Graphitic carbon nitride (g-C₃N₄) is a photocatalyst with wide application in removal of organic pollutants. In this study, we designed a porous g-C₃N₄ (p-g-C₃N₄)/8-quinolinolato iron(III) (Q₃Fe)/H₂O₂ system to enhance the organic pollutant removal efficiency by combining photocatalysis and Fenton interaction under neutral condition. The p-g-C₃N₄ was prepared through a two-step thermal oxidation reaction. Afterwards, Q₃Fe-coupled p-g-C₃N₄ was prepared by an impregnating method. The 2,4-dichlorophenol (2,4-DCP) photodegradation ratio and decomposition rate of the p-g-C₃N₄/Q₃Fe/H₂O₂ system are approximately 5 and 18 times as high as those of individual p-g-C₃N₄ system, respectively. Besides, its degradation rate is 4.3 times as high as that in the p-g-C₃N₄/H₂O₂ system. Meanwhile, Q₃Fe/g-C₃N₄ also exhibits higher activity than individual p-g-C₃N₄ in 2,4-DCP photo-decomposing. On the basis of the results of the radical trapping experiments and the Fe(II) concentration in different systems, the synergistic effect between photocatalysis and Fenton reaction is vital for the efficient pollutant degradation. The coupled system combining p-g-C₃N₄ with Q₃Fe and H₂O₂ shows potential for efficient treatment of recalcitrant organic pollutants. The combined system in this work indicated a new idea for the decomposition of organic pollutants.

A dispersive liquid–liquid microextraction (DLLME) method was optimized for the detection of chlorobenzene (CB) compounds in the drying process of municipal and dyeing sludge. Compared with traditional methods, the optimized DLLME not only has a lower limit of detection but also saves analysis time and requires less amount of organic solvent. Using this method in analyzing CB release during sludge drying, we found that drying temperature is the main factor controlling the amount of chlorobenzene release during sludge drying. In addition, we found that most CBs were released when sludge drying entered into the second falling rate stage, i.e., a period when sludge moisture content was low and temperature was high. By analyzing organic matter content in association with CB release during sludge drying, the relationship between organic matter transformation and chlorobenzene release was established. The results provide scientific basis and technical support for assessing the risks of the secondary pollution of CBs from sludge drying.

We demonstrated a method to form magnetic antimicrobial POHABA (poly-N,N′-[(4,5-dihydroxy-1,2-phenylene)bis(methylene)]bisacrylamide)-based core-shell nanostructure by free-radical polymerization of OHABA on the Fe₃O₄ core surface. The magnetic antimicrobial agent Fe₃O₄@POHABA can be used in domestic water treatment against bacterial pathogens. The thickness of POHABA shell could be controlled from 10.4 ± 1.2 to 56.3 ± 11.7 nm by the dosage of OHABA. The results of antimicrobial-activity test indicated that POHABA-based core-shell nanostructure had broad-spectrum inhibitory against Gram-negative, Gram-positive bacteria and fungi. The minimum inhibitory concentration (MIC) values of Fe₃O₄@POHABA nanostructure against Escherichia coli and Bacillus subtilis were both 0.4 mg/mL. Fe₃O₄@POHABA nanostructures responded to a permanent magnet and were easily recycled. Fe₃O₄@POHABA nanoparticles retained 100% antimicrobial efficiency for both Gram-negative and Gram-positive bacteria throughout eight recycle procedures.

Acid deposition and temperature variation could lead to changes of physiological characteristics of plants in response to stress. In this paper, Medicago sativa CV. Dongmu–1 was investigated to test the effects of freeze-thaw circle and acid deposition upon the changes of osmotic adjustment substances, biological membrane permeability, and antioxidant enzymes. The experiment was conducted under laboratory conditions, and the seedlings were divided into four groups (group I: no treatment, group II: acid stressed only, group III: freeze-thaw stressed only, group IV: both freeze-thaw and acid stressed). Results indicated that under freeze-thaw circle and acid deposition, the contents of malondialdehyde (MDA) and proline increased respectively by 0.6~203.4 and 19.3~68.8% when compared with group I, while protein content declined by 4.1~31.7%, and the effects were even significant than freeze-thaw-only stressed groups. In the freeze-thaw process, superoxide dismutase (SOD) activity dropped at first and then increased with the increase of temperature, peaking at − 3 °C by 1118.45 U g⁻¹; peroxidase (POD) activity showed a brief rise and declined rapidly below 0 °C. By increasing the potentials of antioxidant enzymes and MDA, the membrane lipid peroxidation inside alfalfa was prevented; meanwhile, several indexes changed adaptively in resisting hurts. Variation of SOD and POD was induced by the defense mechanism, which showed alfalfa’s satisfactory cold resistance and acid tolerance. Further research on acid deposition and freeze-thaw circle would be beneficial for the global cultivation of forage grass.

In this study, the degradation of benzene by the means of an optimized surface/packed-bed hybrid discharge (SPBHD) plasma combined with γ-Al₂O₃-supported MO ₓ (M = Ag, Mn, Cu, or Fe) catalysts in post plasma-catalysis (PPC) system. The effects of Ag loading amount and gas hourly space velocity (GHSV) for plasma-catalysis degradation of benzene have been systematically investigated. The experimental result showed that the benzene degradation was improved and the mineralization process was greatly enhanced towards total oxidation after the combination of plasma with all MO ₓ /γ-Al₂O₃ catalysts. The AgO ₓ /γ-Al₂O₃ catalyst exhibited the best catalytic activity in benzene degradation than the other catalysts in PPC system. The highest benzene degradation efficiency of 96% and CO ₓ selectivity of 99% can be obtained for AgO ₓ /γ-Al₂O₃ catalyst with optimum Ag loading amount and GHSV of 15% and 22,856 h⁻¹, respectively. Time course of benzene degradation during PPC process indicated that the plasma-induced catalytic activity of AgO ₓ /γ-Al₂O₃ catalyst was temporary rather than lasting over a period after the plasma off. FT-IR analysis results revealed that the intermediate products (such as CO, HCOOH) and unwanted by-products (O₃ and NO ₓ) generated in plasma process could be significantly inhibited by PPC process with AgO ₓ /γ-Al₂O₃ catalyst.

Bisphenol B (BPB) exhibited higher estrogenic activity and anti-androgenic effects than bisphenol A (BPA) in vitro assays. This result indicates that BPB has higher priority for entry into expensive and stressful testing on animals. However, the disrupting mechanisms of BPB on steroid hormone signaling pathway by in vivo assay have not been investigated yet. In this study, the potential disrupting mechanisms of BPB on the hypothalamic–pituitary–gonadal (HPG) axis and liver were probed by employing the Organization for Economic Co-operation and Development (OECD) 21-day short-term fecundity assay with zebrafish. We found that BPB exposure (1 mg/L) could impair the reproductive function of zebrafish and decline the egg numbers, hatching rate, and survival rate. This finding is related to modifications of the testis and ovary histology of the treated zebrafish. The homogenate T levels in male zebrafish decreased in a concentration-dependent manner, and the E2 level significantly increased when exposed to 0.01, 0.1, and 1 mg/L BPB. Real-time polymerase chain reaction (PCR) was performed to examine the gene expressions in the HPG axis and liver. Hepatic vitellogenin (vtg) expression was upregulated in all exposure males, suggesting that BPB possesses estrogenic activity. The disturbed hormone balance was contributed by the significant alteration of the genes along the HPG axis. These alterations suggest that BPB can lead to adverse effects on the endocrine system of teleost fish, and these effects were more prominent in males than in females.

In the present study, the immobilizing fermentation characteristics and o-chlorophenol biodegradation of Rhodopseudomonas palustris using mycelial pellets as a biomass carrier were investigated. To improve the o-chlorophenol degradation efficiency of the combined mycelial pellets, eight cultivation variables including glucose concentration, yeast extract concentration, spore inoculum size, pH, and agitation speed were optimized with an integrated strategy involving a combination of statistical designs. First, Plackett-Burman experiments identified glucose, yeast extract, and spore inoculum size as three statistically significant factors important for o-chlorophenol removal. Then, the steepest ascent method was used to access the optimal region of these significant factors. Finally, response surface methodology by Box-Behnken optimization was used to examine the mutual interactions among these three variables to determine their optimal levels. The ideal culture conditions for maximum o-chlorophenol removal according to a second-order polynomial model were as follows: 15.60 g/L glucose, 3.09 g/L yeast extract, and 9% (v/v) spore inoculum size, resulting in an expected o-chlorophenol removal rate of 92.60% with an o-chlorophenol initial concentration of 50 mg/L and 96-h culture time. The correlation coefficient (R ² = 0.9933) indicated excellent agreement between the experimental and predicted values, whereas a fair association was observed between the predicted model values and those obtained from subsequent experimentation at the optimized conditions.

Although phosphorus (P) enrichment alone or in combination with other nutrients such as nitrogen (N) and potassium (K) due to anthropogenic activities may modify the nutrient pools and nutrient elemental ratios of terrestrial ecosystems, few studies have revealed the global effects of P alone or in combination with N and K enrichment on terrestrial ecosystems. In this study, we conducted a meta-analysis of the impacts of P addition alone or in combination with N and K on the C, N, and P pools and C/N/P ratios of plants, soils, and microbial biomass in terrestrial ecosystems. The results suggest that the following changes occurred: (1) P addition resulted in a significantly larger plant C pool, which was further enhanced when extra N and K were added. (2) The soil and microbial biomass C pools and the plant, soil, and microbial biomass N pools were minimally affected by P addition at the global scale but were noticeably affected when N and K were simultaneously added. (3) The P pools of the plants, soil, and microbial biomass were significantly and consistently enhanced by the addition of P, NP, and NPK. (4) The plant C/N, N/P, and C/P ratios were significantly reduced when P was added, while the C/N/P ratios in the soil and microbial biomass were minimally affected. These results, which show the inconsistent responses of plant, soil, and microbial biomass nutrient pools and elemental ratios to P, NP, and NPK addition, improve our understanding of terrestrial ecosystem functions under global change scenarios.

Herein, we report the synthesis of carbon spheres (CS) using a relatively low-temperature hydrothermal technique using lactose as precursor pre-treated with HCl. The successful synthesis, spherical morphology, porous morphology, and monodispersed nature of CS were confirmed via scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Isoelectric point (IEP) was determined as 3.8, and at neutral conditions the prepared carbon particles are negatively charged at − 43 ± 2.50 mV. Owing to their spherical morphology, almost uniform distribution and negatively charged surface at neutral conditions, the prepared CS were used as adsorbent for the removal of methylene blue (MB) and Geimsa stain (GS) from aqueous environments at pH 7. It was shown that CS has 97% adsorption capability for GS, whereas for methylene MB, the maximum adsorption capacity was 67% for 0.1-g CS from 50-ppm dye solutions in DI water. The adsorption studies revealed that the Langmuir and modified Fruendlich (MFE) adsorption models resulted in considerably high linear correlation coefficient (r ²) values and the efficient adsorption of positively charged species on CS can be represented better with the MFE model. Graphical Abstract Carbon spheres from D-lactose for environmental application

Nanoscale zero valent iron (NZVI) was synthesized by the reduction of natural limonite under hydrogen conditions. The adsorption performance of the as-prepared NZVI on phosphate was evaluated through batch and column experiments. The removal of phosphate (PO₄³⁻) significantly decreased with an increase of pH from 2.0 to 11, whereas a remarkable increase of PO₄³⁻ removal was observed in the presence of SO₄²⁻ and S₂O₃²⁻. In addition, Cl⁻ and NO₃⁻ also improved phosphate removal at concentrations of more than 0.2 mmol/L. Kinetic studies indicated that the removal process of PO₄³⁻ on NZVI can be easily followed with the pseudo-second-order kinetic model. The removal of phosphate from the oxic system was significantly higher than that of the anoxic system, which was attributed to the formation of the secondary phase by the further oxidization of Fe²⁺. The adsorption capacity of the as-prepared NZVI of the oxic system was 16 mg/g, and the pH was 6.3. The column experiments further demonstrated that the as-prepared NZVI presented a high removal capacity for PO₄³⁻-P. These findings indicated that the as-prepared NZVI displayed an excellent ability to remove phosphate from aqueous solutions.