Design of reaction conditions for the enhancement of microbial degradation of dyes in sequential cycles.

The present study evaluated the potential of white-rot fungal strain Coriolus versicolor to decolorize five structurally different dyes in sequential batch reactors under optimized conditions. The experiments were run continuously for seven cycles of 8 d each. High decolorizing activity was observed even during the repeated reuse of the fungus, especially when the old medium was replaced with fresh medium after every cycle. Biodegradation was the dominating factor as the fungus was able to produce the enzyme laccase mainly, to mineralize synthetic dyes. The nutrients and composition of the medium played important roles in sustaining the decolorisation potential of the fungus. Corncob was found be an easy and cheap substitute for carbon source for the fungus. Glucose consumption by the fungus was in accordance to its decolorisation activity and chemical oxygen demand (COD) reduction.

Removal of lead from aqueous solutions using Cassia grandis seed gum-graft-poly(methylmethacrylate).

Using persulfate/ascorbic acid redox system, a series of Cassia grandis seed gum-graft-poly(methylmethacrylate) samples were synthesized. The copolymer samples were evaluated for lead(II) removal from the aqueous solutions where the sorption capacities were found proportional to the grafting extent. The conditions for the sorption were optimized using copolymer sample of highest percent grafting. The sorption was found pH and concentration dependent, pH 2.0 being the optimum value. Adsorption of lead by the grafted seed gum followed a pseudo-second-order kinetics with a rate constant of 4.64 x 10(-5) g/mg/min. The equilibrium data followed the Langmuir isotherm model with maximum sorption capacity of 126.58 mg/g. The influence of electrolytes NaCl, Na(2)SO(4) on lead uptake was also studied. Desorption with 2 N HCl could elute 76% of the lead ions from the lead-loaded copolymer. The regeneration experiments revealed that the copolymer could be successfully reused for at least four cycles though there was a successive loss in lead sorption capacity with every cycle. The adsorbent was also evaluated for Pb(II) removal from battery waste-water containing 2166 mg/L Pb(II). From 1000 times diluted waste water, 86.1% Pb(II) could be removed using 0.05 g/20 ml adsorbent dose, while 0.5 g/20 ml adsorbent dose was capable of removing 60.29% Pb from 10 times diluted waste water. Optimum Pb(II) binding under highly acidic conditions indicated that there was a significant contribution of nonelectrostatic interactions in the adsorption process. A possible mechanism for the adsorption has been discussed.

Decolorization and partial degradation of monoazo dyes in sequential fixed-film anaerobic batch reactor (SFABR).

Decolorization of two monoazo dyes, acid orange 6 (AO6) and acid orange 7 (AO7), were studied in sequential fixed-film anaerobic batch reactor (SFABR) with varying dye concentrations and 500 mg/L glucose as the co-substrate. More than 90% dye decolorization could be achieved, even at 300 mg/L, with both AO6 and AO7 and dye decolorization rates were 168 mg/L/d and 176 mg/L/d, respectively. COD removals with these two monoazo dyes were significantly different, as 75% and 35% decrease were observed with AO6 and AO7, respectively. UV-visible spectral as well as HPLC analysis of SFABR treated effluent showed the accumulation of 4-aminobenzenesulfonate (4-ABS) from AO6 and AO7. Aminoresorcinol (AR) formed from AO6 decolorization could not be detected at the end of SFABR cycle. This along with high COD removal indicated its further degradation. Formation of pink coloration on exposure to air indicated the presence of 1-amino-2-naphthol (AN) in AO7 fed reactor effluent. Thus both 4-ABS and AN were resistant to further degradation under anaerobic conditions. Presence of nitrate did not decrease the observed decolorization at the end of 24h SFABR cycle, although initial rate was decreased. This indicates the suitability of SFABR configuration for the treatment of azo-dye containing wastewaters in the presence of nitrate.

Novel chitosan derivative for the removal of cadmium in the presence of cyanide from electroplating wastewater.

Chitosan was chemically modified by introducing xanthate group onto its backbone using carbondisulfide under alkaline conditions. The chemically modified chitosan flakes (CMC) was used as an adsorbent for the removal of cadmium ions from electroplating waste effluent under laboratory conditions. CMC was found to be far more efficient than the conventionally used adsorbent activated carbon. The maximum uptake of cadmium by CMC in batch studies was found to be 357.14 mg/g at an optimum pH of 8.0 whereas for plain chitosan flakes it was 85.47 mg/g. Since electroplating wastewater contains cyanide in appreciable concentrations, interference of cyanide ions in cadmium adsorption was found to be very significant. This problem could be easily overcome by using higher doses of CMC, however, activated carbon was not found to be effective even at higher doses. Due to the high formation constant of cadmium with xanthate and adsorption was carried out at pH 8, cations like Pb(II), Cu(II), Ni(II) and Zn(II) did not interfere in the adsorption. Dynamics of the sorption process were studied and the values of rate constant of adsorption were calculated. Desorption of the bound cadmium from CMC was accomplished with 0.01 N H(2)SO(4). The data from regeneration efficiencies for 10 cycles evidenced the reusability of CMC in the treatment of cadmium-laden wastewater.

Sequential batch culture studies for the decolorisation of reactive dye by Coriolus versicolor.

The white rot fungus Coriolus versicolor could decolorise reactive dye Remazol Brilliant Violet to almost 90%. The fungal mycelia removed color as well as COD up to 95% and 75%, respectively, in a batch reactor. Decolorising activity was observed during the repeated reuse of the fungus. It was possible to substantially increase the dye decolorising activity of the fungus by carefully selecting the operational conditions such as media composition, age of fungus and nitrogen source. The fungal pellets could be used for eight cycles during the long term operation, where medium and dye was replenished at the end of each cycle and the fungus was recycled. Presence of a nitrogen source and nutrient content of media played an important role in sustaining the decolorisation activity of the fungus. The form of nitrogen source (e.g. peptone vs. urea) was also important to maintain the decolorising activity with peptone showing better decolorisation.

Use of Cassia javahikai seed gum and gum-g-polyacrylamide as coagulant aid for the decolorization of textile dye solutions.

Investigations were carried out for possible exploitation of Cassia javahikai seeds as potential source of commercial gum for the textile wastewater treatment. Graft copolymerization with acrylamide was done to modify the seed gum for the favorable properties. C. javahikai seed gum, and its copolymer grafted with acrylamide were synthesized in the presence of oxygen using potassium persulphate/ascorbic acid redox system. Both C. javahikai seed gum (CJ) and its grafted-polyacrylamide (CJG), were found to be good working substitutes as coagulant aids in conjunction with PAC, for the decolorization of all the dyes in varying ratios. CJ and CJG alone could effectively decolorize direct dyes (DBR and DO) and in conjunction with a very low dose of PAC could decolorize all the dyes (DBR, DO, ASR, and PBB) to more than 70%. Grafting also increased the decolorizing ability of CJ gum.

Removal of hexavalent chromium using a novel cross linked xanthated chitosan.

Suitability of a novel cross linked, chemically modified chitosan as highly efficient adsorbent for the recovery of toxic chromium(VI) was studied. After cross linking with glutaraldehyde, xanthate group was grafted onto the back bone of chitosan. Sorption was found to be both pH and concentration dependent, with pH 3 being the optimum value. Both, chemically modified beads (CMCB) and flakes (CMCF) followed a pseudo-second-order kinetics with a rate constant of 2.037 and 4.639 g/mg/min, respectively. The equilibrium data followed the Langmuir isotherm model with maximum capacities of 625 mg/g and 256.4 mg/g and for CMCF and CMCB respectively. Desorption studies revealed the reusability of the sorbent for at least 10 cycles without any significant change in adsorption capacities.

Organochlorine and organophosphorous pesticide residues in ground water and surface waters of Kanpur, Uttar Pradesh, India.

A survey undertaken in Kanpur, northern India, has shown the presence of high concentrations of both organochlorine and organophosphorous pesticides in the surface and ground water samples. Liquid-liquid extraction followed by GC-ECD was used for the determination of these compounds. Among the various pesticides analyzed, high concentrations of gamma-HCH (0.259 microg/l) and malathion (2.618 microg/l) were detected in the surface water samples collected from the River Ganges in Kanpur. In the ground water samples collected from the various hand pumps located in agricultural and industrial areas, apart from gamma-HCH and malathion, dieldrin was also detected. The maximum concentration values of gamma-HCH, malathion and dieldrin were 0.900, 29.835 and 16.227 microg/l, respectively. Especially, the concentration of malathion was found to be much higher than the EC water quality standards in the ground water samples from industrial area posing a high risk to the common people. Pesticides like DDE, DDT, aldrin, ethion, methyl parathion and endosulfan were not detected in both the surface and ground water samples.

Organochlorine and organophosphorus pesticide residues in breast milk from Bhopal, Madhya Pradesh, India.

HCH isomers, endosulfan, malathion, chlorpyrifos, and methyl-parathion were monitored in human milk samples from Bhopal, Madhya Pradesh. The endosulfan concentrations were highest and exceeded the sigma-HCH, chlorpyrifos, and malathion concentrations by 3.5-, 1.5-, and 8.4-fold, respectively. Through breast milk, infants consumed 8.6 times more endosulfan and 4.1 times more malathion than the average daily intake levels recommended by the World Health Organization. A correlation analysis (r values) between mothers' age and the content of the chemicals accumulated in breast milk indicated a substantial degree of correlation for malathion (r = 0.5). The other chemicals showed low to negligible correlation with donor age.

A modeling study on the role of fungi in removing inorganic pollutants.

In this paper, a non-linear mathematical model for removing an inorganic pollutant such as chromium from a water body using fungi is proposed and analyzed. It is assumed that the inorganic pollutant is discharged in a water body with a constant rate, which is depleted due to natural factors as well as by fungal absorption using dissolved oxygen in the process. The model is analyzed by using stability theory of differential equations and simulation. The analysis shows that the inorganic pollutant can be removed from the water body by fungal absorption, the rate of removal depends upon the concentration of inorganic pollutant, the density of fungal population and various interaction processes. The simulation analysis of the model confirms the analytical results. It is noted here this theoretical result is qualitatively in line with the experimental observations of one of the authors (Sanghi).

Biomimetic synthesis and characterisation of protein capped silver nanoparticles.

A controlled and up-scalable route for the biosynthesis of silver nanopartilces (NPs) mediated by fungal proteins of Coriolus versicolor has been undertaken for the first time. The fungus when challenged with silver nitrate solution accumulated silver NPs on its surface in 72h which could be reduced to 1h by tailoring the reaction conditions. Under alkaline conditions, the reaction was much faster and could easily proceed at room temperature even without stirring. The resulting Ag NPs displayed controllable structural and optical properties depending on the experimental parameters such as pH and reaction temperatures. The average size, morphology, and structure of particles were determined by AFM, TEM, XRD and UV/Visible absorption spectrophotometry. Fourier transform infrared study disclosed that the amino groups were bound to the particles, which was accountable for the stability of NPs. It further confirmed the presence of protein as the stabilizing and capping agent surrounding the silver NPs. Experiments were conducted both with, media in which fungus was initially harvested and that of pristine fungal mycelium alone. Under normal conditions, in the case of media extracellular synthesis took place whereby other than the fungal proteins, glucose was also responsible for the reduction. In the case of fungal mycelium, the intracellular formation of Ag NPs, could be tailored to give both intracellular and extracellular Ag NPs under alkaline conditions whereby the surface S-H groups of the fungus played a major role.

Fungal bioremediation of chromates: conformational changes of biomass during sequestration, binding, and reduction of hexavalent chromium ions.

This paper highlights the mechanistic aspects of white rot fungus Coriolus versicolor as a complexing/reducing agent for chromium bioremediation. The chemical reduction of Cr(VI) to Cr(III) via the formation of Cr(VI) thio ester as an intermediate, is pH dependent and controls the overall chromium adsorption kinetics. The strong adsorption affinity of the biomass towards Cr(VI) anions was evaluated by the Freundlich and the Langmuir adsorption isotherms. The FTIR spectroscopic analysis suggested the involvement of amino, carboxylate, and thiol groups from fungal cell wall in chromium binding and reduction. The mechanism of the adsorption was preferential sequestration along with binding of the metal to the ligating groups present in the biomass followed by reduction to trivalent state. The results indicate step-wise progression of overall reaction dictated and modulated by structural and conformation effects in the biomass that lead to saturation, acceleration, and ultimate saturation kinetics effects.

Poly(acrylamide) functionalized chitosan: an efficient adsorbent for azo dyes from aqueous solutions.

In the present communication we report on the optimization of persulfate/ascorbic acid initiated synthesis of chitosan-graft-poly(acrylamide) (Ch-g-PAM) and its application in the removal of azo dyes. The optimum yield of the copolymer was obtained using 16 x 10(-2)M acrylamide, 3.0 x 10(-2)M ascorbic acid, 2.4 x 10(-3)M K(2)S(2)O(8) and 0.1g chitosan in 25 mL of 5% aqueous formic acid at 45+/-0.2 degrees C. Ch-g-PAM remained water insoluble even under highly acidic conditions and could efficiently remove Remazol violet and Procion yellow dyes from the aqueous solutions over a pH range of 3-8 in contrast to chitosan (Ch) which showed pH dependent adsorption. The adsorption data of the Ch-g-PAM and Ch for both the dyes were modeled by Langmuir and Freundlich isotherms where the data fitted better to Langmuir isotherms. To understand the adsorption behavior of Ch-g-PAM, adsorption of Remazol violet on to the copolymer was optimized and the kinetic and thermodynamic studies were carried out taking Ch as reference. Both Ch-g-PAM and Ch followed pseudo-second-order adsorption kinetics. The thermodynamic study revealed a positive heat of adsorption (Delta H degrees), a positive DeltaS degrees and a negative Delta G degrees, indicating spontaneous and endothermic nature of the adsorption of RV dye on to the Ch-g-PAM. The Ch-g-PAM was found to be very efficient in removing color from real industrial wastewater as well, though the interfering ions present in the wastewater slightly hindered its adsorption capacity. The data from regeneration efficiencies for ten cycles evidenced the high reusability of the copolymer in the treatment of waste water laden with even high concentrations of dye.

Ipomoea dasysperma seed gum: an effective natural coagulant for the decolorization of textile dye solutions.

An investigation of dye decolorization from synthetic dye solutions using the non-ionic, water-soluble, high molecular weight seed gums Ipomoea dasysperma and guar gum as coagulants was undertaken. The use of galactomannans derived from plants in this system presents a sustainable method of textile effluent treatment. These natural coagulants extracted from plants proved to be workable alternatives to conventional coagulants like polyaluminum chloride, as they are biodegradable, safe to human health, are cost effective when compared to imported chemicals and have a wider effective dosage range for flocculation of various colloidal suspensions. Coagulant dose and coagulation pH are important factors influencing the mechanism of coagulation. Also the type and chemical structure of the dye plays an important role in the coagulation process. The seed gums alone were found to be effective for decolorization of direct dye and in combination with PAC their coagulation efficiency was well extended even for reactive and acid dyes.

Poly(acrylonitrile) grafted Ipomoea seed-gums: a renewable reservoir to industrial gums.

Plants of Ipomoea genus are widely distributed in India as wild vegetation and are reported source for the seed gums. Seed gums from Ipomoea dasysperma, Ipomoea hederacea, and Ipomoea palmata plants were grafted with polyacrylonitrile (PAN) using potassium persulfate/ascorbic acid redox initiator for modifying their properties for potential industrial applications. Under identical grafting conditions, the extent of the grafting was observed to be dependent on the galactose-to-mannose ratio and the degree of the branching in the galactomannans. Viscosity, gel formation, film formation, and the shelf life of the grafted gum solutions and water and saline retention capacity of the grafted seed gums were determined and compared with the parent gums. Water retention of the alkalie hydrolyzed grafted seed gums were also studied. Grafted gums were characterized using FTIR, NMR, and XRD analysis.