Electrocoagulation of blue reactive,red disperse and mixed dyes,and application in treating textile effluent

This study investigated the efficiency of electrocoagulation in removing color from synthetic and real textile wastewater. Two representative dye molecules were selected for the synthetic dye wastewater: a blue reactive dye (Reactive Blue 140) and a disperse dye (Disperse Red 1). The electrochemical technique showed satisfactory color removal efficiency and reliable performance in treating both individual and mixed dye types. The removal efficiency and energy consumption data showed that, for a given current density, iron was superior to aluminum in treating both the reactive dye and the disperse dye. With an initial dye concentration of 100 mg L^?1, the energy cost in achieving >95% color removal was on the order of 1 kWh m^?3 for both dyes. The effect of changing the initial pH of the samples on the removal efficiency and energy consumption was also studied. It was found that the design parameters used for the synthetic wastewater were less effective for treatment of real textile wastewater, with 1 in 5 tests on real wastewater failing.     

Effect of salinity on metal-complex dye biosorption by Rhizopus arrhizus

In this study the biosorption of Yellow RL, a metal-complex anionic dye, by dried Rhizopus arrhizus, a filamentous fungus, was investigated as a function of initial solution pH, initial dye concentration and initial salt (sodium chloride) concentration. The fungus exhibited the maximal dye uptake at pH 2 in the absence and in the presence of salt. Dye uptake increased with the dye concentration up to 1000 mg l^?1 and diminished considerably in the presence of increasing concentrations of salt up to 50 g l^?1. The fungus biosorbed 85.4 mg dye g^?1of dried biomass at 100 mg l^?1 initial dye concentration in the absence of salt. When 50 g l^?1 salt was added to the biosorption medium, this value dropped to 60.8 mg g^?1 resulting in 28.8% reduction in biosorption capacity. The Redlich–Peterson and Langmuir–Freundlich were the most suitable adsorption models for describing the biosorption equilibrium data of the dye both individually and in salt containing medium. The pseudo-second-order and saturation type kinetic models depicted the biosorption kinetics accurately for all cases studied. Equilibrium and kinetic constants varied with the level of salt were expressed as a function of salt concentration.     

Lead accumulation in different Chinese cabbage cultivars and screening for pollution-safe cultivars

Recently, the concept of pollution-safe cultivars (PSCs) was proposed to minimize the influx of pollutants to the human food chain. Variations in lead (Pb) uptake and translocation among Chinese cabbage (Brassica pekinensis L.) cultivars were investigated in a pot-culture experiment and a field-culture experiment to screen out Pb-PSCs for food safety. The results of the pot-culture experiment showed that shoot Pb concentrations under two Pb treatments (500 and 1500 mg kg^?1) varied significantly (p < 0.05) between cultivars, with average values of 3.01 and 6.87 mg kg^?1, respectively. Enrichment factors (EFs) and translocation factors (TFs) in cultivars were less than 0.50 and varied significantly (p < 0.05) between cultivars. Shoot Pb concentrations in 12 cultivars under treatment T₁ (500 mg kg^?1) were lower than 2.0 mg kg^?1. The field-culture experiment further confirmed Qiuao, Shiboqiukang and Fuxing 80 as Pb-PSCs, which were suitable to be cultivated in low-Pb (<382.25 mg kg^?1) contaminated soils and harmless to human health as foods.     

Subsoil TPH contamination in two oil pipeline pumping stations and one pipeline right-of-way in north Mexico

This investigation deals with the characterization carried out in zones around two pipeline pumping stations and one pipeline right-of-way in the north of Mexico. In particular those areas where contamination was evaluated: (a) south area of the separation ditch in the Avalos station, (b) the area between the separation ditch at the Avalos station, (c) km 194 + 420 of the Moctuzma station, and (d) km 286 + 900 in the Candelaria station. Results of this investigation showed that only four samples showed TPH values higher than the Mexican limit for 2004: AVA 1B, with 21,191 mg kg^?1; AVA 1C, with 9348 mg kg^?1; AVA 2B, with 13,970 mg kg^?1; and MOC 2A, with 4108 mg kg^?1.None of the sampled points showed the presence of PAHs at values higher than those found in the Mexican or American legislations. PAH were detected in the range of 0.0004 and 13.05 mg kg^?1.It is suggested to implement surfactant soil washing as a remediation technique for the approximately 600 m³ that need to be treated.     

Preparation of activated carbons from unburnt coal in bottom ash with KOH activation for liquid-phase adsorption

In this work, unburnt coal (UC) in bottom ash from coal-fired power plants was soaked in KOH solution and activated for 1 h at 780 °C. The yield of activated carbons varied from 47.8 to 54.8% when the KOH/UC weight ratio changed from 2 to 4. Pore properties of these activated carbons including the BET surface area, pore volume, pore size distribution, and pore diameter were characterized based on N₂ adsorption isotherms. It was shown that the isotherms for the adsorption of methylene blue, acid blue 74, and 4-chlorophenol from aqueous solutions on these activated carbons at 30 °C were well fitted by the Langmuir equation (correlation coefficient r² > 0.9968). The adsorption capacities of methylene blue, acid blue 74, and 4-chlorophenol were obtained to be 2.40–2.88, 0.57–1.29, and 2.34–5.62 mmol/g, respectively. Moreover, the adsorption kinetics could be suitably described by the Elovich equation.     

Effect of feeding strategy and COD/sulfate ratio on the removal of sulfate in an AnSBBR with recirculation of the liquid phase

The objective of this work was to analyze the effect of the interaction between feeding strategy and COD/sulfate ratio on the removal efficiency of sulfate and organic matter from a synthetic wastewater. An anaerobic sequencing batch reactor with recirculation of the liquid phase and containing immobilized biomass on polyurethane foam (AnSBBR) was used. The AnSBBR with a total volume of 3.7 L, treated 2.0 L synthetic wastewater in 8-h cycles at 30 ± 1 °C and was inoculated with anaerobic biomass from a UASB. Two feeding strategies were assessed: (a) batch and (b) batch followed by fed-batch. In strategy (a) the reactor was fed in 10 min with 2 L wastewater containing sulfate and carbon sources. In strategy (b) 1.2 L wastewater (containing only the sulfate source) was fed during the first 10 min of the cycle and the remaining 0.8 L (containing only the carbon source) in 240 min. The COD/sulfate ratios assessed were 1 and 3. Based on these values and on the concentrations of organic matter (0.5–11.25 gCOD/L) and sulfate (0.5 and 2.5 gSO₄^2?/L), the sulfate and organic matter loading rates applied equaled 1.5 and 4.5 gSO₄^2?/L d for sulfate and 1.5, 4.5 and 13.5 gCOD/L d for organic matter. After stabilization of the system time profiles were run of monitored parameters (COD, sulfate, sulfide and sulfite). In general, the reactor showed to be robust for use in the anaerobic treatment of wastewaters containing sulfate. Gradual feeding (strategy b) of the carbon source favored sulfate reduction, resulting in sulfate removal efficiencies of 84–98% and organic matter removal efficiencies of 48–95%. The best results were observed under COD/sulfate ratio equal to 1 (loading rates of 1.5 and 4.5 gSO₄^2?/L d for sulfate, and 1.5 and 4.5 gCOD/L d for organic matter). When COD/sulfate ratio was 3 (loading rates of 1.5 and 4.5 gSO₄^2?/L d for sulfate, and 4.5 and 13.5 gCOD/L d for organic matter) the effect of feed mode became less significant. These results show that the strategy batch followed by fed-batch is more advantageous for COD/sulfate ratios near the stoichiometric value (0.67) and higher organic matter and sulfate concentrations.     

Adsorption of basic dye from aqueous solution onto fly ash

The fly ash treated by H₂SO₄ was used as a low-cost adsorbent for the removal of a typical dye, methylene blue, from aqueous solution. An increase in the specific surface area and dye-adsorption capacity was observed after the acid treatment. The adsorption isotherm and kinetics of the treated fly ash were studied. The experimental results were fitted using Langmuir and Freundlich isotherms. It shows that the Freundlich isotherm is better in describing the adsorption process. Two kinetic models, pseudo-first order and pseudo-second order, were employed to analyze the kinetic data. It was found that the pseudo-second-order model is the better choice to describe the adsorption behavior. The thermodynamic study reveals that the enthalpy (ΔH⁰) value is positive (5.63 kJ/mol), suggesting an endothermic nature of the adsorption.     

Novel lithium-based sorbents from fly ashes for CO2 capture at high temperatures

In this work several Li₄SiO₄-based sorbents from fly ashes for CO₂ capture at high temperatures have been developed. Three fly ash samples were collected and subjected to calcination at 950 °C in the presence of Li₂CO₃. Both pure Li₄SiO₄ and fly ash-based sorbents were characterised and tested for CO₂ sorption at different temperatures between 400 and 650 °C and adding different amounts of K₂CO₃ (0–40 mol%). To examine the sorbents performance, multiple CO₂ sorption/desorption cycles were carried out. The temperature and the presence of K₂CO₃ strongly affect the CO₂ sorption capacity for the sorbents prepared from fly ashes. When the sorption temperature increases by up to 600 °C both the CO₂ sorption capacity and the sorption rate increase significantly. Moreover when the amount of K₂CO₃ increases, the CO₂ sorption capacity also increases. At optimal experimental conditions (600 °C and 40 mol% K₂CO₃), the maximum CO₂ sorption capacity for the sorbent derived from fly ash was 107 mg CO₂/g sorbent. The Li₄SiO₄-based sorbents can maintain its original capacity during 10 cycle processes and reach the plateau of maximum capture capacity in less than 15 min, while pure Li₄SiO₄ presents a continual upward tendency for the 15 min of the capture step and attains no equilibrium capacity.     

Analytical solution for Joule–Thomson cooling during CO2 geo-sequestration in depleted oil and gas reservoirs

Mathematical tools are needed to screen out sites where Joule–Thomson cooling is a prohibitive factor for CO₂ geo-sequestration and to design approaches to mitigate the effect. In this paper, a simple analytical solution is developed by invoking steady-state flow and constant thermophysical properties. The analytical solution allows fast evaluation of spatiotemporal temperature fields, resulting from constant-rate CO₂ injection. The applicability of the analytical solution is demonstrated by comparison with non-isothermal simulation results from the reservoir simulator TOUGH2. Analysis confirms that for an injection rate of 3 kg s^?1 (0.1 MT yr^?1) into moderately warm (>40 °C) and permeable formations (>10^?14 m² (10 mD)), JTC is unlikely to be a problem for initial reservoir pressures as low as 2 MPa (290 psi).     

Kinetic studies on the adsorption of phenol, 4-chlorophenol,and 2,4-dichlorophenol from water using activated carbons

This study uses rate parameters in pseudo-first-order (PFO) and pseudo-second-order (PSO) equations (k₁ and k₂q_e, respectively) to judge the extent for approaching equilibrium in an adsorption process. Out of fifty-six systems collected from the literature, the adsorption processes with a k₂q_e value between 0.1 and 0.8 min^?1 account for as much as 70% of the total. These are classified as fast processes. This work compares the validity of PFO and PSO equations for the adsorption of phenol, 4-chlorophenol (4-CP), and 2,4-dichlorophenol (2,4-DCP) on activated carbons prepared from pistachio shells at different NaOH/char ratios. The activated carbons, recognized as microporous materials, had a surface area ranging from 939 to 1936 m²/g. Findings show that the adsorption of phenol, 4-CP, and 2,4-DCP on activated carbons had a k₂q_e value of 0.15–0.58 min^?1, reflecting the fast process. Evaluating the operating time by rate parameters revealed that k₂q_e was 1.6–1.8 times larger than k₁. These findings demonstrate the significance of using an appropriate kinetic equation for adsorption process design.     

Nitrogen critical loads and management alternatives for N-impacted ecosystems in California

Empirical critical loads for N deposition effects and maps showing areas projected to be in exceedance of the critical load (CL) are given for seven major vegetation types in California. Thirty-five percent of the land area for these vegetation types (99,639 km²) is estimated to be in excess of the N CL. Low CL values (3–8 kg N ha^?1 yr^?1) were determined for mixed conifer forests, chaparral and oak woodlands due to highly N-sensitive biota (lichens) and N-poor or low biomass vegetation in the case of coastal sage scrub (CSS), annual grassland, and desert scrub vegetation. At these N deposition critical loads the latter three ecosystem types are at risk of major vegetation type change because N enrichment favors invasion by exotic annual grasses. Fifty-four and forty-four percent of the area for CSS and grasslands are in exceedance of the CL for invasive grasses, while 53 and 41% of the chaparral and oak woodland areas are in exceedance of the CL for impacts on epiphytic lichen communities. Approximately 30% of the desert (based on invasive grasses and increased fire risk) and mixed conifer forest (based on lichen community changes) areas are in exceedance of the CL. These ecosystems are generally located further from emissions sources than many grasslands or CSS areas. By comparison, only 3–15% of the forested and chaparral land areas are estimated to be in exceedance of the NO₃^? leaching CL. The CL for incipient N saturation in mixed conifer forest catchments was 17 kg N ha^?1 yr^?1. In 10% of the CL exceedance areas for all seven vegetation types combined, the CL is exceeded by at least 10 kg N ha^?1 yr^?1, and in 27% of the exceedance areas the CL is exceeded by at least 5 kg N ha^?1 yr^?1. Management strategies for mitigating the effects of excess N are based on reducing N emissions and reducing site N capital through approaches such as biomass removal and prescribed fire or control of invasive grasses by mowing, selective herbicides, weeding or domestic animal grazing. Ultimately, decreases in N deposition are needed for long-term ecosystem protection and sustainability, and this is the only strategy that will protect epiphytic lichen communities.     

Physicochemical characterization of hydroxyapatite and its application towards removal of nitrate from water

A laboratory study was conducted to investigate the efficiency of hydroxyapatite (HAP) towards removal of nitrate from synthetic nitrate solution. In the present research HAP synthesized from egg-shell was characterized using SEM, XRD, FTIR and TGA–DSC. The removal of nitrate was 96% under neutral conditions, using 0.3 g of adsorbent in 100 mL of nitrate solution having an initial concentration of 100 mg/L. An adsorption kinetic study revealed that the adsorption process followed first order kinetics. Adsorption data were fitted to a linearly transformed Langmuir isotherm with correlation coefficient (R²) > 0.98. Thermodynamic parameters were also calculated to study the effect of temperature on the removal process. In order to understand the adsorption type, equilibrium data were tested with the Dubinin–Radushkevich isotherm. The process was rapid and equilibrium was established within the first 40 min.     

Transfer characteristics of cobalt from soil to crops in the suburban areas of Fujian Province,southeast China

The bioavailability of cobalt and its transfer from soil to vegetables and rice were investigated. Among 312 soils collected from vegetable and paddy fields in the suburban areas of some major cities of Fujian Province, southeast China, total soil Co ranged from 3.5 to 21.7 mg kg^?1, indicating a slight accumulation compared with the background value of the province. DTPA extracted 0.1–8.5% of soil total Co. Total and DTPA-extractable Co correlated with soil pH, CEC, free Fe, total Mn, clay and silt content more significantly in paddy soils than in the soils from vegetable fields. The average Co concentrations in the edible parts of vegetables and rice were 15.4 μg kg^?1 and 15.5 μg kg^?1, respectively. The transfer factor (the ratio of plant Co to soil DTPA-extractable Co, TF_DTPA) ranged from 0.003 to 0.126 with a median of 0.049. The TF_DTPA decreased in the order of leafy vegetables > fruit vegetables > root vegetables > rice. The TF_DTPA of all crops decreased with increasing DTPA-extractable Co. Increase in pH, CEC, organic matter, clay, silt, free iron and total Mn limited the soil-to-plant transfer of Co to varying degrees. The transfer of Co from the soils to the edible parts of the crops was lower than that of Zn, Cu and Cd, but higher than that of Pb in the same areas. The concentrations of Co in rice and vegetables in the study areas were considered to be safe for the local residents because of the slight anthropogenic input and the low transfer potential to the edible parts of Co from the soils.     

Equilibrium studies of copper ion adsorption onto palm kernel fibre

The equilibrium sorption of copper ions from aqueous solution using a new adsorbent, palm kernel fibre, has been studied. Palm kernel fibre is obtained in large amounts as a waste product of palm oil production. Batch equilibrium studies were carried out and system variables such as solution pH, sorbent dose, and sorption temperature were varied. The equilibrium sorption data was then analyzed using the Langmuir, Freundlich, Dubinin–Radushkevich (D–R) and Temkin isotherms. The fit of these isotherm models to the equilibrium sorption data was determined, using the linear coefficient of determination, r², and the non-linear Chi-square, χ² error analysis.The results revealed that sorption was pH dependent and increased with increasing solution pH above the pH_PZC of the palm kernel fibre with an optimum dose of 10 g/dm³. The equilibrium data were found to fit the Langmuir isotherm model best, with a monolayer capacity of 3.17 × 10^?4 mol/g at 339 K. The sorption equilibrium constant, K_a, increased with increasing temperature, indicating that bond strength between sorbate and sorbent increased with temperature and sorption was endothermic. This was confirmed by the increase in the values of the Temkin isotherm constant, B₁, with increasing temperature. The Dubinin–Radushkevich (D–R) isotherm parameter, free energy, E, was in the range of 15.7–16.7 kJ/mol suggesting that the sorption mechanism was ion exchange. Desorption studies showed that a high percentage of the copper was desorbed from the adsorbent using acid solutions (HCl, HNO₃ and CH₃COOH) and the desorption percentage increased with acid concentration. The thermodynamics of the copper ions/palm kernel fibre system indicate that the process is spontaneous and endothermic.     

Treatment of municipal wastewater using a contact oxidation filtration separation integrated bioreactor

A new contact oxidation filtration separation integrated bioreactor (CFBR) was used to treat municipal wastewater. The CFBR was made up of a biofilm reactor (the upper part of the CFBR) and a gravitational filtration bed (the lower part of the CFBR). Polyacrylonitrile balls (50 mm diameter, 237 m²/m³ specific surface, 90% porosity, and 50.2% packing rate) were filled into the biofilm reactor as biofilm attaching materials and anthracite coal (particle size 1–2 mm, packing density 0.947 g/cm³, non-uniform coefficient (K₈₀ = d₈₀/d₁₀) < 2.0) was placed into the gravitational filtration bed as filter media. At an organic volumetric loading rate of 2.4 kg COD/(m³ d) and an initial filtration velocity of 5 m/h in the CFBR, the average removal efficiencies of COD, ammonia nitrogen, total nitrogen and turbidity were 90.6%, 81.4%, 64.6% and 96.7% respectively, but the treatment process seemed not to be effective in phosphorus removal. The average removal efficiency of total phosphorus was 60.1%. Additionally, the power consumption of the CFBR was less than 0.15 kWh/m³ of wastewater treated, and less than 1.5 kWh/kg BOD₅ removal.     

Closing the water cycle for industrial laundries: An operational performance and techno-economic evaluation of a full-scale membrane bioreactor system

To reduce the consumption of freshwater in the laundry industry, a new trend of closing the water cycle has resulted in the reuse/recycling of water. In this study, the performance of a full-scale submerged aerobic membrane bioreactor (9 m³) used to treat/reuse industrial laundry wastewater was examined over a period of 288 days. The turbidity and total solids (TS) were reduced by 99%, and the chemical oxygen demand (COD) effluent removal efficiencies were between 70% and 99%. The levels of COD removed by the membrane were significantly greater than the levels of biodegraded COD. This enabled the bioreactor to sustain COD levels that were below 100 mg/L, even during periods of low wastewater biodegradation due to bioreactor sludge. An economic evaluation of the membrane bioreactor (MBR) system showed a savings of 1.13 € per 1 m³ of water. The payback period for this system is approximately 6 years. The energy and maintenance costs represent only 5% of the total cost of the MBR system.     

Ash and deposit formation from oxy-coal combustion in a 100 kW test furnace

Ash deposition is still an unresolved problem when retrofitting existing air-fired coal power plants to oxy-fuel combustion. Experimental data are quite necessary for mechanism validation and model development. This work was designed to obtain laboratory combustor data on ash and deposits from oxy-coal combustion, and to explore the effects of oxy-firing on their formation. Two bituminous coals (Utah coal and Illinois coal) and one sub-bituminous coal (PRB coal) were burned on a down-fired combustor under both oxy- and air-firing. Two oxy-fired cases, i.e., 27 vol% O₂/73 vol% CO₂ and 32 vol% O₂/68 vol% CO₂, were selected to match the radiation flux and the adiabatic flame temperature of air combustion, respectively. Once-through CO₂ was used to simulate fully cleaned recycled flue gas. The flue gas excess oxygen was fixed at 3 vol%. For each case, both size-segregated fly ash and bulk fly ash samples were obtained. Simultaneously, ash deposits were collected on an especially designed un-cooled deposition probe. Ash particle size distributions and chemical composition of all samples were characterized. Data showed that oxy-firing had insignificant impacts on the tri-modal ash particle size distributions and composition size distributions in the size range studied. Bulk ash compositions also showed no significant differences between oxy- and air-firing, except for slightly higher sulfur contents in some oxy-fired ashes. The oxy-fired deposits were thicker than those from air-firing, suggesting enhanced ash deposition rates in oxy-firing. Oxy-firing also had apparent impacts on the deposit composition, especially for those components (e.g., CaO, Fe₂O₃, SO₃, etc.) that could contribute significantly to ash deposition. Based on these results, aerodynamic changes in gas flow and changes in combustion temperature seemed more important than chemical changes of ash particles in determining deposit behavior during oxy-coal combustion.     

Butyltin occurrence and risk assessment in the sediments of the Iberian Peninsula

The occurrence of butyltin (BT) compounds in more than 50 recent sediment samples of the Iberian Peninsula, collected in the harbours of the western Mediterranean Sea (Spain) and the North Atlantic Ocean (Portugal), including domestic and industrial sewage disposal sites, has been assessed. The highest levels of tributyltin (TBT) (7673 μg kg^?1 dry wt.) were detected in commercial harbours associated with inputs from large vessels. However, relatively high TBT values (about 2150 μg kg^?1 dry wt.) were also detected in fishing and recreational boating areas. Spanish marinas and harbours are more polluted in terms of TBT (5–7673 μg kg^?1 dry wt.) compared to those in Portugal (4–12 μg kg^?1 dry wt.). Generally, the Mediterranean sediments show a BT distribution characterized by the predominance of TBT over the degradation products dibutyl (DBT) and monobutyltin (MBT), indicating the presence of recent inputs, in contrast to the Portuguese coastal distribution. Calculation of butyltin degradation indexes (BDI) confirmed a different trend, depending on the area. Furthermore, a comparative study of the occurrence of BT in different sewage sludge disposal sites shows that domestic primary sewage sludge effluents can contribute to coastal BT pollution, but to a lesser extent when compared with harbours. Historical trends (1995–2003) for Barcelona harbour reveal that BT regulations on the use of TBT-based antifouling paints have not been fully effective. Finally, a comparison against the existing sediment quality guidelines (SQGs) indicated that acute toxic effects could only be expected for TBT in some Mediterranean harbours; conversely, in every North Atlantic Ocean station, a lesser environmental threat for the harbour benthic community is expected.     

Airborne manganese concentrations on the Korean peninsula from 1991 to 2006

In this study, the distribution of airborne manganese (Mn) bound with particulate matters (PM) was investigated using data sets collected from 15 major cities in Korea over a 16-year time span (1991–2006). The mean Mn concentration measured from all the major cities in Korea throughout the entire study period was 71 ng m^?3, while the annual mean values of different cities ranged from 10.5 ng m^?3 in Yeosu (2003) to 615 ng m^?3 in Wonju (2006). The Mn levels were considerably larger in industrialized areas than in other land-use types. The Mn concentrations in the major industrial cities of Pohang, Incheon, and Ansan averaged 255, 98.2, and 84.6 ng m^?3, respectively; these values were far higher than those measured typically at most cities, e.g., 20–60 ng m^?3. Seasonal patterns characterized by the peak occurrence in spring and the noticeable drop in summer reflected the effects of the massive PM inflow from China (spring) and effective washout by summer monsoon in East Asia, respectively. Examination of Mn data over a long-term period indicated that the temporal trends of Mn seen in most cities were fairly constant through time since the 1990s, although some abnormalities were observed in cities of strong man-made activities (e.g., Pohang and Wonju). In light of the severity of airborne Mn pollution in many urban areas, it is desirable to establish an abatement strategy that can help effectively reduce Mn levels.