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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 1407-1412 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 2130-2135 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 6147-6155 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cancer Genetics and Cytogenetics 31 (1988), S. 285-289 
    ISSN: 0165-4608
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric radiology 15 (1985), S. 207-208 
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A ureter entering a bladder diverticulum almost always has associated vesico-ureteric reflux but rarely obstruction. We present the clinical and radiologic data on a patient with an ectopic ureteral insertion into a bladder diverticulum, with associated obstruction but not vesico-ureteric reflux. Periureteral fibrosis secondary to chronic inflammation is thought to be the underlying cause.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 270 (1992), S. 652-658 
    ISSN: 1435-1536
    Keywords: Deformation ; fracturebehavior ; polystyreneionomers ; ionomerblends ; microstructure of theionomer ; ioncontent
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The deformation and fracture behavior of sulphonated polystyrene ionomers, and of blends of these with polystyrene have been investigated. The microstructure of the ionomer, which varies with ion content, appears to have a significant effect on mechanical properties. Both tensile strength and toughness increase appreciably at ion contents near 5 mol%, where clusters become dominant over ion pairs and multiplets. In blends of the ionomers and polystyrene, phase separation occurs and the ionomer component appears in the form of fine particles dispersed in the polystyrene matrix. These particles possess a greater effective entanglement density than the matrix, as a result of ionic crosslinking, and they provide reinforcement against early craze breakdown and fracture. Tensile strength and fracture energy increase rapidly as the ionomer concentration in the blend is increased and they become essentially independent of blend ratio above about 10 wt% of the ionomer. Tests carried out on thin film specimens of the blends show that the dispersed ionomer particles adhere well to the matrix and contribute to the fracture energy both by inducing matrix crazing and by internal fibrillation within the particles.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 46 (1995), S. 361-366 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relaxation behavior of polyamide 4 was investigated as a function of absorbed moisture using dynamic mechanical measurements. Two relaxations, α at 81 °C and γ at  -  111°C, were observed in the “dry” sample at a frequency of 1 Hz. The addition of water resulted in the depression of the α relaxation (αw) of the “wet” polyamide and the appearance of a second α relaxation (αd), slightly depressed from that of the “dry” specimen, reflecting the movements of the polymer chains after water has evaporated during the heating scan of the experiment. A second run was performed, resulting in the appearance of a single relaxation peak (α) at temperature very close to that of “dry” polyamide 4. Additionally, a β transition was observed whose temperature decreased with increasing water content. Similar results were obtained for specimens of polyamide 6. From plots of the depression of the glass transition temperature, ΔTg, as a function of the ratio of the number of water molecules to the number of accessible amide groups in the amorphous regions, R, one observes a sharp depression in the glass transition temperature with increasing water content up to some critical value, above which additional water molecules do not significantly change the glass transition temperature. Based on existing models for the sorption of water in polyamides, we propose a model whereby the environment of the polymer - water complex varies with the amount of water added to the system. At low water contents, both loosely and tightly bound water exist at the sorption centers, or amide groups. Above the critical water concentration, additional water molecules form clusters at these sorption centers. Additional aspects of the model explain the appearance of two α or primary relaxation peaks (αw and αd) due to the changing environments as a consequence of the heating scan of the dynamic mechanical measurements.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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