Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 7086-7089 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 1009-1010 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of materials science 7 (1988), S. 1241-1242 
    ISSN: 1573-4811
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 413-419 
    ISSN: 0887-624X
    Schlagwort(e): 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
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 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
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 605-611 
    ISSN: 0887-624X
    Schlagwort(e): poly(arylene ether)s ; pendant benzoyl groups ; 2,5-difluoro-4-benzoyl-benzophenone ; hydroquinone derivatives ; thermostability ; semi-crystalline polymer ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Poly(arylene ether)s (3) containing pendant benzoyl groups were prepared by the aromatic substitution reaction of 2,5-difluoro-4-benzoylbenzophenone (2) with hydroquinone (1a) and methylhydroquinone (1b) in the presence of potassium carbonate in N,N-dimethylacetamide. The polycondensation proceeded smoothly at 165°C and produced poly(arylene ether)s with inherent viscosities up to 0.8 dL/g. The polymer (3b) derived from methylhydroquinone was quite soluble in common organic solvents and could be processed into uniform films from solutions. On the other hand, the polymer (3a) derived from hydroquinone was only soluble in pentafluorophenol and methanesulfonic acid and had a high crystallinity. These polymers showed 10% weight losses at around 420 and 490°C in nitrogen. Polymer 3b also showed good tensile strength and tensile moduli. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 605-611, 1997
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 853-858 
    ISSN: 0887-624X
    Schlagwort(e): poly(ether sulfone) ; sodium sulfonate group ; aromatic nucleophilic substitution ; thermal degradation ; glass transition ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 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.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1415-1421 
    ISSN: 0887-624X
    Schlagwort(e): 4-(4-acetoxyphenoxy) benzoic acid ; polycondensation ; thermotropic liquid-crystalline polymer ; phase transition ; schlieren texture ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 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.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 3049-3062 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: 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.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1049-1056 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Films of wholly aromatic copolyester composed of 4-hydroxybenzoic acid (HBA) and 2-hydroxy-6-naphthoic acid (HNA) were prepared by a solution-casting method using a mixed solution of pentafluorophenol (PFP) and chloroform (weight ratio: PFP/chloroform = 3/7). Using five samples with different copolymer compositions (HBA/HNA [mol%] = 25/75, 40/60, 55/45, 62/38, 73/27), the effects of the copolymer composition on the fine structures of the films were investigated using thermal analyses, density measurements, X-ray diffraction methods, and tensile tests. The as-cast films obtained were shown to be trans-parent and highly amorphous in spite of changing the copolymer composition. When the films were heated above the Tg (100°C), cold crystallization first occurred during the heating process and they had melting points. The densities of the films increased with increasing annealing temperature throughout the cold crystallization. The elongation percentages of the as-cast films reached high values of 30-74% at room temperature, indicating their maximum of elongation at 55 mol% of HBA. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 3409-3422 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: 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.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...