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  • Wiley-Blackwell  (7)
  • American Association for the Advancement of Science (AAAS)  (1)
  • 1975-1979  (4)
  • 1970-1974  (4)
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  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1979-12-07
    Description: Rats, with their fur clipped, pressed a lever to turn on an infrared lamp while in a cold chamber. When they were exposed to continuous-wave microwaves at 2450 megahertz for 15-minute periods, the rate at which they turned on the infrared lamp decreased as a function of the microwave power density, which ranged between 5 and 20 milliwatts per square centimeter. This result indicates that behaviorally significant levels of heating may occur at an exposure duration and intensities that do not produce measurable changes in many other behavioral measures or in colonic temperature. Further study of how microwaves affect thermoregulatory behavior may help us understand such phenomena as the reported "nonthermal" behavioral effects of microwaves.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stern, S -- Margolin, L -- Weiss, B -- Lu, S T -- Michaelson, S M -- New York, N.Y. -- Science. 1979 Dec 7;206(4423):1198-201.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/505008" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/*radiation effects ; Body Temperature Regulation/*radiation effects ; Male ; *Microwaves ; Rats
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 25 (1979), S. 903-905 
    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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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 23 (1977), S. 567-578 
    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 permeation of oxygen, nitrogen, argon, and synthetic air through hollow silicon rubber fibers was studied between 0° and 40°C and at gauge pressures of up to 3.45 × 105 N/m2 (50 lb/in.2 abs). The study was conducted in a permeator module in which the hollow fibers were pressurized externally. Strain measurements with single fibers showed this mode of operation to be preferable to internal pressurization. The gas permeation rates were markedly affected by dimensional changes of the hollow fibers under external pressure. These changes were predicted satisfactorily by a modification of Varga's (1966) deformation analysis of thick-walled elastic tubes. The extent of air separation achieved in the permeator was in agreement with that calculated from theoretical models. It is conjectured that the performance of such a permeator may be improved in certain cases if the fibers are under suitable initial tension.
    Additional Material: 12 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-2: Polymer Physics 10 (1972), S. 295-305 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Permeability and diffusion coefficients for dimethyl sulfoxide (DMSO) in polyethylene have been measured by the “time-lag” technique and found to be affected by the adsorption of DMSO vapor in the low-pressure side of the apparatus. An analytical method is described for correcting the apparent permeability coefficients for such adsorption effects. “True” permeability coefficients for DMSO in polyethylene, expressed in units of cm3(STP) - cm/(sec-cm2-cmHg), vary from 0.92 X 10-7 at 30°C to 1.7 X 10-7 at 45°C, and their dependence on relative DMSO pressure appears to be small. The energy of activation for the permeation process is 7.1 kcal/mole. The described correction method is also applicable to the permeation of water vapor through polyethylene and poly-(phenylene oxide). The apparent diffusion coefficients could not be corrected by this method. The solubility of DMSO in polyethylene was measured with a Bakr-McBain balance and found to be very small; solubility coefficients are less than 0.8 cm3(STP) DMSO/(cm3 polymer-cmHg). It is concluded that the transport and solution behavior of DMSO in polyethylene is more similar to that of water vapor than to the corresponding behavior of organic vapors.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 575-575 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 201-219 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The present work is a continuation of a general study of the effect of pressure on gas and vapor permeation through nonporous polymeric membranes. Permeability coefficients have been measured for 1,1-difluoroethylene (C2H2F2) and fluoroform (CHF3) in polyethylene at penetrant pressures up to 35 atm and at temperatures between -18 and 70°C. The permeability coefficient P̄ for the 1,1-difluoroethylene - polyethylene system was found to increase with increasing pressure differential Δp across the membrane. Isothermal plots of log ΔP versus Δp are generally linear and can be represented by empirical relations of the form ΔP = P(0)exp{m Δp}, where P(0) and m are constants. The slope m of these isotherms decreases with increasing temperature. Plots of log P̄ versus Δp for the fluoroform - polyethylene system are also linear, but exhibit negative slopes, i.e., P̄ decreases with increasing Δp. An extension of Fujita's “free volume” theory of diffusion in polymers shows that the dependence of P̄ on pressure reflects how the free volume of the polymer is affected by this pressure. An increase in the penetrant pressure may result in two opposing effects: (a) the concentration of the penetrant dissolved in the membrane is increased, thereby increasing the free volume, and (b) the hydrostatic pressure on the membrane is also increased, which causes a decrease in the free volume. If the overall effect is an increase in the free volume of the polymer, then P̄ will also increase, and vice versa.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 663-681 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Permeability, solubility, and diffusion coefficients have been determined for halothane (CF3CHClBr) and methoxyflurane (CHCl2CF2OCH3) in silicone rubber at temperatures from 17 to 60°C and at relative pressures from 0.05 to 0.96. The solubility of both penetrants in silicone rubber is a strong function of penetrant concentration (or relative pressure), and can be represented satisfactorily by the Flory-Huggins relation with single values of the interaction parameter χ. The solubility coefficients decrease with increasing temperature at constant pressure. Mutual diffusion coefficients exhibit maxima when plotted against penetrant concentration; these maxima are attributed to the mass flow of polymer together with dissolved penetrant. Intrinsic diffusion coefficients increase linearly with increasing concentration. The energies of activation for diffusion are low, probably because of the ease of segmental motion about the Si—O linkage. The diffusivity data are examined in terms of Fujita's “free volume” model and of transition-state theory. Permeability coefficients for the two penetrants are large, of the order of 10-6-10-5 cm3(STP)-cm/(sec-cm2-cm Hg), and increase markedly with increasing concentration or decreasing temperature. This behavior is regarded as a consequence of the low energies of activation for diffusion.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 735-751 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The solubility of carbon dioxide in symmetric (dense) cellulose 2.4-acetate has been measured at temperatures from 0 to 70°C and pressures up to 45 atm. The polymer samples were prepared by slowly drying asymmetric reverse osmosis membranes. The solubility isotherms can be described satisfactorily up to 60°C by the “dual-sorption” model for glassy polymers. The model cannot represent the experimental data above 60°C, possibly because of a second-order transition in the polymer between 60 and 70°C. An analysis of the dual-sorption parameters and of the heats of solution and “hole filling” suggests that the polymer samples contained a relatively large volume of microcavities. Gas solution appears to occur predominantly in microcavities, a large fraction of the penetrant moleculers being immobilized or partially immobilized. The solubilities obtained in this work are compared with similar data computed from time-lag measurements of other investigators, and the validity of the dual-sorption model is examined for the present case.
    Additional Material: 6 Ill.
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