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  • Chemistry  (3)
  • THERMODYNAMICS AND COMBUSTION  (3)
  • 1960-1964  (6)
Collection
Keywords
Publisher
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 45 (1962), S. 1799-1803 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1The condensation of dichloropyromellitic acid dianhydride (I) with substituted anilines (o-, p-chloro-, p-fluoro) gave new derivates of dianilino-pyromellitic acid di-phenylimide (II, VI, VII).2The condensation of dichloropyromellitic acid di-methylimide (IX) or of compound I with ethylamine yielded 1,4-di-ethylamino-pyromellitic acid di-ethylimide (X).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 48 (1960), S. 175-188 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This report is concerned with the kinetics of the emulsion polymerization of styrene initiated by the thermal decomposition of oil-soluble initiators particularly cumene hydroperoxide (CHP). Only those systems are considered in which the latex particles are so small that two radicals cannot coexit for a significant length of time. Polymerization rate, particle size, and molecular weight of the polymer have been determined at 40, 50, and 70°C. as a function of initiator concentration. At low CHP concentrations the polymerization rate per particle conforms to Smith-Ewart kinetics, i.e., on the average one polymer radical propagates during half the time in each particle. Therefore it is concluded that, although CHP may decompose into radical pairs, polymer radicals are formed one by one. It is shown that even very low rates of transfer of single radicals from the particles to the aqueous phase, or vice versa, suffice to account for the observed polymerization rates per particle. An alternative mechanism is considered in which CHP decomposes on the surface of the particle, the organic radical enters the particle, and the hydroxyl radical remains in the aqueous phase. The rate of polymerization per particle is observed to decrease with increasing CHP concentration. The fact that the transfer coefficient of this initiator is several orders of magnitude higher than that of cumene sustains the supposition that the polystyryl radical abstracts the periodic hydrogen from the peroxide. The decrease in polymerization-rate is attributed to the inactivity of the resulting ROO·radical. The Mayo formula for the reciprocal degree of polymerization is reformulated to incorporate this kinetic feature. The dependence of polymerization rate on CHP concentration, derived from the new formula, generally agrees with experimental results. Transfer coefficients of the polystyryl radical to CHP and other organic peroxides are given. From the data it can also be concluded that the decomposition rate of CHP in emulsion polymerization is an order of magnitude larger than in styrene solution.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Emulsion polymerizations of styrene were carried out at different phase ratios. The initial soap concentration was varied from below to above the critical micelle concentration (CMC). Above the CMC the number of particles formed agrees with values calculated from the Smith-Ewart theory. As the soap concentration is reduced below the CMC the number of particles decreases sharply. In this concentration range the number of particles is independent of the amount of initiator but depends strongly on soap concentration. Kinetic features suggest a similarity between particle formation in these polymerizations and in homogeneous precipitation of inorganic insoluble salts. The coefficient of variation of particle diameter distribution below the CMC is about 2.5% and at high soap concentration about 15%. Bimodal distributions are obtained when the initial soap concentration is near the CMC. The initiation efficiency of persulfate is calculated from the rate and degree of polymerization and also from the number of particles formed. The efficiency increases from 0.2 to 0.6 with decreasing persulfate concentration. When the particles are smaller than about 0.12 μ, polymerization kinetics follow the Smith-Ewart theory. Values are reported for the monomer concentration in the particles and for the constant of propagation. Larger particles exhibit a gel effect, i.e., more than one radical can coexist in a particle for a significant lenght of time. From polymerization rate data and molecular weight measurements the rate constants for the transfer reaction to monomer and for termination are calculated. The latter constant is found to be two to three orders of magnitude smaller than values obtained in solution polymerization. The difference is attributed to the high viscosity of the interior of the particles which causes the termination reaction to be diffusion-controlled.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2019-05-11
    Description: Large deflection theory for determining the buckling pressure of spherical shells
    Keywords: THERMODYNAMICS AND COMBUSTION
    Format: text
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  • 5
    Publication Date: 2019-05-11
    Description: Buckling of a free edge of an axially compressed circular cylindrical shell
    Keywords: THERMODYNAMICS AND COMBUSTION
    Format: text
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  • 6
    Publication Date: 2019-05-11
    Description: Hydrostatic buckling pressure calculations for spherical shells
    Keywords: THERMODYNAMICS AND COMBUSTION
    Type: NASA-CR-50600 , SUDAER-133
    Format: application/pdf
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