Removal of arsenic from water by electrocoagulation

In the present study electrocoagulation (EC) has been evaluated as a treatment technology for arsenite [As(III)] and arsenate [As(V)] removal from water. Laboratory scale experiments were conducted with three electrode materials namely, iron, aluminum and titanium to assess their efficiency. Arsenic removal obtained was highest with iron electrodes. EC was able to bring down aqueous phase arsenic concentration to less than 10 microgl(-1) with iron electrodes. Current density was varied from 0.65 to 1.53 mAcm(-2) and it was observed that higher current density achieved rapid arsenic removal. Experimental results at different current densities indicated that arsenic removal was normalized with respect to total charge passed and therefore charge density has been used to compare the results. Effect of pH on arsenic removal was not significant in the pH range 6-8. Comparative evaluation of As(III) and As(V) removal by chemical coagulation (with ferric chloride) and electrocoagulation has been done. The comparison revealed that EC has better removal efficiency for As(III), whereas As(V) removal by both processes was nearly same. The removal mechanism of As(III) by EC seems to be oxidation of As(III) to As(V) and subsequent removal by adsorption/complexation with metal hydroxides generated in the process.     

Dissipation behavior of propargite--an acaricide residues in soil, apple (Malus pumila) and tea (Camellia sinensis)

Propargite, recently introduced in India, is an effective acaricide on a large number of crops most of which are consumed by human beings directly or after processing. Therefore, it has become important to check the dissipation behavior of propargite in edible raw commodities, processed products and in the environment. In the present study, dissipation of residue of this acaricide in soil, apple fruit and tea (green tea leaves, manufactured tea, infusion and spent leaves) was studied. Analysis was carried out using high performance-liquid chromatography with UV detection system. The dissipation rate was found to vary with the nature of studied crop/sample. In soil, half-life ranged from 43 to 45 days, while in plant matrices (tea and apple) it ranged 1.66-2.61 days. The percent transfer of propargite residue from manufactured tea to infusion was 23.60-40.00; however, 35.71-53.20% of the residues remained stuck to the spent leaves.     

Lead induced changes in antioxidant metabolism of horsegram (Macrotyloma uniflorum (Lam.) Verdc.) and bengalgram (Cicer arietinum L.)

One-month old horsegram (Macrotyloma uniflorum (Lam.) Verdc. cv VZM1) and bengalgram (Cicer arietinum L. cv Annogiri) were exposed to different regimes of lead stress as Pb(NO3)2 at 0, 200, 500 and 800 ppm concentrations. The extent of oxidative damage as the rate of lipid peroxidation, antioxidative response and the accumulation of lead in roots and shoots of both plants were evaluated after 12 days of lead stress. Lead (Pb) treated plants showed increased levels of lipid peroxidation as evidenced from the increased malondialdehyde content coupled with the increase in the activities of superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), glutathione reductase (GR), glutathione S-transferase (GST) compared to control (untreated) plants. Lead stress caused significant changes in the activity of antioxidative enzymes. The effect of lead was found to be concentration dependent. Higher concentration of lead (800 ppm) resulted 2- to 3-fold increase in SOD, catalase and peroxidase activities, 3- to 5-fold increase in GR activity and 3- to 4-fold increase in GST activity in roots and leaves of both horsegram and bengalgram plants. Lead stress caused a significant increase in the rate of peroxidation as showed in the levels of malondialdehyde content in roots and leaves of both plant species. Horsegram registered lower Pb accumulation than bengalgram, however localization of Pb was greater in roots than leaves in both plants. In general, lipid peroxide levels and antioxidative enzyme activities were higher in horsegram than bengalgram and also more in roots than leaves which best concordance with the lead contents of both the plants and organs. These results suggest that Pb toxicity causes oxidative stress in plants and the antioxidative enzymes SOD, CAT, POD, GR, GST could play a pivotal role against oxidative injury.     

Improved light extinction reconstruction in interagency monitoring of protected visual environments

The U.S. Environmental Protection Agency (EPA) published the Regional Haze Rule (RHR) in 1999. The RHR default goal is to reduce haze linearly from the baseline period of 2000 through 2004 to natural background in 2064. EPA-recommended method for estimating baseline and natural haze uses the Interagency Monitoring of Protected Visual Environments (IMPROVE) light extinction formula. The IMPROVE formula predicts light extinction from measured aerosol chemical concentrations and estimates of the relative humidity multiplier. On average, the IMPROVE formula overpredicts 6156 nephelometer days (24-hr average measured particle light scattering, bsp) of data by 25%. A new IMPROVED method that reconstructs light extinction using a concentration power law model overpredicts these nephelometer days of data by just 2%. Ignoring the 20% lowest light scattering days, this new IMPROVED formula has a 3% underprediction bias over the 4925 highest nephelometer days with light scattering > or =8 inverse megameters. For comparison, the IMPROVE formula has a 12% overprediction bias for the same days. The IMPROVE formula overprediction averages 77%, 27%, 17%, 9%, and -5% broken down by quintile from lowest to highest nephelometer measured light scattering days. The new IMPROVED formula average overprediction is 21%, -5%, -5%, -2%, and 0%. So, agreement between measured and predicted light scattering improves by modifying the current IMPROVE light extinction formula.     

Bioleaching of zinc and copper from anaerobically digested swine manure: effect of sulfur levels and solids contents.

Anaerobically digested swine manure (ADSM) generally contains high concentrations of zinc (Zn) and copper (Cu). These metals levels exceed the land application regulations of municipal biosolids of many European countries and are on the borderline of exceptional quality in the U.S. Environmental Protection Agency (U.S. EPA) 40 CFR part 503 standards. From this perspective, a series of batch tests were conducted to evaluate the feasibility of bioleaching of Zn and Cu from ADSM so that the produced biosolids could safely be applied to land. The effect of different substrate levels (sulfur) and total solids content (as high as 9%) on metal solubilization was investigated. The results showed that metal solubilization efficiency for both Zn and Cu declined significantly with an increase in total solids from 3 to 6% and then to 9% at the same substrate level. Metal solubilization increased proportionately with increases in substrate concentration up to 6% of total solids content. However, at 9% total solids content, metal solubilization was insignificant at all substrate levels tested. At a 6% total solids level and 10 000 mg/L of substrate, 94% of Zn and 72% of Cu were solubilized. Bioleaching was also found to be effective in destruction of pathogens with approximately 2.5 log-scale reduction. The residual biosolid was found to meet the Class A biosolids standands of U.S. EPA 40 CFR part 503.     

Removal of congo red from aqueous solution by bagasse fly ash and activated carbon: kinetic study and equilibrium isotherm analyses

Present investigation deals with the utilisation of bagasse fly ash (BFA) (generated as a waste material from bagasse fired boilers) and the use of activated carbons-commercial grade (ACC) and laboratory grade (ACL), as adsorbents for the removal of congo red (CR) from aqueous solutions. Batch studies were conducted to evaluate the adsorption capacity of BFA, ACC and ACL and the effects of initial pH (pH(0)), contact time and initial dye concentration on adsorption. The pH(0) of the dye solution strongly affected the chemistry of both the dye molecules and BFA in an aqueous solution. The effective pH(0) was 7.0 for adsorption on BFA. Kinetic studies showed that the adsorption of CR on all the adsorbents was a gradual process. Equilibrium reached in about 4h contact time. Optimum BFA, ACC and ACL dosages were found to be 1, 20 and 2 g l(-1), respectively. CR uptake by the adsorbents followed pseudo-second-order kinetics. Equilibrium isotherms for the adsorption of CR on BFA, ACC and ACL were analysed by the Freundlich, Langmuir, Redlich-Peterson, and Temkin isotherm equations. Error analysis showed that the R-P isotherm best-fits the CR adsorption isotherm data on all adsorbents. The Freundlich isotherm also shows comparable fit. Thermodynamics showed that the adsorption of CR on BFA was most favourable in comparison to activated carbons.     

Performance evaluation of waste activated carbon on atrazine removal from contaminated water

In this study, the potential of spent activated carbon from water purifier (Aqua Guard, India) for the removal of atrazine (2 chloro-4 ethylamino-6-isopropylamino-1, 3, 5 triazine) from wastewaters was evaluated. Different grades of spent activated carbon were prepared by various pretreatments. Based on kinetic and equilibrium study results, spent activated carbon with a grain size of 0.3-0.5 mm and washed with distilled water (designated as WAC) was selected for fixed column studies. Batch adsorption equilibrium data followed both Freundlich and Langmuir isotherm. Fixed bed adsorption column with spent activated carbon as adsorbent was used as a polishing unit for the removal of atrazine from the effluent of an upflow anaerobic sludge blanket (UASB) reactor treating atrazine bearing domestic wastewater. Growth of bacteria on the surface of WAC was observed during column study and bacterial activity enhanced the effectiveness of adsorbent on atrazine removal from wastewater.     

Characterizing the source/sink behavior of double-layer building materials

A model is developed to predict the rate of mass transfer between a double-layer material and indoor air. The model allows non-uniform initial material-phase concentrations in each of the two layers and a transient influent gas-phase concentration to be considered. This model builds on a recently validated single-layer model and should prove useful in predicting the behavior of double-layer material assemblies. Many indoor furnishings and building structures are comprised of layers of different material. The approach taken here represents a first step in the development of a more generally applicable multi-layer model. An analytical solution to the double-layer model is obtained and a parametric analysis is performed illustrating the behavior of the model as a function of the primary model parameters. The paper concludes by examining the potential use of thin diffusion barriers to reduce material emission rates and a hypothetical example of emissions from an adhesive that is part of an adhesive/material assembly.     

Persistence of alpha and beta isomers of endosulphan and endosulphan sulphate in diverse soils of India as influenced by flooding

Laboratory studies were undertaken to evaluate the persistence of alpha-endosulphan, beta-endosulphan and endosulphan sulphate in four diverse soils under non-flooded and flooded conditions. Significant variations were observed in the extent of persistence of the three chemicals in different non-flooded soils with maximum persistence observed in Alfisol and the least in Mollisol having near neutral pH and higher organic matter. Degradation was more in all the flooded soils than in the non-flooded counterpart but in Vertisol under flooded and non-flooded conditions, the rate of degradation of endosulphan sulphate was found to be nearly same.