This study addressed the removal performance of RR2 from aqueous solutions in adsorption columns experiments by comparing the potential of activated carbon alone (ACA) and microbially inoculated (MIAC), prepared from barks of a largely available tree in Brazilian Cerrado biome, Hymenaea courbaril L. or “Jatobá,” presenting the kinetics, isotherms, breakthrough curves, and dissolved organic carbon removal. ACA presented strong interaction to RR2 dye, evidenced at the first 20 min when absorbance already attained 66.4%. The removal percentage gradually increased with time and the equilibrium occurred around 91.7% within 120 min. Langmuir model best fitted the isotherm data, indicating a maximum adsorption capacity of 4.068 mg g⁻¹ for the amount of 0.5 g of adsorbent. The Langmuir’s model parameters KL, RL, and R² corresponded to 0.0234 L mg⁻¹, 0.4159, and 0.9663, respectively, indicating a favorable adsorption process (0 < RL < 1). The experiments in adsorption columns revealed maximum adsorption capacities of 14.38 and 11.43 mg g⁻¹ for MIAC and ACA, respectively, where the microbial activity favorably retarded the adsorption breakpoint in approximately 20 min and enhanced the RR2 consumption in 25.8%. Effectiveness of DOC removal attained above 90% for both ACA and MIAC, reducing the content from 86.1 to 7.84 mg L⁻¹ and 4.82 mg L⁻¹, respectively.

The Rhodamine B adsorption was realized in batch using calcined bentonite clay. The effects of Rhodamine B initial concentration, pH, and temperature were evaluated and the conditions where the adsorption was favored were in 500 mg L⁻¹, pH 3, and 35 °C. The equilibrium isotherms studied were from Langmuir and Freundlich. The coefficients of determination (R² > 0.99) were found to confirm the best fitted to Langmuir isotherm, with a monolayer adsorption capacity (qₘₐₓ) of 552.49 mg g⁻¹. The kinetic data agreed well with the pseudo-second order model (R² > 0.99). The in natura and calcined clay were characterized by the techniques of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), N₂ physisorption (BET), and scanning electron microscopy (SEM). Thermodynamic parameters including Gibbs free energy (ΔG°), enthalpy change (ΔH°), and entropy change (ΔS°) were calculated to estimate the nature of Rhodamine B adsorption in clay. The results suggested that the adsorption was endothermic and spontaneous, with the enthalpy adsorption increasing with the increase of temperature. Therefore, calcined bentonite can be used as an efficient adsorbent for discoloration of large volume of residual water, presenting low-cost and high adsorptive capacity.

Graphene oxide (GO) was synthetized from graphite oxidation via the modified Hummers method. Afterwards, the GO was functionalized with diethylenetriamine (DETA) and FeCl₃ to obtain the novel amino-iron oxide functionalized graphene (GO-NH₂-Fe₃O₄). FTIR, XRD, SEM with EDX, and Raman spectroscopy were performed to characterize both GO and GO-NH₂-Fe₃O₄. The GO-NH₂-Fe₃O₄ was then evaluated as adsorbent of the cationic dye Methylene Blue (MB); analysis of the point of zero net charge (pHPZC) and pH effect showed that the GO-NH₂-Fe₃O₄ pHPZC was 8.2; hence, the MB adsorption was higher at pH 12.0. Adsorption kinetics studies indicated that the system reached the equilibrium state after 5 min, with adsorption capacity at equilibrium (qₑ) and kinetic constant (kS) of 966.39 mg g⁻¹ and 3.17∙10⁻² g mg⁻¹ min⁻¹, respectively; moreover, the pseudo-second-order model was better fitted to the experimental data. Equilibrium studies showed maximum adsorption capacity of 1047.81 mg g⁻¹; furthermore, Langmuir isotherm better fitted the adsorption. Recycling experiments showed that the GO-NH₂-Fe₃O₄ maintained the MB removal rate above 95% after 10 cycles. All the results showed sorbent high adsorption capacity and outstanding regeneration capability and evidenced the employment of novel GO-NH₂-Fe₃O₄ as a profitable adsorbent of textile dyes.

Yeast biomass from ethanol industry (YB) was evaluated as a biosorbent to 17α-ethinylestradiol (EE) alone and along with estrone (EST). This material is rich in sorption sites and has a good cost-benefit ratio, since it is an industrial residue largely produced (around 30 g for each liter of ethanol). A 2ᵏ-factorial design was carried out to evaluate the sorption capacity of YB for EE considering the variables pH, biosorbent dose (BD), and ionic strength (IS), at two hormone concentration (HC) levels. The best conditions assessed for individual EE adsorption (pH = 10, IS = 0.1 mol/L, and BD = 0.5 mg/L) were also established for adsorption carried out in the presence of EST. Individuals EE and EST experimental sorption capacities (SCₑₓₚ) were, respectively, 24.50 ± 0.07 and 0.80 ± 0.07 mg/g, fairly similar to Qₘₐₓ (EE, 21.41 ± 1.27 mg/g; EST, 0.93 ± 0.075 mg/g) from Langmuir model. The Freundlich model best fitted the experimental data for EE adsorption (r² = 0.9925; χ² = 0.5575). The study carried out in the presence of EST showed an associative/competitive sorption process between EE and EST, which may be explained by their similar chemical structures and organic carbon-water partition coefficients Kₒc.

During this research, chemometric approaches were applied for optimization of the low-temperature partitioning extraction (LTPE) for the simultaneous analysis of the pesticides: acephate, difenoconazole, fenamidone, fluazifop, fluazinam, methamidophos, and thiamethoxam from surface water samples and determination by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry. It was used the 2³ full factorial and the Doehlert experimental designs. The extraction technique was optimized by evaluating the effects of the three variables: sample pH, ionic strength (addition of Na₂HPO₄), and organic solvent volume. Considering the interest to find an optimal condition for all analytes simultaneously, the best extraction parameters found were as follows: pH = 5.33, concentration of Na₂HPO₄ = 0.0088 mol L⁻¹ and organic phase volume = 4.5 mL. The optimized methodology showed LOD and LOQ levels from 0.33 to 8.13 ng L⁻¹ and from 1.09 to 26.84 ng L⁻¹, respectively. The recovery values ranged from 38.37 and 99.83% and the RSD values varied from 2.33 to 18.92%. The method was applied to surface water analysis sampled in areas with intensive agricultural practices in Ouro Branco City, Minas Gerais, Brazil. The difenoconazole was detected in concentrations between 12.53 and 94.76 ng L⁻¹.

Current economic policy planning places much emphasis on balancing development and environmental protection. Hence, it is important to determine the drivers of environment pollution from the theoretical, scientific, and policymaking aspects in the context of continuous economic growth. This paper investigates the factors affecting per capita CO₂ emissions in 30 provinces in Iran from 2009 to 2014 with emphasis on spatial spillover effects using the Spatial Durbin Model. The findings show that per capita CO₂ emissions are positively and significantly affected by per capita GDP, industrialization, and urbanization but negatively affected by changes in population. The results of the spatial section of the model indicate that both the more and the less-polluted provinces tend to cluster together, indicating positive spatial dependence for CO₂ emissions in the provinces. Also, the spatial spillover of per capita GDP and the growth of urbanization have a negative and significant effect on per capita CO₂ emissions in the provinces, while the spatial effect of changes in population is significant but positive. In other words, the economic development and rise in urbanization in one province are the results of changes in pollution levels in neighboring provinces.

Dissolved organic matter (DOM) extracted from wheat straw (SDOM) and cow manure (MDOM) were used to investigate their effects on the solubilization, uptake, and translocation of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47). Partition coefficients (KDOC) of BDE 47 between water and the two types of DOM were measured by the solubility enhancement method. The uptake and translocation of BDE 47 by wheat plants were explored by hydroponic exposure experiments. In the range of 0 to 100 mg/L of DOM, the solubility of BDE 47 increased with increasing concentrations of DOM. The log [KDOC] values of BDE 47 in SDOM and MDOM solutions were 5.77 and 5.31, respectively. The log [KDOC] values of BDE 47 in SDOM solutions were higher than those in MDOM solutions, which might be ascribed to the higher content of aliphatic carbon and lower molecular weight of SDOM. The addition of DOM (50 mg/L) significantly increased the accumulation of BDE 47 in the shoots of wheat plants. Wheat straw DOM had greater effect than MDOM in enhancing the accumulation of BDE 47. This study demonstrated the potential risk of BDE 47 to plants resulting from DOM-facilitated transport or the changes in metabolic properties.

The chiral herbicide imazethapyr (IM) is frequently used to control weeds in soybean fields in northeast China. However, the impact of IM enantiomers on microbial communities in soil is still unknown. Genetic markers (16S rRNA V3-V4 regions) were used to characterize and evaluate the variation of the bacterial communities potentially effected by IM enantiomers. Globally, the bacterial community structure based on the OTU profiles in (−)-R-IM-treated soils was significantly different from those in (+)-S-IM-treated soils, and the differences were enlarged with the treatment dose increasing. Interestingly, the Rhizobiaceae family and several other beneficial bacteria, including Bradyrhizobium, Methylobacterium, and Paenibacillus, were strongly enriched in (−)-R-IM treatment compared to (+)-S-IM treatment. In contrast, the pathogenic bacteria, including Erwinia, Pseudomonas, Burkholderia, Streptomyces, and Agrobacterium, were suppressed in the presence of (−)-R-IM compared to (+)-S-IM. Furthermore, we also observed that the bacterial community structure in (−)-R-IM-treated soils was more quickly restored to its original state compared with those in (+)-S-IM-treated soils. These findings unveil a new role of chiral herbicide in the development of soil microbial ecology and provide theoretical support for the application of low-persistence, high-efficiency, and eco-friendly optical rotatory (−)-R-IM.

To estimate the impact of mercury discharged from artisanal and small-scale gold mining (ASGM) activity, variations in the concentrations of elemental mercury (Hg0), mercury ion (Hg2+), particulate mercury (P-Hg), and total mercury in filtered river water (FT-Hg) were investigated from sampling locations extending from 10 km upstream to 30 km downstream of ASGM operations in West Java, Indonesia. The average of the annual concentrations at the ASGM site from 2013 to 2017 were 0.14–0.85 μg L⁻¹, 0.27–12.9 μg L⁻¹, 4.3–49.5 μg L⁻¹, and 1.2–12.5 μg L⁻¹ for Hg0, Hg²⁺, P-Hg, and FT-Hg, respectively. The concentration of mercury species decreased as the distance from the ASGM site increased, while the ratio of P-Hg increased towards the lower reaches of the river system, with the percentage of P-Hg estimated at 90% of Hg at the sample location furthest downstream. A high mercury concentration of 600 mg kg⁻¹ was observed for suspended particulate matter (SPM) at the ASGM site. The SPM maintained a high concentration of mercury, even in the downstream area. In the annual variations of the mercury species from 2013 to 2017, FT-Hg and P-Hg concentrations tended to decrease from 2016, which suggested a decline of ASGM activity in this area. However, SPM and river sediment showed no apparent changes in their mercury concentrations over this period, indicating that the contamination in the river system is persistent and does not recover quickly.

The seasonal succession of phytoplankton functional groups (PFGs), their ecological preferences, relationships between environmental variables and PFGs, and ecological status were investigated in the Batman Dam Reservoir, a warm monomictic reservoir, located in the Tigris River basin of Turkey. Altogether 60 species, 19 functional groups, and 10 prevailing functional groups were identified, and prevailing functional groups showed strong seasonal changes. Centric diatoms Cyclotella ocellata (group B) and Aulacoseira granulata (group P) were dominant in the spring, with water mixing and low temperature. Groups F (Elakatothrix gelatinosa, Elakatothrix gelatinosa, and Sphaerocystis schroeteri), J (Pediastrum simplex and Coelastrum reticulatum), G (Eudorina elegans and Volvox aureus), LM (Ceratium and Microcystis), and H1 (Aphanizomenon flos-aquae and Anabaena spiroides) dominated the phytoplankton community from summer to mid-autumn, with thermal stratification. Groups H1 and P became dominant in the late autumn, with the breakdown of stratification. With the deepening of the mixing zone, groups P and T (Mougeotia sp.) were dominant in the winter. The reservoir was meso-eutrophic according to trophic state index values based on total phosphorus (TP), chlorophyll a, Secchi depth and total nitrogen, habitat preferences of PFGs, and diversity indices of phytoplankton. Redundancy analysis (RDA) revealed that NO₃–N, SiO₂, TP, pH, and water temperature (WT) were the most important environmental factors controlling PFGs in the BDR. Weighted averaging regression results indicated that among PFGs, groups F and T had a narrower tolerance range for WT, pH, and SiO₂, while groups G and T had a narrower tolerance range for TP and NO₃–N.