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  • 1
    Electronic Resource
    Electronic Resource
    Swelling of model networks (1987)
    s.l. : American Chemical Society
    Macromolecules 20 (1987), S. 1088-1096 
    Details
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1021/ma00171a036
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Rheology of model polyurethanes at the gel point (1986)
    s.l. : American Chemical Society
    Macromolecules 19 (1986), S. 2146-2149 
    Details
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1021/ma00162a007
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  • 3
    Electronic Resource
    Electronic Resource
    The application of size exclusion chromatography equipped with RI and LALLS detectors to study network formation (1991)
    Springer
    Polymer bulletin 27 (1991), S. 281-287 
    Details
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The accuracy of the SEC/LALLS/RI method for measuring molecular weight and molecular weight distribution of the polymerizing system, consisting of a triisocyanate and a diol was examined. It has been found that both Mn and Mw were higher than theoretical up to about 60% conversion. Above this conversion Mw was considerably lower and molecular weight distribution narrower than predicted by gelation theory.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00294533
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  • 4
    Electronic Resource
    Electronic Resource
    Mechanical and dielectric properties of segmented polyurethane elastomers containing chemical crosslinks in the hard segment (1998)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 237-251 
    Details
    ISSN: 0887-6266
    Keywords: segmented ; polyurethanes ; crosslinked ; mechanical ; dielectric properties ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mechanical and dielectric properties of two series of segmented polyurethanes having soft segment concentration of 50 and 70% and a varying degree of crosslinking through the hard segment were studied. The degree of crosslinking in each series was varied by varying the butane diol/trimethylol propane ratio in the chain extender mixture. Tensile strength, elongation at break decrease, but elastic recovery increases monotonically with increasing crosslinking. The plateau modulus in the dynamic mechanical test decreases and then increases with increasing TMP content. Crosslinking causes broadening of the soft segment glass transition as seen by permittivity and loss factor measurements. It also affects high temperature behavior (above the glass transition of the hard segment); it lowers permittivity, loss factor, and ionic conductivity. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 237-251, 1998
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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    Paper (German National Licenses)
  • 5
    Electronic Resource
    Electronic Resource
    Structure and physical properties of segmented polyurethane elastomers containing chemical crosslinks in the hard segment (1998)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 221-235 
    Details
    ISSN: 0887-6266
    Keywords: segmented ; polyurethanes ; crosslinked ; properties ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two series of segmented polyurethanes, one containing 50% soft segments and the other with 70% soft segments were synthesized. Chemical crosslinks were introduced through the hard segment in a controlled way. Chemical polyurethane networks were characterized by swelling. The effect of the degree of crosslinking on properties was examined. It was found that chemical crosslinks in the hard segment reduce the mobility of the soft phase and destroy the crystallinity of the hard phase, but they improve heat stability of the hard domains. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 221-235, 1998
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    The effect of soft-segment length and concentration on phase separation in segmented polyurethanes (1989)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 545-560 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three series of polyurethanes, based on three polyols, diphenylmethane diisocyanate (MDI), and three chain extenders were synthesized. Polypropylene glycol (PPG) soft-segment length (MW 1000, 2000, and 3000), soft-segment concentration (30%, 50%, and 70%), and the type of chain extender (ethylene glycol, butane diol, and hexane diol) were varied and their effect on the amount of phase separation studied. Methods for assessing phase separation quantitatively, based on shifts of the glass transition temperature Tg and the enthalpy jump at the glass transition were tested. It was shown that they give incorrect results, especially with PPG 1000 as the soft segment. Dependence of the soft segment Tg on the polyol length was explained by the “network effect.” True phase mixing was found only with PPG 1000 series at low soft-segment concentration, whereas, no clear indication of the phase mixing with PPG 2000 and PPG 3000 based polyurethanes was observed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1989.090270305
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  • 7
    Electronic Resource
    Electronic Resource
    Dielectric properties of segmented polytetramethyleneoxide-based polyurethanes (1989)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 38 (1989), S. 1929-1940 
    Details
    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: Three series of segmented polyurethanes, based on polytetramethylene oxide (PTMO) soft segments, having molecular weights of 650, 1000, and 2000 and MDI/butane diol hard segments, were synthesized and their dielectric properties examined. The effect of the soft segment length, soft segment concentration (ssc) as structural variables, and frequency and temperature as experimental variables, on relative permittivity and tan δ, were examined. The results were discussed in terms of the structural parameters such as the degree of phase separation and soft segment phase state. It was found that both soft segment length and ssc strongly affect dielectric behavior.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1989.070381014
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  • 8
    Electronic Resource
    Electronic Resource
    The effect of crosslinking on properties of polyurethane elastomers (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 391-398 
    Details
    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 segmented polyurethanes from two polyols, 4,4′-diphenylmethane diisocyanate (MDI) and butane diol was synthesized. The degree of chemical crosslinking was controlled by varying the ratio of poly(oxypropylene) diol to poly(oxypropylene/oxyethylene) triol. The samples were prepared at the stoichiometric ratio of NCO to OH groups and at a constant concentration of hard segments (butane diol; MDI) equal 50 wt %. At low concentrations of the triol the molecular weight of the polyurethanes increases; at higher concentrations (above 9 mol %) crosslinked products are obtained. All samples show a distinct two-phase structure and in the region of 0-150°C the dynamic mechanical behavior is affected by the hard phase. Chemical crosslinking was found to increase the tensile strength and strain at break, but did not affect appreciably the tear strength, hardness, and soft segment glass transition. The stress relaxation rate at room temperature was found to depend both on the elongation and on the degree of crosslinking. A comparison of the sol fractions ws found for crosslinked samples with the predictions of the theory of branching processes proved that the achieved conversions of reactive groups in networks are high (∼ 0.98).
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1991.070420211
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  • 9
    Electronic Resource
    Electronic Resource
    Polypropylene-Carbon black interaction in conductive composites (1993)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 1659-1669 
    Details
    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: Interaction between polypropylene matrix and carbon black was examined by measuring physical, mechanical, and electrical properties. It has been shown that presence of carbon black influences the morphology and crystallinity of the matrix. Strong interaction was observed directly by electron microscopy and indirectly by the rise of the modulus of elasticity. The effect of carbon black on strength and physical properties of the composites is discussed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1993.070490919
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  • 10
    Electronic Resource
    Electronic Resource
    Thermal degradation of segmented polyurethanes (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 1087-1095 
    Details
    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: Thermal degradation of polyurethane samples was studied by a thermogravimetric method. The effect of soft-segment length and soft-segment concentration on activation energy of the degradation process was measured. Three methods of calculation gave activation energies at different stages of the very complex weight loss process. It was shown that at initial stages of the weight loss the process was dominated by hard-segment degradation. Activation energy of the whole process calculated by the Ozawa-Flynn method did not offer clear insight into the structure-stability relationship of polyurethanes. The second method showed that activation energy of the initial stage of degradation increased with decrease in hard-segment length. The Flynn method of calculating activation energy produced fairly constant activation energy of the first 40% degradation, at around 150 kJ/mol, for polymers in the C series. Generally, calculation of kinetic parameters of a complex degradation process as in polyurethanes gives results that are not easy to interpret. It has been shown qualitatively that polymers with higher soft-segment concentration display lower initial weight loss and higher onset temperatures of degradation. © 1994 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1994.070510615
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