Please note that the colours on this document are
for demonstration purposes only as colours vary
with individual monitors and therefore cannot be
guaranteed as accurate.
Mordant dyes are
those dyes which require a mordant in their application
and which upon combination with the mordant deposit
insoluble color on the substrate, e.g., dyes with
metal chelating groups. Like the name suggests these
dyes require a mordant. Mordants are substances of
organic or inorganic origin which combine with the
coloring matter and are used to fix the same in the
production of the color. For the purpose of this class,
such materials as oils and sulfonated oils, soaps,
fats and higher acids, are not generally considered
as mordants, but as coming within the scope of “assistants”
in dyeing. The mordant substances include such acids
as tannic acid, sumac, gall nuts, bark extracts, oleic
and stearic acids, and Turkey red oil; and metallic
substances such as various combinations or soluble
salts of chromium, aluminum, iron, copper, and tin.
The latter, the metallic mordants, are more used than
the acid mordants. Mordant improves the fastness of
the dye on the fibre such as water, light and perspiration
fastness. The choice of mordant is very important
as different mordants can change the final colour
significantly. Most natural dyes are mordant dyes
and there is therefore a large literature base describing
dyeing techniques.
Dyes are generally
defined along the lines of being coloured, aromatic
compounds that can ionise. Although this definition
infers that ionic interaction with oppositely charged
tissue constituents is the norm, there are exceptions.
Some dyes require the presence of a metal to properly
develop their colour or staining selectivity. These
are termed mordant dyes. The Colour Index uses this
as a classification and naming system. Each dye is
named according to the pattern: mordant + base colour
+ number
These dyes are thereby
specifically identified as dyes of the stated colour,
and whose primary staining mechanism requires the
presence of metal atoms. Note that this is a functional
and colour classification. It contains no chemical
information neither does it imply that dyes with similar
names but unique numbers are in any way related. It
should also be noted that the classification refers
to the primary mechanism of staining. Other mechanisms
may also be possible.
The most commonly
used mordant dyes have hydroxyl and carboxyl groups
and are negatively charged, i.e. anionic. It is convenient
to view these as a specialised subgroup of acid dyes.
Some other mordant dyes may possess amino groups,
and are cationic overall. Despite this, they must
still have hydroxyl or carboxyl groups, since lake
formation requires it. Mordant dyes can usually stain
by ionic interaction in the same way as other ionisable
dyes. The colour is often pale, sometimes so pale
that the results have no value.
It is often noted
that when a mordant dye forms a lake with a metal,
there is a strong colour change. This is because metals
have low energy atoms. The incorporation of these
low energy atoms into the delocalised electron system
of the dye causes a bathochromic shift in the absorption.
It is this delocalised electron system which is fundamentally
responsible for colour in dyes. Since different metal
atoms have differing energy levels, the colour of
the lakes may also differ.
The most commonly
used mordant dye is undoubtedly hematein (natural
black 1), whose status as a natural product supercedes
its mode of dyeing, apparently. Others are eriochrome
cyanine R (mordant blue 3) and celestine blue B (mordant
blue 14), both used as substitutes for alum hematoxylin
but with a ferric salt as the mordant. Alizarin red
S (mordant red 3) is valuable for the demonstration
of calcium, particularly in embryo skeletons.
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