Review paperRemediation of dyes in textile effluent: a critical review on current treatment technologies with a proposed alternative
Introduction
Textile industries consume large volumes of water and chemicals for wet processing of textiles. The chemical reagents used are very diverse in chemical composition, ranging from inorganic compounds to polymers and organic products Mishra and Tripathy, 1993, Banat et al., 1996, Juang et al., 1996. The presence of very low concentrations of dyes in effluent is highly visible and undesirable (Nigam et al., 2000). There are more than 100,000 commercially available dyes with over 7×105 ton of dye-stuff produced annually Meyer, 1981, Zollinger, 1987. Due to their chemical structure, dyes are resistant to fading on exposure to light, water and many chemicals Poots and McKay, 1976a, McKay, 1979. Many dyes are difficult to decolourise due to their complex structure and synthetic origin. There are many structural varieties, such as, acidic, basic, disperse, azo, diazo, anthroquinone based and metal complex dyes. Decolouration of textile dye effluent does not occur when treated aerobically by municipal sewerage systems (Willmott et al., 1998).
Through the formation, in 1974 of the Ecological and Toxicological Association of the Dyestuffs Manufacturing Industry (ETAD), aims were established to minimise environmental damage, protect users and consumers and to co-operate fully with government and public concerns over the toxicological impact of their products (Anliker, 1979). Over 90% of some 4000 dyes tested in an ETAD survey had LD50 values greater than . The highest rates of toxicity were found amongst basic and diazo direct dyes (Shore, 1996).
In Great Britain, such matters are regulated by the Environment Agency (EA) for England and Wales, and the Scottish Environment Protection Agency (SEPTA), (Willmott et al., 1998). Government legislation is becoming more and more stringent, especially in the more developed countries, regarding the removal of dyes from industrial effluents. Environmental policy in UK, since September 1997, has stated that zero synthetic chemicals should be released into the marine environment. Enforcement of this law will continue to ensure that textile industries treat their dye-containing effluent to the required standard. European Community (EC) regulations are also becoming more stringent (O’Neill et al., 1999).
There are many structural varieties of dyes that fall into either the cationic, nonionic or anionic type. Anionic dyes are the direct, acid and reactive dyes (Mishra and Tripathy, 1993). Brightly coloured, water-soluble reactive and acid dyes are the most problematic, as they tend to pass through conventional treatment systems unaffected (Willmott et al., 1998). Municipal aerobic treatment systems, dependent on biological activity, were found to be inefficient in the removal of these dyes (Moran et al., 1997).
Nonionic dyes refer to disperse dyes because they do not ionise in an aqueous medium. Concern arises, as many dyes are made from known carcinogens such as benzidine and other aromatic compounds (Baughman and Perenich, 1988). Weber and Wolfe (1987) demonstrated that azo- and nitro-compounds are reduced in sediments, and similarly Chung et al. (1978) illustrated their reduction in the intestinal environment, resulting in the formation of toxic amines. Anthroquinone-based dyes are most resistant to degradation due to their fused aromatic ring structure. The ability of some disperse dyes to bioaccumulate has also been demonstrated (Baughman and Perenich, 1988).
This review illustrates the critical study of the most widely used methods of dye removal from dye-containing industrial effluents. These methods have been discussed under three categories: chemical, physical and biological. Currently the main methods of textile dye treatment are by physical and chemical means (Table 1) with research concentrating on cheaper effective alternatives.
Section snippets
Oxidative processes
This is the most commonly used method of decolourisation by chemical means. This is mainly due to its simplicity of application. The main oxidising agent is usually hydrogen peroxide (H2O2). This agent needs to be activated by some means, for example, ultra violet light. Many methods of chemical decolourisation vary depending on the way in which the H2O2 is activated (Slokar and Le Marechal, 1997). Chemical oxidation removes the dye from the dye-containing effluent by oxidation resulting in
Adsorption
Adsorption techniques have gained favour recently due to their efficiency in the removal of pollutants too stable for conventional methods. Adsorption produces a high quality product, and is a process which is economically feasible (Choy et al., 1999). Decolourisation is a result of two mechanisms: adsorption and ion exchange (Slokar and Le Marechal, 1997), and is influenced by many physio-chemical factors, such as, dye/sorbent interaction, sorbent surface area, particle size, temperature, pH,
Decolourisation by white-rot fungi
White-rot fungi are those organisms that are able to degrade lignin, the structural polymer found in woody plants (Barr and Aust, 1994). The most widely studied white-rot fungus, in regards to xenobiotic degradation, is Phanerochaete chrysosporium. This fungus is capable of degrading dioxins, polychlorinated biphenyls (PCBs) and other chloro-organics Chao and Lee, 1994, Reddy, 1995. Davis et al. (1993) also showed the potential of using P. sordida to treat creosote contaminated soil. Kirby
Conclusions and suggestion for dye removal
Physical and chemical methods of dye removal are effective only if the effluent volume is small. This limits the use of physio-chemical methods, such as membrane filtration and cucurbituril, to small-scale in situ removal. A limiting factor of these methods is cost. This is true even in lab-scale studies, and methods, therefore, are unable to be used by large-scale industry. Biological activity, in liquid state fermentations, is incapable of removing dyes from effluent on a continuous basis.
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