Adsorption is one of the best methods for arsenic removal from water which is established in the last few decades. Biosorption by natural biosorbents and agricultural by-product is an environmental friendly approach and has proved to be a cost-effective and non-hazardous technology for the removal of heavy metals from water. This paper describes batch test findings conducted to evaluate the feasibility of using sugarcane bagasse (SCB) as an industrial by-product of sugar industry to remove arsenic (As) from water and compare the results with the efficiency of activated carbon (AC) for arsenic (As) removal. The effects of three parameters, such as pH, adsorbent dosage (Cₐ), and initial metal concentration (C₀) on the adsorption of arsenic were evaluated by using response surface methodology (RSM). It is discovered that AC and SCB removed up to ~89 and ~98 % of arsenic, respectively. The uptake capacities yielded from the batch experiment were about 31.25 mg/g for AC at pH ~7.4 and 11.9 mg/g for SCB at pH ~9. The equilibrium times achieved were 120 and 150 min for SCB and AC, respectively. This study shows that SCB is an efficient low-cost biosorption for arsenic removal from water.

The potential for bioremediation of chromium pollution using bacteria was investigated in this study. Five chromium-removing bacteria strains were successfully isolated from Cr(VI)contaminated soils and identified by their 16S rRNA gene sequences. The optimum growth temperature (30–40 °C) and pH (8.5–11) for the five isolates were investigated. The effect of initial Cr(VI) concentrations (0–1,575 mg L⁻¹) on bacterial growth was also studied. Results showed that Pseudochrobactrum saccharolyticum strain W1 had high chromium-removing ability and could grow at Cr(VI) concentrations from 0 to 1,225 mg L⁻¹. To our knowledge, this is the first report of chromium removal by a member of the Pseudochrobactrum genus. Sporosarcina saromensis W5 had the highest chromium-removing rate of 0.79 mg h⁻¹ mg⁻¹biomass. Exopolysaccharide (EPS) production and components of the five bacteria strains were also investigated, and a positive relationship was found between the bacterial chromium removal and EPS production.

Investigations on the pollution of groundwater with pathogenic microorganisms, e.g. tracer studies for groundwater transport, are constrained by their potential health risk. Thus, microspheres are often used in groundwater transport studies as non-hazardous surrogates for pathogenic microorganisms. Even though pathogenic microorganisms occur at low concentrations in groundwater, current detection methods of microspheres (spectrofluorimetry, flow cytometry and epifluorescence microscopy) have rather high detection limits and are unable to detect rare events. Solid-phase cytometry (SPC) offers the unique capability of reliably quantifying extremely low concentrations of fluorescently labelled microorganisms or microspheres in natural waters, including groundwater. Until now, microspheres have been used in combination with SPC only for instrument calibration purposes and not for environmental applications. In this study, we explored the limits of the SPC methodology for its applicability to groundwater transport studies. The SPC approach proved to be a highly sensitive and reliable enumeration system for microorganism surrogates down to a minimum size of 0.5 μm, in up to 500 ml of groundwater, and 0.75 μm, in up to 1 ml of turbid surface water. Hence, SPC is proposed to be a useful method for enumerating microspheres for groundwater transport studies in the laboratory, as well as in the field when non-toxic, natural products are used.

The bacterial communities in the intestinal tracts of earthworm were isolated by culture-dependent approaches. In total, 72 cultures were isolated and purified from the gut of an earthworm under aerobic culture condition, out of which 25 isolates were laccase positive. Isolate 33, a good laccase producer was identified as Bacillus safensis DSKK5, using both biochemical and molecular approaches. It was found to produce maximum laccase activity at 0.75 % of wheat bran, 37 °C, and pH 6.2. Further, copper sulfate and copper chloride showed a maximum laccase production. In order to understand the affinity of binding and interaction between toxic dyes and bacterial laccase, homology models were generated. The resulted models were further validated and used for docking studies with commonly used industrial dyes. Molecular docking using CCDC GOLD software gave a good score with all the textile dyes. Further, validation using molsoft ICM software showed a good binding energy of −104.25, −106.00, −113.98, and −100.36, with commercial dyes, i.e., procion blue, procion green, procion red, and reactive yellow 86, respectively. Experimental data showed a maximum decolorization with procion green (85.66 %) and procion red (85.58 %), which validate the molsoft ICM results, i.e., −106.00 and −113.98, respectively.

A wide variety of semi-volatile organic chemicals (SVOCs) are still in use in agricultural practices. A proper understanding of the environmental fate and ecotoxicological risk associated with these compounds can aid decision making, particularly regarding product registration and licensing. The aim of this paper is to expand the use of a previously developed Multimedia Agricultural Fate and Risk Assessment Model (MAFRAM) to SVOCs by adopting the fugacity concept as a second criterion to the existing MAFRAM partitioning criterion (i.e., aquivalence). Volatilization processes from surface compartments into the atmosphere were also included. For example, the application of the generalized model was illustrated using an average annual application rate of 4.48 kg/ha of chlorpyrifos over a typical homogeneous region. Chlorpyrifos emissions were assumed to take place in three environmental compartments (i.e., soil, air, and aboveground plants) with fractions of 0.1, 0.3, and 0.6, respectively. The trends seen in the modeling results were in good agreement with the existing experimental data. Validation issues in MAFRAM were also discussed. Comprehensive experimental validation is unattainable because of the large scale of the areas covered, the lack of boundaries for the system considered, and the uncertainty in the input parameters.

The study presented here focuses on the use of monolayer covers for reclaiming two acid-generating tailings sites located in Quebec, Canada. One of these covers is made of non-acid-generating tailings, and the other is made of a silty sand (till). The covers are part of the closure plans that aim at controlling acid mine (rock) drainage at these two sites. Reactive tailings and cover material samples were collected in situ and characterised in the laboratory. Large-size columns (230 cm in height) were set up to evaluate the hydrogeological and geochemical response of the tailings and cover systems. Monthly wetting and drying cycles were repeated over nearly 2 years to simulate climatic conditions. Water content, suction, and oxygen concentrations were monitored, and chemical analyses were performed on the leachate collected at the base during each cycle to follow the evolution of water quality, in terms of pH and concentrations of sulfates and metals. In addition, small columns (45 cm in height) were also set up, with a similar testing program, to assess the hydrogeochemical behaviour of exposed tailings. The specific objective of this experimental program was to evaluate the hydrogeological and geochemical behaviour of the tailings-cover systems under controlled conditions. The results indicate that, for the imposed conditions, the monolayer covers became significantly desaturated, thus insufficiently limiting the oxygen diffusion flux. Consequently, these covers do not efficiently prevent sulfide oxidation within the tailings. The implications of these results are also discussed.

The influence of structure on degradation of five halogenated phenols (XPs) by UV/H₂O₂process was investigated. The combined influence of type or number of substituents and UV/H₂O₂process parameters (pH and [H₂O₂]) on the degradation kinetics of 2-fluorophenol (2-FP), 2-chlorophenol (2-CP), 2-bromophenol (2-BP), 2,4-dichlorophenol (2,4-DCP), and 2,4,6-trichlorophenol (2,4,6-TCP) was studied using modified miscellaneous 3³full factorial design and response surface modeling (RSM). Studied XPs obey first-order degradation kinetics within the investigated range of process parameters. Determined degradation rate constants (kₒbₛ) were correlated with process and structural parameters by the quadratic polynomial models. Analysis of variance (ANOVA) demonstrated RSM models’ accuracy and showed that, in addition to pH and [H₂O₂], model terms related with the pollutant structure are highly influential. kₒbₛof mono-XPs follow the decreasing order 2-FP, 2-CP, and 2-BP, while CPs follow the decreasing order 2-CP, 2,4-DCP, and 2,4,6-TCP. Biodegradability (biochemical oxygen demand (BOD)₅/chemical oxygen demand (COD)) and toxicity (TU) were evaluated prior to the treatment and at the reference time intervals. The observed differences are correlated with the structural characteristics of studied XPs.

This study evaluates the degree of pollution of marine sediments using two methods: standard (physico-chemical parameters) and instrumental techniques: thermogravimetric analysis (TG) and infrared spectroscopy (ATR-FTIR). ATR-FTIR proved to be a tool capable of identifying the organic and inorganic compounds in sediments such as organic carbon, clay, and carboxylate groups which can bind metal contaminants. TG results of 14 sediment samples were compared with organic matter (OM), organic carbon (OC), total nitrogen (TN), clay, and carbonate (CaCO₃) contents obtained by standard methods. The results showed that weight losses for a specific range of temperatures are closely correlated with the content of OM (R ² = 0.92), OC (R ² = 0.82), TN (R ² = 0.96), clay content (R ² = 0.87), and CaCO₃ (R ² = 0.9) for sediment samples. It is concluded that TG and ATR-FTIR allows a simultaneous, rapid, and reliable screening of sediment properties.

A nitrate-dominant synthetic wastewater simulating slightly polluted water with low C/N and poor biochemical availability was treated in lab-scale vertical-flow (VF)-constructed wetlands, which had Phragmites australis planted with different types of external carbon sources: Platanus acerifolia leaf litters, P. australis litters, glucose and a blank test with no external carbon sources. A comparison of the TN removal and N₂O flux performances among the four wetland reactors indicated higher TN removal efficiencies and N₂O release fluxes in the VF wetland columns with external carbon sources, as measured by the percentage removal of TN (P. acerifolia leaf litters 82.49 %, P. australis litters 70.55 %, glucose 62.50 % and blank 46.45 %) and N₂O flux (P. acerifolia leaf litters 2275.22 μg · m⁻² · h⁻¹, P. australis litters 1920.53 μg · m⁻² · h⁻¹, glucose 1598.57 μg · m⁻² · h⁻¹and blank 1192.08 μg · m⁻² · h⁻¹). This was primarily because of an improved supply of organic carbon from the external carbon sources for heterotrophic denitrification. And, the nitrogen released from the decomposition of plant materials resulted in the N₂O release fluxes to some extent. However, employing P. acerifolia leaf litters and P. australis litters as external carbon sources caused net increases in organics of the final effluent water. Overall, the results not only demonstrated the potential of using external plant carbon sources in VF wetlands to enhance the TN removal efficiency but also showed a risk of excessive organic release and greater N₂O flux feedback to global warming. Hence, future studies are needed to optimise the quantity and method for adding external carbon sources to VF-constructed wetlands so that sufficient nitrate removal efficiency is achieved and the N₂O flux and organic pollution are minimised.

Oil spills impose serious damage to the environment. A spilled crude oil or its products affect aquatic flora and fauna and influence the atmosphere as well. Such pollutants are especially dangerous for the water ecosystems, where biological self-purification processes are slower (for example the Baltic Sea), than in warmer regions. In this paper, we evaluate a sorption capacity of ecologically friendly natural sorbents, when the crude oil and diesel are spilled on the surface of water. The experiments are carried out in the laboratory, and the water from the Lithuanian Baltic Sea coastline and Curonian Lagoon is used. Moss, straw, wool, sawdust, and peat are the natural sorbents evaluated during the experiments. Chromatographic analysis of crude oil and diesel during the process of sorption was conducted as well. An experiment with some synthetic sorbents was carried out to compare the results with natural ones. The experiments showed that the most suitable material for crude oil or diesel fuel spilled on the water surface is peat. As well, Lagergren’s model was adopted to the case of the sorption processes we have investigated. It can be exploited as a decision support tool while deciding the required time interval to achieve maximum sorption capacity of the sorbent in use.