This study focused on the ion release and microstructure of slag during its degradation following erosion by different pH solutions. It focused on controlling factors such as slag particle size range, pH value of the solution, and soaking time. The surface microstructure and particle size distribution of slag with the particle size of 0.075–5.0 mm, the mineral composition of suspended pollutants larger than 0.45 μm, and the phenomenon of nano-scale ion release were examined. When slag was soaked in solutions with different pH values for 30 days, the pH value of leachate tended to be neutral, the release amount of Ca, Mg, Fe, and Cd ions increased and the release rate gradually decreased. The dissolution process of slag in the alkaline solution was slower than that in acid, but suspension and gels formed more easily in an alkaline environment. Nitric acid accelerated the chemical reaction of akermanite, gehlenite, and hawleyite, and released Ca, Mg, and Cd ions. There were clear damage cracks and various irregular pores on the slag surface. Under the attack of alkali solution, the weight of akermanite in slag increased, the Mg ion content in solution decreased, and the suspended solids of calcite and portlandite increased. At pH 12, unlike at pH 3, there were no large surface cracks in the slag and the interface damage was small. Compared with pH 7, there were more irregular substances, such as flakes and spheres. The particle size of slag was mainly 0.1–0.5 mm, the content before and after leaching was 52.80%–55.87% and 55.00%–58.27%, and the slag was in a poor grading state. The findings of this study act as an important reference for understanding the influence of slag leaching on water and soil pollution.

Garden pruning waste is becoming a problem that intensifies the garbage siege. It is of great significance to purify polluted water using biochar prepared from garden pruning waste. Herein, the interaction mechanism between BPS and oriental plane tree biochar (TBC) with different surface functional groups was investigated by adsorption experiments, spectroscopic analysis and theoretical calculations. Adsorption kinetics and isotherm of BPS on TBC can be satisfactorily fitted into pseudo-second-order kinetic and Langmuir models, respectively. A rapid adsorption kinetic toward BPS was achieved by TBC in 15 min. As compared with TBC prepared at low temperature (300 °C) (LTBC), the maximum adsorption capacity of TBC prepared at high temperature (600 °C) (HTBC) can be significantly improved from 46.7 mg g⁻¹ to 72.9 mg g⁻¹. Besides, the microstructure and surface functional groups of HTBC were characterized using SEM, BET-N₂, and XPS analysis. According to density functional theory (DFT) theoretical calculations, the higher adsorption energy of HTBC for BPS was mainly attributed to π-π interaction rather than hydrogen bonding, which was further supported by the analysis of FTIR and Raman spectra as well as the adsorption thermodynamic parameters. These findings suggested that by improving π-π interaction through high pyrolysis temperature, BPS could be removed and adsorbed by biochar with high efficacy, cost-efficiency, easy availability, and carbon-negative in nature, contributing to global carbon neutrality.

In order to study the effect of cadmium ions on the mechanical properties and micro-structure characteristics of the red clay in Guilin, we have conducted triaxial test and the scanning electron microscope tests to analyze the effects of cadmium ion concentration and the number of dry and wet cycles on the mechanical properties and micro-structure changes of the red clay. The results showed the effects of cadmium ions and dry-wet cycles destroy the structure of red clay. The cohesive force of red clay decreases with the increase of cadmium ion concentration, and the internal friction angle first increases and then decreases. With the rise in the number of dry and wet cycles, the cohesive force of cadmium-contaminated red clay first increases and then decreases, and the angle of internal friction rises gradually. Under the action of different cadmium ion concentrations, the stress-strain curve is strain hardening. With the concentration of cadmium ions increases, the strain hardening becomes more apparent; the peak value reached faster. and the axial strain corresponding to the peak value of the line decreases. With the increase in the number of wet and dry cycles, the volume of cadmium-contaminated red clay shrinks and its compactness increases; it gets the peak shear strength faster during the shearing process, and its peak value becomes larger and larger. The main reason for the phenomenon is that cadmium ions destroy the cementation between the particles. The soil particles are mainly in point contact which loosens the structure of the soil; on the other hand, the thickness of the surface diffusion layer of the clay particles increases through chemical action, The exchange of cations increases the porosity of the soil and weakens its strength. The dry-wet cycle shrinks the volume of the red clay, and the soil particles are mainly in surface contact; as the number of dry-wet cycles increases, the soil particles connection is closer, the soil porosity decreases and the strength increases.

Air pollution exposure during early-life is associated with altered brain development, but the precise periods of susceptibility are unknown. We aimed to investigate whether there are periods of susceptibility of air pollution between conception and preadolescence in relation to white matter microstructure and brain volumes at 9–12 years old. We used data of 3515 children from the Generation R Study, a population-based birth cohort from Rotterdam, the Netherlands (2002–2006). We estimated daily levels of nitrogen dioxide (NO2), and particulate matter (PM2.5 and PM2.5absorbance) at participants’ homes during pregnancy and childhood using land-use regression models. Diffusion tensor and structural brain images were obtained when children were 9–12 years of age, and we calculated fractional anisotropy and mean diffusivity, and several brain structure volumes. We performed distributed lag non-linear modeling adjusting for socioeconomic and lifestyle characteristics. We observed specific periods of susceptibility to all air pollutants from conception to age 5 years in association with lower fractional anisotropy and higher mean diffusivity that survived correction for multiple testing (e.g., −0.85 fractional anisotropy (95%CI -1.43; −0.27) per 5 μg/m³ increase in PM2.5 between conception and 4 years of age). We also observed certain periods of susceptibility to some air pollutants in relation to global brain and some subcortical brain volumes, but only the association between PM2.5 and putamen survived correction for multiple testing (172 mm³ (95%CI 57; 286) per 5 μg/m³ increase in PM2.5 between 4 months and 1.8 year of age). This study suggested that conception, pregnancy, infancy, toddlerhood, and early childhood seem to be susceptible periods to air pollution exposure for the development of white matter microstructure and the putamen volume. Longitudinal studies with repeated brain outcome measurements are needed for understanding the trajectories and the long-term effects of exposure to air pollution.

Lead (Pb) is a toxic metal in industrial production, which can seriously threat to human health and food safety. Thus, it is particularly crucial to reduce the content of Pb in the environment. In this study, raw fly ash (FA) was used to synthesise a new active silicate materials (IM) employing the low-temperature-assisted alkali (NaOH) roasting approach. The IM was further synthesised to form zeolite-A (ZA) using the hydrothermal method. The physicochemical characteristics of IM and ZA amendments before and after Pb²⁺ adsorption were analysed using the Scanning electron microscope-Energy Dispersive Spectrometer (SEM-EDS), Fourier Transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD) apparatuses. The results revealed the considerably change in the microstructure and functional groups of IM and ZA amendments, conducive to Pb²⁺ removal. Moreover, a 3-year field experiment revealed that the IM and ZA significantly improved the growth of rice and reduced available Pb by 21%–26.8% and 9.7%–16.9%, respectively. After 3 years of remediation, the Pb concentration of the rice grain reached the national edible standard (≤0.2 mg kg⁻¹) of 0.171 mg kg⁻¹ and 0.179 mg kg⁻¹, respectively. Meanwhile, the concentration of acid-exchangeable Pb reduced, while those of reducible and residual fractions of Pb increased. There was no significant difference between the IM and ZA treatments. The potential mechanisms of remediation by the amendments were ion-exchange, complexation, precipitation, and electrostatic attraction. Overall, the results indicate that IM is suitable for the remediation of contaminated soil and promotes safe food production, and develops an environmentally friendly and cost-effective amendment for the remediation of polluted soil.

This paper investigated the impacts of various real microplastics (MPs), i.e., polyethylene (PE) and polyethylene terephthalate (PET) with different sizes (1000–2000 and 100–200 μm) and different dosages (0.5 and 5% on a dry weight basis), on the toluene removal during the thermally enhanced air injection treatment. First, microscopic tests were carried out to determine the MPs' microstructure and behavior. The PE was mainly a small block, and PET appeared filamentous and sheeted with a larger slenderness ratio. Second, the interactions between MPs and toluene-contaminated soils were revealed by batch adsorption equilibrium experiments and low-field magnetic resonance. The morphological differences and dosage of the MPs impacted soils’ total porosity (variation range: 39.2–42.7%) and proportion of the main pores (2–200 μm). Third, the toluene removal during the air injection consisted of compaction, rapid growth, rapid reduction, and tailing stages, and the MPs were regarded as an emerging solid state to affect these removal stages. The final cumulative toluene concentrations of soil-PET mixtures were influenced by total porosity, and those of soil-PE mixtures were controlled by total porosity (influence weight: 0.67) and adsorption capacity (influence weight: 0.33); meanwhile, a self-built comprehensive coefficient of MPs can reflect the relationship between them and cumulative concentrations (correlation coefficient: 0.783).

As particulate matter and heavy metals in the atmosphere affect the atmospheric quality, they pose a threat to human health through the respiratory system. Vegetation can remove airborne particles and purify the atmosphere. Plant leaves are capable of effectively absorbing heavy metals contained by particulates. To evaluate the effects of different garden plants on the particulate matter retention and heavy metal accumulation, the seasonal changes of dust retention of five typical garden plants were compared in the industrial and non-industrial zones in Hangzhou. Results revealed that these species differed in dust retention with the descending order of Loropetalum chinense > Osmanthus fragrans > Pittosporum tobira > Photinia × fraseri > Cinnamomum camphora, which were related to the microstructure feature of the leaf. These species also showed seasonal variation in dust retention, with the highest in summer, followed by winter, autumn, and spring, respectively. The total suspended particle per unit leaf area was higher in the industrial site (80.54 g m⁻²) than in the non-industrial site (19.77 g m⁻²). Leaf particles in different size fractions differed among species, while coarse particles (d > ten μm) predominated in most cases. The L. chinense and C. camphora plants accumulated the greatest Pb and Ni compared to other plants. Overall, L. chinense was the best suitable plant species to improve the air quality.

Bioplastics have emerged to minimize the ecological footprint of non-degradable plastics. However, the effect of their degradation in aquatic systems, including the interaction with toxic metals, is still unexplored. In this work, the influence of UV-aging on structure, chemistry, wettability, rigidity, and Hg-sorption of commercially available bioplastic (BIO)- and polyethylene (PE)-based films was studied. To mimetize the materials disposal in fresh-/saltwaters, non-saline/saline aqueous solutions were used in Hg-sorption studies. ATR-FTIR spectra revealed that the BIO film was a coblended starch/polyester-based material, whose microstructure, physicochemical, and mechanical properties changed after UV-aging to a higher extent than in PE film. AFM and kinetic modelling pointed out electrostatic interactions/complexation as the mechanisms involved in the increased Hg-sorption by the UV-aged BIO film. An increased salinity did not impair its Hg-sorption. Therefore, when disposed in aquatic systems, starch/polyester-based bioplastics can play a potential vector for amplifying Hg along the food chain.

In this paper, Pd-Sn modified Ru-Ir electrode was prepared by thermal oxidation method, and the effects of doping amount of Pd-Sn and synthesis conditions on Pd-Sn modified Ru-Ir electrode performance were studied. Linear sweep voltammetry(LSV), cyclic voltammetry(CV), and the Tafel curve were used to study the electrochemical performance of the Pd-Sn modified Ru-Ir electrode materials. The effects of the doping amount of Pd-Sn on the microstructure and valence states of Pd-Sn modified Ru-Ir electrode materials were investigated by SEM, TEM, XRD, and XPS. When the mass of Pd-Sn accounted for 1.5% of the total mass of the elements, the molar ratio of Ru-Ir was 2:1, and the molar ratio of Pd-Sn was 3:1; the LSV, CV, and the Tafel curves indicated that Pd-Sn modified Ru-Ir electrode had the lowest chlorine evolution potential (1.0640 V vs. SCE), the best CV curve coincidence, and the smallest corrosion current density (6.5 × 10⁻⁴ A/cm²), showing the best chlorine evolution performance, the best durability, and corrosion resistance; the characterization of SEM, TEM, XRD, and XPS showed that Pd-Sn was successfully doped into Ru-Ir electrode materials; the crystallinity of Pd-Sn modified Ru-Ir electrode was the highest, and the binding energy was the lowest, but the crystal form of Ru-Ir solid solution did not have changed. The optimal synthesis conditions of Pd-Sn modified Ru-Ir electrode material were as follows: Pd-Sn molar ratio was 3:1, calcination temperature was 500 ℃, calcination time was 4 h, and water was used as solvent. Pd-Sn modified Ru-Ir electrode can efficiently treat high chlorine ammonia–nitrogen wastewater, when the reaction volume was 200 mL, the initial concentration of NH₃-N was 100 mg/L, the concentration of chloride ion was 5000 mg/L, the current was 0.75 A, and the reaction time was 40 min; the removal rate of ammonia nitrogen can reach 100%.Responsible editor: Weiming Zhang.

The treatment of coal gangue solid waste and microbially induced calcium carbonate precipitation (MICP) consolidate technology is a focus of research at home and abroad. MICP technology was used to solidify and cement coal gangue particles and endows them with a certain strength. The process does not use the traditional cementitious material (Portland cement) and is eco-friendly and pollution-free. The mechanical properties including unconfined compressive strength, CaCO₃ content, scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and infrared spectroscopy (FTIR) were used for macroscopic and microscopic analyses. The results show that the average strength of CG-based bio-mineralized backfill materials reaches 1.55 MPa and the maximum strength is 2.17 MPa, suggesting the potential for its use as an underground fill. Compared with unmineralized gangue, the CaCO₃ crystal content in CG-based mineralized material is increased by 8.75% on average, and the maximum content is 13.34%. In the process of bacterial liquid perfusion, there is uneven distribution of bacteria in the material, which results in fewer CaCO₃ crystals being locally generated in the mineralized material and affects the overall compressive strength of gangue columns. Moreover, the greater the amount of calcium carbonate, the larger the strength of the mineralized material. SEM analysis results indicate that the gaps between gangue particles are filled with CaCO₃ crystals, and the calcium carbonate crystals are mostly polyhedral, showing stacked growth and contain a small number of spherical crystals that exist alone. The results of FTIR and EDS analysis show that the CaCO₃ crystals in the mineralized material are mainly in the form of calcite, followed by a small amount of vaterite. Comprehensive analysis demonstrates that the preparation of CG-based bio-mineralized backfilling materials is successful, and this experiment provides new ideas and methods for the treatment of solid waste such as coal gangue and building material waste.