VOLUMETRIC ANALYSIS
Standard Volumetric Apparatus
Volumetric Apparatus
Use volumetric apparatus
We
have seen that volumetric analysis involves determinations of
quantities of substances, usually acids and alkalis, present in volumes
of solutions. This is usually done by using measuring apparatus.
Apparatus
used in volumetric analysis is based on volume measurements and since
the analysis demands high accuracy, the apparatus has to be calibrated
with the highest possible accuracy. It is for this reason that all
apparatus for volumetric analysis are specifically for this and not
other purposes.
Apparatus
used for volumetric analysis include, burette, pipette, burette stand,
white tile, conical flask, filter funnel, reagent bottle, watch glass,
beaker, measuring cylinder and measuring flask (or volumetric flask).
For approximate measurements, measuring cylinders may be used. For
accurate measurements of volumes, volumetric flasks are used.
Burette
This
is a long glass tube with a narrow lower part, which is fitted with a
tap that controls the amount of solution let out of the burette. This
instrument is calibrated from 0 to 50 cm3.Before measuring
the solution, rinse the burette with distilled water, then with the
solution it is going to hold. It has to be filled to the tip and all gas
bubbles removed. Thus, the burette is an apparatus used for
transferring the solution to the titration vessel (normally a flask).
Pipette
This
apparatus has a wider middle part with narrow parts at either ends. The
upper narrow part has a mark which marks the volume of all the space
below it. If, say, the pipette is one that is marked 25 cm3, we can say that a solution, when filled in the pipette up to this mark, will have a volume of 25 cm3.
The
pipette is used in transferring a standard solution to the titration
flask. There are many types of pipettes depending on their volume
capacity. The common ones are the 25-cm3 and 20-cm3 capacity pipettes. Less common ones are the 10-cm3
capacity.Before measuring the solution, rinse the pipette several times
with distilled water and then with the solution to be measured; suck
the rinsing solution above the graduated mark, then discard the rinsing.
The
pipette is commonly filled by mouth suction but the use of pipette
fillers is highly recommended. When using a pipette, never blow out the
last drop.
Measuring (Volumetric) flask
The
flask is made of glass and has a mark at the upper part of the narrow
tube. The space in the flask up to this mark represents a certain
volume. If a solution is filled up to this mark, the volume of the
solution is equal to the volume indicated by inscriptions on the flask
e.g. 50 cm3, 100 cm3, 150 cm3, 250 cm3, 500 cm3, etc.
Filter funnel
A
filter funnel is required for effective transfer of the weighed solid,
liquid or solution into the volumetric flask or burette.
Wash bottle
Wash
bottle contains water and when squeezed, water squarts out. This is
used in washing down the remains of the weighed solid into the
volumetric flask.
A weighing bottle
This is used in weighing the solute. It is a stoppered bottle. A watch glass can also be used to serve the same purpose.
Retort stand
A burette stand is used for holding the burette in place while carrying out volumetric analysis experiments.
Dropper
A dropper is used to add the indicator dropwise into the solution.
White tile or paper
A
white tile or piece of paper is placed under the flask to give a clear
background for accurate observation of the colour change at the end of
the reaction (end point).
Standard Solutions
The Steps for Preparation of Standard Solutions of Common Acids
Explain the steps for preparation of standard solutions of common acids
A standard solution is a solution of known concentration. For example, a solution containing 15g of sulphuric acid in 1 dm3 of solution is a standard solution.
It has now been approved that volumetric work should be based upon the molar (M) solution. A 1 molar (1M) solution of a compound is a solution which contains one mole of that compound in 1 dm3 of the solution. For example, 58.5g of sodium chloride (NaCl) dissolved in 1 dm3 of the solution makes a molar solution of sodium chloride (1M NaCl). Likewise, 106g of sodium carbonate (Na2CO3) in 1 dm3
of the solution gives a molar solution of sodium carbonate. Therefore, a
1 molar sodium carbonate solution contains 106g of the salt in 1 dm3 of the solution.
1 molar solution of some compounds commonly used in titration contain the following masses of the compounds in 1 dm3 of solution:
Derivative concentrations are also used e.g. 0.1M, 0.5M. 2M, etc.
Preparation of standard solutions
A
standard solution is required as a starting point for volumetric
analysis. We learned early that in order to find the unknown
concentration of a substance in volumetric analysis, the concentration
of one of the solutions must be known.
A
small range of substances are suitable for direct preparation of
accurately standard solutions. Substances that cannot be used for direct
preparation of standard solutions include sodium hydroxide, potassium
hydroxide and concentrated sulphuric acid. These substances absorb water
vapour from the air and hence cannot be weighed out precisely without
taking extra precautions. Apart from absorbing water vapour from the
air, sodium and potassium hydroxides react with carbon dioxide of the
air to form respective carbonates.
2NaOH(s) + CO2(g)→ Na2CO3(s) + H2O(l)
2KOH(s) + CO2(g)→ K2CO3(s) + H2O(l)
Some
solutions are volatile in nature and so are likely to change slowly in
concentration during ordinary use. These include concentrated
hydrochloric acid and ammonia.
A
compound commonly used for preparation of a precisely standard solution
is anhydrous sodium carbonate. It is best prepared from highly pure
sodium carbonate. This is achieved by heating sodium bicarbonate to
constant mass to make sure the compound is fully decomposed.
2NaHCO 3(s) →Na2CO3(s) + H2O(g) + CO2(g)
The
sodium carbonate so formed is suitable for preparation of a standard
solution and can be weighed without undergoing any appreciable change in
composition.
Precautions to be observed while preparing a standard solution
- Transference of the substance from the weighing bottle to the beaker or flasks should be done with outmost care so that not a single particle of the substance is lost.
- Undissolved substance should not be transferred to the measuring flask. Make sure all the solid dissolves into solution before transferring the solution to flask.
- During making up of the volume, the last drop of the water should be added carefully. Do not blow out the final drop.
Standard Solutions of Bases
Prepare standard solutions of bases
Preparation of 0.1M sodium carbonate solution
The molecular mass of sodium carbonate (Na2CO3) is 106g. Therefore, a molar (1M) solution of sodium carbonate contains 106g in 1 dm3 (1000 cm3) of solution.
In
order to prepare 0.1M solution of the carbonate, we have to weigh 10.6g
of the carbonate and put it into a volumetric flask, which has a
capacity of 1000 cm3.
However, normally 250 cm3 flasks are used. This means, in a 250 cm3 flask we have to add 10.6/4= 2.65g calcium of sodium carbonate.
Thus, 1000 cm3 ≡ 10.6g
250 cm3 ≡ X g
X = 250/1000×10.6 = 10.6/4 = 2.65g
The same procedure can be followed when preparing 0.25M, 0.5M, 2M, etc. of the solutions.
Procedure
- Weigh exactly 2.65g of sodium carbonate using a common balance and put it onto a watch glass.
- Transfer it slowly into a beaker of 500-cm3 capacity containing about 50 cm3 of hot distilled water.
- Wash down the watch glass with a jet of hot distilled water from a wash bottle and allow the washings to fall into the beaker (figure 5.7). Make sure all the sodium carbonate is washed into the beaker.
- Stir with a glass rod until all the solid is completely dissolved, and then cool the solution to room temperature. Leave the rod standing in the solution.
- Pour the solution carefully down the glass rod into a 250 cm3 measuring flask.
- Wash the beaker out at least twice with jets of cold distilled water directed round the slides and pour the washings down the glass rod into the measuring flask (figure 5.8).
- Shake the flask gently and fill it up with cold distilled water almost to the mark.
- Add more distilled water drop by drop from a pipette until the meniscus is on the graduation mark (figure 5.9).
- Stopper the measuring flask and shake well. The liquid should then be exactly 0.1M sodium carbonate solution.
Preparation
of standard solutions of other bases of different molarities e.g. 0.2M,
0.5M, 1.0M, 2.0M, etc. can be achieved by using the above procedures.
The only variable will be the weight of the solids and volume of water
as stated early.
Acid-base Titration Experiments
Carry out acid-base titration experiments
Preparation of 0.1M sulphuric acid solution
A
standard solution of sulphuric acid cannot be prepared directly because
concentrated sulphuric acid is hygroscopic in nature (it tends to
absorb water vapour from the air diluting itself) and is never reliably
pure. A solution a little above 0.1M is prepared and then standardized
and diluted with distilled water to exactly 0.1M.A molar solution of H2SO4 contains 98g of pure acid in 1 dm3. Therefore, the 0.1M acid contains 9.8g of the acid in 1 dm3 of the solution. The pure concentrated acid has a density (concentration) of about 1.8g/cm3. So, 9.8g of it occupy about 9.8/1.8 = 5.5cm3
The preparation of a standard solution of sulphuric acid involves two stages:
- Diluting a concentrated solution of the acid to an approximate molarity.
- Finding the exact concentration of the acid (standardizing it) by titrating it against a standard solution of a base (previously prepared).
Dilution of concentrated sulphuric acid
Caution: Make sure you wear safety goggles and gloves before carrying out this experiment.
Procedure
- Cautiously, because the acid is very corrosive, take 5.5 – 6.0 cm3 of concentrated sulphuric acid in a small measuring cylinder.
- Pour the acid carefully, with stirring, into a 250-cm3 volumetric flask containing about 100 cm3 of cold distilled water.
- Pour this solution into, say, 700cm3 of cold distilled water in a measuring flask of capacity 1000cm3.
- Wash out the acid solution remaining in the measuring cylinder with cold distilled water twice and add the washings into the measuring flask.
- Then add distilled water approximately to the mark on the measuring flask, stopper it, and shake well.
This
should give sulphuric acid of concentration a little above 0.1M. The
diluted acid is now standardized with the 0.1M sodium carbonate solution
prepared above.
Determination
of the molarity (standardization) of sulphuric acid solution by
titrating it against 0.1M sodium carbonate solution
The estimation of the concentration of a solution of an acid by reacting the acid with a standard alkali solution is known as titration. The end-point of an acid-base reaction is commonly determined by using a substance known as an indicator.
Procedure
- Measure 25 cm3 of 0.1M sodium carbonate solution and transfer it into a conical flask, using a pipette. Add a few drops of methyl orange indicator. This will turn the sodium carbonate solution yellow.
- Set up the apparatus as shown in figure 5.10
- Pour the acid into a 50-cm3 burette. Read and note the level of the acid in the burette.
- By means of a tap at the base of the burette, drip the acid slowly into the conical flask, swirling the flask continuously until the colour of the liquid in the flask turns orange. This is the end-point of titration. Record the new level of acid in the burette.
- Repeat the titration three to four times, noting the initial and final reading of the burette each time.
- Find the volume of the acid as shown below:
Titration | Rough titration (Pilot) | Titre 1 | Titre 2 |
Final burette reading | 24.20 | 23.65 | 23.55 |
Initial burette reading | 0.00 | 0.00 | 0.00 |
Volume of acid added | 24.20 | 23.65 | 23.55 |
Neglecting the first (rough) trial run, the average titration is 23.60 cm3
Calculation
The
first step in calculating the molarity of any solution from the results
of an acid-base titration is to write the equation for the reaction.
From the equation, find the number of reacting moles of the acid and
base.
Na2CO3(aq)1 mole+ H2SO4(aq)1 mole→Na2SO4(aq) + CO2(aq) + H2O(l)
Now we have the following data.
- Volume of acid, Va = 23.60 cm3
- Volume of base, Vb = 25.00 cm3 (this is the average amount of the base that was added to the flask in titration)
- Molarity of acid, Ma = ?
- Molarity of base, Mb = 0.1M
- Number of moles of acid, Na = 1
- Number of moles of base, Nb = 1
The molarity of the acid can be calculated from the following general formula:
The concentration of sulphuric acid is 0.106M.
To
make the molar concentration of the sulphuric acid solution exactly
equal to that of the sodium carbonate solution (0.1M), 23.6 cm3of the acid must be diluted to 25 cm3, that is, 1.4 cm3of distilled water must be added to 23.6 cm3of the acid.
Remember
it was stated early that in order to prepare 0.1M sulphuric acid
solution, you need to dissolve 9.8g of the acid in 1000 cm3 (1 dm3) of distilled water. Assume that some of the acid was wasted through spillage and mishandling and that only 920 cm3 of the acid was left. If, say, 920 cm3 of the acid was left, it can be made exactly 0.1M by the addition of 920×1.4/23.6 = 55cm3of distilled water. This gives exactly 0.1M of the acid. This is the same as saying that, if 23.6 cm3 of the acid were diluted with 1.4cm3 of distilled water, then 920cm3 of the acid would be diluted with
If, for instance, the volume of acid left was, say, 850 cm3, the amount of distilled water to be added would be = 850×1.4/23.6 = 50.4cm3. This, also, would give exactly 0.1M of the acid.
In
principle, the amount of distilled water to be added is always
calculated based on the amount of the acid left as exemplified above.
These
two standard alkaline and acidic solutions can be used to standardize
other solutions, e.g. sodium hydroxide, potassium hydroxide,
hydrochloric acid, nitric acid, etc. You may dilute any base or
commercial acid to some required concentration e.g. 0.2M, 0.5M, 0.25M,
etc and then standardize it by similar procedures.
Choice of indicators in acid-base titration
We
learned early that the estimation of the concentration of a solution of
an acid or base by reaction with a standard alkali or acid solution
respectively, is known as titration. The end-point of an acid-base
titration is commonly determined using substances known as indicators,
which usually portray certain characteristic colours when in alkaline or
acid solutions.
The
indicators in acid-base titrations must be chosen carefully because the
choice of an inappropriate indicator would lead to an incorrect result.
The choice of an indicator is based on the strength of an acid or base
involved in the reaction.
There
are three common indicators which are used in titration experiments
involving acids and bases namely, methyl orange, litmus and
phenolphthalein. The other indicators in less common use are as included
in the table below. The table shows the colours which each of these
indicators take up in acid or alkaline solution.
Indicator Colour of indicator |
acid solution alkaline solution |
Methyl orange pink yellow |
Litmus red blue |
Phenolphthalein colourless pink |
Malachite green yellow blue/green |
Thymol blue red yellow |
Bromocresol green yellow blue |
Bromothymol blue yellow blue |
Indicators suitable for particular types of acid-base reactions are as given in the table below: