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  • Wiley-Blackwell  (45)
  • Oxford University Press  (13)
  • American Institute of Physics (AIP)
  • American Chemical Society (ACS)
  • 1970-1974  (48)
  • 1955-1959  (10)
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Years
Year
  • 1
    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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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 17 (1971), S. 536-541 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The processes of absorption and desorption with reversible reaction are compared theoretically for reactions of the type A ⇌ nB. With the same concentration difference between bulk and interface, it is found that in general, the rate of desorption is lower than that of absorption. Under certain conditions the difference may be as much as 35%.The analysis is based on the penetration theory. The numerical solution introduces a new transformation of the time and distance variables (based on the error function) which reduces the computing time required. An analytical examination of the penetration theory equations provides an explanation of the results of the numerical solution.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 33 (1958), S. 447-455 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The nitrosation of nylon 66, with the use of four different nitrosating agents, has been investigated. By the more vigorous nitrosating reactions, heterogeneous nitrosation of nylon yarn occurs rapidly and proceeds to completion in a few hours. In this reaction the amide hydrogen is substituted by a nitroso group to give the structure By heating the nitrosated polyamides, nitrogen is evolved, and polyesters are formed. The kinetics of this change have been fully investigated. Caustic alkali reacts rapidly with nitrosated nylon. Free radicals are produced on exposure of the nitrosated nylon to visible radiation. Partial nitrosation of nylon yarns has been carried out with the use of a running threadline system; the physical properties of the resulting yarns have been examined.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 12 (1974), S. 361-362 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 90 (1957), S. 957-962 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Kondensation, welche Catechine unter der Einwirkung von Säuren erleiden, besteht in der Substitution einer reaktionsfähigen CH-Gruppe des einen -Moleküls durch das Kohlenstoffatom 2 (Phenylcarbinoläthergruppe) des anderen. Dieses Ergebnis wird an vereinfachten Modellen aus der Gruppe der Catechine abgeleitet.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 605-618 
    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 theoretical model for drying of a thin gel film is presented. The model is based upon the premise that as solvent is removed from any portion of a gel structure which is permeable by the solvent, the structure shrinks locally to fill the voids left by the solvent. The diffusion coefficient of solvent through the gel film is assumed to be an exponential function of concentration and temperature. The governing equations for the model indicate that for nonisothermal drying, the results of drying and shrinkage rates are functions of 13 independent dimensionless system variables. These results are obtained with the help of a computer solution of the proposed model. The computer results indicate that, except under extreme temperature conditions, the drying and shrinkage rates are most influenced by dimensionless groups M, P, and P̄, defined by eq. (9) of the paper. Furthermore, the drying and shrinkage rates are essentially independent of groups M and P for the values of M and P greater than approximately 100 and 10, respectively. The effect of variable solvent diffusivity on approximate time to achieve the steady-state drying and shrinkage rates is approximately handled by defining a dimensionless time variable τ in terms of average solvent diffusivity. Finally, some experimental data on drying and shrinkage rates of isothermal drying of lyphogel film under natural convection condition are obtained. These data are found to be in qualitative agreement with similar computer predictions by the proposed model.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 2761-2770 
    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 nature and magnitude of mechanical reactions of polystyrene in capillary flow has been examined in a model extrusion process. Studies on polystyrene quantify the sensitive increase in shear degradation tendency with increasing polymer molecular weight. A molecular weight spectrum caused by the shear stress profile was measured across the extrudate radius by the new technique of solvent coring. It was further determined that an appreciable fraction of the mechanical reaction is shear induced in the capillary reservoir. This is confirmed by precision determinations of molecular weights and distributions by gel permeation chromatography on samples taken from concentric layers in the capillary reservoir after 50% sample extrusion. These results, involving traces of oxygen as a chemical probe, describe the stress profile in the reservoir and in the capillary during the pressure extrusion of high molecular weight polystyrene. Thus, changes in molecular weight and distribution may be attributable to changes in different portions of the shear geometry rather than the uniform changes generally considered. Clear evidence is also presented showing the dramatic effects of oxygen on these shear-induced changes in molecular weight and distribution.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 1805-1819 
    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: Isoprene was polymerized in batch reactors by use of bottle polymerization techniques at 30°, 40°, and 50°C at concentrations from 1 to 5 molar. Butyllithium concentration was varied from 0.005 to 0.03 molar. Isoprene and n-butyllithium conversions and molecular weight distributions were determined for different reaction times. Rate equations for the initiation and propagation reactions are presented. The importance of the association reactions in obtaining a narrow molecular weight distribution is illustrated.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 2697-2706 
    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 survey of viscoelastic data on amorphous polymer melts indicates that the steady-state shear compliance, Je, of many systems can be approximated from a knowledge of their flow response. For systems with monomodel molecular weight distributions, the absolute value of the reduced complex viscosity, η*/η0, is found to equal 0.67 ± 0.03 at the frequency ω, where ωη0Je = 1. This result applies to a variety of polymer systems and to a wide range of molecular weights and distributions as long as the highest molecular weight dispersion of the distribution constitutes more than 20 weight per cent of the sample. This relationship determines Je from non-Newtonian flow data and thus provides a consistent way to relate differently shaped reduced variable curves and to calculate compliances from characteristic times reported in the literature. The connection between some commonly used times and Je is given. The method of calculating Je is successfully applied to capillary measurements of melt viscosities and to characteristic times determined from steady-state shear measurements of concentrated polymer solutions.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 3509-3514 
    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 glass transition temperatures of the poly(alkyl α-cyanocrylates) were determined by the dilatometric technique, and some of the values were checked by differential thermal analysis. The data indicate that the Tg's appear to decrease with increase in the size of the alkyl group, for a given molecular weight range. It was also found that the Tg of poly(methyl or butyl α-cyanoacrylate) increased with molecular weight. All cyanoacrylates, excepting methyl and ethyl esters, formed only low molecular weight polymers in aqueous surroundings. Therefore, they have characteristic low glass transition temperatures, causing coalescence at low temperatures.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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