Polybrominated diphenyl ethers in sediments of the Daliao River Estuary, China: levels, distribution and their influencing factors

The concentrations, compositional profiles, possible sources of polybrominated diphenyl ethers (PBDEs) in sediments of the Daliao River Estuary as well as the factors influencing the distribution of PBDEs were investigated. The total concentrations of PBDEs ranged from 0.13 to 1.98 ng g⁻¹ d.w. BDE209 was the dominating congener in all sediment samples, indicating the pollution of PBDEs in the Daliao River Estuary mainly came from the use of deca-BDE commercial mixtures. The intrusion of sea waters promoted the deposition of the colloid-associated PBDEs in the estuary. There were significantly negative correlations between PBDE concentration in sediment with pH value and salinity in the bottom water. The higher river flow in the flood season (summer) obviously accelerated the transport of PBDEs, and thereby increased the risk of PBDE contamination to the deep ocean. Moreover, a positive correlation between TOC and PBDE distributions was observed, suggesting that TOC regulated the distributions of PBDEs in sediments of Daliao River Estuary.     

A novel application of H2O2-Fe(II) process for arsenate removal from synthetic acid mine drainage (AMD) water

Batch experiments were carried out to investigate the influences of H₂O₂/Fe(II) molar ratio, pH, sequence of pH adjustment, initial As(V) concentration, and interfering ions on As(V) removal in H₂O₂-Fe(II) process from synthetic acid mine drainage (AMD). The optimum H₂O₂/Fe(II) molar ratio was one for arsenate removal over the pH range of 4-7. Arsenate removal at pH 3 was poor even at high Fe(II) dosage due to the high solubility of Fe(III) formed in situ. With the increase of Fe(II) dosage, arsenate removal increased progressively before a plateau was reached at pH 5 as arsenate concentration varied from 0.05 to 2.0 mg L⁻¹. However, arsenate removal was negligible at Fe/As molar ratio <3 and then experienced a striking increase before a plateau was reached at pH 7 and arsenate concentration ≥1.0 mg L⁻¹. The co-occurring ions exerted no significant effect on arsenate removal at pH 5. The experimental results with synthetic AMD revealed that this method is highly selective for arsenate removal and the co-occurring ions either improved arsenate removal or slightly depressed arsenate removal at pH 5-7. The extended X-ray absorption fine structure (EXAFS) derived As-Fe length, 3.27-3.30 Å, indicated that arsenate was removed by forming bidentate-binuclear complexes with FeO(OH) octahydra. The economic analysis revealed that the cost of the H₂O₂-Fe(II) process was only 17-32% of that of conventional Fe(III) coagulation process to achieve arsenate concentration below 10 μg L⁻¹ in treated solution. The results suggested that the H₂O₂-Fe(II) process is an efficient, economical, selective and practical method for arsenate removal from AMD.     

Bioaccessibility of polychlorinated biphenyls in different foods using an in vitro digestion method

Bioaccessibility of organic pollutants in food is important for exposure estimation and risk assessment. An in vitro enzyme digestion experiment was carried out to analyze the bioaccessibility of PCBs in different foods including freshwater fish (bighead carp and oriental weather fish) and vegetables (spinach and cabbage). The results indicated that the bioaccessibility of PCBs in freshwater fish (3%) was much lower than that in leafy vegetables (25%). Based on field survey, the daily exposure TEQ value from these two types of food was 17.9 pg/kg bw/day. However, when bioaccessibility was taken into consideration, the value decreased to 0.61 pg/kg bw/day. Therefore, the forms of PCBs existing in food strongly influenced the bioavailability for humans, which may have important implications on dietary exposure. To our knowledge, this is the first paper to illustrate the bioaccessibility of PCBs in different foods using an in vitro digestion method.     

Vertical distribution and environmental significance of sulfur and oxygen heterocyclic aromatic hydrocarbons in soil samples collected from Beijing, China

Vertical distribution of the concentration and composition of some sulfur and oxygen heterocyclic aromatic hydrocarbons (SOHAHs), such as, fluorene, dibenzofuran, dibenzothiophene and their alkyl homologues in 10 soil profiles in Beijing have been investigated. The results showed that the concentrations and composition of SOHAHs in topsoil (0-30cm) from different profiles are different. The concentrations of SOHAHs in topsoils are much higher than that in bottom soils where the concentrations are relatively constant. The fingerprints of SOHAHs from same profile are similar in topsoil samples, which are obviously different at the deep part, which suggested that the sources of these compounds are consistent in topsoil and are discriminating between surface and bottom soils. The main sources of SOHAHs in surface soil were fossil fuel combustion, petroleum and wastewater irrigation, while those at deep part were likely derived from the degradation products of soil organic matters.     

草莓蚜虫防治用药对蜜蜂的急性毒性与风险评价

为明确草莓蚜虫防治用药对蜜蜂的影响,按照《化学农药环境安全评价试验准则》和《化学品测试方法》要求测定了20%啶虫脒SP、10%氟啶虫酰胺WG和22%氟啶虫胺腈SC对意大利蜜蜂(Apis mellifera L.)的急性毒性,并采用危害商值(HQ)法进行了风险评价。急性毒性结果显示:20%啶虫脒SP、10%氟啶虫酰胺WG和22%氟啶虫胺腈SC对蜜蜂的急性经口毒性试验结果(48 h-LD50值)分别为4.47μg a.i.·蜂~(-1)、11.2μg a.i.·蜂~(-1)和0.0601μg a.i.·蜂~(-1),对蜜蜂的急性接触毒性试验结果(48 hLD50值)分别为11.0μg a.i.·蜂~(-1)、13.9μg a.i.·蜂~(-1)和0.643μg a.i.·蜂~(-1)。按《化学农药环境安全评价试验准则》中毒性等级划分标准,20%啶虫脒SP、10%氟啶虫酰胺WG和22%氟啶虫胺腈SC对蜜蜂的毒性等级分别为中毒、低毒和高毒。风险评价结果表明,22%氟啶虫胺腈SC对蜜蜂存在中等风险(HQ值为1 622),20%啶虫脒SP和10%氟啶虫酰胺WG对蜜蜂的风险为低风险,其HQ值分别为40.3和6.70。因此,草莓生产中可优先选用10%氟啶虫酰胺WG来防治蚜虫,20%啶虫脒SP次之。而使用22%氟啶虫胺腈SC时,应注意采取措施降低其对蜜蜂的毒性风险,以免造成危害。     

不同测试方法评估48%毒死蜱乳油对玉米田施药者的人体暴露风险

本研究选取3种不同暴露环境,分别为玉米株高达到施药者膝盖左右(暴露环境1)、达到施药者腰部左右(暴露环境2)和高于施药者身高(暴露环境3),采用手动背负式喷雾器,在这3种暴露环境中施喷48%毒死蜱乳油(EC,稀释500倍),通过贴片法和全身整体测试法(whole body dosimetry,WBD)分析了施药者农药皮肤暴露量(dermal exposure,DE)。依据试验结果,发现在暴露环境1和2中,2种测试方法的农药潜在皮肤暴露量(potential dermal exposure,PDE)无显著性差异,但在暴露环境3中,2种测试方法的PDE之间存在显著性差异(LSD0.05=57.9);对施药者的主要暴露部位进行分析,发现在暴露环境1和暴露环境2中2种测试方法的暴露部位类似,但在暴露环境3中显示,贴片法为手部,全身测试法为上半身(头、颈、前胸、后背及手臂)。使用全身测试法测定PDE同时测定直接皮肤暴露量(actual dermal exposure,ADE),并利用ADE和PDE计算外穿防护服(运动服)渗透率的结果,3种暴露环境分别为4.69%、5.19%和5.54%,比通常假设的防护服或工作服的10%渗透率小。     

连续流反应器污水硝化过程中的N_2O释放

污水生物脱氮硝化阶段是温室气体一氧化二氮（N2O）的重要释放源。采用连续流反应器在2种进水氨氮（NH4-N,低氮反应器60 mg/L和高氮反应器180 mg/L）浓度条件下驯化硝化菌,并研究了不同初始NH4-N浓度和不同初始亚硝酸盐（NO2-N）浓度条件下所驯化硝化菌释放N2O的特征。结果表明在反应器运行过程中2个反应器释放N2O较少,均小于去除NH4-N浓度的0.01%;N2O的释放均随着初始NH4-N浓度或初始NO2-N浓度的升高而增加;不同初始NH4-N浓度条件下,低氮反应器驯化硝化菌的N2O释放率在0.51%~1.40%之间,高氮反应器驯化硝化菌在0.29%~1.27%之间;不同初始NO2-N浓度条件下,低氮反应器驯化硝化菌的N2O释放率在1.38%~3.78%之间,高氮反应器驯化硝化菌在1.16-5.81%之间。     

黄铁矿还原固定水中的高铼酸根

以铼作为放射性锝的替代元素,用黄铁矿粉末对高铼酸根的还原固定进行了研究。采用球磨法制备出黄铁矿粉末。分别研究了不同固液比、不同的初始p H值和不同粒径条件下,黄铁矿粉末对高铼酸根的还原固定效果。结果显示,固液比为1∶10(g/m L)为宜,在体系初始p H为12时,形成铁氧体,吸附高铼酸根,提升还原固定效果。对产物进行XPS表征,证明还原产物为Re O2。在乙醇介质中机械活化后利用超声分散可得到具有大的比表面积和晶格畸变的粒径较小的黄铁矿粉末,使其反应的活性位点增多,处理效果明显好于大粒径的黄铁矿粉末,在相对较短的时间内,铼的去除率可以达42%。在缺氧环境下黄铁矿能够长期保持有效性,在地质处置库应用中有实际意义。     

纳米铁酸盐光催化剂的制备及其在废水处理中的应用综述

概括了纳米铁酸盐(以ZnFe2O4和BiFeO3为代表)光催化剂的制备方法;综述了其在废水处理中的应用现状;讨论了催化反应中铁酸盐的特性及工艺条件(初始反应p H、初始污染物浓度、H2O2的加入等)对有机污染物降解率的影响;介绍了光助-类Fenton氧化反应的机理;对纳米铁酸盐在废水处理应用中存在的问题进行了总结,并对今后的研究方向进行了展望。     

稳定态纳米零价铁-厌氧菌联合处理法降解2,4,6-三氯苯酚

利用SEM、XRD、FTIR等手段对稳定态纳米零价铁（NH₂-SiO₂@NZVI）进行表征,并考察NH₂-SiO₂@NZVI-厌氧菌体系对2,4,6-三氯苯酚（2,4,6-TCP）的降解效果。实验结果表明：NH₂-SiO₂@NZVI具有较强的抗氧化能力及较好的分散性;当2,4,6-TCP质量浓度 50 mg/L、NH₂-SiO₂@NZVI加入量1 g/L、初始 pH 7.00、反应120 h时,2,4,6-TCP的去除率为34.76%,一级降解速率常数为0.022 1,均远大于普通纳米零价铁颗粒;在NH₂-SiO₂@NZVI-厌氧菌体系中,2,4,6-TCP的去除率可达82.70%,NH₂-SiO₂@NZVI与厌氧微生物之间表现出明显的协同效应,能有效缓解2,4,6-TCP对厌氧微生物的抑制作用,稳定体系pH,提高微生物的降解活性和产甲烷活性。