Zastosowanie metody chromatografii cienkowarstwowej do oznaczania pigmentów nieorganicznych THE USE OF THIN LAYER CHROMATOGRAPHY IN THE DETERMINATION OF INORGANIC PIGMENTS
It was in 1978 that a scientific and research laboratory of the
State Enterprise for Monuments Conservation in Warsaw used —
for the first time — thin layer chromatography to identify inorganic
pigments.
Basing on comprehensive literature on the analysis of inorganic
ions by means of thin layer chromatography (TLC) nearly 50
methods of the determination of simple ions and their combinations
were studied, partially restricting the task to methods of distribution
on the most popular carriers. 15 cations entering into the composition
of 28 pigments and 1 2 anions entering into the composition of
20 pigments were identidfied. To give all results of the examinations
set up in more than 2 0 big tables would exceed the framework
of this article. Therefore some details of the examined methods
of distribution have been quoted and briefly discussed as representative.
When working out methods of the distribution of individual ions
or their groups standard pigments and — for comparison purposes
— standard salts available in the laboratory were used. Both
pigments and standard salts were prepared for spreading on plates
by means of proper solvents. Most frequently it was a diluted or
concentrated acid and only occasionally a flux or a diluted base.
Pigment solutions were prepared and their concentration did not
exceed a few per cent (usually 1 per cent solution was employed).
Solutions of the examined pigments or corresponding standard
salts were spread on plates covered with a layer of a carrier. As
a rule Merck’s plates with silicone gel (Kieselgel 60 F22) and a carrier
layer (0.25 mm thick) cut from the plates of 20 X 20 cm down
to 4 X 9 cm or Merck’s plates with a cellulose carrier (Cellulose F)
of 0 .1 mm in thickness and also cut down to 4 x 9 cm were used.
Before spreading standards, plates with cellulose were activated
in a dryer at 105° С for 10 minÿ plates with silicone gel were activated
at 110° С for 1 hour. Standards were spread on plates by means
of capillaries, the diameter of which was 0.5 mm. The plates were
numbered and then developed in small chromatographic cells
(5x3x11 cm) saturated with vapours of the developing system.
After developing a chromatogram, the plates were dried in a dryer
and developed by spraying with special reagents. Developed chromatograms
were photographesd with a Polaroid camera.
The obtained results of the studies make it possible to introduce
the analysis of pigments by means of thin layer chromatography
as a method supplementary to other traditional methods of determination,
particularly when only a small quantity of the sample is
available and it is composed of several pigments and their determination
by traditional methods is impossible.
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