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Concept of Dyeing
Concept of Dyeing
The process in the course of which, a textile material placed in contact with the solution or dispersion of a dye, absorbs the said dye in such a way that the dyed material opposes a certain resistance to releasing the dye from the material in which it has been absorbed.
Phases in Dyeing:
1. 2. 3. 4. 5. Disaggregation of the dye Exhaustion Movement of the dye from dye-bath towards the textile material Adsorption of the dye on the surface of the textile material Diffusion/absorption/penetration of the dye within the textile material Fixation of the dye in the textile material
Generally these linear chains of polymers are oriented along the axis of fibriller filaments Dyeability of fibers depends on the orientation of these molecular chains
In crystalline regions of the fiber, the chains are highly oriented posing difficulties in the dye penetration In amorphous regions of the fiber, the chains are less oriented posing less difficulties in the dye penetration Amorphous regions may be considered functioning as pores, thus allowing the dye penetration The size of the fiber pores in relation with the size of the dye molecule determines the ease of penetration
The size of pores in some fibers increases due to fiber swelling in the presence of water, thus further facilitating the dye penetration Pore size of dry viscose rayon fibers is 5 A while 20-30 A when wet Pore size of different cellulosic fibers range from 20-100 A Porosity of viscose rayon > mercerized cotton > Un-mercerized cotton In the same dyeing bath, colour intensity of viscose rayon > mercerized cotton > Un-mercerized cotton
Pore size of wool fiber in dry state is 6A which increases to 41A when wet Synthetic fibers have high orientation and crystallinity and poor swelling in wet state; consequently dye penetration is comparatively difficult in synthetic dyes
1. Dye structure linearity Linear dyes have higher substantivity than the branched Coplanarity Dyes having coplanar aromatic nuclei have higher substantivity Capability to form hydrogen bonds Separation of hydrogen bond-capable entities by a distance of 10.3 Angstrom or a multiple thereof Existence of a system of conjugated double bonds The presence of solublizing (sulphonic or carboxylic) groups in the minimum possible quantity