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  • 1
    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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  • 2
    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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  • 3
    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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  • 4
    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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  • 5
    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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  • 6
    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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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 44 (1960), S. 275-278 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 54 (1961), S. 201-208 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The γ-ray-induced polymerization of isoprene was investigated in the temperature range of -78° to 40°C. The following variables were studied: the dependence of polymerization rate on temperature; the effects of DPPH and pyridine on the polymerization at various temperatures; the dependence of the polymerization rate on dose rate at -78° and 20°C.; and the structure of the polyisoprenes obtained at various temperatures. the following results were obtained: (1) Although the Arrhenius plot of the polymerization rate did not yield a linear relation, the total polymerization rate was successfully separated into radical and ionic contributions. (2) The polymerization rate was proportional to the square root of dose rate at 20°C., whereas it was proportional to the first power of the dose rate at -78°C. (3) The structure of polyisoprene prepared at -78°C. is closely similar to that of cationically polymerized polyisoprene. The partially ionic mechanism of the radiation-induced polymerization of isoprene was elucidated in this investigation. It was concluded that a cationic mechanism is operative at low temperatures whereas a radical mechanism predominates at higher temperatures.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 43 (1960), S. 459-465 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of acrylonitrile induced by ionizing radiation was investigated in bulk in the temperature range 15 to -196°C. It was found from this investigation that two different mechanisms could exist in the polymerization under the same conditions in different temperature regions. The two polymerization phenomena at room and at very low temperatures were studied from the point of view of radical and ionic polymerization mechanisms. It has been well known that the polymerization at room temperature proceeds by radical mechanism. In the solid state polymerization at very low temperatures the following results were obtained: first, the activation energy is very low, i.e., ca. 0.4 kcal./mole; second, an induction period was not observed under various conditions; third, the monomer containing a radical scavenger was easily polymerized. The authors believe that the facts described above indicate that polymerization in the solid state should proceed by an ionic mechanism.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 20 (1956), S. 567-577 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The ion exchange equilibrium constants were obtained by measurements of infrared spectra of the ion exchange resin phase, using carboxymethylcellulose film (degree of etherification 0.66) as ion exchanger. The apparent constants are calculated by the following equation: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm p} K_a = r_{\rm B} \log {\rm \varepsilon }_{\rm A} \log k\varepsilon _{\rm B} - (r_{\rm B} - r_{\rm A} ){\rm }\log {\rm }(\varepsilon _{\rm A} + k\varepsilon _{\rm B} ) + r_{\rm A} \log B^{ + r_{\rm B} } - r_{\rm B} \log A^{ + r_{\rm A} } + \log {\rm }(\gamma _{\rm B}^{r_{\rm A} } /\gamma _{\rm A}^{r_{\rm B} } )$$\end{document} where A and B are the concentrations of the two exchangeable cations, respectively, rA is the valence of the A ion, γA is the activity coefficient of the A ion in the electrolyte solution, ∊A is absorption intensity of carbonyl band of the carboxy radical having the A ion in an exchanger, and k is a constant. The dependence of the apparent equilibrium constants on pH and the ionic concentration in the electrolyte was investigated in the Na-H, K-H, NH4-H, Ca-H, and Sr-H exchange systems. Further, the activity coefficients of the exchangeable ions in the resin phase were evaluated in both the uniunivalent and unidivalent exchange systems. It is concluded that the abnormal behavior of the coefficients in the resin phase would be explained by the interaction energy between the ion pairs in the resin phase, independent of the concentration of the electrolyte solutions, in the range of comparatively dilute electrolyte solutions.
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