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  • 1
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dendritic polymers are highly branched structures with globular shape and high number of functionalities. In a divergent or convergent stepwise synthesis perfect macromolecules with controlled size and architecture are obtained. From the broad variety of dendrimer structures some examples are given and the properties of these unusual polymers are illustrated. For comparison the hyperbranched polymers, dendritic structures with defects made in a one-pot polycondensation reaction, are discussed. Differences and conformities of properties like molecular weight distributions, functionalities, solubility, viscosity behavior and glass transition temperatures for both globular polymer structures are explained.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 176 (1975), S. 501-506 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 2073-2084 
    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 pyrolysis of acrylic fiber up to 400°C in an inert atmosphere at 1° and 6°C/min was studied by means of thermogravimetric and differential thermal analysis. The exothermic reaction occuring at 180-300°C was shown to be due to the reaction of nitrile groups by comparing the extent of exotherm with the number of nitrile groups present, determined by infrared spectroscopy. In addition, results of single-fiber tensile measurements, density, and elemental analysis of the pyrolyzed fibers are interpreted in terms of possible molecular structures. The gases evolved on pyrolysis were analyzed for both ammonia and hydrogen cyanide and the liberation of ammonia was attributed to a termination reaction of the polymerization of nitrile groups. The critical conditions necessary for the production of high strength and modulus carbon fiber are discussed briefly in ralation to the chemical changes occurring on pyrolysis.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 45-56 
    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 argument is presented that a primary determinant for polymer ignition is the rate of heat input during thermal decomposition. An experimental protocol is described in which a conventional thermogravimetric analyzer is used to monitor the behavior of polymeric solids brought to ignition by exposure to preheated air. The data obtained are used to establish the minimum heating rate required for ignition and the initial decomposition temperature at that critical rate. These two properties are then combined to give a numerical ranking value which seems to be a reasonable indicator of a material's ignitability hazard potential. Data for a variety of polymers and mixed systems are presented.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 601-629 
    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 series of four TDI-polypropylene oxide (PO) water-blown flexible polyurethane foams was produced in which the water content was varied from 2 to 5 pph at a constant isocyanate index of 110. A portion of each foam was thermally compression molded into a plaque. The morphology of both the foams and plaques was investigated using dynamic mechanical spectroscopy (DMS), differential scanning calorimetry (DSC), transmission electron microscopy (TEM), scanning electron microscopy (SEM), swelling, wide angle X-ray scattering (WAXS), and small angle X-ray scattering (SAXS). A high degree of microphase separation occurs in these foams, and its degree is nearly independent of water (hard segment) content. In the foam with the lowest water content the morphology possesses many similarities to that of typical linear segmented urethane elastomers. Small hard segment domains are present with a correlation distance of about 7.0 nm. When the water content is increased a binodal distribution of hard segment material appears. There are the small hard segment domains typical of segmented urethane elastomers as well as larger “hard aggregates” greater than 100 nm in size. The larger domains are thought to be aggregates of rich polyurea that develop by precipitation during the foaming reaction. WAXS patterns of the foams suggest urea and possibly hard segment ordering that may be of a paracrystalline nature but certainly lacking in true 3-dimensional crystallinity.
    Additional Material: 15 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 25 (1987), S. 1971-1979 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mixtures of poly(methyl methacrylate) (PMMA) and plasticizer were made by γ-irradiation of mixtures of methyl methacrylate with diethyl phthalate or with dioctyl phthalate. The glass transition temperature Tg was determined by differential scanning calorimetry. Plots of Tg versus volume fraction of PMMA were found to conform to the simple free volume theory of Kelley and Bueche, using physical property values either reported in the literature or else calculated by Bondi's procedures.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 2 (1959), S. 340-344 
    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: When purified rubber is exposed in vacuo to high energy radiation, very few conjugated triene groups are formed relative to the number of molecules of hydrogen evolved. This indicates that less than 4% of the hydrogen is evolved from adjacent carbon atoms in the same molecule, a reaction which would have no immediate crosslinking potential. Rather more conjugated diene groups have been detected, but when these are compared together with triene groups relative to the yield of chemical crosslinks it can be calculated that less than 10% of the allylic radical precursors disproportionate. Infrared absorption spectra do not indicate the marked decrease in unsaturation reported by some previous workers. Slight changes in the infared spectra may indicate some cis-trans isomerization. There is qualitative evidence for a small increase in vinylidene unsaturation.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 3 (1960), S. 366-367 
    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: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 1401-1439 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Model butanediol-MDI-polypropylene oxide polymers have been synthesized to explore the structure-property relationships in urethane/polyether polymers. The results of mechanical, thermal, and spectroscopic analyses agree remarkably well. The phase mixing in these polymers decreases with increasing hard-segment length, while the hard-segment stability increases with increasing hard-segment length. This is demonstrated clearly by dynamic mechanical, differential scanning calorimetry, infrared, and NMR studies. The importance of hydrogen bonding to the stability of the hard segment is strongly supported by the variable-temperature infrared experiments. The critical hard-segment size for phase segregation was shown to be two butanediols per hard segment. The temperature limit of the flatness of the storage modulus was tied to the thermal stability of the hard-segment hydrogen bonding which is controlled largely by the length of the hard segment and the extent of the hydrogen bonding.
    Additional Material: 22 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 26 (1988), S. 1795-1799 
    ISSN: 0887-6266
    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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