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Author Topic: How does laboratory scale differ from industrial scale opeartions?  (Read 14270 times)

Offline omid

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apologies for my wrong assumption
yeah thats what i am looking for if you can please help ???
 

Offline Chemistry4me

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Here's is one on distillation
 

Offline Chemistry4me

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But for some reason I can't post the link, here is half of it:

Laboratory scale distillation
Laboratory scale distillations are almost exclusively run as batch distillations. The device used in distillation, sometimes referred to as a still, consists at a minimum of a reboiler or pot in which the source material is heated, a condenser in which the heated vapour is cooled back to the liquid state, and a receiver in which the concentrated or purified liquid, called the distillate, is collected. Several laboratory scale techniques for distillation exist (see also distillation types).

Simple distillation
In simple distillation, all the hot vapors produced are immediately channeled into a condenser which cools and condenses the vapors.

As a result, simple distillation is usually used only to separate liquids whose boiling points differ greatly (rule of thumb is 25 C), or to separate liquids from involatile solids.

Fractional distillation
For many cases, the boiling points of the components in the mixture will be sufficiently close that Raoult's law must be taken into consideration.

As the solution to be purified is heated, its vapors rise to the fractionating column. A spinning band distillation system uses a spinning band of Teflon or metal to force the rising vapors into close contact with the descending condensate, increasing the number of theoretical plates.

Steam distillation
Like vacuum distillation, steam distillation is a method for distilling compounds which are heat-sensitive.

Steam distillation of various aromatic herbs and flowers can result in two products;

Vacuum distillation
Some compounds have very high boiling points. Once the pressure is lowered to the vapor pressure of the compound (at the given temperature), boiling and the rest of the distillation process can commence.

This technique is also very useful for compounds which boil beyond their decomposition temperature at atmospheric pressure and which would therefore be decomposed by any attempt to boil them under atmospheric pressure.

Air-sensitive vacuum distillation
Some compounds have high boiling points as well as being air sensitive. A simple vacuum distillation system as exemplified above can be used, whereby the vacuum is replaced with an inert gas after the distillation is complete.

The Perkin triangle, has means via a series of glass or teflon taps to allows fractions to be isolated from the rest of the still, without the main body of the distillation being removed from either the vacuum or heat source, and thus can remain in a state of reflux. A fresh collection vessel can then be added to the system, evacuated and linked back into the distillation system via the taps to collect a second fraction, and so on, until all fractions have been collected.

Azeotropic distillation
Interactions between the components of the solution create properties unique to the solution, as most processes entail nonideal mixtures, where Raoult's law does not hold. At an azeotrope, the solution contains the given component in the same proportion as the vapor, so that evaporation does not change the purity, and distillation does not effect separation.

If the azeotrope is not considered sufficiently pure for use, there exist some techniques to break the azeotrope to give a pure distillate.

Short path distillation
Short path distillation is a distillation technique that involves the distillate traveling a short distance, often only a few centimeters. A classic example would be a distillation involving the distillate traveling from one glass bulb to another, without the need for a condenser separating the two chambers. Advantages are that the temperature of the boiling liquid does not have to be much higher than the boiling point of the distilling substance, and the gases only have to travel a short distance while in the gas-phase before they can be cooled again to a lower temperature.

Other types
In rotary evaporation a vacuum distillation apparatus is used to remove bulk solvents from a sample. In a kugelrohr a short path distillation apparatus is typically used (generally in combination with a (high) vacuum) to distill high boiling (> The apparatus consists of an oven in which the compound to be distilled is placed, a receiving portion which is outside of the oven, and a means of rotating the sample. The process of reactive distillation involves using the reaction vessel as the still. Destructive distillation involves the strong heating of solids (often organic material) in the absence of oxygen (to prevent combustion) to evaporate various high-boiling liquids, as well as thermolysis products. The gases evolved are cooled and condensed as in normal distillation. The destructive distillation of wood to give methanol is the root of its common name - wood alcohol. Dry distillation, despite its name, is not truly distillation, but rather a chemical reaction known as pyrolysis in which solid substances are heated in a strongly reducing atmosphere and any volatile fractions are collected. 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. Freeze distillation is an analogous method of purification using freezing instead of evaporation. It is not truly distillation, and does not produce products equivalent to distillation.

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Google some of those words and you should find it.
 

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