Tapered Element Oscillating Microbalance Monitor Research Articles

Field and laboratory comparison of PM10 instruments in high winds

Abstract Instruments capable of measuring PM10 (particulate matter ≤10 µm in aerodynamic diameter) concentrations may vary in performance as a result of different technologies utilized in measuring PM10. Therefore, the performance of five instruments capable of measuring PM10 concentrations above eroding soil surfaces was tested during high wind events at field sites in the Columbia Plateau and inside a wind tunnel. Comparisons among the Big Spring Number Eight (BSNE) sampler, DustTrak monitor, E-sampler, High-Volume sampler, and Tapered Element Oscillating Microbalance (TEOM) monitor were made at field sites during nine wind erosion events and inside a wind tunnel at two wind speeds (7 and 12 m s−1) and two ambient PM10 concentrations (2 and 50 mg m−3). PM10 concentrations were similar for the High-Volume sampler and TEOM monitor as well as for the BSNE samplers and DustTrak monitors but higher for the High-Volume sampler and TEOM monitor than the E-sampler during field erosion events. Based upon wind tunnel experiments, the TEOM monitor measured the highest PM10 concentration while the DustTrak monitor typically measured the lowest PM10 concentration as compared with other instruments. In addition, PM10 concentration appeared to lower for all instruments at a wind speed of 12 as compared with 7 m s−1 inside the wind tunnel. Differences in the performance of instruments in measuring PM10 concentration poses risks in comparing PM10 concentration among different instrument types or using multiple instrument types to jointly measure concentrations in the field or laboratory or even the same instrument type subject to different wind speeds.

진주시 대기중 PM10및 PM2.5의 질량농도 특성

Ambient particulate matters(PM10 and PM2.5) were investigated at GNTECH university in Jinju city. Samples were collected using a dichotomous sampler(series 240, Andersen Corp.) and a TEOM(Tapered Element Oscillating Microbalance) monitor period from November 2012 to October 2013. For the dichotomous sampler measurements, daily 24-h integrated PM2.5 and PM10.2.5 ambient air samples were collected at a total flow rate of 16.7 L /min. For the TEOM monitor measurements, daily 1-h integrated PM10 ambient air samples were collected at a flow rate of 16.7 L /min. The annual average concentrations of PM10-2.5 and PM2.5 by a dichotomous sampler were 10.0±6.1 μg/m3 and 22.6±9.3 μg/m3, respectively. And PM10 concentration by dichotomous sampler were similar to TEOM monitor by 32.7±12.9 μg/m3 and 31.7±11.3 μg/m3, respectively. And good correlation (R2=0.964) between the two methods was observed. The annual average of PM2.5/PM10 ratio was 0.70±0.12.

Temporal characteristics of black carbon concentrations and its potential emission sources in a southern Taiwan industrial urban area

This study investigates the temporal characteristics of black carbon and its potential emission sources, as well as the fractions of BC in PM2.5 levels in Kaohsiung urban area, which is an industrial city in southern Taiwan. Concentrations of BC and PM2.5 are monitored continuously from March 2006 to February 2010, using an aethalometer and a tapered element oscillating microbalance monitor. Additionally, the presence of organic compounds (or UV enhanced species) in particles at the sampling site is determined using the Delta-C (UVBC-BC) value. According to long-term measurement results, BC and PM2.5 concentrations are 3.33 and 34.0 μg m(-3), respectively, in the Kaohsiung urban area. The ratio of BC/PM2.5 is approximately 11 %. Low concentration of BC and PM2.5 in the summer of this study period is mostly likely owing to meteorological conditions that favored dispersion of local air pollutants. Nevertheless, BC concentrations peaked markedly during morning hours (7:00-11:00), likely owing to local traffic congestion. Measurement results suggest that BC is released from local traffic activities and emitted from industrial activities at this sampling site. Additionally, Delta-C values are significantly higher than zero during January-March and November-December periods in this industrial urban area, implying that UV enhanced species can be observed. At this sampling site, these UV enhanced species do not only originate from household activity and solid waste burning but also release from industrial activities. The elevated Delta-C values during nighttime (18:00-6:00) in the autumn and winter seasons are likely related to those UV enhanced species in the atmosphere, which can be condensed on particle surface under low temperature conditions. According to long-term measurement results, significantly positive Delta-C values can be observed under temperatures <20 °C and relative humidity of 60-75 % in this study. Despite the household activity and solid waste burning, the major sources of particles that are bound with UV enhanced species in this sampling site are industrial parks and a coal-fired power plant.

Measurement of light scattering in an urban area with a nephelometer and PM2.5 FDMS TEOM monitor: Accounting for the effect of water

The U.S. Environmental Protection Agency (EPA) has proposed a new secondary standard based on visibility in urban areas. The proposed standard will be based on light extinction, calculated from 24-hr averaged measurements. It would be desirable to base the standard on a shorter averaging time to better represent human perception of visibility. This could be accomplished by either an estimation of extinction from semicontinuous particulate matter (PM) data or direct measurement of scattering and absorption. To this end we have compared 1-hr measurements of fine plus coarse particulate scattering using a nephelometer, along with an estimate of absorption from aethalometer measurements. The study took place in Lindon, UT, during February and March 2012. The nephelometer measurements were corrected for coarse particle scattering and compared to the Filter Dynamic Measurement System (FDMS) tapered element oscillating microbalance monitor (TEOM) PM2.5 measurements. The two measurements agreed with a mass scattering coefficient of 3.3 ± 0.3 m2/g at relative humidity below 80%. However, at higher humidity, the nephelometer gave higher scattering results due to water absorbed by ammonium nitrate and ammonium sulfate in the particles. This particle-associated water is not measured by the FDMS TEOM. The FDMS TEOM data could be corrected for this difference using appropriate IMPROVE protocols if the particle composition is known. However, a better approach may be to use a particle measurement system that allows for semicontinuous measurements but also measures particle bound water. Data are presented from a 2003 study in Rubidoux, CA, showing how this could be accomplished using a Grimm model 1100 aerosol spectrometer or comparable instrument. Implications: Visibility is currently based on 24-hr averaged PM mass and composition. A metric that captures diurnal changes would better represent human perception. Furthermore, if the PM measurement included aerosol bound water, this would negate the need to know particulate composition and relative humidity (RH), which is currently used to estimate visibility. Methods are outlined that could accomplish both of these objectives based on use of a PM monitor that includes aerosol-bound water. It is recommended that these techniques, coupled with appropriate measurements of light scattering and absorption by aerosols, be evaluated for potential use in the visibility based secondary standard.

Design and Characterization of a Two-Stage Human Subject Exposure Chamber

ABSTRACT A human subject exposure chamber, designed to hold six to eight subjects, coupled to an approximately 30-m3 Teflon reaction bag was designed and built to provide exposures that mimic the production and photochemical oxidation of atmospheric pollutants resulting from the combustion of coal or wood from a stove. The combustion products are introduced into the Teflon bag under atmospheric conditions. Photochemical oxidation of this mixture is accomplished by exposure to tropospheric sun-like radiation from an array of ultraviolet and black lamps. The aerosol in the Teflon reaction bag is then transferred into the exposure room to maintain a constant, lower exposure level. Continuous and semicontinuous monitoring of the gas and particulate matter (PM) pollution in the exposure room and the reaction bag is accomplished using a suite of instruments. This suite of instruments allows for the measurement of the concentrations of total and nonvolatile PM, nitric oxide, nitrogen dioxide, carbon monoxide, carbon dioxide, and ozone. The concentration of the particles was monitored by an R&P tapered element oscillating microbalance monitor. The chemical composition of the PM and its morphological characterization is accomplished by collecting samples in filter packs and conducting ion chromatography, elemental X-ray fluorescence, and scanning electron microscopy analyses. The concentration and composition of emissions from combustion of wood and coal is described. The results of this study suggest that although the bulk compositions of particulate emissions from the combustion of coal or wood in a stove have many similarities, the wood smoke aerosol is photochemically reactive, whereas the coal smoke aerosol is not. IMPLICATIONS The presence of high concentrations of PM and ozone in air has been linked to exacerbation of cardiovascular and cerebrovascular health problems. This manuscript describes the design of a human subject exposure chamber that allows for the production and control of PM and atmospherically important gases and characterizes pollutants present in the exposure chamber from the combustion of wood and coal. Fresh and photochemically aged pollutants are characterized. The chamber thus allows for studies to be conducted to quantify the effects of short-term PM and gas exposure on human subjects.

Temperature effect of tapered element oscillating microbalance (TEOM) system measuring semi-volatile organic particulate matter

The tapered element oscillating microbalance (TEOM) system is widely used to measure continuous particle mass concentrations in air quality networks. However, the semi-volatile aerosol material is lost under normal operation conditions (50 °C). This study has evaluated the error in the organic fraction of the TEOM-measured secondary organic aerosols formed from the degradation of biogenic pollutants. Experiments were carried out under controlled, water-free conditions in a fully equipped, high volume atmospheric simulator--the European PhotoReactor (EUPHORE). The ozonolysis of α-pinene, β-pinene and limonene provided a reproducible source of organic aerosol. Particulate matter concentration profiles were registered for different TEOM operating temperatures. When these values were compared with values from a filter-based gravimetric method and a scanning mobility particle sizer (SMPS), they showed that the differences between monitoring systems increased with increasing TEOM temperature. According to our results, when the TEOM is operated at 50 °C, it fails to measure 32-46% of the organic particulate material, depending on the aerosol precursor. This study has also identified and quantified the multi-oxygenated organic compounds lost in the TEOM monitoring by using a method based on the gas chromatography-mass spectrometry technique. Important losses have been calculated for relevant ambient aerosol compounds such as pinonic acid, pinonaldehyde, norpinone and limonalic acid. In conclusion, the present study has demonstrated that a high operating temperature of the TEOM monitor reduces the humidity interference but underestimates the semi-volatile organic fraction.

The Measurement of Fine Particulate Semivolatile Material in

Ammonium nitrate and semivolatile organic material (SVOM) are significant components of fine particles in urban atmospheres. These components, however, are not properly determined with methods such as the fine particulate matter (PM2.5) Federal Reference Method (FRM) or other single filter samplers because of significant losses of semivolatile material (SVM) from particles collected on the filter during sampling. The R&P tapered element oscillating microbalance (TEOM) monitor also does not measure SVM, because this method heats the sample to remove particle bound water, which also results in evaporation of SVM. Recent advances in monitoring techniques have resulted in samplers for both integrated and continuous measurement of total PM2.5, including the particle concentrator Brigham Young University organic sampling system (PC-BOSS), the real time total ambient mass sampler (RAMS), and the R&P filter dynamics measurement system (FDMS) TEOM monitor. Results obtained using these samplers have been compared with those obtained with either a PM2.5 FRM sampler or a TEOM monitor in studies conducted during the past five years. These studies have shown the following: (1) the PC-BOSS, RAMS, and FDMS TEOM are all comparable. Each instrument measures both the nonvolatile material and the SVM. (2) The SVM is not retained on the heated filter of a regular TEOM monitor and is not measured by this sampling technique. (3) Much of the SVM is also lost during sampling from single filter samplers such as the PM2.5 FRM sampler. (4) The amount of SVM lost from single filter samplers can vary from less than one-third of that lost from heated TEOM filters during cold winter conditions to essentially all during warm summer conditions. (5) SVOM can only be reliably collected using an appropriate denuder sampler. (6) A PM2.5 speciation sampler can be easily modified to a denuder sampler with filters that can be analyzed for semivolatile organic carbon (OC), nonvolatile OC, and elemental carbon using existing OC/elemental carbon analytical techniques. The research upon which these statements are based for various urban studies are summarized in this paper.

New York State Urban and Rural Measurements of Continuous PM2.5 Mass by FDMS, TEOM, and BAM

Field evaluations and comparisons of continuous fine particulate matter (PM2.5) mass measurement technologies at an urban and a rural site in New York state are performed. The continuous measurement technologies include the filter dynamics measurement system (FDMS) tapered element oscillating microbalance (TEOM) monitor, the stand-alone TEOM monitor (without the FDMS), and the beta attenuation monitor (BAM). These continuous measurement methods are also compared with 24-hr integrated filters collected and analyzed under the Federal Reference Method (FRM) protocol. The measurement sites are New York City (the borough of Queens) and Addison, a rural area of southwestern New York state. New York City data comparisons between the FDMS TEOM, BAM, and FRM are examined for bias and seasonality during a 2-yr period. Data comparisons for the FDMS TEOM and FRM from the Addison location are examined for the same 2-yr period. The BAM and FDMS measurements at Queens are highly correlated with each other and the FRM. The BAM and FDMS are very similar to each other in magnitude, and both are ∼25% higher than the FRM filter measurements at this site. The FDMS at Addison measures ∼9% more mass than the FRM. Mass reconstructions using the speciation trends network filter data are examined to provide insight as to the contribution of volatile species of PM2.5 in the FDMS mass measurement and the fraction that is likely lost in the FRM mass measurement. The reconstructed mass at Queens is systematically lower than the FDMS by ∼10%.

Comparison of Measured Total Suspended Particulate Matter Concentrations Using Tapered Element Oscillating Microbalance and a Total Suspended Particulate Sampler

A comparison of the concentration of the total suspended particulate (TSP) matter measured by the tapered element oscillating microbalance (TEOM) monitor and the isokinetic TSP samplers developed at the University of Illinois was carried out in several types of confinement livestock buildings. In a majority of the measurements done, the dust concentration measured by the TEOM monitor was lower than the University of Illinois at Urbana-Champaign (UIUC) isokinetic TSP sampler; the TEOM monitor tended to underestimate the total dust concentration by as much as 54%. The difference in measurements can be attributed to the sampling efficiency of the TEOM monitor sampling head and the loss of some semivolatile compounds and particle-bound water because of heating of the TEOM monitor sampling stream to 50 °C. Although several articles in the literature supported the latter argument, this study did not investigate the effect of heating the sampling stream or the effect of moisture on the relative difference in dust concentration measurements. The model that best describes the relationship between the two methods was site specific, that is, the linear regression model was applicable only to four of the sites monitored. The measured total dust concentration in livestock buildings range from ∼300 to 4000 μg/m3; a higher correlation coefficient between TEOM-TSP and UIUC-TSP monitors was obtained in swine facilities than those obtained in a laying facility.

Continuous Determination of Fine Particulate Matter Mass in the Salt Lake City Environmental Monitoring Project: A Comparison of Real-Time and Conventional TEOM Monitor Results

Fine particulate matter (PM2.5) mass was determined on a continuous basis at the Salt Lake City Environmental Protection Agency Environmental Monitoring for Public Awareness and Community Tracking monitoring site in Salt Lake City, UT, using three different monitoring techniques. Hourly averaged PM2.5 mass data were collected during two sampling periods (summer 2000 and winter 2002) using a real-time total ambient mass sampler (RAMS), sample equilibration system (SES)-tapered element oscillating microbalance (TEOM), and conventional TEOM monitor. This paper compares the results obtained from the various monitoring systems, which differ in their treatment of semivolatile material (SVM; particle-bound water, semivolatile ammonium nitrate, and semivolatile organic compounds). PM2.5 mass results obtained by the RAMS were consistently higher than those obtained by the SES-TEOM and conventional TEOM monitors because of the RAMS ability to measure semivolatile ammonium nitrate and semivolatile organic material but not particle-bound water. The SESTEOM monitoring system was able to account for an average of 28% of the SVM, whereas the conventional TEOM monitor loses essentially all of the SVM from the single filter during sampling. Occasional mass readings by the various TEOM monitors that are higher than RAMS results may reflect particle-bound water, which, under some conditions, is measured by the TEOM but not the RAMS.

Measurement of total PM2.5mass (nonvolatile plus semivolatile) with the Filter Dynamic Measurement System tapered element oscillating microbalance monitor

Field studies have been performed in Lindon, Utah (February 2003) and Rubidoux, California (July 2003) to determine if the Rupprecht and Patashnick (R&amp;P) Filter Dynamic Measurement System (FDMS) determines total fine particulate mass, including the semivolatile ammonium nitrate and organic material. Collocated measurements were made with the FDMS, a conventional tapered element oscillating microbalance (TEOM) monitor with a heated filter, an R&amp;P differential TEOM monitor, the Brigham Young University (BYU) Real‐Time Total Ambient Mass Sampler (RAMS), the BYU particle concentrator‐organic sampling system (PC‐BOSS), a PM2.5Federal Reference Method (FRM), a PM2.5speciation sampler, an R&amp;P continuous nitrate monitor, and two Sunset continuous carbon monitors (one to measure quartz filter‐retained particulate carbon and one to measure particulate semivolatile carbonaceous material lost from the particles on a filter during sampling). The RAMS and PC‐BOSS samplers have been shown to determine fine particulate material, including both the semivolatile and the nonvolatile components. Linear regression analysis at the Lindon site between the FDMS (X) and the PC‐BOSS (Y), and the FDMS (X) and the RAMS (Y), resulted in zero‐intercept slopes of 1.01 ± 0.06 (r2= 0.63) and 1.00 ± 0.01 (r2= 0.69), respectively. At the Rubidoux sampling site, linear regression analysis between the PC‐BOSS (X) and the FDMS (Y) gave a zero‐intercept slope of 0.96 ± 0.02 (r2= 0.90). Linear regression analysis between the FDMS (X) and the RAMS (Y) resulted in a zero‐intercept slope of 0.99 ± 0.01 (r2= 0.80). Measurements made at the two sites indicate that the FDMS and the R&amp;P differential TEOM monitors do measure total fine particulate mass, including the semivolatile ammonium nitrate and organic material. Both the heated TEOM monitor and PM2.5FRM did not measure the semivolatile material. The difference between the FDMS and a heated TEOM monitor was explained by the semivolatile ammonium nitrate and organic material measured by the various chemical composition monitors.

Long-Term Field Characterization of Tapered Element Oscillating Microbalance and Modified Tapered Element Oscillating Microbalance Samplers in Urban and Rural New York State Locations

Long-term field comparisons of continuous and integrated filter measurements of mass concentrations of par-ticulate matter (PM) with an aerodynamic diameter less than or equal to 2.5 μm (PM2.5) were performed at rural and urban sites in New York State. Two versions of the continuous tapered element oscillating microbalance (TEOM) mass monitor are deployed at each site, in addition to Federal Reference Method filter samplers. Data are grouped into monthly averages to retain and demonstrate seasonal differences. Strong seasonal dependence is observed—the TEOM monitors with the heated sensors are biased systematically low with respect to the Federal Reference Method measurements during the cold season. For the rural site, the average bias for the sample equilibration system (SES)-equipped and standard TEOM monitors is 14 and 24%, respectively. At this location, the TEOM monitor measurements were biased low for all 34 months. For the urban site, the average bias for the SES and standard TEOM monitors is 8 and 18%, respectively. At this location, the TEOM monitor measurements are as likely to be biased high as low during the warm-season months. The hour averaged data from the two versions of the TEOM monitor are also compared, and also indicate that the SES-equipped version of the TEOM monitor captures 7-11% more PM2.5 mass at these locations.

Laboratory Characterization of Modified Tapered Element Oscillating Microbalance Samplers

Laboratory tests with generated aerosols were conducted to test the efficacy of two recent design modifications to the well-established tapered element oscillating microbalance (TEOM) continuous particulate matter (PM) mass monitor. The two systems tested were the sample equilibration system-equipped TEOM monitor operating at 30 °C, which uses a Nafion dryer as part of the sample inlet, and the differential TEOM monitor, which adds a switched electrostatic precipitator and uses a self-referencing algorithm to determine “true PM mass.” Test aerosols included ammonium sulfate, ammonium nitrate, sodium chloride, copper (II) sulfate, and mixed aerosols. Aerosols were generated with an atomizer or a vibrating orifice generator and were equilibrated in a 450-L slow flow chamber before being sampled. Relative humidity in the chamber was varied between 10 and 90%, and step changes in humidity were executed while generating aerosol to test the response of the instruments. The sample equilibration system-equipped TEOM monitor does reduce, but not totally eliminate, the sensitivity of the TEOM mass monitor to changes in humidity. The differential TEOM monitor gives every indication of being a very robust technique for the continuous real-time measurement of ambient aerosol mass, even in the presence of semi-volatile particles and condensable gases.

Trends in PM 2.5 composition at the Department of Energy OST NETL fine particle characterization site in Pittsburgh, PA, USA

This paper reports on the results from the first 6 months (from November 1999 to April 2000) of an ongoing monitoring study of fine particulate air pollutants at the Department of Energy's Office of Science and Technology (OST) NETL sampling site, 30 km southwest of Pittsburgh city center, Pennsylvania. This study is part of a 2-year sampling program for PM characterization, under the auspices of The University Coal Research Program of the National Energy Technology Laboratory (NETL), US Department of Energy in Pittsburgh, PA, USA. Samples were collected daily with a Particle Concentrator-Brigham Young University Organic Sampling System (PC-BOSS) to determine PM 2.3 composition, including the semi-volatile organic compounds (SVOC) and ammonium nitrate lost from particles during sampling. Average fine particulate composition during the 6-month period was: constructed PM 2.3, 19.4 μg m −3; ammonium sulfate 4.3 μg m −3; non-volatile organic material, 6.9 μg m −3; elemental carbon, 0.4 μg m −3; SVOC lost from particles during sampling, 6.1 μg m −3; retained ammonium nitrate, 1.4 μg m −3; lost ammonium nitrate, 0.3 μg m −3. Results from the PC-BOSS sampler are also compared with those obtained from a Federal Reference Method PM 2.5 sampler, and a Tapered Element Oscillating Microbalance monitor, both of which tended to not measure the semi-volatile particulate matter. SVOC concentrations were highest in the spring. Episodes of fine particulate non-volatile organic material occurred throughout the 6-month period. Average ammonium sulfate concentrations were higher in November and January than the other months for the study period.

Evaluation of the RAMS Continuous Monitor for Determination of PM2.5 Mass Including Semi-Volatile Material in Philadelphia, PA

The real-time ambient mass sampler (RAMS) is a continuous monitor based on particle concentrator, denuder, drier, and tapered element oscillating microbalance (TEOM) monitor technology. It is designed to measure PM2.5 mass, including the semi-volatile species NH4NO3 and semi-volatile organic material, but not to measure PM2.5 water content. The performance of the RAMS in an urban environment with high humidity was evaluated during the July 1999 NARSTO-Northeast Oxidant and Particles Study (NEOPS) intensive study at the Baxter water treatment plant in Philadelphia, PA. The results obtained with the RAMS were compared to mass measurements made with a TEOM monitor and to constructed mass obtained with a Particle Concentrator-Brigham Young University Organic Sampling System (PC-BOSS) sampler designed to determine the chemical composition of fine particles, including the semi-volatile species. An average of 28% of the fine particulate material present during the study was semi-volatile organic material lost from a filter during particle collection, and 1% was NH4NO3 that was also lost from the particles during sampling. The remaining mass was dominantly nonvolatile (NH4)2SO4 (31%) and organic material (37%), with minor amounts of soot, crustal material, and nonvolatile NH4NO3. Comparison of the RAMS and PC-BOSS results indicated that the RAMS correctly monitored for fine particulate mass, including the semi-volatile material. In contrast, the heated filter of the TEOM monitor did not measure the semi-volatile material. The comparison of the RAMS and PC-BOSS data had a precision of ±4.1 μg/m3 (±9.6%). The precision of the RAMS data was limited by the uncertainty in the blank correction for the reversible adsorption of water by the charcoal-impregnated cellulose sorbent filter of the RAMS monitor. The precision of the measurement of fine par-ticulate components by the PC-BOSS was ±6-8%.

Development of a Sample Equilibration System for the TEOM Continuous PM Monitor

ABSTRACT In recent years, scientific discussion has included the influence of thermodynamic conditions (e.g., temperature, relative humidity, and filter face velocity) on PM retention efficiency of filter-based samplers and monitors. Method-associated thermodynamic conditions can, in some instances, dramatically influence the presence of particle-bound water and other light-molecular-weight chemical components such as particulate nitrates and certain organic compounds. The measurement of fine particle mass presents a new challenge for all PM measurement methods, since a relatively greater fraction of the mass is semi-volatile. The tapered element oscillating microbalance (TEOM) continuous PM monitor is a U.S. Environmental Protection Agency (EPA) PM10 equivalent method (EQPM-1090-079). Several hundred of these monitors are deployed throughout the United States. The TEOM monitor has the unique characteristic of providing direct PM mass measurement without the calibration uncertainty inherent in mass surrogate methods. In addition, it provides high-precision, near-real-time continuous data automatically. Much attention has been given to semi-volatile species retention of the TEOM method. While using this monitor, it is desirable to maintain as low an operating temperature as practical and to remove unwanted particle-bound water. A new sample equilibration system (SES) has been developed to allow conditioning of the PM sample stream to a lower humidity and temperature level. The SES incorporates a special low-particle-loss Nafion dryer. This paper discusses the configuration and theory of the SES. Performance results include high time-resolved PM2.5 data comparison between a 30 °C sample stream TEOM monitor with SES and a standard 50 °C TEOM monitor. In addition, 24-hr integrated data are compared with data collected using an EPA PM2.5 Federal Reference Method (FRM)-type sampler. The SES is a significant development because it can be applied easily to existing TEOM monitors.

Comparison between a personal PM 10 sampling head and the tapered element oscillating microbalance (TEOM) system

A new personal PM 10 sampling head has been developed by the Institute of Occupational Medicine (IOM), Edinburgh. The purpose of this study was to compare its performance in the field with the accepted fixed-location PM 10 sampler, the tapered element oscillating microbalance (TEOM). The comparisons were carried out on three separate occasions during 1997 at each of two city centre locations in the UK. On each occasion two personal IOM PM 10 sampling heads were located adjacent to a TEOM monitor and four successive sets of 24-h filter samples were collected. The data was compared with 24-h average TEOM concentrations, calculated as the arithmetic mean of the recorded hourly averages. There was a statistically significant linear relationship between the two types of monitor, although the concentrations from the IOM PM 10 samplers were consistently higher than the TEOM data. It is therefore possible to use the regression equations presented in this paper to correct ambient PM 10 concentrations measured by either method to equivalent values. Further research is needed to properly understand the reason for the difference between the TEOM and filter samplers.