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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Energy & fuels 6 (1992), S. 635-642 
    ISSN: 1520-5029
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European archives of oto-rhino-laryngology and head & neck 230 (1981), S. 49-55 
    ISSN: 1434-4726
    Keywords: Tissue culture ; Human parotid gland ; Parotin ; Autoradiography ; Isoproterenol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We investigated the origin of the non-specialized cells proliferated in primary expiant culture of human parotid gland. The predominant cells in surface layer were morphologically epithelial origin with desmosomes and intercellular digitations. The cultured cells did not show any specific affinity to parotin isolated from bovine parotid gland, which seemed to be one of the marker for duct cell. However, it was demonstrated autoradiographycally that DNA synthesis in the cells was rapidly induced by isoproterenol, a potent stimulator of acinar cell. From these results, the non-specialized epithelial cells in expiant culture seemed to be derived from acinar cell in human parotid gland.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2741-2747 
    ISSN: 0887-6266
    Keywords: FTIR spectroscopy ; poly(ethylene-2,6-naphthalate) ; crystallization process ; induction period ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In situ Fourier transform infrared (FTIR) measurements were carried out to elucidate conformation changes occurring during the isothermal melt crystallization of poly(ethylene-2,6-naphthalate) (PEN). Based on the band assignments for the components of the amorphous, α-crystal form, and β-crystal form of PEN in film samples, the in situ data was analyzed in terms of the amorphous- and crystal-trans conformations. It was observed at a higher isothermal crystallization temperature that the formation of amorphous-trans conformations precedes the growth of crystals. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2741-2747, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1227-1233 
    ISSN: 0887-6266
    Keywords: FTIR spectroscopy ; isotactic polystyrene ; crystallization process ; induction period ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The melt crystallization process of isotactic polystyrene (i-PS) was studied by means of in situ Fourier transform infrared (FTIR) spectroscopy, with a focus on the conformational changes during the induction period. The spectra obtained during the induction period suggested the occurrence of some ordered structure that is characterized by higher regularity and packing of the helical moieties than observed in the melt. This ordered structure was clearly different from the amorphous structure, and close to the crystal structure. The Avrami analysis indicated that the formation process of the ordered structure at the late stage of the induction period is similar to the growth process of the crystallites after the induction period. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1227-1233, 1998
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 3193-3201 
    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: Many papers have reported on the thermal shrinkage mechanism of drawn polymers. The cause of the thermal shrinkage is very complex, because that relates to many factors. In this study, atactic polystyrene, a noncrystalline polymer, was used to eliminate factors related to the melting and crystallization effects, and it is considered that there is a relation between the change of the polymer's structure due to heat treatment and thermal shrinkage. It is observed in a certain temperature range that the thermal shrinkage of drawn polystyrene is not caused by increase of the entropy but results in decrease of the entropy.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 2145-2157 
    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: In previous articles, we reported the change in physical properties of hydrophobic polymers caused by absorption of a very small amount of water. This article describes the changes in physical properties of three polyesters owing to absorption of water. The tested polymers were poly(ethylene terephthalate) (PET), poly(butylene terephthalate) (PBT), and polyethylene 2,6-naphthalate (PEN). PBT has more flexible main chains than that of PET, and PEN has more rigid main chains. The dielectric measurements revealed that water absorption results in shortening the relaxation time for PET, while the relaxation time for moist PBT becomes longer. The larger amount of absorbed water yields the higher density of PET and the lower density of PBT. The water absorption of the polyesters also yields increments in dielectric constants and relaxation strength. Distribution of relaxation time of the polyesters is narrowed by absorption of water.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 1143-1149 
    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: In this paper, we report the changes in physical properties of polycarbonate caused by absorbed water and supply basic data for the application of this effect. Absorbed water increases monotonously with increase in relative humidity. Along with the increase in absorbed water, the relaxation time of the β process increases, the glass transition temperature rises, the area of the endothermic peak at the glass transition temperature increases, and the dynamic Young's modulus decreases. We conclude that the absorbed water fills holes but does not function as a crosslinking agent.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 2313-2320 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study of the effect of drawing on the glass transition temperature Tg of amorphous polycarbonate was carried out. The Tg attains a maximum at a draw ratio in the range from 1.6 to 2.0. The relationship between the change of structure and Tg is discussed in terms of the configurational entropy and the rate of molecular motion in local mode relaxation. The variation of Tg with drawing may be explained by using the iso-entropy theory. The frequency of the maximum in the dielectric loss fmax and the dielectric relaxation strength Δε of the β mechanism changed with drawing in the same way as that of Tg. Based on the parallel behavior in these results, it is reasonable to consider that the β process of local mode relaxation of polyesters such as PC and PET reflects the structure of the glassy state.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 701-706 
    ISSN: 0887-6266
    Keywords: dielectric relaxation in PET and ethylene isophthalate terephthalate copolyester ; copolymers, ethylene isophthalate terephthalte, dielectric relaxation in ; poly(ethylene terphthalate) and related copolyesters, dielectric relaxation in ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dielectric β-relaxation in poly(ethylene terephthalate) and ethylene isophthalate terephthalate copolyesters with various ethylene isophthalate contents was investigated over a wide range of frequencies. Isothermal spectra and normalized plots show that the dielectric β-relaxation is characterized by the molecular structure between the aromatic rings. The equilibrium polarizability of the motional segment, which was estimated from the dielectric increment obtained by the best fit of the Havriliak-Negami equation to the Cole-Cole plot, indicates that torsional vibrations of the main chain are correlated over a length corresponding to one monomer.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1477-1483 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of drawing on the glass-transition temperature of amorphous poly(ethylene terephthalate) has been studied. The Tg decreases to a minimum at a draw ratio of 1.5, then increases to a maximum at a draw ratio of about 2.0, and again decreases with increasing draw ratio. The relationship between the change of structure and Tg is discussed in terms of the configurational entropy and the rate of molecular motion in local-mode relaxation. On the basis of configurational entropy, the decrease of Tg at the beginning of drawing depends on the increase of configurational entropy, while at draw ratios above 2.0 it depends on the increase of entropy associated with intermolecular interaction. From the point of view of molecular motion, it is concluded that the change of Tg is determined by local oscillations in the amorphous region.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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