Coloration process
AssigneeImperial Chemical Industries PLC
InventorHerbert G. Connor
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AssigneeImperial Chemical Industries PLC
InventorHerbert G. Connor
Estimating the term…
Process for the coloration of cellulose textile materials which comprises applying a dyestuff containing one or more s-triazinyl groups bearing a quaternary nitrogen substituent, or the precursors of such a dyestuff, in the absence of an acid-binding agent and heating the treated textile material to 150.degree. C. or higher to fix the dyestuff to the cellulose. Improved coloration is often achieved by applying urea or dicyandiamide with the dyestuff. The process is particularly valuable for the coloration of cellulose in polyester/cellulose unions when a disperse dye may be applied simultaneously with less problems than encountered with conventional alkali fixed reactive dyes.
A process for the colouration of cellulose or wool textile materials which comprises applying a dyestuff containing one or more s-triazinyl groups bearing a quaternary nitrogen substituent, or the precursors of such a dyestuff, in the absence of an acid-binding agent and heating the treated textile material to 150.degree. C. or higher to fix the dyestuff to the cellulose or wool, the dyestuff being selected from the group consisting of
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With the reactive group directly attached to a heterocyclic ring: to a triazine ring
Natural or regenerated cellulose: using reactive dyes
Mixtures of fibres containing hydroxyl and ester groups: using one kind of dye
Natural fiber dyeing: wool or silk
Term ended 5 Jun 2000 (estimated)
USPTO file history isn’t available for this patent, so only indexed dates are shown.
This invention relates to a colouration process in particular to a process for colouring cellulose and wool textiles.
It is now well-established to colour cellulose with dyestuffs containing groups which are believed to react to form a bond between dyestuff and hydroxyl groups of the cellulose. Many such dyestuffs are available having a wide range of groups capable of reacting with the cellulose such as haloheterocyclic compounds, e.g. fluoro-, chloro and bromo-s-triazinyl, chloro- and fluoro-pyrimidinyl, chloroquinoxaline and chloropyridazine. To obtain good levels of colouration it is usually found necessary to include a treatment with an acid-binding agent in the colouration process. The acid-binding agents are typically sodium bicarbonate, carbonate or hydroxide and are usually associated with an alkaline pH. Fixation is normally achieved at temperatures from 25.degree.-100.degree. C.
Similar reaction can occur between these dyestuffs and amino groups in wool though an alkaline treatment is not usually employed in this instance since it is not necessary to ensure reaction and wool may be adversely affected by the alkaline conditions. Thus it is not usually possible to colour wool/cellulose blends satisfactorily with conventional reactive dyestuffs since each component requires conditions incompatible with those required by the other.
Print pastes are prepared with the composition given in the following Table:
______________________________________ 1 2 3 4 5 6 7 8 9 ______________________________________ Dyestuff 5 5 5 5 5 5 5 5 5 Water 45 25 43 23 44.5 24.5 42.5 22.5 22 Manutex F 50 50 50 50 50 50 50 50 50 (alginate thickener 10% aqueous soln.) Urea -- 20 -- 20 -- 20 -- 20 20 Nicotinic -- -- -- -- 0.5 0.5 0.5 0.5 1 acid Dicyan- -- -- 2 2 -- -- 2 2 2 diamide ______________________________________
The dyestuff has the structure (in free acid form): ##STR9##