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  • Polymer and Materials Science  (163)
  • AERODYNAMICS  (97)
  • GENERAL
  • 1975-1979  (267)
  • 1955-1959
  • 1975  (267)
  • 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
    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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  • 3
    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.
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  • 4
    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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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 1829-1835 
    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: A new apparatus is described for measuring the permeability of polymer films to sulfur dioxide at partial pressures down to 2 Pa. It employs a permeation tube technique for establishing the partial pressure gradient and a detection system based on the absorption of light at 213.8 nm. Data on the permeability to sulfur dioxide of a range of polymer films are presented and discussed.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 2545-2562 
    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 fracture behavior of a piperidine/bisphenol A diglycidyl ether (A) resin has been determined in bulk and as an adhesive using the linear elastic fracture methods developed by Mostovoy1. The effect of adding carboxy-terminated butadiene-acrylonitrile (CTBN) elastomer to resin A was investigated. The opening-mode fracture energy () of resin A was 120 to 150 J/m2, and largely attributable to plastic deformation. Fractographic evidence was obtained for plastic flow at the crack tip during crack initiation. Propagation was unstable due to the rate dependence of the plasticity. There were no significant differences in the bulk and adhesive fracture behavior. Addition of 5-15% CTBN to resin A produced minute elastomer particles which increased to ∼4000J/m2 (at 15%). Further CTBN addition resulted in an elastomer-epoxy blend and a decrease in fracture energy. Fractography again indicated that crack initiation involved plastic deformation but that the elastomer had greatly increased the volume in which the deformation occurred. The adhesive fracture of the elastomer-epoxy was found to be strongly dependent on the crack-tip deformation zone size (ryc) in that was a maximum when bond thickness was equal to 2 ryc. At bond thicknesses less than 2 ryc, there was a restraint on the development of the plastic zone resulting in lower values.
    Additional Material: 13 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 2933-2945 
    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: A chromatograph employing five columns packed with porous glass of pore size 1250 Å to 75 Å provided peak retention volumes (VR) that were reproducible and essentially independent of sample size and flow rate when aqueous eluents were used. Calibration was carried out with a series of dextran fractions and polystyrene sulfonate samples, both of moderately narrow molecular weight distribution. The universal calibration method, based on hydrodynamic volume, was tested for four different polymer types. All four types produced a common curve within experimental error, which indicates that absolute molecular weight distributions may be derived from aqueous exclusion chromatography data for at least these polymer types. Additional study using a higher salt concentration produced hydrodynamic-volume plots that superposed with those above. The use of the same set of porous glass columns with polystyrene standards in three different organic solvents produced calibration curves that agreed well with the aqueous curves after corrections were made for differences in available pore volumes.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 3093-3106 
    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: A study of the kinetics, failure mechanism, and fracture surfaces of PMMA/methanol crazes has been made on notched circular bar specimens subjected to constant tensile loads. Failures were by void growth and coalescence inside the craze away from the notch tip and near to the specimen center. Two distinct features of void coalescence were observed; the first a cluster of very small voids (each of the order of 3.4 × 103 Å) and the second, separate larger voids which usually caused final failure.An analysis of craze growth, based on fracture mechanics concepts in conjunction with simple flow analysis, suggests that the growth is controlled mainly by the ability of the environment to flow through the voided structure of the craze. Good agreement has been obtained between predicted behavior and experimental data.
    Additional Material: 14 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 1387-1401 
    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 characteristics of Monvelle, a new biconstituent fiber from nylon 6 and a segmented polyurethane, are reviewed briefly, and some of the technical problems inherent in producing such a fiber are discussed. The characterization of two series of polyurethanes which can be melt spun is given in detail. The chemical composition of the hard segment was maintained constant, being derived from 4,4′-diphenylmethane diisocyanate (MDI) and 1,4-butanediol, in all polymers. In one series using poly(butylene adipate) of MW 2000 as the soft segment, the average hard segment content was varied from 33% to 54%. In the other series, the hard segment content was held at 43%, and three additional soft segments, each at MW 2000, were used: poly(ethylene adipate), polycaprolactone and poly-1,4-oxybutylene glycol (PBG). Characterizations include molecular weight distributions, thermal analysis, rheological studies, and selected small-angle and wide-angle x-ray diffraction and polarized light microscopy. Crystallinity, melt viscosity, and activation energy of flow increased with increasing hardsegment content. Changes in the polyester soft segments had little effect on the properties studied, but with PBG the crystalline melting point of the polymer, without annealing, was higher and the melt viscosity was slightly higher than corresponding polyester-based samples, in agreement with previous reports of sharper phase separation in polyether urethanes, compared to polyester urethanes.
    Additional Material: 8 Ill.
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  • 10
    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.
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