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Acrylate Copolymers (acrylate + copolymer)
Selected AbstractsToughening of Epoxy Resin by Methyl Methacrylate/2-Ethylhexyl Acrylate Copolymers: The Effect of Copolymer CompositionMACROMOLECULAR MATERIALS & ENGINEERING, Issue 12 2007Soraia Zaioncz Abstract MMA-EHA copolymers with different compositions and with a low amount of AA were synthesized and used as impact modifier for epoxy networks. The effect of the copolymers on the tensile and dynamic mechanical properties as well as impact resistance of the epoxy network was evaluated. The addition of 10 phr of low-molar-mass MMA-EHA copolymer with defined composition resulted in a significant increase in impact resistance without any significant changes in the tensile strength, modulus, and glass transition temperature. The morphology of the modified epoxy network depends upon the copolymer composition. [source] Simultaneous enhancement of cosmetic function and feel via molecular investigation of stickinessINTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 2 2006H. Kudoh Moisturizing performance is often a very important factor in cosmetics. However, incorporating high concentrations of moisturizing agents often causes products to become sticky, a feel that consumers dislike. We suspected that the reason why high moisturizer content generates strong stickiness is that the polar group of the molecule is exposed at the surface. Thus, we began with a hypothesis that stickiness could be prevented through coexistence with a substance minimizing the exposure of polar group. Using glycerine as a moisturizing agent, we screened a large number of conventional materials for reducing stickiness but failed to find an effective compound. We then considered the use of a polymer for this purpose and synthesized a custom-made polymer, polyoxyethylene methacrylate 2-hydroxyethyl methacrylate fluoroalkyl acrylate copolymer (Polymer SR). Our experiments revealed that Polymer SR reduces the stickiness of glycerine by forming a hydrophobic film without hindering moisturizing performance. To clarify the mechanism by which Polymer SR reduces stickiness, we investigated the interaction between the Polymer SR and glycerine in solution using NMR and static light scattering measurements. We learned that Polymer SR and glycerine form a complex via hydrogen bonding of glycerine that results in orientation of the hydrophobic group of Polymer SR towards the outside. Subjective sensory tests supported the hypothesis that this hydrophobic orientation was maintained on the dermal surface even after application to skin. We believe that by taking into account the intended function and feel our technique for reducing the stickiness of moisturizers can be adopted for use with other substances and will contribute to future cosmetic research. [source] A novel route for preparation of PVC sheets with high UV irradiation resistanceJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010Xianke Ye Abstract A novel acrylonitrile acrylate copolymer coating was proposed to improve the UV irradiation resistance of poly(vinyl chloride) (PVC) sheets. Its effect on the photoageing properties of the sheets was evaluated by means of Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), yellowness index test, and the oxygen permeability coefficient and mechanical properties measurement. The experimental results show that the novel acrylonitrile acrylate copolymer coating significantly improves the UV irradiation resistance of PVC sheets. Compared with the PVC sheets without coating, the coated PVC sheets show better mechanical properties, lower yellowness index, and smaller oxygen permeability coefficient after UV irradiation. The analysis on the SEM images of the PVC sheets indicates that the coating acts as a film to prevent the PVC sheets from UV energy and oxygen that can accelerate the photochemical reactions of PVC. The FTIR analysis confirms that the coating can slow down the microstructures development of the PVC sheets, also indicating that the coating impeded the photochemical reactions of PVC. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Miniemulsion polymerization of a fluorinated acrylate copolymer: Kinetic studies and nanolatex morphology characterizationJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007Qinghua Zhang Abstract A stable fluoroacrylate copolymer emulsion was successfully prepared by miniemulsion polymerization with fluoroacrylate, lauryl methylacrylate, and methyl methacrylate as monomers. Extremely hydrophobic fluoroacrylate, instead of conventional cosurfactants, was used as a reactive cosurfactant to stabilize the miniemulsions. The results indicated that fluoroacrylate retarded Ostwald ripening and allowed the production of stable miniemulsions. The chemical compositions of the copolymer were studied with Fourier transform infrared and 1H-NMR. The average composition of the copolymers prepared with miniemulsions was in good agreement with the feed ratio according to 1H-NMR from the integration ratios corresponding to typical protons of the individual monomers. The particle size distribution and morphology of the latex particles were determined with laser particle analysis and transmission electron microscopy. The particle size of the latex underwent no change in the process of miniemulsion polymerization, but the particle size distributions were broader than those of conventional emulsion polymerization. The effects of various reaction parameters, including the temperature and concentrations of the emulsifier and initiator, on the miniemulsion polymerization were also investigated, and the polymerization rate and conversion increased with increasing concentrations of nonylphenol polyethoxylate (with an average of 40 ethylene oxide units per molecule), cetyltrimethylammonium, and 2,2,-azobisisobutyronitrile. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 641,647, 2007 [source] Fabrication, structures, and properties of acrylonitrile/methyl acrylate copolymers and copolymers containing microencapsulated phase change materialsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2007Na Han Abstract The polyacrylonitrile-methyl acrylate (AN/MA mole ratio 100/0,70/30) copolymers and copolymers (AN/MA mole ratio 85/15) containing up to 40 wt % of microencapsulated n -octadecane (MicroPCMs) are synthesized in water. The MicroPCMs were incorporated at the step of polymerization. The effect of the MA mole ratio and MicroPCMs content on structures and properties of the copolymers were studied by using Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (1H NMR), scanning electronic microscope (SEM), differential scanning calorimetry (DSC), thermogravimetry analysis (TG), gel permeation chromatography (GPC), and X-ray diffraction (XRD). The feeding ratio agreed well with the composition of the AN/MA copolymers. The copolymers are synthesized in the presence of MicroPCMs. The melting point moves to lower temperature (206°C), while the decomposition temperature moves to higher temperature (309°C) with increasing of the MA mole ratio and microcapsules content. The number,average molecular weight of the copolymer is ,30,000. The crystallinity of the copolymer decreases with increasing of the MA mole ratio and microcapsules content. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2776,2781, 2007 [source] Frontal free-radical copolymerization of urethane,acrylatesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 9 2006Ting Hu Abstract We report the first synthesis of urethane,acrylate copolymers via free-radical frontal polymerization. In a typical run, the appropriate amounts of the reactants (urethane,acrylate macromonomer and 2-hydroxyethyl acrylate) and initiator (ammonium persulfate) were dissolved in dimethyl sulfoxide. Frontal polymerization was initiated by the heating of the wall of the tube with a soldering iron, and the resultant hot fronts were allowed to self-propagate throughout the reaction vessel. Once it was initiated, no further energy was required for the polymerization to occur. The dependence of the front velocity and front temperature on the initiator concentration was investigated. The front temperatures were between 55 and 65 °C, depending on the persulfate concentration. Thermogravimetric analysis indicated that the urethane,acrylate copolymers had higher thermal stability than pure frontally prepared polyurethane. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3018,3024, 2006 [source] Compositional and configurational sequence determination of methyl methacrylate/ethyl acrylate copolymers by one- and two-dimensional nuclear magnetic resonance spectroscopyJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 2 2003A. S. Brar Abstract Ethyl acrylate (E)/methyl methacrylate (M) copolymers of different compositions were prepared, and their compositions were determined with 1H NMR spectra. The complete spectral assignments, in terms of the compositional and configurational sequences of these copolymers, were made with the help of distortionless enhancement by polarization transfer and two-dimensional heteronuclear single quantum coherence spectroscopy. The ,-(CH3)M, CH (E), CH2, and ,CO carbons of both M and E units were found to be sensitive to various compositional and configurational sequences. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 313,326, 2003 [source] Characterization of Ethylene Copolymers with Liquid Chromatography and Melt Rheology MethodsMACROMOLECULAR SYMPOSIA, Issue 1 2009Yefim Brun Abstract Summary: Melt rheology and polymer chromatography methods were applied to characterize molecular heterogeneities in products of free radical copolymerization of ethylene with methyl acrylate and vinyl acetate comonomers performed in continuously stirred tank and tubular reactors. We found that the ethylene,vinyl acetate copolymers made in both reactors had similar linear viscoelastic properties typical to branched products of the high pressure process. But the ethylene,methyl acrylate copolymers obtained in the tubular reactor had unusually high melt viscosity at low shear rate and much lower onset of shear thinning despite the narrower molecular weight distribution and the lower overall amount of long-chain branches compare to their autoclave counterparts with similar average molecular weight and chemical composition. Using interaction polymer chromatography method called gradient elution at critical point of adsorption we found that ethylene-acrylate copolymers from the tubular reactor had very broad chemical composition distribution, which was consistent with a significant difference in reactivity ratios between ethylene and acrylate comonomers. Such chemical composition heterogeneity can be a reason for the observed unusual rheological properties of these copolymers. [source] | ||||||||||