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  • Polymer and Materials Science  (6)
  • *Action Potentials
  • 1980-1984  (4)
  • 1975-1979  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 50 (1976), S. 9-14 
    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: Verbindungen der Strukturformeln [π-C5H5M(CO)nX] (M = Fe, n = 2; M = Mo, n = 3; X = CH3, CH2C6H5, CH2Si(CH3)3, CH2OCH3, Sn(C6H5)3, SnCl3, HgCl, I), [Mn(CO)5CH3], und [(π-CH3C5H4)Mn(CO)3] wurden als Katalysatoren für die Härtung von Epoxidharzen unter verschiedenen Bedingungen geprüft. Es wurde gefunden, daß die Verbindungen [π-C5H5Fe(CO)2R] (R = CH3, CH2C6H5) und [π-C5H5Mo(CO)3CH3] wirksame lichtempfindliche Beschleuniger für die Anhydridhärtung von Expoxidharzen sind. Der Aktivierungsmechanismus wird diskutiert.
    Notes: Compounds of the types [π-C5H5M(CO)nX] (M = Fe, n = 2; M = Mo, n = 3; X = CH3, CH2C6H5, CH2Si(CH3)3, CH2OCH3, Sn(C6H5)3, SnCl3, HgCl, I), [Mn(CO)5CH3], and [(π-CH3C5H4)Mn(CO)3] have been examined as catalysts for the cure of epoxy resins under various conditions. It was found that the compounds [π-C5H5Fe(CO)2R] (R = CH3, CH2C6H5) and [π-C5H5Mo(CO)3CH3] are active photosensitizing agents for the anhydride cure of certain epoxy resins. The mechanism of the process is discussed.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 56 (1976), S. 157-162 
    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: 13C-und 1H-NMR-Untersuchungen haben überzeugend gezeigt, daß die Hauptkomponente des Epoxidharzes aus Phenolphthalein und Epichlorhydrin ein aromatischer Diglycidyläther mit einem Lactonring ist und nicht eine chinoide Verbindung mit Glycidylätherund Glycidylesterstruktur.
    Notes: 13C- and 1H-NMR studies have shown conclusively that the main component of the epoxy resin derived from phenolphthalein and epichlorohydrin is an aromatic diglycidyl ether containing a lactone ring, rather than a glycidyl ether-glycidyl ester compound containing a quinoid ring.
    Additional Material: 1 Tab.
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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 modification of epoxy resins by reactions involving their hydroxyl groups is described. For example, reactions with enol ethers, acrylonitrile, ethyl acetoacetate and certain other carboxylic esters, or triethyl orthoformate, gave products which had reduced reactivities towards various hardeners, and which therefore gave lower peak temperatures on cure and/or longer usable lives. Suitable modification of epoxy resins with various other reagents(certain acid anhydrides, epichlorohydrin, or N-hydroxymethylacrylamide) introduces additional useful functional groups. The uses of a diisocyanate and of α-naphthyl isocyanate to modify epoxy resins or their mixtures prior to GPC analysis are also mentioned.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 13 (1979), S. 339-342 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 56 (1984), S. 853-855 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 33 (1982), S. 9-13 
    ISSN: 0323-7648
    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 surface contaminations on isothermal charge decay of electrets of (tetrafluoroethylene-hexafluoropropylene) copolymer was investigated. Carefully rinsed samples showed increased charge stability in comparison with not treated or open stored samples. The results are explained by the partial destruction of the isolating properties of FEP by dust particles.
    Notes: Der Einfluß von Oberflächenverunreinigungen auf den isothermen Ladungsabbau bei Elektreten aus Tetrafluorethylen-Hexafluorpropylen-Copolymer (FEP) wird untersucht. An sorgfältig gespülten Proben ist eine deutliche Erhöhung der Ladungsstabilität im Vergleich zu unbehandelten bzw. offen gelagerten Proben zu beobachten. Die Ergebnisse werden mit der teilweisen Zerstörung der Isolationseigenschaften des FEP durch eindringende Staubpartikel in Verbindung gebracht.
    Additional Material: 7 Ill.
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  • 7
    Publication Date: 1982-08-20
    Description: Action potentials were silenced in one eye of neonatal kittens by repeated intraocular injections of tetrodotoxin for 5 to 8 weeks. After tetrodotoxin blockade was allowed to wear off, receptive field properties of individual relay cells in the lateral geniculate nucleus were examined. The many ON-OFF and binocular fields found in the layers that receive input from the treated eye suggest that these cells had extremely abnormal retino-geniculate synaptic connections. These effects were different in kind from those seen after deprivation rearing that does not silence action potentials. Lack of action potential activity was concluded to lead to abnormal development in the central nervous system.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Archer, S M -- Dubin, M W -- Stark, L A -- 7F32 EY 05442/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 1982 Aug 20;217(4561):743-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7100921" target="_blank"〉PubMed〈/a〉
    Keywords: *Action Potentials ; Animals ; Animals, Newborn ; Cats/*growth & development ; Evoked Potentials, Visual ; Facial Nerve/*growth & development ; Geniculate Ganglion/*growth & development ; Optic Nerve/growth & development ; Retina/*growth & development ; Sensory Deprivation ; Synapses/physiology ; Tetrodotoxin/pharmacology ; Visual Pathways/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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