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  • Chemical Engineering  (115)
  • Wiley-Blackwell  (115)
  • Institute of Physics
  • International Union of Crystallography
  • 1985-1989
  • 1980-1984  (75)
  • 1970-1974  (40)
  • 1940-1944
  • 1984  (75)
  • 1970  (40)
Collection
Publisher
  • Wiley-Blackwell  (115)
  • Institute of Physics
  • International Union of Crystallography
Years
  • 1985-1989
  • 1980-1984  (75)
  • 1970-1974  (40)
  • 1940-1944
Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 679-682 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 492-494 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 967-973 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A general equation is derived that predicts the evolution of pore volume distribution during isothermal gasification in the regime of kinetic control, starting from a given initial condition. The development takes into account pore enlargement as well as pore intersections. Equations are also derived for the special cases of (1) uniform pore size and (2) bimodal distribution. The results are used to interpret the experimental data of Tomkow et al. (1977) and Kawahata and Walker (1962).
    Additional Material: 7 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 56-62 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Rate studies are reported of the effect of rehydration-dehydration cycling on the vapor hydration behavior of solid K2CO3. Isothermal rate data were obtained at different temperatures and water vapor pressures for the reaction of narrowlysized anhydrous particles. Effects of different particle preparation histories on the rehydration rate were investigated and correlations of rate with particle pore structure explored. Rehydration rates of dehydrated K2CO3·3/2H2O were found to depend on the conditions of the prior dehydration. Rehydration is comparatively very slow at relative pressures below P/Peq ≃ 1.5; rates increase linearly with pressure above P/Peq ≃ 3. Hydration rates of K2CO3 particles obtained as anhydrous are substantially slower than those of identically-sized crystals produced by prior dehydration of K2CO3·3/2H2O; after one rehydration-dehydration cycle, rehydration rates are increased by as much as two orders of magnitude and this distinction between sources virtually disappears. Diffusional resistances based on calculated water vapor diffusivities are qualitatively consistent with the observed effects of cycling but do not by themselves account fully for the observations.
    Additional Material: 10 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 557-563 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A mechanism is proposed for the dehydration-rehydration process in solid inorganic salts, and model rate equations are derived and applied to the observed behavior of potassium carbonate. Quantitative expressions for the effect of pressure on the reaction rates are derived using basic principles from nucleation and heterogeneous phase transformation theory. Model equation predictions agree with experimental dehydration and rehydration rate data at all but extreme pressures. The basic rate equation is also used to interpret the data of Eckhardt and Flanagan (1964) for the effect of pressure on the dehydration of manganous formate dihydrate. The mechanism on which the model equations are based is also consistent with the observed effects of cycling and of high temperature pretreatment on the K2CO3 rehydration rate.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 849-853 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 30 (1984), S. 829-831 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 16 (1970), S. 420-425 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Thermodynamic properties of the chemically reactive system N2O4 ⇌ 2NO2 ⇌ 2NO + O2 have been evaluated over a pressure range of 0.005 to 200.0 atm. and a temperature range of 200° to 900°K. by making use of Lennard-Jones potential. In these calculations, the dissociation of nitrogen tetroxide to nitrogen dioxide, nitric oxide and oxygen, and the effect of pressure on the equilibrium constants for the system of reactions N2O4 ⇌ 2NO2 and 2NO2 ⇌ 2NO + O2 have been taken into account.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 24 (1984), S. 127-134 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 technique of Thermo Stimulated Creep (TSC) has been applied to the study of anelastic properties of polyethylene, polypropylene, their copolymers and blends. In the temperature range -200 to 100°C, complex TSC peaks were observed in all samples, namely around 0°C, about the same temperature as for the homopolypolymer polypropylene. By applying “fractional stresses”, with a convenient choice or the loading program, these peaks have been experimentally resolved. Two components can be distinguished: 1. The “low temperature” component is characterized by mechanical retardation times following a compensation law. It has been attributed to microbrownian motions of polypropylene sequences liberated at the glass transition of the “true” amorphous regions. 2. The “high temperature” component which is influenced by thermal treatment has been assigned to microbrownian motions of polypropylene sequences liberated at the glass transition of the “constrained” amorphous regions. In block polymers, an additional TSC peak is observed around -50°C: it has been associated with the glass transition of ethylene-propylene-rubber (EPR) interphase. The coupling of this interphase with polyethylene and polypropylene phases is insured by diffusion of some ethylene and propylene sequences in-EPR. At about -140°C, a TSC peak associated with the low temperature component of the glass transition of polyethylene can be distinguished in all the materials studied.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 10 (1970), S. 86-93 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Boron fiber reinforced composites have been extensively evaluated in epoxy resin matrix materials, which are satisfactory for applications in comparatively moderate environments, and are usually inapplicable at temperatures in excess of 400°F. For use in high temperature environments in excess of this figure, it is necessary to use more thermally stable resins. A modified phenolic resin was selected for this application because of the versatility of the material and the successful performance of phenolics in glass fiber reinforced structures. The modifications increased the viscosity and tack of the formulation so that consolidation could not be readily accomplished by a combination of tension and heat during the winding process, so that a multi-stage winding process with intermediate consolidation steps became necessary. Winding a complex path to make a uniformly thick wall on a frustrum required further modifications to the basic winding process. The successful solution of these problems and the development of structurally sound composites was the primary object of this work.
    Additional Material: 15 Ill.
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