--%>

Problem on relative volatility

In vapor-liquid equilibrium the relative volatility αij is defined to be the ratio of the separation or K factor for species i to that for species j, that is,

 αij = Ki/Kj = (yi/xi)/(yj/xj)

In approximate distillation column calculations, the relative volatility is sometimes assumed to be a constant (independent of composition, temperature, and pressure). Test this assumption for the ethanol-ethyl acetate system using the following data:

RT ln γi = 8.163 xj2 KJ/mol

lm PvapEOH = (-4728.98/T) + 13.4643

lm PvapEOH = (-3570.58/T) + 10.4575

   Related Questions in Chemistry

  • Q : Dipole attractions-London dispersion

    Describe how dipole attractions, London dispersion forces and the hydrogen bonding identical?

  • Q : Problem on Osmotic Pressure of solution

    The osmotic pressure of a 5% solution of cane sugar at 150oC  is (mol. wt. of cane sugar = 342)(a) 4 atm (b) 3.4 atm (c) 5.07 atm (d) 2.45 atmAnswer: (c) Π = (5 x 0.0821 x 1000 x 423)/(342 x 100) = 5.07 atm

  • Q : What is schrodinger wave equation? The

    The Schrodinger wave equation generalizes the fitting-in-of-waves procedure.The waves that "fit" into the region to which the particle is contained can be recognized "by inspection" only for a few simple systems. For other problem a mathematical procedure

  • Q : Relative reactivity Which is more

    Which is more reactive towards nucleophilic substitution aryl halide or vinyl halides

  • Q : Calculating weight of acid Give me

    Give me answer of this question. The formula weight of H2SO4 is 98. The weight of the acid in 400mi of solution is: (a)2.45g (b) 3.92g (c) 4.90g (d) 9.8g

  • Q : Basicity order order of decreasing

    order of decreasing basicity of urea and its substituents

  • Q : Organic structure of cetearyl alcohol

    Show the organic structure of cetearyl alcohol and state what the organic family is? Briefly state it.

  • Q : What is ortho effect? Orthosubstituted

    Orthosubstituted anilines are generally weaker bases than aniline irrespective of the electron releasing or electron withdrawing nature of the substituent. This is known as ortho effect and may probably be due to combined electronic and steric factors.The overall basic strength of ort

  • Q : BASIC CHARACTER OF AMINES IN GAS PHASE,

    IN GAS PHASE, BASICITIES OF THE AMINES IS JUST OPPOSITE TO BASICITY OF AMINES IN AQEUOUS PHASE .. EXPLAIN

  • Q : Modern periodic table and Mendeleevs

    Differentiate between the modern periodic table and Mendeleevs table?