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Kjeldahl - A Brief History
Kjeldahl is the common name given to the analytical method of
determining the amount of Nitrogen in organic substances.
The method was originally developed by a Danish chemist, Johan
Kjeldahl, 1849-1900. Johan Kjeldahl was part of the innovative
laboratory team at the Carlsberg Brewery, also famous in microbiology
for isolating the famous beer yeast Saccharomyces carlsbergensis,
still used today.
Johan Kjeldahl was given the job of finding a way to prevent
problems in the brewing process caused by differing amounts of
protein in the grain supplied to the brewery. The lower the amount
of protein in the mash the higher the volume of beer produced.
As a start in solving the problem Johan needed a way of calculating
the amount of protein in the grain supplied to the brewery quickly
and accurately.
Johan developed a method which reduces the protein by breaking
all the bonds in the molecule and converting the nitrogen from
the protein into ammonium ions. Sulphuric acid is used for this
purpose. However, Sulphuric acid alone is too slow in breaking
down these bonds and the reaction needed some help. To speed up
the process a combination of heat, salt and catalyst are used.
Heating alone can only get the Sulphuric acid to its boiling point
of 338ºC. The addition of salt can raise this to the critical
temperature for decomposition of 373ºC. Addition of a catalyst
(Johan used Mercury, today most people use Copper) speeds the
reaction even further. Today the normal operating temperature
for Kjeldahl heating systems, KJELDATHERM
and TURBOTHERM is between 380 - 420ºC.
Infrared heaters, TURBOTHERM, speed the
reaction even further by heating and cooling quickly providing
additional efficiency, safety and programmability.
Gerhardt are the unique manufacturers of both traditional
and modern heating systems for the digestion of the sample in
acid.
Once the ammonium ions had been formed, Johan needed some means
of measuring the amount ammonium in the solution. This resulted
in the second phase of Kjeldahl analysis, the distillation. At
this stage, after diluting the acid with water, Sodium Hydroxide
is added to the solution. This frees the ammonium ions from their
salt complex and forms free volatile ammonia which with the steam
from the distillation is carried out of the solution and condensed
into a collection vessel containing Boric acid buffer solution.
The Boric acid captures the ammonia and its pH increases. An indication
in the Boric Acid, usually 4.5 indicator, changes colour as the
pH increases. At the end of the distillation, 40 minutes for the
traditional heaters and about 4 minutes for the rapid distillation
unit, the VAPODEST. The Boric acid solution is then titrated
back to its original start point with acid.
The amount of acid used in the titration can be directly compared
to the amount of Ammonia, which in turn can be directly linked
to the amount of Nitrogen in that Ammonia and finally to the amount
of protein in the original sample. Modern equipment uses automated
titration based on pH rather than colour. External or internal
titration systems may be used to calculate the end point rather
than relying on subjective colourmetric colour techniques.
Johan Kjeldahl produced his method for Nitrogen and protein
analysis at the Carlsberg brewery over 100 years ago and his method
is still the universally accepted method for this analysis and
although other methods claim to be faster and more efficient,
none can cope with the variety of sizes or conditions of samples
than Johan Kjeldahl's original method. Kjeldahl equipment is used
extensively all over the world and provides essential information
for customers as well as supplying manufacturers and distributors
of kjeldahl equipment with their livelihoods.
Cheers Johan!
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C.Gerhardt.....All
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