This method is for the determination of nitric and ammoniacal nitrogen with reduction according to Devarda (modified for each of the variants (a), (b) and (c)).
See Method 3a.
Reduction of nitrates and nitrites to ammonia in a strongly alkaline solution by means of a metallic alloy composed of 45% A1, 5% Zn, and 50% Cu (Devarda alloy). Distillation of the ammonia and determination of the yield in a known volume of standard sulphuric acid; titration of the excess sulphuric acid by means of a standard solution of sodium or potassium hydroxide.
Hydrochloric acid solution, 50% (V/V): dilute an appropriate volume of hydrochloric acid (d = 1.18 g/ml) with an equal volume of water.
Sulphuric acid, 0.1 N solution. Sodium or potassium hydroxide, 0.1 N solution, carbonate free.) | for variant (a) (page 19) |
Sulphuric acid, 0.2 N solution. Sodium or potassium hydroxide, 0.2 N solution, carbonate free. | for variant (b) (page 19) (See Note on page 18) |
Sulphuric acid, 0.5 N solution. Sodium or potassium hydroxide, 0.5 N solution, carbonate free. | for variant (c) (page 19) (See Note on page 18) |
Devarda’s alloy—powdered so that 90 to 100% will pass through a sieve with apertures less than 0.25 mm square, 50 to 75% will pass through a sieve with apertures of less than 0.075 mm square. (Pre-packed bottles containing a maximum of 100 g are recommended).
Sodium hydroxide solution, 30 g per 100 ml ammonia free.
Indicator solutions:
4.10.1 Solution A: dissolve 1 g methyl red in 37 ml 0.1 N sodium hydroxide solution and make up to 1 litre with water.
Solution B: dissolve 1 g methylene blue in water and make up to 1 litre. Mix 1 volume of A with 2 volumes of B.
This indicator is violet in acid solution, grey in neutral solution and green in alkaline solution. Use 0.5 ml (10 drops).
4.10.2 dissolve 0.1 g methyl red in 50 ml 95%, ethanol. Make up to 100 ml with water and filter if necessary.
This indicator (4 to 5 drops) may be used instead of the preceding one.
Ethanol, 95%.
Sodium nitrate.
Distillation apparatus consisting of a round bottomed flask of suitable capacity, connected to a condenser by means of a splash head, equipped, in addition, with a bubble trap on the receiving flask to prevent any loss of ammonia.
An example of the type of apparatus recommended for this determination is reproduced in Figure 5 in the Appendix.
See Method 1.
7.1 See Method 2.
7.2 According to the variant chosen, place in the receiving flask an exactly measured quantity of standard sulphuric acid as indicated in the Table. Add the appropriate quantity of the chosen indicator solution (4.10.1 or 4.10.2) and finally, sufficient water to give a volume of 50 ml. The end of the extension tube of the condenser must be below the surface of the solution. Fill the bottle trap with distilled water.
Using a pipette, take an aliquot part of the clear solution as indicated in the Table and place in the distillation flask. Add sufficient water to the distillation flask to obtain a volume of 250-300 ml, 5 ml ethanol (4.11) and 1 g Devarda’s alloy (4.8).
In the presence of calcium salts such as calcium nitrate and calcium ammonium nitrate, it is necessary to add, before distillation for each gram of sample present in the aliquot, 0.700 g disodium hydrogen phosphate (Na2HPO4.2H2O) to prevent the formation of calcium hydroxide).
Taking the necessary precautions to avoid loss of ammonia, add to the flask about 30 ml 30% sodium hydroxide solution (4.9) and finally, in the case of acid soluble samples an additional quantity sufficient to neutralise the quantity of hydrochloric acid (4.1) present in the aliquot part taken for the analysis. Connect the distillation flask to the apparatus, ensuring the tightness of connections. Carefully shake the flask to mix the contents.
Warm gently, so that the release of hydrogen decreases appreciably over about half an hour and the liquid will boil. Continue the distillation, increasing the heat so that at least 200 ml liquid distils in about 30 minutes. (Do not prolong the distillation beyond 4.5 minutes).
When the distillation is complete, disconnect the receiving flask from the apparatus, carefully wash the extension tube and bubble trap, collecting the rinsings in the titration flask. Titrate the excess acid according to the procedure in Method 2.
7.3 Carry out a blank test under the same conditions omitting only the sample and allow for this in the calculation of the final results.
7.4 Before carrying out the analysis, check that the apparatus is working properly and that the correct application of the method is used, using an aliquot of a freshly prepared solution of sodium nitrate (4.12) containing, according to the variant chosen, 0.050 g to 0.150 g nitrate nitrogen.
Express the results of analysis as a percentage of nitric nitrogen or combined ammoniacal and nitric nitrogen contained in the fertiliser as received for analysis.