Tamarind fruit shell was used as a low-cost biosorbent for the removal of methylene blue from aqueous solution. The various factors affecting adsorption, such as agitation, pH, initial dye concentration, contact time, and temperature, were investigated. The dye adsorption capacity was strongly dependent on solution pH as well as temperature. The Langmuir isotherm model showed good fit to the equilibrium adsorption data, and the maximum adsorption capacity obtained was 1.72 mg g⁻¹ at 303 K. The kinetics of adsorption followed the pseudo-second-order model and the rate constant increased with increase in temperature, indicating endothermic nature of adsorption. The Arrhenius equation was used to obtain the activation energy (E a) for the adsorption system. The activation energy was estimated to be 19.65 kJ mol⁻¹. Thermodynamic parameters such as Gibbs free energy (ΔG ⁰), enthalpy (ΔH ⁰), and entropy (ΔS ⁰) were also investigated. Results suggested that adsorption of methylene blue onto tamarind fruit shell was a spontaneous and endothermic process. The present investigation suggests that tamarind fruit shell may be utilized as a low-cost adsorbent for methylene blue removal from aqueous solution.

Urban drainage transports a complex and heterogeneous mixture of aqueous-phase chemicals and also solid-phase particulate matter (PM). In this study, event-scale particle size distribution (PSD) of wet and dry weather flows are measured, modeled, and compared. The flows are generated from a complex urbanizing sewershed (Liguori catchment) in Cosenza, Italy. Results indicate PSDs are heterodisperse, ranging from colloidal to sand-size PM. On an event scale, dry weather PSDs are coarser than wet weather flows, yet within each flow class results indicate flow-limited behavior and only nominal variability during and between events. PSDs from each event and flow category are modeled with a cumulative gamma distribution. Results produced nonparametric distributions of shape (γ) and scaling (α) parameters as well as a d ₅₀ index. Wet weather flows generated statistically significantly higher distributions of γ and α and statistically significantly lower d ₅₀. Nonparametric parameter distributions illustrate greater, yet still nominal variability for wet weather flows.

Mercury pollution in the Second Songhua River (SSR) was serious in the last century due to effluent from a chemical corporation. Effects of riverine self-purification on mercury removal were studied by comparing monitoring data of mercury concentrations varieties in water, sediment, and fish in the past, about 30 years. The present work suggested that a river of such a size like the SSR possessed the potential ability to recover from mercury pollution under the condition that mercury sources were cut off, though it needs a very long time, which might be several decades or even a century of years. During the 30 years with no effluent containing mercury input, total mercury (T-Hg) of water and sediment in some typical segments, mostly near the past effluent outlet, had decreased radically but still higher than the background values, though the decrease amplitudes were over 90% compared with that in 1975. T-Hg had decreased by more than 90% in most fishes, but some were still not suitable for consumption. Methylmercury concentrations (MeHg) of water, sediment, and fish were higher or close to the background levels in 2004. In the coming decades, the purification processes in the SSR would be steady and slow for a long period.

Decolorization of six synthetic dyes and two raw textile effluents (A and B) by eight basidiomycetous fungi was investigated. Among eight basidiomycetous fungi, fungal isolate RCK-1 decolorized textile effluent A maximally (42%), while fungal isolate RCK-3 was found to decolorize more of Congo Red (69%), Xylidine Ponceau 2R (100%), Poly R-478 (96%), Indigo Carmine (99%), Lissamine Green B (90%), Toluidine Blue (57%) and textile effluent B (54%), than the rest of fungi. Percentage decolorization of all synthetic dyes and textile effluents by the new fungal isolates RCK-1 and RCK-3 was higher compared to the most widely studied simultaneous lignin degrader, Phanerochaete chrysosporium and selective lignin degrader, Pycnoporus cinnabarinus, when tested in liquid cultures. A statistically significant positive correlation between laccase production and decolorization of dyes and effluents was obtained as compared to other ligninolytic enzymes (lignin peroxidase and manganese peroxidase) production. This showed the importance of the differential contribution of the different ligninolytic enzymes towards the decolorization of the synthetic dyes and textile effluents. The substantially higher ligninolytic enzyme production by the fungal isolates RCK-1 and RCK-3 also suggested their potential use for textile effluent treatment and other possible biotechnological applications.

Semi-solid Fenton process (SSFP) was firstly conducted on hazardous solid waste detoxication. Batch tests, Box-Behnken designs, and response surface methodology were applied to optimize the key factors including the pH, the initial Fe(II) content, and the liquid-to-solid ratio (L/S). It shows that the optimal pH, the initial Fe(II) content, and the L/S in SSFP are 3.5, 0.062 mol kg⁻¹ dry weight and 1.77, respectively. Correspondingly, the removal efficiencies of ONA and ArNH₂ are 98.5 ± 0.5% and 100% which agree well with the results of an established polynomial model. It suggests that SSFP is an efficient and environment-friendly method for hazardous solid waste detoxication without wastewater generation.

A strong base anion exchange resin Amberlite IRA-400 Cl⁻ and its hybrids with Mn(OH)₂ and Cu(OH)₂ are used for the removal of chromium from the synthetic spent tannery bath. The recovery is examined by varying the experimental conditions, viz., resin dosage, stirring speed, and temperature. The rate of chromium removal by Amberlite IRA-400 Cl⁻ increased almost four times when the resin dosage was increased from 0.2 to 1.0 g. Furthermore, the rate of chromium sorption almost doubled when the stirring speed was increased from 100 to 1,000 rpm, suggesting that the sorption is a diffusionally controlled process. The chromium removal capacity also increased with the rise of temperature, showing the endothermic nature of the process. The results are explained with the help of film diffusion, particle diffusion, and Lagergren pseudo-first-order kinetic models. The kinetics results of the Amberlite IRA-400 Cl⁻ are compared with its hybrid anion exchange resins IRA-400 Mn(OH)₂ and IRA-400 Cu(OH)₂. It is found that the hybrid ion exchangers have greater removal ability and fast kinetics as compared to the parent exchanger.

Hydroponics culture generates large amounts of wastewater that are highly concentrated in nitrate and phosphorus but contains almost no organic carbon. Constructed wetlands (CWs) have been proposed to treat this type of effluent, but little is known about the performance of these systems in treating hydroponic wastewater. In addition, obtaining satisfactory winter performances from CWs operated in cold climates remains a challenge, as biological pathways are often slowed down or inhibited. The main objective of this study was to assess the effect of plant species (Typha sp., Phragmites australis, and Phalaris arundinacea) and the addition of organic carbon on nutrient removal in winter. The experimental setup consisted of 16 subsurface flow CW mesocosms (1 m², HRT of 3 days) fed with 30 L d¹ of synthetic hydroponics wastewater, with half of the mesocosms fed with an additional source of organic carbon (sucrose). Carbon addition had a significant impact on nitrate and phosphate removal, with removal means of 4.9 g m⁻² d⁻¹ of NO₃-N and 0.5 g m⁻² d⁻¹ of PO₄-P. Planted mesocosms were generally more efficient than unplanted controls. Furthermore, we found significant differences among plant treatments for NO₃-N (highest removal with P. arundinacea) and COD (highest removal with P. australis/Typha sp.). Overall, planted wetlands with added organic carbon represent the best combination to treat hydroponics wastewater during the winter.

A study on pH and chemical composition of precipitation was carried out in two Italian sites, one urban (site 1) and one rural (site 2), located approximately 30 km far from Bologna, during a 3-year period. No significative site variation was found. In both locations, bulk deposition pH ranged from slightly acid to slightly alkaline, despite the volume weighted mean concentration of acidic species, NO ₃ ⁻ and SO ₄ ²⁻ (67.4 and 118.4 μeq l⁻¹ in site 1 and 88.7 and 103.8 μeq l⁻¹ in site 2), that were similar to those of typical acidic rainfall region. This might be ascribed to the neutralization reaction of the Ca²⁺, attributed to the calcareous soil and the frequent dusty air mass intrusion from the Sahara. The pair correlation matrix and the analysis of the main components suggested also ammonium and other crustal elements as neutralization agents. The depositional rate of SO ₄ ²⁻ and NO ₃ ⁻ , chemical elements of agricultural interest, amounted to 38 and 28 and 32 and 35 kg ha⁻¹ for site 1 and site 2, respectively. These supplies of nutrient were not negligible and had to be considered on cultivated lands. NH ₄ ⁺ deposition rate on site 2 was 7 kg ha⁻¹, 23% over site 1, probably due to nitrogen fertilization in the fields around the monitoring station. In site 1, SO ₄ ²⁻ presented a seasonal trend, indicating that its principal source was the residential heating. Results emphasized that the entity of the bulk deposition acidification is linked not only to the ions local emission sources (fossil fuel combustions, heating, and fertilizers) but also to the surrounding territory and the prevalent wind that transports through kilometers air masses which may contain acidic and alkaline species.

This study is the first to report nitrite occurrence and variability in surface water across an agricultural watershed in the province of Quebec, Canada. Nitrite (NO₂ ⁻) concentrations were monitored across a 2.4 km² watershed during 2 years. Water samples were collected at the outlet from April to November and in three contrasted stream branches (six stations) during three hydrological regimes (summer low water levels, fall recharge, and snowmelt). Our study clearly demonstrates that NO₂ ⁻ levels observed at the outlet are not representative of NO₂ ⁻ variability across the micro-watershed. Surface water collected in cropped areas presents high NO₂ ⁻ concentrations during summer low water levels, often exceeding guidelines for aquatic life, with NO₂ ⁻ means ranging from 0.022 to 0.107 mg N L⁻¹ and maximum value reaching 0.156 mg N L⁻¹. Furthermore, the two stream branches in cropped area have demonstrated significant differences in NO₂ ⁻ concentrations and other water quality parameters. The importance of groundwater discharge to streams in the micro-watershed Bras d'Henri may potentially generate different in-stream sources of NO₂ ⁻ and water quality parameters. However, further studies are essential to determine sources and processes related to in-stream NO₂ ⁻ peaks.

Distribution of ¹³⁷Cs and ²³⁹,²⁴⁰Pu in the forest soils horizons of the Opole Anomaly was established. Gamma and alpha spectrometry was used for determination of these isotopes. It was found that the ¹³⁷Cs activity was approx. 1,000 times higher than that of ²³⁹,²⁴⁰Pu. The highest activities of both radioisotopes were found close to the boundary region in soil profile where the organic horizon turns into the inorganic one. Cluster analysis did not clearly indicate the group's existence in data in respect to ¹³⁷Cs and ²³⁹,²⁴⁰Pu activities and organic matter content. Distributions of ¹³⁷Cs and ²³⁹,²⁴⁰Pu in soil horizons were non-normal but similar to each other. These distributions were substantially different from that one for organic matter content. The data were separated into two groups, for organic and inorganic soil horizons, respectively. Data transformation using Box-Cox formula was performed following by standardization. Mutual relationships between variables were investigated using ordinary and robust regression methods. Good correlation between ¹³⁷Cs and ²³⁹,²⁴⁰Pu was found. No significant relationship between organic matter content and radioisotopes activity was asserted.