FIELD OF INVENTION
[0001] This invention relates to a process for dyeing of wool, silk or their blends (fibre/yarn/fabric)
in tandem with indigo. In particular, this invention relates to a pretreatment of
wool, silk or their blends in order to render it receptive to indigo dyeing.
BACKGROUND OF THE INVENTION
[0002] The literature on wool discloses that the molecular grid of wool (Keratin) consists
of polypeptide chains bound together by salt linkages and the covalent disulphide
(-S-S) linkages. Such a literature further discloses that the disulphide bond is easily
and readily degraded in the presence of alkali. Alkali disrupts the disulphide bonds
and the fission of disulphide bonds results in the formation of thiol groups, which
are very labile.
It is known that as a natural polyamide or polypeptide, silk Fibroin (degummed silk)
exhibits free amino, carboxyl and phenolic substitutes with accessible hydroxyl groups.
Silk and wool have a slightly cationic character with an isoelectric point at about
pH 5.0. Thus, in an acidic solution, silk fibroin or wool takes on a positive charge
through absorption of hydrogen ions. The resulting electric charge can be counter
balanced with negatively charged anions of the dye, whilst dyeing with anionic dyes
such as acid, metal complex, direct and reactive dyes.
[0003] It is known that indigo dyeing is carried out under highly alkaline pH values and
that leuco indigo has an anionic charge. However, silk and wool have a tendency to
lose their cationic property in presence of alkali. Both fibre and the dye being anionic
under alkaline conditions, the net result is loss of dye-fibre affinity, lighter dyeing
and poor fastness.
[0004] Two of the silk properties that determine its colour behaviour are, firstly, very
fine fibre fibrils and, secondly high fiber orientation. These fine fibrils produce
a large fiber surface. Such a large fiber surface results in the colour yield being
very low and about twice as much dye is required for achieving a given dark shade.
Further, the fastness is poor. A large fiber surface also leads to a high dye-strike
rate even at very low temperature resulting into rapid saturation at the fiber surface
and unlevel dyeing. The high orientation of the fibres, which is a barrier to diffusion,
causes a very slow rate of further dye absorption, after the first rapid saturation.
[0005] Further, the surface of silk is very easily chafed by abrasion particularly when
the material is in wet swollen state.
[0006] The polypeptide chains of silk fibroin may hydrolyze in boiling water or in steam.
This becomes critical in the presence of acids or alkalis. Higher concentrations of
alkalis rapidly dissolve silk and wool. Degradation of silk and wool is determined
by pH and the type of alkali. The mechanical stress leads to splicing of silk threads,
which is severe and irreparable damage.
[0007] Thus, it would be apparent that the normal known steps of dyeing of silk cannot be
employed for indigo dyeing of silk (and wool) in general. Firstly, indigo dyeing is
conventionally carried out under highly alkaline pH values. Both silk and wool would
cease to be cationic under alkaline conditions and would assume anionic character
losing electrostatic affinity for anionic leuco indigo. The result would be lighter
and skittery dyeing and poor fastness.
[0008] The rope/slasher indigo dyeing machine is a long battery of several dip-squeeze-air
modules with pre-wet, Pre-wet washes and post-dye-wash off boxes. The yarn passage
through the said machine would be as long as 400-500 mtrs. At dyeing speed of for
example 18-20 mtrs/minute, the yarn runs through hostile environment; for 25 minutes
including long exposure to caustic soda, hot washes and mechanical stresses. All these
could deteriorate the mechanical properties of silk and wool.
[0009] GB 448,272 discloses a process for dyeing fibrous materials suitable for the textile industry
with vat dyestuffs consisting of pre-treating the fibrous material with quaternary
ammonium compounds.
[0010] GB 372,325 discloses a process for improving the softness or purity of fibrous materials such
as textiles by treatment with aqueous solutions of amines or ammonium bases which
contain at least one alkyl or cycloalkyl radical with at least eight carbon atoms,
or water-soluble salts of the bases.
[0011] US 2,254,965 discloses a process for dyeing fibrous materials.
[0012] US 4,615,709 discloses cationic compounds used for improving the dyeing properties of a textile
material by treating the textile material before or after dyeing with an anionic dye.
OBJECTS OF THE INVENTION
[0013] An object of this invention is to propose a novel process for the dyeing of wool,
silk or blends thereof with indigo in conventional dyeing machines.
[0014] Yet another object of this invention is to propose a novel pretreatment process for
dyeing of wool, silk or blends thereof with indigo.
[0015] Still another object of this invention is to propose a novel process for the dyeing
of wool, silk or blends thereof with indigo, which reduces the severity of dyeing
conditions.
[0016] A further object of this invention is to propose a novel process for the dyeing of
wool, silk or blends thereof with indigo, which avoids any damage being caused to
wool or silk.
[0017] A still further object of this invention is to propose a novel process for the dyeing
of wool, silk or blends thereof with indigo, which provides a dark and level indigo
shade.
[0018] Yet further object of this invention is to propose a novel process for the dyeing
of wool, silk or blends thereof with indigo, which provides adequate fastness.
[0019] Still a further object of this invention is to propose a novel process for the dyeing
of wool or silk or blends thereof with indigo, which is efficient.
DESCRIPTION OF THE INVENTION
[0020] It is known that alkali disrupts the disulphide bonds in wool and results in the
formation of thiol groups. Such a reaction is utilized in the present invention in
that before the labile thiol groups recombine or form fresh cross links, the thiol
groups are, in situ, brought in contact with (leuco) indigo, some hydrogen bonds/salt
linkages between the dye and the thiol groups in the substrate are effected. Thus,
the total dye-combining capacity of the substrate is increased by generating additional
dye-combining groups or sites by the action of alkali on wool. The rate and extent
of dye absorption is enhanced by virtue of increased accessibility of the fibre to
the dye.
[0021] In accordance with this invention, a mordanting of wool and silk in the form of cationization
on line enhances dye-fibre affinity by virtue of imparted cationic dye-combining sites
for indigo which is anionic in alkaline media. Such mordanting also reduces the heterogeneity
in the substrate and offer thereby level dyeing.
[0022] Wool and silk are sensitive to alkali and might degrade significantly when in contact
with alkali particularly caustic soda for any appreciable length of time. In case
of wool, such a normally negative point is instead taken advantage of by using generated
thiol groups as additional dye combining sites.
[0023] Thus, to overcome the disadvantages of the prior art, cationization of wool and silk
or deposition of insitu generated cationic polymer/oligomer within fibre provides
the required result in that the cationic charge in the substrate could attract the
anionic leuco indigo dye
[0024] According to this invention there is provided a process for the pretreatment of wool,
silk or blends thereof comprising the step of online cationization of silk, wool or
blends thereof to render it receptive to indigo dyeing by imparting a cationic charge
and generating dye-combining sites.
[0025] Thus, the invention provides a process for the on-line pre-treatment of a substrate
comprising wool, silk or blends thereof rendering the substrate receptive for a subsequent
step of indigo dyeing, the pre-treatment step comprising generating dye combining
sites by: (i) cationisation on the substrate; and (ii) treatment with caustic soda;
for a period sufficient to generate said sites, wherein pre-treatment step (i) includes
the step of cationising the substrate by passing the substrate through a pre-treatment
bath containing a cationising compound solution followed by aeration such that the
cationising compound can penetrate into the substrate, and wherein the pre-treatment
step is carried out for 5 to 30 seconds and the aeration is carried out for 30 to
180 seconds. The treatment comprises in the step of cationization by passing wool,
silk or blends thereof through pre-treatment baths and then subjecting to the step
of a passage in air, which is online. The online pre-treatment could be effected either
at ambient temperature or at subambient temperature, for example, at 12-15°C. The
pre-treatment bath comprises 3- to 120 gpl, and preferably 3 to 80 gpl of cationizing
compound and 3 to 25 gpl of caustic soda either separately or in admixture.
Reference is now made to the step of dyeing of silk or wool with indigo subsequent
to the pretreatment step in a manner known in the art, but the step of dyeing comprises
in passing in tandem the pretreated silk, wool or blend through a plurality of indigo
dye baths following the dip-squeeze-air (oxidation) steps.
In accordance with this invention, the dye bath contains (leuco) indigo, soda ash
sodium hydroxide, sodium hydrosulphite and
known chemical auxiliaries. As described hereinabove, wool and silk have a tendency
to lose its cationic charge in the presence of alkali. Simultaneously, the addition
of alkali to the dye bath is necessary in order to render the dye soluble. However,
the pretreatment step renders silk or wool receptive to anionic leuco dye by virtue
of imparted cationization and generated dye combining sites in the substrate. Thus,
each dye bath contains 1.0 to 3.5 gpl indigo and upto 8 dye baths may be provided.
The passage of wool or silk through each dye bath is for a period of 5 to 30 seconds
each followed by the step of squeez and oxidation for a period of 30 to 180 seconds
for each step of oxidation. The dye-bath recipe contains soda ash mostly and between
15-20 gp1, in place of caustic soda. The latter is used for fine tuning of dye bath
pH. The caustic soda and the cationizing chemical in the pre-treatment are kept at
subambient treatment in accordance with on embodiment of this invention. This is to
reduce the severity of the process and help substrate retain its original strength.
[0026] Reference is made to the online pretreatment step in distinction to a batch process.
One of the aspects of the present invention resides in the online pretreatment step
which provides a short period of contact of wool, silk of its blends with caustic
soda and cationizing chemicals. It is known that wool, silk or its blend is sensitive
to caustic soda. Thus, one of the aspects of the present invention is to ensure that
the wool, silk or its blends is not deteriorated or damaged by the pretreatment step,
which is ensured by a reduced contact period with the cationizing chemicals by such
an online step.
EXAMPLE
[0027] The wool yarn was subjected to online cationization. The original sample as well
as the cationized sample were then analyzed for their nitrogen contents by Kjeldahl
method. The sample showed increase in nitrogen content over the control by 0.35%.
The nitrogen content of the cationizing chemical viz., 3-chloro-2-hydroxy propyl trimethyl
ammonium chloride is 9.18%.
[0028] The 0.35% increase in nitrogen content in cationized sample would therefore mean
5.8 gram of cationizing chemical was added up to 100 grams of wool.
[0029] The spectral study indicated no major change in the structural pattern of wool.
[0030] The nitrogen increase in case of silk was 0.2% which means 3.3 gms of cationizing
chemical was deposited onto 100 gms of silk.
DESCRIPTION WITH REFERENCE TO ACCOMPANYING DRAWING
[0031] Reference is made to fig. 1 of the accompanying drawing which illustrates a schematic
line diagram of a known rope dyeing apparatus but modified to contain the pretreatment
steps.
[0032] As shown in fig. 1, the pretreatment apparatus contains Box 1 and Box 2 with squeeze
rollers SR1 therebetween.
[0033] First box Box 1 may contain cationizing chemical solution followed by aeration thereafter
which allows time for cationizing chemical to penetrate well into wool/silk substrate.
[0034] The second box Box 2 may contain caustic soda solution also followed by aeration.
[0035] Aeration allows time for reaction between wool/silk and cationizing chemical in the
presence of caustic soda. Alternatively, Box 1 may contain both cationizing chemicals
and caustic soda.
[0036] After impregnation of wool/silk with the said cationizing chemical, an aeration is
effected which allows for the time for the reaction between wool/silk and cationizing
chemical in the presence of caustic soda.
[0037] The second box Box 2 in such an instance could be empty-or could be used for a water-rinse
[0038] Indigo dyeing then follow in tandem, with conventional and known steps of indigo
dyeing, viz., dip-squeeze-air.
As shown in fig. 1, the pretreated substrate then passes through a plurality of dye
boxes, for example 1 to 8 dye boxes, followed each time by aeration. The substrate
is then subjected to post dyeing wash off in wash boxes and then passed through drying
cans.
1. A process for the on-line pre-treatment of a substrate comprising wool, silk or blends
thereof rendering the substrate receptive for a subsequent step of indigo dyeing,
the pre-treatment step comprising generating dye combining sites by:
(i) cationisation on the substrate; and
(ii) treatment with caustic soda;
for a period sufficient to generate said sites,
wherein pre-treatment step (i) includes the step of cationising the substrate by passing
the substrate through a pre-treatment bath containing a cationising compound solution
followed by aeration such that the cationising compound can penetrate into the substrate,
and
wherein the pre-treatment step is carried out for 5 to 30 seconds and the aeration
is carried out for 30 to 180 seconds.
2. The process according to claim 1, wherein the pre-treatment bath comprises 3 to 80
grams/litre of cationising compound and 3 to 25 grams/litre of caustic soda.
3. The process according to claim 1, wherein the pre-treatment step is carried out at
ambient temperature.
4. The process according to claim 1 or claim 2, wherein the pre-treatment step is carried
out at 12 to 15°C.
5. The process according to claim 1, wherein the cationising compound comprises 3-chloro-2-hydroxypropyl
trimethyl ammonium chloride.
1. Verfahren zur On-Line-Vorbehandlung eines Substrats, das Wolle, Seide oder Gemische
davon umfasst, wodurch das Substrat für einen anschließenden Schritt des Indigofärbens
empfänglich gemacht wird, wobei der Vorbehandlungsschritt das Erzeugen von Farbstoffkombinationsstellen
durch:
(i) Kationisierung auf dem Substrat und
(ii) Behandlung mit Ätznatron
für einen Zeitraum, der dazu ausreicht, die Stellen zu erzeugen, umfasst,
wobei der Vorbehandlungsschritt (i) den Schritt des Kationisierens des Substrats durch
Leiten des Substrats durch ein Vorbehandlungsbad, das eine kationisierende Verbindungslösung
enthält, gefolgt von Belüften, so dass die kationisierende Verbindung in das Substrat
eindringen kann, beinhaltet und
wobei der Vorbehandlungsschritt für 5 bis 30 Sekunden durchgeführt wird und das Belüften
für 30 bis 180 Sekunden durchgeführt wird.
2. Verfahren nach Anspruch 1, wobei das Vorbehandlungsbad 3 bis 80 Gramm/Liter kationisierende
Verbindung und 3 bis 25 Gramm/Liter Ätznatron umfasst.
3. Verfahren nach Anspruch 1, wobei der Vorbehandlungsschritt bei Umgebungstemperatur
durchgeführt wird.
4. Verfahren nach Anspruch 1 oder 2, wobei der Vorbehandlungsschritt bei 12 bis 15 °C
durchgeführt wird.
5. Verfahren nach Anspruch 1, wobei die kationisierende Verbindung 3-Chlor-2-hydroxypropyltrimethylammoniumchlorid
umfasst.
1. Procédé pour le prétraitement en ligne d'un substrat comprenant de la laine, de la
soie ou des mélanges de celles-ci sensibilisant le substrat pour une étape subséquente
de teinture à l'indigo, l'étape de prétraitement comprenant la production de sites
de combinaison de colorant par :
(i)cationisation sur le substrat ; et
(ii) traitement avec de la soude caustique ;
pendant une durée suffisante pour produire lesdits sites,
dans lequel l'étape de prétraitement (i) comprend l'étape de cationisation du substrat
par passage du substrat dans un bain de prétraitement contenant une solution de composé
de cationisation suivi d'une aération de façon telle que le composé de cationisation
peut pénétrer dans le substrat et
dans lequel l'étape de prétraitement est effectuée pendant 5 à 30 secondes et l'aération
est effectuée pendant 30 à 180 secondes.
2. Procédé selon la revendication 1, dans lequel le bain de prétraitement comprend 3
à 80 grammes/litre de composé de cationisation et 3 à 25 grammes/litre de soude caustique.
3. Procédé selon la revendication 1, dans lequel l'étape de prétraitement est effectuée
à température ambiante.
4. Procédé selon la revendication 1 ou la revendication 2, dans lequel l'étape de prétraitement
est effectuée à 12 à 15 °C.
5. Procédé selon la revendication 1, dans lequel le composé de cationisation comprend
du chlorure de 3-chloro-2-hydroxypropyltriméthylammonium.