Skip to main content

Renin Angiotensin Mechanism.

Pharmaceutical Sieves.

 Pharmaceutical Sieves.


  • Sieves are the simplest and sieving is the most frequently used method for size separation.

Construction:

  • Sieves for pharmaceutical testing are constructed from wire cloth with square meshes, woven from wire ,of brass, bronze, 'stainless'' steel or any suitable materials.

  • Sieves should not be coated or plated.

  • There must be no reaction between the material of the sieve and the substance to be sieved

Types of Sieves:

  1. Woven wire sieves.

  2. Plain weave

  3. Twilled weave

  4. Bolting cloth sieves.

  5. Bar screens.

  6. Punched  plates (Perforated Screens)

Standards of Sieves:

  • Common standards used for sieves are: 

    • (a) Tyler standard sieve series (in USA) 

    • (b) US standard. sieve series (in USA) 

    • (c) British standard sieve series (in UK) 

    • (d) German DIN (Deutsche lndustrienormein) (in Germany"and Europe) 

    • (e) IP standard sieve series (in India) 

    • (f) International test sieve series (ISO) (World wide).

  • It is required that wire-mesh sieves will be made from wire of uniform, circular cross-section and for each sieve the following particulars are stated.

Sieve Number:

  • This is the number of meshes in a length of 25.4mm (i.e. 1 inch), in each direction.

Nominal size aperture:

  • This is the distance between the wires, so that it represents the length of the side of the square aperture. 

Nominal diameter of the wire:

  • The wire diameter is selected to give a suitable aperture size. 

  • It is also required to give the necessary strength to avoid distortion.

  • The diameter of the wire is represented by Standard Wire Gauge.


Approximate screen area:

  • This standard expresses the area of the meshes as a percentage of the total area of the sieve.

  • It is governed by the diameter of the wire. 

  • It is generally kept within 35 to 45% of the total area of the sieve.

  • This represents the useful area of a sieve. Greater screen area is preferred.

Aperture tolerance average:

  • Some variation in the aperture size is unavoidable and this variation is expressed as a percentage, known as aperture tolerance average.

  • It is the maximum limit within which the dimension of meshes can be allowed to vary and still be acceptable for sieving.

  • Finer wires are likely to be subject to a greater proportional variation in diameter than coarse mesh.

Commonly Asked Questions.

  1. Define,

    1. Aperture tolerance average.

    2. Approximate screen area.

    3. Nominal diameter of the wire.

    4. Sieve Number.

    5. Nominal size aperture.

  2. Write a short note on “Pharmaceutical Sieves”.

Popular posts from this blog

Rate of Drying Curve.

  Definition Drying is defined as the removal of liquid from a product usually with application of heat. Rate of Drying Curve. Drying process can be divided into three periods Initial Adjustment Period. Constant drying rate period. First falling drying rate period. Second falling rate period. Initial Adjustment Period (A-B): Also called the “ Heating up” period . In this period the substance gets heat and increases in temperature. Drying has not yet started. Constant drying rate period (B-C): During this period the temperature of the solid and the rate of drying remain constant. The moisture evaporating from the surface is replaced by water diffusing from the interior of the solid at a rate equal t o the rate of evaporation.  The moisture content at the end of constant rate (point C) is referred to as the critical moisture content (CMC).  At CMC, dry spots start appearing and drying rate starts falling . First falling drying rate period (C-D): This period is also called the period of

Heat Exchangers and Heat Interchangers.

  In pharmaceutical industries many types of equipments are used for transfer of heat, they can be classified as follows, Heat Exchangers. Heat Interchangers. Heat Exchangers: These devices are used for transferring heat from a fluid (Hot Gas or Steam) to another fluid (Liquid) through a metal wall. Heat Interchangers: These devices are used for transferring heat from a One liquid to another liquid or one gas to another gas through a metal wall. HEAT EXCHANGERS; The equipment used for heat transferring are known as heat exchangers. Some of the processes that involves heat transfer in pharmaceutical industries are: Preparation of starch paste (in steam jacketed kettle). Crystallization. Evaporation. Distillation.  Classification of heat exchangers On the basis of transfer of heat, heat exchangers are classified as: Direct transfer type:  The hot and cold fluids are separated by a metal wall through which the heat is transferred from hot fluid to cold fluid. E.g. shell and tube heater, 

Flash Distillation.

  Principle: When a hot mixture is allowed to enter from a high-pressure zone into a low pressure zone, the entire liquid mixture is suddenly vaporized. This process is known as flash vaporization .  During this process, the chamber is cooled.  The less volatile fraction is condensed and the more volatile component remains in the vapor phase .  This process requires time, hence liquid and vapor are kept in intimate contact until equilibrium is achieved. Flash distillation is also called equilibrium distillation because separation of two liquids takes place when liquid and vapor phases are at equilibrium. Equipment used for Flash Distillation: Construction: It consists of a pump, which is connected to a feed reservoir.  Pumps help in pumping the feed into the heating chamber.  The heating chamber is heat supplied by steam.  The other end of the pipe is directly introduced into the vapor-liquid separator through a reducing valve.  The vapor outlet is provided at the top of the separato