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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 34 (1994), S. 23-33 
    ISSN: 0959-8103
    Keywords: polyesters ; diacetylenes ; cross-polymerisation ; DSC ; Raman spectroscopy ; tensile deformation ; Raman shift factors ; 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 series of diacetylene-containing polyesters with number-average molar masses (GPC) in the range 900-4200 g mol-1 were prepared from terephthaloyl chloride and hexa-2,4-diyne-1,6-diol using benzoyl chloride as a monofunctional reactant for control of molar mass. Degrees of crystallinity were estimated from WAXD to be up to 29%. Correlations between molar mass, melting behaviour, degree of crystallinity and thermal cross-polymerisation of diacetylene-containing polyesters have been established using hot-stage microscopy, DSC and resonance Raman spectroscopy. The polyester with M̄n of 1264 g mol-1 gave the best balance between processability and the ability to cross-polymerise efficiently. Its degree of crystallinity before cross-polymerisation was estimated from WAXD measurments to be 24%, a value coincident with the percentage conversion of diacetylene units to polydiacetylene chains measured by 13C solid-state NMR. The optimum conditions for compression moulding the polyester to produce a material with a strong Raman spectrum involved heating under vacuum at 120°C for 6h after an initial 3 h heat-up period. The material thus produced gave an intense Raman C=C stretching band, which upon tensile deformation shifted linearly with strain to lower wavenumber by 12.0 cm-1 %-1. The potential use of the diacetylene-containing polyesters in the preparation of model blends for use in quantitative micromechanics studies of stress transfer between phases is briefly discussed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2019-07-13
    Description: Structure and kinematics of carbon monoxide in the upper stratosphere and lower mesosphere (10-0.03 hPa) are studied for the early northern winter 1991/92 using the Upper Atmosphere Research Satellite Improved Stratospheric and Mesospheric Sounder (ISAMS) measurements. The study is aided by data from a 6-week parameterized-chemistry run of the Goddard Space Flight Center 3D Chemistry and Transport Model (CTM), initialized on 8 December 1991. Generally, CO mixing ratios increase with height due to the increasing source contribution from CO, photolysis. In the tropical upper stratosphere. however, a local maximum in CO mixing ratio occurs. A simple photochemical model is used to show that this feature results largely from methane oxidation. In the extratropics the photochemical lifetime of CO is long, and therefore its evolution is dictated by large-scale motion of air. evidenced by strong correlation with Ertel potential vorticity. This makes CO one of the few useful observable tracers at the stratopause level and above. Thus CO maps are used to study the synoptic evolution of the polar vortex in early January 1992. Modified Lagrangian mean mixing diagnostics are applied to ISAMS and CTM data to examine the strength of the mixing barrier at the polar vortex edge. It is demonstrated that planetary wave activity weakens the barrier. promoting vortex erosion. The vortex erosion first appears in the lower mesosphere and subsequently descends through the upper stratosphere. and is attributed to effects of planetary wave dissipation. Agreement between ISAMS and CTM is good in the horizontal distribution of CO throughout the examined period, but vertical CO gradients in the CTM weaken with time relative to the ISAMS observations.
    Keywords: Environment Pollution
    Type: Journal of the Atmospheric Sciences; 56; 563-583
    Format: text
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