Removal of arsenic by pilot-scale vertical flow constructed wetland

• VFCWs are effective for the treatment of arsenic-containing wastewater. • Arsenic removal did not affect the removal of nutrients, except for TP in CW500. • Arsenic removal was highest when the temperature peaked and the reed was in bloom. • Substrate accumulation contributed more to arsenic removal than plant absorption. Four pilot-scale Vertical Flow Constructed Wetlands (VFCWs) filled with gravel and planted with Phragmites australis were operated for seven months in the field to study the efficiency of arsenic removal in contaminated wastewater. The average arsenic removal efficiency by the VFCWs was 52.0%±20.2%, 52.9%±21.3%, and 40.3%±19.4% at the theoretical concentrations of 50 μg/L (CW50), 100 μg/L (CW100), and 500 μg/L (CW500) arsenic in the wastewater, respectively. The results also showed no significant differences in the removal efficiency for conventional contaminants (nitrogen, phosphorus, or chemical oxygen demand) between wastewater treatments that did or did not contain arsenic (P>0.05), except for phosphorus in CW500. The highest average monthly removal rate of arsenic occurred in August (55.9%–74.5%) and the lowest in November (7.8%–15.5%). The arsenic removal efficiency of each VFCW was positively correlated with temperature (P<0.05). Arsenic accumulated in both substrates and plants, with greater accumulation associated with increased arsenic concentrations in the influent. The maximum accumulated arsenic concentrations in the substrates and plants at the end of the experiment were 4.47 mg/kg and 281.9 mg/kg, respectively, both present in CW500. The translocation factor (TF) of arsenic in the reeds was less than 1, with most of the arsenic accumulating in the roots. The arsenic mass balance indicated that substrate accumulation contributed most to arsenic removal (19.9%–30.4%), with lower levels in plants (3.8%–9.5%). In summary, VFCWs are effective for the treatment of arsenic-containing wastewater.     

酞酸酯暴露及风险评价研究进展

酞酸酯的暴露及健康风险研究日趋深入。在综述了酞酸酯的物化性质、接触机会两方面特性,以及体内代谢、健康危害两方面的最新研究进展基础上,比较了其国内外相关标准现状,总结了酞酸酯暴露评估现状及健康风险研究现状,提出并分析了存在的问题,并对其今后的研究进行了展望。     

Biodegradability of Atrazine,Cyanazine and Dicamba under methanogenic condition in three soils of China

Persistence and degradation of the herbicides Atrazine, Cyanazine and Dicamba were measured in laboratory microcosms incubated under methanogenic condition using three soils of China. Results showed that Atrazine was more resistant to degradation than Cyanazine and Dicamba for the 300 days of incubation. Between 30% and 40% of the initially introduced chemicals were found to be not recoverable through solvent extraction of the incubated soils. Our results also indicated that the half-life of these herbicides in the three soils generally followed: Atrazine>Cyanazine>Dicamba. Biodegradation of Cyanazine and Dicamba was further substantiated by establishing enrichment cultures in which the degradation of the respective herbicides could be accelerated by the microorganisms. Our results suggest that biodegradation of xenobiotics can be established through enrichment culture transfer technique and non-extractability of chemicals should be taken into account in evaluation of chemicals' fate and risk.     

Heavy metal accumulation by panicled goldenrain tree （Koelreuteria paniculata） and common elaeocarpus （Elaeocarpus decipens） in abandoned mine soils in southern China

Phytoremediation can be used as a sustainable technology for mine spoil remediation to remove heavy metals. This study investigated the concentration of 7 heavy metal contamination in soil and plant samples at an abandoned mine site. We found that, after vegetation remediation at the abandoned mine site, the reduction rates for 7 heavy metals were in the range of 4.2%–86%, where reduction rates over 50% were achieved for four heavy metals (Zn, Mn, Cd, Ni). Transfer coe cients of the panicled goldenrain tree (Koelreuteria paniculata Laxm) and the common elaeocarpus (Elaeocarpus decipens) for Zn, Mn, Ni, and Co were more than 1. Enrichment coe cients of both trees for Mn were higher than 1. Our results suggest that the panicled goldenrain tree and the common elaeocarpus tree may act as accumulators in remediation. Moreover, the woody vegetation remediation in abandoned mining areas play an important role in improving scenery besides removing heavy metal from contaminated soil.     

Relation of lead adsorption on birnessites with di erent average oxidation states of manganese and release of Mn2+/H+/K+

The characteristics of Pb2+ adsorption on the surface of birnessites with di erent average oxidation states (AOS) of Mn, synthesized under acidic and alkali conditions, were investigated. The results indicated that the amount of adsorbed Pb2+ increased with the increase of Mn AOS in birnessites. The amount of Pb2+ adsorbed positively correlated with the amount of released Mn2+, H+, and K+ (r = 0.9962 > 0.6614, n = 14, = 0.01). The released Mn2+, H+, and K+ were derived mostly from the corresponding cations adsorbed on the vacant sites. The maximum amount of adsorbed Pb2+ increased with the increasing vacant cation sites, leading to an increase of the total amount of released Mn2+, H+, and K+, and the increased likelihood for two Pb2+ adsorbed in the region of one side of a vacant site.     

Application of enriched stable isotope technique to the study of copper bioavailability in Daphnia magna

The biokinetics of Cu in Daphnia magna, including dissolved uptake, assimilation and e ux, has been determined using a gamma 67Cu radiotracer methodology. However, this gamma emitting radioisotope is not readily available due to its very short half-life. In the present study, we employed a stable isotope tracer (65Cu) to determine the Cu biokinetics and compared our results to those determined using 67Cu. The dissolved uptake rate constant of 65Cu was 3.36 L/(g day), which is higher than that of 67Cu (1.32 L/(g day)). With increasing food concentrations from 2 104 to 1 105 cells/mL, the Cu assimilation e ciency (AE) decreased from 46% to 11%, compared to a decrease from 27% to 16% when determined using 67Cu. The e ux of Cu from Daphnia magna was quantified following both dissolved and dietary uptake. The e ux of waterborne Cu was comparable to that of dietborne Cu and the e ux rate constant (0.32–0.52 day??1) was higher than that determined by 67Cu (0.19–0.20 day??1). By considering di erent water properties and handling procedure between the two experiments, we believe that these di erences are reasonable. Overall, this study demonstrated that the enriched stable isotope tracer technique is a powerful tool to investigate metal bioavailability and maybe a good alternative to radioactive measurements.     

Humification characterization of biochar and its potential as a composting amendment

Biochar has received increasing attention due to its applications as a soil amendment. Here, the chemical properties of solid and water-extractable fractions of four biochar samples were investigated. The results showed that wood biochar and bamboo biochar samples were 60%–80% more hydrophobic than those of rice husk biochar and rice husk ash. In addition, the acidity was 3.88 mmol/g from the total functional groups and 1.03 mmol/g from the carboxyl groups/lactones/phenols found in the wood biochar sample, which were about 1.5 times greater than those of the bamboo biochar sample. These functional groups could be used to determine the sorptive capacity of biochar for ionic solutes and water content and to increase the degradation of compost organics. The wood biochar sample was found to have the most humification materials(fulvic acid-like material + humic acid-like material) in the water-extractable fraction, which was 3–10 times higher than that in the rice husk biochar and rice husk ash; humified materials were not detected in the bamboo biochar sample. Humification materials in biochar may be involved in increasing the proportion of humic acid-like materials in humic-like substances within the compost product. Wood biochar had better hydrophobic, sorptive, aromatic, and humification properties compared to other biochars, suggesting that it may be used in composting in order to exert its effect as both a bulking agent and a composting amendment during the solid waste composting process.     

Review of the progress in preparing nano TiO2: An important environmental engineering material

TiO2 nanomaterial is promising with its high potential and outstanding performance in photocatalytic environmental applications, such as CO2 conversion, water treatment, and air quality control. For many of these applications, the particle size, crystal structure and phase,porosity, and surface area influence the activity of TiO2 dramatically. TiO2 nanomaterials with special structures and morphologies, such as nanospheres, nanowires, nanotubes, nanorods,and nanoflowers are thus synthesized due to their desired characteristics. With an emphasis on the different morphologies of TiO2 and the influence factors in the synthesis, this review summarizes fourteen TiO2 preparation methods, such as the sol–gel method, solvothermal method, and reverse micelle method. The TiO2 formation mechanisms, the advantages and disadvantages of the preparation methods, and the photocatalytic environmental application examples are proposed as well.     

In situ bioelectrokinetic remediation of phenol-contaminated soil by use of an electrode matrix and a rotational operation mode

In situ bioremediation is a safe and cost-effective technology for the cleanup of contaminated sites, but its remediation rate is usually very slow. This study attempted to accelerate the process of bioremediation by employing non-uniform electrokinetic transport processes to mix organic pollutants and degrading bacteria in soils under in situ conditions (namely, in situ bioelectrokinetic remediation) by use of an electrode matrix and a rotational operation mode. A bench-scale non-uniform electrokinetic system with periodic polarity-reversal was developed for this purpose, and tested by using a sandy loam spiked with phenol as a model organic pollutant. The results demonstrated that non-uniform electrokinetic processes could enhance the in situ biodegradation of phenol in the soil, the efficiency of which depended upon the operational mode of the electric field. Compared with the unidirectional operation and the bidirectional operation, the rotational operation could effectively stimulate the biodegradation of phenol in the soil if adopting appropriate time intervals of polarity-reversal and electrode matrixes. A reversal interval of 3.0 h and a square-shaped electrode matrix with four electrode couples appeared appropriate for the in situ biodegradation of phenol, at which a maximum phenol removal of 58% was achieved in 10d and the bioremediation rate was increased about five times as compared to that with no electric field applied. The results also showed that adopting a small polarity-reversal interval and an appropriate electrode array could produce a high and uniform removal of phenol from the soil. It is believed that in situ bioelectrokinetic remediation holds the potential for field application.     

Modeling the crystallization of magnesium ammonium phosphate for phosphorus recovery

The crystallization of magnesium ammonium phosphate (MAP) is one of the main processes for recovering P and N from wastewater. Chemically defined solution systems were designed; the saturation indices (SIs) of the solution systems with respect to MAP were derived by using a geochemical aqueous model Program, PHREEQC 2.11; the effects of the solution conditions were evaluated using thermodynamic theories. The concentrations of P and Mg in the tested solutions were 10-600 mg l(-1) and 24-720 mg l(-1), respectively, the molar ratios of N/P and pH values of the solutions varied in the ranges of 1-40 and 6.0-12.0, respectively. The temperature of all the tests was set at 25 degrees C. The test results show that the SI value of MAP is the logarithmic functions of the concentrations of P, ammonium-N and Mg, and increases with the increase of the concentration of each element. The SI value of MAP is a polynomial function of pH value of the solution, and the optimum pH value for the crystallization of MAP is 9.0 but increases slightly with the increase of the N/P. Moreover, the SI value of MAP is a power law function of the ionic strength of solutions but decreases with its increase. The adjustment of the Mg concentration and the control of solution pH are two effective methods for the control of the crystallization of MAP. The results obtained from the research can be used to guide the design and control of MAP crystallization process for the removal and recovery of P.