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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 3 (1957), S. 242-248 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Heat transfer and friction measurements were made for air flow through a smooth copper pipe and six other commercial pipes, with a ratio of diameter to equivalent sand roughness varying from 640 to 64. The Reynolds number range was 10,000 to 80,000. Though some increase in heat transfer coefficients with roughness was found, the heat transmission per unit power loss always decreased.The momentum-heat-transfer anlogies of Reynolds and Colburn are shown to be inadequate for handling the experimental data. Those of Prandtl and Taylor, von Kármán, and Pinkel fail to show a required Reynolds number dependence of jh when friction factor has become independent of Reynolds number for a rough pipe. Martinelli's equation shows such dependence and, even in approximate form, gives good prediction of the experimental results.
    Additional Material: 13 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 20 (1974), S. 678-687 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Growth and dissolution rates of nickel sulfate α-hexahydrate were measured as functions of the concentration driving force in a laboratory-scale fluidized-bed crystallizer for the temperature range 35° to 50°C and the crystal size range 0.5 to 4.0 mm.Dissolution rates at a given temperature and crystal size were first order in the concentration driving force. Growth rates were about one-quarter of dissolution rates and depended on a higher exponent (around 1.3) of the concentration driving force. This exponent was not significantly affected by variations in crystal size, but decreased as temperature increased. The apparent variation of growth rate itself with crystal size at constant temperature was slight. Growth rates were found to be insensitive to solids concentration.
    Additional Material: 12 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 26 (1957), S. 399-401 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 23 (1957), S. 23-46 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Osmotic pressure, initial phase separation, and viscosity results are presented for dilute solutions of cellulose nitrate, cellulose acetate, and ethyl cellulose, using polymers of similar molecular weight and degree of substitution. A fairly wide range of solvents has been used in each case. Osmotic pressure results suggest molecular dispersion of polymer in most solvents but there is evidence for association of ethyl cellulose in aromatic hydrocarbons. Values of the Huggins μ are obtained and, for systems involving cellulose nitrate and ethyl cellulose in homologous series of ketones and acetates, seem to fall to a minimum and then increase on ascent of each series. It is suggested that the heat term in μ should include an exothermic contribution arising from solvation in addition to an endothermic contribution resulting from mixing of solvated polymer and solvent. It is tentatively suggested that, in a homologous series of solvents, the entropy and exothermic contributions may not vary much and that the variation of μ may arise from varying endothermic contributions. The volumes of hexane required to cause initial phase separation of the nitrate and acetate from solution increase with solvent power, as estimated from μ, but with ethyl cellulose the volumes tend to decrease. It is suggested that solvated polymer may separate from solutions involving polar solvents and, making certain assumptions, estimates are made of the solubility parameters of the polymers separating. Those for cellulose nitrate vary markedly with solvent. The variation of solubility parameter with solvent is less with cellulose acetate and ethyl cellulose but in the latter case values for polymer separating from polar solvents are less than from nonpolar. Comparison of these estimated solubility parameters with those of the solvents and hexane suggests that the volumes of hexane required to cause initial phase separation will only serve as measures of solvent power if the solubility parameters of solvents and precipitant all lie on the same side of that of the polymer separating. This seems to be so for cellulose acetate and possibly the nitrate but not for ethyl cellulose. Comparison of viscosity parameters and values of μ suggests that in certain cases both [η] and the initial slope of the plot of ηsp/c against c increase with solvent power. Other suggested viscosity measures of solvent power do not seem to be generally applicable. Some variation of chain configuration with solvent seems probable. Solvation, solvent type and association of polymer may also affect the viscosities of dilute solutions of cellulose derivatives.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 31 (1958), S. 399-414 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The hydrolysis rate of the nerve gas Sarin in aqueous solution may be accelerated by strongly acidic and strongly basic ion exchange resins. Basic resins are more effective than acid resins. Depending on the resin type and internal structure, a diffusional process or the chemical reaction may be rate determining. In distilled water, cationic resins behave as true catalysts, whereas the products of decomposition of Sarin destroy the effectiveness of anion resins. Dissolved salts in the water lower the useful life of both types of resins by replacement of the active hydrogen or hydroxyl groups.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 849-861 
    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 modulus of a fiber can be increased by plying with it a higher-modulus fiber. In this case, the modulus of the combination is characterized by a springs-in-parallel model, and the modulus of the composite is a linear function of the per cent of the second fiber in the composite. Another method of obtaining reinforcement is to melt-blend a higher-modulus polymer with the substrate polymer. With polyamides, this leads to a certain degree of amide interchange and block copolymer formation which depends on the compatibility of the polymers as well as on the usual kinetic factors. If the dispersion of the higher-modulus polymer is such that aggregate size is relatively large (e.g., ≥500 Å) and if the adhesion between the two polymers is good, a springs-in-parallel-type reinforcement is the best which can be obtained. In melt-blend polyamides, a “nonclassical” phenomenon in reinforcement has been noted when the diameters of the dispersed aggregates are ≤500 Å and when there are a relatively high number of hydrogen bonding sites on both polymer components. In this case, it appears that moduli appreciably higher than predicted from a springs-in-parallel model are obtained as well as higher than expected Tg values. A mechanism is proposed to account for this “nonclassical” behavior along with data to support it. Another type of anomaly is observed when the components of the blend are isomorphous. In this case, the reinforcement is considerably less than expected.
    Additional Material: 16 Ill.
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  • 7
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dilute solution properties of copolymers are briefly discussed in relation to those of the parent homopolymers. It is shown that copolymer molecules are usually more expanded in solution than would be expected from the averaged behavior of the pure polymers, because of repulsive interactions between the unlike monomer units. A thermodynamic parameter χAB characterizing these interactions can be derived from measurements of the dilute solution properties of copolymers. In favorable cases this parameter can be independently evaluated from studies of ternary systems composed of the two parent homopolymers and a solvent, thus allowing prediction of the behavior of the copolymer. Light scattering and viscosity measurements on fractions of approximately equimolal copolymers of styrene and methyl methacrylate are presented and analyzed. The values of χAB deduced from the results in two solvents agree satisfactorily with each other, but are somewhat larger than those earlier obtained from measurements on ternary systems.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 81 (1909), S. 85-93 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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