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  • AERODYNAMICS  (97)
  • Physics  (44)
  • FLUID MECHANICS AND HEAT TRANSFER  (43)
  • GENERAL
  • 1975-1979  (191)
  • 1965-1969
  • 1955-1959
  • 1975  (191)
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  • 1975-1979  (191)
  • 1965-1969
  • 1955-1959
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  • 1
    Publication Date: 2019-07-13
    Keywords: AERODYNAMICS
    Type: SAE PAPER 750703 , West Coast Meeting; Aug 11, 1975 - Aug 14, 1975; Seattle, WA
    Format: text
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  • 2
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Partial molar excess free enthalpies (or excess chemical potentials) at infinite dilution were obtained over a large temperature range by gas chromatography. Data on n-alkenes in Apiezon M are interpreted by the Prigogine-Patterson theory; data on normal and branched alkanes in squalane and polydimethylsiloxane (PDMS) are discussed in terms of the Prigogine-Patterson theory and the solution theory of Flory, Orwoll, and Vrij. For the alkane-PDMS systems heats of dilution and partial excess heat capacity data are given.The aim of this work is to get some insight in the applicability of these solution theories to mixtures of fluids, the properties of which may slightly violate the basic assumptions of these theories. It is shown that orientational order in and a large cross-sectional chain diameter of the polymer solvent do not affect their applicability to the partical molar excess free enthalpies of apolar mixtures, whereas large dissimilarities between the force fields around the segments of the mixture components and/or dissimilar chain flexibilities detract from the applicability of these theories (alkanes in PDMS).Special attention has been paid to the effects of dissimilar size and shape of the segments of the mixture compounds on the magnitude of the interchange interaction parameter. It is shown that the multiple-connected segment model after Lichtenthaler et al. does not warrant a reliable combinatorial contribution. Comparison of the interaction parameters obtained for n-alkanes in n-alkanes, Apiezon, squalane, and polyisobutylene and for branched alkanes in squalane reveals that the magnitude of this parameter is affected by small end-effects due to the relative weakness of methyl-methylene interactions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1783-1787 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When a mixture of two monodisperse samples of poly-α-methylstyrene is thermally degraded, the components behave independently, as a first approximation, as shown by GPC and rate of volatilization data. The ratio Mw/Mn, before approaching the ultimate value of 2.0, first goes through a minimum at a much lower value.
    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 Physics Edition 13 (1975), S. 1159-1166 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fundamental vibrational frequencies of an isolated chain of trans-1,4-polychloroprene have been calculated. The agreement between the calculated and experimentally observed crystalline frequencies supports the molecular model for the structure of trans-1,4-polychloroprene and the force field employed in the calculations. The results of the normal coordinate analysis indicate that there is essentially no coupling between adjacent translational repeat units of trans-1,4-polychloroprene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1145-1158 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Infrared spectra have been obtained for the crystalline regions of samples of predominantly trans-1,4-polychloroprenes polymerized at -20, 0, and 40°C. Spectral differences among the polychloroprenes are interpreted in terms of the increase in structural irregularities that occur as the polymerization temperature is increased. Results of this study indicate that crystallization occurs with random inclusion of these structural irregularities into the crystalline domains. The conclusion is supported by the spectra of the crystalline regions of a chloroprene copolymer containing known impurities in the form of 2,3-dichloro-2-butenylene units in addition to the normal 2-chloro-2-butenylene units.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 815-824 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fourier transform infrared spectra have been obtained for polyethylene irradiated in oxygen and nitrogen atmospheres. The spectra before and after irradiation have been compared by digital subtraction. The difference spectra are indicative of changes caused by irradiation. Crosslinking and chain scission reactions produce the observed changes.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1619-1643 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolymerization of propylene oxide (PO) with tetrahydrofuran (THF) in dichloroethane (DCE) has been studied at -10, 0, +10, and +20°C. The reactions were initiated by triphenylmethyl cations associated with the following gegenions: PF6-, SbF6-, and AsF6-. The overall energies of activation (Eα of PO and Ea of THF) obtained with the three gegenions increase as one passes from PF6- to AsF6- then to SbF6-, though the magnitude of the increase in each case is not substantial. On the other hand, the associated frequency factors A show a considerable variation with the gegenion. The bimodal distributions of the molecular weights, obtained by GPC with the copolymer produced from reactions initiated with triphenylmethyl hexafluorophosphate, show that the proportions of the lower molecular weight component (L) decrease as the solvent is changed from DCE to toluene, and this is even more marked when bulk polymerization conditions are adopted. The proportions of the higher molecular weight component (H) however increase, as does its molecular weight. The GPC molecular weight distributions of the copolymers initiated with triphenylmethyl hexafluorophosphate in DCE to which water has been added, show that the molecular weight of component H decreases with increasing concentration of water, while that of component L remains practically unchanged at a value of 308. This corresponds to an average degree of polymerization (DP) of 4 to 5. The NMR and infrared spectra of copolymers prepared in the presence of still higher initial water concentrations indicate that the PO-based polymer segments are present in excess of those required for a 1:1 copolymer.
    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 Chemistry Edition 13 (1975), S. 961-972 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermosetting arylimides were prepared by reaction of sulfone ether diamines with maleic anhydride followed by chemical imidization of the intermediate polyamic acid with acetic anhydride/sodium acetate. These arylimides could be thermally cured to afford heat stable systems possessing high glass transition temperatures (Tg) and moderate to high modulus plateaus above the Tg, depending upon the molecular weight between maleimide sites. The addition type curing process alleviates problems associated with the fabrication of other polyimide systems, since volatiles are not liberated and lowviscosity, high-solids solutions can be prepared in common organic solvents. Thermal, mechanical, adhesive and fabrication characteristics are reported for the sulfone-based arylimides, which indicate utility in spectrum of high-temperature applications.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 271-288 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymerizations at -10 to +20°C of propylene oxide (PO) with tetrahydrofuran (THF) were carried out in 1,2-dichloroethane (DCE) under dry, inert atmospheric conditions. Reactions were initiated by triphenylmethyl hexafluorophosphate (TPM-HFP) and subsequently followed by vapor-phase chromatography. Vacuum-dried residual copolymer products (RCP) were analyzed by gel-permeation chromatography (GPC), vapor-pressure osmometry (VPO) and nuclear magnetic resonance spectrometry (NMR). Attempts to homopolymerize THF in equimolar mixtures of DCE and THF at THF/TPMHFP ratios of 1:1 × 10-3 proved futile, while the homopolymerization of PO under identical operating conditions took place quite readily. Copolymerizations of PO-THF mixtures were easily carried out with high and often complete consumption of both monomers though, more often than not, THF was the principal residual monomer at the end of the 24 hr reaction period since, under no circumstances could additional THF be polymerized when the PO charged was completely consumed. Linearity of plots of -ln (C0/C) versus time showed the reactions to be first order with respect to both PO and THF concentrations. Influence of temperature reveals, via Arrhenius plots and overall activation energies (16.0 kcal/mole for PO and 13.0 kcal/mole for THF), that the initiator system functions similarly to other reported systems. Reactivity ratios (0.26 for PO and 0.80 for THF) indicate that monomer units tend to alternate along the chains rather than form extended segments of a given kind. This is supported by NMR analyses of RCP samples. Bimodal GPC distributions observed in the present study suggest that the copolymerization reaction may be proceeding by either a dual mechanism or a two-step process.
    Additional Material: 9 Ill.
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  • 10
    Publication Date: 2011-10-14
    Description: A method is developed for solving the laminar and turbulent compressible boundary layer equations for separating and reattaching flows. Results of this method are compared with experimental data for two laminar and three turbulent layer, shock wave interactions. Several Navier-Stokes solutions are obtained for each of the laminar boundary layer, shock wave interactions considered. Comparison of these solutions indicates a first order sensitivity in C sub f to the computational mesh selected in both the viscous and inviscid portions of the flow. Comparison of the present boundary layer solutions with the Navier-Stokes solutions and with data for a given Mach number indicates that as long as the separation bubble is small, the boundary layer approximation yields solutions whose accuracy is comparable to the Navier-Stokes solutions.
    Keywords: AERODYNAMICS
    Type: AGARD Flow Separation; 12 p
    Format: text
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