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The cloudiness or haziness of water, caused by suspended particles and colloids that are
invisible to naked eyes, is known as turbidity.
Turbidity measurements is performed using Nephelometric instruments. The Nephelometric
apparatus is designed to measure the suspended particles present in water samples that scatter a
portion of the light pass through the water. The scattered light is captured by a photodiode kept at
90 in the light path produce electronic signals that converted into turbidity in comparison with a
reference standard.
The Formazin solution is used as a standard for turbidity measurements as the particles of Formazin
are uniform in size and shape. The stock standard of 400 NTU.
Experiment No 2: Alkalinity
The alkalinity is defined as the amount of hydrogen ions (in moles) required to neutralise the
proton acceptor in 1 L of water.
if Phenolphthalein indicator is added to a sample with pH greater than 8.3, the colour of the sample
will turn to pink due to the presence of OH ions. If pH of the sample further reduced by adding a
sulphuric acid - H2SO4, the pink colour disappears at a pH of 8.3 due to the neutralization of OH
ions. Further, if Bromocresol green indicator is added to the sample at this point, colour will turn to
green, and titrated against H2SO4 the colour will from green to reddish violet at pH of 4.3 where all
the remaining chemical species contributing alkalinity will be neutralized.
Reagents
Winkler Reagent – I (Manganese Sulphate, MnSO4 solution)
Winkler Reagent – II (Alkaline Potassium Iodide, KI, solution)
Sulphuric acid (H2SO4)
Sodium Thiosulfate solution
Potassium Iodate standard
Starch Indicator solution
In two BOD bottles, fill them with water sample. fix one of the BOD bottles, by adding 1 mL of
Winkler Reagent – I and Winkler Reagent – II a brown precipitate will form (Initial DO)
Allow the precipitate to settle two third of the way to the bottom. Add I mL of sulphuric acid through
the wall of the bottle to dissolve the precipitate completely. Keep the other BOD bottle for
incubation at 20oC for 5 days. After five days of incubation, repeat the steps above steps and titrate
the sample. Take 50-mL of sample in flask. Check the burette to ensure that it is filled with of
thiosulfate solution. Place the flask under the burette and add thiosulfate solution drop-by-drop until
the solution turn pale yellow colour - STOP titration
Add 3 drops of starch solution into the flask, continue to titrate by adding thiosulfate
drop-by-drop just until the solution turns clear and colourless
Record the volume of thiosulfate added.
BOD = DO(in) – DO(final).
Initially EBT forms a weak EBT-Ca2+/Mg2+ complex that provide wine red colour with Ca2+/Mg2+
ions present in the hard water. On addition of EDTA solution, Ca2+/Mg2+ ions preferably form a
stable EDTA Ca2+/Mg2+ complex with EDTA, leaving the free EBT indicator in solution which is steel
blue in colour in the presence of ammonia buffer.
Vol of EDTA solution consumed (mL) × 1000
Total Hardness (ppm) = ---------------------------------------------------------
Volume of water taken (mL)
Temporary hardness = Total hardness - Permanent hardness (ppm)
Experiment No 7: Iron concentration in water
WHO limit the amount of iron to less than 0.3 ppm (0.3 mg/L) in drinking water.
A commonly used method for the determination of trace amounts of iron involves the
complexation of Ferrous ion (Fe2+) with 1,10-phenanthroline (phen) to produce an intensely
red orange coloured complex:
Fe2+ + 3 phen → Fe(phen)32+
The determination of the iron-phen complex is performed with a spectrophotometer at a fixed
wavelength of 510 nm using external calibration based on iron standard solutions.