Heterogeneous Fenton oxidation of dissolved organics in salt-laden wastewater from leather industry without sludge production

This is the first report on the heterogeneous oxidation of dissolved organics in wastewater with little consumption of Fenton’s reagent and without sludge production. The salt-laden wastewater discharged from leather industry has poor biodegradability due to the presence of high total dissolved solids. This wastewater is evaporated in solar evaporation pans. The evaporated residue faces disposal problem due to high concentration of organic and inorganic salts. The present study demonstrates the preparation, characterization and application of mesoporous activated carbon matrix along with Fenton’s reagent for the removal of dissolved organics in wastewater. Free electron-rich mesoporous activated carbon matrices (MAC₇₀₀, MAC₈₀₀ and MAC₉₀₀) were prepared and characterized for surface area, C, H, N, ash content, free electron density and energy gap value. Results show that heterogeneous catalytic oxidation of dissolved organics in the wastewater decreased biochemical oxygen demand, chemical oxygen demand, total organic carbon and dissolved protein, respectively, by 74, 69, 61 and 80% at optimum pH (3.5), H₂O₂ (7.5 mmol/l), FeSO₄.7H₂O (0.3 mmol/l) and MAC₈₀₀ (10 g/l).     

Assessment of potential hazards of fluoride contamination in drinking groundwater of an intensively cultivated district in West Bengal, India

We assessed the potential of fluoride (F) contamination in drinking groundwater of an intensively cultivated district in India as a function of its lithology and agricultural activities. Three hundred and eight groundwater samples were collected at different depths from various types of wells and analyzed for pH, EC, NO(3)-N load and F content. A typical litholog was constructed and database on fertilizer and pesticide uses were also recorded for the district. The water samples were almost neutral in reaction and non-saline in nature with low NO(3)-N content (0.02 to 4.56 microg mL(-1)). Fluoride content in water was also low (0.01 to 1.18 microg mL(-1)) with only 2.27% of them exceeding 1.0 microg mL(-1) posing a potential threat of fluorosis. On average, its content varied little spatially and along depth of sampling aquifers because of homogeneity in lithology of the district. The F content in these samples showed a significant positive correlation (r = 0.12, P < or = 0.05) with the amount of phosphatic fertilizer (single super phosphate) used for agriculture but no such relation either with the anthropogenic activities of pesticide use or NO(3)-N content, pH and EC values of the samples was found. The results suggest that the use of phosphatic fertilizer may have some role to play in F enrichment of groundwater.     

Characterization of different road dusts in opencast coal mining areas of India

Dust from haul and transport roads are the major source of air pollution in opencast coal mining areas. Dust generated during mining operations pollutes air which causes different health problems. Various available techniques are implemented in the field to minimize and control dust in mining areas. However, they are not very effective because dust deposited on road surfaces are not removed by these techniques. For effective control of dust in opencast mining areas, it has to be regularly collected from road surfaces and may be converted into solid form, and subsequently can be used as a domestic fuel considering its physicochemical properties. The present paper describes a comparative study of qualitative and quantitative aspects of road dust samples of four coalfields of India. The pH of the dust was found to be in the range of 5.1–7.7. Moisture, ash, volatile matter, fixed carbon, water-holding capacity, bulk density, and specific gravity of dust samples were found to be in the range of 0.5–3.0%, 45–76%, 12.6–20.0%, 10.2–45.3%, 21.17–31.71%, 1.15–1.70, and 1.73–2.30 g cm⁻³, respectively. Observing the overall generation and characteristics of coal dust, it is suggested that coal dust from haul and transport roads of mining areas can be effectively collected and used as domestic fuel.     

Removal efficiency of fluoride by novel Mg-Cr-Cl layered double hydroxide by batch process from water

The fluoride ion removal from aqueous solution using synthesized Mg-Cr-Cl layered double hydroxide has been reported.Mg-Cr-Cl was characterized by X-ray powder diffraction,Fourier-transform infrared,thermo-gravimetric analysis,differential thermal analysis,and scanning electron microscope.Adsorption experiments were carried out in batch mode as a function of adsorption dosages,contact time,pH,and initial fluoride concentration to get optimum adsorption capacity.The adsorption kinetic study showed that the adsorption process followed first order kinetics.The fluoride removal was 88.5% and 77.4% at pH 7 with an adsorbent dose of 0.6 g/100 mL solution and initial fluoride concentration of 10 mg/L and 100 mg/L,respectively.The equilibrium was established at 40 min.Adsorption experiment data were fitted well with Langmuir isotherm with R 2 = 0.9924.Thermodynamic constants were also measured and concluded that the adsorption process was spontaneous and endothermic in nature.The removal percentage decreased slowly with increasing pH.This process is suitable for industrial effluents.The regeneration of the material is not possible.     

Chemical characteristics and source apportionment of PM<Subscript>2.5</Subscript> using PCA/APCS,UNMIX, and PMF at an urban site of Delhi,India

The present study investigated the comprehensive chemical composition [organic carbon (OC), elemental carbon (EC), water-soluble inorganic ionic components (WSICs), and major & trace elements] of particulate matter (PM_2.5) and scrutinized their emission sources for urban region of Delhi. The 135 PM_2.5 samples were collected from January 2013 to December 2014 and analyzed for chemical constituents for source apportionment study. The average concentration of PM_2.5 was recorded as 121.9 ± 93.2 μg m^?3 (range 25.1–429.8 μg m^?3), whereas the total concentration of trace elements (Na, Ca, Mg, Al, S, Cl, K, Cr, Si, Ti, As, Br, Pb, Fe, Zn, and Mn) was accounted for ～17% of PM_2.5. Strong seasonal variation was observed in PM_2.5 mass concentration and its chemical composition with maxima during winter and minima during monsoon seasons. The chemical composition of the PM_2.5 was reconstructed using IMPROVE equation, which was observed to be in good agreement with the gravimetric mass. Source apportionment of PM_2.5 was carried out using the following three different receptor models: principal component analysis with absolute principal component scores (PCA/APCS), which identified five major sources; UNMIX which identified four major sources; and positive matrix factorization (PMF), which explored seven major sources. The applied models were able to identify the major sources contributing to the PM_2.5 and re-confirmed that secondary aerosols (SAs), soil/road dust (SD), vehicular emissions (VEs), biomass burning (BB), fossil fuel combustion (FFC), and industrial emission (IE) were dominant contributors to PM_2.5 in Delhi. The influences of local and regional sources were also explored using 5-day backward air mass trajectory analysis, cluster analysis, and potential source contribution function (PSCF). Cluster and PSCF results indicated that local as well as long-transported PM_2.5 from the north-west India and Pakistan were mostly pertinent.     

Assessment of the potential hazards of nitrate contamination in surface and groundwater in a heavily fertilized and intensively cultivated district of India

We made an inventory of nitrate (NO3-N) enrichment in surface and groundwater systems in the Hooghly district of India owing to intensive farming with high fertilizer doses as a function of quantity of fertilizers use, soil characteristics, types of crop grown, depth of groundwater sampling and also N-load in soil profiles. Water samples were collected from different sources at 412 odd sites spread over in 17 blocks of the district along with representative soil profiles. On average, the study area had high clay and NO3-N in soil profiles with an increasing and decreasing trends along depth, respectively. The NO3-N content both in surface and groundwater varied from 0.01 microg mL(-1) to 4.56 microg mL(-1), being well below the threshold limit of 10 microg mL(-1) fixed by WHO for drinking purpose. The content decreased with increasing depth of wells (r = -0.39**) and clay content of soil profiles (r = -0.31**). It, however, increased with increasing rate of fertilizer application (r = 0.72**), NO3-N load in soil profiles (r = 0.85**) and was higher in areas where shallow--rather than deep-rooted crops are grown. Results indicated even under fairly high quantity of fertilizer use, groundwater of the study area is safe for drinking purpose.     

Sub-chronic oral toxicity of acetamiprid in Wistar rats

Acetamiprid is a neoncotinoid insecticide that acts as an agonist to the nicotinic acetylcholine receptor used as insecticide in crops and to control fleas on dogs and cats. The objectives of this study are (1) to evaluate the sub-chronic toxicity of orally administered acetamiprid, (2) to estimate the tissue residue levels and (3) to assess the reactive oxygen species induction in Wistar rats. Clinical signs of toxicity and changes in the haematological parameters were not observed in the acetamiprid-treated groups. Biochemically, increases in the levels of alanine aminotransferase, aspartate aminotransferase, cholesterol and decreases in body weight, feed consumption, reduced glutathione, catalase, superoxide dismutase, glutathione peroxidase, and AchE were observed. Lipid peroxidation was increased in liver and kidney. Acetamiprid residues persisted in liver, kidney, spleen, muscles, brain, fat and histopathology revealed lesions in the liver. The no observable adverse effect level of acetamiprid was found to be ≤55 mg/kg body weight.     

A preliminary study on the nature of particulate matters in vehicle fuel wastes

Powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and tunneling electron microscopy (TEM) studies of two solid vehicle wastes (pollutants) from petrol- and diesel-fueled engines of Kolkata (India) have detected a significant amount of ultrafine particles in the nanometer scale in these wastes. Both powder XRD and selected area electron diffraction from TEM have confirmed the existence of inhomogeneous distribution of nanocrystallites in these pollutants. Energy dispersive X-ray spectrometry shows that these wastes contain mainly carbon and oxygen as the constituent components. These pollutants are magnetic in nature as seen with SQUID magnetometry, and the presence of a high amount of carbon presumably is likely the origin of the magnetic property.     

Effect of magnetic field on the removal of copper from aqueous solution using activated carbon derived from rice husk

Adsorptive removal of copper by activated carbon derived from modified rice husk (ACRH) was studied in the presence and absence of magnetic field (MF). The ACRH was prepared from the normal rice husk treated by NaOH solution and subsequent pyrolysis at 450 °C in the absence of oxygen. The physicochemical properties of ACRH's were determined before and after the adsorption process to delineate the adsorption mechanism. The BET analysis confirmed that the fabricated ACRH has a specific surface area of 8.244 m²/g with a mesopore to micropore ratio of 0.974. It was observed that the micropore structure gradually replaced the mesopores, and the surface area of the micropore increased (from 0.9219 to 4.1764 m²/g), and the pore diameter was also decreased from 180.381 to 46.249 Å after pyrolysis. The CHNO/S test result reveals that the carbon content was increased from 42 to 67.8% in the ACRH after pyrolysis. The batch sorption studies were performed by varying the initial adsorbate concentration, temperature, agitation speed, pH, adsorbent dose and contact time for magnetic and non-magnetic conditions to analyze the effect of the magnetic field. The univariate studies show that the maximum experimental adsorption capacity was 4.522 mg/g and 3.855 mg/g, respectively, for these two conditions (representing the magnetic impact) at 25 °C with an adsorbent dose of 2 g/L and an agitation speed of 150 rpm. It was also observed that the removal efficiency was 94.55% and 77.96% (magnetic and non-magnetic condition) at pH 7 with a concentration of 10 mg/L in 2 h. The test result on the impact of exposure time on the magnetic field suggested that the magnetic memory influenced the removal efficiency; after 40 to 60 min, the maximum removal efficiency was achieved, around 80 to 90%. The pseudo-second-order kinetic model was best fitted with the experimental data with a rate constant as 0.1749 and 0.1006 g/mg/min for these two conditions. The Temkin model delineates the adsorption isotherm suggesting the heat generated during the adsorption process is linearly abate with the coverage of the surface area of the adsorbent. The thermodynamic model confirms that the copper adsorption is spontaneous (ΔG = ? 3.91 kJ/mol and ? 6.02 kJ/mol), wherein the negative enthalpy value (ΔH = ? 36.74 kJ/mol and ? 25.74 kJ/mol) suggested that the process is exothermic irrespective of magnetic interference. The significant enhancement of copper removal was observed by incorporating the magnetic field, showing an increase in sorption capacity by 17.48% and a reduction of reaction time by 88.12%.