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The distillation column is fed with a mixture containing the mole fraction xf of the desired compound. The overhead mixture is a gas or an aerosol which contains the mole fraction xD of the desired compound and the bottom product contains a mixture with the fraction xB of the desired compound.
The McCabe–Thiele method is a technique that is commonly employed in the field of chemical engineering to model the separation of two substances by a distillation column. [ 1 ] [ 2 ] [ 3 ] It uses the fact that the composition at each theoretical tray is completely determined by the mole fraction of one of the two components.
The vacuum distillation column internals must provide good vapor–liquid contacting while, at the same time, maintaining a very low-pressure increase from the top of the column top to the bottom. Therefore, the vacuum column uses distillation trays only where products are withdrawn from the side of the column (referred to as side draws ).
A fractionating column or fractional column is equipment used in the distillation of liquid mixtures to separate the mixture into its component parts, or fractions, based on their differences in volatility. Fractionating columns are used in small-scale laboratory distillations as well as large-scale industrial distillations.
Modeling and simulation of batch distillation unit is done with the help of one of the most important process simulators (aspen plus) used in chemical industry with the following data given in the table and check the simulation result. Various steps are involved in the simulation of batch distillation column using aspen plus software is :
Distillation column in a cryogenic air separation plant. The cryogenic separation process [4] [5] [6] requires a very tight integration of heat exchangers and separation columns to obtain a good efficiency and all the energy for refrigeration is provided by the compression of the air at the inlet of the unit.
The concept of theoretical plates in designing distillation processes has been discussed in many reference texts. [2] [3] Any physical device that provides good contact between the vapor and liquid phases present in industrial-scale distillation columns or laboratory-scale glassware distillation columns constitutes a "plate" or "tray". Since an ...
The pressure at the top is maintained at 1.2–1.5 atm [2] so that the distillation can be carried out at close to atmospheric pressure, and therefore it is known as the atmospheric distillation column. [3] The vapors from the top of the column are a mixture of hydrocarbon gases and naphtha, at a temperature of 120 °C–130 °C.