Showing posts with label Limit test. Show all posts
Showing posts with label Limit test. Show all posts

Saturday, October 16, 2021

Limit test for chlorides in sodium bicarbonate

Learn the limit test for chlorides in sodium bicarbonate through a laboratory experiment or practical.

Aim:

To perform the limit test for chlorides for the given sample and report its compliance /non-compliance with standards of I.P.

Sample: Sodium bicarbonate

Requirements:

Glasswares and miscellaneous: Nessler cylinders, measuring cylinder, pipette, pipette bulb, dropper, test-tube stand, glass rod, volumetric flask, and balance.
Chemicals: Sodium bicarbonate (NaHCO3), silver nitrate (AgNO3), nitric acid (HNO3), and sodium chloride (NaCl).

Principle:

We already discuss the principle of the limit test for chloride in the previous article. Click here to get the detailed reaction involved in this test.

Preparation of reagents:

Preparation of dilute HNO3:

Click here to get the procedure.

Preparation of 0.1M AgNO3:

Click here to get the procedure.

Preparation of 25 ppm standard NaCl solution:

Click here to get the procedure.


Procedure:

Standard opalescence:
  • Take 10.00 ml of 25 ppm chloride standard solution using a pipette into a Nessler cylinder and label it as standard.
  • Add 05.00 ml of water.
  • Add 10.00 mL of dilute HNO3 solution to the above preparation and dilute to 50 ml with water.
  • Then add 01.00 ml of prepared 0.1 M silver nitrate solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this standard preparation under a black background.

Test opalescence:

  • Take 01.20 gm of sodium bicarbonate into a Nessler cylinder and label it as a test.
  • Add 02.00 ml of dilute HNO3 solution to the above preparation and dilute to 50 ml with water.
  • Then add 01.00 ml of prepared 0.1 M silver nitrate solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this standard preparation under a black background.

Observations:

The test solution produces less or same or more opalescence than the standard solution.


Results:

The sample passes/fails the limit test as per Indian Pharmacopoeia.



FAQ (Frequently Asked Questions)


Which precipitate is obtained in the limit test for chloride?
The reaction of the Cl- with AgNO3 in the presence of weak HNO3 produces a silver chloride precipitate as a limit test for chloride.

Which acid is used in the limit test of chloride?
Nitric acid is used in the chloride limit test, which makes the solution acidic and aids silver chloride precipitation, which causes the solution to become turbid at the end of the process.

Which standard solution is used for the limit test of chloride?
Standard sodium chloride solution of specific concentration (PPM) is used for limit test of chloride.


Limit test for chlorides for water insoluble substances

Learn the limit test for chlorides for water-insoluble substances through a laboratory experiment or practical.

Aim:

To perform the limit test for chlorides for water insoluble activated charcoal

Sample: Activated charcoal

Requirements:

Glasswares and miscellaneous: Nessler cylinders, measuring cylinder, pipette, pipette bulb, dropper, test tube stand, glass rod, volumetric flask, and balance.
Chemicals: silver nitrate (AgNO3), nitric acid (HNO3), and sodium chloride (NaCl).

Principle:

The test opalescence produced by chloride impurities reacting with AgNO3 is compared to the standard opalescence produced by a known amount of chloride reacting with silver nitrate. If other impurities are present, a dilute HNO3 solution is used to dissolve them.

Limit test for chlorides for water insoluble substances

The precipitate formed is AgNO3 insoluble in dilute HNO3 solution and provides opalescence. The key objective here is to determine chloride impurities in charcoal rather than actual charcoal. Chloride salts are generally water-soluble. Chloride salt dissolves when charcoal is treated with H2O, however charcoal does not. As a result, the suspension filtrate is used for the limit test for chloride.

Preparation of reagents:

Preparation of dilute HNO3:

Take 10.60 ml of concentrated HNO3 using a pipette, dilute in 100 ml of distilled water in a volumetric flask, and properly mixing it.

Preparation of 0.1M AgNO3:

Take 17.00 gm of silver nitrate and dissolve in 70 ml of distilled water in a volumetric flask, and properly mixing it. Once it has completely dissolved, make up the volume with distilled water to 100 ml. Light-resistant containers should be used for storage.

Preparation of 0.0824% w/v standard NaCl solution:

Take 0.0824gm of sodium chloride and dissolve in 50 ml of distilled water in a volumetric flask, and properly mixing it. Once it has completely dissolved, make up the volume with distilled water to 100 ml.

Preparation of 25 ppm standard NaCl solution:

Take 05 volumes of 0.0824% w/v sodium chloride solution using a pipette and dilute to 100 volumes of distilled water in a volumetric flask.

Procedure:

Standard opalescence:
  • Take 10.00 ml of 25 ppm chloride standard solution using a pipette into a Nessler cylinder and label it as standard.
  • Add 05.00 ml of water.
  • Add 10.00 mL of dilute HNO3 solution to the above preparation and dilute to 50 ml with water.
  • Then add 01.00 ml of prepared 0.1 M silver nitrate solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this standard preparation under a black background.
Test opalescence:
  • Take 03.00 gm of activated charcoal in 75.00 ml distilled water, boil it for 5 minutes then cool.
  • Make up the volume with distilled water to 100 ml and filter.
  • Take 06.00 ml of the filtrate using a pipette into a Nessler cylinder and label it as a test.
  • Add 10.00 mL of dilute HNO3 solution to the above preparation and dilute to 50 ml with water.
  • Then add 01.00 ml of prepared 0.1 M silver nitrate solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this standard preparation under a black background.

Observations:

The test solution produces less or same or more opalescence than the standard solution.

Results:

The sample passes/fails the limit test as per Indian Pharmacopoeia.



FAQ (Frequently Asked Questions):


What is the inference for the chloride test?
When compared to a standard solution, the provided substance passes or fails the chloride limit.

Limit test of chloride is based on which reaction?
The chloride limit test is based on the reaction of soluble chloride with AgNO3 in the presence of dilute HNO3 to form AgNO3, which appears in the solution as solid particles.


Wednesday, October 13, 2021

Limit test for lead

Learn the limit test of lead through a laboratory experiment or practical.

Aim:

To perform the limit test for lead of the given samples.

Requirements:

Glasswares and miscellaneous:
Separating funnel, separating-flask ring, measuring cylinder, pipette, dropper, beaker, volumetric flask, rubber stopper, test tube, glass rod, and balance, etc.
Chemicals:
Ammonium citrate (C6H5+4yFexNyO7), ammonium cyanide(CH4N2), potassium cyanide (KCN), ammonia solution (NH4OH), hydroxylamine hydrochloride (HONH2·HCl), phenol red (C19H14O5S), nitric acid (HNO3), chloroform(CHCl3), and dithizone (C13H12N4S), etc.

Principle of limit test for lead:

The reaction of lead and diphenyl thiocabazone in an alkaline solution produces a lead dithizone complex, which has color-red.

Because dithizone is green in chloroform and the lead-dithizone complex is violet, the final color at the end of the process is red.

Preparation of chemicals:

Preparation of 0.1 % lead standard solution:

In a volumetric flask, dissolve 0.400 gm of lead nitrate in 250.00 ml of distilled water containing 02.00 ml of nitric acid, properly mixing it.

Preparation of 100 ppm lead standard solution:

Take 01 volume of 1% lead standard solution using a pipette and dilute to 10 volume of distilled water in a volumetric flask, and properly mixing it.

Preparation of 10 ppm lead standard solution:


Take 01 volume of 100 ppm lead standard solution using a pipette and dilute to 10 volume of distilled water in a volumetric flask, and properly mixing it.

Preparation of 01 ppm lead standard solution:

Take 01 volume of 10 ppm lead standard solution using a pipette and dilute to 10 volume of distilled water in a volumetric flask, and properly mixing it.

Preparation of 1% v/v nitric acid:

Take 01 volume of nitric acid using a pipette and dilute to 100 volume of distilled water in a volumetric flask, and properly mixing it.

Preparation of ammonium citrate solution:

Take 40.00 gm of citric acid in 90.00 ml of distilled water, add 2 drops phenol red solution, followed by gradual addition of strong ammonia solution until the solution turns a reddish color.

Remove any lead from the solution by extracting it with 30.00 ml increments of dithizone extraction solution until the dithizone solution retains its orange-green color.

Preparation of dithizone extraction solution:

Take 30.00 mg of dithizone in a 1-liter volumetric flask, add 05.00 ml of 95% ethanol, and make up the volume with chloroform. The solution should be kept in the refrigerator. Shake an appropriate volume of the solution with about half the volume of a 1 percent v/v HNO3 before using, and then discard the acid.

Preparation of dithizone standard solution:

Take 10.00 mg dithizone and dissolve to 1000 ml of distilled water in a volumetric flask, and properly mixing it.

Procedure of limit test for lead:

Standard:
  • Take the desired amount of lead standard solution in the separating funnel, which is equivalent to the amount of lead allowed in the substance being tested.
  • Add 06.00 ml of prepared ammonium citrate solution.
  • Add 02.00 ml hydroxylamine hydrochloride and 02.00 ml potassium cyanide.
  • Then add 2 drops of phenol red.
  • Add ammonia solution to make the solution alkaline.
  • Extract instantly with numerous volumes of dithizone extraction solution, each of 05.00 ml, until it becomes green.
  • Combine the dithizone extracts with 30.00 ml of nitric acid solution (1 % v/v), shake for 30 seconds, and discard the chloroform layer. (Dithizone remains in the layer of chloroform and lead nitrate is in the aqueous layer)
  • Add 05.00 ml of standard dithizone solution to this acid solution.
  • Add 04.00 ml of ammonium cyanide solution.
  • Shake well for a half-hour, and observe the color of the chloroform layer after separation.
Test:
  • Take the desired amount of sample in the separating funnel.
  • Add 06.00 ml of prepared ammonium citrate solution.
  • Add 02.00 ml hydroxylamine hydrochloride and 02.00 ml potassium cyanide.
  • Then add 2 drops of phenol red.
  • Add ammonia solution to make the solution alkaline.
  • Extract instantly with numerous volumes of dithizone extraction solution, each of 05.00 ml, until it becomes green.
  • Combine the dithizone extracts with 30.00 ml of nitric acid solution (1 % v/v), shake for 30 seconds, and discard the chloroform layer. (Dithizone is remains in the layer of chloroform and lead nitrate is in the aqueous layer)
  • Add 05.00 ml of standard dithizone solution to this acid solution.
  • Add 04.00 ml of ammonium cyanide solution.
  • Shake well for a half-hour, and observe the color of the chloroform layer after separation.

Observation:

Test color of the chloroform layer is more/not more intense than the standard color of the chloroform layer.

Results:

The given sample passes/fails the limit test for lead.


FAQ (Frequently Asked Questions):


What is the role of ammonium citrate, potassium cyanide, and hydroxylamine hydrochloride in the limit test for lead?
Ammonium citrate, potassium cyanide, and hydroxylamine hydrochloride are used to adjust the pH to the optimum, removing interference and effects of other impurities.

How many methods are there for the limit test of heavy metals?
The four different methods are used for the limit test of heavy metals; generally, it is based on the reaction of metallic impurities with H2S in an acidic medium to form a colored solution.

Why phenol red is used in the limit test for iron?
Phenol red is used as an indicator, which produces the color at the end of the process.


Monday, October 11, 2021

Limit test for arsenic

Learn the limit test for arsenic through a laboratory experiment or practical.

Aim:

To perform the arsenic limit test for chloride of the given samples as per IP.

Sample: Sodium acetate (CH3COONa)
Reference: Indian Pharmacopoeia (IP) 2010, www.web-formulas.com


Requirements:

Glasswares and miscellaneous: Measuring cylinder, pipette, glass rod, dropper, rubber stopper, test tube stand, mercuric chloride paper, cotton wool, balance, and arsenic limit test apparatus, etc.
Chemicals: Arsenic trioxide (As2O3), sodium hydroxide (NaOH), sodium acetate (C2H3NaO2), hydrochloric acid (HCL), stannous chloride (SnCl2), potassium iodide (KI), lead acetate (Pb(C2H3O2)2), and zinc (Zn+2), etc

Principle of limit test for Arsenic:

The limit test for arsenic is also known as the Gutzeit test which is based on the reaction of arsenic gas with hydrogen ions to form a yellow stain on paper of mercuric chloride in the presence of reducing agents such as KI is used to determine the limit of arsenic.

Limit test for arsenic

Arsenic present in the form of arsenic acid in the sample is reduced to arsenic acid by reducing agents such as KI, SnCl2, zinc, and HCL. Arsenious acid is further reduced to arsine (gas) by hydrogen and reacts with mercuric chloride paper to give a yellow stain.

The depth of yellow stain on mercuric chloride paper will depend upon the quality of arsenic present in the sample.

Preparation of chemicals:

How to prepare 10 ppm arsenic standard solution:

Take 00.33 gm of arsenic trioxide in 05.00 ml of 2 M NaOH and dilute to 250.00 ml of distilled water in a volumetric flask, and properly mixing it. Take 01 volume of this solution and to 100 volumes with distilled water.

How to prepare 02 ppm arsenic standard solution:

Take 02 volumes of prepared 10 ppm arsenic trioxide standard and dilute to 10 volumes with distilled water.

Preparation of stannous chloride solution:

Take 330.00 gm of stannous chloride in 100.00 ml of hydrochloric acid in a volumetric flask, and properly mixing it, add this solution in 500 ml of distilled water, and make up the volume to 1000 ml with water.

How to prepare stannated hydrochloric acid:

Take 01.00 ml of stannous chloride solution and dilute to 100.00 ml of HCL.

Preparation of sodium acetate test solution:

Take 05.00 gm of sodium acetate in 50.00 ml distilled water and add 15.00 ml of stannated hydrochloric acid.

How to prepare 1M potassium iodide solution:

Take 01.66 gm of potassium iodide and dissolve in 50.00 ml of distilled in a volumetric flask and properly mixing it. Once it has completely dissolved, make up the volume to 100 ml.

How to prepare 2M sodium hydroxide solution:

Take 08.00 gm of NaOH and dissolve in 70.00 ml of distilled in a volumetric flask and properly mixing it. Once it has completely dissolved and cool, make up the volume to 100 ml.

Procedure of limit test for arsenic:

Standard:
  • Take 01.00 ml of prepared 2 ppm arsenic standard solution using a pipette into a glass bottle flask, dilute to 50.00 ml with water and label it as standard.
  • Then add 15.00 ml of stannated hydrochloric acid.
  • Add 05.00 ml of prepared 1M potassium iodide solution.
  • Then add 10.00 gm of zinc and properly mixed it.
  • Assemble the apparatus as soon as possible, and place the bottle in a water bath at a temperature that ensures a uniform gas evolution.
  • Allow 40 minutes for the reaction to occur.

Test:
  • Take 05.00 gm sodium acetate diluted with 50.00 ml of water in a glass bottle flask and label it as standard.
  • Then add 15.00 ml of stannated hydrochloric acid.
  • Add 05.00 ml of prepared 1M potassium iodide solution.
  • Then add 10.00 gm of zinc and properly mixed it.
  • Assemble the apparatus as soon as possible, and place the bottle in a water bath at a temperature that ensures a uniform gas evolution.
  • Allow 40 minutes for the reaction to occur, any stain formed by the sample on mercuric chloride paper is compared to that of the standard.

Observations:

The stain produced in the sodium acetate test sample is less/same/more than the stain produced in standard.

Results:

The given sample of sodium acetate compile/does not comply the limit test for arsenic as per the Indian Pharmacopoeia.


FAQ (Frequently Asked Questions):


Why Lead acetate is used in the limit test for arsenic?
In the limit test of arsenic, lead acetate cotton wool is used to form a stain that is used to compare the results.

How to prepare mercuric chloride paper?
Take a smooth white filter paper which has less than 25 mm in width. Soak it in a saturated mercuric chloride solution, squeezed it to remove excess solution, and dried in the dark place at 60°C.

When used in the limit test for arsenic, a paper that has been exposed to sunlight or ammonia vapor produces a lighter stain or no stain at all. Therefore it needs to be store in a stoppered bottle in a dark place.

How to prepare lead acetate paper?
Prepare it with a solution of lead acetate and dry the impregnated paper at 100°.

How to prepare lead acetate cotton?
Immerse absorbent cotton in a mixture of 10 volumes of 10% w/v lead acetate solution and 1 volume of 2 M acetic acid. Remove excess fluid without squeezing the cotton wool, just lay it on several layers of filter paper. Allow time for air drying at room temperature and protect from moisture when storing.


Limit test for heavy metals

Learn the limit test for heavy metals through 3 different methods as a laboratory experiment or practical.

Aim:

To perform the limit test for heavy metals of the given samples as per IP.

Reference: Indian Pharmacopoeia (IP) 1996, 2006.


Requirements:

Glasswares and miscellaneous: Nessler cylinder, measuring cylinder, pipette, dropper, rubber stopper, test tube stand, pH paper, balance, and glass rod, etc.

Chemicals: Lead nitrate (Pb(NO3)2), nitric acid (HNO3), acetic acid (CH3COOH), hydrogen sulphide solution, and ammonia solution (NH4OH), etc.

Principle of limit test for heavy metals:

The reaction of metallic impurities with hydrogen sulphide to produce a brownish solution in an acidic medium is the basis for the heavy metals limit test. Lead, arsenic, bismuth, copper, mercury, antimony, silver, tin, cadmium, and molybdenum are among the metals that respond to this test. Parts of lead per million parts of the substance are used to measure metallic impurities. The usual limit, according to the IP, is 20 ppm.

Limit test for heavy metals

Preparation of chemicals:

Preparation of dilute acetic acid:

Take 05.70 ml of concentrated glacial acetic acid and dissolve in 50 ml of distilled water in a volumetric flask, and properly mixing it. Once it has completely dissolved and cool, make up the volume to 100 ml.

Preparation of dilute ammonia:

Take 42.50 ml of strong ammonia solution and dissolve in 50 ml of distilled water in a volumetric flask, and properly mixing it. Once it has completely dissolved and cool, make up the volume to 100 ml.

Preparations of 0.1% lead standard solution:

Take 0.40 gm of lead nitrate and dissolve in 150.00 ml of distilled water containing 2 ml of nitric acid in a volumetric flask, and properly mixing it. Once it has completely dissolved, make up the volume to 250.00 ml.

Preparations of 100 ppm lead standard solution:

Take 01 volume 0.1% lead standard solution and dilute to 10 volumes with distilled water.

Preparations of 20 ppm lead standard solution:

Take 01 volume 100 ppm lead standard solution and dilute to 05 volumes with distilled water.


The Indian Pharmacopoeia offers three methods for determining heavy metal limits.

Method I:
It refers to and is used for a substance that, under certain conditions, produces a clear, colorless solution.

Method II:
It refers to and is used for a substance that, under certain conditions, does not produce a clear, colorless solution.

Method III:
It refers to and is used for a substance that, under certain conditions, produces a clear, colorless solution in sodium hydroxide medium.

Procedure of limit test for heavy metals as per method I:

Standard:
  • Take 02.00 ml of prepared standard lead solution using a pipette into a Nessler cylinder, dilute to 25.00 ml with water and label it as standard.
  • Adjust the pH of this solution to between 03.00 and 04.00, using dilute acetic acid or dilute ammonia solution.
  • Then, dilute it with water to 35.00 ml.
  • Add 10.00 ml of freshly prepared hydrogen sulphide solution.
  • Add sufficient water to make 50.00 ml and allow standing for five minutes.
  • Observe this standard preparation under a white background or over a white surface.
Test:
  • Take 25.00 ml of the prepared solution according to the monograph using a pipette into a Nessler cylinder and label it as a test.
  • Adjust the pH of this solution to between 03.00 and 04.00, using dilute acetic acid or dilute ammonia solution.
  • Then, dilute it with water to 35.00 ml.
  • Add 10.00 ml of freshly prepared hydrogen sulphide solution.
  • Add sufficient water to make 50.00 ml and allow standing for five minutes.
  • Observe this test preparation under a white background or over a white surface.
Observations:
The test solution produces less or same or more opalescence than the standard solution.

Results:
The sample passes/fails the limit test as per Indian Pharmacopoeia.

Procedure of limit test for heavy metals as per method II:

Standard:
  • Take 02.00 ml of prepared standard lead solution using a pipette into a Nessler cylinder, dilute to 25.00 ml with water and label it as standard.
  • Adjust the pH of this solution to between 03.00 and 04.00, using dilute acetic acid or dilute ammonia solution.
  • Then, dilute it with water to 35.00 ml.
  • Add 10.00 ml of freshly prepared hydrogen sulphide solution.
  • Add sufficient water to make 50.00 ml and allow standing for five minutes.
  • Observe this standard preparation under a white background or over a white surface.
Test:
  • Weigh a specific amount of test substance, moisten it with H2So4, then ignite it over a low flame until it is charred.
  • Add few drops of nitric acid and heat to 500 °C.
  • Allow cooling before adding 04.00 ml of HCL and evaporate to dryness.
  • Moisten the residue with 10.00 ml of HCL and digest for 2 minutes.
  • Neutralize it using ammonia solution and just acidified with acetic acid.
  • Adjust the pH of this solution to between 03.00 and 04.00, and filter if necessary
  • Then, dilute it with water to 35.00 ml.
  • Add 10.00 ml of freshly prepared hydrogen sulphide solution.
  • Add sufficient water to make 50.00 ml and allow standing for five minutes.
  • Observe this test preparation under a white background or over a white surface.
Observations:
The test solution produces less or same or more opalescence than the standard solution.

Results:
The sample passes/fails the limit test as per Indian Pharmacopoeia.

Procedure of limit test for heavy metals as per method III:

Standard:
  • Take 02.00 ml of prepared standard lead solution using a pipette into a Nessler cylinder and label it as standard.
  • Add 05.00 ml of dilute NaOH solution and make up the volume to 50.00 ml with water.
  • Add five drops of freshly prepared hydrogen sulphide solution and allow standing for five minutes.
  • Observe this standard preparation under a white background or over a white surface.
Test:
  • Take 25.00 ml of the prepared solution according to the monograph using a pipette into a Nessler cylinder and label it as a test. Or weigh a specific amount of test substance, dissolve it in 20 ml of water, then add 5 ml of dilute sodium hydroxide solution.
  • Add sufficient water to make 50.00 ml and allow standing for five minutes.
  • Observe this test preparation under a white background or over a white surface.
Observations:
The test solution produces less or same or more opalescence than the standard solution.

Results:
The sample passes/fails the limit test as per Indian Pharmacopoeia.

Sunday, October 10, 2021

Limit test for Iron

Learn the limit test for iron through a laboratory experiment or practical.

Aim:

To perform the limit test for iron of the given samples as per IP 2010.

Sample: Sodium chloride (NaCl)
Reference: Indian Pharmacopoeia (IP) 2010

Requirements:

Glasswares and miscellaneous: Nessler cylinder, measuring cylinder, pipette, dropper, rubber stopper, test tube stand, pH paper, balance, and glass rod, etc.
Chemicals: Ferric ammonium sulphate (NH4Fe (SO4)2), sulphuric acid (H2SO4), citric acid (C6H8O7), thioglycolic acid (C2H4O2S), and ammonia solution (NH4OH).

Principle of limit test for iron:

The reaction between ferrous ions (Fe2+) and thioglycolic acid in the presence of citric acid is the basis for the limit test. By reacting with the same thioglycolic acid, iron in the ferric state (Fe3+) is converted to a ferrous state (Fe2+).

Fe2+ reacts with C2H4O2S to form a coordination complex called ferrous-thioglycolate. The formation of ferrothioglycolate ion gives this complex a deep reddish color under basic conditions.

In the presence of NH4OH, C6H8O7 forms a soluble complex with iron, preventing the precipitation of iron as Fe(OH)2 or Fe(OH)3.

Chemical reaction involved in limit test for iron:


Limit test for Iron

Preparation of chemicals:

How to prepare 20 ppm iron standard solution:

Take 1 volume of 0.1726 % w/v ferric ammonium sulphate solution in 0.05 M H2SO4 and dilute to 100 volume of distilled water in a volumetric flask, and properly mixing it. (Contains iron in the ferric state)

How to prepare 20 % w/v iron-free citric acid solution:

Take 20.00 gm of citric acid and dissolve in 50 ml of distilled water in a volumetric flask, and properly mixing it. Once it has completely dissolved, make up the volume to 100 ml.

Procedure of limit test for iron:

Standard:
  • Take 02.00 ml of prepared 20 ppm iron standard solution using a pipette into a Nessler cylinder and label it as standard.
  • Add 02.00 ml of prepared 20 % w/v iron-free citric acid solution.
  • Then, add 0.10 ml of thioglycolic acid, and properly mixed it.
  • Make it alkaline using an iron-free ammonia solution.
  • Add sufficient water to make 50.00 ml and allow standing for five minutes.

Test:
  • Take 02.00 gm of sodium chloride into a Nessler cylinder containing 20.00 ml of water and label it as a test.
  • Add 02.00 ml of prepared iron-free citric acid solution (20 % w/v).
  • Then, add 0.10 ml of thioglycolic acid, and properly mixed it.
  • Make it alkaline using an iron-free ammonia solution.
  • Add sufficient water to make 50.00 ml and allow standing for five minutes.
  • Observe this test preparation and compare the opalescence of this solution to that of a standard solution.

Observations:

The sodium chloride test solution produces less or same or more opalescence than the standard solution.

Results:

The sample passes/fails the limit test as per Indian Pharmacopoeia.



FAQ (Frequently Asked Questions):


What is the importance of the iron limit test?
The purpose of a limit test is to find impurities in a substance and compare them to a standard. In general, it is a quantitative or semi-quantitative chemical test.

What is the role of citric acid in the limit test for iron?
Citric acid helps in the precipitation of iron by ammonia by forming a complex with it, which is why it is used in the limit test for iron.

Why thioglycolic acid is used in a limit test of iron​?
Thioglycolic acid helps to oxidize iron-II to iron III, which is why it is used in the limit test for iron.


Thursday, October 7, 2021

Modified limit test for sulphate

Learn the modified limit test of sulphate through a laboratory experiment or practical.

Aim:

To perform the modified limit test for sulphate of the given samples as per IP 2010.

Sample: Potassium permanganate (KMnO4)
Reference: Indian Pharmacopoeia (IP) 2010

Requirements:

Glasswares and miscellaneous: Nessler cylinder, measuring cylinder, pipette, dropper, rubber stopper, test tube stand, glass rod, and balance.
Chemicals: Potassium sulphate (K2SO4), potassium permanganate (KMn04), barium chloride (BaCl2), ethanol, hydrochloric acid (HCL), glacial acetic acid (CH3COOH).

Principle of modified limit test for sulphate:

The potassium permanganate is de-colored before the limit test because its purple color interferes with the limit test. The BaSO4 precipitate turns pink or violet as it absorbs some of the permanganates. This coloration hinders the identification of impurities in the test solution by comparing the opalescence which is formed in the standard solution.

Modified limit test for sulphate

Potassium permanganate is reduced by heating with ethyl alcohol to decolorize it. Filtration removes the precipitate, and the resulting colorless filtrate is obtained subject to a chloride limit test.

Preparation of chemicals:

How to prepare 600 ppm sulphate standard solution:

Take 60 volume of 0.181 % w/v prepared solution of K2SO4 and dilute to 100 volume of distilled water in a volumetric flask, and properly mixing it.

Preparation of potassium permanganate test solution:

Preparation of 10 ppm ethanolic sulphate standard solution:

Preparation of 25 % w/v barium chloride solution:

Preparation of 5M acetic acid:

We already discussed the preparation of the above solutions in the limit test for sulphate. Click here to get the procedure.

Procedure of limit test for sulphate:

Standard:
  • Take 15.00 ml of prepared 600 ppm standard sulphate solution using a pipette into a Nessler cylinder and label it as standard.
  • Add 1 ml of prepared 25 % w/v barium chloride solution.
  • Allow one minute to stand after adding 1.5 ml of ethanolic sulphate standard solution.
  • Then add 0.15 ml prepared 05 molar acetic acid.
  • Add sufficient water to make 50 ml.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this standard preparation under a black background.
Test:
  • Take 10.00 ml of prepared KMnO4 test solution using a pipette into a Nessler cylinder and label it as a test.
  • Add 15.00 ml of distilled water.
  • Add 1 ml of prepared 25 % w/v barium chloride solution.
  • Allow one minute to stand after adding 1.5 ml of ethanolic sulphate standard solution.
  • Add sufficient water to make 50 ml.
  • Then add 0.15 ml of prepared 5 M acetic acid solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this test preparation under a black background and compare the opalescence of this solution to that of a standard solution.

Observations:

The KMnO4 test solution produces less or same or more opalescence than the standard solution.

Results:

The sample passes/fails the modified limit test as per Indian Pharmacopoeia.


Wednesday, October 6, 2021

Limit test for sulphate

Learn the limit test of sulphate through a laboratory experiment or practical.

Aim:

To perform the limit test for sulphate of the given samples as per IP 2010.

Sample: Calcium gluconate (C12H22CaO14).
Reference: Indian Pharmacopoeia (IP) 2010.


Requirements:

Glasswares and miscellaneous: Nessler cylinder, measuring cylinder, pipette, dropper, rubber stopper, test tube stand, glass rod, and balance.

Chemicals: Calcium gluconate (C12H22Ca014), potassium sulphate (K2SO4), barium chloride (BaCl2), glacial acetic acid (CH3COOH), ethanol.

Principle of limit test for sulphate:

The limit test for sulfate relies on the reaction of SO4²- with BaCl2 in the presence of alcohol and acid (HCL or CH3COOH) to form BaSO4, which appears as solid particles in the solution. The opalescence of precipitate that is observed in the test is compared with the standard solution in dark background.

Chemical reaction:

Limit test for sulphate

Preparation of chemicals:

How to prepare 150 ppm sulphate standard solution:

Take 15 volume of 0.181 % w/v prepared solution of K2SO4 and dilute to 100 volume of distilled water in a volumetric flask, and properly mixing it.

How to prepare 10 ppm ethanolic sulphate standard solution:

Take 1 volume of 0.181 % w/v prepared solution of K2SO4 and dilute to 100 volume of 30 % ethanol in a volumetric flask, and properly mixing it.

How to prepare 25 % w/v barium chloride solution:

Take 25 gm of barium chloride and dilute to 70 ml of distilled water in a volumetric flask, and properly mixing it. Once it has completely dissolved, make up the volume with distilled water to 100 ml.

How to prepare 5 M acetic acid:

Take 28.5 ml concentrated glacial acetic acid and dilute to 100 volume of distilled water in a volumetric flask, and properly mixing it.

Procedure of limit test for sulphate:

Standard:
  • Take 15.00 ml of prepared 150 ppm standard sulphate solution using a pipette into a Nessler cylinder and label it as standard.
  • Add 1 ml of prepared barium chloride solution (25 % w/v).
  • Allow one minute to stand after adding 1.5 ml of ethanolic sulphate standard solution.
  • Then add 00.15 ml of prepared 5 M acetic acid solution.
  • Add enough water to make 50 ml.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this standard preparation under a black background.
Test:
  • Weigh exactly 01.00 gm calcium gluconate and pour 15 ml of distilled water into a Nessler cylinder and label it as a test.
  • To dissolve it, you'll need to stir it for 10 to 15 minutes.
  • Add 1 ml of prepared barium chloride solution (25 % w/v).
  • Allow one minute to stand after adding 1.5 ml of ethanolic sulphate standard solution.
  • Then add 00.15 ml of prepared 5 M acetic acid solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this test preparation under a black background and compare the opalescence of this solution to that of a standard solution.

Observations:

The calcium gluconate test solution produces less or same or more opalescence than the reference solution.

Results:

The sample passes/fails the limit test as per Indian Pharmacopoeia.


FAQ (Frequently Asked Questions):


Why HCl is used in the limit test of sulphate?
Hydrochloric acid is used in the limit test of sulphate since it helps to make the solution acidic. Under acidic conditions, phosphates and carbonates do not precipitate.

What is the importance of ethanolic sulphate solution in the sulphate limit test?
In the sulphate limit test, potassium sulphate is added to increases the sensitivity of the test, and ethanol helps prevent over-saturation of barium sulfate leading to the formation of a precipitate.

Why potassium sulphate is used in the limit test for sulphate?
To increase the test's sensitivity, potassium sulphate is used in the limit test for sulphate.


Monday, October 4, 2021

Modified limit test for chloride

Learn the modified limit test of chloride through a laboratory experiment or practical.

Aim:

To perform the modified limit test for chloride of the given samples as per IP 2010

Sample: Potassium permanganate (KMnO4).
Reference: Indian Pharmacopoeia (IP) 2010.

Requirements:

Glasswares and miscellaneous: Nessler cylinder, measuring cylinder, pipette, dropper, rubber stopper, test tube stand, glass rod, and balance.
Chemicals: Potassium permanganate (KMnO4), sodium chloride (NaCl), silver nitrate solution (AgNO3), nitric acid solution (HNO3),

Principle of modified limit test for chloride:

Before performing the limit test, the KMnO4 is de-colored since the purple color of potassium permanganate interferes with the limit test. The AgNO3 precipitate turns pink as it absorbs some of the permanganates.

This coloration hinders the identification of impurities in the test solution by comparing the opalescence which is formed in the standard solution of chloride. Potassium permanganate is reduced by heating with ethyl alcohol to decolorize it.

Modified limit test for chloride

Filtration removes the precipitate, and the resulting colorless filtrate is obtained subject to a chloride limit test.

Preparation of chemicals:

How to prepare potassium permanganate test solution:

Take 01.50 gm of KMnO4 and dissolve in 50 ml of distilled water in a volumetric flask, and properly mixing it. Heat on a water bath and gradually add 06.00 ml of 95 % ethanol. Once cooling dilute to 60 ml by distilled water and filter it.

How to prepare 250 ppm of chloride standard solution:

Take 50 volume of 0.0824% w/v prepared solution of NaCl and dilute to 100 volume of distilled water in a volumetric flask, and properly mixing it.

How to prepare 0.1 M silver nitrate solution:

Take 17.00 gm of AgNO3 and dissolve in 500 ml of distilled water in a volumetric flask, and properly mixing it. Once it has completely dissolved, make up the volume with distilled water to 1000 ml.

How to prepare dilute nitric acid:

Click here to get the procedure of preparation dilute nitric acid.

Procedure of modified limit test for chloride:

Standard:
  • Take 10.00 ml of 250 ppm sodium chloride solution using a pipette into a Nessler cylinder and label it as standard.
  • Add 05.00 ml of distilled water.
  • Add 10.00 ml of dilute nitric acid to the above preparation and properly mixed it.
  • Dilute it to 50.00 ml with distilled water.
  • Then add 01.00 ml of prepared 0.1 M silver nitrate solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this standard preparation under a black background.
Test:
  • Take 40.00 ml of prepared potassium permanganate test solution using a pipette into a Nessler cylinder and label it as a test.
  • Add 10.00 ml of dilute HNO3 solution.
  • Then add 01.00 ml of prepared 0.1 M AgNO3 solution.
  • Stir immediately with a glass rod and let stand for five minutes by protecting from light.
  • Observe this test preparation under a black background.
  • Compare the opalescence produced to the opalescence produced by a standard solution.

Observation:

The KMnO4 test solution produces less or same or more opalescence than the reference solution.

Result:

The sample passes/fails the modified limit test as per Indian Pharmacopoeia.

Precautions:
  • The use of distilled water is required as chloride in tap water will interfere with the result.
  • Do not use the same glass rod for the standard and sample, as this will affect the result.
  • Store silver nitrate in an amber-colored container as it is photosensitive.
  • If silver nitrate is in contact with skin it will be produced black dots.

FAQ (Frequently Asked Questions):

Modified limit test for chloride is done for which compound?
Modified limit test of chloride is done to test colored compounds which are not possible with normal tests.

Is observed in the limit test of chloride and sulphate?
Turbidity is observed in the limit test of chloride and sulphate.

State the reason for use of acidic conditions in the chloride limit test.
Nitric acid is added to the chloride limit test to acidify the solution and aid in silver chloride precipitation, which causes the solution to become turbid at the end of the process.