Basic Principles and methodology of distillation
- 1. DISTILLATION Akanksha Patel Asst prof. Tagore Institute of Pharmacy and Research, Bilaspur (c.g.)
- 2. DEFINITION • "Distillation is an unit operation which involves separation of a vaporizable component from a multi- component system and subsequent condensation of vapours." • "Distillation is a process of separating the component substances from a liquid mixture by selective evaporation and condensation.“ • Applications- • Separation of volatile oils- cloves(EugenoI comprises 7290%, Vanilin, acetyl eugenol). • Separation of drugs obtained from plant and animal sources- Vit. A from fish liver oil. • Purification of organic solvents-absolute alcohol (100%). • Purification of drugs obtained from chemical process. • Manufacture of official preparations -sprit of nitrous ether, sprit of ammonia, D.water and water for inj. • Refining of petroleum products- Petroleum ether 60,80. • Quality control methods- Alcohol content in elixir(4-40%).
- 3. CLASSIFICATION • Simple Distillation (Differential distillation) • Flash Distillation (Equilibrium distillation) • Vacuum distillation (distillation under reduced pressure) IV. • Molecular Distillation (Evaporation distillation or short path distillation.) • Fractional Distillation (Rectification) • Aezotropic and extractive Distillation • Steam Distillation • Destructive Distillation • Compression Distillation
- 4. SIMPLE DISTILLATION Objective: Simple distillation is the process of converting a liquid into its vapors which, are passed through a cooling surface to condense the vapors. The condensed vapors are reformed into liquid which, is collected in a receiver. Apparatus construction for laboratory scale: It consists of a distillation flask with a side arm sloping downward that is connected to a condenser. The condensed vapors are collected in a flask called ‘receiver’. The whole apparatus is made of glass. A thermometer is fitted in the distillation flask to note down the temperature at which, the vapors are distilled. Bumping is avoided by adding small pieces of porcelain or porous pot before distillation. Application of simple distillation in pharmacy i. It is used for the preparation of distilled water and water for injection. ii. Many volatile oils and aromatic waters are prepared by simple distillation e.g. Spirit of nitrous ether and Aromatic Spirit of Ammonia iii. Concentration of liquid and to separate non-volatile solid from volatile liquids such as alcohol and ether.
- 6. EQUILIBRIUM DISTILLATION / FLASH DISTILLATION • Equilibrium distillation or flash distillation This is a single stage operation where a liquid is partially vaporized, the vapors are allowed to come in equilibrium with the residual liquid and the resulting vapors and liquid are separated. • Use: This method is used only when the difference between volatilities of two components is very large.
- 7. FRACTIONAL DISTILLATION Construction- A rectifying unit consists primarily of (a) a still or reboiler, in which vapor is generated, (b) a rectifying or fractionating column through which this vapor rises in counter- current contact with a descending stream of liquid, and (c) a condenser, which condenses all the vapor leaving the top of the column, sending part of this condensed liquid (the reflux) back to the column to descend counter to the rising vapors, and delivering the rest of the condensed liquid as product. As the liquid stream descends the column, it is progressively enriched with the less volatile. Advantages i) Have a low pressure drop per unit of height than bubble cap ii) For very small diameters of column, where it would be difficult to get in more than two or three bubble caps, a packed column can be used. iii) Since Raschig rings can be made of any material, hence packed columns can be used for corrosive materials. iv) The amount of liquid held up in the column is low so thermolabile liquid remains in contact with high temperature for a short time than bubble cap method. Disadvantages i. They are relatively inflexible. ii. Distribution of liquid uniformly in such packed column is difficult. It is found that, as the liquid passes down the tower it tends to concentrate at the walls and leave the center dry.
- 8. STEAM DISTILLATION • Theory: Liquid boils when its vapor pressure is equal to the atmospheric pressure. Liquids, which are decomposed at their boiling point under atmospheric pressure, can be distilled at a much lower temperature than its boiling point if the pressure is reduced on the surface of the liquid. Boiling under reduced pressure will also increase the rate of distillation. • Principle- • A mixture Of immiscible liquids begins to boil when sum Of their vapour pressure is equal to atmospheric pressure. • In case Of mixture Of water and turpentine, mixture boils below the boiling point Of pure water, though the turpentine boils at a much higher temperature than that of water • Limitation Not suitable when two immiscible liquids reacts with each other.
- 10. MOLECULAR DISTILLATION Theory / Principle of Molecular Distillation: In a high vacuum distillation operation, where the material distils from an evaporating surface to a relatively cool condensing-surface. The conditions are such that, the mean free path of the distillation molecules is greater than the distance between the evaporating and condensing surface. Mean free path is defined as the average distance travelled by the molecules in a straight line without any collision.
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