Problems in the sampling and analysis of carbon particulate

Several thermal and wet chemical methods of separating organic from elemental carbon in particulate samples were examined. It is concluded that none of them represents an ideal separation procedure and that only a method-dependent operational definition of organic and elemental carbon is possible at this time. The best separation method appears to be a thermal procedure using 350°C air oxidation followed by pyrolysis in He at 950°C. There are also difficulties in sampling since dual filter techniques show that adsorption of organic compounds on various filter media accounted for at least 15 per cent of the total organic carbon collected during ambient sampling in Warren, MI. This adsorption further confuses the results and needs to be studied at other sampling sites.     

Evaluation of activated carbon fiber filter for sampling of organochlorine pesticides in environmental water samples

A simple method for quantitative analyses of organic chlorine pesticides (OCPs) in environmental water samples such as rainwater, river water and seawater using activated carbon fiber filters (ACFF) is described. ACFF was used as adsorbent to collect the chemicals in water samples. The collection of OCPs was completed almost for one day by stirring the mixture of the sample and the ACFF chips at room temperature. The adsorbed OCPs on the ACFF could be extracted easily with toluene-ethanol (4:1) mixed solvent. The purified extract by a florisil column chromatograph was followed by the analysis using high-resolution gas chromatograph/high-resolution mass spectrometer. Recoveries of OCPs spiked to actual samples such as rainwater, river water and seawater samples were approximately more than 80%, and the coefficients of variations were within 10%. This method was applied to the actual samples and was confirmed to be applicable for monitoring sub-ng/l level OCPs in environmental water samples.     

A holistic passive integrative sampling approach for assessing the presence and potential impacts of waterborne environmental contaminants

As an integral part of our continuing research in environmental quality assessment approaches, we have developed a variety of passive integrative sampling devices widely applicable for use in defining the presence and potential impacts of a broad array of contaminants. The semipermeable membrane device has gained widespread use for sampling hydrophobic chemicals from water and air, the polar organic chemical integrative sampler is applicable for sequestering waterborne hydrophilic organic chemicals, the stabilized liquid membrane device is used to integratively sample waterborne ionic metals, and the passive integrative mercury sampler is applicable for sampling vapor phase or dissolved neutral mercury species. This suite of integrative samplers forms the basis for a new passive sampling approach for assessing the presence and potential toxicological significance of a broad spectrum of environmental contaminants. In a proof-of-concept study, three of our four passive integrative samplers were used to assess the presence of a wide variety of contaminants in the waters of a constructed wetland, and to determine the effectiveness of the constructed wetland in removing contaminants. The wetland is used for final polishing of secondary-treatment municipal wastewater and the effluent is used as a source of water for a state wildlife area. Numerous contaminants, including organochlorine pesticides, polycyclic aromatic hydrocarbons, organophosphate pesticides, and pharmaceutical chemicals (e.g., ibuprofen, oxindole, etc.) were detected in the wastewater. Herein we summarize the results of the analysis of the field-deployed samplers and demonstrate the utility of this holistic approach.     

Field sampling of soil pore water to evaluate trace element mobility and associated environmental risk

Monitoring soil pollution is a key aspect in sustainable management of contaminated land but there is often debate over what should be monitored to assess ecological risk. Soil pore water, containing the most labile pollutant fraction in soils, can be easily collected in situ offering a routine way to monitor this risk. We present a compilation of data on concentration of trace elements (As, Cd, Cu, Pb, and Zn) in soil pore water collected in field conditions from a range of polluted and non-polluted soils in Spain and the UK during single and repeated monitoring, and propose a simple eco-toxicity test using this media. Sufficient pore water could be extracted for analysis both under semi-arid and temperate conditions, and eco-toxicity comparisons could be effectively made between polluted and non-polluted soils. We propose that in-situ pore water extraction could enhance the realism of risk assessment at some contaminated sites.     

环境影响评价中部分标准存在的问题及对策

环境标准是环境影响评价的准则.结合环境影响评价的实际,探讨中国主要环境标准在执行中存在的3大问题,即环境标准中控制的环境因子数远远小于企业实际生产中排放的污染因子数,简单引用《工业企业设计卫生标准》(TJ 36-79)不适合中国国情,部分因子的标准限值没有日均浓度等.针对这些问题,笔者提出利用美国环保局多介质环境模型,或根据《大气污染物综合排放标准》(GB 16297-1996)、TJ 36-79和《环境影响评价技术导则大气环境》(HJ/T 2.2-93)进行计算或推导的对策.     

我国土壤环境管理名录制度实施中的问题分析和对策

我国污染地块土壤环境管理的基本制度包括疑似污染地块名单制度、污染地块名录制度、建设用地土壤污染风险管控和修复名录制度。分析了3项制度的主要内容和执行现状,提出了实施中存在的6个问题,阐述了6个方面的对策建议。分析认为,目前疑似污染地块名单和污染地块名录制度未明确“退出”程序和要求;制度的实际执行情况与管理办法的要求不一致;各地纳入疑似污染地块名单的地块数量明显偏少;信息公开的渠道与内容未做统一要求;初步调查报告的编制和评审要求在现行技术规范中缺乏足够阐述;风险管控和修复名录制度对工程实施的变更程序、是否明确设置工程设计环节等未做出明确规定。最后,提出在污染地块环境管理办法修订过程中应增加“退出”疑似污染地块名单和污染地块名录的条件和要求、信息公开渠道与内容,明确由项目业主单位自行确定是否开展工程设计,将疑似污染地块名录的制定和信息公开责任调升为市级生态环境主管部门负责,并细化《建设用地土壤环境调查评估技术指南》中的初步调查布点要求和采样深度要求,加快省级风险评估报告和效果评估报告评审细则文件的制定等建议,以期为我国土壤环境管理部门提供决策参考。     

Conditional sampling for measuring mercury vapor fluxes

Surface–atmosphere mercury fluxes are difficult to measure accurately. Current techniques include dynamic flux chambers and micrometeorological gradient and aerodynamic approaches, all of which have a number of intrinsic problems associated with them. We have adapted conditional sampling (relaxed eddy accumulation), a micrometeorological technique commonly used to measure other trace gas fluxes, to measure surface–air mercury fluxes. Our initial flux measurement campaign over an agricultural soil consisted of two 1-week measurement periods, and was longer in duration than previously reported mercury flux measurement periods. Fluxes during both measurement periods ranged between 190.5 (evolution) and –91.7 ng m⁻² h⁻¹ (deposition) with an average evolution of 9.67 ng m⁻² h⁻¹. The data showed significant diurnal trends, weakly correlated with shallow soil temperatures and solar radiation. This initial trial run indicates that conditional sampling has much promise for the accurate quantification of both short and long-term mercury fluxes.     

A fabric denuder for sampling semi-volatile species

A new style of diffusion denuder has been evaluated specifically for sampling HNO3. A coated fabric is used as the denuder substrate, which can be loaded directly into a standard filter holder. This approach allows direct denuder sampling with no additional capital costs over filter sampling and simplifies the coating and extraction process. Potential denuder materials and coatings were evaluated in the laboratory to test the removal efficiency. NaCl coatings were used to assess more than 20 materials for HNO3 collection efficiency. Particle retention, which would cause a denuder to have a positive bias for gas concentration measurements, was evaluated by ambient air sampling using particulate sulfate as the reference aerosol. Particle retention varied from 0 to 15%, depending on the denuder material tested. The best performing material showed an average particle retention of less than 3%. Denuder efficiency of four fabric materials was tested under ambient conditions to determine removal efficiency. The fabric denuder method was compared with a long path-length Fourier transform infrared (FTIR) spectrometer, a tunable diode laser absorption spectrometer (TDLAS), and a denuder difference sampler to independently measure HNO3. HNO3 collection efficiency was typically 90% for the denuders, whether coated with NaCl or not. For 10-L/min sampling rates with the fabric denuder, the square of the correlation coefficient with the FTIR spectrometer was 0.73, compared to 0.24 with the TDLAS.     

Objective sensor placement for sampling regional turbidity

Objective sensor-placement techniques are applied to the process of selecting locations for a network of ten pyranometers, which will be used to investigate regional patterns of high turbidity across the northeastern United States. The techniques involve adjusting via nonlinear programming methods the values of coefficients in a continuous function that describes correlations between turbidity values separated by temporal and spatial intervals, in order to best describe the structure of turbidity. With the correlation structure function that is found, sensor locations are evaluated by calculating the normalized residual variance obtained from objective analyses performed at gridpoints across the region of interest. Sensor positions are shifted by nonlinear programming methods until residual variance is minimized. A comparison is made between simultaneous and sequential methods of sensorplacement optimization, in which the incremental value of adding sensors is determined objectively.     

The EU environmental policy context for monitoring for and with raptors in Europe

This paper outlines the importance of the policy context for monitoring with and for raptors, and, conversely, of the importance of such monitoring for policy. It then outlines two key areas of European Union (EU) environmental policy most relevant to monitoring for and with raptors, namely biodiversity policy and pollution policy. For each of the policy areas, the pertinent objectives and actions of the current EU policy are identified, and their relevance for raptor monitoring is discussed. The potential contribution of raptor monitoring to the further development of these policy areas is also addressed.     

An automated systems for air sampling with annular denuder systems at a remote site

An automated air sampling system has been designed for use with the annular denuder system (ADS). The automated air sampling system allows for accurate measurements of air volume and day-night sampling while preventing the accumulation of moisture within the ADS caused by condensation or cloud events. The sampling system consists of air flow, monitoring and control subsystems. Calibration of the sampling system against a Hoffer turbine flow meter indicated accurate measurement of air flow volumes. Field testing and preliminary data have shown that the sampling system functions well in a remote mountain forest site, and was relatively unaffected by condensation, fog, or cloud events.     

Optimized method for dissolved hydrogen sampling in groundwater

Dissolved hydrogen concentrations are used to characterize redox conditions of contaminated aquifers. The currently accepted and recommended bubble strip method for hydrogen sampling (Wiedemeier et al., 1998) requires relatively long sampling times and immediate field analysis. In this study we present methods for optimized sampling and for sample storage. The bubble strip sampling method was examined for various flow rates, bubble sizes (headspace volume in the sampling bulb) and two different H2 concentrations. The results were compared to a theoretical equilibration model. Turbulent flow in the sampling bulb was optimized for gas transfer by reducing the inlet diameter. Extraction with a 5 mL headspace volume and flow rates higher than 100 mL/min resulted in 95-100% equilibrium within 10-15 min. In order to investigate the storage of samples from the gas sampling bulb gas samples were kept in headspace vials for varying periods. Hydrogen samples (4.5 ppmv, corresponding to 3.5 nM in liquid phase) could be stored up to 48 h and 72 h with a recovery rate of 100.1+/-2.6% and 94.6+/-3.2%, respectively. These results are promising and prove the possibility of storage for 2-3 days before laboratory analysis. The optimized method was tested at a field site contaminated with chlorinated solvents. Duplicate gas samples were stored in headspace vials and analyzed after 24 h. Concentrations were measured in the range of 2.5-8.0 nM corresponding to known concentrations in reduced aquifers.     

Passive air sampling theory for semivolatile organic compounds

The mathematical modelling underlying passive air sampling theory can be based on mass transfer coefficients or rate constants. Generally, these models have not been inter-related. Starting with basic models, the exchange of chemicals between the gaseous phase and the sampler is developed using mass transfer coefficients and rate constants. Importantly, the inter-relationships between the approaches are demonstrated by relating uptake rate constants and loss rate constants to mass transfer coefficients when either sampler-side or air-side resistance is dominating chemical exchange. The influence of sampler area and sampler volume on chemical exchange is discussed in general terms and as they relate to frequently used parameters such as sampling rates and time to equilibrium. Where air-side or sampler-side resistance dominates, an increase in the surface area of the sampler will increase sampling rates. Sampling rates are not related to the sampler/air partition coefficient (K(SV)) when air-side resistance dominates and increase with K(SV) when sampler-side resistance dominates.     

Towards optimal sampling schedules for integral pumping tests

Ethanol use as a gasoline additive is increasing, as are the chances of groundwater contamination caused by gasoline releases involving ethanol. To evaluate the impact of ethanol on dissolved hydrocarbon plumes, a field test was performed in which three gasoline residual sources with different ethanol fractions (E0: no ethanol, E10: 10% ethanol and E95: 95% ethanol) were emplaced below the water table. Using the numerical model BIONAPL/3D, the mass discharge rates of benzene, toluene, ethylbenzene, xylenes, trimethylbenzenes and naphthalene were simulated and results compared to those obtained from sampling transects of multilevel samplers. It was shown that ethanol dissolved rapidly and migrated downgradient as a short slug. Mass discharge of the hydrocarbons from the E0 and E10 sources suggested similar first-order hydrocarbon decay rates, indicating that ethanol from E10 had no impact on hydrocarbon degradation. In contrast, the estimated hydrocarbon decay rates were significantly lower when the source was E95. For the E0 and E10 cases, the aquifer did not have enough oxygen to support complete mineralization of the hydrocarbon compounds to the extent suggested by the field-based mass discharge. Introducing a heterogeneous distribution of hydraulic conductivity did little to overcome this discrepancy. A better match between the numerical model and the field data was obtained assuming partial degradation of the hydrocarbons to intermediate compounds. Besides depending on the ethanol concentration, the impact of ethanol on hydrocarbon degradation appears to be highly dependent on the availability of electron acceptors.     

Conjoint analysis for environmental evaluation

BACKGROUND, AIM AND SCOPE: Conjoint analysis and the related choice-modelling methods have been used for many years in marketing research to evaluate consumer behaviour and preferences for different kinds of product attributes. Recently, the number of applications in environmental science and management has started to grow. Conjoint analysis is found in many different forms, and the environmental studies evaluated in this review display the same range of methods as in other fields. The key characteristic of all these methods is that trade-offs are evaluated by jointly considering a number of important attributes. MAIN FEATURES: This paper is a review of the literature on environmental applications of conjoint analysis and assesses in which environmental area conjoint analysis has been most successful. The method and the design of the studies are reviewed as well. RESULTS: A total of 84 studies were found, dealing with environmental issues that were evaluated by conjoint analysis. The studies concern agriculture, ecosystem management, energy, environmental evaluation, forestry, land management, pollution, products, recreation, environmental risk analysis and waste management. DISCUSSION: Choice experiments seem to have a comparatively stronger position in environmental studies than elsewhere. Most of the environmental applications are related to natural resource management. This is somewhat surprising, but a number of reports have appeared also on product evaluation, which could be a key application area in the future. CONCLUSIONS: Compared to marketing and transportation, the number of environmental conjoint studies is rather small but increasing, and the method has proven to work effectively in eliciting preferences on environmental issues. In environmental issues, experimenters often use choice experiments, especially concerning ecosystem management and environmental evaluations. When it comes to evaluating preferences concerning agriculture, forestry, energy and products, a more traditional approach of conjoint analysis is favoured. RECOMMENDATIONS AND PERSPECTIVES: Two new areas of application are identified in this review--environmental communication and expert elicitation. Conjoint analysis can thus be developed into a useful instrument for environmental risk analysis and communication, both of which are necessary for an efficient approach to risk governance.     

Designing of sampling programmes for industrial effluent monitoring

Introduction  

Monitoring of effluent discharges from industrial establishments discharging directly into municipality sewers is one of the major water pollution control activities conducted by municipalities. For largely industrialised municipalities, the task can be quite expensive and not effective if sampling programmes are not properly designed. In most cases, samples are randomly collected without proper knowledge of the discharge patterns of various industries. As a result, the information obtained does not give a good reflection of the quality of effluent being discharged.