A considerable number of studies have been conducted to investigate the effect of physical and chemical variables on the transport of nanoscale zerovalent iron (nZVI) in granular media. However, the role of soil grain size as a crucial factor in nanoparticle mobility is less understood. The present research work sought to examine the simultaneous effects of soil grain size and particle concentration on the transport of nZVI coated with carboxymethyl cellulose (CMC-nZVI), using saturated sand packed column experiments. To this end, a total of 12 tests were conducted by combining four different particle concentrations (C = 10, 200, 3000, 10,000 mg/l) and three grain sizes (dc = 0.297–0.5 mm, 0.5–1 mm, 1–2 mm). The effluent nZVI concentration and water pressure drop along the column were measured. The results showed that during the injection time, decreasing the grain size and increasing the particle concentration reduces the mobility of CMC-nZVI due to ripening phenomena, while during the flushing time (introducing deionized water), such changes in grain size and particle concentration increase the mobility of CMC-nZVI due to a release from the secondary energy minimum well (in the DLVO theory).

Previous pilot-scale studies have shown outstanding levels of efficiency in phosphorus removal by using hydrated oil shale ash (HOSA) sediments in horizontal subsurface flow (HSSF) filters with low greenhouse gas emissions. However, no long-term full-scale experiment has been conducted using this material. From September 2013 to December 2015, two HSSF filters with different hydraulic loading regimes (NH1 with a stable loading regime and NH2 with a fluctuating regime), used to treat municipal wastewater, were analysed to estimate greenhouse gas (GHG) fluxes and to develop a treatment system with minimised GHG emissions. The fluxes of CO₂, CH₄ and N₂O, as well as their emission factors were significantly lower when compared with studies where regular filter materials (sand, gravel, etc.) are in use. The fluctuating loading regime significantly increased CO₂ and N₂O fluxes (median values of −3.3 and 2.6 mg CO₂−C m⁻² h⁻¹, and 5.7 and 8.6 μg N₂O−N m⁻² h⁻¹ for NH1 and NH2 regimes, respectively), whereas no impact could be seen on CH₄ emissions (median 93.3 and 95.6 μg CH₄−C m⁻² h⁻¹, for NH1 and NH2, respectively). All GHG emissions were strongly affected by the chemical composition of the water entering into the system. The water purification efficiency of the system was satisfactory for most water quality parameters and excellent for phosphorus. Thus, the HOSA-filled filters have a good potential for municipal wastewater treatment with low GHG emission.

The objective of this research was to determine the process of atrazine transport compared to bromide and δO¹⁸ transport in sands near Denver. Three 1.5 × 2 × 1.5-m plots were installed and allowed to equilibrate for 2 years before research initiation and were instrumented with 1.5 × 2-m zero-tension pan lysimeters installed at 1.5-m depths. Additionally, each plot was instrumented with suction lysimeters, tensiometers, time domain reflectometry (TDR) moisture probes, and thermocouples (to measure soil temperature) at 15-cm depth increments. All plots were enclosed with a raised frame (of 8-cm height) to prevent surface runoff. During the 2-year period before research began, all suction and pan lysimeters were purged monthly and were sampled for fluids immediately prior to atrazine and KBr application to obtain background concentrations. Atrazine illustrated little movement until after a significant rainfall event, which peaked concentrations at depths of about 90 to 135 cm. Both Br⁻ and δO¹⁸ moved rapidly through the soil, probably owing to soil porosity and anion exclusion for Br⁻. Concentrations of atrazine exceeding 5.0 μL⁻¹ were observed with depth (90 to 150 cm) after several months. It appears that significant rainfall events were a key factor in the movement of atrazine in the sand, which allowed the chemicals to move to greater depths and thus avoid generally found biodegradation processes.

Biochar produced from agricultural residues through pyrolysis has the characteristics of large specific surface area and porous structure and thus can be used as an adsorbent for various contaminants. In this study, five types of agricultural residues, peanut shells (PS), mung bean shells (MBS), rice husk (RH), corn cob (CC), and cotton stalks (CS), were selected as feedstocks to prepare biochars. Magnesium chloride (MgCl₂; 5 mol L⁻¹ m) solution was used as a modifier to prepare pre-modified and post-modified biochar adsorbents. The modified biochars were used in adsorption experiment to test their sorption ability to phosphate from aqueous solution. Model simulations and analysis were used to determine phosphorus removal mechanisms. Experimental results showed that the phosphate removal efficiency of the pre-modified cotton stalk paralyzed at 600 °C (Pre-CS600) was the best with adsorption capacity of 129.9 mg g⁻¹. The results also showed that the adsorption capacity of the biochar pre-modified by MgCl₂ was much better than that of unmodified and post-modified ones, suggesting the pre-modification method can be used to prepare modified biochars for the removal of phosphorus from aqueous solution.

The aim of this study is to evaluate the fluoride removal from contaminated water using a new adsorbent material of high efficiency to obtain drinking water. The ZrCl₄-graphene supported on vegetal activated carbon composite (G-ZrCl₄/VAC) was synthesized and characterized using transmission and scanning electron microscopy, N₂ physisorption, energy dispersive X-ray spectrometry, Fourier transform-infrared spectroscopy, X-ray diffraction, and Raman spectroscopy. Furthermore, the point of zero charge was determined. The G-ZrCl₄/VAC was evaluated for fluoride adsorptive removal from water under several operating conditions in batch system. The results indicated that fluoride adsorption by G-ZrCl₄/VAC is favored at low pH values with the maximum adsorption at pH 2, corresponding to 97.22% removal. Among the conditions of temperature and agitation evaluated, the best results were achieved at 30 °C and 130 rpm, with removal percentages equal to 47.78 and 48.48%, respectively. The equilibrium of the system was achieved in 5 h of operation. The pseudo-first order kinetic model was the one that best described the kinetic data, while the equilibrium data were best described by the Langmuir isotherm with maximum adsorption capacity equal to 3.89 mg g⁻¹. Therefore, the results obtained show that the material synthesized has a great capacity for adsorption and demonstrate the viability of use of G-ZrCl₄/VAC in the removal of fluoride to obtain drinking water.

This paper attempts to investigate the emissions embodied in Australia’s economic growth and disaggregate primary energy sources used for electricity production. Using time series data over the period of 1990–2012, the ARDL bounds test approach to cointegration technique is applied to test the long-run association among the underlying variables. The regression results validate the long-run equilibrium relationship among all vectors and confirm that CO₂ emissions, economic growth, and disaggregate primary energy consumption impact each other in the long-run path. Afterwards, the long- and short-run analyses are conducted using error correction model. The results show that economic growth, coal, oil, gas, and hydro energy sources have positive and statistically significant impact on CO₂ emissions both in long and short run, with an exception of renewables which has negative impact only in the long run. The results conclude that Australia faces wide gap between emission abatement policies and targets. The country still relies on emission intensive fossil fuels (i.e., coal and oil) to meet the indigenous electricity demand.

Pesticides are used for controlling the development of various pests in agricultural crops worldwide. Despite their agricultural benefits, pesticides are often considered a serious threat to the environment because of their persistent nature and the anomalies they create. Hence removal of such pesticides from the environment is a topic of interest for the researchers nowadays. During the recent years, use of biological resources to degrade or remove pesticides has emerged as a powerful tool for their in situ degradation and remediation. Fungi are among such bioresources that have been widely characterized and applied for biodegradation and bioremediation of pesticides. This review article presents the perspectives of using fungi for biodegradation and bioremediation of pesticides in liquid and soil media. This review clearly indicates that fungal isolates are an effective bioresource to degrade different pesticides including lindane, methamidophos, endosulfan, chlorpyrifos, atrazine, cypermethrin, dieldrin, methyl parathion, heptachlor, etc. However, rate of fungal degradation of pesticides depends on soil moisture content, nutrient availability, pH, temperature, oxygen level, etc. Fungal strains were found to harbor different processes including hydroxylation, demethylation, dechlorination, dioxygenation, esterification, dehydrochlorination, oxidation, etc during the biodegradation of different pesticides having varying functional groups. Moreover, the biodegradation of different pesticides was found to be mediated by involvement of different enzymes including laccase, hydrolase, peroxidase, esterase, dehydrogenase, manganese peroxidase, lignin peroxidase, etc. The recent advances in understanding the fungal biodegradation of pesticides focusing on the processes, pathways, genes/enzymes and factors affecting the biodegradation have also been presented in this review article.

Activated carbon fiber-supported cobalt phthalocyanine photocatalyst (Co-TDTAPc-F) was prepared in this study, and its performance for dye wastewater decoloration was investigated, and Acid Orange II (AO7) was selected as the target pollutant. The morphology analysis of Co-TDTAPc-F was conducted, and the effects of catalyst loading, H₂O₂ addition, solution pH, and catalyst reuse on AO7 decoloration efficiency were evaluated. The results showed that AO7 decoloration efficiency increased by 23.2% during the Co-TDTAPc-F photocatalytic process as compared with solely Co-TDTAPc-F adsorption, and the decoloration process was fitted by pseudo first-order reaction. The increase of catalyst loading and H₂O₂ content both benefitted AO7 decoloration. Strong photocatalytic activities were observed at both acidic and alkaline conditions; however, total organic carbon (TOC) removal efficiency decreased with the increase of solution pH. Strong photocatalytic activity was still observed after four times reuse. The mechanisms of AO7 photocatalytic decomposition by Co-TDTAPc-F were proposed.

The surface morphology of biocathode was one of the limiting factors for microbial fuel cell (MFC) design. Up-flow membrane-less single-chambered MFC (UFML MFC) was used to investigate the effect of surface morphology of carbon material as aqueous biocathode. Pt-loaded carbon paper, carbon felt, and carbon plate were examined and compared on the power output, surface morphology for biofilm formation, Coulombic efficiency (CE), and chemical oxygen demand (COD) reduction. The COD reduction was up to 90 % in UFML MFC with Pt-loaded carbon paper, carbon felt, and carbon plate as aqueous biocathodes. The results obtained showed that the performance in voltage output was not related to internal resistance but mainly due to the ability of cathode material in oxygen reduction process. The performance of voltage output with different materials as aqueous biocathode was mainly based on to the surface morphology as it was related to the ability of biofilm formation. Roughness of aqueous biocathode’s surface morphology could prompt the biofilm growth, while biofilm overgrowth on aqueous biocathode could decrease voltage output. Therefore, smoother surface morphology of aqueous biocathode is more suitable for long-term operation.

Mercury (Hg), aside from having high toxicity, is characterized by its ability to biomagnify in the marine trophic chain. This is an important problem especially in estuaries, or in the coastal zone, particularly near the mouths of large rivers. This study was conducted in the years 2001–2011, in the coastal zone of the Baltic Sea near to the mouth of the River Vistula, which is the second biggest river discharging into the Baltic. Mercury concentration was measured in the tissues and organs of cod, flounder, herring, seals (living in the wild and in captivity), great black-backed gulls, and African penguins from Gdańsk Zoo, and also in human hair. Penguins and seals at the seal sanctuary in Hel were fed only herring. In marine birds and mammals and in the pelagic herring, the highest Hg concentration was observed in the kidney and in the liver, while in cod and flounder (located on a higher trophic level) the muscles were the most contaminated with mercury. In gray seals living in the seal sanctuary, Hg concentration in all analyzed tissues and organs except the kidneys was lower in comparison with seals living in the wild. The comparatively small share of fish in the diet of local Polish people and their preference towards the consumption of herring contributed to low concentration of Hg in their hair. The protective mechanisms related to detoxification and elimination of mercury were shown to be more effective in the seals than in the penguins, despite the former consuming around 10 times more food per day.