Chemical techniques for assessing bioavailability of sediment-associated contaminants: SPME versus Tenax extraction

The traditional approach for predicting the risk of hydrophobic organic contaminants (HOCs) in sediment is to relate organic carbon normalized sediment concentrations to body residues or toxic effects to organisms. However, due to the multiple variables controlling bioavailability, this method has limitations. A matrix independent method of predicting bioavailability needs to be used in order to be universally applicable. Both chemical activity (freely dissolved chemical concentrations) measured by solid-phase microextraction (SPME) and bioaccessibility (rapidly desorbing fraction) estimated by Tenax extraction have been developed to predict bioavailability of sediment-associated HOCs. The objectives of this review are to summarize a number of studies using matrix-SPME or Tenax extraction to estimate bioavailability and/or toxicity of different classes of HOCs and evaluate the strengths and weakness of these two techniques. Although the two chemical techniques assess different components of the matrix, estimates obtained from both techniques have been correlated to organism body residues. The advantages of SPME fibers are their applicability for use in situ and their potential usage for a wide array of contaminants by selection of appropriate coatings. Single time-point Tenax extraction, however, is more time- and labor-effective. Tenax extraction also has lower detection limits, making it more applicable for highly toxic contaminants. This review also calls for additional research to evaluate the role of sequestrated contaminants and ingestion of sediment particles by organisms on HOC bioavailability. The use of performance reference compounds to reduce SPME sampling time and linking chemical based bioavailability estimates to toxicological endpoints are essential to expand the applications of these methods.     

Short-range transport of contaminants released from e-waste recycling site in South China

The transport behaviors of a suite of contaminants released from electronic waste (e-waste) recycling operations, including polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and heavy metals, were evaluated by analyzing the contaminant residues in surface soils sampled in the surrounding area of an e-waste recycling site in South China. Concentrations of PBDEs and PCBs in the soil samples ranged from 0.565 to 2908 ng g(-1) dw and from 0.267 to 1891 ng g(-1) dw, respectively, while soil residues were 0.082-2.56, 3.22-287, and 16.3-162 μg g(-1) dw for Cd, Cu, and Pb, respectively. Concentrations of PBDEs and PCBs in soil decreased with increasing distance from the source of pollution, indicating possible PBDE and PCB contamination in the surrounding areas due to the short-range transport of these compounds from the e-waste recycling site. Although no significant difference in the short-range transport potential among PBDE and PCB congeners was observed, reductions in concentrations of the highly-brominated-BDEs and highly-chlorinated-CBs were slightly quicker than those of their less-halogen-substituted counterparts. Conversely, heavy metals showed the lowest transport potential due to their low vapor pressure, and results showed metals would remain near the pollution source instead of diffusing into the surrounding areas. Finally, mass inventories in areas near the e-waste site were 0.920, 0.134, 0.860, 4.68, 757, and 673 tons for BDE209, PBDEs (excluding BDE209), PCBs, Cd, Cu, and Pb, respectively.     

Status of mercury pollution during resources development in Guizhou Province, China

1　ＩｎｔｒｏｄｕｃｔｉｏｎＧｕｉｚｈｏｕＰｒｏｖｉｎｃｅｉｓｌｏｃａｔｅｄｉｎｓｏｕｔｈｗｅｓｔＣｈｉｎａｗｉｔｈａｔｏｔａｌａｒｅａｏｆ 176.2 8ｔｈｏｕｓａｎｄｓｑｕａｒｅｋｉｌｏｍｅｔｅｒｓ,ｏｆｗｈｉｃｈ 87%ｉｓｍｏｕｎｔａｉｎ ,10 %ｉｓｈｉｌｌｓ,3%ｉｓｒｉｖｅｒ,ｂａｓｉｎａｎｄｐｌａｉｎ .Ｇｕｉｚｈｏｕｉｓａｍｏｕｎｔａｉｎｏｕｓｐｒｏｖｉｎｃｅｗｉｔｈｒｉｃｈｍｉｎｅｒａｌｒｅｓｏｕｒｃｅｓ,ａｍｏｎｇｗｈｉｃｈｍｅｒｃｕｒｙｒｅｓｅｒｖｅｒａｎｋｓｆｉｒｓｔｉｎＣｈｉｎａ,ｅｖｅｎｉ…     

Effect of placement angles on wireless electrocoagulation for bipolar aluminum electrodes

A new electrocoagulation process based on bipolar aluminum electrode is proposed. The placement angles of bipolar electrode are key parameter. The numerical simulations support the experimental results. We in our previous study reported the wireless electrocoagulation (WEC) based on bipolar electrochemistry for water purification. One of the most important advantages of WEC is the omission of ohmic connection between bipolar electrode (BPE) and power supply, and thus the electrochemical reactions on BPE are driven by electric field in solution induced by driving electrodes. In this study, the impact of placement angle of bipolar aluminum electrode on WEC was investigated to provide a detailed analysis on the correlations between the bipolar electrode placement angle and bipolar electrocoagulation reactions. The results showed that the WEC cell with a horizontal BPE placed at 0° produced the maximum dissolved aluminum coagulant, accounting for 71.6 % higher than that with a vertical one placed at 90°. Moreover, the finite element simulations of current and potential distribution were carried out along the surface of BPE at different placement angles, revealing the mechanism of different BPE placement angles on aluminum dissolution rates in WEC system.     

乳状液膜分离法预处理垃圾渗滤液氨氮的试验研究

用span-80表面活性剂制作的乳状液处理垃圾渗滤液中氨氮,考察了表面活性剂span-80用量、膜内相硫酸浓度、膜增强剂用量、油内比、乳水比、外相水pH值因素对氨氮去除率的影响。结果表明,在最佳反应条件下,用乳状液膜分离法预处理垃圾渗滤液中的氨氮,分离速度快,处理效果达到87%以上。     

Field assessment of straw pellet combustion in improved heating stoves in rural Northeast China

Straw pellets are widely promoted and expected to be a cleaner alternative fuel to unprocessed crop residues and raw coal in rural China.However,the effectiveness of these dissemination programs is not well evaluated.In this?eld study,emission characteristics of burning straw pellets,raw coal,and unprocessed corn cobs in heating stoves were investigated in a pilot village in Northeast China.Emission measurements covering the whole combustion cycle (ignition,?aming,and smoldering phases) shows th...     

Effect of NOx and SO2 on the photooxidation of methylglyoxal: Implications in secondary aerosol formation

Methylglyoxal(CH₃COCHO,MG),which is one of the most abundant α-dicarbonyl compounds in the atmosphere,has been reported as a major source of secondary organic aerosol(SOA).In this work,the reaction of MG with hydroxyl radicals was studied in a 500 L smog chamber at(293±3) K,atmospheric pressure,(18±2)% relative humidity,and under different NOx and SO₂.Particle size distribution was measured by using a scanning mobility particle sizer(SMPS) and the results showed that the ad...     

Research progress on distribution,sources, identification,toxicity, and biodegradation of microplastics in the ocean,freshwater, and soil environment

• Microplastics are widely found in both aquatic and terrestrial environments. • Cleaning products and discarded plastic waste are primary sources of microplastics. • Microplastics have apparent toxic effects on the growth of fish and soil plants. • Multiple strains of biodegradable microplastics have been isolated. Microplastics (MPs) are distributed in the oceans, freshwater, and soil environment and have become major pollutants. MPs are generally referred to as plastic particles less than 5 mm in diameter. They consist of primary microplastics synthesized in microscopic size manufactured production and secondary microplastics generated by physical and environmental degradation. Plastic particles are long-lived pollutants that are highly resistant to environmental degradation. In this review, the distribution and possible sources of MPs in aquatic and terrestrial environments are described. Moreover, the adverse effects of MPs on natural creatures due to ingestion have been discussed. We also have summarized identification methods based on MPs particle size and chemical bond. To control the pollution of MPs, the biodegradation of MPs under the action of different microbes has also been reviewed in this work. This review will contribute to a better understanding of MPs pollution in the environment, as well as their identification, toxicity, and biodegradation in the ocean, freshwater, and soil, and the assessment and control of microplastics exposure.     

Recent advances in antimony removal using carbon-based nanomaterials: A review

• The synthesis and physicochemical properties of various CNMs are reviewed. • Sb removal using carbon-based nano-adsorbents and membranes are summarized. • Details on adsorption behavior and mechanisms of Sb uptake by CNMs are discussed. • Challenges and future prospects for rational design of advanced CNMs are provided. Recently, special attention has been deserved to environmental risks of antimony (Sb) element that is of highly physiologic toxicity to human. Conventional coagulation and ion exchange methods for Sb removal are faced with challenges of low efficiency, high cost and secondary pollution. Adsorption based on carbon nanomaterials (CNMs; e.g., carbon nanotubes, graphene, graphene oxide, reduced graphene oxide and their derivatives) may provide effective alternative because the CNMs have high surface area, rich surface chemistry and high stability. In particular, good conductivity makes it possible to create linkage between adsorption and electrochemistry, thereby the synergistic interaction will be expected for enhanced Sb removal. This review article summarizes the state of art on Sb removal using CNMs with the form of nano-adsorbents and/or filtration membranes. In details, procedures of synthesis and functionalization of different forms of CNMs were reviewed. Next, adsorption behavior and the underlying mechanisms toward Sb removal using various CNMs were presented as resulting from a retrospective analysis of literatures. Last, we prospect the needs for mass production and regeneration of CNMs adsorbents using more affordable precursors and objective assessment of environmental impacts in future studies.     

Measurement of air exchange rates in different indoor environments using continuous CO2 sensors

A new air exchange rate (AER) monitoring method using continuous CO₂ sensors was developed and validated through both laboratory experiments and field studies. Controlled laboratory simulation tests were conducted in a 1-m³ environmental chamber at different AERs (0.1-10.0 hr^-1). AERs were determined using the decay method based on box model assumptions. Field tests were conducted in classrooms, dormitories, meeting rooms and apartments during 2-5 weekdays using CO₂ sensors coupled with data loggers. Indoor temperature, relative humidity (RH), and CO₂ concentrations were continuously monitored while outdoor parameters combined with on-site climate conditions were recorded. Statistical results indicated that good laboratory performance was achieved: duplicate precision was within 10%, and the measured AERs were 90%-120% of the real AERs. Average AERs were 1.22, 1.37, 1.10, 1.91 and 0.73 hr^-1 in dormitories, air-conditioned classrooms, classrooms with an air circulation cooling system, reading rooms, and meeting rooms, respectively. In an elderly particulate matter exposure study, all the homes had AER values ranging from 0.29 to 3.46 hr??1 in fall, and 0.12 to 1.39 hr^-1 in winter with a median AER of 1.15.