Separation operations achieve their objective by the creation of two or more coexisting zones which differ in temperature, pressure, composition, and/or phase state. Each molecular species in the mixture to be separated reacts in a unique way to differing environments offered by these zones. Consequently, as the system moves toward equilibrium, each species establishes a different concentration in each zone, and this results in a separation between the species.
The separation operation called distillation utilizes vapor and liquid phases at essentially the same temperature and pressure for the coexisting zones. Various kinds of devices such as random or structured packings and plates or trays are used to bring the two phases into intimate contact. Trays are stacked one above the other and enclosed in a cylindrical shell to form a column. Packings are also generally contained in a cylindrical shell between hold-down and support plates. A typical tray-type distillation column plus major external accessories is shown schematically in Fig. 13-1.
The feed material, which is to be separated into fractions, is introduced at one or more points along the column shell. Because of the difference in gravity between vapor and liquid phases, liquid runs down the column, cascading from tray to tray, while vapor flows up the column, contacting liquid at each tray.
Liquid reaching the bottom of the column is partially vaporized in a heated reboiler to provide boil-up, which is sent back up the column. The remainder of the bottom liquid is withdrawn as bottoms, or bottom product. Vapor reaching the top of the column is cooled and condensed to liquid in the overhead condenser. Part of this liquid is returned to the column as reflux to provide liquid overflow. The remainder of the overhead stream is withdrawn as distillate, or overhead product. In some cases only part of the vapor is condensed so that a vapor distillate can be withdrawn.
This overall flow pattern in a distillation column provides counter-current contacting of vapor and liquid streams on all the trays through the column. Vapor and liquid phases on a given tray approach thermal, pressure, and composition equilibriums to an extent dependent upon the efficiency of the contacting tray.
The lighter (lower-boiling) components tend to concentrate in the vapor phase, while the heavier (higher-boiling) components tend toward the liquid phase. The result is a vapor phase that becomes richer in light components as it passes up the column and a liquid phase that becomes richer in heavy components as it cascades downward. The overall separation achieved between the distillate and the bottoms depends primarily on the relative volatilities of the components, the number of contacting trays, and the ratio of the liquidphase flow rate to the vapor-phase flow rate.
If the feed is introduced at one point along the column shell, the column is divided into an upper section, which is often called the rectifying section, and a lower section, which is often referred to as the stripping section. These terms become rather indefinite in multiple-feed columns and in columns from which a liquid or vapor sidestream is withdrawn somewhere along the column length in addition to the two end-product streams.
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