Jhimli Paul

Decoloration and degradation of Reactive Red-120 dye by electron beam irradiation in aqueous solution.

The decoloration and degradation of aqueous solution of the reactive azo dye viz. Reactive Red-120 (RR-120) was carried out by electron beam irradiation. The change in decoloration percentage, removal of chemical oxygen demand (COD) and total organic carbon (TOC), solution pH and five-day biochemical oxygen demand (BOD(5)) were investigated with respect to the applied dose. However, the concentration of the dye in the solution showed a great influence on all these observables. During the radiolysis process, it was found that the decoloration of dye was caused by the destruction of the chromophore group of the dye molecule, whereas COD and TOC removal were depended on the extent of mineralization of the dye. The decrease in pH during the radiolysis process indicated the fragmentation of the large dye molecule into smaller organic components mostly like smaller organic acids. The BOD(5)/COD ratio of the unirradiated dye solution was in the range of 0.1-0.2, which could be classified as non-biodegradable wastewater. However, the BOD(5)/COD ratio increased upon irradiation and it indicated the transformation of non-biodegradable dye solution into biodegradable solution. This study showed that electron beam irradiation could be a promising method for treatment of textile wastewater containing RR-120 dye.

An insight into the influence of low dose irradiation pretreatment on the microbial decolouration and degradation of Reactive Red-120 dye.

The influence of low dose irradiation pretreatment on the microbial decolouration and degradation of Reactive Red-120 (RR-120) dye was investigated in detail by using Pseudomonas sp. SUK1. About 27%, 56% and 66% decolouration of 150 ppm RR-120 dye solution was observed by applying 0, 0.5 and 1 kGy doses, respectively, in the first step followed by microbial treatment for 24 h under static condition. Similarly, about 70%, 88% and 90% TOC removal was observed by applying 0, 0.5 and 1 kGy doses, respectively, in the first step followed by the microbial treatment for 96 h under static condition. The radiation induced fragmented products of RR-120 at doses of 0.5 and 1 kGy were investigated by FTIR and electrospray ionization-MS analysis. The induction of the enzymes viz. laccase, tyrosinase, azoreductase and NADH-2,6-dichlorophenol indophenol reductase was studied in the decolourised solution obtained after irradiating 150 ppm RR-120 dye solution with 0 and 1 kGy doses followed by the microbial treatment for 96 h under static condition. The enzymatic degradation products were studied by FTIR, HPLC and GC-MS. The toxicity study of the treated dye solution on plants revealed the degradation of RR-120 into non-toxic products by combined radiation-microbial treatment. This study explores a reliable and promising way to use industrially viable dose (≤1 kGy) and microbial strain viz. Pseudomonas sp. SUK1 for permissible safe disposal of dye solutions from textile industries.

Studies on production of fructo-oligosaccharides (FOS) by gamma radiation processing of microbial levan

Microbial levan, a natural polymer of fructose, was produced and purified by alcohol precipitation from culture supernatants of Bacillus megaterium type 1 grown in an optimized liquid sucrose medium. GPC analysis showed that the yield of the major fraction of levan having molecular weight ~5000 D increased with increase in sucrose concentration in the broth. Levan subjected to (60)Co-gamma radiation as well as acid hydrolysis was investigated by rheometry, UV-visible spectrophotometry and gel permeation chromatography (GPC) techniques. Unlike most of the polysaccharides, levan powder exhibited good radiation degradation stability up to 150 kGy. Gamma irradiation of 10% levan aqueous solution at 250 kGy yielded 63.0% fructo-oligosaccharide (FOS) with an average molecular weight of 1250 D. Acid hydrolysis of levan using 0.5 N HCl for 60 min treatment time gave rise to the desired FOS with lower yield (23.1%) as compared to that obtained in gamma radiolysis process.