Development of an electrochemical separation-Rhodopseudomonas palustris electrolysis cell-coupled system for resourceful treatment of mature leachate landfill.

Electrochemical technology is a promising technique for separating ammonia from mature landfill leachate. However, the accompanying migration and transformation of coexisting pollutants and strategies for further high-value resourceful utilization of ammonia have rarely received attention. In this study, an electrochemical separation-Rhodopseudomonas palustris electrolysis cell coupled system was initially constructed for efficient separation and conversion of nitrogen in mature landfill leachate to microbial protein with synchronously tracking the transport and conversion of coexisting heavy metals accompanying the process. The results revealed that ammonia concentration in the cathode increased from 40.3 to 49.8% with increasing the current density from 20 to 40 mA/cm2, with less than 3% of ammonia transformation to NO2--N and NO3--N. During ammonia separation, approximately 95% of HM-DOMs (Cr, Cu, Ni, Pb, and Zn) were released into the anolyte due to humus degradation and further diffused to the cathode. A significant correlation was observed between the releases of HM-DOMs. Cu-DOMs accounted for 70.2% of the total Cu content, which was the highest proportion among the heavy metals (HMs). Among the HMs in anolyte, 57.4% of Pb, 52.5% of Ni, and 50.6% of Zn diffused to the cathode, and most of the HMs were removed in the form of hydroxide precipitations due to heavy alkaline catholyte. Compared with the open-circuit condition, the utilization efficiency of NH4+-N in the R. palustris electrolysis cell increased by 445.1% with 47% and 50% increases in final NH4+-N conversion rate and R. palustris biomass, respectively, due to bio-electrochemical enhanced phototrophic metabolism and acid generation for buffering the strong alkalinity of the electrolyte to maintain suitable growth conditions for R. palustris.

Photochemical behaviors of sludge extracellular polymeric substances from bio-treated effluents towards antibiotic degradation: Distinguish the main photosensitive active component and its environmental implication.

Activated sludge extracellular polymeric substances (ASEPSs) comprise most dissolved organic matters (DOMs) in the tail water. However, the understanding of the link between the photolysis of antibiotic and the photo-reactivity/photo-persistence of ASEPS components is limited. This study first investigated the photochemical behaviors of ASEPS's components (humic acids (HA), hydrophobic substances (HOS) and hydrophilic substances (HIS)) separated from municipal sludge's EPS (M-EPS) and nitrification sludge's EPS (N-EPS) in the photolysis of sulfadiazine (SDZ). The results showed that 60% of SDZ was removed by the M-EPS, but the effect in the separated components was weakened, and only 24% - 39% was degraded. However, 58% of SDZ was cleaned by HOS in N-EPS, which was 23% higher than full N-EPS. M-EPS components had lower steady-state concentrations of triplet intermediates (3EPS*), hydroxyl radicals (·OH) and singlet oxygen (1O2) than M-EPS, but N-EPS components had the highest concentrations (5.96 ×10-15, 8.44 ×10-18, 4.56 ×10-13 M, respectively). The changes of CO, C-O and O-CO groups in HA and HOS potentially correspond to reactive specie's generation. These groups change little in HIS, which may make it have radiation resistance. HCO-3 and NO-3 decreased the indirect photolysis of SDZ, and its by-product N-(2-Pyrimidinyl)1,4-benzenediamine presents high environmental risk.

A novel alginate-embedded magnetic biochar-anoxygenic photosynthetic bacteria composite microspheres for multipollutant removal: Mechanisms of photo-bioelectrochemical enhancement and excellent reusability performance.

Existing wastewater treatment technologies face the key challenge of simultaneously removing emerging contaminants and nutrients from wastewater efficiently, with a simplified technological process and minimized operational costs. In this study, a novel alginate-embedded magnetic biochar-anoxygenic photosynthetic bacteria composite microspheres (CA-MBC-PSB microspheres) was prepared for efficient, cost-effective and one-step removal of antibiotics and NH4+-N from wastewater. Our results demonstrated that the CA-MBC-PSB microspheres removed 97.23% of sulfadiazine (SDZ) within 7 h and 91% of NH4+-N within 12 h, which were 21.23% and 38% higher than those achieved by pure calcium alginate-Rhodopseudomonas palustris microspheres (53% and 45.7%), respectively. The enhanced SDZ and NH4+-N removal were attributed to the enhanced photoheterotrophic metabolism and excretion of extracellular photosensitive active substances from R. Palustris through the photo-bioelectrochemical interaction between R. Palustris and magnetic biochar. The long-term pollutants removal performance of the CA-MBC-PSB microspheres was not deteriorated but continuously improved with increasing ruse cycles with a simultaneous removal efficiency of 99% for SDZ and 92% for NH4+-N after three cycles. The excellent stability and reusability were due to the fact that calcium alginate acts as an encapsulating agent preventing the loss and contamination of R. palustris biomass. The CA-MBC-PSB microspheres also exhibited excellent performance for simultaneous removal of SDZ (89% in 7 h) and NH4+-N (90.7% in 12 h) from the secondary effluent of wastewater treatment plant, indicating the stable and efficient performance of CA-MBC-PSB microspheres in practical wastewater treatment.

Magnetic Fe-doped silicon carbide induced microwave activated persulfate for decabromodiphenyl ether removal: Mechanism and unique degradation pathway.

In this work, the magnetic nanocomposite Fe@SiC was prepared by a hydrothermal method and determined by SEM, XRD, XPS, FTIR and VNA. Fe3O4 particles were loaded onto SiC with great success, and the synthesized composites had favorable microwave absorption properties. Fe@SiC was used to activate persulfate in a microwave field for the degradation of BDE209 in soil. Specifically, the synergistic interaction between microwaves and Fe@SiC showed excellent catalytic performance in activating PS to degrade BDE209 (90.1% BDE209 degradation in 15 min). The presence of •OH, O2•- and 1O2 was demonstrated based on quench trapping and EPR experiments. LC‒MS was applied to determine the intermediates and propose the possible degradation pathway for BDE209 in the MW/Fe@SiC/PS system, and it was found that BDE209 produced almost no lower brominated diphenyl ethers. Therefore, the toxicity of BDE209 was found to be reduced using toxicity assessment software. Overall, this work provides an effective approach for the degradation of BDE209 in environmental remediation.

Simultaneous adsorption of As(III) and Pb(II) by the iron-sulfur codoped biochar composite: Competitive and synergistic effects.

Simultaneous elimination of As(III) and Pb(II) from wastewater is still a great challenge. In this work, an iron-sulfur codoped biochar (Fe/S-BC) was successfully fabricated in a simplified way and was applied to the remediate the co-pollution of As(III) and Pb(II). The positive enthalpy indicated that the adsorption in As-Pb co-pollution was an endothermic reaction. The mechanism of As(III) removal could be illustrated by surface complexation, oxidation and precipitation. In addition to precipitation and complexation, the elimination mechanism of Pb(II) also contained ion exchange and electrostatic interactions. Competitive and synergistic effects existed simultaneously in the co-contamination system. The suppression of As(III) was ascribed to competitive complexation of the two metals on Fe/S-BC, while the synergy of Pb(II) was attributed to the formation of the PbFe2(AsO4)2(OH)2. Batch experiments revealed that Fe/S-BC had outstanding ability to remove As(III) and Pb(II), regardless of pH dependency and interference by various coexisting ions. The maximum adsorption capacities of the Fe/S-BC for As(III) and Pb(II) were 91.2 mg/g and 631.7 mg/g, respectively. Fe/S-BC could be treated as a novel candidate for the elimination of As(III)-Pb(II) combined pollution.

Remediation of cadmium and lead contaminated soils using Fe-OM based materials.

Iron oxide-lignin composites (GLS) were prepared based on the significant role of Fe-OM in the environmental behaviour of heavy metals and lignin binding with iron oxide preferentially in soil. GLS was applied in Cd/Pb immobilization and the stability under acid rain was investigated. The results show that the iron oxide appeared weakly crystalline or amorphous similar to 2-line ferrihydrite after the addition of lignin. Agglomerates of nanoparticles with higher adsorption capacity were observed for GLS. The mobility factor (MF) of Cd/Pb in the soil decreased rapidly after adding GLS. At the 3% dosage, the MF of Cd and Pb in the soil was decreased by 58.94% and 78.15% respectively, which was approximately 5 times that of goethite (GE). The mobile and exchangeable Cd/Pb were converted to organic, amorphous Fe oxide-bound and residue fractions. Under acid rain conditions, MF continues to decline for the GLS group, increasing the organic and amorphous Fe oxide-bound fractions, while for control group (CK) and GE, the trend was the opposite. Lignin could inhibit iron oxide dissolution and stabilize the combination of Cd/Pb and iron oxides in soil. The better stability performance of GLS for Cd/Pb may be related to the higher adsorption capacity and microstructural difference after iron oxide combined with lignin.

Peroxydisulfate activation by nano zero-valent iron graphitized carbon materials for ciprofloxacin removal: Effects and mechanism.

Since the discovery of the potential hazards of ciprofloxacin (CIP) to the ecosystem and human health, there has been an urgent need to develop effective technologies to solve the severe issue. In this work, the nanozero-valent iron graphitized carbon matrix (xFe@CS-Tm) were prepared via a hydrothermal method to activate peroxydisulfate (PDS) for degradation of CIP. Specifically, 0.5Fe@CS-T7 exhibited the excellent catalytic performance for PDS activation to degrade CIP. Moreover, the catalyst exhibited vigorous interference resistance at various pH values, in the presence of various inorganic anions and under humic acid conditions. The characterization results demonstrated that Fe was successfully embedded on the carbon matrix and became the active sites to promote ROS production. It is demonstrated that O2•- was the main active species rather than •OH and SO4•-, based on quench trapping, EPR experiments and steady state concentrations calculations. The possible pathways of CIP degradation were proposed using LC-MS results and density functional theory. The outcomes of the toxicity estimation software tool found that the toxicity of CIP was reduced. This study not only investigated a novel methodology for the degradation of antibiotic wastewater but also provides a feasible pathway for carbon-neutral wastewater treatment.

Role of sulfide-modified nanoscale zero-valent iron on carbon nanotubes in nonradical activation of peroxydisulfate.

Sulfamethoxazole (SMX) is highly persistent and difficult to remove, making it urgent to find an efficient method for alleviating the enormous environmental pressure of SMX. In this study, sulfide-modified nanoscale zero-valent iron on carbon nanotubes (S-nZVI@CNTs) was prepared to activate peroxydisulfate (PDS) for the degradation of SMX. The results showed that SMX was completely removed within 40 min (kobs=0.1058 min-1) in the S-nZVI@CNTs/PDS system. By analyzing quenching experiments and electron paramagnetic resonance (EPR), singlet oxygen (1O2) was the main active species of the S-nZVI@CNTs/PDS system. 1O2 might be mediated by the abundant carbonyl groups (CO) on carbon nanotubes through spectroscopic analyses. In addition, sulfur doping transitioned the activation pathway to a nonradical pathway. Spectroscopic analyses and electrochemical experiments confirmed that the formation of CNTs-PDS complexes and S-nZVI could promote electron transfer on the catalyst surface. Furthermore, the main degradation intermediates of SMX were identified, and five possible transformation pathways were proposed. The S-nZVI@CNTs/PDS system possessed advantages including high anti-interference (Cl-, NO3-, HA), a strong applicability, recyclability and a low PDS consumption, offering new insight into the degradation of antibiotic wastewater.

Carbon materials in persulfate-based advanced oxidation processes: The roles and construction of active sites.

Many researchers have paid more attention to the progress of carbon materials owing to their advantages, such as high activity, low cost, large surface area, high conductivity and high stability. Carbon materials have been widely used in persulfate-based advanced oxidation processes (PS-AOPs), especially for graphene (G), carbon nanotubes (CNTs) and biochar (BC). Various strategies are applied to promote their activity, however, up to now, the relationship between the structures of carbon materials and their activities in PS-AOPs has not been specifically reviewed. The methods to switch reaction pathway (radical and nonradical pathways) in carbon-persulfate-based AOPs have not been systematically explored. Hereon, this review illustrated the active sites of G, CNTs, BC and other carbon materials, and generalized the modification methods to promote the activity of carbon materials and to switch reaction pathway in PS-AOPs. The roles of carbon materials in PS-AOPs were discussed around reactive oxygen species (ROS) and the structures. ROS are frequently complex in AOPs, but main ROS generation is related to the active sites on carbon materials. The structures of carbon materials (e.g., metal-carbon bonds, the electron-deficient C atoms, unbalanced electron distribution and graphitized structures) play a decisive role in the nonradical pathway. Finally, future breakthroughs of carbon materials were proposed for practical engineering and multi-field application.

Quantitative analysis on the mechanism of Cd2+ removal by MgCl2-modified biochar in aqueous solutions.

In this study, a pristine biochar (BC) and MgCl2-modified biochar (MBC) were prepared using Pennisetum sp. straw for removing Cd2+ from aqueous solutions. Scanning electron microscope (SEM) imaging combined with energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), as well as the surface area and porosity analyses were used to reveal the physico-chemical characteristics of the pristine and modified adsorbents. Results suggested that MgCl2 impregnation during the synthesis had enhanced the specific surface area and pore volume of the biochar. Batch adsorption experiments indicated that the Cd2+ adsorption data of MBC fitted the Langmuir isothermal and pseudo-second order kinetic models, indicating a chemical adsorption was undergoing in the system. The maximum adsorption capacity of Cd2+ on MBC was 763.12 mg/g, which was 11.15 times higher than that of the pristine BC. The Cd2+ removal by MBC was mainly attributed to the mechanisms in an order: Cd(OH)2 precipitation (73.43%) > ion exchange (22.67%) > Cd2+-π interaction (3.88%), with negligible contributions from functional group complexation, electrostatic attraction and physical adsorption. The MBC could thus be used as a promising adsorbent for Cd2+ removal from aqueous solutions.

Removal of Cd from aqueous solution by chitosan coated MgO-biochar and its in-situ remediation of Cd-contaminated soil.

In this study, magnesium oxide biochar-chitosan composite (MgO-BCR-W) prepared through modification with MgCl2 and chitosan was investigated as an adsorbent for the removal of Cd from the aquatic and soil environment. Kinetic and thermodynamics revealed that the Cd(II) adsorption onto MgO-BCR-W was well fitted by pseudo-second-order and the Langmuir adsorption isotherm. The adsorption capacities of rice husk biochar (BCR) and MgO-BCR-W for Cd(II) reached 11.09 mg/g and 59.66 mg/g, respectively. Attractively, the computed values of RL ranged between 0 and 1, suggesting that the adsorption of Cd(II) onto MgO-BCR-W is favourable. Characterisations of the adsorbents revealed that the synergistic effect of surface complexation and precipitation mechanisms played a major role in the removal of Cd. In soil incubation experiment, the addition of MgO-BCR-W at the level of 2% was most effective in Cd stabilization compared to the control, which reduced the content of bioavailable Cd by 22.32%. Furthermore, it reduced the acid extractable Cd by 24.77%, while increased the residual Cd content by 22.24%. The results demonstrated that MgO-BCR-W could be used as an effective and eco-friendly adsorbent for Cd remediation in both water and soil environment.

Key roles of the crystal structures of MgO-biochar nanocomposites for enhancing phosphate adsorption.

The affinity of biochar (BC) adsorbing phosphate was weak, while generation of magnesium oxide (MgO)-BC nanocomposites that transformed the crystal structures of BC would change the adsorption processes in improving the phosphate adsorption. Hereon, four different crystal structure of absorbents were selected to illustrate why the crystal structures and surface properties of absorbents were of great importance for the phosphate adsorption. The results showed that MgO/KBC with higher combination degree between MgO and KBC could change the normal crystal structure (MgO/KBC1, MgO phase (dominant)) to C-Mg-O phase (dominant). Therefore, MgO/KBC could achieve highest adsorption rate (k2, 8.059 g mg-1 min-1) and qm (maximal adsorption capacity, 121.950 mg g-1) for phosphate adsorption among absorbents, and even it had high anti-interference capacity for anions and natural organic matter (NOM). The mechanisms of MgO/KBC for phosphate adsorption were hydrogen-bond interaction, inner-sphere complexation and surface chemical adsorption; adsorption of phosphate on MgO/KBC1 was mainly controlled by inner-sphere complexation (Mg-O-PO3H2-, Mg-O-PO3H2- species). In addition, the adsorbability of MgO/KBC for phosphate could be restored after recalcination, which further proved that an efficient nanocomposite, calcinated from waste biomass (fallen leaves), was proposed to control eutrophication.

Removal of Cu and Pb from contaminated agricultural soil using mixed chelators of fulvic acid potassium and citric acid.

This study investigated the application of a specific soil washing method to remove Cu and Pb from contaminated agricultural soil. To develop an efficient leaching agent of heavy metal compounds for use in farmland soil, a mixed chelator (MC) was prepared using potassium fulvic acid (PFA, 3.2%) and citric acid (CIT, 0.16 M) in a volume ratio of 4:1 (PFA:CIT = 4:1); the optimal solid-liquid ratio (S/L = 1:20), initial pH value (4.51) and contact time (360 min) were also explored. Under optimal conditions, the removal efficiencies of MC for Cu and Pb were 42.92% and 50.46%, respectively, both of which performed better than PFA (27.86% of Cu and 17.91% of Pb) and CIT (42.04% of Cu and 41.46% of Pb). The effective states, bioavailability and relative mobilities of Cu and Pb in soil were also efficiently reduced by MC, which also increased the stability of these elements, thereby lowering the risk to soil health. More importantly, MC not only had little effect on the soil physicochemical properties (e.g., pH, organic matter (OM), cation exchange capacity (CEC), ammonium nitrogen (AN), available phosphorus (AP) and rapidly available potassium (AK)), but also improved the restored soil. Furthermore, soil structure, surface elements and the enzyme activity did not exhibit significantly loss. Therefore, MC has great potential for remediating agricultural soil.

Effect of lignosulfonate on the adsorption performance of hematite for Cd(II).

Lignin is a precursor of humus in soil and sediment. Lignin can be separated from vascular plants in the form of lignosulfonate via pulping processes. On the other hand, composites of iron oxide and organic matter can adsorb heavy metals, and thus influence the migration of these heavy metals in the environment. In this paper, a hematite/lignosulfonate composite (HLS) was prepared via coprecipitation to compare the adsorption performance of hematite (α-Fe2O3) toward Cd(II) before and after the incorporation of lignosulfonate (LS). The HLS is found to exhibit a weakly crystalline structure and possess a large number of nanoscale particles. Specific surface area of HLS (291.97 m2/g) is about 11 times that of α-Fe2O3, and the pore volume of HLS (0.22 cm3/g) is twice that of α-Fe2O3. The adsorption of Cd(II) is well illustrated by the pseudo-second-order adsorption kinetics and the initial adsorption rate (h) of HLS is 13.83 times that of α-Fe2O3. The maximum adsorption capacities are significantly improved from 4.89-6.35 mg/g (α-Fe2O3) to 39.03-53.65 mg/g (HLS). A greater affinity and more favorable association between Cd(II) and HLS is observed via fitting models. The incorporation of LS provides HLS with significantly better adsorption properties toward Cd(II) than α-Fe2O3, as is further confirmed by FT-IR and XPS characterization. Fe-O-O-H and Fe-O-H structures as well as more hydroxyl groups are observed, which promote the adsorption performance since the process are mainly influenced by complexation via coordination bonds.

[Immobilization Impact of Goethite-Fulvic Acid Composites on Pb-Cd Contaminated Soil].

The Pearl River Delta region is the major economic zone of the Greater Bay Area:it presents a large number of industrial-mining enterprises and is interested by severe heavy metal pollution (mainly caused by Pb and Cd). The research and development of safe and efficient heavy metal remediation materials and technologies is fundamental in order to guarantee regional environmental quality and habitat safety. Goethite-fulvic acid composites were prepared using goethite minerals present in the red soils of the Pearl River Delta region by passivation repair, and were applied to immobilize Pb and Cd in a co-contaminated soil. The results showed that a higher ratio of fulvic acid in the composites enhanced the immobilization effect on Pb and Cd:the immobilization efficiency (IE) of Pb and Cd increased with the passivation time, and then stabilized. Additionally, the exchangeable and carbonate-bound fractions of Pb and Cd in the soil decreased, while the Fe-Mn oxide-bound and residual fractions increased. The cation exchange capacity (CEC), as well as the available K and NH4+-N in the soil increased after the application of the composite materials. We conclude that goethite-fulvic acid composites can be effectively applied to the remediation of Pb-Cd contaminated soil.

Di-(2-Ethylhexyl) Phthalate as a Chemical Indicator for Phthalic Acid Esters: An Investigation into Phthalic Acid Esters in Cultivated Fields and E-Waste Dismantling Sites.

Phthalic acid esters (PAEs) represent an ongoing pollution problem and have attracted extensive attention due to their ubiquitous presence in the environment. We investigated the distribution of 6 PAEs (benzyl butyl phthalate [BBP], dibutyl phthalate [DBP], di-(2-ethylhexyl) phthalate [DEHP], diethyl phthalate [DEP], dimethyl phthalate [DMP], and di-n-octyl phthalate [DnOP]) in cultivated soils, including vegetable fields and paddy fields, as well as the soils of E-waste dismantling sites. We also explored the relationship between the particle size of soils and the distribution of PAEs, put forward a novel method to forecast the occurrence and fate of PAEs in soils with DEHP used as a chemical indicator, and made a preliminary assessment of the potential ecological risks of the 6 target compounds in soils. The results showed that the detection rate of target PAEs was 100%, and that the concentrations of ∑6 PAEs ranged from 1.2 to 7.3 mg/kg in vegetable fields, 1.2 to 1.5 mg/kg in paddy fields, and 11.8 to 17.9 mg/kg in E-waste dismantling sites. In addition, DEHP exhibited the maximum concentrations (0.480-15.34 mg/kg) in all soil samples. The results also showed that in the wake of decreasing particle size, increasing soil organic carbon would enhance the sorption of PAEs in soils. Moreover, the correlation formula of DEHP successfully predicted the concentrations of other PAEs and ∑ 6 PAEs in soils, suggesting that DEHP could be a dependable chemical indicator for forecasting the environmental occurrence of PAEs in soils. Based on the residual levels in the trial sites and limited toxicity data, high risks to soil organisms are expected for DBP, DEP, and DEHP, and low-medium risks for BBP, DnOP, and DMP. Environ Toxicol Chem 2019;00:1-11. © 2019 SETAC.

Characterization of goethite-fulvic acid composites and their impact on the immobility of Pb/Cd in soil.

The coprecipitation of organic matter (OM) and minerals is a relatively common phenomenon in soil, and it has a significant influence on the surface properties and reactivity of minerals. In turn, the fate of pollutants in soil is greatly affected by the organic-mineral composites. In this study, goethite-fulvic acid (Ge-FA) composites with varying FA mass ratios in the range of 0-15% were synthesized by coprecipitation. The sample properties were studied using XRD, FTIR, SEM-EDS and N2 gas adsorption techniques. The influence of Ge-FA on the mobility of Pb/Cd in soil was investigated. The crystal forms of Ge-FA changed from goethite (FA≤4%) to hematite (FA≥5%), and the FA affected the FeO bond vibrations. These results demonstrated that FA was successfully introduced into the iron oxide. Ge-FA changed from a filamental morphology to an aggregate as the FA ratio increased. The coprecipitation resulted in blockages of iron oxides, thereby decreasing the specific surface area and pore volume. The adsorption amount of Pb(II) on Ge-FA increased as the FA ratio increased, but no significant change was observed for Cd(II). With the application of Ge-FA, the exchangeable concentrations of Pb and Cd in contaminated soil decreased by 42.4%-93.6% and 15.8%-43.7%, respectively. The exchangeable and carbonate bound fractions of Pb and Cd decreased and were transformed into the FeMn bound and residual fractions.

Adsorption of Cd(II) from aqueous solution by Pennisetum sp. straw biochars derived from different modification methods.

The adsorption mechanism of Cd (II) was investigated by Pennisetum sp. straw biochars (JBC) that were modified by two different methods: KMnO4 impregnation (JMB1) and H2O2 impregnation (JMB2). A scanning electron microscope and energy-dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), a Fourier transform infrared spectrometer (FTIR), and a Brunauer-Emmett-Teller (BET) specific surface area analysis were employed to examine the physicochemical characteristics of biochars. The Cd(II) adsorption kinetic fit, the Langmuir model well, and the maximum adsorption capacity occurred in the following order: JMB1 (90.32 mg/g) > JMB2 (45.18 mg/g) > JBC (41.79 mg/g), suggesting that JMB1 had an excellent adsorption performance. Finally, X-ray photoelectron spectroscopy (XPS) was used to explore the main adsorption mechanism. Our results showed that JMB1 was an excellent adsorbent in removing Cd(II) from aqueous solution.

The combined effects of surfactant solubilization and chemical oxidation on the removal of polycyclic aromatic hydrocarbon from soil.

A method for the remediation of polycyclic aromatic hydrocarbons (PAHs) contaminated soils was proposed involving a combination of surfactant-aided soil washing and chemical oxidation by activated persulfate (SP). In this study, Triton X-100 (TX-100) and SP was applied to the soil, either concurrently or sequentially. Results indicated that surfactant followed by amendment with a solution of SP, TX-100 + SP(l), was most effective in decreasing PAHs concentrations in a sandy loam soil (SS) and a silty clay soil (NS) from 1220 mg/kg and 2730 mg·kg-1 to 414 mg·kg-1 and 180 mg·kg-1, respectively. Compared with extraction alone and oxidation alone, TX-100 + SP(l) increased the removal of PAHs by 10-20%. TX-100 improved the degradation of 3-4 ring PAHs (M-PAHs) and 5-6 ring PAHs (H-PAHs) in SS, by approximately 8%-11%. The oxygenated polycyclic aromatic hydrocarbons (oxy-PAHs) including furans and xanthene exhibited greater reductions in soil when amended with the TX-100 and SP, than under TX-100 extraction or SP oxidation alone. Overall, increased removal of PAHs in contaminated soil can occur through simultaneous application of TX-100 and SP, relative to the sole use of TX-100 or SP. The sequential combination of surfactant and oxidant was most effective for the elimination of PAHs, especially for M-PAHs and H-PAHs in sandy loam contaminated soil.

Activation of persulfate with 3D urchin-like CoO-CuO microparticles for DBP degradation: A catalytic mechanism study.

Rational modification of the surface structure and interface structure can effectively optimize the catalytic performance and stability of a heterogeneous catalyst. A CoO-CuO bimetallic catalyst with a special urchin-like structure was prepared by a hydrothermal urea precipitation method. This carbon nanosphere template method significantly improves the dispersibility of the material. The special urchin-like nanorod structure expands the specific surface area, resulting in excellent adsorption performance and high catalytic performance. The materials were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The oxidative degradation mechanism of dibutyl phthalate (DBP) using sodium persulfate (SPS) activated by the CoO-CuO double metal oxide catalyst was explored. The synergy between the two metals gives the material a stable and highly catalytic ability.