB mixtures. Upon heating past T(m), vesicle/polymer mixtures undergo an irreversible conversion into mixed DODAB/F127 micelles and/or F127-bearing vesicles, depending on the relative amount of each component, together with, in some cases, residual intact F127 micelles or DODAB vesicles. Sample preparation protocol is shown to have little impact on the composition of mixed systems once they are heated above T(m). 相似文献
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Abdelrahman AI Thickett SC Liang Y Ornatsky O Baranov V Winnik MA 《Macromolecules》2011,44(12):4801-4813
Lanthanide-encoded polystyrene particles synthesized by dispersion polymerization are excellent candidates for mass cytometry based immunoassays, however they have previously lacked the ability to conjugate biomolecules to the particle surface. We present here three approaches to post-functionalize these particles, enabling the covalent attachment of proteins. Our first approach used partially hydrolyzed poly(N-vinylpyrrolidone) as a dispersion polymerization stabilizer to synthesize particles with high concentration of -COOH groups on the particle surface. In an alternative strategy to provide -COOH functionality to the lanthanide-encoded particles, we employed seeded emulsion polymerization to graft poly(methacrylic acid) (PMAA) chains onto the surface of these particles. However, these two approaches gave little to no improvement in the extent of bioconjugation. In our third approach, seeded emulsion polymerization was subsequently used as a method to grow a functional polymer shell (in this case, poly(glycidyl methacrylate) (PGMA)) onto the surface of these particles, which proved highly successful. The epoxide-rich PGMA shell permitted extensive surface bioconjugation of NeutrAvidin, as probed by an Lu-labeled biotin reporter (ca. 7 × 10(5) binding events per particle with a very low amount of non-specific binding) and analyzed by mass cytometry. It was shown that coupling agents such as EDC were not needed, such was the reactivity of the particle surface. These particles were stable and the addition of a polymeric shell was shown did not affect the narrow lanthanide ion distribution within the particle interior as analyzed by mass cytometry. These particles represent the most promising candidates for the development of a highly multiplexed bioassay based on lanthanide-labeled particles to date. 相似文献
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S.L. Winnik 《Nuclear Physics A》1975,247(2):382-394
The transfer of nucleonic Cooper pairs during the scattering of two superfluid nuclei just below the Coulomb barrier is discussed microscopically. Break-up of pairs, especially by Coulomb excitation of vibrational states, and competition from other channels reduce the transfer probability. 相似文献
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