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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 20 (1991), S. 531-538 
    ISSN: 1572-8927
    Keywords: Molecular interaction ; excess Gibbs free energy of mixing ; ideal associated model ; equilibrium constants ; thermodynamics of mixtures ; binary mixtures ; interactions in solutions ; applicability of Flory theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The excess Gibb's free energy of mixing, GE, for ethyl iodide+toluene at 25°C have been obtained from the measured vapor pressuure data. The HE and GE values for ethyl iodide+toluene are positive throughout the ethyl iodide concentration range and GE〉HE. The results have been analyzed in terms of Flory and ideal associated model theory of nonelectrolyte solutions. It has been observed that the ideal associated model approach which assumes the presence of AN and A2B molecular species describes well (within±10 J-mol−1 in the worst case) the general dependence of HE on XA (mole fraction of ethyl iodide) over the whole composition range for ethyl iodide+toluene mixtures. The equilibrium constants for A+A⇆ AB and 2A+B⇆A2B reactions along with the enthalpies of formation of AB and A2B molecular species have been calculated.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 268 (1990), S. 645-648 
    ISSN: 1435-1536
    Keywords: β-picolinium-p-chlorophenacylide ; α-α azobisisobutyronitrile ; N-vinyl pyrrolidone ; dilatometry ; retarder ; kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract β-Picolinium-p-chlorophenacylide (β-PCFY) acts as a retarder for polymerization of N-vinyl pyrrolidone. The polymerization runs were carried out at 60°C using benzene as an inert solvent. The kinetic equation for the present system may be written asR p α[β-PCPY]−1.0 [AIBN]0.66[N-VP]1.0. The value of overall energy of activation for polymerization in presence and absence ofβ-PCPY was computed as 44.0 and 42.3 kJ mol−1, respectively. The inverse relationship ofR p and¯M v withβ-PCPY suggests thatβ-PCPY acts as a polymerization retarder. The retarding effect is also evidenced by higher initiator exponent value and higher value of energy of activation in presence of ylide. A mechanism is also proposed in which polymer propagating chain combines with one ylide component to give resonance stabilized radical.
    Type of Medium: Electronic Resource
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