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Distillation I: Principles
Definition & Purpose:
Distillation is the most widely used separation process in the chemical industry. It is
also known as fractional distillation or fractionation. It is normally used to separate
liquid mixtures into two or more vapor or liquid products with different compositions.
Distillation is an equilibrium stage operation. In each stage, a vapor phase is
contacted with a liquid phase and mass is from vapor to liquid and from liquid to
vapor. The less volatile, "heavy" or "high boiling", components concentrate in the
liquid phase; the more volatile, "light", components concentrate in the vapor. By using
multiple stages in series with recycle, separation can be accomplished.
Operating Principles:
The feed to a
distillation column
may be liquid, vapor,
or a liquid-vapor
mixture. It may enter
at any point in the
column, although the
optimal feed tray
location should be
determined and used.
More than one stream
may be fed to the
system, and more than
one product may be
drawn.
A column is divided
into a series of stages.
These correspond to a
cascade of equilibrium
stages. Liquid flows
down the column from
stage to stage and is
contacted by vapor
flowing upward.
Traditionally, most columns have been built from a set of distinct "trays" or "plates",
so these terms end up being essentially interchangeable with "stages". Each tray in a
distillation column is designed to promote contact between the vapor and liquid on the
stage. Distillation can be conducted in a packed column (just as absorption can be
done in a trayed column), but we will focus on trayed columns for the present.
Stages may be numbered from top down or bottom up. When analyzing a stage, flows
and compositions take the number of the stage they leave. The text for this class calls
the top tray of the column "Tray 1" and numbers downward - - this is the convention
we will use. MSH also denote the streams between the column top and condenser with
an "a" subscript and those at the bottom with "b". Personally, I generally prefer to let
"Tray 1" be the bottom tray of the column, the reboiler "Tray 0" and number upward
(so if you catch me doing this, don't panic). I like this way of numbering because it
tends to simplify computer based calculations.
The product leaving the top of the column is called the overhead product, the
"overhead", the "top product", the distillate, or "distillate product". Distillate product
may be liquid or vapor (or occasionally both) depending on the type
of condenserused. Most of the time the distillate flow rate is assigned the symbol D,
and the composition xD or yD.
The product leaving the bottom of the column is called the bottom product or
"bottoms", and given the symbol B, with composition xB.
In some situations, notably petroleum refining, one or more intermediate or
"sidedraw" products may be removed from the column.
Vapor leaving the top of the column passes through a heat exchanger, the condenser,
where it is partially or totally condensed. The liquid which results is temporarily held
in the "accumulator" or reflux drum. A liquid stream is withdrawn from the drum and
returned to the top tray of the column as reflux (R or L) to promote separation.
The portion of the column above the feed tray is called the rectification section. In this
section, the vapor is enriched by contact with the reflux.
The portion of the column below the feed tray is called the stripping section. The
liquid portion of the feed serves as the reflux for this section.
The operating pressure of the column is typically controlled by adjusting heat removal
in the condenser.
The base of the column is typically used as a reservoir to hold liquid leaving the
bottom tray. A heat exchanger, the reboiler, is used to boil this liquid. The vapor
which results, the "boilup" (V) is returned to the column on one of the bottom three or
four trays.
In normal operation, there are five "handles" that can be adjusted to manipulate the
behavior of a distillation column -- the feed flow, two product flows, the reflux flow,
and the boilup flow (or reboiler heat input).
A normal column has a temperature gradient and a pressure gradient from bottom to
top.

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Distillation i

  • 1. Distillation I: Principles Definition & Purpose: Distillation is the most widely used separation process in the chemical industry. It is also known as fractional distillation or fractionation. It is normally used to separate liquid mixtures into two or more vapor or liquid products with different compositions. Distillation is an equilibrium stage operation. In each stage, a vapor phase is contacted with a liquid phase and mass is from vapor to liquid and from liquid to vapor. The less volatile, "heavy" or "high boiling", components concentrate in the liquid phase; the more volatile, "light", components concentrate in the vapor. By using multiple stages in series with recycle, separation can be accomplished. Operating Principles: The feed to a distillation column may be liquid, vapor, or a liquid-vapor mixture. It may enter at any point in the column, although the optimal feed tray location should be determined and used. More than one stream may be fed to the system, and more than one product may be drawn. A column is divided into a series of stages. These correspond to a cascade of equilibrium stages. Liquid flows down the column from stage to stage and is contacted by vapor flowing upward.
  • 2. Traditionally, most columns have been built from a set of distinct "trays" or "plates", so these terms end up being essentially interchangeable with "stages". Each tray in a distillation column is designed to promote contact between the vapor and liquid on the stage. Distillation can be conducted in a packed column (just as absorption can be done in a trayed column), but we will focus on trayed columns for the present. Stages may be numbered from top down or bottom up. When analyzing a stage, flows and compositions take the number of the stage they leave. The text for this class calls the top tray of the column "Tray 1" and numbers downward - - this is the convention we will use. MSH also denote the streams between the column top and condenser with an "a" subscript and those at the bottom with "b". Personally, I generally prefer to let "Tray 1" be the bottom tray of the column, the reboiler "Tray 0" and number upward (so if you catch me doing this, don't panic). I like this way of numbering because it tends to simplify computer based calculations. The product leaving the top of the column is called the overhead product, the "overhead", the "top product", the distillate, or "distillate product". Distillate product may be liquid or vapor (or occasionally both) depending on the type of condenserused. Most of the time the distillate flow rate is assigned the symbol D, and the composition xD or yD. The product leaving the bottom of the column is called the bottom product or "bottoms", and given the symbol B, with composition xB. In some situations, notably petroleum refining, one or more intermediate or "sidedraw" products may be removed from the column. Vapor leaving the top of the column passes through a heat exchanger, the condenser, where it is partially or totally condensed. The liquid which results is temporarily held in the "accumulator" or reflux drum. A liquid stream is withdrawn from the drum and returned to the top tray of the column as reflux (R or L) to promote separation. The portion of the column above the feed tray is called the rectification section. In this section, the vapor is enriched by contact with the reflux. The portion of the column below the feed tray is called the stripping section. The liquid portion of the feed serves as the reflux for this section. The operating pressure of the column is typically controlled by adjusting heat removal in the condenser.
  • 3. The base of the column is typically used as a reservoir to hold liquid leaving the bottom tray. A heat exchanger, the reboiler, is used to boil this liquid. The vapor which results, the "boilup" (V) is returned to the column on one of the bottom three or four trays. In normal operation, there are five "handles" that can be adjusted to manipulate the behavior of a distillation column -- the feed flow, two product flows, the reflux flow, and the boilup flow (or reboiler heat input). A normal column has a temperature gradient and a pressure gradient from bottom to top.