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  • 1
    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: The influence of coupling agents in E-glass cellulose acetate composites was investigated by stereoscan photographs, that have been taken from the surfaces of broken test bars, and correlated with mechanical properties of the systems. Furthermore some stereoscan photographs show the different types of adhesion in glass reinforced nylon-6, poly(ethyleneterephthalate) and polyester resin.
    Notes: Der Einfluß der Schlichte von E-Glasfasern auf die Haftung bei Celluloseacetat wurde mit Hilfe von Stereoscan-Aufnahmen der Bruchflächen gespritzter Normkleinstäbe sichtbar gemacht und mit den mechanischen Eigenschaften der Systeme korreliert. Weiterhin zeigen Bruchflächenaufnahmen von glasfaserverstärktem 6-Polyamid, Polyäthylenglykolterephthalat und Polyester verschiedene Formen der Benetzung der geschlichteten Glasfaser durch das Polymere.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anionic ring-opening polymerization of mixtures of 2,2-dimethyltrimethylene carbonate and ∊-caprolactone in toluene as solvent, with sec-butyllithium or potassium dihydronaphthylide as initiator, results in the formation of polymers of the (A-X-B)n type, where A represents a poly(2,2-dimethyltrimethylene carbonate) block, B represents a poly(∊-caprolactone) block and X stands for a block of the two monomers with a composition gradient; n represents the number of portions by which the monomer mixture is added to the initiator or the living system. From the time-conversion curves it follows that the reactivity of the carbonate monomer is higher than that of the lactone. This difference in reactivity of the monomers is the reason for the special polymer architecture represented by (A-X-B)n. The properties of these polymers depend upon the ratio of the monomers and the number n of additions. The polymers are characterized by spectroscopic, thermoanalytical, and thermomechanical measurements.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anionic ring-opening polymerization of mixtures of 2,2-dimethyltrimethylene carbonate (5,5-dimethyl-1,3-dioxan-2-one) (1) and pivalolactone (2,2-dimethyl-3-propanolide) (3) in toluene as a solvent and with potassium dihydronaphthylide as initiator, results in formation of block copolymers with yields of ca. 90%. In tetrahydrofuran as a solvent the polymer yields are ca. 65% only. In toluene, 1 polymerizes first and subsequently 3 resulting in a blocky structure of the copolymer. According to a mechanistic study, the active species is first a 1-alcoholate, later a 3-alcoholate and finally a 3-carboxylate. The copolymers are soluble in deuterochloroform up to a mole fraction of pivalolactone of ca. 0,40. By means of 13C NMR spectroscopy the blocky structure of the copolymers prepared in toluene was confirmed. In tetrahydrofuran as a solvent 1-3 and 3-1-diads are formed to a significant extent. The copolymers were characterized by thermoanalytical and thermomechanical measurements.
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 103 (1991), S. 1626-1638 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei den Technischen Thermoplasten gehört Polycarbonat zusammen mit den Acrylnitril/Butadien/Styrol-Copolymeren und den Polyamiden zur Spitzengruppe; weiteres dynamisches Mengenwachstum wird ihm vorhergesagt. Ein wesentlicher Grund für diesen “Höhenflug” ist - neben einer herausragenden Kombination von Basiseigenschaften und einem günstigen Preis/Leistungsverhältnis - das in der Grundstruktur liegende chemische und physikalische Potential. Diese Übersicht zeigt Beispiele dafür, wie dieses Potential durch den Einbau eigenschaftsbestimmender alternativer Monomere, die Änderung der linearen Struktur, die Variation von Endgruppen, die Zugabe spezieller Additive sowie durch Legierungsbildung zur Herstellung neuer Polycarbonat-Werkstoffe genutzt werden kann. Besonders herausgestellt wird die Entwicklung hochwärmeformbeständiger Polycarbonate mit weiteren technisch wertvollen Eigenschaften. Von wissenschaftlichem wie praktischem Interesse ist das dabei erkannte neue Kriterium für hochwärmeformbeständige und zugleich ausreichend zähe Polycarbonate.
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 94 (1982), S. 159-169 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zur Modifizierung der Eigenschaften von Polymer-Werkstoffen gewinnt zunehmend das „Legieren“ von Polymeren an Bedeutung. Kennzeichnend für Polymerlegierungen ist ihre Phasigkeit. Vollständige, partielle oder fehlende Verträglichkeiten von Polymeren führen zu unterschiedlichen Phasigkeiten der Legierungen. Zur Analyse der Phasigkeit eignen sich unter anderem dynamisch-mechanische Methoden: Danach sind Polymerlegierungen einphasig, wenn nur ein diskreter Schubmodul-Abfall zu beobachten ist, auch wenn sich dieser über einen breiteren Temperaturbereich erstreckt als bei den Mischungskomponenten. Aliphatische (Polyester)-polycarbonate und Tetramethylbisphenol-A-polycarbonat sind neuartige, mit PVC verträgliche Polymer-Modifikatoren. Die (Polyester)-polycarbonate (aus Adipinsäure, 1,6-Hexandiol, Neopentandiol und Diphenylcarbonat) ergeben mit PVC einphasige Legierungen, die oberhalb der Mischungs-Glasübergangstemperaturen die Charakteristiken von Weich-PVC und weit unterhalb dieser Temperatur noch Zähigkeitseigenschaften aufweisen. Das besondere Hochtemperaturverhalten des harzartigen Tetramethylbisphenol-A-polycarbonats ermöglicht die Herstellung von Legierungen mit erhöhter Wärmeformbeständigkeit.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 21 (1982), S. 174-184 
    ISSN: 0570-0833
    Keywords: Polymer alloys ; Polyvinyl chloride ; Polyblends ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymer alloying is acquiring ever increasing significance for the modification of polymeric materials. Polymer alloys are defined by their phase character, which in turn is determined by the mutual compatibility or incompatibility of the components. Suitable techniques for the analysis of the phase character include, inter alia, dynamic-mechanical methods, according to which a polymer alloy may be considered in a simplified manner as single-phase when only one glass transition is observed, even if it extends over a broader temperature range than in the case of the pure components. Aliphatic (polyester)-polycarbonates and tetramethylbisphenol-A polycarbonate are new, PVC-compatible, polymer modifiers. The (polyester)-polycarbonates (from adipic acid, hexane-1,6-diol, neopentanediol, and diphenyl carbonate) yield with PVC single-phase alloys that at temperatures above the glass transitions of the mixture display the characteristics of soft PVC and that are tough far below this temperature. The special high-temperature properties of the resin-like tetramethylbisphenol-A polycarbonate permits the preparation of alloys with increased dimensional stability under heat (higher deflection temperatures under load).
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 30 (1991), S. 1598-1610 
    ISSN: 0570-0833
    Keywords: Materials science ; Polymers ; Polycarbonates ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polycarbonate together with the acrylonitrile/butadiene/styrene copolymers, and the poly amides constitute the leading groups of engineering thermoplastics; for polycarbonate in particular, continued dynamic growth is prophesized.The underlying reason for this lies not only in its outstanding combination of technical properties and excellent price/performance balance, but also in the chemical and physical potential inherent in the basic structure of polycarbonate. The following review demonstrates with examples how this potential can be used in the development of new polycarbonates through the incorporation of alternative monomers, changes in the linear structure, end group variation, addition of special additives, and blending. The main emphasis of this articles lies in the development of polycarbonates resistant to high temperature, with a good balance of technologically valuable properties. For scientific and practical interests a new criterion is offered for polycarbonates having both high-temperature stability and impact strength.“One must not only make a discovery, but also realize that a discovery has been made.”Hermann Schnell [1]
    Additional Material: 9 Ill.
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