2005年中国气态α HCH的人体暴露和健康风险分析

为评估由我国大气中α HCH所导致的人体健康风险,利用CanMETOP 模拟的2005年日均α HCH大气浓度,基于吸入因子和致癌风险进行研究。结果表明年吸入因子呈东部>西部,北部>南部的特征，东中和东北部地区的吸入因子分别主要由人口密度和α HCH大气浓度贡献，东中和东南部地区的个体健康损失小于东北地区，东中和东南部地区年内逐月吸入因子分配较为均匀,而东北地区主要集中的夏季，东北地区个体致癌风险系数明显高于中部和南部。推测由其它污染物所形成的暴露风险具有类似的时空分布。加之夏季东北地区集中降水所形成的湿沉降以及气温升高等因素,使摄食暴露和皮肤接触暴露增大,东北地区人群的复合暴露风险将显著大于其它地区     

焦化苯初馏份蒸馏釜发生爆炸的原因探讨

通过对某企业的一起典型爆炸事故案例进行分析,找出其产生的原因,提出了预防措施。     

Predicting the aquatic risk of realistic pesticide mixtures to species assemblages in Portuguese river basins

Although pesticide regulatory tools are mainly based on individual substances, aquatic ecosystems are usually exposed to multiple pesticides from their use on the variety of crops within the catchment of a river. This study estimated the impact of measured pesticide mixtures in surface waters from 2002 and 2008 within three important Portuguese river basins (‘Mondego’, ‘Sado’ and ‘Tejo’) on primary producers, arthropods and fish by toxic pressure calculation. Species sensitivity distributions (SSDs), in combination with mixture toxicity models, were applied. Considering the differences in the responses of the taxonomic groups as well as in the pesticide exposures that these organisms experience, variable acute multi-substance potentially affected fractions (msPAFs) were obtained. The median msPAF for primary producers and arthropods in surface waters of all river basins exceeded 5%, the cut-off value used in the prospective SSD approach for deriving individual environmental quality standards. A ranking procedure identified various photosystem II inhibiting herbicides, with oxadiazon having the relatively largest toxic effects on primary producers, while the organophosphorus insecticides, chlorfenvinphos and chlorpyrifos, and the organochloride endosulfan had the largest effects on arthropods and fish, respectively. These results ensure compliance with European legislation with regard to ecological risk assessment and management of pesticides in surface waters.     

Immobilization of lead in anthropogenic contaminated soils using phosphates with/without oxalic acid

Understanding the effects of oxalic acid(OA) on the immobilization of Pb(Ⅱ) in contaminated soils by phosphate materials, has considerable benefits for risk assessment and remediation strategies for the soil. A series of phosphate amendments with/without oxalic acid were applied to two anthropogenic contaminated soils. We investigated the immobilization of Pb(Ⅱ) by KH2PO4, phosphate rock(PR), activated phosphate rock(APR) and synthetic hydroxyapatite(HAP) at different phosphate:Pb(P:Pb) molar ratios(0, 0.6, 2.0 and 4.0) in the presence/absence of 50 mmol oxalic acid/kg soil, respectively. The effects of treatments were evaluated using single extraction with deionized water or Ca Cl2, Community Bureau of Reference(BCR) sequential extraction and toxicity characteristic leaching procedure(TCLP)methods. Our results showed that the concentration of water extractable, exchangeable and TCLP-Pb all decreased with incubation time. The concentration of water-extractable Pb after120 days was reduced by 100% when soils were amended with APR, HAP and HAP + OA, and the TCLP-Pb was 5 mg/L for the red soil at P:Pb molar ratio 4.0. Water-soluble Pb could not be detected and the TCLP-Pb was 5 mg/L at all treatments applied to the yellow-brown soil. BCR results indicated that APR was most effective, although a slight enhancement of water-soluble phosphate was detected at the P:Pb molar ratio 4.0 at the beginning of incubation. Oxalic acid activated phosphates, and so mixing insoluble phosphates with oxalic acid may be a useful strategy to improve their effectiveness in reducing Pb bioavailability.     

Pesticide residue dynamics in passion fruits: Comparing field trial and modelling results

We evaluated the exposure to pesticides from the consumption of passion fruits and subsequent human health risks by combining several methods: (i) experimental field studies including the determination of pesticide residues in/on passion fruits, (ii) dynamic plant uptake modelling, and (iii) human health risk assessment concepts. Eight commonly used pesticides were applied onto passion fruits cultivated in Colombia. Pesticide concentrations were measured periodically (between application and harvest) in whole fruits and fruit pulp. Measured concentrations were compared with predicted residues calculated with a dynamic and crop-specific pesticide uptake model, namely dynamiCROP. The model accounts for the time between pesticide application and harvest, the time between harvest and consumption, the amount of spray deposition on plant surfaces, uptake processes, dilution due to crop growth, degradation in plant components, and reduction due to food processing (peeling). Measured and modelled residues correspond well (r² = 0.88-0.99), with all predictions falling within the 90% confidence interval of the measured values. A mean error of 43% over all studied pesticides was observed between model estimates and measurements. The fraction of pesticide applied during cultivation that is eventually ingested by humans is on average 10⁻⁴-10⁻⁶, depending on the time period between application and ingestion and the processing step considered. Model calculations and intake fractions via fruit consumption based on experimental data corresponded well for all pesticides with a deviation of less than a factor of 2. Pesticide residues in fruits measured at recommended harvest dates were all below European Maximum Residue Limits (MRLs) and therefore do not indicate any violation of international regulatory thresholds.     

南昌市扬尘PM2.5中多环芳烃的来源解析及健康风险评价

为了解南昌市道路扬尘和土壤风沙尘PM_2.5中多环芳烃（PAHs）的来源和健康风险,利用颗粒物再悬浮系统采集PM_2.5样品,测定了PM_2.5中16种优先控制的多环芳烃的含量.结果表明,南昌市道路扬尘PM_2.5中ΣPAHs含量范围为48.85~166.16μg·kg^-1,平均值为（114.22±39.95）μg·kg^-1,土壤风沙尘PM_2.5中ΣPAHs含量范围为31.05~62.92μg·kg^-1,平均值为（40.79±9.39）μg·kg^-1.道路尘和土壤风沙尘PM_2.5中的PAHs都是以4~5环组分为主.主成分分析/多元线性回归分析结果表明,南昌市道路扬尘PM_2.5中PAHs的来源包括机动车的排放和燃煤源与石油泄漏,贡献率分别为51.7%和48.3%,总估计值与实际值的线性拟合有很好的一致性.对于儿童和成年男性,不同暴露途径的PAHs致癌风险值从大到小依次是皮肤接触 > 摄食 > 呼吸吸入,而成年女性则表现为摄食 > 皮肤接触 > 呼吸吸入.各暴露途径中,PAHs对成人的致癌风险均高于儿童.所有人群中,PAHs的总致癌风险值均低于美国EPA推荐的致癌风险阈值10^-6,没有致癌风险.     

滇西北剑湖沉积物钒空间分布特征和生态风险

用电感耦合等离子体发射光谱仪（ICP-OES）测定剑湖表层及柱状沉积物钒（V）含量,采用改进BCR连续提取法提取V各形态,并对V空间分布特征和生态风险进行了分析,揭示了粒度对剑湖沉积物V及形态含量的影响.结果表明,剑湖表层沉积物和柱状沉积物颗粒均以粉砂粒和细砂为主,细颗粒V含量更高.表层沉积物V含量为（117.82±63.31）mg/kg,其水平空间分布差异较大.V可交换态、可还原态、可氧化态和残渣态含量分别为（8.91±8.91）,（18.36±10.53）,（7.67±7.67）,（80.22±58.71）mg/kg,主要以残渣态形式存在,且黏粒和粉砂粒对V可还原态和残渣态影响较大.V垂直分布差异大,底层V含量高于表层,少部分区域受黏粒和粉砂粒影响.剑湖沉积物V污染程度小,大部分地区潜在生态风险较低,底层沉积物污染程度和潜在生态风险都高于表层.     

Removal of polycyclic aromatic hydrocarbons from different soil fractions by persulfate oxidation

Removal of polycyclic aromatic hydrocarbons (PAHs) from different soil fractions of contaminated soil was investigated by using activated persulfate oxidation remediation in our research. The results showed that the light fraction, which accounted for only 10% of the soil, contained 30% of the PAHs at a concentration of 4352?mg/kg. The heavy fraction contained more high-molecular-weight PAHs, and the total PAH concentration was 625?mg/kg. After being oxidized, the removal rate of PAHs was 39% in the light fraction and nearly 90% in the heavy fraction. Among the different fractions of the heavy fraction, humic acid contained the highest concentration of PAHs, and consequently, the highest removal efficiency of PAHs was also in humic acid. Compared with the light fraction, the heavy fraction has more aromatic compounds and those compounds were broken down during the oxidation process, which may be the removal mechanism involved in the oxidation of high-ring PAHs. Similarly, the enhancement of C = C bonds after oxidation can also explain the poor removal of high-ring PAHs in the light fraction. These results imply that different fractions of soil vary in composition and structure, leading to differences in the distribution and oxidation efficiencies of PAHs.     

可燃气体燃爆特性综合试验装置构建与甲烷试验

为研究半开敞空间内可燃气体爆炸过程,设计带有泄压面的气体爆炸室,并在此基础上构建一套可燃气体燃爆特性综合试验装置。运用该试验装置,研究预混塔内甲烷气体分层现象以及甲烷爆炸浓度与最小点火能之间的变化规律。甲烷分层试验结果表明:静置一段时间后,预混塔中甲烷浓度随高度的增加而增大。最小点火能试验结果显示,当甲烷的试验爆炸体积分数在10%～13%时,其浓度与点火能之间呈现比较平缓的变化关系,而当其体积分数小于10%或大于13%时,浓度稍微变化,其点火能将发生明显变化。     

Lower flammability limits of flammable ternary organic mixtures: Synergistic behavior

Organic flammable liquids and their mixtures, which possess high risk of combustion and explosion, are widely used as raw materials and solvents in chemical and pharmaceutical industries. Lower flammability limits (LFL) is one of the most important parameters to characterize the combustion and explosion hazards of combustible gases and liquid vapors. The LFL of various ternary organic mixtures consist of ketone (acetone and butanone), ester (ethyl acetate) and alcohol (ethanol and isopropanol) were tested at 25 °C and atmospheric pressure. The results showed that resulted LFL values of the experiment were always lower than those calculated by volume fraction weighting method when the volume fraction of alcohol was less than 20 vol% but more than 10 vol%. The co-existence of alcohol and ethyl acetate had synergistic effect on reducing the LFL values of ternary organic mixtures and thus increased their explosive risk. The mechanism of synergistic effect was analyzed, and the results showed that the OH· and H· radicals produced by the oxidation decomposition of alcohols and esters accelerated the oxidation process of ternary organic mixtures, which led to the decrease of experimental LFL values and thus corresponding increased of their explosive risk. This study would be expected to provide some guidance for designing or choosing safer and more suitable ternary organic mixtures prior to their applications for engineering.