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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 65 (1961), S. 1645-1647 
    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 4 (1971), S. 79-81 
    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.] : Nature Publishing Group
    Nature 188 (1960), S. 315-316 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Isotactic polypropylene ('Moplen') powder was used. The molecular weight determined from viscosity was 2.7 X 105. The degree of crystallinity is reported to be 75 per cent. Rods were prepared by melting the powder in the glass ampoule under high vacuum. The materials were irradiated at 25 C. (in ...
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurde ein Übergang 2. Ordnung von Cellulosetriacetat bei ca. 30°C mit Hilfe der Polarisations-Infrarot-Spektroskopie untersucht. Die Temperaturabhängigkeiten des IR Dichroismus der Banden bei 900 cm-1 (C1—H Biegeschwingung) und 600 cm-1 (Acetyl-Gruppenfrequenz) wurden untersucht. Die 900 cm-1 Bande zeigte einen Übergang bei ca. 30°C, während die 600 cm-1 Bande keine bemerkenswerte Änderung zeigte. Diese Ergebnisse legen nahe, daß der hier beobachtete Übergang wahrscheinlich einem Konformationswechsel des Pyranoserings zugeordnet werden kann. Es wird angenommen, daß der Übergangsmechanismus einer Sessel (C 1)-Wannen (B) Konformationsänderung des Pyranoserings bei der Faltung des Cellulosemoleküls zukommt.
    Notes: A second-order transition of cellulose triacetate at approximately 30°C was studied by polarized infrared spectroscopy. The temperature dependences of infrared dichroismus were examined for the 900cm-1 (C1—H bending vibration) and 600 cm -1 (acetyl group frequency) bands. The former changed at about 30°C, whereas the latter did not show any remarkable change. These results suggest that the transition observed here is probably related to the conformational change of the pyranose ring. The transition mechanism is supposed to be associated with the chair (C 1)-boat (B) transformation of the pyranose ring at the folding of the cellulose molecule.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 1390-1393 
    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: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 2 (1959), S. 66-70 
    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: Crystallization and orientation of isotactic polypropylene film by stretching were investigated. The specimen used was a film of thickness 0.03 mm. and had ca. 30% crystallinity in the initial state. It was observed both by x-ray examination and measurement of density that the crystallization of the stretched film increased proportionally to the stretching ratio. And it was confirmed that a quasi-crystalline structure was already developed in the low stretching ratio coexisting with the ordinary stable crystalline structures. This quasi-crystal structure can be easily transformed into the ordinary stable state at above 100°C., as well as the quasi-crystal structure in melt spinning filament, as described in a previous paper. It was also confirmed that the ordinary stable crystalline part was biaxially oriented by high stretching at room temperature, that is, (110) plane of the crystallite was preferentially oriented perpendicular to the surface plane of the film in the cross section perpendicular to the stretching axis. This phenomenon was elucidated from both the cohesive interactions between lattice planes and the compressive stress in the stretching process.
    Additional Material: 10 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. 62-65 
    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 highly biaxially oriented isotactic polypropylene was obtained by stretching and rolling repeatedly. In such treatment, it was confirmed by x-ray examination that the 010 spacing was oriented parallel to the plane of rolling.
    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 4 (1960), S. 244-245 
    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
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 2657-2670 
    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 infrared spectra of chlorinated polypropylene (CPP) are interpreted and tentative assignments of C - Cl stretching vibration of CPP are proposed. Recently, infrared spectrophotometry has been applied as a useful tool for the investigation of polymer transitions. The solid-state transition in isotactic polypropylene (IPP) was studied by infrared method in the range of -50° to 30°C; and from the temperature dependence of the peak absorbance, transition at -10°C was detected. This temperature of -10°C agrees well with the Tg2 detected by other methods. From these results, it is presumed that Tg2 is attributed to a motion (thermal expansion) of IPP segments in either crystalline and amorphous region. The thermal transition of chlorinated isotactic polypropylene (CIPP) was also examined with differential scanning calorimetry and infrared method, and two thermal transitions were observed. A higher transition (TH) has a minimum at a degree of chlorination of about 39 wt-%; and a lower transition (TL) changes linearly with increasing degree of chlorination. Infrared results indicate that TH may be associated with a motion (thermal expansion) in chlorinated segments, and TL may be associated with a motion in unchlorinated segments. These results of infrared studies also suggest that CIPP may have a block structure.
    Additional Material: 12 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2079-2088 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The glass transition in styrene-based ionomers was investigated by means of infrared spectroscopy and differential scanning calorimetry (DSC). Transition temperatures were determined from the temperature dependence of the peak absorbances of the 1700 and 1745 cm-1 bands. These transition temperatures agreed with glass transition temperatures (Tg) determined by DSC. With increasing degree of ionization, Tg and the enthalpy ΔH of the residual intermolecular hydrogen bonding increased. The values of Tg obtained were analyzed by the theory of Fox and Loshaek for the effect of crosslinks. It is concluded that sodium ions probably from ionic domains and act as crosslinks to reinforce the residual hydrogen bonding and may increase Tg. The absorbance at 1560 cm-1 (νCOO-) did not change at Tg. This suggests that the glass transition observed here is not due to the onset of the mobility in ionic domains, as has been proposed for ethylene-based ionomers on the basis of dielectric measurements.
    Additional Material: 8 Ill.
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