User Manual
Appendix C: Total Kjeldahl Nitrogen Method 
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the flask neck on the fume removal system. If necessary 
lower the burner heat setting to prevent sample from 
foaming up into neck of flask. Once, the sample comes to 
a smooth rolling boil return heat setting to maximum. 
When digestion sample clears (no black specs with pale 
green tint color), continue to boil for an equal length of 
time as required to reach the clear point, (total time 
approx. 1 hr). If black specs occur in the flask neck, rotate 
the flask 180 degrees to allow refluxing acid to rinse the 
internal flask surface. Allow digestion mixture to cool and 
carefully add 50 ml of distilled water to prevent K
2
S0
4
 salt 
solids from forming. All salt crystals must be dissolved 
before proceeding to the next step. If necessary partially 
reheat sample and agitate to dissolve crystals. 
6.  Distillation 
6.1. The distillation burners should be preheated and condenser cooling 
water turned on. The receiving flask should be in-place with enough 
boric acid H
3
BO
3 
plus the mixed indicator solution to submerge the 
tip of condenser delivery tube well below the level of the boric acid 
receiving solution in the receiving flask. (Erlenmeyer 250 ml flasks 
recommended) 
6.2. In a fume hood, carefully adding of 100 ml of 45% sodium 
hydroxide solution without mixing to make the digested sample 
alkaline. Tilt the flask in to the hood while adding the sodium 
hydroxide to the sulfuric acid digestion solution. Slowly add the 
heavy sodium hydroxide solution down the neck of the flask. The 
heavier sodium hydroxide solution will slip under the aqueous 
sulfuric acid solution without mixing and with out loss of free-
ammonia. Do not mix until the flask has been connected to the 
distillation apparatus. 
6.3. Immediately connect the flask to a condenser using the rubber 
stopper on the distillation connecting bulb attached to a condenser 
column. 
6.4. Vigorously swirl the Kjeldahl flask to mix contents thoroughly; heat 
until all NH
3
 has been distilled (>8-10 minutes). During the ammonia 
transfer the receiving solution with change color from purple to 
green. Lower receiving flask and let liquid drain from condenser tip. 
Turn off distillation burners. 
6.5. For nitrogen concentrations above 1 mg/1, the ammonia can be 
determined titrimetrically. For concentrations below this level, 
colorimetric or potentiometric determination methods are 
recommended. 










