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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 21 (1982), S. 551-558 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 21 (1982), S. 55-61 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1536
    Keywords: Key wordsBlock-copolymers ; polyethylene oxide ; polybutylene oxide ; reactive surfactants ; emulsion polymerization ; dispersion polymerization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  A variety of nonionic reactive surfactants have been prepared from block copolymer precursors. These precursors are formed from a commercially available polyoxyethylene glycol monomethylether as the hydrophilic sequence of the surfactant; this product is used as initiator of ring opening anionic polymerization of butylene oxide. Finally the reactive surfactants are obtained after proper functionalization of the precursor. The reactive surfactants are an inisurf with an asymmetric azo compound, a transurf with a thiol group, and a few surfmers with acrylic, methacrylic, styrenic and α-methyl styrenic reactive groups. These compounds have been engaged in styrene emulsion or dispersion polymerization. Several of them have been found to be useful for preparing stable latices.
    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. 3569-3587 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new approach is presented to calculate both the distribution of particles with iradicals and the average number of radicals per particle in emulsion polymerizations carried out using oil-soluble initiators. The convergence and accuracy of the approach were examined. It was found that, in agreement with previously published experimental results, the present approach predicts a kinetic behavior similar to that found for water-soluble initiators. This effect is primarily due to the desorption of initiator radicals from the polymer particles rather than the contribution of the fraction of oil-soluble initiator dissolved in the aqueous phase.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 987-1009 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mathematical model for the unseeded emulsion copolymerization of styrene and methyl methacrylate has been developed. This model, which includes a new rate coefficient for radical desorption, was used to analyze the effect of the styrene/methyl methacrylate molar ratio in the initial charge on the number of particles, overall conversion and copolymer composition. It was found that the number of particles increased with the methyl methacrylate content and that a drift of the copolymer composition resulted during the polymerization of styrene/methyl methacrylate molar ratios other than 50/50. Good agreement between experimental results and model predictions was achieved.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 3903-3913 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The derivation of a radical desorption coefficient in emulsion polymerization is presented, which takes into account the possible reactions of the desorbed radical in the aqueous phase as well as the competition between desorption and termination in polymer particles containing more than one radical. This model overcomes some important limitations of the previous models and is able to explain previously reported experimental results that the other models were unable to explain.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 4241-4255 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetic analysis of the transesterification of ethylene glycol (EG) and dimethyl terephthalate (DMT) was studied in a semibatch reactor under nonisothermal conditions. The effect of the temperature profile, EG/DMT ratio, and catalyst concentration on the reaction rate was studied. Models were fitted by using an algorithm of parameter estimation in differential equations based on the Gauss-Newton method improved with the Marquardt extension. It was found that, unlike previous authors, the reaction rate was not a classical third order reaction of first order with respect to EG, DMT, and catalyst concentration, but the EG reaction order was 0.6 and a hyperbolic function was found to fit the relationship between reaction rate and catalyst concentration. Also, it was found that, at high conversions, the effect of the reverse reaction should not be neglected.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 309-311 
    ISSN: 0887-624X
    Keywords: radical desorption ; exit ; emulsion polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No abstract.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 1869-1877 
    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 rate coefficient for entry of radicals into the polymer particles and the radical exit rate coefficient were estimated in seeded emulsion polymerization of styrene. The dependence of both coefficients on the particle size was used in an attempt to discriminate between the models proposed for these coefficients. The results obtained were found to be consistent with a model in which the entry of radicals into the polymer particles occurs by the propagational mechanism and the radicals desorb from the polymer particles by diffusion. A comparison between the estimated values of the coefficients and those calculated theoretically using the equations derived from the corresponding mechanisms was performed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 39 (1990), S. 1183-1213 
    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: A new method for the estimation of kinetic parameters in emulsion polymerization systems is presented. This method is based on studies of the evolution of monomer conversion in chemically initiated seeded emulsion polymerization systems. In this paper, homopolymerization under zero - one conditions is considered. The method is based on a fundamental model that includes the free radical balance in the aqueous phase and fundamental parameters such as the entry and exit rate coefficients, the termination rate constant in the aqueous phase, and the rate coefficient for initiator decomposition. These parameters, as well as the propagation rate constant, are the estimable parameters. This method, which uses all available data simultaneously in order to estimate the parameters, is checked by using simulated experimental data generated with exact values of the parameters. The criteria for deciding the usefulness of the present approach are the closeness of the fit to the original data and the match of the estimated kinetic parameters to the exact values of the parameters. It was found that accurate values of the parameters are obtained with the present approach provided that a sufficient number of experiments with a minimum range of variation are available. A study of both the minimum number of experiments and the minimum range of variation of the experimental conditions needed to estimate reliable parameters is presented. Also, the effect of both random and systematic errors is included in this study. Finally, a comparison between the present approach and those previously published in the literature is presented.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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