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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3083-3086 
    ISSN: 0887-624X
    Keywords: vinylidene ; scission ; polypropylene ; controlled-rheology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2371-2380 
    ISSN: 0887-624X
    Keywords: Alder Ene reaction ; polypropylene ; Lewis acid ; maleation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the parameters that affect the Alder Ene reaction with respect to the synthesis of a terminally anhydride-functionalized polypropylene was carried out over a temperature range of 220-250°C using maleic anhydride concentrations of 2-12 mol equivalence with respect to the vinylidene group. As previously observed, a Lewis acid (i.e., SnCl2 · 2H2O) had a catalytic effect on the reaction at these temperatures, thereby improving anhydride content in the polymer for short reaction times. Increased temperature and maleic anhydride concentration had a positive effect on improving the incorporation of the succinyl anhydride moiety at the terminal site in polypropylene. Lower SnCl2 · 2H2O concentrations, likewise, improve the functionality of the product. The application of a second-order kinetic model to the measured succinyl anhydride results was not valid over the entire temperature range studied due to side reactions, particularly vinylidene isomerization, and homopolymerization of maleic anhydride. Ruthenium chloride has been examined as another possible catalyst candidate in the reaction and has been found to improve the level of anhydride incorporation in polypropylene compared to stannous chloride. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2371-2380, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Advances in Polymer Technology 14 (1995), S. 87-96 
    ISSN: 0730-6679
    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
    Notes: The chemical modification of high density polyethylene (HDPE) in a counter-rotating nonintermeshing twin screw extruder is modeled using a simultaneous random scission and cross-linking integro-differential equation. The roles of mixing and kinetics in the free-radical reaction are investigated. The modification experiments use a masterbatch feed of HDPE with various concentrations of 2,5-dimethyl-2,5-(t-butylperoxy)-3-hexyne. The extruder operating parameters studied were barrel temperature, screw speed, and the degree of screw flight stagger. The reaction model is fit using the molecular weight averages and the gel content measured experimentally. The reaction time for HDPE is determined by use of the residence time distribution of the extruder with a segregation (macromixing) assumption. The segregation model is compared against the plug flow assumption, where the mean residence time of the measured distribution is used for the length of reaction of all polymer species within the extruder. The calculated molecular weight distributions are insensitive to the mixing model used. © 1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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