Binding characteristics of Pb and Zn to low-temperature feces-based biochar-derived DOM revealed by EEM-PARAFAC combined with general and moving-window two-dimensional correlation analyses.

Pyrolysis carbonization of human feces has shown potential for converting feces biomass into a soil amendment. However, little is known about the interactions of DOM derived from feces-based biochar produced at low-temperature with heavy metals (HMs). In this study, the binding properties of Pb(II) and Zn(II) with DOM derived from feces-based biochar produced at low pyrolysis temperatures were investigated using EEM-PARAFAC combined with general, and moving-window two-dimensional correlation analyses (2D-COS). The results revealed that DOM from biochar produced at 280 °C exhibited a higher Pb(II) and Zn(II) affinity and more binding sites than DOM produced at 380 °C. The fulvic-like and humic-like components exhibited obvious fluorescence quenching after the heavy metal addition, and the complexes formed with Pb(II) and Zn(II) were more stable. C-H groups exhibited the fastest response to Pb(II) and Zn(II) binding in the FB280 DOM, while the COO- groups of carboxylic acids in the FB380 DOM exhibited the fastest response to Pb(II) and Zn(II). Moreover, the mutation concentration range of components and functional groups in DOM, as analyzed by MW2D-COS, was greater for Zn(II) than for Pb(II). These results provide a more detailed molecular-level understanding of the interaction mechanisms between heavy metals and feces-based biochar-derived DOM and the effect of HM concentration on DOM binding. Further, these results will help to provide a reasonable reference for feces management and feces-based biochar in controlling soil HMs.

Enhanced denitrification of dispersed swine wastewater using Ca(OH)2-pretreated rice straw as a solid carbon source.

In a pilot-scale packed bed reactor, the denitrification performance and microbial community structure of the dispersed swine wastewater treatment using calcium hydroxide (Ca(OH)2) pretreated rice straw as a carbon source were investigated. In a Ca(OH)2-pretreated rice straw supported denitrification system (Ca(OH)2-RS), the removal efficiency of NO3--N was 96.39% at an influent NO3--N load of 0.04 kg/(m3•d). Meanwhile, there was no obvious accumulation of NO2--N or chemical oxygen demand (COD) in the effluent of Ca(OH)2-RS. The contents of soluble microbial byproduct-like substances and tryptophan-like substances in the effluent of Ca(OH)2-RS were reduced by 46.2% and 43.4%, respectively, compared with the influent. Overall, the Ca(OH)2-pretreated rice straw system had a strong resistance to fluctuations in water quality conditions, such as influent NO3--N and COD concentrations. According to the microbial assay results, the Ca(OH)2 pretreatment enriched more denitrifying bacteria. Among them, Proteobacteria (42.33%) and Bacteroidetes (35.28%) were the dominant bacteria. Moreover, the main denitrifying functional bacteria, generanorank_f_Saprospiraceae (13.32%), norank_f_Porphyromonadaceae (4.22%), and Flavobacterium (3.25%), were enriched in Ca(OH)2-RS. This suggested that using Ca(OH)2-pretreated rice straw as a carbon source was a stable and efficient technology to enhance the denitrification performance of dispersed swine wastewater.

The Associations Between White Matter Disruptions and Cognitive Decline at the Early Stage of Subcortical Vascular Cognitive Impairment: A Case-Control Study.

OBJECTIVE: Emerging evidence suggests that white matter (WM) disruption is associated with the incidence of subcortical vascular cognitive impairment (SVCI). However, our knowledge regarding this relationship in the early stage of SVCI is limited. We aimed to investigate the associations between WM disruptions and cognitive declines at the early stage of SVCI. METHOD: We performed a case-control study, involving 22 cases and 19 controls. The cases were patients at the early stage of SVCI, which was defined as subcortical ischemic vascular disease with normal global cognitive measures (pre-SVCI). The controls were healthy people matched by age, sex, and education years. We assessed the differences in a battery of neuropsychological tests between the two groups, investigated the diffusion changes in 40 WM tracts among the participants via an atlas-based segmentation strategy, and compared the differences between the cases and controls by multiple linear regression analysis. We then evaluated the relationships between diffusion indices and cognitive assessment scores by Pearson's correlation. RESULTS: The pre-SVCI group exhibited significant differences in the Montreal cognitive assessment (MoCA), Rey-Osterrieth Complex Figure (R-O)-copy, and Trail Making Test (TMT)-B test compared with the controls. Compared with the controls, some long associative and projective bundles, such as the right anterior corona radiata (ACR), the right inferior fronto-occipital fasciculus (IFOF), and the left external capsule (EC), were extensively damaged in cases after Bonferroni correction (p < 0.05/40). Damages to specific fibers, such as the right ACR, IFOF, and posterior thalamic radiation (PTR), exhibited significant correlations with declines in MoCA, R-O delay, and the Mini-Mental State Examination (MMSE), respectively, after Bonferroni correction (p < 0.05/14). CONCLUSION: Long WM tracts, especially those in the right hemisphere, were extensively damaged in the pre-SVCI patients and correlated with declines in executive functions and spatial processing. Patients of pre-SVCI are likely at an ultra-early stage of SVCI, and there is a very high risk of this condition becoming SVCI.

A novel method based on membrane distillation for treating acid mine drainage: Recovery of water and utilization of iron.

Rapid and highly efficient treatment of acid mine drainage (AMD) is still challenging due to the low pH and high metal concentrations in it. This research focuses on a novel treatment method of AMD using direct contact membrane distillation (DCMD) and photocatalysis to recover water and utilize iron. In the DCMD process without pretreatment, the flux decreased by 93.38%. If pretreated by adding sodium oxalate, scale formation potential was effectively mitigated due to the removal of calcium and complexing of iron. For the treatment of the pretreated AMD (PAMD), 60% of water was recovered in the DCMD process with the flux decrease of 22%. The concentrate obtained from the DCMD process demonstrated high photocatalytic activity in the methylene blue (MB) degradation in an aqueous solution. In addition, the Fe (III)-oxalate complexes in the concentrate were reduced to insoluble Fe (II)-oxalate with visible light irradiation, which could be separated by sedimentation and used as a Fenton catalyst. Hence, this novel method exhibits great advantages on effectively inhibiting DCMD membrane fouling during AMD treatment, producing high-quality distillate with low conductivity, and realizing near zero-discharge of AMD.

Disrupted White Matter Networks from Subjective Memory Impairment to Amnestic Mild Cognitive Impairment.

BACKGROUND AND OBJECTIVE: Subjective memory impairment (SMI) is a preclinical stage prior to amnestic mild cognitive impairment (aMCI) along with the Alzheimer's disease (AD) continuum. We hypothesized that SMI patients had white matter (WM) network disruptions similar to those in aMCI patients. METHODS: We used diffusion-tensor magnetic resonance imaging and graph theory to construct, analyze, and compare the WM networks among 20 normal controls (NC), 20 SMI patients, and 20 aMCI patients. RESULTS: Compared with the NC group, the SMI group had significantly decreased global and local efficiency and an increased shortest path length. Moreover, similar to the aMCI group, the SMI group had lower nodal efficiency in regions located in the frontal and parietal lobes, limbic systems, and caudate nucleus compared to that of the NC group. CONCLUSION: Similar to aMCI patient, SMI patients exhibited WM network disruptions, and detection of these disruptions could facilitate the early detection of SMI.

A review of clay based photocatalysts: Role of phyllosilicate mineral in interfacial assembly, microstructure control and performance regulation.

Over the past decades, inspired by the outstanding properties of clay minerals such as abundance, low-cost, environmental benignity, high stability, and regularly arranged silica-alumina framework, researchers put much efforts on the interface assembly and surface modification of natural minerals with bare photocatalysts, i.e. TiO2, g-C3N4, ZnO, MoS2, etc. The clay-based hybrid photocatalysts have resulted in a rich database for their tailor-designed microstructures, characterizations, and environmental-related applications. Therefore, in this study, we took a brief introduction of three representative minerals, i.e. kaolinite, montmorillonite and rectorite, and discussed their basic merits in photocatalysis applications. After that, we summarized the recent advances in construction of stable visible-light driven photocatalysts based on these minerals. The structure-activity relationships between the properties of clay types, pore structure, distribution/dispersion and light absorption, carrier separation efficiency as well as redox performance were illustrated in detail. Such representative information would provide theoretical basis and scientific support for the application of clay based photocatalysts. Finally, we pointed out the major challenges and future directions at the end of this review. Undoubtedly, control and preparation of novel photocatalysts based on clays will continue to witness many breakthroughs in the arena of solar-driven technologies.

Clinoptilolite mediated activation of peroxymonosulfate through spherical dispersion and oriented array of NiFe2O4: Upgrading synergy and performance.

Inspired by the features of both transition metal oxide and natural clinoptilolite (flaky structure with suitable pore diameter and open skeleton structure), we adopted a robust strategy by immobilization of nickel ferrite nanoparticles (NiFe2O4) on the clinoptilolite surface via typical citric acid combustion method. The hybrid catalyst exhibited enhanced peroxymonosulfate (PMS) activation efficiency and bisphenol A (BPA) degradation performance. Calculated by effective equivalent of NiFe2O4, it is found that the reaction rate constant (k) of NiFe2O4/clinoptilolite/PMS system (0.1859 min-1) was 11.9 times higher than that of bare NiFe2O4/PMS system (0.0156 min-1), which demonstrated that catalyst would be conjugated to PMS or contaminant efficiently and renders the rapid degradation and mineralization in the presence of clinoptilolite. After comprehensive characterization analysis and DFT simulations, natural mineral carrier effect (i.e. decreased crystalline size, increased oxygen vacancy content, etc.), abundant surface-bonded and structural hydroxyl groups as well as effective bonding with iron or nickel ions charged for the potential activation mechanism of PMS by NiFe2O4/clinoptilolite composite. And it is indicated that not only •OH and SO4•-, but also 1O2 was involved into series reactions. Overall, this study put forward a green and promising technology for high-toxic wastewater treatment.

Immobilization of Cr(VI) in Soil Using a Montmorillonite-Supported Carboxymethyl Cellulose-Stabilized Iron Sulfide Composite: Effectiveness and Biotoxicity Assessment.

A novel composite of montmorillonite-supported carboxymethyl cellulose-stabilized nanoscale iron sulfide (CMC@MMT-FeS), prepared using the co-precipitation method, was applied to remediate hexavalent chromium (Cr(VI))-contaminated soil. Cr(VI)-removal capacity increased with increasing FeS-particle loading. We tested the efficacy of CMC@MMT-FeS at three concentrations of FeS: 0.2, 0.5, and 1 mmol/g, hereafter referred to as 0.2 CMC@MMT-FeS, 0.5 CMC@MMT-FeS, and 1.0 CMC@MMT-FeS, respectively. The soil Cr(VI) concentration decreased by 90.7% (from an initial concentration of 424.6 mg/kg to 39.4 mg/kg) after 30 days, following addition of 5% (composite-soil mass proportion) 1.0 CMC@MMT-FeS. When 2% 0.5 CMC@MMT-FeS was added to Cr(VI)-contaminated soil, the Cr(VI) removal efficiency, as measured in the leaching solution using the toxicity characteristic leaching procedure, was 90.3%, meeting the environmental protection standard for hazardous waste (5 mg/kg). The European Community Bureau of Reference (BCR) test confirmed that the main Cr fractions in the soil samples changed from acid-exchangeable fractions to oxidable fractions and residual fractions after 30 days of soil remediation by the composite. Moreover, the main complex formed during remediation was Fe(III)-Cr(III), based on BCR and X-ray photoelectron spectroscopy analyses. Biotoxicity of the remediated soils, using Vicia faba and Eisenia foetida, was analyzed and evaluated. Our results indicate that CMC@MMT-FeS effectively immobilizes Cr(VI), with widespread potential application in Cr(VI)-contaminated soil remediation.

Photo-electrocatalytic degradation of cyclic volatile methyl siloxane by ZnO-coated aluminum anode: Optimal parameters, kinetics, and reaction pathways.

Cyclic volatile methylsiloxanes (cVMSs) are widely used in industrial processes and consumer products, which have been reported to be potentially toxic to human health due to their persistence and bioaccumulation. In this study, a novel photo-catalytic zinc oxide (ZnO)-coated aluminum (ZnO@Al) anode was prepared by a facile hydrothermal epitaxial process for the purpose of degrading cVMSs in practical wastewater. Morphological data and compositional analysis showed a compact coating layer that had the characteristic peaks of ZnO. To optimize the degradation process, central composite design combined with response surface methodology was applied to acquire the optimum parameters of cVMSs removal, and results indicated the cVMSs removal efficiency was approximately 63.3% at the conditions of current density = 17.3 mA/cm2, initial pH of electrolyte = 7.8, plate distance = 18 mm, UV intensity = 90 W, and reaction time = 80 min. Furthermore, the photo-electrocatalytic degradation of cVMSs obeys the pseudo-first order kinetic reaction, and the anode exhibited high durability as the attenuation of cVMSs removal efficiency was <6% after four times reuse. It was also observed that with the application period of the anode was extended, the electroflocculation reaction gradually occurred. The FT-IR of the generated flocs and the total ion gas chromatograms mass spectrometer analysis unraveled the methyl groups in Si-CH3 could be easily attacked by hydroxyl radicals to form the intermediates of monohydroxy substituted products (m/z = 298, 372, and 446) and eventually short-chain carboxylic acids, alkyl radical and silicate. The effective removal of cVMSs by photo-electrocatalytic process using ZnO@Al anode provide significant implication in treatment of practical wastewater.

The Immobilization Effect of Natural Mineral Materials on Cr(VI) Remediation in Water and Soil.

The effects of sepiolite, montmorillonite, and attapulgite on the removal and immobilization of Cr(VI) in water and soil were studied. X-ray diffraction (XRD) characterizations showed that the purities of these three mineral materials decreased in the following order: montmorillonite > attapulgite > sepiolite, and that their surface molecular bond types were similar. The adsorption potential of Cr(VI) in aqueous solutions of the three mineral materials was in the following order: sepiolite > attapulgite > montmorillonite. The adsorption mechanism for attapulgite was consistent with the Freundlich isotherm adsorption model, whereas that for montmorillonite was more consistent with the Langmuir model. Sepiolite had a good fitting effect for both isothermal adsorption models. For montmorillonite and attapulgite, a lower pH corresponded to a higher removal of Cr(VI). For sepiolite, however, the removal efficiency of Cr(VI) from an aqueous solution was the lowest at a pH of approximately 5.0. The results of the soil toxicity characteristic leaching procedure showed that, following the addition of 15% sepiolite, attapulgite, or montmorillonite to the contaminated soil, Cr(VI) concentrations in the leachates decreased by 16.8%, 18.9%, and 15.9%, respectively, and the total Cr concentrations in the leachates were reduced by 21.2%, 29.2%, and 17.6%. Of the three mineral materials, attapulgite demonstrated the highest Cr(VI) immobilization efficiency in soil. This study emphasizes the effect of attapulgite on the immobilization of Cr(VI) in soil and aqueous solutions, thus providing a theoretical basis for the potential application of natural mineral material remediation of Cr(VI)-contaminated aqueous solutions and soils.

Network topology and machine learning analyses reveal microstructural white matter changes underlying Chinese medicine Dengzhan Shengmai treatment on patients with vascular cognitive impairment.

With the increasing incidence of cerebrovascular diseases and dementia, considerable efforts have been made to develop effective treatments on vascular cognitive impairment (VCI), among which accumulating practice-based evidence has shown great potential of the traditional Chinese medicine (TCM). Current randomized double-blind controlled trial has been designed to evaluate the 6-month treatment effects of Dengzhan Shengmai (DZSM) capsules, one TCM herbal preparations on VCI, and to explore the underlying neural mechanisms with graph theory-based analysis and machine learning method based on diffusion tensor imaging (DTI) data. A total of 82 VCI patients were recruited and randomly assigned to drug (45 with DZSM) and placebo (37 with placebo) groups, and neuropsychological and neuroimaging data were acquired at baseline and after 6-month treatment. After treatment, compared to the placebo group, the drug groups showed significantly improved performance in Alzheimer's Disease Assessment Scale-Cognitive subscale (ADAS-cog) score (p < 0.001) and the other cognitive domains. And with the reconstruction of white matter structural network, there were more streamlines connecting the left thalamus and right hippocampus in the drug groups (p < 0.001 uncorrected), with decreasing nodal efficiency of the right olfactory associated with slower decline in the general cognition (r = -0.364, p = 0.048). Moreover, support vector machine classification analyses revealed significant white matter network alterations after treatment in the drug groups (accuracy of baseline vs. 6-month later, 68.18 %). Taking together, the present study showed significant efficacy of DZSM treatment on VCI, which might result from white matter microstructure alterations and the topological changes in brain structural network.

Comparison of four test methods for toxicity evaluation of typical toxicants in petrochemical wastewater on activated sludge.

The shock impact of toxic pollutants in petrochemical wastewater on the activated sludge in biological treatment system is a key factor restricting the treatment efficiency. It is necessary to evaluate the toxicity of these pollutants by appropriate methods. In this study, four test methods were used to evaluate the toxicity of characteristic organic pollutants in petrochemical wastewater including 2,4-dichlorophenol, formaldehyde and pyridine, as well as one frequently-used reference toxicant 3,5-dichlorophenol. The sensitivity, accuracy and response time were compared among these methods: the oxygen consumption rate inhibition method (OCRIM), the dehydrogenase activity inhibition method (DAIM), the nitrification rate inhibition method (NRIM) and the growth rate inhibition method (GRIM). Principal component analysis was used to evaluate the correlation among the results of different methods. The OCRIM was comprehensively outstanding with the highest correlation between concentration and inhibition ratio (R2 values were all higher than 0.9854), good sensitivity, best accuracy (error value of the effective concentrations below 0.15 mg/l) and fastest response (<40 min). The sensitivity of the NRIM was found to be the highest in this study (10% effective inhibition concentration (EC10) value of 3,5-dichlorophenol was only 0.03 mg/l). Therefore, combined tests of OCRIM and NRIM were suggested.

Effective mineralization of quinoline and bio-treated coking wastewater by catalytic ozonation using CuFe2O4/Sepiolite catalyst: Efficiency and mechanism.

In this study, CuFe2O4 nanocomposite loaded on natural sepiolite (CuFe2O4/SEP) was prepared by the citrate sol-gel method. CuFe2O4/SEP was characterized by X-ray diffraction, Brunauer-Emmett-Teller adsorption analysis, scanning electron microscopy, and energy dispersive spectroscopy. The CuFe2O4/SEP composite was stable and showed an excellent catalytic activity for ozonation. The efficiency of quinoline mineralization in the catalytic ozonation with CuFe2O4/SEP was 90.3%, and this value was 5.4 times higher than that of the uncatalyzed ozonation (16.8%). The quinoline mineralization followed a pseudo first-order kinetics with all the catalysts. The rate constant for the mineralization of quinoline by ozonation in the presence of CuFe2O4/SEP was 0.0885 min-1, which was 16.7 times higher than that in ozone alone (0.0053 min-1). Radical scavenging tests revealed that hydroxyl radical (OH) and superoxide radical (O2-) were the reactive oxygen species (ROS) in the quinoline degradation. In the presence of CuFe2O4/SEP, ozone and hydrogen peroxide were rapidly converted into the ROS. Although neutral and alkaline pH were more beneficial for the quinoline mineralization, CuFe2O4/SEP exhibited significant catalytic activity even under acidic conditions. Meanwhile, five-cycle successive tests suggested that CuFe2O4/SEP was recyclable and hence, stable. Furthermore, the feasibility of the catalytic ozonation for the treatment of biologically treated coking wastewater was evaluated. The catalytic ozonation resulted in 57.81% total organic carbon removal efficiency at 60 min, which was 2.9 times higher than that in the uncatalyzed ozonation (19.99%).

Spectroscopic study on transformations of dissolved organic matter in coal-to-liquids wastewater under integrated chemical oxidation and biological treatment process.

A large amount of wastewater containing various toxic organic contaminants is produced during coal-to-liquids process. In this study, several spectroscopic methods were used to monitor the transformation of organic pollutants during an integrated chemical oxidation and biological process. The results showed that the hydrophobic acid fraction increased after Fenton oxidation, which was likely due to the production of small-molecule organic acids. Soluble microbial products were generated during biological treatment processes, which were degraded after ozonation; meanwhile, the hydrophilic base and acid components increased. Ultraviolet-visible spectroscopic analysis indicated that peaks at the absorption wavelengths of 280 and 254nm, which are associated with aromatic substances, were detected in the raw water. The aromatic substances were gradually removed, becoming undetectable after biological aeration filter (BAF) treatment. Fourier transform infrared spectroscopy analysis revealed that the functional groups of phenols; benzene, toluene, ethylbenzene, and xylene (BTEX); aromatic hydrocarbons; aliphatic acids; aldehydes; and esters were present in raw wastewater. The organic substances were oxidized into small molecules after Fenton treatment. Aromatic hydrocarbons were effectively removed through bioadsorption and biodegradation after BAF process. Biodegradable organic matter was reduced and finally became undetectable after anoxic-oxic treatment in combination with a membrane bioreactor. Four fluorescent components were fractionated and obtained via excitation-emission matrix parallel factor analysis (EEM-PARAFAC). Dissolved organic matter fractionation in conjunction with EEM-PARAFAC was able to monitor more precisely the evolution of characteristic organic contaminants.

Evaluating tetracycline degradation pathway and intermediate toxicity during the electrochemical oxidation over a Ti/Ti4O7 anode.

Tetracycline (TC) is one of the most widely used antibiotics with significant impacts on human health and thus it needs appropriate approaches for its removal. In the present study, we evaluated the performance and complete pathway of the TC electrochemical oxidation on a Ti/Ti4O7 anode prepared by plasma spraying. Morphological data and composition analysis indicated a compact coating layer on the anode, which had the characteristic peaks of Ti4O7 as active constituent. The TC electrochemical oxidation on the Ti/Ti4O7 anode followed a pseudo-first-order kinetics, and the TC removal efficiency reached 95.8% in 40 min. The influential factors on TC decay kinetics included current density, anode-cathode distance and initial TC concentration. This anode also had high durability and the TC removal efficiency was maintained over 95% after five times reuse. For the first time, we unraveled the complete pathway of the TC electrochemical oxidation using high-performance liquid chromatograph (HPLC) and gas chromatograph (GC) coupled with mass spectrometer (MS). ·OH radicals produced from electrochemical oxidation attack the double bond, phenolic group and amine group of TC, forming a primary intermediate (m/z = 461), secondary intermediates (m/z = 432, 477 and 509) and tertiary intermediates (m/z = 480, 448 and 525). The latter were further oxidized to the key downstream intermediate (m/z = 496), followed by further downstream intermediates (m/z = 451, 412, 396, 367, 351, 298 and 253) and eventually short-chain carboxylic acids. We also evaluated the toxicity change during the electrochemical oxidation process with bioluminescent bacteria. The bioluminescence inhibition ratio peaked at 10 min (55.41%), likely owing to the high toxicity of intermediates with m/z = 461, 432 and 477 as obtained from quantitative structure activity relationship (QSAR) analysis. The bioluminescence inhibition ratio eventually decreased to 16.78% in 40 min due to further transformation of TC and intermediates. By comprehensively analyzing the influential factors and complete degradation pathway of TC electrochemical oxidation on the Ti/Ti4O7 anode, our research provides deeper insights into the risk assessment of intermediates and their toxicity, assigning new perspectives for practical electrochemical oxidation to effectively eliminate the amount and toxicity of TC and other antibiotics in wastewater.

Impact of dissolved oxygen on the microbial community structure of an intermittent biological aerated filter (IBAF) and the removal efficiency of gasification wastewater.

A novel IBAF system (altered conventional biological aerated filter (BAF) for intermittent aeration) was used to treat BDD anodes electrochemical oxidation gasification wastewater effluent, after which 454 pyrosequencing was applied to investigate the bacterial community of IBAF and demonstrate the relationship between dissolved oxygen (DO) and the bacterial community. The results showed that the concentration of COD, NH4+-N and NO3--N reached 55.08, 7.64 and 7.76 mg/L, respectively, in IBAF effluent because of changes in the DO concentration at 30 days after system start-up. The bacterial community results revealed that the 40 cm sample had the highest bacterial diversity. The bacterial species were approximate in total samples at phylum and family level, but the relative abundance was significantly different because of change in DO concentration. In addition, sample distance analysis indicated that the similarity of different samples was related to the DO concentration at different heights.

Quicklime-induced changes of soil properties: Implications for enhanced remediation of volatile chlorinated hydrocarbon contaminated soils via mechanical soil aeration.

Mechanical soil aeration is used for soil remediation at sites contaminated by volatile organic compounds. However, the effectiveness of the method is limited by low soil temperature, high soil moisture, and high soil viscosity. Combined with mechanical soil aeration, quicklime has a practical application value related to reinforcement remediation and to its action in the remediation of soil contaminated with volatile organic compounds. In this study, the target pollutant was trichloroethylene, which is a volatile chlorinated hydrocarbon pollutant commonly found in contaminated soils. A restoration experiment was carried out, using a set of mechanical soil-aeration simulation tests, by adding quicklime (mass ratios of 3, 10, and 20%) to the contaminated soil. The results clearly indicate that quicklime changed the physical properties of the soil, which affected the environmental behaviour of trichloroethylene in the soil. The addition of CaO increased soil temperature and reduced soil moisture to improve the mass transfer of trichloroethylene. In addition, it improved the macroporous cumulative pore volume and average pore size, which increased soil permeability. As soil pH increased, the clay mineral content in the soils decreased, the cation exchange capacity and the redox potential decreased, and the removal of trichloroethylene from the soil was enhanced to a certain extent. After the addition of quicklime, the functional group COO of soil organic matter could interact with calcium ions, which increased soil polarity and promoted the removal of trichloroethylene.

Fe and Mn removal from mining drainage using goaf filling materials obtained from coal mining process.

Coal gangue, sandy soil and clay (mass ratio 45:4:1) as goaf filling materials acquired from coal mining processes were applied to remove Fe and Mn effectively from mining drainage. The results of an adsorption kinetic study showed that the Fe adsorption equation was y=21.454y+8.4712, R2=0.9924 and the Mn adsorption equation was y=7.5409x+0.905, R2=0.9957. Meanwhile, the goaf filling materials had low desorption capacity (Fe 6.765 µg/g, Mn 1.52 µg/g) and desorption ratio (Fe 8.98%, Mn 11.04%). Experiments demonstrated that Fe and Mn from mining drainage could be removed stably at a flow rate of 1.2 L/min, Fe inlet concentration of less than 40 mg/L, Mn inlet concentration of less than 2 mg/L and neutral or alkaline conditions. During a procedure of continuous experiments, the effluent quality could meet the requirement of the 'Code for Engineering Design of Sewage Regeneration-GB503352-2002'. A real-application project using goaf filling materials to treat mining drainage in Shendong coal mine showed that the average cost per ton of mining drainage was about 0.55 RMB, which could bring about considerable economic benefit for coal mining enterprises.

Catalytic wet air oxidation of phenol with functionalized carbon materials as catalysts: reaction mechanism and pathway.

The development of highly active carbon material catalysts in catalytic wet air oxidation (CWAO) has attracted a great deal of attention. In this study different carbon material catalysts (multi-walled carbon nanotubes, carbon fibers and graphite) were developed to enhance the CWAO of phenol in aqueous solution. The functionalized carbon materials exhibited excellent catalytic activity in the CWAO of phenol. After 60 min reaction, the removal of phenol was nearly 100% over the functionalized multi-walled carbon, while it was only 14% over the purified multi-walled carbon under the same reaction conditions. Carboxylic acid groups introduced on the surface of the functionalized carbon materials play an important role in the catalytic activity in CWAO. They can promote the production of free radicals, which act as strong oxidants in CWAO. Based on the analysis of the intermediates produced in the CWAO reactions, a new reaction pathway for the CWAO of phenol was proposed in this study. There are some differences between the proposed reaction pathway and that reported in the literature. First, maleic acid is transformed directly into malonic acid. Second, acetic acid is oxidized into an unknown intermediate, which is then oxidized into CO2 and H2O. Finally, formic acid and oxalic acid can mutually interconvert when conditions are favorable.

[Health-based risk assessment in the excavating process of VOCs contaminated site].

The dissipative concentration test of VOCs in the remediation process of a typical contaminated site was operated, and three routes of exposure were set up for health risk assessment in the repair process. Analysis showed that carbon tetrachloride was the single pollutant with highest multi-route cumulative non-carcinogenic index, which was as high as 8.86E + 01, and its contribution rate to the integrated non-carcinogenic effects was 74.45%. Respiratory exposure was the exposure route with highest multi-pollutant hazard index, which was 1.01E + 02, accounting for 84. 87% of the comprehensive risk index, and the index of integrated non-carcinogenic damage was 1.19E + 02. 1,2-dichloroethane was the single pollutant with highest multi-route cumulative carcinogenic index, which was as high as 3.08E-02, and its contribution rate to the integrated carcinogenic effects was 69.53%. Respiratory exposure was the exposure route with highest multi-pollutant hazard index, which was 3.96E -02, accounting for 89.39% of the comprehensive risk index, and the index of integrated carcinogenic damage was 4.43E-02.