Flash Distillation
Flash distillation is defined as a process in which the
entire liquid mixture is suddenly vaporized (flash) by passing the feed from a
high pressure zone to a low pressure zone. Flash distillation is also known as
equilibrium distillation, i.e., separation is attempted when the liquid and
vapour phases are in equilibrium. This method is frequently carried out as a
continuous process.
Principle
• When a hot liquid mixture is allowed to enter from a
high-pressure zone into a low-pressure zone, the entire liquid mixture is
suddenly vaporised. This process is known as flash vaporisation. During this
process the chamber gets cooled.
• The individual vapour phase molecules of high boiling
fraction get condensed, while low boiling fraction remains as vapour.
Working
• The feed is pumped through a heater at a certain
pressure. The liquid gets heated, which enters the vapour-liquid separator
through a pressure-reducing valve. Due to the drop in pressure, the hot liquid
flashes, which further enhances the vaporisation process.
• The sudden vaporisation induces cooling. The
individual vapour phase molecules of high boiling fraction get condensed, while
low boiling fraction remains as vapour. The mixture is allowed for a sufficient
time, so that vapour and liquid portions separate and achieve equilibrium.
• The vapour is separated through a pipe from above
and liquid is collected from the bottom of the separator. By continuously
feeding into the still, it is possible to obtain continuous flash distillation.
• The operating conditions can be adjusted in such a
way that the amount of feed exactly equals the amount of material removed.
Therefore, vapour and liquid concentrations at any point remain constant in the
unit.
Uses: Flash distillation is used for separating components,
which boil at widely different temperatures. It is widely used in petroleum
industry for refining crude oil.
Advantages: Flash distillation is a continuous
process.
Disadvantages: Flash distillation is not effective in separating components of comparable volatility. It is not an efficient distillation when nearly pure components are required, because the condensed vapour and residual liquid are far from pure.
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