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  • 1
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    A New Polyurethane Millable Gum (1969)
    American Chemical Society
    Details
    Publication Date: 1969-06-01
    Print ISSN: 0196-4321
    Electronic ISSN: 1541-4841
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Published by American Chemical Society
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    PAPER CURRENT
  • 2
    Electronic Resource
    Electronic Resource
    A New Polyurethane Millable Gum (1969)
    s.l. : American Chemical Society
    Industrial and engineering chemistry 8 (1969), S. 182-184 
    Details
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1021/i360030a017
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Elastomers from castor oil (1967)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 11 (1967), S. 629-638 
    Details
    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: Castor oil has been used to prepare millable elastomers by using 2,4-toluene diisocyanate, 4,4′-diphenylmethane diisocyanate, and 1,5-naphthalene diisocyanate, respectively. These elastomers are vulcanized with sulfur and 4,4′-diphenylmethane diisocyanate separately by using the standard methods of rubber technology, and the properties of these vulcanizates are reported.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1967.070110502
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  • 4
    Electronic Resource
    Electronic Resource
    Effects of low molecular weight aliphatic diols on the polyurethane elastomers prepared from hydroxyl-terminated polybutadienesNCL Communication No. 3251. (1983)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 3559-3563 
    Details
    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: Hydroxyl-terminated polybutadienes were prepared by using azo initiators such as di(4-hydroxybutyl)-2,2′-azobisisobutyrate and di(3-hydroxybutyl)-2,2′-azobisisobutyrate, one of which contains primary and the other secondary hydroxyl groups. The effects of aliphatic diols and 2,4-toluene diisocyanate (TDI) in the presence of dibutyltindilaurate (DBTDL) as catalyst, on crosslinking of primary and secondary hydroxyl groups, were studied. Polyurethane elastomers from these polymers are prepared by using different ratios of diols, 2,4-toluene diisocyanate and catalyst. Physical properties such as hardness, tensile strength, 100% modulus, and elongation at break of these polymers were studied with a view to compare them with the physical properties of elastomers prepared from ARCO R-45M.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1983.070281119
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  • 5
    Electronic Resource
    Electronic Resource
    Isocyanate-terminated polybutadiene prepolymers: Synthesis, characterization, and end-group modifications (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 1433-1441 
    Details
    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: Telechelic prepolymers of butadiene with aliphatic isocyanate end-groups were prepared by the solution polymerization of butadiene under free radical initiation. 4,4′-Azobis (4-cyanopentanoyl azide) was used as the initiator. Liquid prepolymers were obtained with molecular weights of 1450 to 6000 and functionalities 1.9 to 2.2. The prepolymers were characterized by their number-average molecular weight, isocyanate content, functionality, infrared, and nuclear magnetic resonance spectra and microstructure. The storage stability of the prepolymers was checked and they were found to be quite stable under ambient conditions. Isocyanate-terminated polybutadienes were reacted with N,N-dimethylamino ethanol and t-butyl hydroperoxide to obtain useful dimethylamino-terminated and peroxycarbamate-terminated prepolymers, respectively.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070360613
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  • 6
    Electronic Resource
    Electronic Resource
    Decomposition rate studies of azobisnitriles containing functional groups (1988)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 953-958 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1988.080260321
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  • 7
    Electronic Resource
    Electronic Resource
    Preparation of silicon-containing polymers IV. Thermally stable organosilicon poly-1,2,4-triazoles (1986)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 103-107 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel silicon-containing poly-1,2,4-triazoles have been synthesized by the reaction of polyhydrazide precursors and aniline in polyphosphoric acid (PPA) at 260°C. The polyhydrazide intermediates were prepared from aromatic dihydrazides and silicon-containing acid dichlorides via interfacial polycondensation. These polymers and their intermediates were characterized by infrared spectroscopy (IR), solubility, and by solution viscosity. The thermal behavior of these polytriazoles has been studied by dynamic thermogravimetry.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1986.080240109
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  • 8
    Electronic Resource
    Electronic Resource
    Syntheses of ultraviolet light absorbers for polyvinylchloride (PVC). Part I (1971)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 20 (1971), S. 165-174 
    Details
    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: Synthesen für folgende Verbindungen, die als UV-Absorber dienen können, werden beschrieben:2-(2′-Pentadecenyl-4′-hydroxy-phenyl)-benzotriazol, 2-(2′-Pentadecyl-4′-hydroxy-phenyl)-benzotriazol, 2-(2′-Pentadecyl-3′-carboxy-4′-hydroxy-phenyl)-benzotrlazol, 2-(2′Hydroxy-4′-pentadecyl-5′-chlor-phenyl)-benzotriazol, 2-Hydroxy-4-pentadecyl-benzophonon, 3-Pontadecyl-phenyl-salicylat und Nickelkomplex von Di-(4-pentadecyl-6-hydroxy-phenyl)-sulfid.
    Notes: The syntheses of the following ultravilot light absorbers from cashewnutshell liquid are described:2-(2′-pentadecenyl-4′-hydroxy-phenyl)-benzotriazole, 2-(2′-pentadecyl-4′-hydroxy-phenyl)-benzotriazole, 2-(2′-pentadecyl-3′-carboxy-4′-hydroxy-phenyl)-benzotriazole, 2-(2′hydroxy-4′-pentadecyl-5′-chloro-phenyl)-benzotriazole, 2-(2′-hydroxy-4′-pentadecyl-benzophenone, 3-pentadecyl-phenyl-salicylate and nickel complex of di-(4-pentadecyl-6-hydroxy-phenyl)-sulfide.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1971.050200114
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  • 9
    Electronic Resource
    Electronic Resource
    Plasticizer extenders for PVC. Part I - esters and ethers (1975)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 43 (1975), S. 1-10 
    Details
    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: Die Synthese von Estern und Äthern aus Cardanol (3-Pentadecenylphenol) wird beschrieben. Ihre Anwendung als sekundäre Weichmacher am Beispiel der Compoundierung von PVC wird gezeigt. Am geeignetsten erwies sich 3-Pentadecenylphenyllinoleat.
    Notes: The synthesis of esters and ethers from cardanol (3-pentadecenyl phenol) is described. Their application as secondary plasticizers (extenders) is shown for the compounding of PVC. The most suitable extender on this basis is 3-pentadecenyl phenyl linoleate.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1975.050430101
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  • 10
    Electronic Resource
    Electronic Resource
    Polyimides from diamines and dianhydridesNCL Communication No. 2272. (1979)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 79 (1979), S. 93-106 
    Details
    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: Neue Polyimide wurden aus 3,3′,4,4′-Benzophenon-tetracarbonsäuredianhydriden und drei verschiedenen Diaminen hergestellt, die die folgende allgemeine Struktur haben: Die thermischen und elektrischen Eigenschaften von Filmen dieser Polyimide wurden ermittelt. Die thermische Stabilität der hergestellten Polyimide hangt von der Struktur der Diamine ab. Der spezifische Volumenwiderstand war in der Größenordnung von 1015 Ω cm für alle Polyimide.
    Notes: Novel polyimides have been synthesized by reacting 3,3′,4,4′-benzophenone tetracarboxylic acid dianhydride with three diamines having the general structure: Polyimide films obtained have been evaluated for their thermal and electrical properties. The dependence of the thermal stability of the polyimides on the structure of the diamine component has been established. The specific volume resistivity has been found to be of the order of 1015 Ω cm for all the polyimides.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1979.050790108
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