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  • 2020-2024
  • 1965-1969  (7)
  • 1935-1939
  • 1920-1924
  • Physics  (4)
  • Chemical Engineering  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 14 (1968), S. 415-420 
    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 packed bed model has been adopted to develop a general correlation applicable to the flow of Newtonian fluids through all types of woven metal screens. Both of the main theoretical approaches to studying pressure drop in packed systems have been used by visualizing the screen as a collection of submerged objects with surface area to unit volume ratio a for laminar flow, and as a bundle of tubes of diameter D for turbulent flow. In the usual manner viscous and inertial energy losses are added to give an expression for the total pressure loss. Rearrangement of the general equation to the form of a friction factor yields a unique definition of the Reynolds number for screens NRe = ρu/μa2D. Procedures are described for collection of pressure drop-velocity data for the flow of nitrogen and helium through plain square, full twill, fourdrinier, plain dutch, and twilled dutch weaves. The data are used to derive a viscous resistance coefficient α = 8.61 and an inertial resistance coefficient β = 0.52. The validity of the correlation equation is tested by using additional data from the literature. The correlation successfully predicts pressure drop for a Reynolds number range of 0.1 to 1,000, void fractions from 0.35 to 0.76, screen pore diameters from 5 to 550 μ, mesh sizes from 30 to 2,400 wires/in., and surface area to unit volume ratios from 1,200 to 29,000 ft.-1.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 12 (1966), S. 986-994 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Capillary phenomena arising from vapor phase condensation in porous media are discussed in the light of an exact interface curvature theory and a self-consistent thermodynamic theory. The system studied consists of liquid condensed in the form of pendular rings at the contact points between identical spherical particles. The geometrical parameters - the curvature, the confined volume, and the surface area of the liquid-vapor interface - must be expressed in terms of incomplete elliptic integrals. In addition several corrections are introduced for the classical Kelvin relation for lowering of vapor pressure. One of these is based on the density dependence of the isothermal thermodynamic susceptibility. Since the susceptibility vanishes at large negative pressures, an upper limit to the curvature is established. The balance equation for the extensive free energy is considered from the point of view of hydrostatic principles.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 13 (1967), S. 657-662 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This paper presents theoretical studies of a method of using a radioactive tracer technique to evaluate the kinetic data of heterogeneous catalytic reactions that are coupled with a Knudsen type of pore diffusion. By superimposing a transient radioactive tracer response over the steady state concentration profile in the catalyst particle, one can establish an implicit relation between the total amount of radioactive components diffused out of the particle and the kinetic data of the reaction system. This relation can then be used to evaluate kinetic data of the reaction system. A detailed study of general monomolecular complex systems is given. Use of the method for nonlinear systems is also included.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 375-379 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyethylene hydroperoxide (PEH) was prepared by low-temperature autoxidation initiated by AIBN. Over 85% of the total hydroperoxyl groups decompose by a rapid process, the remainder dissociate at about one-tenth of that rate. The results are the same whether PEH is decomposed in solution or in the solid state. Large amounts of scavenger have no effect on these decompositions; there is no radical-induced processes. The results suggest mechanisms of decomposition involving neighboring group assistance.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 3091-3101 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants for the autoxidation of polypropylene were determined by a combined ESR, volumetric, and chemical method. The values of ki, kp, and kt at 110°C. are 3 × 10-4 sec.-1, 1.9 l./mole-sec., and 3 × 106 l./mole-sec., respectively. The values of ki and its activation energy are the same as those for the decomposition of polypropylene hydroperoxide, thus identifying the latter as the principal initiation process. The values of the temperature-independent kt suggest that secondary peroxy radicals are the terminating species. The rate constants are compared with rate constant ratios for initiated autoxidations of squalane and other related systems.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 393-402 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of polypropylene hydroperoxide (PPH) consists of two consecutive reactions. The initial, faster reaction has rates up to 60 times that of the slower process. The former is largely suppressed by the addition of an excess of 2,6-di-tert-butyl-p-cresol. The course of reaction is the same in either solid state or in solution. The results are consistent with an intramolecular radical-induced mechanism for the initial reaction. This faster reaction consumes about 70-95% of the total hydroperoxides. The decomposition of PPH yields a maximum of about 1.8 radicals. Samples prepared from crystalline and amorphous polypropylenes have identical decomposition kinetics.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 381-392 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation of polypropylene introduces hydroperoxide groups into the polymer. Infrared spectroscopy has determined that more than 90% of these groups are intramolecularly hydrogen bonded. The sequential lengths and sequence distributions of these neighboring hydroperoxides were estimated from the electronic spectra of the polyenes derived from the polypropylene hydroperoxide by two methods: (1) reduction, acetylation, and pyrolysis, and (2) reduction and dehydration. The results indicate that all the hydroperoxide groups are present in sequences of length two and greater. Intramolecular hydrogen abstraction during oxidation could account for the formation of these neighboring hydroperoxides.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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