Faculty of engineering, Alexandria university
Gas and petrochemical department
Safety
Phase diagram of nitric acid
Done by: Engy Mahmoud Gahin
ID: 7056
Submitted to: Dr. Hassan Farag
Using the diagram
Distilling dilute nitric acid
Start with a dilute solution of nitric
acid with a composition of
C1 and trace through what
happens.
The vapour produced is richer in
water than the original acid. If you
condense the vapour and reboil it, the new vapour is even richer in
water. Fractional distillation of dilute nitric acid will enable you to
collect pure water from the top of the fractionating
column.
As the acid loses water, it becomes more concentrated. Its concentration
gradually increases until it gets to 68% by mass of nitric acid. At that point, the
vapour produced has exactly the same concentration as the liquid, because
the two curves meet.
You produce a constant boiling mixture (or azeotropic mixture or azeotrope). If
you distil dilute nitric acid, that's what you will eventually be left with in the
distillation flask. You can't produce pure nitric acid from the dilute acid by
distilling it.
Distilling nitric acid more concentrated than 68% by mass
This time you are starting with a concentration C2 to the right of the azeotropic
mixture.
The vapour formed is richer in nitric acid. If you condense and reboil this, you
will get a still richer vapour. If you continue to do this all the way up the
fractionating column, you can get pure nitric acid out of the top.
As far as the liquid in the distillation flask is concerned, it is gradually losing
nitric acid. Its concentration drifts down towards the azeotropic composition.
Once it reaches that, there can't be any further change, because it then boils
to give a vapour with the same composition as the liquid.
Distilling a nitric acid / water mixture containing more than 68% by mass of
nitric acid gives you pure nitric acid from the top of the fractionating column
and the azeotropic mixture left in the distillation flask.