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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 60 (1956), S. 1250-1254 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Industrial and engineering chemistry 2 (1963), S. 273-278 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 169-182 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Experiments were conducted on samples of crosslinked rubbers filled with poly(tetrafluoroethylene) powder or small glass beads. Volume changes on elongation were measured in a dilatometer. Slow deformation cycles showed considerable hysteresis, the volume on elongation being smaller than on contraction. There is much less hysteresis if the sample is degassed before the experiment. These observations suggest that, to a large extent, the volume of the cavities is determined by the availability of gases dissolved in the elastomer matrix. When the samples were saturated with carbon dioxide, nitrogen, and helium, it was indeed found that the degree of cavitation increased in order with the solubility of these gases.The initial rate of cavitation is high. After about 1 min, dilatation is proportional to the logarithm of time. This rate is inversely related to the solubility of the gas present.When a sample is subjected to a constant tensile stress under vacuum and the external pressure is suddenly brought to atmospheric, the elongation at first decreases due to compression of the cavities and then increases slowly as gas diffuses into them. Even unfilled compounds mixed mechanically contain submicroscopic holes. These enlarge on deformation thus causing dilatation. Only for samples prepared by evaporation from solution is there no pressure dependence of the apparent modulus.It is demonstrated that the relation between the volume of vacuum cavities and the external pressure resembles that of volume and inflation pressure of a spherical hole in an infinite elastic medium.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 2373-2384 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: High molecular weight polyisobutylene samples were degraded by milling at 320 K. The degradation process was followed by determining the course of the changes in molecular weight distributions (MWD) that were obtained by gel permeation chromatography. After long milling times degradation stops or at least the rate of rupture becomes extremely small, the molecular weight approaching an apparent minimum value (Mm) of 0.4 × 106. The rate of degradation decreases in the course of the first ½ to 1 hr from an initial value to one constant up to at least 3 hr if the maximum shear rate is higher than about 6 s-1. At lower shear rates the rate of scission is constant from the start. When milling is stopped for 24 hr, high initial rupture rate is observed on resumption of milling at high shear rate, again followed by a drop in rate to the same value as before the interruption. The initial rates are independent of shear rate, whereas the subsequent constant rates are proportional to the rate of shear. These observations are discussed in terms of an equilibrium between the formation of multimolecular “rheological units” and the tendency, due to thermal motion, to form a homogeneous entanglement network. The MWDs are compared with those calculated from a model based on a given relation between probability of scission (P) and molecular weight and an assumed probability distribution (Q) of rupture site along the length of the polymer moelecules. The observed MWDs are incompatible with those calculated from models in which Mm = 0 or in which breakage near the center of the molecule is favored. They agree rather well with computed MWDs based on the assumptions that P ∞ MW and Q is the symmetrical beta function between points along the molecule Mm removed from the ends, where Mm is (0.4-0.5) × 106. The mechanism of rupture appears to be the same for low and for high shear rates.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 24 (1979), S. 2087-2100 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Intrinsic viscosities of polymers are most often estimated using the Huggins equation, which relates the quotient ηsp/c to intrinsic viscosity and concentration c. It is shown that when this method is used, the error structure is distorted by the presence of concentration in the quotient. The result is that when dilution series experiments are analyzed, the estimates are ordinarily poorer the more dilutions are made. A rearrangement of the Huggins equation is introduced which allows precise estimation from any experiment. It is also shown that dilution series experiments with more than three different concentrations including that of the pure solvent are inefficient by any method of analysis, and convenient experiments which may be considered practical optima are described. When they are used the conventional analysis is restored to full efficiency. Design and analysis of experiments where there is important uncertainty in polymer concentration are also studied.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 297-311 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Stress-strain behavior in extension and the swelling of polymer networks with different lenghts of crosslinks is reported. These networks were prepared by copolymerization of butyl acrylate with different amounts of various difunctional comonomers which yield crosslinks of 4, 7, 10, and 16 bonds in length. The efficiency of the comonomers in crosslinking is low, improving with increasing length of the chain between their unsaturated endgroups. Analysis of a large number of stress-strain data obtained at elongations between 2 and 8% elongation showed that in this deformation range the stress-strain relation based on the statistical theory of elasticity represents the data better than does Hooke's law or the Mooney-Rivlin relation. It was found that the relation between the modulus at small deformations and the swelling ratio of the various samples inindependent of the length of the crosslinks. Also the shapes of the Mooney-Rivlin curves are the same for all networks. Furthermore, the creep behavior of various networks with different crosslink lengths is the same for networks compared at the same elastically effective chain concentration. It is concluded that the lenght of the crosslinks, at least up to 16 bonds, does not affect the elastic response of polymer networks.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 487-490 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 48 (1960), S. 175-188 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 9
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 493-502 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Radical chain-transfer constants can be deduced from corresponding measurements of rates and degrees of polymerization in copolymerization experiments. It is particularly useful to carry out such copolymerization in emulsion systems where the normal termination reactions are relatively less important and chain-transfer processes are significant in determining the number-average degree of polymerization. The method is illustrated for copolymerization of styrene and α-methylstyrene at three temperatures. Rate constants for transfer of styryl and α-methylstyryl radicals to either monomer were measured. All the rate constants are consistent with the relative stabilities of the product radicals which could be formed by the various transfer reactions. The procedure described here can be extended for measurements of rate constants for reactions of other potential transfer agents.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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