粤港澳大湾区典型化工地块地下水分层调查与风险评估

以粤港澳大湾区某典型有机化工地块为研究对象,采用丛式井分层调查不同深度地下水苯含量,并通过分层评估明确不同深度地下水的人体健康风险水平,确定苯的修复目标值、修复范围及相应策略.结果表明:该地块上层地下水苯最大质量浓度为7440.0μg/L,下层为30000.0μg/L,说明地下水受到苯污染,且下层地下水污染程度较上层更...     

连续管式原位注入化学氧化技术对某有机污染场地地下水的修复效果

针对传统地下水原位注入化学氧化技术存在注入深度浅、效率低等问题,采用连续管和高压水射流技术实现地下水原位修复药剂钻注一体化和水射流钻进,以提高效率和深层修复。以某退役化工厂地下水中的氯苯为目标污染物,基于自主开发的连续管式原位注入化学氧化技术开展了中试规模的实验研究,基于现场实验确定原位注入药剂影响半径并评估了修复效果。结果表明,药剂影响半径可达2 m,且药剂扩散趋势与场地总体地下水流场的流向基本吻合;经原位化学氧化处理后,实验区地下水中氯苯检测质量浓度低于400 μg·L⁻¹,即采用连续管式原位注入化学氧化技术实现了实验区地下水中氯苯的有效去除。本研究可为连续管注入技术在地下水原位修复中的应用提供参考。     

基于2种采样方法的北京市夏季道路扬尘的监测及积尘负荷分布特征

为探究不同采样方法对积尘负荷结果的影响,使用样方采样法和以克论净车采样法采集2018年夏季样品的数据,对北京市3个行政区的11条道路扬尘样品进行现场监测,计算不同道路类型及不同车道的积尘负荷,并对积尘负荷的变化规律进行分析。结果表明：基于样方采样法和以克论净车采样法的北京市夏季不同道路类型积尘负荷从大到小顺序依次为次干道(0.46 g·m⁻²、0.99 g·m⁻²) >支路(0.31 g·m⁻²、0.88 g·m⁻²)>主干道(0.24 g·m⁻²、0.78 g·m⁻²);2种采样方法所得积尘负荷差异的检验结果具有显著性(P=0.00<0.05)且存在线性关系;北京市夏季道路积尘负荷(0.34 g·m⁻²)稍高于天津市(0.24 g·m⁻²),低于石家庄市(1.06 g·m⁻²)、乌鲁木齐市(0.96 g·m⁻²)和西安市(0.70 g·m⁻²);基于样方采样法和以克论净车采样法采集的不同城区道路积尘负荷水平排序为大兴区(0.39 g·m⁻²、1.83 g·m⁻²)>朝阳区(0.38 g·m⁻²、1.00 g·m⁻²)>东城区(0.26 g·m⁻²、0.92 g·m⁻²),朝阳区、东城区和大兴区积尘负荷差异的检验结果均不具有显著性(P>0.05);基于样方采样法的机动车慢车道与机动车快车道积尘负荷分别为0.04~1.30 g·m⁻²和0.02~1.08 g·m⁻²;慢车道积尘负荷略高于快车道,但二者差异的检验结果不具有显著性(P=0.51>0. 05)。本研究成果可为遴选道路扬尘采样方法、构建北京市道路扬尘排放清单和制定管控措施提供参考。     

A Monitoring Network Design Procedure for Three-Dimensional (3D) Groundwater Contaminant Source Identification

Finding the location and concentration of contaminant sources is an important step in groundwater remediation and management. This discovery typically requires the solution of an inverse problem. This inverse problem can be formulated as an optimization problem where the objective function is the sum of the square of the errors between the observed and predicted values of contaminant concentration at the observation wells. Studies show that the source identification accuracy is dependent on the observation locations (i.e., network geometry) and frequency of sampling; thus, finding a set of optimal monitoring well locations is very important for characterizing the source. The objective of this study is to propose a sensitivity-based method for optimal placement of monitoring wells by incorporating two uncertainties: the source location and hydraulic conductivity. An optimality metric called D-optimality in combination with a distance metric, which tends to make monitoring locations as far apart from each other as possible, is developed for finding optimal monitoring well locations for source identification. To address uncertainty in hydraulic conductivity, an integration method of multiple well designs is proposed based on multiple hydraulic conductivity realizations. Genetic algorithm is used as a search technique for this discrete combinatorial optimization problem. This procedure was applied to a hypothetical problem based on the well-known Borden Site data in Canada. The results show that the criterion-based selection proposed in this paper provides improved source identification performance when compared to uniformly distributed placement of wells.     

固定污染源污水排放口及监测点位规范设置技术

为规范我国固定污染源污水排放口及监测点位设置,以保障污水样品采集和流量监测的准确性与代表性,在调研与查阅国内外技术文献的基础上,总结了我国现有固定污染源污水排放口和监测点位设置中存在的主要问题,探讨了国内外相关标准规定的缺陷和不足;基于保障实际监测工作需要和便于监督管理的原则,兼顾流量监测的准确性、样品采集的代表性与监测人员采样安全考虑,探讨了排污单位污水排放口与监测点位数量、位置设置技术。结果表明：排污单位不得通过暗管排放污水,应在厂界10 m以内设置1个污水总排放口和1个雨水总排放口及监测点位,排放第1类污染物及其他有毒有害或需优先控制的污染物指标时需同时在车间或车间处理设施出口设置排放口和监测点位;污水日排放量超过50 t·d⁻¹的排放口应按国家标准规范要求选择修建或安装适宜的标准化量水堰槽;其他排放口应修建满足污水采样监测和流量监测、长度不少于3 m的顺直排水明渠及高度不少于0.1 m的垂直跌水落差;通过压力管道排放污水时,应修建长度不少于15倍管径且需时刻满管的直管段,以安装管道流量计和取样阀门。排污单位须设置污水排放口环境保护图形标志与监测点位信息标志,制定污水排放口和监测点位的保障监测安全的防护措施及日常维护和管理的规定。污水排放口和监测点位的有关构筑物及相关设施应作为环境保护设施的组成部分,与主体工程“同时设计、同时施工、同时投产和使用”,且应作为建设项目竣工环境保护验收的必要条件。相关研究结果可为污水排放口和监测点位规范化整治提供技术依据,并为保证污水采样、监测与监管的安全有效实施提供技术保障。     

Ozonation of azo dye Acid Red 14 in a microporous tube-in-tube microchannel reactor: decolorization and mechanism

Despite the great success of time-weighted average passive sampling of hydrophobic contaminants, such as PCBs and PAHs, the sampling of polar organic compounds still presents a challenge because the equilibrium between water and most sampling phases is attained in a relatively short time. In this study, we proposed a new time-integrative sampler using in situ solvent extraction (TISIS) for polar organic chemicals. The sampler was composed of a 15 cm poly(dimethylsiloxane) (PDMS) tubing, with an internal diameter of 0.5 mm and wall thickness of 0.5 mm, through which an extraction solvent (acetonitrile) was passed. Four polar organic contaminants, caffeine, atrazine, diuron and 17α-ethynylestradiol, were chosen for the evaluation of the performance of the sampler. Without the use of in situ solvent extraction, the PDMS tubing when exposed to a constant aqueous concentration of the four model compounds was able to linearly accumulate those compounds for less than 12 h and equilibrium between the PDMS tubing and water was attained in 2 d under our laboratory conditions. However, TISIS when exposed to a constant aqueous concentration was able to linearly accumulate all the model compounds without any exposure time limitation. The measured sampling rates at three different extraction flow rates (0.2, 0.5, 1.5 mL min⁻¹) were similar, regardless of the chemicals, indicating that the overall mass transfer from aqueous solution to the extraction solvent was most likely dominated by partitioning to the PDMS tubing and the internal diffusion within PDMS. In addition, a pulsed exposure experiment confirmed that TISIS operated in a time-integrative mode when the environmental concentration was highly fluctuated.     

Effect of housing geometry on the performance of Chemcatcher passive sampler for the monitoring of hydrophobic organic pollutants in water

Passive sampling of pollutants in water has been gaining acceptance for environmental monitoring. Previously, an integrative passive sampler (the Chemcatcher) was developed and calibrated for the measurement of time weighted average concentrations of hydrophobic pollutants in water. Effects of physicochemical properties and environmental variables (water temperature and turbulence) on kinetic and thermodynamic parameters characterising the exchange of analytes between the sampler and water have been published. In this study, the effect of modification in sampler housing geometry on these calibration parameters was studied. The results obtained for polycyclic aromatic hydrocarbons show that reducing the depth of the cavity in the sampler body geometry increased the exchange kinetics by approximately twofold, whilst having no effect on the correlation between the uptake and offload kinetics of analytes. The use of performance reference compounds thus avoids the need for extensive re-calibration when the sampler body geometry is modified.     

远距离多通道的无组织排放VOCs连续在线监测系统

研制了一套远距离多通道VOCs连续采样在线监测系统.监测系统主要由远距离多通道VOCs连续采样装置与真空紫外灯单光子电离源飞行时间质谱仪组成.通过PAMS与有机硫标准气体对该系统进行了性能表征测试.结果表明:各物质连续7次实验RSD≤7％;最优检测限为0.004 μmol?mol-1;在0.01～1.00 μmol?m...     

Pesticide residues in products of plant origin in the European Union

The results of a co-ordinated monitoring programme for pesticide residues in the European Union and Norway carried out in 1996 and 1997 are presented. The aim of this programme is to work towards a system, which makes it possible to estimate actual dietary pesticide intake for the population of the European Union. Based on a statistically dérived sampling plan and within the limited number of pesticides/commodities analysed, the most critical pesticides (benomyl group and dithiocarbamates) and commodities (mandarine and lettuce) were identified. In case of detected non-compliances, repeated sampling and, if necessary, enforcement actions are to be taken by national authorities. The programme will be continued in the next years.     

Recovery of a marker strain of Salmonella typhimurium in litter and aerosols from isolation rooms containing infected chickens

Abstract

Screening of poultry flocks for foodborne pathogen Salmonella contamination is critical for Salmonella control in preharvest stages of poultry production. In this study, two sampling methods (litter and air filter) were compared for detection of S. typhimurium from experimentally infected chicks some of which had received either a probiotic competitive exclusion culture or transfer of cecal contents from salmonellae‐free adult birds. At 4, 9, and 11 days after inoculation, S. typhimurium samples were enumerated by selective plating. For both types of sampling, the control birds yielded the greatest levels of environmental contamination followed by the samples from the probiotic inoculated birds with the birds receiving the cecal transfer culture having the lowest levels of contamination. Although the two sampling methods responded in a similar fashion, detection sensitivity needs to be increased for air filter sampling.     

Passive water sampling for polynuclear aromatic hydrocarbons using lipidcontaining semipermeable membrane devices (SPMDs): Application to contaminant residence times

Lipid-containing semipermeable membrane devices are applied to the quantitative determination of the persistence of polynuclear aromatic hydrocarbons (PAH) in an irrigation water canal, a representative waterway. The uniform and reproducible sampling of the USGS design of lipid-containing SPMDs is exploited to measure PAH half-lives without requiring calculation of water concentrations. The trend in calculated PAH half-lives agrees with that expected if volatilization is a significant mechanism for loss from the canal with more volatile PAHs having shorter half-lives. The higher persistence of phenanthrene compared to anthracene is consistent with the greater stability of phenanthrene and suggests, with other physicochemical evidence, that other (reactive) mechanisms may be involved. The results of this study demonstrate the feasibility of the SPMD method for the measurement of residence times in aquatic and other compartments. Such information is essential for quantifying contaminant behavior in the environment and providing insights into contaminant fate.     

National baseline survey of soil quality in the Netherlands

To determine background values of the 252 chemical compounds listed in Dutch legislation, a survey was designed with the aim of estimating percentiles of the cumulative frequency distributions and areal fractions exceeding the former, legislative reference values. Sampling locations were selected by probability sampling, so that in estimating the target quantities no model assumptions on the spatial variation were required, and valid estimates could be obtained by design-based inference. Strata in random sampling were formed by overlaying an aggregated soil map and land use map. For most of the heavy metals the areal fraction with concentrations in the topsoil (0-10 cm) exceeding the reference value was smaller than the allowable maximum of 5%. For these compounds a background value was determined smaller than the reference value. Exceptions were V, Co, Ba and Cu, for which a background value was defined (slightly) larger than the reference value.