Jump to content



Featured Articles

Check out the latest featured articles.

File Library

Check out the latest downloads available in the File Library.

New Article

Product Viscosity vs. Shear

Featured File

Vertical Tank Selection

New Blog Entry

Low Flow in Pipes- posted in Ankur's blog

Distillation Column Energy And Material Balance


This topic has been archived. This means that you cannot reply to this topic.
5 replies to this topic
Share this topic:
| More

#1 raanii89

raanii89

    Junior Member

  • Members
  • 11 posts

Posted 15 June 2013 - 11:55 AM

Hi,

 

Currently I am in my final year doing chemical engineering.Were a given a project to design a styrene plant.We are required to do manual calculation and also simulation.

 

Is there any spreadsheet for material and energy balance of fractional distillation column?I have difficulties to draw x-y graph (ethylbenzene-styrene) to find no of plates as the boiling points of this two components are very near..Is there any ways to separate two components which have almost similar boiling point.

 

How to reduce no of plates fr this column.



#2 Mirco

Mirco

    Brand New Member

  • Members
  • 2 posts

Posted 15 June 2013 - 12:19 PM

  hi raanii have you try to increase reflux ratio? in this way you may reduce the number of trays. Alternatively you may reduce operating pressure,this will increase relative volatility of components and the effect is the same,but it is a much more expensive solution.



#3 Bobby Strain

Bobby Strain

    Gold Member

  • Members
  • 3,529 posts

Posted 15 June 2013 - 03:07 PM

The two components are easily separated at low pressure.

 

Bobby



#4 raanii89

raanii89

    Junior Member

  • Members
  • 11 posts

Posted 16 June 2013 - 07:39 PM

Thank you.



#5 Ahsan67

Ahsan67

    Veteran Member

  • Members
  • 40 posts

Posted 22 June 2013 - 06:00 PM

hi,
i suppose you are talking about azetropic distillation, if is the case try to find the solvent which is able to absorb one component of your feed then mix it with your feed & then try to seperate them via other method that may not be distallation, what i am talking about that may be extraction or some other. or kindly share there boiling points, if it is not a azetropic distillation u can use phensky, & underwood equation to find min no. of plates & min reflux, the method you mentioned is mecab-theal for this you need the K values at each stage or you have to decide earlier the top & bottom temp . i also suggest you to use hysys for this.


Regards
Ahsan



#6 thorium90

thorium90

    Gold Member

  • Members
  • 1,073 posts

Posted 22 June 2013 - 06:25 PM

Ahsan, ethylbenzene and styrene separation is not an azeotropic distillation. Also, I believe you are referring to the method know as FUG method, or Fenske Underwood Gilliland method to designing a distillation column.
The graphical method the OP is referring to is known as McCabe Thiele method, of which a link to a spreadsheet created by Samir Khan I posted a while back can be found in this forums or by google.
K values, for relative volatility is technically not a needed value but a calculated value.
Component normal boiling points can easily be found on nist website.
 
To the OP, the following article may be of your interest
http://www.google.co...tents/US5386075

 

Edit: Attached the file by Samir Khan.

Attached Files


Edited by thorium90, 22 June 2013 - 11:33 PM.





Similar Topics