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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 34 (1987), S. 677-687 
    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
    Additional Material: 9 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 34 (1988), S. 1568-1572 
    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: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 509-512 
    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: 5 Ill.
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  • 4
    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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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 26 (1986), S. 1254-1263 
    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: Solid state rolling of semicrystalline polymers represents a high speed process for producing oriented, high modulus films, tapes, and sheets. The important process variables include roll temperature, thickness of initial sheet, roll speed, take-up tension, roll diameter, and initial morphological state of the polymer. Roll temperature controls both the extent of maximum deformation and the rate of rolling. A minimum temperature exists for each polymer below which the orientation process is sharply limited. This condition is similar to the limitation present in the hydrostatic extrusion process, in which the alpha crystallization temperature limits the orientation process. Roll speeds as high as 20 m/min have been realized. It is apparent that film thickness and thickness reduction ratio have a strong effect on the ultimate rolling rate. The process, as currently practiced, is adiabatic, and therefore, heat transfer limited. The take-up tension influences the extant of orientation in the amorphous phse of of the polymer. This in turn affects its thermal and chemical stability. The effect of roll diameter is to limit the extent of thickness reduction by causing roll-film slippage when the roll dianmeter to thickness reduction ratio is below some as yet undetermined value. The initial morphological state of the polymer affects the amount of crystalline deformation possible, the surface texture of the rolled film, and the tear resistant of the oriented film.
    Additional Material: 17 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 23 (1989), S. 253-266 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: We report the biocompatibility in the rat brain of a controlled-release, biodegradable polymer, the polyanhydride poly-[bis(p-carboxyphenoxy)propane-sebacic acid] copolymer (PCPP-SA) in a 20:80 formulation. The biodegradable polyanhydride can be used for drug delivery directly into the brain, circumventing the difficulties posed by the blood - brain barrier and avoiding the consequences of having to administer toxic doses systemically to reach therapeutic doses in the central nervous system. The tissue reaction in the presence of PCPP-SA was compared to that seen with other standard neurosurgical implants. Fifty-six adult Sprague-Dawley rats were assigned to one of seven groups and underwent bilateral frontal lobe implantation of PCPP-SA (42 hemispheres), Surgicel (oxidized regenerated cellulose) (35 hemispheres), or Gelfoam (absorbable gelatin sponge) (35 hemispheres). None of the animals showed any behavioral changes or neurological deficits suggestive of either systemic or localized toxicity from the biodegradable polyanhydride, all surviving to the scheduled data of sacrifice. PCPP-SA evoked a well localized inflammatory reaction, comparable to that of Surgicel, which resolved as the PCPP-SA polymer degraded over five weeks. The biodegradable polyanhydride has been shown in this study to be nontoxic and biocompatible in the rat brain, when compared to standard neurosurgical implants.
    Additional Material: 10 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 99 (1987), S. 332-339 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Der Austausch von Kationen gegen Neutralmoleküle ähnlicher Form und Polarisierbarkeit in einem hochleitfähigen („metallischen“) organischen Charge-Transfer-Komplex ermöglicht die gezielte Einstellung von dessen elektronischer Struktur vom viertel- zum halbgefüllten Band. Verwirklicht wurde dieses Konzept in idealer Weise am N-Methylphenazinium(NMP)-Salz des Tetracyanchinodimethan(TCNQ)-Anions; bei diesem Salz läßt sich das Kation partiell gegen Phenazin austauschen. Eine detaillierte Untersuchung der optischen, elektrischen und magnetischen Eigenschaften der so erhaltenen leitfähigen molekularen Festkörper führte zu einem besseren Verständnis der Physik eindimensionaler organischer Leiter und zur Neuinterpretation des Mechanismus des Elektrontransports in diesen Festkörpern. Es wurden Phänomene wie der Übergang von einem „Zwei-Ketten-Leiter“ mit niedriger Coulomb-Abstoßung zum „Ein-Ketten-Leiter“ mit hoher Coulomb-Abstoßung und ein durch Solitonen unterstützter Elektronentransport beobachtet.
    Additional Material: 10 Ill.
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  • 8
    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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  • 9
    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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  • 10
    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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