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  • Wiley-Blackwell  (181)
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  • 1975-1979  (55)
  • 1970-1974  (126)
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  • 1
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 18 (1972), S. 1268-1271 
    ISSN: 0001-1541
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 20 (1974), S. 653-659 
    ISSN: 0001-1541
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: The purpose of this study was to investigate the influence of seed crystal size on the rate of nucleation in batch stirred-tank crystallizers. Experimental results confirm the existence of such an effect. Nucleation rate data are correlated with a second-order polynomial in seed crystal size; coefficients of the correlation are functions of the solute-solvent system, crystallizer geometry, and mixing conditions. The empirical correlation is incorporated into a population balance model for determining the nucleation rate in multi-seed crystallizers. The observed results are explained in terms of variations in impact energy, circulation frequency, and target efficiency.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 24 (1978), S. 1029-1035 
    ISSN: 0001-1541
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: The mixing of particles and gases in confined, coaxial jets in the presence of recirculation was studied. Particle and gas mixing rates were measured for conditions simulating processes involving pulverized coal combustion and entrained gasification. The effects of mixing chamber diameter, gas velocity, particle size, and particle loading level on mixing rates were determined from particle mass flux and gas tracer measurements. In every case, the gas mixed much faster than did the particles. Introduction of an expanded mixing chamber of larger diameter (with recirculation zone) significantly increased both gas and particle mixing rates over that for a smaller mixing chamber without recirculation. However, this observed increase was not strongly dependent upon the diameter of the larger mixing chamber. Increasing secondary velocity also increased mixing rates significantly.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 1117-1126 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Compressive fatigue experiments have been designed to compare this long term mechanical life property with shorter term stress-strain behavior. Fatigue lifetime curves can be represented by three distinct regions. The fatigue failure curves shift to shorter lifetimes and lower stresses as temperature is increased. The results are discussed in terms of the Zhurkov model of static fatigue failure. Using a Coulomb-Navier yield criterion modified rate expression, it is clear that activation energy and activation volume are functions of temperature. A change in temperature dependence of activation energy and endurance limiting stress occurs near the β transition suggesting that this molecular process is related to the fatigue process. The nearly identical dependence of fatigue and stress-strain activation energies and activation volumes with temperature suggest that both deformation processes may be controlled by a similar mechanism, i.e., localized plastic deformation. Utilizing these concepts, a simple model of fatigue allows correlation of the endurance limiting stress and the number of stress cycles at the endurance limiting stress with measures of resistance to plastic flow as determined from stress-strain data for this polystyrene. These data are used to project the longest and shortest mechanical fatigue lifetimes for these deformation conditions.
    Zusätzliches Material: 17 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 14 (1974), S. 161-161 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 14 (1974), S. 806-809 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The flow and processing behavior of commercial plastics is determined not only by the characteristics of the base resin but also by the presence of additives of various kinds. In this study the influence of a number of additives on the rheological behavior of molten ABS was investigated using a capillary extrusion rheometer and a Weissenberg rheogoniometer. The additives studied included molding lubricants, rubber impact modifiers, flame-retardant additives, and residual unreacted components remaining from the polymerization process. The mechanisms by which these species affect flow characteristics are described.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 1109-1116 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The compressive stress-strain behavior of a commercial polystyrene has been studied and the effect of deformation temperature on modulus, yield stress, percent yield strain and yield energy was determined. Yield energy is the only one of these parameters that is linear with temperature in the ductile region. A change in the mode of failure from ductile to brittle occurs between 5-30°C at a strain rate of O.1/in./in./min. At all temperatures studied, the yield or fracture stress varied linearly with the rate of deformation for strain rates ranging from 0.1 to 1.0 in./in./min. The yield data as a function of temperature were analyzed via a rate expression modified to incorporate the Coulomb-Navier yield criterion, Activation energy was found to be a function of deformation temperature with a change in slope occurring near the β transition. Activation volume increased linearly with deformation temperature, for the range studied. Agreement of dynamic mechanical and yield activation energies imply that the type of motion and the height of the energy barrier are similar for both. However, an increase in activation volume for stressed vs unstressed conditions suggests that a greater number of chain segments move as a result of stress biasing. Also the increase of both activation volume and activation energy with temperature implies that the correlated length of chain movement increases as temperature is increased. Similar to activation energy, yield stress exhibits a change in temperature dependence near the β transition. Data on other glassy polymers suggest that the highest temperature sub-Tg, transition is related to the change in the temperature dependence of yield stress.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 293-298 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: In this paper the effect of temperature and filler content φ on electrical resistivity of styrene-acrylonitrile polymer filled with iron or aluminium powders has been investigated. The resistivity of such composites decreases suddenly by several orders of magnitude at a critical volume concentration φc, which depends on the size distribution of particles and on thermal history. For filler content lower than φc, the resistivity decreases with increasing temperature, whereas for φ 〉 φc there is a sudden increase in resistivity at temperatures near the glass transition temperature of the polymeric matrix. This effect is more pronounced than the previously reported data on other composite systems.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 829-848 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The chemical reactions of SO2(3B1) molecules with cis- and trans-2-butene have been studied in gaseous mixtures at 25°C by excitation of SO2 within the SO2(3B1) → SO2(+, 1A1) ‘forbidden’ band using 3500-4100-Å light. The initial quatum yields of olefin isomerization were determined as a function of the [SO2]/[2-butene] ratio and added gases, He and O2. The kinetic treatment of these data suggests that there is formed in the SO2(3B1) quenching step with either cis- or trans-2-butene, some common intermediate, probably a triplet addition complex between SO- and olefin. It decomposes very rapidly to form the 2-butene isomers in the ratio [trans-2-butene]/[cis-2-butene] = 1.8. In another series of experiments SO2 was excited using a 3630 ± 1-Å laser pulse of short duration, and the SO2(3B1) quenching rate constants with the 2-butenes were determined from the SO2(3B1) lifetime measurements. The rate constants at 21°C are (1.29 ± 0.18) × 1011 and (1.22 ± 0.15) × 1011 l/mole·sec with cis-2-butene and trans-2-butene, respectively, as the quencher molecule. Within the experimental error these quenching constants equal those derived from the quantum yield data. Thus the rate-determining step in the isomerization reaction is suggested to be the quenching reaction, presumably the formation of the triplet SO2-2-butene addition complex. In a third series of experiments using light scattering measurements, it was found that the aerosol formation probably originates largely from SO3 and H2SO4 mist formed following the reaction SO2(3B1) + SO2 → SO3 + SO(3Σ-). Aerosol formation from photochemically excited SO2-olefin interaction is probably unimportant in these systems and must be unimportant in the atmosphere.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The total decomposition rates of the chemically activated alkanes n-butane, n-pentane, isopentane, and neohexane were measured using an internal comparison technique. Chemical activation was by the C—H insertion reaction of excited singlet-state methylene radicals. A total of ten rate constants ranging from 4.6 × 105 to 2.3 × 107 sec-1 were measured for these alkanes at different excitation energies. These rates correlate via RRKM theory calculations with thermal A-factors in the range of 1016.1 to 1017.1 sec-1 for free rotoractivated complex models and in the range of 1016.4 to 1017.8 sec-1 for vibrator-activated complex models. It was found that high critical energies for decomposition, “tight” radical models, and activated complex models with free internal rotations were required to correlate the decomposition rates of these alkanes with estimated alkyl radical recombination rates. The correlation is just barely possible even for these favorable extremes, indicating that there may be a basic discrepancy between the recombination rate and decomposition rate data for alkanes.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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