A novel assembly method was used to prepare the sulfhydryl functionalized magnetic SBA-15 (SH-M-SBA-15). The physicochemical properties of SH-M-SBA-15 were characterized by TEM, XRD, EDS, FT-IR, BET, and VSM. Batch adsorption experiments were conducted to investigate the influence of initial uranium concentration, dosage of adsorbent, pH values, contact time, and temperature on the adsorption efficiency and behaviors. The adsorption types were analyzed from the aspects of kinetic, isotherms, and thermodynamic. The results show that the specific surface area of SH-M-SBA-15 is 316.67 m²/g, which is smaller than that of SBA-15 (692.18 m²/g). However, compared with SBA-15, SH-M-SBA-15 has more surface sulfhydryl functional groups. The addition of this group can improve the adsorption of uranyl ions by SH-M-SBA-15. The optimal adsorption conditions were adsorption dosage 40 mg/L, pH 6, temperature 35 °C, contact time 180 min, and initial uranium concentration 35 mg/L. Under this condition, the maximum adsorption amount of uranyl ion by SH-M-SBA-15 can reach 804.79 mg/g, which is much higher than the highest adsorption capacity of uranyl ion by SBA-15 (146.23 mg/g). The adsorption process was better depicted by the Langmuir isotherm model. The process was consistent with the quasi-second-order model. ΔG was negative and ΔH was positive, indicating spontaneous and endothermic adsorption.

The pollutants’ emissions from on-road transport are critical pressure on the climate change scenario, and most developing countries rely on mostly diesel transportation. The current study aimed to estimate the environmental impact of the distance from the agricultural production area of fresh food (papaya, potato, and tomato) to a fresh food distribution center located in Campinas, Sao Paulo, Brazil. The way the products were carried was assessed for calculating the total transported volume. The total amount carried was measured, considering the number of trips multiplied by the total distance traveled within a year of supply. An online calculator was used to evaluate the amount of CO₂ emission, and to allow the estimative of the amount of CO₂-eq, that is the Global Warming Impact (GWP) in 100 years. The highest CO₂ emission was identified in the potato transported from Paraná State to the distribution center, with a CO₂-eq emission of 3237 t/year (64% of contribution), followed by the papaya from Bahia State (2723 t/year, 42% of contribution), and the tomato from Sao Paulo State (625 t/year, 71% of contribution). However, when computing the GWP, the highest value was found in the transport of potato from the Minas Gerais State (8 × 10⁻² in 100 years) followed by the papaya from Rio Grande do Norte State (5 × 10⁻² in 100 years) and the papaya from Bahia (3 × 10⁻² in 100 years). The higher the amount of product transported by a trip, the smaller the environmental impact in the long run. A proper strategy to reduce the environmental impact would be to have large freight volume when transporting food from vast distances within continental countries.

Diclofenac (DCF), a widely used non-steroidal anti-inflammatory drug, has been detected in effluents of conventional wastewater treatment plants worldwide. The presence of this compound in various water resources even at very low concentrations poses a big threat both to human health and aquatic ecosystems. In this study, the removal of diclofenac from aqueous solution using Fe–Mn binary oxide (FMBO) adsorbents was investigated. FMBO adsorbents were prepared at varying Fe/Mn molar ratios (1:0, 3:1, and 1:1) through simultaneous oxidation and co-precipitation methods. Batch adsorption experiments were conducted to evaluate the effects of important parameters, such as initial DCF concentration, FMBO dosage, solution pH, and Fe/Mn molar ratio, on DCF removal. Acidic to neutral pH conditions were more favorable for DCF adsorption, while increasing initial DCF concentration and adsorbent dosage resulted in higher DCF removal efficiencies for the three oxides. Lower Fe/Mn molar ratio during FBMO synthesis favored higher DCF removals of up to 99% within a wide pH range. Optimization of operating parameters (initial DCF concentration, FMBO dosage, and solution pH) by Box–Behnken design resulted in up to 28.84 mg g⁻¹ DCF removal for 3:1 FMBO. Freundlich isotherm best described the experimental data, indicating that adsorption occurred on heterogeneous adsorbent surface. Chemisorption was the rate-limiting step of the DCF removal, as best described by the pseudo-second-order kinetic model.

Polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) are ubiquitous and toxic contaminants. Their atmospheric deposition fluxes on the regional scale were quantified based on simultaneous sampling during 1 to 5 years at 1 to 6 background/rural sites in the Czech Republic and Austria. The samples were extracted and analysed by means of gas chromatography coupled to mass spectrometry. For all seasons and sites, total deposition fluxes for Σ₁₅PAHs ranged 23–1100 ng m⁻² d⁻¹, while those for Σ6PCBs and Σ12OCPs ranged 64–4400 and 410–7800 pg m⁻² d⁻¹, respectively. Fluoranthene and pyrene were the main contributors to the PAH deposition fluxes, accounting on average for 19% each, while deposition fluxes of PCBs and OCPs were dominated by PCB153 (26%) and γ-hexachlorobenzene (30%), respectively. The highest deposition flux of Σ₁₅PAHs was generally found in spring, while no seasonality was found for PCB deposition. For deposition fluxes for Σ₁₂OCPs, no clear spatial trend was found, confirming the perception of long-lived regional pollutants. Although most OCPs and PCBs hardly partition to the particulate phase in ambient air, on average, 42% of their deposition fluxes were found on filters, confirming the perception that particle deposition is more efficient than dry gaseous deposition. Due to methodological constraints, fluxes derived from bulk deposition samplers should be understood as lower estimates, in particular with regard to those substances which in ambient aerosols mostly partition to the particulate phase.

Heavy metal lead poses a great threat to organisms and the environment; the removal of lead has drawn more and more attention in recent years. In this paper, the sulfur-containing functional group was grafted onto the walnut shell with xanthate to synthesize a low-cost biosorbent (SWM) for the removal of lead in water. The synthesized adsorbent was characterized by Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and Brunner−Emmet−Teller (BET). The effects of pH, adsorbent dosage, contact time, initial Pb (II) concentration, and temperature on adsorption were investigated, and the adsorption properties of walnut shells before and after modification were compared. Moreover, adsorption kinetics, adsorption isotherms, and adsorption thermodynamics were studied. The sulfur-containing functional group was confirmed to be successfully grafted onto the walnut shell. The results showed that the adsorption performance of SWM was much better than the unmodified walnut shell due to complexation by sulfur-containing functional group and ion exchange. The Pb (II) adsorption onto SWM was found to follow Temkin isotherm model and has a good correlation with the pseudo-second-order kinetic model. In addition, the adsorption process was spontaneous and exothermic. All the results showed that the high adsorption performance and low cost of SWM make it a potential biosorbent in the treatment of lead-contaminated water.

NaY and Na13X zeolites were modified by different modification manners including H⁺ modification, metal ion modification (Cu²⁺, Ni²⁺, or Ce³⁺), and H⁺ modification followed by metal ion modification to investigate their deep desulfurization behavior in gasoline. The sorbents were characterized by X-ray diffraction, FTIR of chemisorbed pyridine, N₂ adsorption, and scanning electron microscope (SEM). The desulfurization performance of these sorbents was evaluated in model gasoline containing thiophene and cyclohexane with thiophene concentration of 500 mg/L, and the results were analyzed to investigate the effect of preparation methods on adsorption desulfurization behavior. The result indicates that H⁺ modification or metal ion modification could all improve the desulfurization performance of both NaY and Na13X zeolites, except for Na13X modified by Cu²⁺ and Ni²⁺. For Cu²⁺ or Ni²⁺ ion exchanging, the crystal structure of Na13X would be destroyed, resulting in a much lower desulfurization efficiency than that of the parent Na13X. The desulfurization efficiency of sorbents prepared via H⁺ modification followed by metal ion modification is higher than that of sorbents prepared by single H⁺ modification or single metal ion modification, because the former is more conducive to improve the content of metal elements on the sorbents than the latter. In addition, the increase of the specific surface area and pore volume of the sorbents would directly lead to the improvement of desulfurization performance of the sorbents. Compared with Na13X, the H⁺ modification on NaY zeolite can significantly enhance the desulfurization performance of the sorbents. Among those prepared sorbents, the CuHY has the highest desulfurization efficiency. The influence of thiophene concentration (100–1000 mg/L) on desulfurization efficiency of CuHY sorbent was evaluated. The results indicate that the desulfurization efficiency of CuHY sorbent is nearly 100% at room temperature, when the thiophene concentration is lower than 300 mg/L. Moreover, its desulfurization behavior could be described by Langmuir isothermal equation. Graphic abstract .

Long-distance inter-basin water transfer solves the problem of unbalanced water resources in different regions. However, it also changes the natural water chemistry characteristics as well as the bioavailability of heavy metals in the receiving water. In this study, taking the South-to-North Water Transfer Project in China as an example, the basic physicochemical characteristics of the source water (in the Danjiangkou (DJK) Reservoir) and receiving water (in the Beitang (BT) Reservoir) were studied. The BLM (biotic ligand model) was used to study the effect of long-distance inter-basin water transfer on the bioavailability of Cu in receiving waters. The results showed that the TOC (total organic carbon) and TDS (total dissolved solids) in the BT Reservoir water were 10 times and 4.6 times greater than those of the DJK Reservoir water, respectively. The ions in the BT Reservoir were mainly (K⁺+Na⁺)–(SO₄²⁻+CI⁻), while the ions in the DJK Reservoir were mainly (Ca²⁺+Mg²⁺)–HCO₃⁻. The results from the BLM showed that the main species of Cu in the water was total organic Cu (Torg Cu), which accounted for 98.69% and 99.77% of the Cu in the DJK Reservoir and BT Reservoir, respectively. The LC50 of Cu for Daphnia magna was 1203.40 ± 57.70 μg/l in the BT Reservoir and only 101.93 ± 7.60 μg/l in the DJK Reservoir. The criteria maximum concentration value of the BT Reservoir was 13.75 times that of the DJK Reservoir, while the criteria continuous concentration value of the BT Reservoir was 13.76 times that of the DJK Reservoir. These results showed that the heavy metals content in water bodies should not be used as the only consideration for water ecological security in the inter-basin water transfer process, and that differences in water quality criteria values caused by differing water environmental qualities in the river basins must be taken into consideration.

Anticoagulant rodenticides (ARs) have been used for decades for rodent control worldwide. Research on the exposure of the environment and accumulation of these active substances in biota has been focused on terrestrial food webs, but few data are available on the impact of ARs on aquatic systems and water organisms. To fill this gap, we analyzed liver samples of bream (Abramis brama) and co-located suspended particulate matter (SPM) from the German Environmental Specimen Bank (ESB). An appropriate method was developed for the determination of eight different ARs, including first- and second-generation ARs, in fish liver and SPM. Applying this method to bream liver samples from 17 and 18 sampling locations of the years 2011 and 2015, respectively, five ARs were found at levels above limits of quantifications (LOQs, 0.2 to 2 μg kg⁻¹). For 2015, brodifacoum was detected in 88% of the samples with a maximum concentration of 12.5 μg kg⁻¹. Moreover, difenacoum, bromadiolone, difethialone, and flocoumafen were detected in some samples above LOQ. In contrast, no first generation AR was detected in the ESB samples. In SPM, only bromadiolone could be detected in 56% of the samples at levels up to 9.24 μg kg⁻¹. A temporal trend analysis of bream liver from two sampling locations over a period of up to 23 years revealed a significant trend for brodifacoum at one of the sampling locations.

Oyster shells are a type of biogenic materials with excellent characteristics in surface area, porosity, sorption capacity, and high concentration of CaCO₃ (up to 90 wt%), and can be easily converted into a calcium-based alkali adsorbent. In this research, oyster shells calcined at 900 °C were applied as an adsorbent for acid green 25 (AG25) removal from aqueous solutions. The adsorption performances were evaluated, and the FTIR, SEM, and BET techniques were employed to characterize this material. Results showed that AG25 removal performance depended on adsorbent dosage, pH, adsorption temperature, contact time, and initial concentration. Adsorption capacity was maximized at 34.1 mg g⁻¹ at pH of 11.0, an adsorbent dosage of 2.0 g L⁻¹, an AG25 concentration of 70 mg L⁻¹, and adsorption temperature of 40 °C. Both the Ho-McKay model and the pseudo-second-order model correlated with the adsorption kinetics well with the values of R² > 0.99 (closer to unity). The Langmuir isotherm showed an excellent correlation coefficient of R² > 0.99 with the equilibrium data. The thermodynamics study indicates that the adsorption was spontaneous and endothermic. These results demonstrate that the calcined oyster shells has the potential to be used as an eco-friendly and low-cost effective adsorbent for anionic dye removal from water.

Phytoremediation of heavy metal-contaminated soil is considered to be one ecological environmental protection way that is effective and economical. The selection of suitable hyperaccumulators is a key issue for phytoremediation of heavy metal-contaminated soil. Pot experiments were conducted to study the effects of different Cd levels (0, 75, 150, 300, and 600 mg kg⁻¹ Cd) on the dry weight, antioxidant enzyme activities, malondialdehyde (MDA) contents, Cd concentration, Cd accumulation, and soil Cd form distribution ratio (FDC) of alfalfa (Medicago sativa L.) and Indian mustard (Brassica juncea L.). The correlations between Cd concentration in shoots and roots of alfalfa and Indian mustard and soil Cd form were also investigated. The results showed that with the increase of soil Cd levels, dry weight of shoot and root of alfalfa and Indian mustard significantly decreased, which decreased by 50.0–71.8% and 29.6–59.3% (alfalfa), 59.6–89.0% and 64.3–74.8% (India mustard), respectively, compared with the control. With the increase of soil Cd level, superoxide dismutase (SOD) activity in shoot of alfalfa significantly increased. Catalase (CAT) activity and malondialdehyde contents in shoots and roots of alfalfa and Indian mustard, as well as superoxide dismutase activity in the roots of alfalfa and Indian mustard increased first and then decreased with the increase of soil Cd level. With increasing Cd stress, Cd concentration in shoots and roots of alfalfa and Indian mustard significantly increased. At soil Cd level of 75 mg kg⁻¹, Cd concentrations in shoots of alfalfa and Indian mustard exceeded the critical value of Cd-hyperaccumulator (100 mg kg⁻¹), which was 356.46 mg kg⁻¹ and 308.74 mg kg⁻¹, respectively. Cadmium concentrations in shoots and roots of plants were in the order of that of alfalfa > Indian mustard; total Cd accumulation in the aboveground tissues and roots of the plants was in the order of that of Indian mustard > alfalfa at the same Cd level. With increasing soil Cd level, Cd concentrations of exchangeable form (EXC-Cd), carbonate-bound form (CAB-Cd), iron-manganese oxide-bound form (FeMn-Cd), organic-bound form (OM-Cd), and residual form (RES-Cd) showed an increasing trend. The form distribution ratio of soil Cd forms in alfalfa’s rhizosphere was in the order of that of exchangeable form Cd > carbonate-bound form Cd > iron-manganese oxide-bound form Cd > residual form Cd > organic-bound form Cd. Except for organic-bound form Cd, soil Cd forms were significantly positively correlated with Cd concentration in shoot and root (P < 0.01). Comprehensively considering the biomass and Cd accumulation, Indian mustard is more suitable as remediation material for soil Cd pollution.