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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4421-4438 
    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: The second stage of batch poly(ethylene terephthalate) (PET) reactor with bis(2-hydroxyethyl) terephthalate (BHET) as the feed has been simulated. In this stage, the overall polymerization is not diffusion limited and is known to be a complex reaction. In this work it has been assumed to consist of polycondensation, reaction with monofunctional compounds (cetyl alcohol), redistribution, and cyclization reactions. The forward and reverse steps of each of these have been modelled in terms of the rate constants involving functional groups and the reacted bonds. The equations for the calculation of the molecular weight distribution (MWD) in batch reactors have been written and solved numerically. The MWD reported in this work is assumed to include the monofunctional products only, and, for the case where ethylene glycol is not removed from the reaction mass, it was found to be unaffected by the choice of the redistribution rate constant (kr). Since the removal of ethylene glycol is not mass transfer controlled, its concentration in the reaction mass is assumed be given by the vapor-liquid equilibrium existing at the pressure applied on the reactor. In this work, the level of ethylene glycol concentration, yg (≡[G]/[P1]0), has been taken as a parameter, and, on application of vacuum, the MWD results were found to vary with kr with the sensitivity increasing with yg. It was then shown that the importance of the redistribution reaction is enhanced when the cyclization reaction also occurs. The effect of vacuum on the performance of the reactor has been studied by varying yg. For yg less than 0.01, the change in the MWD of the polymer becomes very small. The effects of polymerization temperature and initial concentration of monofunctional compounds on MWD were found to be small.
    Additional Material: 10 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 22 (1982), S. 1184-1189 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Application of shear is found to increase the rate of solution polymerization of acrylonitrile in N,N-dimethyl formamide (DMF) initiated by benzoyl peroxide by as much as 400 percent of the value in absence of shear. The solvent DMF acts as an inert and maintains a homogeneous reaction mass during the entire course of polymerization. To study the effect of shear systematically, a special dilatometer has been constructed such that a constant shear rate, \documentclass{article}\pagestyle{empty}\begin{document}$ \mathop \gamma \limits^. $\end{document} could be applied to the reaction mass. The rule of solution polymerization has been measured under the variation of \documentclass{article}\pagestyle{empty}\begin{document}$ \mathop \gamma \limits^. $\end{document} and monomer concentration in the system. The measurements of induction time on the addition of a strong inhibitor, hydroquinone, reveal that the increase in the rate of polymerization with shear rate can be largely attributed to the change in the initiator efficiency. As a further confirmation of the above hypothesis, the decomposition of benzoyl peroxide in nitrobenzene at 80°C was measured and was found to increase significantly on application of shear. This confirms the importance of mass-transfer resistance in removal of CO2, and the increase in the rate of polymerization of acrylonitrile occurs because the decomposition of benzoyloxy radicals is favored in the forward direction. Since the polymerization of acrylonitrile is preferentially initiated by phenyl radicals, the rate of polymerization is found to increase.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 471 (1980), S. 203-207 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemie substituierter Schwefelsäuren. X. Lösungen von Säuren und Basen in MethansulfonsäurenMethansulfonsäure ist schwächer als Schwefelsäure. Eine Zahl von anorganischen protonischen Säuren wirken in Methansulfonsäure gelöst als Säuren, während starke Basen vollständig protoniert werden. Säure-Base-Titrationen in Methansulfonsäure zeigen bei starken Säuren, daß die elektrische Leitung über CH3SO3H2+ - und CH3SO3- - Ionen erfolgt. Leitfähigkeitsmessungen zeigen die Reihenfolge der Säurestärken, s. Abstract.
    Notes: Methanesulphuric acid is weaker than sulphuric acid. A number of inorganic protonic acids act as acids in it while the strong bases are fully protonated. The acid-base titrations in it with strong acids indicate that the bulk of the current is carried by CH3SO3H2+ and CH3SO3- ions. The conductance measurements indicate that the order of the acid strength is: H[B(HSO4)4] 〉 HSO3F 〉 H2S2O7 〉 HAs(HSO4)4 〉 HSO3Cl 〉 H2SO4 〉 HX (X=Br 〉 Cl) 〉 H2SeO4.
    Additional Material: 1 Ill.
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