Major ion chemistry and identification of hydrogeochemical processes controlling groundwater in and around Neyveli Lignite Mines, Tamil Nadu, South India

Groundwater geochemistry was studied in and around the Neyveli lignite mining region of Tamil Nadu, India. Representative groundwater samples (168) were collected from bore wells during June 2004, October 2004, January 2005, and March 2005 to broadly cover seasonal variation. Higher electrical conductivity values were observed in the southeastern and southwestern part of the study area. During the southwest monsoon (June) and postmonsoon (January) seasons, bicarbonate?+?chloride dominated the anions, with few representations for sulphate. Sodium?+?potassium were the dominant cations in all the seasons except in summer (March). The data reveals that the region is a complex hydrogeochemical system with proportional interplay of ions from leaching of ions, ion exchange, agricultural return flow, and stagnant waters. The influence of mine waters and weathering of minerals varies according to the season and spatial distribution of the sources. The water quality can be used for drinking and irrigation, except in a few locations.     

Magnetic measurements and pollutants of sediments from Cauvery and Palaru River,India

Rock-magnetic techniques have become a useful tool in environmental issues; in particular, magnetic studies constitute an alternative way to study pollution in different media. The present contribution focuses on magnetic parameters as pollution indicators, especially from their relationship with contents of heavy metals. The work was carried out in two Indian rivers located in Tamil Nadu, southern India. Several sediment samples were collected and studied in the laboratory using magnetic techniques, magnetic susceptibility, anhysteric remanent magnetization, isothermal remanent magnetization, and chemical techniques to determine contents of heavy metals. Magnetic mineralogy indicates the predominance of ferrimagnetic minerals; although magnetite-like minerals are the main magnetic carriers, antiferromagnetic minerals can be present as subordinate carriers. Concentration-dependent magnetic parameters revealed noticeable differences between both rivers, e.g. magnetic susceptibility is four times higher in Cauvery than in Palaru River. Moreover, such increase can be interpreted as “magnetic enhancement” and therefore related to the pollution status. This magnetic enhancement indicated a different pollutant contribution in both rivers, and also, a different spatial distribution along these rivers, where critical (or more polluted) sites were identified. On the other hand, univariate and multivariate statistical analyses—e.g. PCoordA, Multifactorial Analysis of distance, PCA and RDA—were examined, revealing a link between magnetic and chemical variables. Among magnetic parameters, the concentration-dependent magnetic parameters (e.g. magnetic susceptibility) seem to be the most relevant for this study.     

Adsorption of Metal Ions onto the Chemically Modified Agricultural Waste

This paper discusses about the adsorption of metal ions such as Cu(II), Cd(II), Zn(II), and Ni(II) from aqueous solution by sulfuric acid treated cashew nut shell (STCNS). The adsorption process depends on the solution pH, adsorbent dose, contact time, initial metal ions concentration, and temperature. The adsorption kinetics was relatively fast and equilibrium was reached at 30 min. The adsorption equilibrium follows Langmuir adsorption isotherm model. The maximum adsorption capacity values of the modified cashew nut shell (CNS) for metal ions were 406.6 mg/g for Cu(II), 436.7 mg/g for Cd(II), 455.7 mg/g for Zn(II), and 456.3 mg/g for Ni(II). The thermodynamic study shows the adsorption of metal ions onto the STCNS was spontaneous and exothermic in nature. The kinetics of metal ions adsorption onto the STCNS followed a pseudo‐second‐order kinetic model. The external mass transfer controlled metal ions removal at the earlier stages and intraparticle diffusion at the later stages of adsorption. A Boyd kinetic plot confirms that the external mass transfer was the slowest step involved in the adsorption of metal ions onto the STCNS. A single‐stage batch adsorber was designed using the Langmuir adsorption isotherm equation.     

Characterisation of groundwater chemistry in an eastern coastal area of Cuddalore district,Tamil Nadu

The groundwater quality detoriation due to various geochemical processes like saline water intrusion, evaporation and interaction of groundwater with brines is a serious problem in coastal environments. Understanding the geochemical evolution is important for sustainable development of water resources. A detailed investigation was carried out to evaluate the geochemical processes regulating groundwater quality in Cuddalore district of Tamilnadu, India. The area is entirely underlined by sedimentary formations, which include sandstone, clay, alluvium, and small patches of laterite soils of tertiary and quaternary age. Groundwater samples were collected from the study area and analyzed for major ions. The electrical conductivity (EC) value ranged from 962 to 11,824 μS/cm, with a mean of 2802 μS/cm. The hydrogeochemical evolution of groundwater in the study area starts from Mg-HCO₃ type to Na-Cl type indicating the cation exchange reaction along with seawater intrusion. The Br/Cl ratio indicates the evaporation source for the ion. The Na/Cl ratios indicate groundwater is probably controlled by water-rock interaction, most likely by derived from the weathering of calcium-magnesium silicates. The plot of (Ca+Mg) versus HCO₃ suggests ions derived from sediment weathering. The plot of Na+K over Cl reflects silicate weathering along with precipitation. Gibbs plot indicates the dominant control of rock weathering. Factor analysis indicates dominance of salt water intrusion, cation-exchange and anthropogenic phenomenon in the study.     

Hydrochemistry of groundwater in a coastal region of Cuddalore district, Tamilnadu, India: implication for quality assessment

A hydrogeochemical investigation was conducted in a coastal region of Cuddalore district to identify the influence of saltwater intrusion and suitability of groundwater for domestic and agricultural purposes. The geology of the study area comprises of sandstone, clay, alluvium, and laterite soils of Tertiary and Quaternary age. A total of 18 groundwater samples were analyzed for 14 different water quality parameters and the result indicates higher concentrations of ions like Cl (3,509 mg/l), Na (3,123 mg/l), and HCO₃ (998 mg/l) when compared with WHO, BIS, and ISI standards. A positive correlation (r ²?=?0.82) was observed between Na and Cl, indicating its sources from salt water intrusion. Three factors were extracted with a total variance of 64% which indicates the sources of salinization, cation exchange, and anthropogenic impact to the groundwater. The Piper trilinear diagram indicates both Na–Cl and mixed Na–HCO₃–Cl-type, indicating that groundwater was strongly affected by anthropogenic activities. The plot of (Ca?+?Mg)/(K?+?Na) indicates evidences of cation exchange and salt water intrusion. The (Ca–0.33*HCO₃)/ SO₄ plot indicates salt water intrusion for elevated SO₄ levels rather than gypsum dissolution. The spatial distribution of total dissolved solid indicates the saline water encroachment along the SW part of the study area. As per sodium adsorption ratio (SAR), 50% of the samples with <10 SAR are suitable for irrigation and >10 SAR indicates that water is unsuitable for irrigation purposes. The residual sodium carbonate classification indicates that 50% of the samples fall in safe and 50% of the samples fall in bad zones and prolonged usage of this water will affect the crop yield. The Chloro Alkaline Index of water indicates disequilibrium due to a higher ratio of Cl?>?Na–K, indicating the influence of salt water intrusion. The Permeability Index of the groundwater indicates that the groundwater from the study area is moderate to good for irrigation purposes.     

Kinetics of Methyldiethanolamine Mineralization by Using UV/H2O2 Process

The UV/H₂O₂ is one of the popular techniques in the advanced oxidation processes (AOPs) and has been applied in the wastewater treatment during recent two decades. UV exposure on the H₂O₂ generate highly reactive hydroxyl radicals (OH^?), which are used to degrade organic contaminants through oxidation processes in wastewater. This present study involves the estimation of hydroxyl radical rate constants of methyldiethanolamine (MDEA) mineralization at different temperatures by using UV/H₂O₂ in aqueous solution. Laboratory experiments have been conducted and the profile of MDEA mineralization has been established. The hydroxyl radical rate constants and the activation energy of mineralization process have been calculated. The estimated hydroxyl rate constants and the activation energy are in good agreement with those reported in the literature.     

Assessment of groundwater quality with special emphasis on fluoride contamination in crystalline bed rock aquifers of Mettur region, Tamilnadu, India

Groundwater samples were collected from Mettur taluk of Salem district, Tamilnadu, India for two different seasons (pre-monsoon and post-monsoon) and analyzed for fluoride ion along with other chemical parameters. The major litho units of the study area are Charnockites, peninsular gneiss, and calc gneiss of meta-sedimentary group. The fluoride concentration ranges from 0.1 to 2.8?mg/L and 0.4 to 4.0?mg/L during pre-monsoon (PRM) and post-monsoon (POM) seasons, respectively. Results showed that collected water samples were contaminated by the presence of fluoride ion. During PRM and POM, 21% and 56% of samples recorded higher fluoride when compared with Indian Drinking Water Standard (1?mg/L) and (9% and 35%) of samples recorded higher fluoride when compared with World Health Organization tolerance limit (1.5?mg/L). The ratio of Na/Ca indicates high sodium content in groundwater enhances the dissolution of fluoride at higher pH. Hydrogeochemical facies indicates water-rock interaction as main source for high fluoride in groundwater. A positive correlation between pH, Mg, and F indicates high alkaline nature of water promotes fluoride leaching from source rocks into ground water. Factor analysis indicates hydro-geochemical processes like weathering, ion exchange, and anthropogenic contributes to groundwater chemistry. The saturation index indicates dissolution and precipitation contributes fluoride dissolution along with mixing.