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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 14 (1981), S. 608-613 
    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 27 (1994), S. 7689-7694 
    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
    Amsterdam : Elsevier
    Sensors and Actuators B: Chemical 8 (1992), S. 249-252 
    ISSN: 0925-4005
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 8669-8674 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 19 (1971), S. 121-134 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Verschiedene copolymere Anhydridimide wurden aus Dicarbonsäuren mit vorgebildeter Imidgruppe erhalten. Dazu wurde zunächst Trimellitsäureanhydrid mit verschiedenen aromatischen und aliphatischen Aminen zu den entsprechenden Dicarbonsäuren mit Imidgruppen umgesetzt. Dann wurden aus diesen Dicarbonsäuren durch Reaktion mit Essigsäureanhydrid die entsprechenden gemischten Anhydride hergestellt. Unter bestimmten Bedingungen wurden daraus dann unter Abspaltung von Essigsäureanhydrid polymere Anhydride gewonnen.Die Polymeren sind kristallin und zeigen hohe thermische Stabilität und gute elektrische Eigenschaften. Ihre Struktur wurde IR-spektroskopisch und durch Elementaranalyse bestimmt; Beziehungen zwischen Struktur und Eigenschaften wurden untersucht.
    Notes: Various copolyanhydride-imides have been obtained from diacids containing the preformed imide group by directly reacting of trimellitic anhydride with various aromatic and aliphatic amines. The polymerization process took place in several stages. In the first stage the diacetyl derivatives were obtained from the corresponding diacids by reactions with acetic anhydride. Under special temperature and pressure conditions, polymers were obtained from these derivatives and the chain grew by developing acetic anhydride between contiguous molecules.The polymers obtained are crystalline, have high thermal stability and good electrical properties. Their structures were determined by IR spectroscopy and elementary analysis and the relationships between their properties and the polymer structures were investigated.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 21 (1972), S. 65-77 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Eine Reihe vollständig geordneter Copolyamide-imide und Copolyester-imide wurde durch Reaktion von aliphatischen oder aromatischen Diaminen mit symmetrischen Monomeren mit reaktiven Imidgruppen erhalten.Die aromatischen Diimidamid- und Diimidester-Monomeren wurden dazu durch Acidolyse zwischen Trimellitsäureimid und Essigsäurederivaten von aromatischen Diaminen und Diphenolen hergestellt.Die Diimidester-Monomeren mit aliphatischen Substituenten wurden durch Umesterung von Glycolen mit Trimellitimid-methylester erhalten.Die Polykondensationen wurden in polaren Lösungsmitteln durchgeführt; die isolierten Polymeren wurden im Hinblick auf einen Zusammenhang zwischen Struktur und Eigenschaften charakterisiert.
    Notes: A group of copolyamide-imides and copolyester-imides completely ordered has been obtained by the reaction of aliphatic and aromatic diamines with symmetrical monomers possessing reactive imide group.The aromatic diimide-amide and diimide-ester monomers were prepared by means of the reaction of acidolysis between trimellitic acid imide and acetoxy derivative of aromatic diamines and diphenols.The diimide-ester monomers with aliphatic substitutes were obtained by ester interchange between glycols and the methyl ester of trimellitimide.The polymerization reactions were carried out in a solution of polar solvents and the solated polymers were characterized with the object of estabilishing a relation between the properties and the structure of each one.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 457-468 
    ISSN: 0887-6266
    Keywords: poly(ether amide)s ; mechanical relaxation ; dielectric relaxation ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical and dielectric relaxation of a set of aromatic-aliphatic polyamides containing ether linkages have been examined as a function of temperature (-140 to 190°C) and frequency (3 to 106 Hz). The polymers differ in the orientation (meta and para) of the aromatic rings, in the length of the aliphatic chain, and in the number of ether linkages per repeating unit. Dynamic mechanical experiments showed three main relaxation peaks related to the glass transition temperature of the polymers (α relaxation), the subglass relaxations associated to the absorbed water molecules (β) and to the motion of the aliphatic moieties (γ). Dielectric experiments showed two subglass relaxation processes (β and γ) that correlates with the mechanical β and γ relaxations, and a conduction process (σ) above 50°C that masks the relaxation associated to the glass transition. A molecular interpretation is attempted to explain the position and intensity of the relaxation, studying the influence of the proportion of para- or meta- oriented phenylene rings, the presence of ether linkages and the length of the aliphatic chain. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 457-468, 1997
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 3377-3385 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cationic copolymerization of tetrahydrofuran-(A)-3,3-dimethyloxetane (B) was studied at 0°C with BF3·OEt2-epichlorhydrin and acetylhexafluoroantimonate as initiators. The values of the reactivity ratios, calculated by the Fineman-Ross and Kelen-Tüdos methods, were rA = 0.13, rB = 8.1 and rA = 0.13, rB = 7.9, respectively. These values are in satisfactory agreement with those obtained with a kinetic scheme in which depropagation reactions were considered. The product rArB was approximately equal to unity, which indicated an ideal random copolymerization. The copolymers were also analyzed by 1H-NMR spectroscopy. Their spectra presented a doublet at 3.1 and 3.15 ppm that corresponded to the methylene protons of the dimethyloxetane units and allowed the determination of the probabilities P(AA), P(AB), and P(BB). Good agreement was found between the values calculated by spectroscopic methods and those obtained by using the classical probability theory of copolymerization.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 38 (1989), S. 1745-1759 
    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 series of imide end-capped oligoesters were prepared by reacting a number of hydroxylterminated poly(diethyleneglycol terephthalate) oligomers (X̄n ranging from 1 to 20) with N-(4-chlorocarbonylphenyl)maleimide and N-(4-chlorocarbonylphenyl)nadimide. All the oligomers were characterized by vapor pressure osmometry, 1H- and 13C-NMR and GPC. The thermal properties were also investigated and a correlation of the thermal behavior with molecular weight and the type of reactive end groups was established. Molecular models were also synthesized and characterized to obtain reliable analytical data for the determination of the oligomers composition.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 313-317 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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