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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 132 (1985), S. 197-201 
    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: Das Polymere aus (NPCl2)3 wurde durch Substanzpolymerisation erhalten. Insbesondere wurde überwiegend lineares Polymeres gebildet, wenn Wolframphosphat als Katalysator verwendet wurde.
    Notes: The polymer of (NPCl2)3 was obtained by bulk polymerization. Especially, linear polymer was predominantly formed when tungsten phosphate as catalyst was used.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 119 (1983), S. 209-212 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymers were prepared by the reaction of poly(dichloro phosphazene), phenoxide, and trifluoro ethoxide in THF. Elastic copolymers having lower Tg than that of poly(trifluoroethoxy phosphazene) were formed when the ratio of phenoxide: trifluoro ethoxide was between 0.5:1.5 and 1.5:0.5.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 42 (1975), S. 55-61 
    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: Tetrachlordiphenylcyclotriphosphazen N3P3Cl4(C6H5)2 (TPC) wurde durch Friedel-Crafts-Reaktion hergestellt. Die Polykondensation von TPC mit aromatischen Diaminen wurde in Pyridin durchgeführt. Die erhaltenen Produkte waren wenig löslich in polaren Lösungsmitteln. Die durch Endgruppenanalyse ermittelten Molekulargewichte lagen zwischen 2800 und 10 800. Es handelte sich um amorphe, braune, gelbe oder farblose Feststoffe; ihre Erweichungspunkte lagen zwischen 100 und 120°C. Die elektrische Leitfahigkeit der aus TPC mit p-Phenylendiamin und p,p′-Diaminodiphenylsulfon erhaltenen Produkte wurde zu 5 × 1012 (Ωcm)-1 bzw. 1 × 1015 (Ω cm)-1 bestimmt.
    Notes: Tetrachlorodiphenyl cyclotriphosphazene N3P3Cl4(C6H5)2 (TPC) has been synthesized by Friedel-Crafts reaction. The polycondensation of TPC with aromatic diamine compounds has been carried out in pyridine. The products obtained from the reaction of TPC with aromatic diamine compounds were slightly soluble in polar organic solvents. The molecular weights measured by the method of end group analysis were about 2800 to 10800. The products were amorphous, brown, yellow or white coloured solids. The softening points of all polycondensation products were found to be in the region of 100°C to 120°C. The electrical conductivity of the products obtained from TPC with p-phenylenediamine and p,p′-diaminodiphenyl sulfone was determined to 5 × 1012 (Ωcm)-1 and 1 × 1015 (Ωcm)-1, respectively.
    Additional Material: 2 Ill.
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  • 4
    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: Cyclophosphazenoligomere (I) wurden durch Erhitzen von Tetrabutyloxydianilinocyclophosphazen und Dichlordiphenylsilan auf 100°C bis 160°C dargestellt. Diese Oligomeren sind in den meisten organischen Lösungsmitteln löslich. Molekulargewicht und Erweichungsbereich von (I) liegen bei 1 700 bis 37000 bzw. bei 95°C bis 180°C. Molekulargewicht und Erweichungsbereich der Cyclophosphazenpolymeren (II), die durch Erhitzen von (I) auf 190°C erhalten wurden, liegen bei 3 000 bis 180 000 bzw. bei 78°C bis über 300°C. Thermischer Abbau dieser Polymeren tritt im Bereich von 100°C bis 300°C ein. Durch thermogravimetrische Messungen wurde gefunden, daß das thermisch stabilste Polymere der Reihe (II) in Luft einen Gewichtsverlust von 15% bei 800°C aufweist.
    Notes: Cyclophosphazene oligomers (I) have been formed by heating tetrabutoxydianilinocyclophosphazene and dichlorodiphenylsilane at temperatures between 100°C to 160°C. These oligomers are soluble in most organic solvents. Molecular weights and softening points of (I) are in the range of 1700 to 37000 and 95°C to 180°C. Molecular weights and softening points of cyclophosphazene polymers (II) obtained by reheating of (I) at 190°C are about 3000 to 180000 and about 78°C to over 300°C. The thermal decomposition of the polymers (II) occurs in the range from 100°C to 300°C. It is shown by thermogravimetry that the weight loss of the thermally most stable polymer of (II) is about 15% in air at 800°C.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Fire and Materials 13 (1988), S. 179-186 
    ISSN: 0308-0501
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Architecture, Civil Engineering, Surveying , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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