Monday, 13 June 2016

Preparation of Some Standard Solutions Used in the Laboratory

A standard solution is a solution whose concentration is known. Standard solutions are prepared in advance or at demand and kept on the bench in the laboratory for use. A standard solution of a substance can be prepared, if the substance can be obtained in pure form state, by weighing accurately a definite mass of the substance, dissolving it in a suitable solvent, usually water, and making up the solution to a known volume in a volumetric flask.

When a substance is not available in pure form, a solution of approximate concentration required is first prepared, and then standardized (that is, its concentration determined) by titrating against a standard solution of a pure substance.
Standard solutions of common acids and alkalis cannot be prepared by direct weighing. Reasons: some of them are volatile and corrosive liquids, for example HCl, HNO3 and ammonia; while H2SO4 is hygroscopic. Others are solids that are deliquescent and hence absorbs moisture and carbon(IV)oxide, from the atmosphere, for example KOH and NaOH pellets.

Types of standard solutions include;

1.     Primary standard: a substance which can be obtained in a high state of purity, anhydrous, non-deliquescent, non-hydroscopic, readily soluble in water or in the required solvent, and hence suitable for the preparation of standard solution. Examples are anhydrous sodium trioxocarbonate(IV), NaCO3 and benzoic acid C6H5COOH.
2.     A substance which is hydrated, but does not efflorescent can be used in the preparation of a standard solution. An example is the dibasic organic acid called ethanedioic acid. (H2C2O4) (Oxalic acid).
Example of preparation of some solutions

To prepare 2 Molar HCl

From calculation 89ml is dissolved in 1liter of distilled water to get one molar solution of HCl.
NB: HCl is a monobasic acid, therefore its molarity and normality is the same?
89mls of HCl 1Molar 1Litre
2×89mls of HCl 2molar 1Litre
That is, 178mls of HCl 2molar 1Litre.

For tetraoxosulphate (VI) H2SO4

Molecular weight Mw =98
(Mw  %purity) × (100÷specific gravity)
Therefore (98.07 )
54.4ml of H2SO4 1000mls of H2O 1M

To prepare 0.1NaOH (sodium hydroxide)

Molecular weight of NaOH =40g
To get the mass in o.1m =40×0.1=4g
Therefore 4g in 1dm3 of distilled water
4grams of NaOH pellets/crystals will be measured and dissolved and be made up to 1liter of distilled water to get 0.1m concentration.

Stock solution

This is to prepare different concentration from already prepared solution.
Use the following equation V1= (M2V2÷M1)
Were V1=Initial volume; V2=final volume; M1=initial mole; M2=final mole which is the new desired mole.

QUANTITATIVE DETERMINATION OF CAFFEINE IN BEVERAGES AND SOFT DRINKS USING UV. SPECTROSCOPY

·       Determination of caffeine in Igbo kola nut, Hausa kolanut and coca cola.
Caffeine is a naturally occurring alkaloid which is found in the leaves, seeds or fruits of over 63 plant species world wide.
The most common sources of caffeine are
1.     Coffee
2.     Cocoa beans
3.     Colanut
4.     Tea leaves
Method
Reagent used
1. Caffeine
2.Dichloromethane
3.Purified H20
Aim: To extract caffeine from the sample by the use of chloroform.
Procedure
·   Hausa and Igbo kolanut was grated. Then allowed to dry after drying it was grinded with an electric grinder into powder form.
·   2g was measure and poured into a conical flask.
·  Water was boiled and then 200ml of the boiled water was measured and then added to the sample in the beaker and placed in a magnetic stirrer to stir for 30mins.
·  After adding boiled water to the sample and stir for 30min. It was allowed to cool @ room temperature.
·   200ml of coca cola was measured and heated.
·   Allowed to cool.
·   The sample was washed with 25ml of chloroform to extract the caffeine.
Note: Wash for 3 times
After extracting the caffeine from the sample it was taken to uv spectroscopy and then read @ spec. 450nm.
The concentration of caffeine was taken in ppm (part per million) which is as follows 55.358 x ABS.

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