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Diagram of a Batch Rectifier. The simplest and most frequently used batch distillation configuration is the batch rectifier, including the alembic and pot still.The batch rectifier consists of a pot (or reboiler), rectifying column, a condenser, some means of splitting off a portion of the condensed vapour (distillate) as reflux, and one or more receivers.
Here the distillation head and fractionating column are combined in one piece. Differential centrifugation . Fractionation is a separation process in which a certain quantity of a mixture (of gasses, solids, liquids, enzymes , or isotopes , or a suspension ) is divided during a phase transition , into a number of smaller quantities ( fractions ...
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.
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.
For rectification and stripping a countercurrent liquid phase must flow through the column, so that liquid and vapour can contact each other on each stage. The distillation column is fed with a mixture containing the mole fraction xf of the desired compound.
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. To achieve the low distillation temperatures, an air separation unit requires a ...
In this case the mixture components A and B are separated in the first column through the solvent E (recovered in the second column). Extractive distillation is defined as distillation in the presence of a miscible , high-boiling, relatively non-volatile component, the solvent , that forms no azeotrope with the other components in the mixture.
To design a distillation unit or a similar chemical process, the number of theoretical trays or plates (that is, hypothetical equilibrium stages), N t, required in the process should be determined, taking into account a likely range of feedstock composition and the desired degree of separation of the components in the output fractions.