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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 7086-7089 
    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 25 (1992), S. 1009-1010 
    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
    Springer
    Journal of materials science 7 (1988), S. 1241-1242 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    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 28 (1990), S. 303-314 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cationically charged poly(allylamine) (PAA) membranes having various water contents [0.49 〈 H 〈 0.63 (g H2O/g wet membrane)] were prepared. Sorption and permeation of simple salts (sodium chloride and sodium tetraphenylborate) were investigated, taking into account the state of the water in these membranes. The weight ratios of freezable water and free water to total water (Wfz/Wt, and Wf/Wt) in the membranes were estimated by means of DSC and pulsed 1H-NMR measurements, respectively. Partition coefficients K for total water were converted into those in freezable and free water, Kfz and Kf, using Wfz/Wt and Wf/Wt. The permeability of both salts in the membranes could be interpreted satisfactorily by an equation derived from the Teorell-Meyer-Sievers theory using values of Kf. The free water is mainly involved in the permeation of simple salts through PAA membranes while bound water hardly takes part.
    Additional Material: 11 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 28 (1983), S. 3049-3062 
    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: Spherulitic polypropylene (PP) films prepared by a melt-quenched process and then exposed to isothermal annealing treatments at various temperatures ranging from 120°C to 155°C have been dyed at 80°C with C.I. Disperse Yellow 7(Y-7) or p-aminoazobenzene. Different PP films as crystallized isothermally in the range of 60°C to 155°C have also been dyed with the same dyes. The equilibrium dye sorption (Mo) obtained for these films increased slightly with an increase in polymer volume crystallinity (Cu). Using fine structural data of these films, the change in Mo were analyzed in terms of the mosaic-block structural model; e.g., the values of Mo were divided into sorption by the amorphous end region (Me) located between lamella surfaces and sorption by the amorphous side region (Ms) located between crystalline cores parallel to the molecular chain axis. The value of Ms increased with increasing Cv in both cases of the dyeing systems, while the value of Me decreased monotonically in an opposite manner. The amorphous chains in the side region seem to have a strong affinity to a long rodlike dye molecule of Y-7; this feature is considered to be associated with the extended chain conformation of the side region which originates from distorted lattice chains.
    Additional Material: 11 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 30 (1985), S. 3409-3422 
    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: Isotactic polypropylene (PP) films drawn at various temperatures ranging from 100 to 155°C have been dyed at 80°C with p-aminoazobenzene (PAAB) or C.I. Disperse Yellow 7 (Y-7). The equilibrium dye sorption (M0) of PAAB obtained for these films decreased with an increase in draw ratio (λ) of the films. The M0 values of Y-7, however, increased with increasing in λ similarly the crystallinities of these films increased slightly with draw ratios. By use of fine structural data of these films, the change in M0 of Y-7 for drawn PP films were analyzed in terms of a mosaic-block structural model. The increase in M0 with increasing in λ was thus ascribed to enhanced sorption by the amorphous side region between crystalline cores located parallelly in the direction to the molecular axis. The side regions of the drawn systems become rich in interfibrillar tie chains in a higher range of λ. The side region seem to have a strong affinity particularly to a long rodlike dye molecule such as Y-7; this feature is probably associated with the amount of the amorphous chains having extended chain conformation, the fraction of which increases during drawing.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A phenomenological theory of disperse dye sorption is presented in view of the mosaic-block structure model of a crystalline polymer. The sorption model is essentially based on the idea that disperse dyes are dissolved into two kinds of amorphous regions within the polymer: one consists of chains with relatively random conformation (the end region); the other is mainly composed of chains whose molecular arrangement is predominant in parallel alignment (the side region). Experimental findings derived from the equilibrium uptakes at 80°C of four disperse dyes by variously-annealed high-density polyethylene (PE) films are fully examined in terms of this theory. The dye sorption into the end region in every dyeing case decreases monotonically with increasing the crystallinity of PE; whilst that into the side region increases definitely, particularly in the case of rod-like dye molecules. The latter is probably reflected on the increase in the fraction of the amorphous chains with trans-type conformation, the development of which may be accompanied by thickening of lamellae, since straight-type chains of this molecular shape are preferentially effective in binding tightly to the rod-like dye molecules.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1415-1421 
    ISSN: 0887-624X
    Keywords: 4-(4-acetoxyphenoxy) benzoic acid ; polycondensation ; thermotropic liquid-crystalline polymer ; phase transition ; schlieren texture ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly[4-(4-hydroxyphenoxy) benzoic acid] was prepared by the bulk polycondensation of 4-(4-acetoxyphenoxy) benzoic acid. Polycondensation was conducted at 350°C for 3 h under a reduced pressure of 0.1 mmHg and gave a polymer with X̄n of 255. The polymer was characterized by elemental analysis, IR spectroscopy, differential scanning calorimetry, and wide-angle X-ray measurement. The crystal/nematic and nematic/isotropic phase transition temperatures of polymer, which depend on the molecular weight, were observed at about 300°C and 410°C, respectively. The polymers with low molecular weights showed nematic textures above 300°C. This nematic/isotropic phase transition temperature is lower than that of poly (4-hydroxybenzoic acid). This thermal behavior of polymer comes from ether units, which increase the flexibility (the rotation or torsion of skeletal bonds) of the polymer chain. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 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 A: Polymer Chemistry 36 (1998), S. 413-419 
    ISSN: 0887-624X
    Keywords: liquid crystalline polymer ; polyarylates ; 4-hydroxy-2,3,5,6-tetrafluorobenzoic acid ; 6-hydroxy-2-naphthoic acid ; fine structure ; thermal property ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4-Hydroxy-2,3,5,6-tetrafluorobenzoic acid/6-hydroxy-2-naphthoic acid copolymers (FHBA/HNA copolymer) with different copolymer compositions were prepared and the influence of FHBA residue on the thermal properties and structures of the copolymers were investigated. Introduction of FHBA decreased the crystal/nematic phase transition temperatures(TCNs) of the FHBA/HNA copolymers. TCNs of the copolymers were in the temperature range between 200 and 250°C, depending on the copolymer composition. They are approximately 40°C lower than those of 4-hydroxybenzoic acid/HNA copolymers. FHBA/HNA copolymers exhibited low crystallinity, and annealing treatment hardly influenced the crystalline natures. FHBA residue possibly interferes with the recrystallization during annealing. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 413-419, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 853-858 
    ISSN: 0887-624X
    Keywords: poly(ether sulfone) ; sodium sulfonate group ; aromatic nucleophilic substitution ; thermal degradation ; glass transition ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(ether sulfone)s containing pendant sodium sulfonate groups were prepared by the aromatic nucleophilic substitution reaction of 4,4′-dichlorodiphenylsulfone (1) and sodium 5,5′-sulfonylbis (2-chlorobenzenesulfonate) (2) with bisphenols (3) in the presence of potassium carbonate in N,N-dimethylacetamide. A new monomer 2 containing the sodium sulfonate groups was synthesized by the sulfonation of 1 with fuming sulfuric acid. The polycondensation proceeded smoothly at 170°C and produced the desired poly(ether sulfone)s containing the sodium sulfonate with inherent viscosities up to 1.2 dL/g. The polymers were quite soluble in strong acid, dipolar aprotic solvents, m-cresol, and dichloromethane. The thermogravimetry of the polymers showed excellent thermal stability, indicating that 10% weight losses of the polymers were observed in the range above 460°C in nitrogen atmosphere. Both the glass transition temperatures and hydrophilicity of the polymers increased with increasing their concentrations of sodium sulfonate groups. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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