The adsorption properties and mechanisms of methylene blue (MB) onto novel biochars produced by the fallen leaves of Magnolia grandiflora Linn (MGL), at different pyrolysis temperatures (450 °C, 500 °C, 550 °C) were explored. Results of the adsorption experiments revealed that the fallen leaf-biochar of MGL (MGLB) pyrolyzed at 450 °C (MGLB450) had the highest adsorption capacity of MB (114.15 mg g⁻¹) and MGLB pyrolyzed at 500 °C (MGLB500) was lowest (88.13 mg g⁻¹). The characterization results showed that the BET surface area (41.784 m² g⁻¹) and total pore volume (0.043 cm³ g⁻¹) of MGLB450 were low, but the contents of oxygen-containing functional groups were highest. Oxygen-containing functional group might have a greater impact on the adsorption of MB than its physical characteristics. The adsorption capacity increased with reaction temperature, indicating that the MG adsorption onto biochars was endothermic. The higher initial concentrations of MB and pH were beneficial to adsorption. The adsorption kinetics showed that the adsorption followed pseudo-second-order kinetics model. The obtained equilibrium data were fitted better by Langmuir model rather than Freundlich model.

Constructed wetlands (CWs) have been applied to remediate heavy metal pollution effectively in practice. However, the heavy metal release from CWs has not been paid enough attention. In this study, a 5-month experiment was carried out with three parallel lab-scale vertical flow constructed wetlands (VFCWs) with zeolites as fillers. The artificial rainwater was pumped into VFCWs to study the release characteristic and mechanisms of heavy metals (Cu, Zn, Cr, and Pb). The results showed that significant amounts of Zn and Cu were released from the VFCWs at the end of the experiment while Pb and Cr rarely escaped. The upper layer (0–30 cm) of the VFCWs was the most effective area for heavy metal removal due to the presence of sediments, but it was also the most active area for heavy metal release. To explain this result, the sediments were analyzed before and after being leached by the tap water. The results indicated that Zn and Cu existed mainly in the exchangeable state, and they had strong leachability and bioavailability, causing its releases. Also, competitive adsorption of different metals meant that the metal ions with strong adsorption to zeolite caused the metal ions with weak adsorption to be desorbed from zeolites, and thus, a large amount of Zn escaped from VFCWs. The escape of heavy metals from CWs illustrated that it should be paid more attention in the management.

Application of fungicides on grapevines is the main source of soil contamination by copper and zinc. Studies on this issue in relatively young grapevines are common; however, studies that elucidate the metal transfer in a soil-plant-food production system in a centenarian vineyard are scarce. The present work was aimed at tracing the copper and zinc accumulation in three different compartments—soil, plant, and vine products—in young and centenarian vineyards. Soil samples were collected in the middle plant row and rhizosphere positions of the vineyards; samples of root and leaf tissue and of grape juice and wine from these vineyards were also collected. In the centenarian vineyard, the soil available copper, regardless of vineyard position, reached 1100 mg kg⁻¹. Copper in root and leaf tissues reached 12,300 mg kg⁻¹ and 6800 mg kg⁻¹, respectively. In grape juice and wine, copper was 9.08 mg L⁻¹ and 0.78 mg L⁻¹, respectively. The roots retained most part of the metals reducing their transfer through the system. However, Cu levels in the grape juice from the centenarian vineyard exceeded by 908% the limit established by Brazilian and international norms. Zinc concentrations in soil and vine products were within the permitted level. Finally, the magnitude of metal transfer and accumulation is due to decades of cupric fungicide application and varies according to the compartment evaluated. The findings will provide information to rethink the vineyard agricultural practices in order to avoid environmental contamination by metals and compromising the whole food chain.

Contamination with fluoroaromatics (FAs), particularly polyfluorinated aniline, is becoming a serious environmental problem worldwide. To shorten the start-up time, and increase the stability of treatment systems, this work focused on the effects of three seeding sources on treatment performances of 2,3,4-trifluoroaniline (2,3,4-TFA) during start-up and shock, as well as the acclimated strategy. After 246–323 days of acclimation in a stepwise feeding according to the inhibition degree, three sequencing batch reactors (SBRs) successfully achieved efficient removal, i.e., 300.00 mg/L of 2,3,4-TFA, with over 95.00% of degradation efficiency and 60.00–80.00% of defluorination rates. The sludge obtained from the fluorizated hydrocarbon wastewater treatment plant(FHS) without prior exposure to fluoroaniline was determined to be optimal, based on the observed shortest start-up time of 246 days, the highest defluorination rate of 70.00–80.00%, the fastest recovery time of 7 days after shock, and the highest microbial diversity with nine dominant bacterial groups. Furthermore, compared with the sludge obtained from pharmaceutical wastewater containing part of municipal wastewater treatment plant(PMS), the seeding source used in treating the comprehensive wastewater in industrial park (CIS) exhibited earlier defluorination reaction, higher defluorination rate and microbial diversity, but lower shock resistance. High-throughput sequencing demonstrated that microbial diversity was dependent on the origin of the inoculum after acclimation. We identified two predominant phyla in PMS, namely, Deinococcus-Thermus (24.43%) and Bacteroidetes (18.44%), whereas these were Acidobacteria and Chloroflexi in FHS and CIS. During the shock of 400 mg/L 2,3,4-TFA, the predominant bacteria norank_f_Blastocatellaceae and norank_f_Methylobacteriaceae disappeared, and the defluorination reaction hardly occurred, indicating that the bacterial genera could contribute to the defluorination reaction.

This paper presents an experimental study of suspended particle transport through sand layer using a new self-developed sand layer transportation-deposition testing system, and the study aims to identify the effects of temperature on the transport of suspended particles through porous medium. Four typical temperatures (5 °C, 15 °C, 25 °C, and 35 °C) were considered in our study, and the experiments were conducted under four size compositions and three flow velocities (1.5 cm/s, 0.2 cm/s, and 0.04 cm/s). The tests were conducted using quartz sand as the porous medium and quartz powder as particles to monitor the change in turbidity under the different conditions. The breakthrough curves were analyzed, and the results demonstrated that changes in temperature can affect the breakthrough curves, especially at the peak. The influence is particularly significant under lower flow velocities and for smaller particles. In regard to the influence factors on the transport process, water viscosity and adsorption effect can be regarded as promoting factors, while kinetic energy of particles can be classified as constraining factors.

Textile effluents contain a series of dyes and salts, and their decolorization is strongly affected by salinity. In this work, the influence of salinity on methylene blue (MB) adsorption by comminuted raw avocado seeds was investigated. The adsorbent was firstly characterized. The optimal conditions for MB adsorption on the avocado seeds were determined by response surface methodology (RSM). Subsequently, the influence of ten salts in MB adsorption was evaluated using kinetic and equilibrium studies. The optimal conditions for MB adsorption on the avocado seeds were pH = 10 and adsorbent dosage = 1 g L⁻¹. General order model was able to describe the kinetic profile, and its parameters showed that the adsorption rate and capacity were affected by the presence of salts. The equilibrium was adequately represented by the Sips model. The maximum adsorption capacity without the presence of salts was 97.97 mg g⁻¹. The maximum adsorption capacity was found in the presence of sodium carbonate, which was 103.13 mg g⁻¹. The presence of sodium citrate reduced the adsorption capacity to 80.42 mg g⁻¹. Therefore, even in the presence of salts, comminuted raw avocado seeds demonstrated great potential to treat colored effluents containing MB dye.

Brominated diphenyl ethers-209 (BDE-209), a toxic and stably retardant, is a ubiquitous environmental contaminant and commonly used in daily consumer products. The Cenococcum geophilum and Laccaria amethystina were used to inoculate Japanese black pine (Pinus thunbergii Parl) seedlings, using root chamber experiments to check their potential for improving host growth and the capacity in establishing in persistent organic pollutants (POPs)-contaminated environments. The results showed that the inoculation with ectomycorrhizal (ECM) fungi significantly (p < 0.01) improved the growth and reduced the concentrations of BDE-209 in needles and stems of pine seedlings planted in polluted soils. The transfer ratio (calculated as the ratio between the concentrations in needles and roots) and the root concentration factor (calculated as the ratio of the concentration in roots to soil) decreased significantly (p < 0.01), when inoculated with ectomycorrhizal (ECM) fungi compared to without. However, inoculated with ECM fungi (EMF) increased the concentration of BDE-209 in tube soil (soil collected from tube where seedlings were grown) significantly (p < 0.01), especially C. geophilum, which has a rich mycelium system. The capability of EMF accumulation and enrichment of BDE-209 in the contaminated soil, from distance to root zone, reduced the risks of the spread and leaching of organic pollutants to the crops around. The pine inoculated with EMF can be considered to have a potential in forestation and remediating BDE-209 contaminated areas by the way of phytostabilisation pollutants.

The aim of the present study was to isolate several bacterial consortia from a soil sample and to establish if they could colonize zirconium-tin alloy, such as Zircaloy-4. Two bacterial consortia containing aerobic heterotrophic bacteria and anaerobic sulfate-reducing bacteria were isolated from a soil sample. The aerobic heterotrophic bacteria exhibited a higher capability to utilize different sole carbon sources, as compared with anaerobic sulfate-reducing bacteria. Based on a morphological, biochemical, and molecular analysis, bacterial isolates were identified as Pseudomonas putida IBBHA₁, Pseudomonas aeruginosa IBBHA₂, Achromobacter spanius IBBHA₃, Citrobacter freundii IBBSR₁, Citrobacter youngae IBBSR₂, and Citrobacter braakii IBBSR₃. Isolated bacterial consortia which possess distinct DNA fingerprints were able to form biofilms and colonize the surface of zirconium-tin alloy coupons, although the colonization of coupons by the aerobic heterotrophic bacteria or anaerobic sulfate-reducing bacteria alone was lower compared with that observed when the coupon was immersed in a mixture of both bacterial consortia. Coupons immersed in these bacterial consortia revealed changes in the surface characteristics, which can facilitate or accelerate zirconium-tin alloy corrosion. The accumulation of corrosion products on coupons surface was less significant when the coupons were immersed solely in aerobic heterotrophic bacteria or anaerobic sulfate-reducing bacteria, compared with that observed when the coupon was immersed in a mixture of both bacterial consortia.

In this study, a high sensitive metamaterial sensor has been designed to detect quality of water for water treatment centre. The water samples have been obtained and electrical properties have been measured in microwave range to design the proposed sensor. These electrical properties have been assigned in microwave simulator. Water quality has been investigated by using parametric study and genetic algorithm approach to realize high sensitivity in terms of resonance frequency shift. Around 130 MHz frequency shift has been observed between the water samples. This shift is sufficient to detect instantaneously to the quality of water. This is the first study that metamaterial approach has been used to detect water quality in literature.

Coprecipitation of humic acid (HA) with ferrihydrite (Fh) has been proposed to reduce the activity of heavy metals in aqueous solutions. The effect of the amount of HA added to the coprecipitates on the stabilization of Cd in soil is unclear. In this research, five different Fh-HA coprecipitates were synthesized to study the impact of different HA additions on the fractionation of Cd in the soil and the optimal addition ratio of C/Fe. Characterization technique as Fourier transform infrared spectroscopy (FT–IR), X–ray diffraction (XRD), specific surface area analyzer, and scanning electron microscopy (SEM) was used in order to test and analyze of the microstructure and physicochemical property of the coprecipitates. The results showed that the Fh-HA coprecipitate is mainly combined by the coordination exchange of –OH on the surface of the Fh with the carboxyl group of the HA. Adding HA could stabilize Fh and increase its surface roughness. Changes in the fractionation of the Cd were used to evaluate the stabilization effect of the coprecipitate. Before treatment, Cd in different contaminated soils was existed only a small amount of residual fraction. After the addition of the Fh-HA coprecipitate, the proportion of residual Cd in each contaminated soil increased. When the C/Fe ratio was 1.5, the maximum residual fraction were 62.94%, 55.67%, and 52.99% respectively. Residual Cd could remain relatively stable indicating that the Fh-HA coprecipitate is a promising amendment for repairing Cd-contaminated soil. The addition of HA has strengthened the active role of Fh on stabilizing heavy metals.