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Hydrogel adsorbents are promising tools for reducing heavy metals' bioavailability in contaminated soil. However, their practical feasibility remains limited by the low stability, inefficient removal efficiency, and potential secondary pollution. Optimizing the adsorption operation and the functional properties of hydrogel adsorbents could eliminate this method's drawbacks. Herein, three innovative in-situ remediation strategies for Pb/Cu-contaminated soil were adopted based on the concept of novel TEMPO-cellulose (TO-NFCs)/lignin/acrylamide@MIL-100(Fe) nanocomposite hydrogel adsorbent (NCLMH). Characteristic analyses revealed ideal Pb/Cu adsorption mechanisms by swelling, complexation, electrical attraction, and ion exchange via carboxyl/hydroxyl/carbonyl groups and unsaturated Fe(III) sites on ANCMH besides FeOOH formation. The highest maximum theoretical adsorption capacities of Pb(II) and Cu(II) on ANCMH were 416.39 and 133.98 mg/g, under pH 6.5, governed by pseudo-second-order/Freundlich models. Greenhouse pot experiments with contaminated soils amended with two-depth layers of 0.5% NCLMHs (SA@NCLMH) displayed a decline in Pb and Cu bioavailability up to 85.9% and 74.5% within 45 d. Soil column studies simulating continuous water soil flushing coupled with NCLMH layers, instead of conventional extractant fluids, and connected to NCLMH-sand column as purification unit (CF@NCLMH) achieved higher removal rates for Pb, and Cu of 89.5% and 77.2% within 24 h. Alternatively, conducting multiple-pulse soil flushing mode (MF@NCLMH) gained the highest Pb and Cu removal of 96.5% and 85.4%, as the water flushing-stop flux events allowed adequate water movement/residence period, promoting Pb/Cu desorption-adsorption from soil to NCLMH. Also, the NCLMH-sand column conducting and easy separation of the stable/reusable NCLMHs prevented the potential secondary pollution. Interestingly, the three remediated soils reached the corresponding regulation of the permissible limits for Pb and Cu residential scenarios in medium-to-heavily agricultural polluted soils, alleviating the Pb/Cu bioaccumulation and phytotoxicity symptoms in cultivated wheat, especially after MF@NCLMH treatment. This study introduces promising alternative remediation strategies with high sustainability and feasibility in acidic-to-neutral heavy metal-contaminated agricultural soil., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Reducing cadmium (Cd) content from contaminated farmland soils remains a major challenge due to the difficulty in separating commonly used adsorbents from soils. This study synthesized novel millimeter-sized magnetic Fe 3 O 4 /mercapto-functionalized attapulgite beads (MFBs) through a facile one-step gelation process incorporating alginate. The MFBs inherit the environmental stability of alginate and enhance its mechanical strength by hybridizing Fe 3 O 4 and clay mineral components. MFBs can be easily separated from flooded soils by magnets. When applied to 12 Cd-polluted paddy soils and 14 Cd-polluted upland soils, MFBs achieved Cd(II) removal rates ranging from 16.9% to 62.2% and 9.8%-54.6%, respectively, within a 12-h period. The MFBs predominantly targeted the exchangeable and acid soluble, and reducible fractions of Cd, with significantly enhanced removal efficiencies in paddy soils compared to upland soils. Notably, MFBs exhibited superior adsorption performance in soils with lower pH and organic matter (OM) content, where the bioavailability and mobility of Cd are heightened. The reduction of Cd content by MFBs is a sustainable and safe method, as it permanently removes the bioavailable Cd from soil, rather than temporarily reducing its bioavailability. The functional groups such as -SH, -OH, present in attapulgite and alginate of MFBs, played a crucial role in Cd(II) adsorption. Additionally, attapulgite and zeolite provided a porous matrix structure that further enhanced Cd(II) adsorption. The results of X-ray photoelectron spectroscopy suggested that both chemical precipitation and surface complexation contributed to Cd(II) removal. The MFBs maintained 87.6% Cd removal efficiency after 5 regeneration cycles. The surface of the MFBs exposed new adsorption sites and increased the specific surface area during multiple cycles with Cd-contaminated soil. This suggests that MFBs treatment with magnetic retrieval is a potentially effective pathway for the rapid removal of Cd from contaminated farmland soils., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

To investigate watershed remediation within a Total Maximum Daily Load program, this study examined the field-scale filtration performance of two specialty absorbents. The goal was to simultaneously remove nutrients and biological pollutants along Canal 23 (C-23) in the St. Lucie River Basin, Florida. The filtration system installed in the C-23 river corridor was equipped with either clay-perlite with sand sorption media (CPS) or zero-valent iron and perlite green environmental media (ZIPGEM). Both media were formulated with varying combinations of sand, clay, perlite, and/or recycled iron based on distinct recipes. In comparison with CPS, ZIPGEM exhibited higher average removal percentages for nutrients. Findings indicated that ZIPGEM could remove total nitrogen up to 49.3%, total Kjeldahl nitrogen up to 67.1%, dissolved organic nitrogen (DON) up to 72.9%, total phosphorus up to 79.6%, and orthophosphate up to 73.2%. Both ZIPGEM and CPS demonstrated similar efficiency in eliminating biological pollutants, such as E. coli (both media exhibiting an 80% removal percentage) and chlorophyll a (both media achieving approximately 95% removal). Seasonality effects were also evident in nutrient removal efficiencies, particularly in the case of ammonia nitrogen; the negative removal efficiency of ammonia nitrogen from the fifth sampling event could be attributed to processes such as photochemical ammonification, microbial transformation, and mineralization of DON in wet seasons. Overall, ZIPGEM demonstrated a more stable nutrient removal efficiency than CPS in the phase of seasonal changes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

The extensive use of pesticides for better yield of crops have become major human concern over the decades. Pesticides are widely used in the fields to kill weeds and pests on the vegetable and crops to improve the quality and yield of the food knowing the fact that pesticides residue in food are very lethal for human being. Amongst, the hazardous pesticides, mancozeb is widely applied in the protection of crops. Thus the quantification of mancozeb residue is of great importance. This study reports the electrochemical monitoring of mancozeb through tungsten oxide reduced graphene oxide (WO 3 /rGO) nanocomposite. The engineered nanocomposite was characterized though different analytical tools such as FTIR, XRD and TEM to examine crystallinity, internal texture and the size. The FTIR result confirm the functionalities of GO and WO 3 /rGO nanocomposite in finger print and functional group region. Through XRD analysis, the size of the WO 3 /rGO nanocomposite was calculated as 31.6 nm. While the TEM analysis was also exploited to examine the 2D texture of GO and nanometric size of the WO 3 /rGO. To ensure the conductive nature of the WO 3 /rGO nanocomposite, the glassy carbon electrode was modified and exploited for cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Under the optimal conditions, the modified sensor showed exceptional response for mancozeb. The linear dynamic range was set from 0.05 to 70 μM in BRB buffer of pH 4. The LOD and LOQ for proposed method was calculated as 0.0038 and 0.0115 μM. The analytical applicability of chemically modified sensor was investigated in real matrix of different vegetable samples and the recovery values were observed in acceptable range. The electrochemical examination of present work reveals that WO 3 /rGO nanocomposite can be an exceptional aspirant for the determination of mancozeb at commercial level., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Different cyclodextrin-calixarene nanosponges (CyCaNSs) have been characterized by means of FFC-NMR relaxometry, and used as sorbents to remove Pb 2+ ions from aqueous solutions. Considering that the removal treatments may involve polluted waters with different characteristics, the adsorption experiments were performed on solutions without and with the addition of background salts, under different operational conditions. The adsorption abilities and affinities of the nanosponges towards Pb 2+ ions were investigated by measuring the metal ion concentration by means of Inductively Coupled Plasma Emission Spectroscopy (ICP-OES) and Differential Pulse Anodic Stripping Voltammetry (DP-ASV). The acid-base properties of nanosponges and of metal ion as well as their interactions with the other interacting components of the systems have been considered in the evaluation of adsorption mechanism. Recycling and reuse experiments on the most efficient adsorbents were also performed. On the grounds of the results obtained, post-modified CyCaNSs appear promising materials for designing environmental remediation devices., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Heavy metals and metalloids (HMMs) pose a serious threat to both environmental and human health. The unique characteristics and environmental toxicity of HMMs make their removal from the environment a major challenge. Constructed wetlands (CWs) are increasingly being used as an eco-friendly system for the removal of HMMs from aqueous environments. In this review, bibliometric analysis was performed using the Scopus database using VOSviewer software to assess the developing use of CWs in recent years. Heavy metal and metalloid (HMM) removal pathways were reviewed (such as precipitation, co-precipitation, adsorption and ion exchange, plant action and microbial action) along with the impact of key factors (pH, chemical oxygen demand, dissolved oxygen, HMM concentration, and temperature). This review aimed to establish the connections between published results, to help effectively optimize the use of CWs for the removal of HMMs and identify the most critical factors for their effective removal. Important aspects that require further research include assessing the synergistic toxicity between different pollutants and combining the use of CWs with other technologies to optimize pollutant remediation efficiency., (© 2021. The Author(s), under exclusive licence to Springer Nature B.V.)

The petrochemical industry is responsible for many accidental releases of pollutants in soil such as hydrocarbons and toxic metals. This co-contamination is responsible for a delay in the degradation of the organic pollution. Many successful technologies to remove these metals apply extracellular polymeric substances (EPS). In this study, we tested the application of an EPS from a Paenibacillus sp. to aid the bioremediation of soils contaminated with crude oil and nickel. We conducted a microcosm experiment to soils containing combinations of oil, nickel, and EPS. The final concentration of oil was evaluated with an infrared spectrometer. Also, we sequenced the metagenomes of the samples in an ion torrent sequencer. The application of EPS did not aid the removal of hydrocarbons with or without the presence of nickel. However, it led to a smaller decrease in the diversity indexes. EPS decreased the abundance of Actinobacteria and increased that of Proteobacteria. The EPS also decreased the connectivity among Actinobacteria in the network analysis. The results indicated that the addition of EPS had a higher effect on the community structure than nickel. Altogether, our results indicate that this approach did not aid the bioremediation of hydrocarbons likely due to its effect in the community structure that affected hydrocarbonoclastic microorganisms.

Diclofenac is a commercial non-steroidal anti-inflammatory drug commonly present as a pollutant in naturally occurring water sources and wastewaters. In this work, the adsorption of diclofenac onto chitosan-coated magnetic nanosystems is proposed as a possible tool for remediation. Experimental and theoretical studies have been carried out to reveal the mechanisms associated with diclofenac interactions among all the components of the nanosystem. Mechanisms are presented, analyzed and discussed. A toxicological study in mice was carried out to evaluate the parameters associated with neurotoxicity of the nanodevice. The elucidation of the mechanisms implied in the adsorption process of diclofenac onto magnetic chitosan nanocomposites suggests that diclofenac remediation from water is possible by adsorption onto chitosan. The strategy innovates the commonly used methodologies for diclofenac remediation from pharmaceutical wastes. This magnetic nanotechnology would not induce damage on the nervous system in a murine model, in case of traces remaining in water sources.

Restoration is becoming a vital tool to counteract coastal ecosystem degradation. Modifying transplant designs of habitat-forming organisms from dispersed to clumped can amplify coastal restoration yields as it generates self-facilitation from emergent traits, i.e. traits not expressed by individuals or small clones, but that emerge in clumped individuals or large clones. Here, we advance restoration science by mimicking key emergent traits that locally suppress physical stress using biodegradable establishment structures. Experiments across (sub)tropical and temperate seagrass and salt marsh systems demonstrate greatly enhanced yields when individuals are transplanted within structures mimicking emergent traits that suppress waves or sediment mobility. Specifically, belowground mimics of dense root mats most facilitate seagrasses via sediment stabilization, while mimics of aboveground plant structures most facilitate marsh grasses by reducing stem movement. Mimicking key emergent traits may allow upscaling of restoration in many ecosystems that depend on self-facilitation for persistence, by constraining biological material requirements and implementation costs.

Indoor air pollutant is a serious problem due to its wide diversity and variability. The harmful substances from construction materials and decorative materials may make the indoor air pollution become more and more serious and cause serious health problems. In this paper, the review summarizes the advanced technologies for the removal of indoor air pollutants and the development in the treatment of indoor air pollution by catalytic oxidation technologies. Meanwhile, some catalytic oxidation mechanisms of indoor air pollutants are proposed in detail, and suggestions for the indoor air pollution treatment are also presented, in order to provide some reference for subsequent research., (© 2020 Walter de Gruyter GmbH, Berlin/Boston.)

The use of electrokinetic Fenton (EK Fenton) process, as promising soil remediation approach, was investigated by using an iron electrode with different supporting electrolytes (tap water, H 2 O 2 , and citric acid) to depollute soil spiked with petroleum where kaolin was selected as low hydraulic conductivity. The results clearly confirm that, the combination of electrokinetic remediation (EK) and Fenton technologies, is an efficient oxidizing approach for removing hydrocarbons from this kind of soil. In fact, the electrokinetic Fenton reactions and the control of the soil pH conditions by adding citric acid enhanced the oxidation process because the addition of the H 2 O 2 with iron electrode resulted in higher removal efficiencies (89%) for total petroleum hydrocarbons (TPHs). These figures allowed to confirm that EK Fenton process with pH control contributed for the transport of H 2 O 2 and Fe 2+ ions in the soil by electromigration and eletro-osmotic phenomena. Conversely, no control of pH conditions when only EK was applied, achieved lower hydrocarbons removal (27%) after 15 d of treatment due to the precipitation of iron ions. Finally, the efficiency of the EK Fenton remediation prevented the generation of secondary effluent with higher organic content, avoiding its treatment by other advanced oxidation process., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Polycyclic aromatic hydrocarbons (PAHs) in soil are not only detrimental to environment but also to human health. Double dielectric barrier discharge (DDBD) plasma reactor used for the remediation of pyrene contaminated soil was studied. The performance of DDBD reactor was optimized with influential parameters including applied voltage, type of carrier gas, air feeding rate as well as pyrene initial concentration. The analysis of variance (ANOVA) results showed that input energy had a great effect on pyrene remediation efficiency followed by pyrene initial concentration, while, the effect of air feeding rate was insignificant. More specifically, the remediation efficiency of pyrene under air, nitrogen and argon as carrier gas were approximately 79.7, 40.7 and 38.2% respectively. Pyrene remediation efficiency is favored at high level of applied voltages and low level of pyrene initial concentration (10 mgkg -1 ) and air feeding rate (0.85 L/min). Moreover, computation of the energy efficiency of the DDBD system disclosed that an optimal applied voltage (35.8 kV) and higher initial pyrene concentration (200 mgkg -1 ) favored the high energy efficiency. A regression model predicting pyrene remediation under DDBD plasma condition was developed using the data from a face-centered central composite design (FCCD) experiment. Finally, the residual toxicity analysis depicted that the respiratory activity increased more than 21 times (from 0.04 to 0.849 mg O 2 g -1 ) with a pyrene remediation efficiency of 81.1%. The study demonstrated the DDBD plasma technology is a promising method not only for high efficiency of pyrene remediation, but also recovering biological function without changing the physical-chemical properties of soil., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Successful recruitment of new individuals is essential for recovery of degraded coral reefs. Enhancing supply of coral larvae increases initial settlement, however post-settlement survival can be influenced by density-dependent processes. We investigated the influence of larval density on settlement, colony abundance and growth to 24 months for Acropora tenuis in the north-western Philippines, to determine whether larval supply can be optimised to maximise successful recruitment. Thirty different densities of coral larvae were enclosed for five days around settlement tiles and highest total settlement occurred on tiles with highest larval densities. After 12 months, however, colony abundance and coral cover was lower on high density tiles (supplied with ~2,500-5,000 larvae) than tiles supplied with ~1,000-2,000 larvae. Coral cover at 24 months remained highest on tiles supplied with ~1,000-2,500 larvae. Larval density influenced larval substratum selection, with proportionally fewer larvae settling in typically preferred locations as density increased. We conclude that larval density can influence post-settlement colony abundance and coral cover to 12 months, with coral cover trends persisting to 24 months. We show that optimising larval densities can maximise coral recruitment and growth, however oversupply of larvae at very high densities can have negative outcomes for larval restoration.

This study presents the removal of phosphate from aqueous solution using a new silver nanoparticles-loaded tea activated carbon (AgNPs-TAC) material. In order to reduce costs, the tea activated carbon was produced from tea residue. Batch adsorption experiments were conducted to evaluate the effects of impregnation ratio of AgNPs and TAC, pH solution, contact time, initial phosphate concentration and dose of AgNPs-AC on removing phosphate from aqueous solution. Results show that the best conditions for phosphate adsorption occurred at the impregnation ratio AgNPs/TAC of 3% w/w, pH 3, and contact time lasting 150 min. The maximum adsorption capacity of phosphate on AgNPs-TAC determined by the Langmuir model was 13.62 mg/g at an initial phosphate concentration of 30 mg/L. The adsorption isotherm of phosphate on AgNPs-TAC fits well with both the Langmuir and Sips models. The adsorption kinetics data were also described well by the pseudo-first-order and pseudo-second-order models with high correlation coefficients of 0.978 and 0.966, respectively. The adsorption process was controlled by chemisorption through complexes and ligand exchange mechanisms. This study suggests that AgNPs-TAC is a promising, low cost adsorbent for phosphate removal from aqueous solution.

The reduction of ammonia emissions from air was experimentally investigated by advanced oxidation processes (AOPs) utilizing the combination of ultraviolet irradiation with ozone. The influence of operating conditions such as initial ammonia concentration and flow rate of gas on the reduction of ammonia concentration was investigated in homemade photochemical unit. The conversion of ammonia decreased with increasing initial concentration of ammonia and with increasing flow rate of air (decreasing retention time). The highest conversion of ammonia (97%) was achieved under lower initial concentration of ammonia (30 ppm) and lower flow rate of air (28 m 3 /h). The energy per order was evaluated for the advanced oxidation process too. The energy consumption was about 0.037 kWh/m 3 /order for the 97% ammonia conversion at 30 ppm of initial ammonia concentration and 28 m 3 /h flow rate of air. Based on the results, the advanced oxidation process combining the UV irradiation and ozone was effective for mitigation of ammonia concentration and presents a promising technology for the reduction of odor emissions from livestock buildings. Moreover, the AOPs are suitable for application for high flow rate of air, especially for ammonia abatement from livestock buildings, where very high efficiency is expected.

Heavy metals contaminated sediment has become a worldwide environmental issue due to its great harm to human and aquatic organisms. Thus, economical, effective, and environmentally-friendly remediation technologies are urgently needed. Among which, combined remediation technologies have attracted widespread attention for their unique advantages. This paper introduces combined remediation technologies based on physical-, chemical-, and bio-remediation of heavy metal polluted sediments. Firstly, the research progress in physical-chemical, bio-chemical, and inter-organismal (including plants, animals, microorganisms) remediation of heavy metal polluted sediments are summarized. Additionally, the paper analyzes the problems of the process of combined remediation of heavy metals in river sediments and outlooks the future development trends of remediation technologies. Overall, this review provides useful technology references for the control and treatment of heavy metal pollution in river sediments.

Enantioselectivity is usually ignored when assessing potential biochar-based methods of redressing pesticide contamination of soils. In this study, the effect of woodchip biochar (WBC) on the enantioselective dissipation of metalaxyl in soil and its uptake and translocation by lettuce were investigated. S -metalaxyl ( T 1/2 = 29.8 days) dissipated more quickly than R -metalaxyl ( T 1/2 = 36.4 days) in unamended soil. The addition of WBC to the soil decreased the dissipation rate and the enantioselectivity of metalaxyl. Metalaxyl distribution showed opposing enantioselectivity in lettuce, with roots and shoots showing preferences for R -metalaxyl and S -metalaxyl, respectively. Enrichment with WBC decreased the concentrations of metalaxyl and metalaxyl acid enantiomers in lettuce and reduced the ability of the shoots to transport the highly toxic R -metalaxyl from roots. This is the first study to provide evidence that amending soil with biochar affects the enantioselective uptake and translocation of a chiral pesticide.

Xylene is the main component of many volatile industrial pollution sources, and the use of biotechnology to remove volatile organic compounds (VOCs) has become a growing trend. In this study, a biotrickling filter for gaseous xylene treatment was developed using activated sludge as raw material to study the biodegradation process of xylene. Reaction conditions were optimized, and long-term operation was performed. The optimal pH was 7.0, gas-liquid ratio was 15:1 ( v / v ), and temperature was 25 °C. High-throughput sequencing technique was carried out to analyze microbial communities in the top, middle, and bottom layers of the reactor. Characteristics of microbial diversity were elucidated, and microbial functions were predicted. The result showed that the removal efficiency (RE) was stable at 86%-91%, the maximum elimination capacity (EC) was 303.61 g·m -3 ·hr -1 , residence time was 33.75 sec, and the initial inlet xylene concentration was 3000 mg·m -3 , which was the highest known degradation concentration reported. Kinetic analysis of the xylene degradation indicated that it was a very high-efficiency-activity bioprocess. The r max was 1059.8 g·m -3 ·hr -1 , and K s value was 4.78 g·m -3 in stationary phase. In addition, microbial community structures in the bottom and top layers were significantly different: Pseudomonas was the dominant genus in the bottom layer, whereas Sphingobium was dominant in the top layer. The results showed that intermediate metabolites of xylene could affect the distribution of community structure. Pseudomonas sp. can adapt to high concentration xylene-contaminated environments. Implications: We combined domesticated active sludge and reinforced microbial agent on biotrickling filter. This system performed continuously under a reduced residence time at 33.75 sec and high elimination capacity at 303.61 g·m -3 ·hr -1 in the biotrickling reactor for about 260 days. In this case, predomestication combined with reinforcing of microorganisms was very important to obtaining high-efficiency results. Analysis of microbial diversity and functional prediction indicated a gradient distribution along with the concentration of xylene. This implied a rational design of microbial reagent and optimizing the inoculation of different sites of reactor could reduce the preparation period of the technology.

Several industrial activities produce wastewater with high sulfate content that can cause significant environmental issues. Although bioelectrochemical systems (BESs) have recently been studied for the treatment of sulfate contained in this wastewater, the recovery of elemental sulfur with BESs is still in its beginnings. This work proposes a new reactor configuration named BES-EC, consisting of the coupling of a BES with an electrochemical cell (EC), to treat this type of wastewater and recover elemental sulfur. The reactor consisted of four electrodes: i) an abiotic anode, ii) a biocathode for the autotrophic sulfate reduction, iii) an anode of an electrochemical cell (EC) for the partial oxidation of sulfide to elemental sulfur (the biocathode and the EC anode were placed in the same chamber) and iv) an abiotic EC cathode. Several cathode potentials and sulfate loads were tested, obtaining high sulfate removal rates (up to 888 mg SO 4 2- -S L -1  d -1 at -0.9 V vs. SHE with a specific energy consumption of 9.18 ± 0.80 kWh kg -1  SO 4 2- -S). Exceptionally high theoretical elemental sulfur production rates (up to 498 mg S 0 -S L -1  d -1 ) were achieved with the EC controlled at a current density of 2.5 A m -2 . Electron recovery around 80% was observed throughout most of the operation of the integrated system. In addition, short experiments were performed at different current densities, observing that sulfate removal did not increase proportionally to the higher applied current density. However, when the BES was controlled at 30 A m -2 and the EC at 7.5 A m -2 , the proportion of elemental sulfur produced corresponded to 92.9 ± 1.9% of all sulfate removed., (Copyright © 2019. Published by Elsevier B.V.)

Herein we fabricated the supported single-atom silver catalysts using an in situ molten salt method. The Mn 2 O 3 nanowires supported single-atom silver catalyst (i.e., 0.06 wt% Ag/Mn 2 O 3 ) exhibited excellent catalytic activity for toluene combustion, with the temperatures required for 50 and 90% of toluene conversions being 170 and 205 °C, respectively, at a space velocity of 40,000 mL/(g h). However, the toluene conversion at 205 °C quickly decreased from 90 to 30% within 2.5 h of on-stream reaction. Based on the various characterization results, we found that there were no aggregation of Ag particles, no change in crystal structure of the Mn 2 O 3 nanowire support, and no carbon deposition on the catalyst surface, and the quick deactivation of 0.06 wt% Ag/Mn 2 O 3 was mainly associated with the low oxygen activation ability. The proper CeO 2 addition to the 0.06 wt% Ag/Mn 2 O 3 catalyst was found to not only improve the catalytic activity but also significantly enhance the stability of the catalyst. Toluene conversion at 195 °C over 0.63 wt% CeO 2 -0.06 wt% Ag/Mn 2 O 3 decreased by only 10% in 50 h of on-stream reaction. Because Ag and CeO 2 particles were highly dispersed on the Mn 2 O 3 nanowire support, the oxygen species formed at the surface oxygen vacancies of CeO 2 could efficiently migrate to the active sites (i.e., the interface of Ag-Mn 2 O 3 ) and replenish the surface reactive lattice oxygen species. Thus, the present single-atom silver catalyst is an alternative for commercial noble metal catalysts for the removal of VOCs., (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

The ability of standard soils to capture heavy metals or polycyclic aromatic hydrocarbons (PAHs) from ammoniacal copper zinc arsenate (ACZA)- or creosote-treated wood, respectively, was assessed using pressure-treated posts immersed in a freshwater pond. The soil, in heat-sealed, permeable plastic mesh sachets, was able to intercept copper, zinc, arsenic, and PAHs migrating from the posts. Chemical levels were much higher immediately adjacent to the posts and declined with distance from the posts. Metals were consistently detected around ACZA-treated posts, while 10 of the 16 EPA priority pollutants were detected in at least one sachet embedded around creosote-treated posts at each sampling point. These results were consistent with traditional sediment sampling methods. The primary advantages of the sachets were their consistency in terms of soil characteristics and the ease with which they could be retrieved from the pond. Further studies are planned to better understand the role of soil characteristics in the sachets on the ability to capture migrating preservatives.

The present work reconnoitres the feasibility of utilizing class F fly ash and calcined animal bone powder (CABP) as raw material for the synthesis of heterogeneous solid base catalyst with varying ratios (CABP of 10, 20, and 30 mass%), that is subsequently used for transesterification of mustard oil. Physicochemical characterization of CABP revealed crystalline behavior, signifying one of the components as hydroxyapatite (HAP); when calcined at 900 °C transforms to β-tricalcium phosphate having a specific surface area of 100 m 2  g -1 . The synthesized catalyst showed improved catalytic activity when compared to the parental species and the optimal value to achieve the highest conversion of 90.4% would be at CABP loading of 10 mass%, 5.5:1 methanol to oil molar ratio, and 10 mass% catalyst concentration for 6 h. The prepared biodiesel had a calorific value of 36.2 MJ kg -1 with ash content < 0.01 mass%. The catalyst could be reused five times with no loss in its activity. Results indicated that calcium enriched waste materials when impregnated in fly ash might be a potential source of catalyst in biodiesel production., (Copyright © 2019. Published by Elsevier B.V.)

Formaldehyde is one of the most common indoor air pollutants in Chinese residences. This study introduces a novel laminated plate with adjustable surface temperature to remove gaseous formaldehyde. The plate is fabricated with activated carbon, polyimide, and copper foil via thermal compression. The plate can be regenerated in situ by applying a direct current to the copper foil. Adsorption-regeneration cycle tests were conducted to evaluate the plate's formaldehyde removal performance. The overall removal efficiency of the fabricated laminated plate with glue mass fraction of 25% and thickness of 1.5 mm was about 30% at the face velocity of 0.8-1.2 m/s. The pressure drop was about 5 Pa. Its removal ability can be regenerated in situ in 8 minutes by increasing the surface temperature to 80°C. The fabricated laminated plate showed good durability after 52 cycles of adsorption-regeneration tests. The results indicate that the proposed laminated plate can enhance the purifying efficiency and enlarge the life span of ordinary, cheap sorbents. It makes cheap materials with low performance suitable for air purification., (© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

In soil, vanadium (V) contamination is commonly concomitant with chromium (Cr) contamination, which poses potential risks to humans, animals, and plants due to the transfer of toxic metals and the increase in their concentrations via the food chain or through direct exposure. This study applied a multi-step column leaching process using low-molecular-weight organic acids (LMWOAs) to treat V-contaminated soil from a smelter site that contains 2015.1 mg V kg -1 and 1060.3 mg Cr kg -1 . After leaching three times with an equivalent solution/soil ratio of 0.3 mL/g using 1.0 M oxalic acid solution, the total removal rates reached 77.2% and 7.2% for V and Cr, respectively, while the removal rates of the extractable fractions reached 118.6% and 99.2% due to the reduction in residual fraction (F 4 ) of toxic metals. Simultaneously, the distribution and redistribution of geochemical fractions of V and Cr were determined with a sequential extraction technique, and the greater proportion of potential mobile fractions of V (65.1%) may increase its leaching from soil relative to Cr (7.1%). In addition, a lower pH of the leaching agent increased the efficiency of the leaching process to an extent. Compared with batch extraction with a typical solution to soil ratio of 10 mL/g, multi-step column leaching used less agent and hence produced less wastewater. This strategy could reduce the mobilization and bioavailability of toxic metals, and potentially enhance in situ soil flushing for the remediation of V- and Cr- contaminated soil.

Cadmium contamination in soil, water and food has become a global problem since last century's industrial and agricultural revolution. It is a highly toxic metal with serious consequences on human and animal health. Different natural and anthropogenic sources are responsible for Cd release in the soil which ultimately leads to the food chain. Cd persists in soil for long durations due to its minimal microbial or chemical loss. There are various physical, chemical or biological techniques which are helpful to minimize Cd risk in food chain. Among them, in-situ immobilization with organic, inorganic or clay amendments is a cost-effective and an environment friendly strategy to remediate Cd polluted sites. Lime, biochar, organic wastes, phosphorus fertilizers, sepiolite, zeolite, hydroxyapatite and bentonite are commonly used amendments for amelioration of Cd contaminated soils. These amendments reduce Cd uptake and enhance immobilization by adsorption, complexation, and precipitation processes. This review is aimed to provide a comprehensive note on Cd toxicity in humans and environment, its immobilization by different agents through variety of processes, and comparison of technologies for Cd removal from contaminated sites., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Concerning the contamination of phthalate esters (PAEs) in river sediments, this mini-review introduces four recently reported novel "integrated electrokinetic (EK) processes" for the remediation purpose, namely two combined technologies of the EK process and advanced oxidation process (EK-AOP Processes) and two combined technologies of the EK process and biological process (EK-BIO Processes). The following is a comprehensive summary for these remediation processes: (1) the EK process coupled with nano-Fe 3 O 4 /S 2 O 8 2- oxidation process - Test results have shown that nanoscale Fe 3 O 4 played a significant role in activating persulfate oxidation. Even a recalcitrant compound like di(2‑ethylhexyl)phthalate (DEHP), its concentration in test sediment was reduced to 1.97 mg kg -1 , far below the regulatory levels set by Taiwan EPA; (2) the EK process integrated with a novel Fenton-like process catalyzed by nanoscale schwertmannite (nano-SHM) - Test results have revealed that simultaneous injection of nano-SHM slurry and H 2 O 2 into the anode reservoir and sediment compartment is a good practice. 70-99% in removal efficiency was obtained for various target PAEs; (3) enhanced in situ bioremediation coupled with the EK process for promoting the growth of intrinsic microorganisms by adding H 2 O 2 as an oxygen release compound (ORC) - Test results have demonstrated that an intermittent mode of injecting lab-prepared ORC directly into the contaminant zone would be beneficial to the growth of intrinsic microorganisms in test sediment for in situ bioremediation of target PAEs; and (4) coupling of a second-generation ORC (designated 2G-ORC) with the EK-biological process - Test results have proved that 2G-ORC is long-lasting and can be directly utilized as the carbon source and oxygen source for microbial growth resulting in an enhanced biodegradation of PAEs. Except DEHP having a residual concentration of 4 μg kg -1 , all other target PAEs in test sediment were totally removed by this novel combined remediation process., (Copyright © 2019. Published by Elsevier B.V.)

Owing to their high earth-abundance, eco-friendliness, high electrical conductivity, large surface area, structure tunability at the atomic/morphological levels, and excellent stability in harsh conditions, carbon-based metal-free materials have become promising advanced electrode materials for high-performance pseudocapacitors and metal-air batteries. Furthermore, carbon-based nanomaterials with well-defined structures can function as green catalysts because of their efficiency in advanced oxidation processes to remove organics in air or from water, which reduces the cost for air/water purification and avoids cross-contamination by eliminating the release of heavy metals/metal ions. Here, the research and development of carbon-based catalysts in supercapacitors and batteries for clean energy storage as well as in air/water treatments for environmental remediation are reviewed. The related mechanistic understanding and design principles of carbon-based metal-free catalysts are illustrated, along with the challenges and perspectives in this emerging field., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

In our study, plant polyphenol-inspired chemistry is explored to nano-engineer the topological and chemical structures of commercial melamine sponge surface for preparing superhydrophobic sponges. Briefly, tannic acid (TA, a typical plant polyphenol) is applied to induce the co-assembly of silica nanoparticles (SiO 2 ) and silver ions (Ag + ) to form SiO 2 @TA@Ag nanostructures on a melamine sponge surface. After further chemical fluorination, the superhydrophobic sponge with a "lotus leaf-mimic" surface is formed. Surface topological/chemical structures, superhydrophobic property and anti-combustion characteristics of the sponge are examined by a series of characterization techniques, including scanning electron microscopy, X-ray photoelectron spectroscopy, water contact angle measurements, combustion/heating test, etc. The superhydrophobic sponge presents an adsorption capacity of 69-153 times of its own weight toward various oils/organic solvents, and exhibits excellent recycling ability evidenced by over 100-cycled uses. Continuous oil/water separation apparatus is also set up through equipping the superhydrophobic sponge on a peristaltic pump, realizing the clean-up of oils and organic solvents from water continuously. Together with the facile, easy-to-scale-up and substrate non-selective features of plant polyphenol-inspired chemistry, the superhydrophobic sponge and the surface nano-engineering method would hold great promise for the effective treatment of oil spillages and organic discharges, achieving high sustainability to energy and environment., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Acid mine drainage (AMD) is among the most serious threats to water and the typical alkali-based treatment costs are high. This study's main objective was the establishment of a highly efficient biological process using an upflow anaerobic sludge blanket (UASB) reactor to treat AMD based on a shorter hydraulic retention time (HRT) and lower organic matter input. The process was evaluated for a long-term operation (739 days) in terms of the influence of HRT (14-24 h), metal addition, sulfate loading rate (0.5-2.6 g SO 4 2-  l -1  d -1 ), and the COD/SO 4 2- ratio (0.67-1.0) using ethanol as the only electron donor at a pH of 4.0. Neutral effluent pH was achieved throughout the time apart from operational modifications. The reduction in HRT from 24 to 16 h and an increase in the sulfate loading rate (SLR) up to 2.25 g SO 4 2-  l -1  d -1 improved the sulfate removal to (92.1 ± 1.8)% with 80% chemical oxygen demand (COD) removal. However, the sulfate reduction was less than 80% when the HRT and SLR was changed to 14 h and 2.6 g SO 4 2-  l -1  d -1 , respectively. The oxidation of organic matter by sulfate reduction was greater than 50% regardless of the conditions imposed but the use of ethanol to treat AMD was more efficient when either the HRT was 16 h (1.5 g SO 4 2-  l -1  d -1 ) in the presence of Fe, Zn, and Cu or the HRT was 14 h (2.6 g SO 4 2-  l -1  d -1 ) but the COD/SO 4 2- ratio was reduced to 0.67. The fully optimized conditions of the UASB reactor were set at an HRT of 16 h, SLR of 1.5 g SO 4 2-  l -1  d -1 , and a COD/SO 4 2- ratio of 1.0.

Soil and water bioengineering is a technology that encourages scientists and practitioners to combine their knowledge and skills in the management of ecosystems with a common goal to maximize benefits to both man and the natural environment. It involves techniques that use plants as living building materials, for: (i) natural hazard control (e.g., soil erosion, torrential floods and landslides) and (ii) ecological restoration or nature-based re-introduction of species on degraded lands, river embankments, and disturbed environments. For a bioengineering project to be successful, engineers are required to highlight all the potential benefits and ecosystem services by documenting the technical, ecological, economic and social values. The novel approaches used by bioengineers raise questions for researchers and necessitate innovation from practitioners to design bioengineering concepts and techniques. Our objective in this paper, therefore, is to highlight the practice and research needs in soil and water bioengineering for reconciling natural hazard control and ecological restoration. Firstly, we review the definition and development of bioengineering technology, while stressing issues concerning the design, implementation, and monitoring of bioengineering actions. Secondly, we highlight the need to reconcile natural hazard control and ecological restoration by posing novel practice and research questions., (Copyright © 2018. Published by Elsevier B.V.)

In the present article, optimization of process variables has been done to maximize the removal efficiency of toxic HCl gas in a submerged self-priming venturi scrubber. Response surface methodology with central composite design has been chosen to predict the effect of process variables on the removal efficiency. A quadratic equation was found from this study to predict the removal efficiency and from the ANOVA test, the significance of process variables was evaluated. Regression analysis confirmed the suitability of the developed model by the higher R 2 square value (0.9717). Optimum conditions were obtained as 55.18 m s -1 of throat gas velocity, 405.10 ppm of inlet HCl concentration and 0.0038 N of NaOH concentration in scrubbing liquid to achieve 90.80% of the HCl removal efficiency.

Wet electrostatic precipitators (WESPs) are modern-era pollution control systems specifically designed to capture ultrafine particles as well as acid mist, highly resistive and sticky particles; however, this requires the use of expensive corrosion-resistant metal alloys. The work presented here is part of a continuing study at Ohio University aimed at reducing the cost of WESPs by using a novel combination of a polymer collector surfaces with a hybrid composite discharge electrode. In this study, a hybrid composite discharge electrode was tested, for the first time, inside a semi-pilot-scale experimental setup, with collection surfaces consists of a vertical array of strands. Particle laden gases were passed through this array of polymer ropes, which were kept wet by a small flow of water. The discharge electrodes were composite laminates of carbon fibers in a polymer matrix enclosing a metal mesh. The preliminary results showed that this new integrated system of composite discharge electrode and polymer collector surfaces can match or exceed the performance of a conventional metal alloy electrostatic precipitator (ESP) with metal discharge electrodes. There are additional advantages due to the system being compact, lightweight, and highly corrosion resistant. Implications: This study focused on integrating and assessing performance of a novel hybrid composite electrode (HCE) inside semi-pilot novel cross-flow electrostatic precipitator at conditions typically observed in coal-fired power plant exhausts. The results were collected for particulate collection efficiencies and were compared with a rigid metal electrode. The HCE outperformed metal electrode by showing higher particulate collection efficiency. This result showcases substantial potential for these two new technologies (HCE and cross-flow system) as a substitute for conventional metal based wet ESPs.

Enhanced understanding of light non-aqueous phase liquid (LNAPL) infiltration into sandy porous medium is significant to the effective design of remediation strategies. A system for buried pipeline leakage in 2-D sandbox was conducted to investigate the migration of diesel through a sandy porous medium, and the system could also be conducted to investigate groundwater remediation. Two groups of experiments were carried out. The first experiment consisted of diesel infiltration into a fine sand matrix. We could notice that diesel spilled in dry sand layer at a constant speed and the diesel front kept longitudinal movement due to the gravity before it arrived at the edge of the capillary zone. The diesel front broadened as a whole because of the capillary force jacking after it reached the capillary zone. Finally, the bulk of the diesel was contained on top of the capillary zone. To protect groundwater, the second experiment consisted of remediating soils and groundwater. The results indicated that the voltage of electrocoagulation apparatus had a great influence on the treatment effect, and the removal rate of diesel was found to be more than 90% with a constant voltage of 20 V. The efficiency of groundwater remediation was influenced by the flow velocity, and it took 11 h when the flow velocity was 2.089 L/min. To summarize, the research was conducive to the study on diesel pollution control and pollution prediction.

Heavy metal contamination is a severe environmental issue over the world. A lot of work has been done to develop effective stabilizers. In the present work, hydrothermal carbon-modified magnesium silicate (MS-C) was synthesized and used for the remediation of two heavy metal-polluted soils with different physicochemical properties. Soil samples were exposed to different doses of MS-C over 60 days (1, 3, and 5 wt%). The toxicity characteristic leaching procedure (TCLP) and the community bureau of reference sequential extraction procedure (BCR) were used to evaluate the remediation efficiency. The bioavailability of heavy metals in both soils was reduced by 20-86.7%, and the toxicity of heavy metals was reduced by 26.6-73.2% after MS-C added. Meanwhile, soil pH and water soluble organic carbon (WSOC) were increased. In addition, soil microbial biomass was increased, which indicated the improvement of soil condition. The immobilization of heavy metals was mainly caused by electrostatic attraction and cation exchange between MS-C and heavy metals. The significantly negative correlation between extractable heavy metals and pH/WSOC indicated the positive role of pH/WSOC in metal stabilization. Thus, this new stabilizer holds great application potentials for both single and multi-metal-contaminated soil remediation. ᅟ Graphical abstract.

Spent mushroom substrate (SMS) as an organic amendment to plant production has received increasing attention on soil phytoremediation. However, organic amendments are known to contribute to greenhouse gas (GHG) emission from soils. Castor oil plant has a high biomass production and phytoremediation potential for heavy metal-contaminated soils. In the present study, the roles of SMS on phytoremediation efficiency of castor oil plant (Ricinus communis L.) from cadmium (Cd) and nickel (Ni)-contaminated soils were investigated, and the impact of SMS application on methane emission from the contaminated soil were evaluated. Pot experiments with SMS-amended and unamended contaminated soils were conducted to investigate Cd and Ni accumulation in R. communis and CH 4 emission. After growing for 3 months in soils with the addition of Cd (10 mg/kg) and Ni (at rates of 200 and 600 mg/kg), the dry biomass and the concentrations of Cd and Ni in the R. communis were measured, and the mobility factors for Cd and Ni were calculated. To assess methane emission, CH 4 fluxes and potential rates of CH 4 production and oxidation were measured pre- and post-incubation. SMS addition significantly improved the growth of R. communis and gave 19.15~82.46% more dry weight as compared to the single plant cultivation in the contaminated soils. SMS also increased plant Cd uptake and the total amount of Cd accumulation in R. communis increased by 28.1-152.1%, respectively, in signal Cd treatment and Cd-Ni complexation treatment, as compared to the single plant cultivation. The high values of mobility factor for Cd in single plant cultivation and co-application of SMS and R. communis pointed to the potential of R. communis to the Cd mobilization from the contaminated soils. Moreover, the addition of SMS tended to stimulate CH 4 uptake that the average increases in CH 4 uptake rate were 3.84-fold (in controls) and 2.91-fold (in single Cd treated soils) by the co-application of SMS and R. communis as compared to the single plant cultivation. The results suggested that the application of SMS could improve the growth of R. communis in Cd and Ni-contaminated soil, enhance heavy metal bioaccumulation, and stimulate soil CH 4 uptake. Therefore, SMS might be useful for enhancing phytoremediation of heavy metals and mitigate CH 4 emission from the contaminated soil. In addition, results in the study implied that implementing carefully designed management strategies (e.g., application of organic residues) during contaminated soil remediation is a promising solution for agricultural waste management and soil phytoremediation.

Due to their simple layout and adaptability to various environments, straw checkerboards are widely used to control windblown sand in China. To fully understand the wind proofing and sand-fixing benefits of different board specifications, and to determine the restorative effects of straw checkerboard, we tested different sizes of checkerboard, determined their performance as a windbreak and in trapping shifting sand, and constructed models based on wind tunnel tests, enabling the wind speed flow field to be analysed. We also sampled the soil in areas where straw checkerboards had been established for several years and analysed the trends in soil physical and chemical properties over time. We found that all sizes of straw checkerboard effectively reduced the wind speed near the surface and formed a protected area, with the best protective effect achieved for a one-meter board. All sizes of straw checkerboard effectively intercepted windblown sand to form surface accumulation, with the one-meter board again showing the best performance. The use of a straw checkerboard also effectively improved the physical and chemical properties of soil and promoted ecological restoration. These results indicate that straw checkerboards are a low-cost engineering measure that could play an important role in desertification control and the ecological restoration of sandy land ecosystems.

The objective of this paper is to demonstrate an interdisciplinary strategy combining both engineering- and biology-based approaches for stormwater and wastewater treatment. The work involves a novel and environmentally friendly surface material that can withstand urban load over its design service life, allows preliminary treatment through filtration, and diverts water to the subsurface to conduct secondary treatment below the surface through phytoremediation via the extensive rooting systems of trees. The present study highlights an interdisciplinary low-impact development (LID) approach developed for a polluted industrial wastewater site, for a cleaner and greener environment. The LID system involves (i) rhizofiltration and phytoremediation methods for removing heavy metals and organic pollutants using a hybrid poplar and aspen species; (ii) porous infrastructure produced using industrial waste, referred to as geopolymer pavers; and (iii) use of Silva cells as a tree-friendly and load support system. The design of the pavers over the Silva cells is innovative as it can deal with rainwater runoff and urban transportation loads simultaneously. The proposed system has the ability to extract heavy metals that are common in urban runoff or domestic and industrial effluents thus preserving the ecosystem naturally. The test site is only 15 m 2 , but designed for a water-retention capacity of 2 m 3 (roughly 1:100 year design volume draining a 10 × 10 m parking lot), and remediation levels for Cu and Zn are expected to reach 180 mg/kg dry weight and 1200 mg/kg dry weight, respectively.

Modified Hummer's method has been used in this study to synthesize graphene oxide (GO) solution that was utilized for the fabrication of three-dimensional (3D) graphene sponges and their subsequent functionalization through a low-cost and facile vapor-based surface enhancement approach. The functionalized 3D-graphene sponge is an excellent absorbent, which can remove more than 3300 wt.% of crude oil (calculated with respect to the original sorbent mass). The functionalization of the obtained graphene sponges with trichloro (1H,1H,2H,2H-perfluorooctyl)silane enhanced their wettability properties due to the super-hydrophobic nature of the resulting materials characterized by the contact angles in water greater than 150°. Furthermore, their elastic compression modulus (estimated by conducting a series of compression tests) was about 22.3 kPa. The equilibrium modeling of the oil removal process, which was performed by plotting Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich isotherms, confirmed the properties of the fabricated 3D graphene sponges as exceptional absorbents for crude and diesel oil, which could be attributed to the oleophilic nature of graphene. Moreover, the obtained 3D graphene sponges could be regenerated via heat treatment, which was conducted to release the adsorbed species. After five adsorption-desorption cycles, the sorption capacity of the produced 3D graphene sponges towards crude oil reached 95% of the initial value.

Multiple free water surface flow constructed wetlands (multi-FWS CWs) are a variety of conventional water treatment plants for the interception of pollutants. This review encapsulated the characteristics and applications in the field of ecological non-point source water pollution control technology. The roles of in-series design and operation parameters (hydraulic residence time, hydraulic load rate, water depth and aspect ratio, composition of influent, and plant species) for performance intensification were also analyzed, which were crucial to achieve sustainable and effective contaminants removal, especially the retention of nutrient. The mechanism study of design and operation parameters for the removal of nitrogen and phosphorus was also highlighted. Conducive perspectives for further research on optimizing its design/operation parameters and advanced technologies of ecological restoration were illustrated to possibly interpret the functions of multi-FWS CWs.

Indoor pollution poses a serious threat to human health. Plants represent a sustainable but underexploited solution to enhance indoor air quality. However, the current selection of plants suitable for indoors fails to consider the physiological processes and mechanisms involved in phytoremediation. Therefore, the capacity of plants to remove indoor air pollutants through stomatal uptake (absorption) and non-stomatal deposition (adsorption) remains largely unknown. Moreover, the effects of the indoor plant-associated microbiome still need to be fully analyzed. Here, we discuss how a combination of the enhanced phytoremediation capacity of plants together with cutting-edge air-cleaning and smart sensor technologies can improve indoor life while reducing energy consumption., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

The wide occurrence of antibiotics in groundwater has raised serious concerns due to their impacts on humans and the ecosystem. Most of the research in groundwater remediation focuses on the exploitation of nano-materials. However, nano-materials have several disadvantages such as high production cost, rapid reduction in permeability, disposal problems, and high sensitivity to environmental conditions. To solve these issues, novel sodium alginate/graphene oxide hydrogel beads (GSA) were synthesised and their effectiveness as permeable reactive barrier (PRB) backfill material in the remediation of ciprofloxacin (CPX)-contaminated groundwater was tested. The adsorption of CPX onto GSA followed the pseudo-second-order kinetic model. The isotherm data followed the Freundlich model. The maximum adsorption capacity was 100 mg g -1 at pH 7.0. The adsorption process was sensitive to contact time, initial CPX concentration and ionic strength. However, it was not pH sensitive. Hydrophobic interaction, electrostatic interaction, ion exchange, H-bonding, and pore filling were proposed to be the main adsorption mechanisms. The effects of flow rate, influent CPX concentration, and ionic strength on the performance of PRB were confirmed through flow-through column experiments and by using a chemical non-equilibrium two-site model. Accordingly, a proper PRB was designed based on hydrogeological conditions. Finally, the lifetime and cost of the PRBs were calculated. The results obtained provided concrete evidence that GSA is a promising adsorbent material for PRBs applications in the remediation of CPX-contaminated groundwater., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Surveys of restored oyster reefs need to produce accurate population estimates to assess the efficacy of restoration. Due to the complex structure of subtidal oyster reefs, one effective and efficient means to sample is by patent tongs, rather than SCUBA, dredges, or bottom cores. Restored reefs vary in relief and oyster density, either of which could affect survey efficiency. This study is the first to evaluate gear (the first full grab) and survey (which includes selecting a specific half portion of the first grab for further processing) efficiencies of hand-operated patent tongs as a function of reef height and oyster density on subtidal restoration reefs. In the Great Wicomico River, a tributary of lower Chesapeake Bay, restored reefs of high- and low-relief (25-45 cm, and 8-12 cm, respectively) were constructed throughout the river as the first large-scale oyster sanctuary reef restoration effort (sanctuary acreage > 20 ha at one site) in Chesapeake Bay. We designed a metal frame to guide a non-hydraulic mechanical patent tong repeatedly into the same plot on a restored reef until all oysters within the grab area were captured. Full capture was verified by an underwater remotely-operated vehicle. Samples (n = 19) were taken on nine different reefs, including five low- (n = 8) and four high-relief reefs (n = 11), over a two-year period. The gear efficiency of the patent tong was estimated to be 76% (± 5% standard error), whereas survey efficiency increased to 81% (± 10%) due to processing. Neither efficiency differed significantly between young-of-the-year oysters (spat) and adults, high- and low-relief reefs, or years. As this type of patent tong is a common and cost-effective tool to evaluate oyster restoration projects as well as population density on fished habitat, knowing the gear and survey efficiencies allows for accurate and precise population estimates.

Eutrophication of urban rivers has caused severe environmental problems due to the pollution from point and diffuse sources. Although eutrophication can be alleviated by reducing the input to the river system, fast-treating terminal control technologies, especially under emergent situations, should be developed to reduce risks induced by eutrophication. The present study developed an emergency purification device based on dissolved air flotation (DAF) technology. After equipment commissioning and parameter optimization for applications in the field of engineering, the device was found to effectively remove total phosphorus, chlorophyll a, chemical oxygen demand, and turbidity in water by controlling the coagulant dosage and adjusting the gas-liquid mixing pump parameters. Dissolved air in water could enhance dissolved oxygen, and dissolved oxygen in polluted rivers could be raised from 0.2-2 mg/L to 3-3.5 mg/L. Removal of total nitrogen was poor because the majority of nitrogen contents were dissolved. Finally, DAF has been proven to be a promising technology due to its ease of implementation, low equipment investment requirement, and low operation cost.

In this study, the treatment of mature landfill leachate is evaluated by oxidation with hydrogen peroxide (H 2 O 2 ) combined with adsorption in a granular activated carbon (GAC) fixed bed column to determinate the increase in the biodegradability index, the reduction of chemical oxygen demand (COD) as well as the increase in the useful life of the GAC bed. The sample leachate from Loma de Los Cocos Landfill (Cartagena de Indias, Colombia) has a very low biodegradability ratio ranging from 0.034 to 0.048 that makes it difficult to meet the required water quality level according to the regulations. The COD removal is initially monitored in the H 2 O 2 oxidation treatment process. The operating conditions such as pH, H 2 O 2 dosage, and the reaction time are optimized in this process based on the percentage of COD removal. A maximum COD removal of 29.9% is achieved at an initial H 2 O 2 concentration of 5000 mg L -1 with a pH of 8 and the reaction time of 60 min. The hybrid treatment by H 2 O 2 -GAC achieved 97.3% COD removal and 116% increase in the biodegradability ratio (from 0.072 to 0.134) while this ratio was increased by 6.5% with H 2 O 2 alone. Moreover, the useful life of the GAC bed is increased from 45 min in the column fed with raw leachate to 170 min in the column fed with pretreated leachate and 5000 mg L -1 of H 2 O 2 at pH of 8 that subsequently increased the activated carbon adsorption capacity. An adsorption model for leachate treated with H 2 O 2 is also developed.

Among various adsorbents studied, sulfur-impregnated activated carbon is one of the most promising adsorbents for mercury removal from flue gas. However, a large amount of spent activated carbons containing high content of mercury are generated after adsorption. To make the adsorption a more viable option, the regeneration and reuse of the spent activated carbon should be considered. The purpose of this study is to develop a novel technique for bioregeneration of sulfur-impregnated activated carbons after adsorption of mercury from flue gases by sulfur-oxidizing bacteria. The optimal operating parameters for this bioregeneration process were studied using central composite design (CCD) and response surface methodology (RSM). Results showed that the sulfur oxidation rate was increased with increasing activated carbon dosage. Furthermore, the increase of inoculum size only caused a slight increase of sulfur oxidation rate in the bioregeneration. The maximum mercury removal efficiency of more than 50% was obtained at 10% (w/v) activated carbon dosage and 20% (v/v) inoculum size. After the bioregeneration process, Brunauer-Emmett-Teller (BET) surface area and micropore volume of spent activated carbon increased due to the bio-oxidation of mercury bearing sulfur on the surface of activated carbons.

The intensive industrial development and urbanization, as well as the negligible return of hazardous components to the deeper layers of the Earth, increases the contamination load on the noosphere (i.e., the new status of the biosphere, the development of which is mainly controlled by the conscious activity of a human being). The need for reducing the spread and mobility of contaminants is growing. The insights into the role of the tree in the reduction of contaminant mobility through its life cycle are presented to show an important function performed by the living matter and its products in reducing contamination. For maintaining the sustainable development, natural materials are often used as the media in the environmental protection technologies. However, due to increasing contamination intensity, the capacity of natural materials is not sufficiently high. Therefore, the popularity of engineered materials, such as biochar which is the thermochemically modified lignocellulosic product, is growing. The new approaches, based on using the contaminant footprint, as well as natural (biogeochemical) and engineered barriers for reducing contaminant migration and their application, are described in the paper.

Pharmaceuticals and personal care products (PPCPs) are an extraordinary and diverse group of chemicals used in veterinary medicine, agriculture, and for human health and cosmetics care. They are considered emerging contaminants and have raised great concern in recent years. Among the PPCPs, ibuprofen (IBP) is one of the most known non-steroidal anti-inflammatory drugs, which has been found at a high concentration in irrigation water in the USA and showed harmful effect for organisms. This study examined IBP degradation performance by an electrokinetic process coupled with 24-96 cm 2 of RuO 2 /Ni foam (RN) electrodes applied 1-3 V cm -1 potential gradient for 5-9 days. The electroosmosis permeabilities (k e ) and the treatment efficiency of IBP increased from 1.5 × 10 -4 to 1.8 × 10 -4  cm 2  V -1  s -1 and from 65.4 to 78.4%, respectively, as the potential gradient increased from 1 to 3 V cm -1 . The k e values also increased with electrode area, but it was much less insignificant than that of the potential gradient. Prolonging the treatment time and increasing the electrode area only enhanced the IBP remediation efficiency by a trivial amount. The degradation mechanism was more critical for IBP remediation than was the electrokinetic (EK) removal mechanism. A cost analysis revealed that processing fluid accounted for 84.1-87.6% of the operation cost. The electrode characteristics and the treatment mechanism are also discussed. This study confirmed that the IBP-contaminated soil was successfully remediated by electrokinetic process coupled with RN electrodes.

Two prominent polybrominated diphenyl ether (PBDE) congeners have been included in the persistent organic pollutant list, 2,2',4,4',5-tetrabromodiphenyl ether (BDE-99) and 2,2,4,4'-tetrabromodiphenyl ether (BDE-47), which have been detected in treated municipal wastewater, river water, and sediments in China. A lab-scale column experiment was established to investigate the effects of the competitive sorption of BDE-47 on BDE-99 biodegradation and migration in two types of river-based aquifer soils during groundwater recharge with reclaimed water. Two types of recharge columns were used, filled with either silty clay (SC) or black carbon-amended silty clay (BCA). The decay rate constants of BDE-99 in the BCA and SC systems were 0.186 and 0.13 m -1 in the single-solute system and 0.128 and 0.071 m -1 in the binary-solute system, respectively, showing that the decay of BDE-99 was inhibited by the coexistence of BDE-47. This was particularly evident in the SC system because the higher hydrophobicity of BDE-99 determined the higher affinity and competition for sorption sites onto black carbon. The biodegradation of BDE-99 was suppressed by the coexistence of BDE-47, especially in the SC system. Lesser-brominated congeners (BDE-47 and BDE-28) and higher-brominated congeners (BDE-100, BDE-153, BDE-154, and BDE-183) were generated in the four recharge systems, albeit at different ratios. Bacterial biodiversity was influenced by the presence of BDE-47 in the SC system, while it had no significant effect on the BCA system, because the high sorption capacity of black carbon on the hydrophobic PBDEs effectively reduced their toxicity. The ranking order of the most abundant classes changed markedly due to the coexistence of BDE-47 in both the SC and BCA systems. The ranking order of the most abundant genera changed from Azospira, Methylotenera, Desulfovibrio, Methylibium, and Bradyrhizobium to Halomonas, Hyphomicrobium, Pseudomonas, Methylophaga, and Shewanella, which could be involved in PBDE degradation.

Groundwater denitrification bioreactors under limited phosphorus conditions were studied in column experiments using four types of plant-chips. When the phosphate-P concentration in the influent increased from 0.04mg/L to 0.4mg/L, the nitrate removal ratio increased from 61.6% to 86.1% in reed, from 7.2% to 12.6% in Japanese cedar, from 37.0% to 73.6% in Moso bamboo, and from 19.2% to 50.5% in Lithocarpus edulis. The carbon source of the denitrifiers' growth was indicated by the content of acid detergent soluble organic matter in the chips. Furthermore, according to the modified Michaelis-Menten-type equation proposed in the study, the denitrification rate was largely limited by the phosphate-P concentration in reed and L. eduilis, and by the dissolved organic carbon (DOC) in Japanese cedar. Denitrification in Moso bamboo was affected by both phosphate-P and DOC. Besides the DOC, phosphorus emerged as an important limiting element of denitrification in some bioreactor plant-chips., (Copyright © 2018 Elsevier B.V. All rights reserved.)