- Key People:
- Friedrich Bayer
- Adolf von Baeyer
- Related Topics:
- saffron
- azo dye
- indigo
- anthraquinone dye
- cochineal
In dyeing operations, the dye must become closely and evenly associated with a specific material to give level (even) colouring with some measure of resistance to moisture, heat, and light—i.e., fastness. These factors involve both chemical and physical interactions between the dye and the fabric. The dyeing process must place dye molecules within the microstructure of the fibre. The dye molecules can be anchored securely through the formation of covalent bonds that result from chemical reactions between substituents on the molecules of the dye and the fibre. These are the reactive dyes, a type introduced in 1956. Many dye-fibre interactions, however, do not involve covalent bond formation. While some dyeing methods have several steps, many dyes can be successfully applied simply by immersing the fabric in an aqueous solution of the dye; these are called direct dyes. In other cases, auxiliary compounds and additional steps are required to obtain the desired fastness. In any event, questions arise as to how and how well the dye is retained within the fibre. The structure of the fibres from which the common fabrics are made provides some guidance for the selection of useful colorants.
Fibre structure
Fibre molecules are polymeric chains of repeating units of five major chemical types. Wool, silk, and leather are proteins, which are polymers of α-amino acids, RCH(NH2)COOH (where R is an organic group). Each chain consists of a series of amide linkages (―CO―NH―) separated by one carbon to which the R group, characteristic of each amino acid, is bonded. These groups may contain basic or acidic substituents, which can serve as sites for electrostatic interactions with dyes having, respectively, acidic or basic groups.
Polyamides (nylons) are synthetic analogs of proteins having the amide groups separated by hydrocarbon chains, (CH2)n, and can be made with an excess of either terminal amino (―NH2) or terminal carboxyl groups (―COOH). These and the amide groups are sites for polar interactions with dyes. Polyester poly(ethylene terephthalate), or PET, is the main synthetic fibre, accounting for more than 50 percent of worldwide production of synthetic fibres. The terminal hydroxyl groups (―OH) can serve as dyeing sites, but PET is difficult to dye because the individual chains pack tightly. Acrylics have hydrocarbon chains bearing polar groups, mainly nitriles, made by copolymerization of acrylonitrile (at least 85 percent) with small amounts (10–15 percent) of components such as acrylamide and vinyl acetate to produce a fibre with improved dyeability. Fibres with 35–85 percent acrylonitrile are termed modacrylics.
Cellulose is found in plants as a linear polymer of a few thousand glucose units, each with three free hydroxyl groups that can be extensively hydrogen-bonded. Cotton fibres are essentially pure cellulose. Wood contains 40–50 percent cellulose that is isolated as chemical cellulose by a process known as pulping. In fibre manufacture, the insolubility of cellulose caused processing problems that were overcome by the development of the viscose process, which produces regenerated cellulose with 300–400 glucose units. This semisynthetic cellulosic is rayon, which is very similar to cotton. The semisynthetic acetate rayon, produced by acetylation of chemical cellulose, has 200–300 glucose units with 75 percent of the hydroxyl groups converted to acetates. The smaller number of free hydroxyls precludes extensive hydrogen bonding, and dyes differing from those for cotton and rayon are needed.
Fibre porosity
Fibres are made by various spinning techniques that produce bundles of up to several hundred roughly aligned strands of polymer chains with length-to-diameter ratios in the thousands. For the dyeing process, an important characteristic of fibres is their porosity. There is a huge number of submicroscopic pores aligned mainly on the longitudinal axis of the fibres such that there are roughly 10 million pores in a cross-section of a normal fibre. The internal surface area therefore is enormous—about 45,000 square metres per kilogram (5 acres per pound) for cotton and wool—some thousand times greater than the outer surface area. To produce deep coloration, a layer of 1,000–10,000 dye molecules in thickness is needed. Upon immersion in a dyebath, the fabric absorbs the aqueous dye solution, and the dye molecules can move into pores that are sufficiently large to accommodate them. Although many pores may be too small, there is an ample number of adequate size to give satisfactory depths of colour.
Dye retention
Various attractive forces play a role in the retention of particular dyes on specific fibres. These include polar or ionic attractions, hydrogen bonding, Van der Waals forces, and solubilities. The affinity of a dye for a given substrate through such interactions is termed its substantivity. Dyes can be classified by their substantivity, which depends, in part, on the nature of the substituents in the dye molecule.
Attractive ionic interactions are operative in the case of anionic (acid) and cationic (basic) dyes, which have negatively and positively charged groups, respectively. These charged groups are attracted to sites of opposite polarity on the fibre. Mordant dyes are a related type. In the mordanting process, the fabric is pretreated with metallic salts, which complex with polar groups of the fibre to form more highly polarized sites for better subsequent interaction with the dye molecules.
Nonionic groups can also be involved in attractive interactions. Since the electronegativities of oxygen, nitrogen, and sulfur are greater than those of carbon and hydrogen, when these elements are part of a compound, the electron densities at their atomic sites are enhanced and those at neighbouring atoms are decreased. An O―H bond is therefore polar, and an attractive interaction between the hydrogen of one bond and the oxygen of a neighbouring bond can occur. Hydrogen bonding may be exhibited by any weakly acidic hydrogen. Although there is no chemical bond, strong attractive forces are involved. Phenolic hydroxyl groups are more highly polarized and, in dyes, can act as auxochromes and as good hydrogen-bonding sites.
Similar, but weaker, attractive forces are operative between other closely spaced polarized groups. These are the Van der Waals interactions, which are effective for dye adsorption if the separation between molecules is small. Such interactions are particularly important for cellulosics, which tend to have relatively large planar areas to which dye molecules are favourably attracted.
Although most dyes are applied as aqueous solutions, the finished goods should not be prone to dye loss through washing or other exposure to moisture. An exception is in the common use of highly soluble dyes to identify different fibres for weaving processes. These are called fugitive tints and are readily removed with water.