A comparison of four gravimetric fine particle sampling methods.

A study was conducted to compare four gravimetric methods of measuring fine particle (PM2.5) concentrations in air: the BGI, Inc. PQ200 Federal Reference Method PM2.5 (FRM) sampler; the Harvard-Marple Impactor (HI); the BGI, Inc. GK2.05 KTL Respirable/Thoracic Cyclone (KTL); and the AirMetrics MiniVol (MiniVol). Pairs of FRM, HI, and KTL samplers and one MiniVol sampler were collocated and 24-hr integrated PM2.5 samples were collected on 21 days from January 6 through April 9, 2000. The mean and standard deviation of PM2.5 levels from the FRM samplers were 13.6 and 6.8 microg/m3, respectively. Significant systematic bias was found between mean concentrations from the FRM and the MiniVol (1.14 microg/m3, p = 0.0007), the HI and the MiniVol (0.85 microg/m3, p = 0.0048), and the KTL and the MiniVol (1.23 microg/m3, p = 0.0078) according to paired t test analyses. Linear regression on all pairwise combinations of the sampler types was used to evaluate measurements made by the samplers. None of the regression intercepts was significantly different from 0, and only two of the regression slopes were significantly different from 1, that for the FRM and the MiniVol [beta1 = 0.91, 95% CI (0.83-0.99)] and that for the KTL and the MiniVol [beta1 = 0.88, 95% CI (0.78-0.98)]. Regression R2 terms were 0.96 or greater between all pairs of samplers, and regression root mean square error terms (RMSE) were 1.65 microg/m3 or less. These results suggest that the MiniVol will underestimate measurements made by the FRM, the HI, and the KTL by an amount proportional to PM2.5 concentration. Nonetheless, these results indicate that all of the sampler types are comparable if approximately 10% variation on the mean levels and on individual measurement levels is considered acceptable and the actual concentration is within the range of this study (5-35 microg/m3).     

The MMT bag for emission source sampling: design and evaluation

This paper presents the design and evaluation results for a metal-coated multilayer Tedlar (MMT) bag that was developed for the collection of source emissions. The applicability of the MMT bag was evaluated for a number of important greenhouse relevant gases: CO, CO2, CH4, N2O, and total hydrocarbons (THCs). The bag was tested for durability and stability for a range of concentrations of the tested compounds using both laboratory-prepared samples and real source samples. The results show that all tested compounds were more stable when stored in the MMT bag than when stored in a regular Tedlar bag. These compounds can be stored at room temperature for at least 3 months without significant changes in concentration. When properly packed, the MMT bag is durable and may be shipped by air. The MMT bag is lower in cost, lighter in weight, and easier to clean, and it requires less devices during the subsequent laboratory analysis compared with a stainless steel canister, which is often used to collect air and source samples.     

Review of receptor modeling methods for source apportionment

Efforts have been made to relate measured concentrations of airborne constituents to their origins for more than 50 years. During this time interval, there have been developments in the measurement technology to gather highly time-resolved, detailed chemical compositional data. Similarly, the improvements in computers have permitted a parallel development of data analysis tools that permit the extraction of information from these data. There is now a substantial capability to provide useful insights into the sources of pollutants and their atmospheric processing that can help inform air quality management options. Efforts have been made to combine receptor and chemical transport models to provide improved apportionments. Tools are available to utilize limited numbers of known profiles with the ambient data to obtain more accurate apportionments for targeted sources. In addition, tools are in place to allow more advanced models to be fitted to the data based on conceptual models of the nature of the sources and the sampling/analytical approach. Each of the approaches has its strengths and weaknesses. However, the field as a whole suffers from a lack of measurements of source emission compositions. There has not been an active effort to develop source profiles for stationary sources for a long time, and with many significant sources built in developing countries, the lack of local profiles is a serious problem in effective source apportionment. The field is now relatively mature in terms of its methods and its ability to adapt to new measurement technologies, so that we can be assured of a high likelihood of extracting the maximal information from the collected data.

Implications: Efforts have been made over the past 50 years to use air quality data to estimate the influence of air pollution sources. These methods are now relatively mature and many are readily accessible through publically available software. This review examines the development of receptor models and the current state of the art in extracting source identification and apportionments from ambient air quality data.     

Application of different RP-HPLC methods for the determination of the octanol/water partition coefficient of selected tetrachlorobenzyltoluenes.

Reversed-phase high-performance liquid chromatography (RP-HPLC) in both, isocratic and gradient elution mode (stationary phase: LiChrospher 100 RP-18; mobile phase: water/methanol or water/acetonitrile) was used for a renewed determination of octanol/water partition coefficients (Kow) of selected tetrachlorobenzyltoluene (TCBT) isomers. Reported Kow values identify this substance class as very hydrophobic but the data are relatively inconsistent. Based on a series of calibration runs with hydrophobic reference substances of different chemical structure at various eluent compositions we tested different approaches for the evaluation of isocratic retention factors (logk) and found substantial differences between the direct calibration procedure at special methanol volume fractions in the mobile phase (0.95-0.80) and the use of retention factors extrapolated to pure water as eluent (logkw). The logKow values obtained for the TCBTs with the latter approach are around 0.5 units higher and closer to literature data. The gradient elution experiments yield slightly better results compared to the isocratic direct calibration procedure, but not as good as the calibration with log kw. In addition, the use of the RP-HPLC retention factors for estimating sorption coefficients (Koc) of TCBT isomers is discussed.     

Intercomparison of methods for sampling and analysis of atmospheric mercury species

An intercomparison for sampling and analysis of atmospheric mercury species was held in Tuscany, June 1998. Methods for sampling and analysis of total gaseous mercury (TGM), reactive gaseous mercury (RGM) and total particulate mercury (TPM) were used in parallel sampling over a period of 4 days. The results show that the different methods employed for TGM compared well whereas RGM and TPM showed a somewhat higher variability. Measurement results of RGM and TPM improved over the time period indicating that activities at the sampling site during set-up and initial sampling affected the results. Especially the TPM measurement results were affected. Additional parallel sampling was performed for two of the TPM methods under more controlled conditions which yielded more comparable results.     

Studies on sampling methods for PCDDs and PCDFs in stack emission

Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) in stack emission exist both as vapor and sorbed onto the surface of particles. The partition between the two phases is of a dynamic nature and changes rapidly with temperature. When monitoring stack emissions, a sampling method must be used that efficiently collects both phases as well as any condensation aerosol formed in the sampling train. In this study, the two sampling methods used in Sweden, the cooled probe polyurethane foam plug (PUFP) sampling train and the sampling train recommended by the Swedish Environmental Protection Board has been tested for particle collection ability. The results show that an aerosol filter has to be introduced after the condensor in order to collect particle bound PCDDs and PCDFs efficiently.     

A comparison of river water quality sampling methodologies under highly variable load conditions

When river water quality fluctuates over relatively short periods of time with respect to the sampling frequency, the collection of grab samples may be inappropriate for characterising average water quality. This paper presents the results of a water quality monitoring study carried out on a stretch of the river Lambro (northern Italy) dominated by a periodically overloaded sewage treatment works (STW) located near its upstream end. Water quality was strongly influenced by a pronounced diurnal cycle in pollutant loads caused by the regular emission of untreated waste water during periods of high domestic flow (daytime). Two different sampling techniques were employed: grab sampling and 24-h composite sampling using automatic samplers. Samples were collected at the plant overflow and at several sites along the river and analysed for two common ingredients of household detergents, linear alkylbenzene sulphonate (LAS) and boron (B) and for routine water quality variables. The results obtained show that: (1) The diurnal variability of point-source-derived chemical concentrations in the river downstream of the undersized STW increased with increasing removal efficiency in sewage treatment. (2) The shape of the diurnal concentration signal remained relatively intact for a considerable distance downstream of the STW for several water quality variables, suggesting that hydrodynamic dispersion plays a relatively minor role in controlling concentration patterns in this river. (3) In-stream degradation of LAS was consistent with first order kinetics with a rate constant of 0.05-0.06 h(-1). (4) Grab sampling is a relatively inefficient methodology for capturing mean concentrations for rivers subjected to highly variable loads, especially when it is restricted to office hours. The inefficiency of grab sampling is more marked for substances (e.g. LAS) which are effectively removed during sewage treatment than for substances which are not. (5) For LAS, diurnal variability in the concentration signal decreases with distance downstream, making grab sampling an increasingly reliable methodology for estimating mean concentrations. (6) 24-h composite sampling is an efficient way of eliminating the effect of diurnal variations in load strength.     

Cost-effective sampling network design for contaminant plume monitoring under general hydrogeological conditions

A new simulation-optimization methodology is developed for cost-effective sampling network design associated with long-term monitoring of large-scale contaminant plumes. The new methodology is similar in concept to the one presented by Reed et al. (Reed, P.M., Minsker, B.S., Valocchi, A.J., 2000a. Cost-effective long-term groundwater monitoring design using a genetic algorithm and global mass interpolation. Water Resour. Res. 36 (12), 3731-3741) in that an optimization model based on a genetic algorithm is coupled with a flow and transport simulator and a global mass estimator to search for optimal sampling strategies. However, this study introduces the first and second moments of a three-dimensional contaminant plume as new constraints in the optimization formulation, and demonstrates the proposed methodology through a real-world application. The new moment constraints significantly increase the accuracy of the plume interpolated from the sampled data relative to the plume simulated by the transport model. The plume interpolation approaches employed in this study are ordinary kriging (OK) and inverse distance weighting (IDW). The proposed methodology is applied to the monitoring of plume evolution during a pump-and-treat operation at a large field site. It is shown that potential cost savings up to 65.6% may be achieved without any significant loss of accuracy in mass and moment estimations. The IDW-based interpolation method is computationally more efficient than the OK-based method and results in more potential cost savings. However, the OK-based method leads to more accurate mass and moment estimations. A comparison of the sampling designs obtained with and without the moment constraints points to their importance in ensuring a robust long-term monitoring design that is both cost-effective and accurate in mass and moment estimations. Additional analysis demonstrates the sensitivity of the optimal sampling design to the various coefficients included in the objective function of the optimization model.     

Comparison of various sampling methods for PCDDs and PCDFs in stack gas

There have been discussions about how complete PCDDs and PCDFs are sampled from stack gas of waste combustion plants by various sampling methods. In Germany, at present, a sampling method is used, which was first proposed by Nottrodt et al.¹, consisting of a filter device, condenser, and an absorption train. Since this sampling procedure complicates sampling and analysis, we compared this “standard procedure” with a “dilution method”, where only a filter, impregnated with paraffin, is used as trapping device, and also tested the effectiveness of XAD-2 as an adsorption trap.

As standard procedure the standard train was always used in parallel to other sampling methods. The results of four parallel sampling periods confirmed, that comparable results are obtained, when parallel sampling is carried out with the standard train.

The result of our investigation can be summarized as follows: The total emission of PCDDs and PCDFs determined by different sampling procedures varies only insignificantly. This means that sampling and analysis for PCDDs and PCDFs in stack gas could be simplified considerably.     

A qualitative UV spectroscopic method as an initial guide to source origins of polycyclic aromatic hydrocarbons

A qualitative method is described, using ultraviolet spectroscopy, to determine the source origins of polycyclic aromatic hydrocarbons present in the environment. The technique takes advantage of the fact that aromatic compounds exhibit strong absorption in the ultraviolet region. It offers a fast and convenient alternative to other methods, which normally require extensive sample clean-up to avoid or limit interference from other materials during analysis. In contrast, this method requires only basic column chromatography to isolate the compounds of interest. Examples of the application of the technique are presented; the results are corroborated by those previously obtained by other methods.     

Formaldehyde source interaction studies under whole-house conditions

This study was designed to determine the effect of source combinations on formaldehyde levels under whole-house conditions. Evaluations were conducted on particleboard (applied as subflooring) and hardwood plywood panelling (applied as a wall covering) both singly and in combination, and on urea-formaldehyde foam insulation and particleboard. Formaldehyde source combination/interaction evaluations revealed several different outcomes, including no augmentation of formaldehyde levels, a slight augmentation (30-50%) and complete addivity. Additivity was observed for regular and low emission grade particleboard and hardwood plywood combinations and for urea-formaldehyde foam insulation and particleboard subflooring. In contrast, controlled chamber studies employing samples of the same wood materials revealed no additive effects. Results of these studies raise questions about the reliability of using laboratory evaluations alone to predict formaldehyde levels under real-world residential conditions.     

An improved algorithm for locating a gas source using inverse methods

We apply an inverse problem approach to locating a known gas source in a desert setting from simultaneous measurements of gas concentration and wind data. We use a random search algorithm with simulated annealing to generate candidate distributions of source strengths and positions. These distributions are then assessed by means of a cost function, which quantifies the degree to which the postulated source distribution accounts for the measured gas concentrations. We present results from using three cost functions with differing regularisation terms. We assess the robustness of these and the differing regularisation terms by the progressive addition of random noise and systematic offsets to the concentration data. We show that for our application, the best reconstructions are obtained by using a multiplicative regularisation parameter defined to minimise the total gas emissions.     

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.     

Understanding the source of water for selected springs within Mojave Trails National Monument,California

While water sources that sustain many of the springs in the Mojave Desert have been poorly understood, the desert ecosystem can be highly dependent on such resources. This evaluation updates the water resource forensics of Bonanza Spring, the largest spring in the southeastern Mojave Desert. The source of spring flow at Bonanza Spring was evaluated through an integration of published geologic maps, measured groundwater levels, water quality chemistry, and isotope data compiled from both published sources and new samples collected for water chemistry and isotopic composition. The results indicate that Bonanza Spring has a regional water source, in hydraulic communication with basin fill aquifer systems. Neighboring Lower Bonanza Spring appears to primarily be a downstream manifestation of surfacing water originally discharged from the Bonanza Spring source. Whereas other springs in the area, Hummingbird, Chuckwalla, and Teresa Springs, each appear to be locally sourced as “perched” springs. These conclusions have important implications for managing activities that have the potential to impact the desert ecosystem.     

Passive sampling of selected endocrine disrupting compounds using polar organic chemical integrative samplers

Two types of polar organic chemical integrative samplers (pharmaceutical POCIS and pesticide POCIS) were examined for their sampling efficiency of selected endocrine disrupting compounds (EDCs). Laboratory-based calibration of POCISs was conducted by exposing them at high and low concentrations of 14 EDCs (4-alkyl-phenols, their ethoxylate oligomers, bisphenol A, selected estrogens and synthetic steroids) for different time periods. The kinetic studies showed an integrative uptake up to 28 days. The sampling rates for the individual compounds were obtained. The use of POCISs could result in an integrative approach to the quality status of the aquatic systems especially in the case of high variation of water concentrations of EDCs. The sampling efficiency of POCISs under various field conditions was assessed after their deployment in different aquatic environments.     

不同类型海岸的溢油清理方法

世界石油资源分布和需求的不均衡性,促进了海上石油工业和石油运输业的快速发展,同时也增加了溢油事故的几率.海上溢油污染问题日趋严重,溢油污染对海洋环境、生态、资源、经济及人类生产生活等造成了巨大的影响,日益引起社会各界的关注.海岸溢油污染清理实践表明,正确的溢油清理方案的制定应综合考虑海岸的敏感性指数、溢油的类型、清理方法可能带来的危害以及支际可操作程度等.对包括盐沼地海岸和红树林海岸,沉积海岸,以及岩石海岸三类典型海岸的国内外现有海岸溢油污染清理技术进行了详细的综述,以期为我国的海岸带管理和溢油应急计划的制订提供技术参考.