Chemical inputs from agricultural activities represent a threat to aquatic biota and its biochemical systems. Among these systems, acid phosphatases are involved in autophagic digestive processes, decomposing organic phosphates, signaling pathways, and other metabolic routes. In vitro tests are helpful to generate hypotheses about pollutant mechanisms of action through comparison of the toxicity effects of these compounds. In this work, we investigated the inhibitory effects of four organic pesticides and three metals on the acid phosphatases extracted from the freshwater microcrustacean Daphnia similis and the fish Metynnis argenteus. Our results demonstrated that only the metals have considerable inhibitory effects (50% or higher) on the enzyme activities. The calculated median effect concentrations (IC50) for the enzyme inhibition were 0.139 mM Hg²⁺ (fish enzyme), 0.652 mM Cu²⁺ (fish enzyme), and 1.974 mM Al³⁺ (Daphnia enzyme). Due to the relatively low value of the inhibition parameter for Hg²⁺, its inhibitory property could be used as a tool for Hg²⁺ detection in environmental samples. The enzyme activities obtained in the presence of the inhibitors are potential data as in vivo biomarkers for metals in both aquatic species.

The goal of this research was the electrooxidation (EO) of a nonionic surfactant nonylphenol decaethoxylate (NP-10) in aqueous solution and denim wastewater. Three different configuration systems were evaluated in batch cells using a boron-doped diamond (BDD) anode; copper, iron, and BDD were used as cathodes. The EO process was carried out in a batch process, in a glass cell with a capacity of 1000 mL. The anode surface area was 0.0307 m² and 1–3 A of current intensity were applied (3, 6, 10 mA/cm²) with an electrolysis time of 240 min for aqueous solution and 780 min for denim wastewater in order to investigate the degradation of the surfactant. The processes were analyzed in terms of chemical oxygen demand (COD) and total organic carbon (TOC). The maximum mineralization efficiency in aqueous solution for the BDD-Cu electrooxidation system was 92.2% for COD and 45.6% for TOC at pH 2 and 3 mA/cm² of current intensity. For denim wastewater, the removal efficiency was 44.1% for COD and 26.5% for TOC at pH 4.5 and 6 mA/cm² of current intensity, using a BDD-BDD system. The raw and treated (aqueous solution and denim) wastewater were characterized by UV-Vis and infrared spectroscopy.

Benzalkonium chloride (BAC) loaded to montmorillonites (Mt) or organomontmorillonites (OMt) generates a functional material that can be incorporated to several systems (polymers, paints, etc) as a controlled release bactericide. Understanding the BAC adsorption sites on these adsorbents is of high importance to clarify their adsorption/desorption characteristics in aqueous media or other solvents. In this work, a thorough study about the adsorption/desorption properties of Mt and OMt with regards to BAC is presented, in order to evaluate further BAC release with the consequent aquatic environment contamination. In this work, the BAC adsorption on two different sites is demonstrated: the interlayer space and the external surface. Depending on BAC concentration in water, sorption of BAC at Mt occurred in two steps. At adsorbed amount <0.5 mmol g⁻¹, there was an Mt interlayer expansion of 0.49 nm with no change of the external charge. At adsorbed amount >0.5 mmol g⁻¹, there was a new interlayer expansion attaining 0.75 nm and the external charge shifted to positive value. In the case of OMt, the introduction of BAC produced changes in the interlayer structure and in the external surface charge. BAC desorption was strongly dependent on the type of Mt or OMt and extraction solvent, knowledge of which will allow its safe use in environmental friendly technological applications.

Nitrogen dioxide (NO₂) is one of the major atmospheric pollutants, and the concentration of NO₂ is regarded as one of the indicators of air quality. In the past decades, China has experienced rapid economic growth and severe NO₂ pollution to match. We evaluate the trends and spatiotemporal patterns of tropospheric NO₂ over mainland China from 2005 to 2014 using vertical column density (VCD) datasets retrieved from the Ozone Monitoring Instrument (OMI). Results show that from 2005 to 2014, NO₂ pollution regions have enlarged at the national scale, and high NO₂ VCDs are mainly concentrated over highly populated regions in eastern China. The year 2011 is the turning point. Tropospheric NO₂ VCDs first significantly increase by 0.19 × 10¹⁵ molec cm⁻² year⁻¹ (R ² = 0.94, P = 0.002) from 2005 to 2011, and then decrease by 0.21 × 10¹⁵ molec cm⁻² year⁻¹ (R ² = 0.97, P = 0.016) from 2011 to 2014. Since 2011, tropospheric NO₂ VCDs over central-east China decrease remarkably. Tropospheric NO₂ VCDs is higher in November (3.630 × 10¹⁵ molec/cm²), December (4.758 × 10¹⁵ molec/cm²), and January (4.863 × 10¹⁵ molec/cm²), while lower in July (1.684 × 10¹⁵ molec/cm²), August (1.627 × 10¹⁵ molec/cm²), and September (1.703 × 10¹⁵ molec/cm²), indicating that winter and spring are the most polluted seasons. Due to the huge gap in population density and industry development between western and eastern China, the spatial pattern of tropospheric NO₂ VCDs shows large west-east difference.

Present study investigates the coagulation ability of Plantago ovata (P. ovata) seed extracts for turbidity removal. The active coagulant agents were successfully extracted from P. ovata seeds using different solvents such as distilled water (PO-DW), tap water (PO-TW), NaCl (PO-NaCl), and ammonium acetate (PO-AA). Experiments were conducted in batch mode for initial turbidity such as 500 NTU (high), 150 NTU (medium), and 50 NTU (low). Results demonstrated that P. ovata extracts are less efficient in low turbidities, while PO-NaCl was found to provide high coagulation activity in all initial turbidity concentrations compared to other extracts. PO-NaCl was able to remove 98.2, 94.9, and 80.2% of turbidity from water having in initial turbidities of 500, 150, and 50 NTU, respectively. Coagulation activity of the extract was the best when the extraction was performed for 50 min at room temperature. Jar test procedure with the coagulation time of 1 min and flocculation time of 30 min was optimized, irrespective of the initial turbidity. The optimum settling time for 500, 150, and 50 NTU water samples were 20, 30, and 90 min, respectively. PO-NaCl was used in different pH turbid solutions and it was found to be working very efficiently in alkaline conditions. The coagulation efficiency of the coagulant stored in refrigerator was higher than that stored at room temperature. Thus, the natural coagulants extracted from P. ovata seeds revealed to be effective for turbidity removal.

Environmental pollution with chromium is due to residues of several industrial processes. Bioremediation is an alternative actually considered to remove Cr (VI) from the environment, using adapted organisms that grow in contaminated places. Have been conducted studies with fungi mechanisms of interaction with chromium, most of which have focused on processes biosorption, characterized it by passive binding of metal components of the cell surface, and bioaccumulation, wherein the metal entry to cells occurs with energy expenditure. The paper presents the results of studies carried out on sorption of chromium (VI) ions from aqueous solutions by Fusarium sp. and Myrothecium sp. Both biomasses have the ability to take up hexavalent chromium during the stationary phase of growth and as well inactive conditions. Fusarium sp. showed 26% of biosorption with active biomass and 64% in inactive biomass; meanwhile, Myrothecium sp. obtained 97 and 82%, respectively. Both fungi showed adjust to pseudo-second-order model in active (Fusarium sp. R ² = 0.99; Myrothecium sp. R ² = 0.96) and inactive biomass assay (Fusarium sp. R ² = 0.99; Myrothecium sp. R ² = 0.99). The data of the active biomass test also confirmed to the intraparticle diffusion model (Fusarium sp. R ² = 0.98; Myrothecium sp. R ² = 0.93). The results obtained through this investigation indicate the possibility of treating waste effluents containing hexavalent chromium using Fusarium sp. and Myrothecium sp.

Road dust impacts almost all terrestrial areas of the planet and may impact vegetation and nearby ecosystems. Therefore, research methods are needed for applying road dust in a controlled manner on targeted areas (e.g. plants). Three dust application methods, sifter, sieve, and sprayer, were investigated for their uniformity in applying dust in a 0.75 m × 0.75 m area. Within the treatment area 196, 37-ml cups were placed in a uniform fashion to collect dust applied at 15.8, 78.8, and 158 g. At the 15.8 and 78.8 g rates, the coefficient of uniformity for each method was >98% indicating a uniform amount of dust applied. At the 158 g rate, the sifter and sieve had coefficient of uniformities >95%, while the sprayer had a significantly lower (p < 0.05) coefficient of uniformity (46%). Although the sifter and sieve were simpler to use and the least expensive options, the sprayer may be more useful when applying dust to larger areas when the exact amount of dust entering and exiting the systems does not need to be controlled. This research is useful to anyone looking to apply road dust or similar sized particulates under controlled field or laboratory conditions.

A method for simultaneously determining the levels of aniline, benzidine, microcystin variants (microcystin-LR, RR, and YR) and carbaryl in water was developed based on ultra-performance liquid chromatography–electrospray ionization tandem mass spectrometry (UPLC-MS/MS). The chromatographic conditions were optimized for the trace determination. Without sample enrichment, the method detection limit for all test compounds ranged from 0.040 to 0.155 μg/L; meanwhile, the recoveries for all test compounds were 83.1–114%. Precision, indicated by the relative standard deviation, was <12.9%. The results meet the requirements for the determination of these compounds. Without the need to clean up the samples, the results of the analysis of samples from wastewater and surface water demonstrated that the UPLC-MS/MS method has the capability to analyze complex matrices in the trace-level monitoring of wastewater samples.

A novel bag filter + powdered activated carbon technique is here proposed to address the low utilization rate of powdered activated carbon and the low dioxin removal rate associated with the conventional activated carbon injection + bag filter technique, better known as the fly ash + activated carbon + bag technique. In this method, dibenzofuran serves as a dioxin simulant. The effect of the adsorption temperature and dibenzofuran inlet concentration on the adsorption performance of activated carbon was studied using a filter cloth adsorption device with an inner diameter of 25 mm, and the adsorption performances of fly ash, activated carbon, and fly ash +5% activated carbon were compared. The results showed that activated carbon exhibited a higher adsorption efficiency and remained highly efficient longer than fly ash +5% activated carbon. When the dibenzofuran inlet concentration was 0.0956 g/m³ (about one million times the concentration of dioxin in the flue gas of incinerated waste), the duration of the high-efficiency (>90%) adsorption of the powdered activated carbon (thickness 1.2 mm) on the filter cloth was over 7 h. These results prove that the replacement of fly ash + activated carbon + filter bag with powdered activated carbon + bag filter can significantly improve the removal efficiency of the dioxin in waste incineration flue gas and the utilization rate of activated carbon.