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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 861-874 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Differences between the emulsion copolymerization and miniemulsion copolymerization processes, in terms of emulsifier adsorption, emulsion stability, polymerization kinetics, copolymer composition and dynamic mechanical properties were studied for the comonomer mixture of 50:50 molar ratio vinyl acetate (VA+) - butyl acrylate (BuA), using sodium hexadecyl sulfate (SHS) as a surfactant and hexadecane (HD) as a co-surfactant. The use of hexadecane with the appropriate SHS initial concentration led to a higher adsorption of surfactant, smaller droplet size, higher stability of the emulsions, lower polymerization rates, and larger latex particle size. The copolymer composition during the initial 70% conversion was found to be less rich in Vac monomer units for the miniemulsion process. The dynamic mechanical properties of the copolymer films showed less mixing between the BuA-rich core and the VAc-rich shell in the miniemulsion latexes compared to the conventional latex films.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 123-127 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 87-109 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of new ionenes was accomplished by the reaction of novel diamines and dihalides. A new class of crosslinkable ionenes was made possible by the synthesis of tertiary diamines with acrylate functionality, generated ultimately from diepoxides and secondary amines. Other tertiary diamines were produced by endcapping of diols with tolylene diisocyanate, followed by reaction with N,N-dimethylethanolamine and also termination of living poly(tetrahydrofuran) polymer with dimethylamine. New dihalides were produced by the opening of diepoxides with ω-bromoacids.These diamines and dihalides underwent Menschutkin reactions providing novel ionenes for structure-property relationship studies. Correlations were drawn concerning amine nucleophilicity, dihalide nucleofugascity, and molecular weight. Stress-strain and thermal data reflected the effects of ionic domains and large flexible segments in the polymers. Also considered were the electrical conductivity, moisture-vapor transmission, and oxygen permeability of these materials.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 193-202 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The role of the cosurfactant (hexadecane) in the miniemulsion copolymerization of 50 : 50 molar ratio vinyl acetate-butyl acrylate monomer mixture is analyzed from an experimental point of view. The main factor responsible for the different kinetic behavior between the miniemulsion and conventional emulsion copolymerization processes was found to be the different particle nucleation mechanism operating in each process. Experimental evidence is presented indicating that in the miniemulsion copolymerization particle nucleation takes place in the preformed stable submicron monomer droplets.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 1155-1167 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Dielectric spectroscopy was used to monitor the curing process of two epoxy resin systems. The basic system (system I) consisted of DGEBA (a difunctional epoxy) and a polyamide in a 50-phr mixture. In addition, a comparative analysis was performed on a high-performance resin system (system II) used primarily in unidirectional composite applications. This system contained TGDDM (a tetrafunctional epoxy) and DDS (a tetrafunctional amine) in a 25-phr mixture. The dielectric data were obtained using a simple yet functional sample cell electrode designed and constructed in the laboratory. For system I, isothermal dielectric data were used to determine apparent activation energies for the temperature range from 22 to 70°C. The data showed that the activation energy was a function of temperature and increased as the temperature of the cure increased. This indicated that the reaction mechanism was also a function of temperature. For system II, data were collected between 140 and 190°C and an overall activation energy for that temperature range was determined. The overall activation energies for both systems, calculated using dielectric spectroscopy, compared favorably to those obtained using differential scanning calorimetry. Also, using a wider frequency range (240 Hz to 2 MHz), Argand diagrams were constructed and modeled with the Cole-Cole empirical equation for systems with a distribution of relaxation times. This justified the calculation of average relaxation times, which could then be related to the bulk physical properties of the polymer, such as viscosity. Modified Argand diagrams, where ε″ is plotted against ε′ at one frequency as a function of time, were also constructed, which aided in the understanding of the curing processes for these thermosetting systems.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 33 (1987), S. 657-667 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polypentafluorostyrene (PPFS), polymethylacrylate (PMA), and poly(pentafluorostyrene-co-methylacrylate), poly(PFS-co-MA) were prepared and the wetting characteristics of polymer blends of PPFS and PMA were compared with that of poly(PFS-co-MA) via contact angle measurements. The critical surface tension of polypentafluorostyrene was found to be 22.6 dyne/cm, which is comparable to the value reported for polytrifluoroethylene (22 dyne/cm). The critical surface tension of poly(PFS-co-MA) is not linearly related to its composition. The polymer blends of PPFS and PMA exhibit significant surface enrichment of the fluoropolymer. The harmonic-mean method1 was employed to determine surface tensions of these polymers and many known polymers. It is found that the method produces useful surface tension data provided the contact angle values are derived from testing liquids of dissimilar polarity.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 5007-5019 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The solubility parameter scheme is an exceptionally useful tool for predicting the solubility behavior of simple polymer systems. However, this scheme is unable to handle well enough complicated systems, such as those involving donor-acceptor interactions and those containing more than two solvents. More advanced thermodynamic treatments and computer techniques, such as UNIFAC, can be a key to solving these kinds of problems.The UNIFAC group-contribution method utilizes a volume parameter and a surface-area parameter for each structural group and a pair of interaction-energy parameters for each pair of groups, which can be deduced from experimental activity data. The method was originally derived for mixtures of ordinary liquids and has been extended to polymer solutions by adding a free-volume correction. The modified UNIFAC method can be used to estimate the activities of solvents in a polymer solution, even when no experimental data are available for the mixture.In the present study, the UNIFAC method was applied to optimize polymer-solvent interactions in three-solvent systems. A three-dimensional plot, displaying polymer activity as a function of the solvent composition, was constructed for each polymer system. The minimum in polymer activity was used as the criterion for maximum polymer-solvent interaction. Dissolution rate and solution clarity were used to test the polymer-solvent interaction experimentally. Comparison of theoretical predictions with experimental results indicated that a better agreement could be obtained by using the UNIFAC method rather than the solubility parameter method.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 20 (1986), S. 273-275 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Gold and platinum ultrathin ring microelectrodes (0.1-0.5 mm thick, 1.5-4 mm diameter) were made by sputtering, from fired metalloorganic paint, and from foil for use as sensors in a thick-layer wall-jet flow cell. An end-on array of three 0.1 μm × 0.5 mm gold band electrodes were mounted parallel to the flow direction in a thin-layer channel cell. These ultrathin sensors, along with a jet-centered carbon microdisk, were evaluated in the amperometric flow-injection mode for temporal stability, calibration sensitivity, detectivity, background signal, and flow rate dependence of the analytical signal using ferrocene samples in acetonitrile containing 10-4-10-2 M TEAP. The detectivity of gold paint ring electrodes made on borosilicate glass was 3-6 nM, an order of magnitude lower than any of the other electrodes tested. Analytical signals from gold paint and foil rings and the carbon microdisk had the best temporal stability. The current for the ultrathin band array in a channel cell was flow rate-independent, and the exponential dependence of cell current on flow rate was 0.11-0.14 for ultrathin rings in the thick-layer wall-jet mode.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Advanced Materials 1 (1989), S. 140-141 
    ISSN: 0935-9648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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