Super capacity of ligand-engineered biochar for sorption of malachite green dye: key role of functional moieties and mesoporous structure.

This study synthesized a new thiomalic acid-modified rice husk biochar (TMA-BC) as a versatile and eco-friendly sorbent. After undergoing chemical treatments, the mercerized rice husk biochar (NaOH-BC) and TMA-BC samples showed higher BET surface area values of 277.1 m2/g and 305.8 m2/g, respectively, compared to the pristine biochar (BC) sample, which had a surface area of 234.2 m2/g. In batch adsorption experiments, it was found that the highest removal efficiency for malachite green (MG) was achieved with TMA-BC, reaching 96.4%, while NaOH-BC and BC exhibited removal efficiencies of 38.6% and 27.9%, respectively, at pH 8. The engineered TMA-BC exhibited a super adsorption capacity of 104.17 mg/g for MG dye at pH 8.0 and 25 °C with a dosage of 2 g/L. The SEM, TEM, XPS, and FTIR spectroscopy analyses were performed to examine mesoporous features and successful TMA-BC carboxylic and thiol functional groups grafting on biochar. Electrostatic forces, such as π - π interactions, hydrogen bonding, and pore intrusion, were identified as key factors in the sorption of MG dye. As compared to single-solution adsorption experiments, the binary solution experiments performed at optimized dosages of undesired ions, such as humic acid, sodium dodecyl sulfate surfactant, NaCl, and NaSCN, reflected an increase in MG dye removal of 2.8%, 8.7%, 5.4%, and 12.7%, respectively, which was attributed to unique mesoporous features and grafted functional groups of TMA-BC. Furthermore, the TMA-BC showed promising reusability up to three cycles. Our study indicates that mediocre biochar modified with TMA can provide an eco-friendly and cost-effective alternative to commercially accessible adsorbents.

Comprehensive metagenomic and enzyme activity analysis reveals the inhibitory effects and potential toxic mechanism of tetracycline on denitrification in groundwater.

The widespread use of tetracycline (TC) inevitably leads to its increasing emission into groundwater. However, the potential risks of TC to denitrification in groundwater remain unclear. In this study, the effects of TC on denitrification in groundwater were systematically investigated at both the protein and gene levels from the electron behavior aspect for the first time. The results showed that increasing TC from 0 to 10 µg·L-1 decreased the nitrate removal rate from 0.41 to 0.26 mg·L-1·h-1 while enhancing the residual nitrite concentration from 0.52 mg·L-1 to 50.60 mg·L-1 at the end of the experiment. From a macroscopic view, 10 µg·L-1 TC significantly inhibited microbial growth and altered microbial community structure and function in groundwater, which induced the degeneration of denitrification. From the electron behavior aspect (the electron production, electron transport and electron consumption processes), 10 µg·L-1 TC decreased the concentration of electron donors (nicotinamide adenine dinucleotide, NADH), electron transport system activity, and denitrifying enzyme activities at the protein level. At the gene level, 10 µg·L-1 TC restricted the replication of genes related to carbon metabolism, the electron transport system and denitrification. Moreover, discrepant inhibitory effects of TC on individual denitrification steps, which led to the accumulation of nitrite, were observed in this study. These results provide the information that is necessary for evaluating the potential environmental risk of antibiotics on groundwater denitrification and bring more attention to their effects on geochemical nitrogen cycles.

Degradation mechanism of Bisphenol S via hydrogen peroxide/persulfate activated by sulfidated nanoscale zero valent iron.

Fenton-like oxidation processes are widely used to degrade recalcitrant organic pollutants, but are limited by narrow application pH and low reaction efficiency. This study investigated the synchronous activation of H2O2 and persulfate (PDS) by sulfidated zero valent iron (S-nZVI) in ambient conditions for Fenton-like oxidation of bisphenol S (BPS), an estrogenic endocrine-disrupting chemical. The activation of S-nZVI induced H2O2 or PDS could be greatly enhanced with the assistance of PDS and H2O2, respectively, even across a wide range of pH value (3-11). The first-order rate constant of S-nZVI/H2O2/PDS, S-nZVI/PDS and S-nZVI/H2O2 systems was found to be 0.2766 min-1, 0.0436 min-1, and 0.0113 min-1, respectively. A significant synergy between H2O2 and PDS was achieved when the PDS-H2O2 molar ratio was above 1:1, and where sulfidation promoted iron corrosion and decreased solution pH were observed in the S-nZVI/H2O2/PDS system. Radical scavenging experiments and electron paramagnetic resonance (EPR) investigations suggest that both SO4•- and •OH were generated and that •OH played a crucial role in BPS removal. Furthermore, four BPS degradation intermediates were detected and three degradation pathways were proposed in line with the HPLC-Q-TOF-MS analysis. This study demonstrated that compared to the traditional Fenton-like system, the S-nZVI/H2O2/PDS system could be a more efficient, advanced oxidation technology capable of being used across a broad pH range for emerging pollutants' degradation.

Biochar enhanced the stability and microbial metabolic activity of aerobic denitrification system under long-term oxytetracycline stress.

Reactors were established to study the feasibility of the direct addition of modified biochar to alleviate the long-term stress of oxytetracycline (OTC) on aerobic denitrification (AD) and improve the stability of the system. The results showed that OTC stimulated at µg/L, and inhibited at mg/L. The higher the concentration of OTC, the longer the system was affected. The addition of biochar, without immobilization, improved the tolerance of community, alleviated the irreversible inhibition effect of OTC, and maintained a high denitrification efficiency. Overall, the main mechanisms of AD enhancement by biochar under OTC stress were: enhancing the bacteria metabolic activity, strengthening sludge structure and substrate transport, and improving the community stability and diversity. This study confirmed that direct addition of biochar could effectively alleviate the negative effect of antibiotics on the microorganisms, strengthen the AD, which provided a new idea to broaden the application of AD technology in livestock wastewater.

Sulfamethoxazole degradation by alpha-MnO2/periodate oxidative system: Role of MnO2 crystalline and reactive oxygen species.

Pollutant degradation via periodate ([Formula: see text]) and transitional metal oxides provides an economical, energy-efficient way for chemical oxidation process in environmental remediation. However, catalytic activation of periodate by manganese dioxide and the associated mechanism were barely investigated. In this study, four MnO2 polymorphs (α-, ß-, γ- and δ-MnO2) were synthesized and tested to activate [Formula: see text] for the degradation of sulfamethoxazole (SMX). The reactivity of different MnO2 structures followed the order of α-MnO2 > ß-MnO2 > γ-MnO2 > δ-MnO2, suggesting that the particular crystalline structure in α-MnO2 would exhibit higher activities via [Formula: see text] activation. Herein, in α-MnO2/[Formula: see text] system, 91.1% of SMX was eliminated within 30 min with degradation rate constant of 0.0649 min-1, and the neutral pH exhibited higher efficiency in SMX degradation compared with acidic and alkaline conditions. Singlet oxygen (1O2) was unveiled to be the dominant ROS according to the results of electron paramagnetic resonance, chemical probes and radical quenching experiments, whereas [Formula: see text] and •OH were mainly acted as a free-radical precursor. Six oxidation products were identified by LC-MS, and the elimination of sulfonamide bond, hydroxylation and direct oxidation were found to be the important oxidation pathways. The study dedicates to the mechanistic study into periodate activation over alpha-MnO2 and provides a novel catalytic activation for selective removal in aqueous contaminants.

Insight into enrichment of anammox bacteria by a polyurethane sponge carrier coupled with iron-carbon micro-electrolysis under no strict anaerobic condition.

A novel composite carrier (ICME-PS) was formed by coupling polyurethane sponge carriers (PS) with different pore sizes (15, 25, 40 ppi) and iron-carbon micro-electrolysis (ICME), which was used for enrichment of anammox bacteria and stable operation under no strict anaerobic condition. An increase of 5.67%-38.55% in specific anammox activity (SAA), an significant enhancement of biofilm stability and an improvement of 14.61%-42.38% in Ca.Brocadia were observed in ICME-PS, compared to PS carriers. ICME played a dual role: 1) contributed to the formation of an anaerobic microenvironment; 2) used for nitrogen cycle reactions. Additionally, small-pore carriers with highest biofilm stability can be used in high shear environments, while medium-pore carriers achieved the highest SAA in stable environments. Extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) analysis indicated that ICME application reduced the energy barrier and improved aggregation performance. This study designed a novel composite carrier to broaden the application of anammox under no strict anaerobic condition.

Microbially-mediated synthesis of activated carbon derived from cottonseed husks for enhanced sulfanilamide removal.

This study provided a novel pathway to develop activated carbon with enhanced adsorption performance via feedstock pretreatment by fungi. The growth of Pleurotus ostreatus on cottonseed husks offered this feedstock an advantageous pore size for porous carbon making. The prepared activated carbons derived from cottonseed husks (CSH-ACs) during different fungal growth periods exhibited extraordinary performance than commercial activated carbon for sulfanilamide adsorptive removal. Their experimental data of adsorption capacities for sulfanilamide were 139.43, 146.15, and 146.16 mg g-1, respectively. The adsorption behaviors of sulfanilamide on CSH-ACs were evaluated by kinetic, isotherm and thermodynamic models. Pore filling, hydrogen-bond forming and π-π staking interactions all contributed to the rapid sulfanilamide removal. The microporous-mesoporous structure, stronger hydrophilicity, and richer functional groups moieties owing to the lignocellulose decomposition in the plant wall significantly strengthened the adsorption process on the microbial-mediated activated carbon. The effects of pH and water impurities (H2PO4-, CO32-, SO42-, Cl-, and humic acid) on sulfanilamide removal were investigated by a single factor experimental design. Results indicated that CSH-ACs were suitable for sulfanilamide removal in actual wastewater treatment with wide pH adaptability and resilience to interference.

Rice straw particles covered with Brevundimonas naejangsanensis DD1 cells can synergistically remove doxycycline from water using adsorption and biotransformation.

Doxycycline (DC) is a second generation tetracycline antibiotic and its occurrence in the aquatic environment due to the discharge of municipal and agricultural wastes has called for technologies to effectively remove DC from water. The objective of the study was to characterize the synergistic benefits of adsorption and biotransformation in removing DC from water using rice straw particles (RSPs) covered with DC degrading bacteria, Brevundimonas naejangsanensis strain DD1. First, optimal experimental conditions were identified for individual processes, i.e., hydrolysis, adsorption, and biotransformation, in terms of their performance of removing DC from water. Then, synergistic effects between adsorption and biotransformation were demonstrated by adding DD1-covered RSPs (DD1-RSPs) to DC-containing solution. Results suggest that DC was quickly adsorbed onto RSPs and the adsorbed DC was subsequently biotransformed by the DD1 cells on RSPs. The adsorption of DC to DD1-RSPs can be well described using the pseudo-second-order kinetics and the Langmuir isotherm. The DD1 cells on RSPs converted DC to several biotransformation products through a series of demethylation, dehydration, decarbonylation, and deamination. This study demonstrated that adsorption and biotransformation could work synergistically to remove DC from water.

Application of electric fields to mitigate inhibition on anammox consortia under long-term tetracycline stress.

The feasibility of applying electric fields to mitigate inhibition of tetracycline (TC) on anammox process and improve system stability was evaluated in this study. Three electric field intensities of 1, 3 and a variable intensity of 1-6 V (VEF) were used to optimize electric field intensity under gradually increasing addition of TC (0.5, 2 and 10 mg L-1). Results showed that the application of electric fields (3 V and VEF) could improve TC tolerance and keep relatively high-efficiency nitrogen removal performance, especially at TC ≥ 2 mg L-1. Furthermore, applying electric fields contributed to mitigate irreversible inhibition and improve the stability of community structure. Underlying mechanism analysis indicated that the main mechanism of applying electric fields to mitigate inhibition relies on sludge structure strengthening. This study explored a novel strategy to reduce the inhibition of antibiotics on microbial denitrification and broaden the application of anammox in industrial water treatment.

Hazardous Heavy Metals Accumulation and Health Risk Assessment of Different Vegetable Species in Contaminated Soils from a Typical Mining City, Central China.

Heavy metal poisoning has caused serious and widespread human tragedies via the food chain. To alleviate heavy metal pollution, particular attention should be paid to low accumulating vegetables and crops. In this study, the concentrations of five hazardous heavy metals (HMs), including copper (Cu), chromium (Cr), lead (Pb), cadmium (Cd), and arsenic (As) were determined from soils, vegetables, and crops near four typical mining and smelting zones. Nemerow's synthetical pollution index (Pn), Potential ecological risk index (RI), and Geo-accumulation index (Igeo) were used to characterize the pollution degrees. The results showed that soils near mining and metal smelting zones were heavily polluted by Cu, Cd, As, and Pb. The total excessive rate followed a decreasing order of Cd (80.00%) > Cu (61.11%) > As (45.56%) > Pb (32.22%) > Cr (0.00%). Moreover, sources identification indicated that Cu, Pb, Cd, and As may originate from anthropogenic activities, while Cr may originate from parent materials. The exceeding rates of Cu, Cr, Pb, Cd, and As were 6.7%, 6.7%, 66.7%, 80.0%, and 26.7% among the vegetable and crop species, respectively. Particularly, vegetables like tomatoes, bell peppers, white radishes, and asparagus, revealed low accumulation characteristics. In addition, the hazard index (HI) for vegetables and crops of four zones was greater than 1, revealing a higher risk to the health of local children near the mine and smelter. However, the solanaceous fruit has a low-risk index (HI), indicating that it is a potentially safe vegetable type.

Evolution of Singlet Oxygen by Activating Peroxydisulfate and Peroxymonosulfate: A Review.

Advanced oxidation processes (AOPs) based on peroxydisulfate (PDS) or peroxymonosulfate (PMS) activation have attracted much research attention in the last decade for the degradation of recalcitrant organic contaminants. Sulfate (SO4•-) and hydroxyl (•OH) radicals are most frequently generated from catalytic PDS/PMS decomposition by thermal, base, irradiation, transition metals and carbon materials. In addition, increasingly more recent studies have reported the involvement of singlet oxygen (1O2) during PDS/PMS-based AOPs. Typically, 1O2 can be produced either along with SO4•- and •OH or discovered as the dominant reactive oxygen species (ROSs) for pollutants degradation. This paper reviews recent advances in 1O2 generation during PDS/PMS activation. First, it introduces the basic chemistry of 1O2, its oxidation properties and detection methodologies. Furthermore, it elaborates different activation strategies/techniques, including homogeneous and heterogeneous systems, and discusses the possible reaction mechanisms to give an overview of the principle of 1O2 production by activating PDS/PMS. Moreover, although 1O2 has shown promising features such as high degradation selectivity and anti-interference capability, its production pathways and mechanisms remain controversial in the present literatures. Therefore, this study identifies the research gaps and proposes future perspectives in the aspects of novel catalysts and related mechanisms.

Biotransformation of doxycycline by Brevundimonas naejangsanensis and Sphingobacterium mizutaii strains.

The fate of doxycycline (DC), a second generation tetracycline antibiotic, in the environment has drawn increasing attention in recent years due to its wide usage. Little is known about the biodegradability of DC in the environment. The objective of this study was to characterize the biotransformation of DC by pure bacterial strains with respect to reaction kinetics under different environmental conditions and biotransformation products. Two bacterial strains, Brevundimonas naejangsanensis DD1 and Sphingobacterium mizutaii DD2, were isolated from chicken litter and characterized for their biotransformation capability of DC. Results show both strains rely on cometabolism to biotransform DC with tryptone as primary growth substrate. DD2 had higher biotransformation kinetics than DD1. The two strains prefer similar pHs (7 and 8) and temperature (30 °C), however, they exhibited opposite responses to increasing background tryptone concentration. While hydrolysis converted DC to its isomer or epimer, the two bacterial strains converted DC to various biotransformation products through a series of demethylation, dehydration, decarbonylation and deamination. Findings from the study can be used to better predict the fate of DC in the environment.

Health Risk Assessment of Heavy Metals Accumulated on PM2.5 Fractioned Road Dust from Two Cities of Pakistan.

The aim of this study is to identify and investigate levels of toxic heavy metals in PM2.5 fractioned road dust to better understand the associated inhalation risk and potential health impacts. To achieve this aim, concentrations of seven traffic generated heavy metals (Cu, Pb, Zn, Cd, Ni, Sb, and Cr) were determined in the PM2.5 fraction of road dust samples from four different locations (offices, residential, hospital, and school) in two cities (Karachi and Shikarpur) of Pakistan using ICP-MS. The average concentration values of heavy metals in Karachi were as follows: 332.9 mg/kg Cu, 426.6 mg/kg Pb, 4254.4 mg/kg Zn, 62.3 mg/kg Cd, 389.7 mg/kg Ni, 70.4 mg/kg Sb, 148.1 mg/kg Cr, whereas the average concentration values of heavy metals in Shikarpur were 245.8 mg/kg Cu, 538.4 mg/kg Pb, 8351.0 mg/kg Zn, 57.6 mg/kg Cd, 131.7 mg/kg Ni, 314.5 mg/kg Sb, 346.6 mg/kg Cr. The pollution level was assessed through two pollution indices enrichment factor (EF) and geoaccumulation index (Igeo). These indices showed moderate to extreme level pollution in studied areas of both cities. The health risk assessment through inhalation contact was conducted according to the United States Environmental Protection Agency's (USEPA) model for children and adults. Both non-cancerous and cancerous risks were characterised in the road dust samples for each location. As yet, there is not a single study on the concentrations of heavy metals in PM2.5 fractions of road dust in Karachi and Shikarpur, findings of this research will facilitate researchers for further investigations in current field.

[Enhanced Chromate (â ¥) Removal Characteristics and Mechanism Using Graphene Oxide Immobilized Nanoscale Zero-Valent Iron Coupled with a Weak Magnetic Field (GO-nFe0/WMF)].

A green, high-efficiency mesoporous magnetic material with strong reusability and oxidation resistance, named graphene oxide immobilized nanoscale zero-valent iron (GO-nFe0), was prepared by a co-precipitation method. The structure, appearance, surface elements, and valence of GO-nFe0 were characterized via FESEM, TEM, FTIR, BET, XRD, and XPS. The characteristics and mechanism of Cr(Ⅵ) treatment in water using a weak magnetic field (WMF) coupled with GO-nFe0 (GO-nFe0/WMF) were studied. Batch experiments established that when the load mass ratio of GO to nFe0 was 1:10 under 20 mT weak magnetic field strength, the GO-nFe0/WMF system could completely remove the 10 mg·L-1 of Cr(Ⅵ) solution in 30 min, consistent with first-order dynamics. With a decrease in initial pH value and an increase in material dosage, the removal efficiency of Cr(Ⅵ) increased significantly by enhancing the release rate of Fe2+. ClO4- had no effect on the reaction, Cl- could encourage corrosion and promote the corrosion of nFe0 to release Fe2+, CO32- restrained the reaction through an increase in initial pH of the solution, and SO42- could promote the dissolution of the nFe0 surface passivation film to accelerate the reaction process. The GO-nFe0/WMF system can maintain high activity after five reuses and 30 days of exposure to air. XRD, XPS, and 1,10-phenanthroline shielding experiments proved that its great conductivity allowed GO to provide electron transfer sites to accelerate the transfer of electrons, and nFe0 could quickly release Fe2+. WMF generated a magnetic gradient force (FΔB) that pushed the paramagnetic Fe2+ ions in the diffusion boundary layer concentrated on the two poles of GO-nFe0, where the most magnetic intensity was present, to exposed active sites on both sides. The high removal rate ability of GO-nFe0 to release Fe2+ continuously was maintained.

Transformation mechanisms of tetracycline by horseradish peroxidase with/without redox mediator ABTS for variable water chemistry.

The threat of antibiotics in the environment causing antibiotics resistance is a global health concern. Enzymes catalyze pollutant transformations, and how commercially available enzymes like horseradish peroxidase (HRP), with or without a redox mediator, may be used to degrade antibiotics in water treatment is of great interest. This work demonstrates tetracycline transformation by HRP, and how it is significantly enhanced by free radicals created from the mediator 2,2-Azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). Water temperature and pH strongly influence the tetracycline removal rate due to their correlation with the enzyme activity, abundance and stability of ABTS•+. Four transformation products were identified in the pure HRP system using a liquid chromatography tandem mass spectrometry hybrid quadrupole-orbitrap mass spectrometer system. Addition of 25 µmol L-1 ABTS not only accelerated the degradation of tetracycline, but also expanded the range of degradation pathways. Potential tetracycline transformation pathways are proposed based on these observations, which include a range of mechanisms such as hydroxylation, demethylation, dehydration, decarbonylation and secondary alcohol oxidation. Despite of decreased efficiency, the HRP/ABTS system was able to degrade tetracycline in a domestic wastewater treatment plant effluent matrix, which demonstrates the potential of the system to be utilized in wastewater treatment.

Application of biochar in advanced oxidation processes: supportive, adsorptive, and catalytic role.

The advanced oxidation processes (AOPs), especially sulphate radical (SO4•-)-based AOPs (SR-AOPs), have been considered more effective, selective, and prominent technologies for the removal of highly toxic emerging contaminants (ECs) due to wide operational pH range and relatively higher oxidation potential (2.5-3.1 V). Recently, biochar (BC)-based composite materials have been introduced in AOPs due to the dual benefits of adsorption and catalytic degradation, but the scientific review of BC-based catalysts for the generation of reactive oxygen species (ROSs) through radical- and non-radical-oriented routes for EC removal was rarely reported. The chemical treatments, such as acid/base treatment, chemical oxidation, surfactant incorporation, and coating and impregnation of minerals, were applied to make BC suitable as supporting materials (SMs) for the loading of Fenton catalysts to boost up peroxymonosulphate/persulphate/H2O2 activation to get ROSs including •OH, SO4•-, 1O2, and O2•- for targeted pollutant degradation. In this review, all the possible merits of BC-based catalysts including supportive, adsorptive, and catalytic role are summarised along with the possible route for the development prospects of BC properties. The limitations of SR-AOPs especially on production of non-desired oxyanions, as well as disinfection intermediates and their potential solutions, have been identified. Lastly, the knowledge gap and future-oriented research needs are highlighted.

Characterization of the copper resistance mechanism and bioremediation potential of an Acinetobacter calcoaceticus strain isolated from copper mine sludge.

Bioremediation is one of the most effective ways for removal of heavy metals and restoration of contaminated sites. This study investigated the copper (Cu) resistance mechanism and bioremediation potential of an Acinetobacter calcoaceticus strain KW3 isolated from sludge of Cu mine. The effect of Cu concentrations on the bacterial growth, biomass, and adsorption capacity, as well as the effect of contact time on the adsorption process was evaluated in a batch biosorption test. The strain exhibited strong tolerance of Cu, and the minimal inhibitory concentration was around 400 mg Cu2+ L-1, at which the maximum adsorption capacity was 14.1 mg g-1 dry cell mass. Cell walls and intracellular soluble components adsorbed 51.2% and 46.6% of Cu2+, respectively, suggesting that the strain not only adsorbed Cu2+ on the surface but also metastasized ions into cells. The adsorption and kinetic data were well fitted with Freundlich isotherm and Pseudo-second-order models, suggesting that cell surface had a high affinity for Cu2+ and the chemisorption could be the main adsorption mechanism. Scanning electron microscope and Fourier transform infrared spectroscopy analysis revealed that hydroxyl, carboxylic, amide, sulfate, and phosphate on cell walls might be involved in the biosorption process. Two-dimensional gel electrophoresis and MALDI-TOF/TOF mass spectrometry revealed that some oxidoreductases, in particular Cu resistance protein A (CopA) expression levels, were upregulated. Antioxidant defense and P1B-type ATPases CopA efflux might play a crucial role in maintaining cellular homeostasis and intracellular detoxification. To our knowledge, this is the first time that Cu resistance mechanisms, especially intracellular enzymatic mechanisms, were identified in an A. calcoaceticus KW3 strain.

Synergistic degradation of PNP via coupling H2O2 with persulfate catalyzed by nano zero valent iron.

H2O2 and persulfate (PDS) activated by iron are attracting much attention due to their strong oxidation capacity for the effective degradation of organic pollutants. However, they face problems such as requiring an acidic reaction pH and difficulty of Fe2+ regeneration. In this study, the simultaneous activation of H2O2 and persulfate by nanoscaled zero valent iron (nZVI) was investigated for the degradation of p-nitrophenol (PNP). The nZVI/H2O2/PDS oxidation system exhibited significantly higher reactivity toward PNP degradation than the systems with a single oxidant. A synergistic effect was explored between H2O2 and PDS during nZVI-mediated activation, and the molar ratio of H2O2/PDS was a key parameter in optimizing the performance of PNP degradation. The nZVI/H2O2/PDS system could function well in a wide pH range, and even 95% PNP was removed at an initial pH 10, thus markedly alleviating the pH limitations of Fenton-like processes. Both hydroxyl radicals and sulfate radicals could be identified during H2O2/PDS activation, in which H+ produced during PDS decomposition promoted H2O2 activation. The increase of oxidant concentration could significantly enhance the PNP degradation, while the presence of HCO3 - and HPO4 2- exerted great inhibition. Furthermore, five degradation intermediates of PNP were detected and its degradation pathways in the nZVI/H2O2/PDS system were presented. This study reveals that the simultaneous activation of H2O2 and PDS by nZVI is a promising advanced oxidation tool as an alternative to typical Fenton processes for recalcitrant pollutant removal.

[Degradation Mechanism of Tetracycline Using Fe/Cu Oxides as Heterogeneous Activators of Peroxymonosulfate].

A green, highly efficient, and porous copper-ferrite heterogeneous catalyst (Fe-Cu-400) with good magnetism was synthesized via a coprecipitation method. The catalysts were characterized using XRD, BET, FESEM, and EDS. The performance of Fe-Cu-400 as a catalyst was evaluated by activating peroxymonosulfate (PMS) for degradation of tetracycline (TC) in aqueous solution and investigating the influence of several water parameters. The Fe-Cu-400/PMS system showed a greater TC degradation ability, and the degradation rate of TC was enhanced with an increase in the PMS concentration and the initial pH of the coupled Fe-Cu-400/PMS system. Anions including H2PO4-, HCO3-, and Cl- promoted TC degradation, whereas NO3- showed a low inhibitory influence. In addition, Fe-Cu-400 exhibited excellent reusability towards activating PMS for TC degradation after five runs of tests. Possible mechanisms of the activation of PMS by Fe-Cu-400 and the main reactive species were proposed based on radical identification tests and XPS analysis. Furthermore, a potential degradation pathway was proposed that included hydrolysis and sequential removal of N-methyl, hydroxyl, and amine functional groups according to the results of LC-MS and TOC detections.

Phytoremediation of heavy metal contaminated soil potential by woody plants on Tonglushan ancient copper spoil heap in China.

Fast-growing metal-accumulating woody plants are considered potential candidates for phytoremediation of metals. Tonglushan mining, one of the biggest Cu production bases in China, presents an important source of the pollution of environment. The sample was collected at Tonglushan ancient copper spoil heap. The aims were to measure the content of heavy metal in the soil and woody plants and to elucidate the phytoremediation potential of the plants. The result showed that soil Cu, Cd and Pb were the main contamination, the mean contents of which were 3166.73 mg/kg, 3.66 mg/kg and 137.06 mg/kg respectively, which belonged to severe contamination. Fourteen species from 14 genera of 13 families were collected and investigated; except for Ligutrum lucidum, the other 13 woody plants species were newly recorded in this area. In addition, to assess the ability of metal accumulation of these trees, we proposed accumulation index. Data suggested that Platanus × acerilolia, Broussonetia papyrifera, Ligutrum lucidum, Viburnum awabuki, Firmiana simplex, Robina pseudoacacia, Melia azedarach and Osmanthus fragrans exhibited high accumulated capacity and strong tolerance to heavy metals. Therefore, Platanus × acerilolia and Broussonetia papyrifera can be planted in Pb contaminated areas; Viburnum awabuki, Firmiana simplex, Robina pseudoacacia and Melia azedarach are the suitable trees for Cd contaminated areas; Viburnum awabuki, Melia azedarach, Ligutrum lucidum, Firmiana simplex, Osmanthus fragrans and Robina pseudoacacia are appropriate to Cu, Pb and Cd multi-metal contaminated areas.