Paragraph 7 PROCEDURE
Preparation of the solution
Weigh to the nearest 0.001 g, 1 g of the prepared sample into the Kjeldahl flask. Add 0.5 g of powdered iron (4.2) and 50 ml of the stannous chloride solution (4.11), stir and leave standing for half an hour. During the time it is left standing, stir again after 10 and 20 minutes. Then add 10 g of potassium sulfate (4.3) and 30 ml of sulfuric acid (4.1). Boil and continue for an hour after the appearance of white fumes. Leave to cool and dilute with 100-150 ml of water. Transfer the suspension quantitatively into a 250 ml graduated flask, cool and make up to volume with water, mix and filter through a dry paper into a dry container. Discard the first portion of the filtrate.
Determination
According to the variant chosen (see Method 2) transfer with a pipette 50, 100 or 200 ml of the solution to the distillation apparatus and add sufficient sodium hydroxide solution (4.12) to ensure a considerable excess. Distil the ammonia and titrate the excess acid as described in Method 2.
Blank test
Make a blank test (omitting only the sample) under the same conditions and allow for this in the calculation of the final result.
Control test
Before carrying out the analysis, check that the apparatus is working properly and that the correct application of the method is used with a standard solution containing quantities of ammoniacal and nitrate nitrogen comparable to the quantities of cyanamide and nitrate nitrogen contained in nitrated calcium cyanamide.