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Abstract Groundwater chemistry is mainly governed by lithological variations, space and resident time. In addition, hydrogeochemical characteristics of groundwater in the lithological contact zones are too complex. Hence, Cretaceous–Tertiary (KT) boundary from Ariyalur district, Tamilnadu, India, was selected for this study to identify the hydrogeochemistry of groundwater. This study includes 284 groundwater samples from four different seasons (pre-monsoon, post-monsoon, southwest monsoon and northeast monsoon). Groundwater samples were collected and analysed for major cations and anions, including physical parameters using standard procedures. High electrical conductivity (EC) showed the longer residence time of groundwater in hard rock region at the central and southern part of the study area. Ca2+, Na+, Cl− and HCO3 − are the dominant ions in all the four seasons. The seasonal composition migration was observed from Na–Ca–Cl–HCO3 type to Na–Mg–Cl–HCO3 type, and Ca-HCO3 is the predominant water type in piper plot. Interpretation of data reveals that the groundwater quality was unsuitable for domestic and irrigation purposes during pre- and southwest monsoon seasons. Rock–water interaction and dissolution of minerals are the main sources of groundwater chemistry. Agriculture activities during monsoonal seasons also play a role in controlling the hydrogeochemistry of groundwater in this region.

Abstract Uranium (U) is formed by the interaction of groundwater in aquifer and the surrounding rocks. The area chosen for this study is a hard rock terrain of various lithology in South India, which releases U in groundwater and affect the groundwater quality. Hence, this study was conducted to understand the geochemistry and temporal variations of U in groundwater with respect to saturation state of minerals for different seasons namely Pre-monsoon (PRM), Northeast monsoon (NEM), Southwest monsoon (SWM) and Post-monsoon (POM). A total of 216 groundwater samples were collected, representing various lithology (Fissile hornblende biotite gneiss, Charnockite, Quartzite, Granite and Flood Plain Alluvium) in the study area. The collected samples were analyzed for physical parameters such as Electrical conductivity, Total dissolved solids, pH and major ions. U was measured using Laser Fluorimeter. The study infers that weathering in SWM, ion exchange in PRM and POM and anthropogenic process in NEM were the three major processes that could dominate the hydrogeochemistry of U. The higher concentration of U has been highlighted, and the water–rock interaction has been studied to know the sources of origin and it has been plotted through bivariate and ternary diagrams. The saturation index study was made and calculated for uranium, carbonate, sulfate, silicate and phosphate minerals using PHREEQC Programme. Uraninite and Coffinite are the dominant saturated states of U minerals which tend to attain near saturation to saturation state irrespective of seasons. With the increase in U concentration irrespective of seasons, it was noticed that the saturation state of minerals is also increasing. Overall, the weathering process and the lithological impact are the sources for higher concentration of U and their minerals occurring in the study area. The outcome of the study will help the policy makers for sustainable management to safeguard the groundwater resource in this region.

Abstract In recent years, the extraction of groundwater (GW) in coastal aquifers has rendered the fragile aquifers more saline due to the sea water intrusion. Groundwater from the coastal aquifers of the Pudhucherry region were sampled to study the process of salinization. An integrated approach was adopted to identify the salinization process, by coordinating the results of borehole geophysics, rainfall pattern, water level variation, hydrochemical characters and multivariate statistical analysis. A total of 136 groundwater samples were collected during two different seasons, southwest monsoon (SWM) and northeast monsoon (NEM). The major cations and anions were analyzed adopting standard procedures. Resistivity and litholog indicate that the southeastern (SE) part of the study region has lower resistivity than in north. Based on electrical conductivity (EC) and total dissolved solids (TDS) values, most of the samples are potable, except for few samples from southeastern region. The study results indicated that higher values of Na, EC, K, SO4, Mg and Cl were observed during NEM, indicating leaching of salt into the aquifer and ion exchange process. The predominant hydrochemical facies of groundwater was Na-Cl and Ca–Mg–Cl type reflecting the saline water and the mixing process of saltwater and fresh groundwater, respectively. Though more number of samples with higher EC was noted in NEM, the results of PCA and correlation analysis indicate the predominance of leaching of salts and intense agricultural activities. The process of sea water intrusion was observed to be dominant during SWM.

The adsorption of methylene blue dye onto acid-treated sugarcane bagasse (ASB) was investigated in batch system. The characterization of ASB was investigated using scanning electron microscopy, X-ray diffractometer and Fourier transform infra-red spectroscopy. The different factors namely adsorbent dosage, solution pH, initial composition of dye solution and temperature on specific dye uptake were examined using ASB in order to evaluate equilibrium kinetic parameters. The suitable variables (dosage = 5 g dm-3; initial pH = 6) for the maximum specific uptake of dye onto ASB. The maximum adsorption capacity of 45.4 mg g-1 was obtained at 25°C using ASB. In order to evaluate decay rate and concentration independent mass transfer parameters namely diffusivity and mass transfer co-efficient for adsorption of methylene blue on ASB, the film pore mass transfer model was considered. In this study, external mass transfer co-efficient and pore diffusivity are ranging between 10-6 and 10-12 m² s-1, respectively. The rate limiting step for the adsorption of MB on ASB was known to be internal pore diffusion owing to the higher value of Biot number. [ABSTRACT FROM AUTHOR]