Air Sampling Measurements Research Articles

Analysis and Modeling of Airborne BTEX Concentrations from the Deepwater Horizon Oil Spill

Concerns have been raised about whether the Deepwater Horizon oil spill cleanup workers experienced adverse health effects from exposure to airborne benzene, toluene, ethylbenzene, and xylene (BTEX) which volatilized from surfaced oil. Thus, we analyzed the nearly 20 000 BTEX measurements of breathing zone air samples of offshore cleanup workers taken during the six months following the incident (made publicly available by British Petroleum). The measurements indicate that 99% of the measurements taken prior to capping the well were 32-, 510-, 360-, and 77-fold lower than the U.S. Occupational Safety and Health Administration's Permissible Exposure Limits (PELs) for BTEX, respectively. BTEX measurements did not decrease appreciably during the three months after the well was capped. Moreover, the magnitudes of these data were similar to measurements from ships not involved in oil slick remediation, suggesting that the BTEX measurements were primarily due to engine exhaust rather than the oil slick. To supplement the data analysis, two modeling approaches were employed to estimate airborne BTEX concentrations under a variety of conditions (e.g., oil slick thickness, wind velocity). The modeling results corroborated that BTEX concentrations from the oil were well below PELs and that the oil was not the primary contributor to the measured BTEX.

In utero exposure to bisphenol-A and its effect on birth weight of offspring

To examine the effect of in utero BPA exposure on the birth weight of offspring, a total of 587 children from families in which parent(s) did or did not have occupational exposure to BPA were examined. Their birth weights were obtained by an in-person interview of the mother. Parental BPA exposure level during the index pregnancy was determined through personal air sampling measurements and exposure history. After controlling for potential confounders, parental exposure to BPA in the workplace during pregnancy was associated with decreased birth weight. The association was stronger for maternal exposure which is statistically significant ( P = 0.02). A dose–response relationship was observed with increased BPA exposure levels in pregnancy associated with greater magnitude of decrease of birth weight in offspring ( P = 0.003). Our findings provide the new epidemiologic evidence suggesting that in utero exposure to BPA during pregnancy may be associated with decreased birth weight in offspring.

Development of a novel methodology for indoor emission source identification

The objective of this study was to develop and evaluate a methodology to identify individual sources of emissions based on the measurements of mixed air samples and the emission signatures of individual materials previously determined by Proton Transfer Reaction-Mass Spectrometry (PTR-MS), an on-line analytical device. The methodology based on signal processing principles was developed by employing the method of multiple regression least squares (MRLS) and a normalization technique. Samples of nine typical building materials were tested individually and in combination, including carpet, ceiling material, gypsum board, linoleum, two paints, polyolefine, PVC and wood. Volatile Organic Compound (VOC) emissions from each material were measured in a 50-liter small-scale chamber. Chamber air was sampled by PTR-MS to establish a database of emission signatures unique to each individual material. The same task was performed to measure combined emissions from material mixtures for the application and validation of the developed signal separation method. Results showed that the proposed method could identify the individual sources under laboratory conditions with two, three, five and seven materials present. Further experiments and investigation are needed for cases where the relative emission rates among different compounds may change over a long-term period. ► Unique emission patterns appear to exist for building materials. ► These unique patterns can be established as emission signatures by PTR-MS. ► VOC mixture emissions among material mixtures appear to be superposed. ► Sorptive effects exist, but can be accurately assessed with the new technique. ► By these identified features, material emission sources can be clearly pointed out.

Mitigation of methane emission from Fakse landfill using a biowindow system

Landfills are significant sources of atmospheric methane (CH 4) that contributes to climate change, and therefore there is a need to reduce CH 4 emissions from landfills. A promising cost efficient technology is to integrate compost into landfill covers (so-called “biocovers”) to enhance biological oxidation of CH 4. A full scale biocover system to reduce CH 4 emissions was installed at Fakse landfill, Denmark using composted yard waste as active material supporting CH 4 oxidation. Ten biowindows with a total area of 5000 m 2 were integrated into the existing cover at the 12 ha site. To increase CH 4 load to the biowindows, leachate wells were capped, and clay was added to slopes at the site. Point measurements using flux chambers suggested in most cases that almost all CH 4 was oxidized, but more detailed studies on emissions from the site after installation of the biocover as well as measurements of total CH 4 emissions showed that a significant portion of the emission quantified in the baseline study continued unabated from the site. Total emission measurements suggested a reduction in CH 4 emission of approximately 28% at the end of the one year monitoring period. This was supported by analysis of stable carbon isotopes which showed an increase in oxidation efficiency from 16% to 41%. The project documented that integrating approaches such a whole landfill emission measurements using tracer techniques or stable carbon isotope measurements of ambient air samples are needed to document CH 4 mitigation efficiencies of biocover systems. The study also revealed that there still exist several challenges to better optimize the functionality. The most important challenges are to control gas flow and evenly distribute the gas into the biocovers.

A cryogen-free refrigerating preconcentration device for the measurement of C2 to C4 hydrocarbons in ambient air

A cryogen-free refrigerating preconcentration device for the enrichment of trace amounts of highly volatile organic compounds in the atmosphere prior to analysis has been designed and evaluated. The device consists of a microtrap housed in an insulated box, which is cooled by a conventional refrigeration unit. Experimental parameters, including adsorbent mass, trapping temperature, and thermal desorption temperature, were optimized. The on-line coupling of the device to a GC allows sufficient enrichment and separation of C2 to C4 hydrocarbons in less than 40 min without a second cryotrap. The target compounds analysis showed good linearity (correlation coefficients >0.99) and repeatability (relative standard deviation <5%). Detection limits for the 10 volatile organic compounds ranged from 14 ppt to 52 ppt, under the conditions of a 500 mL sampling volume and -10 °C trapping temperature. Real air sample measurements were conducted at an urban site, and five VOCs including ethane, ethene, propane, propene and 1-butene were detected and quantified.

Accelerating growth of HFC-227ea (1,1,1,2,3,3,3-heptafluoropropane) in the atmosphere

Abstract. We report the first measurements of 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea), a substitute for ozone depleting compounds, in air samples originating from remote regions of the atmosphere and present evidence for its accelerating growth. Observed mixing ratios ranged from below 0.01 ppt in deep firn air to 0.59 ppt in the current northern mid-latitudinal upper troposphere. Firn air samples collected in Greenland were used to reconstruct a history of atmospheric abundance. Year-on-year increases were deduced, with acceleration in the growth rate from 0.029 ppt per year in 2000 to 0.056 ppt per year in 2007. Upper tropospheric air samples provide evidence for a continuing growth until late 2009. Furthermore we calculated a stratospheric lifetime of 370 years from measurements of air samples collected on board high altitude aircraft and balloons. Emission estimates were determined from the reconstructed atmospheric trend and suggest that current "bottom-up" estimates of global emissions for 2005 are too high by a factor of three.

Emissions of 1,2‐Dichloroethane from Holiday Decorations as a Source of Indoor Air Contamination

Groundwater contamination associated with an industrial facility in Utah has led to concerns about potential vapor intrusion into residences outside the facility boundary. Trichloroethylene (TCE) is the main contaminant of concern with 1,2‐dichloroethane (1,2‐DCA) present in some areas. An air‐monitoring program implemented to detect vapor intrusion of these compounds found 1,2‐DCA in homes outside areas of groundwater contamination, suggesting indoor sources in these cases. Investigative indoor air and product sampling were conducted to isolate consumer products emitting 1,2‐DCA and to quantify the emission rates of identified products. The combination of room‐by‐room air sampling and emission measurements was successfully used to identify molded plastic holiday ornaments, having measured emission rates as high as 0.3 µg 1,2‐DCA/min. Subsequent testing of seven comparable retail items found similar 1,2‐DCA emissions. Screening‐level calculations show that the measured emission rates of 1,2‐DCA from these items can lead to indoor concentrations high enough to be of regulatory concern (0.094 to 9.4 µg/m3 based on 10–6 to 10–4 cancer risk levels).

Assimilation of SCIAMACHY total column CO observations: Global and regional analysis of data impact

Carbon monoxide (CO) total column observations from the Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY) on board Envisat‐1 are assimilated into the Global Modeling and Assimilation Office constituent assimilation system for the period 1 April to 20 December 2004. The impact of the assimilation on CO distribution is evaluated using independent surface flask observations from the National Oceanic and Atmospheric Administration (NOAA)/ESRL global cooperative air sampling network and Measurement of Ozone and Water Vapor by Airbus In‐Service Aircraft (MOZAIC) in situ CO profiles. Assimilation of SCIAMACHY data improves agreement of CO assimilation with both of these data sets on both global and regional scales compared to the free‐running model. Regional comparisons with MOZAIC profiles made in western Europe, the northeastern United States, and the Arabian Peninsula show improvements at all three locations in the free troposphere and into the boundary layer over Arabia and the northeastern United States. Comparisons with NOAA Earth System Research Laboratory data improve at about two thirds of the surface observation sites. The systematic model errors related to the uncertainty of CO surface sources and the chemistry of CO losses are investigated through experiments with increased surface CO emissions over the Arabian Peninsula and/or globally reduced hydroxyl radical (OH) concentrations. Both model changes decrease mean CO errors at all altitudes in comparison to MOZAIC data over Dubai and Abu Dhabi. In contrast, errors in the assimilated CO are reduced by the increased emissions for pressures ≥800 hPa and by the reduced OH for pressures ≤600 hPa. Our analysis suggests that CO emissions over Dubai in 2004 are more than double those in the 1998 emissions inventory.

Comprehensive software for the assessment of 222Rn and 220Rn decay products based on air sampling measurements

A computational tool dedicated to the measurement of 222Rn and 220Rn decay products by air sampling is presented. α- or γ-spectrometry measurements, gross α or β counting, as well as a combination of them are considered. Special attention is given to the evaluation of the uncertainty budget of the results. Besides typical applications in the analysis of experimental data, the software can be used for assessing the expected quality of a measurement protocol and for optimizing it, by generating and analyzing sets of realistic synthetic data.

Children's inhalation exposure to methamidophos from sprayed potato fields in Washington State: Exploring the use of probabilistic modeling of meteorological data in exposure assessment

We examined the significance of meteorology and postspray volatilization of methamidophos (an organophosphorus insecticide) in assessing potential inhalation risk to children in an agricultural community. We combined fluxes from sources and dispersion modeling with a range of possible local meteorology to create output to study the variability in potential community exposure as a result of changing temperature, wind speeds and wind directions. This work is based on an aerial spray drift study where air sampling measurements of methamidophos were made before, during and after a spray event were used to examine acute inhalation risk for children living in an Eastern Washington State community in close proximity (between 15 and 200 m) to sprayed potato fields. We compared the measured average air concentrations of methamidophos in the community to a "no observed adverse effect level" for subchronic inhalation to characterize acute and subchronic inhalation risks. The baseline estimates of inhalation exposure were below Environment Protection Agency's (EPA) level of concern based on a target margin of exposure of 300. As meteorological conditions during and after spraying influence the amount of material moving into areas where children reside we used historical meteorological data to drive model simulations that predicted likely air residue concentrations under different wind and temperature conditions. We also added variability to the decay constant and initial emission fluxes to create a 2-D simulation of estimated air concentrations in the community near the fields. This work provides a methodological framework for the assessment of air concentrations of pesticides from agricultural sprays in the absence of extended measurements, although including variability from meteorological conditions. The deterministic as well as the probabilistic risk analyses in this study indicated that postspray volatilization in the specific spray situation analyzed (methamidophos applied on potato fields in Eastern Washington) did not pose acute or subchronic risks as defined by the EPA. However, this study did not consider any pathway of exposure other than inhalation (e.g. diet, dermal, etc.) and the risk assessment should be evaluated in that context.

Measurement of radon daughters in water and in air using the detection unit “YAPMARE” with a YAP:Ce scintillation detector

With a focus on the detection of the Rn concentration in water in extreme conditions, the detection unit YAPMARE was developed by the company CRYTUR. The main part of the detection unit is a detection probe based on the Ø25×100 mm YAP:Ce detector. The measured water covers approximately 95% of the crystal surface (the detection volume is 12 ml). Measurements of 222Rn and 220Rn standards for determination of individual peaks in the spectra were conducted, including an observation of the 222Rn (and its daughters) behavior. For YAPMARE calibration, fresh water was taken from a drilled well in the Lounovice area (biotitic granodiorite–adamellite). The calibration was carried out with the assistance of radon in water monitor RADIM 4. The results of the water measurements in Lounovice were as follows: detection limit was about 50 Bq/l, and calibration coefficient was 0.0011 imp/s per 1 Bq/l. The results of the fresh water and air sample measurements have demonstrated the main advantages (spectrometric results of the measurement, possibility for water or air samples evaluation) and disadvantages (large size of scintillation crystal increases gamma ray background, calibration for each water with particular composition, and detector cleaning using HCl acid).

Ten years of atmospheric methane observations at a high elevation site in Western China

Abstract In this paper, the continuous (1994–2001) and discrete air sample (1991–2001) measurements of atmospheric CH 4 from the Waliguan Baseline Observatory located in western China (36°17′N, 100°54′E, 3816 m asl) are presented and characterized. The CH 4 time series show large episodic events on the order of 100 ppb throughout the year. During spring, a diurnal cycle with average amplitude of 7 ppb and a morning maximum and late afternoon minimum is observed. In winter, a diurnal cycle with average amplitude of 14 ppb is observed with an afternoon maximum and morning minimum. Unlike most terrestrial observational sites, no obvious diurnal patterns are present during the summer or autumn. A background data selection procedure was developed based on local horizontal and vertical winds. A selected hourly data set representative of “baseline” conditions was derived with approximately 50% of the valid hourly data. The range of CH 4 mixing ratios, annual means, annual increases and mean annual cycle at Waliguan during the 1992–2001 were derived from discrete and continuous data representative of “baseline” conditions and compared to air samples collected at other Northern Hemisphere sites. The range of CH 4 monthly means of 1746–1822 ppb, average annual means of 1786.7±10.8 ppb and mean annual increase of 4.5±4.2 ppb yr −1 at Waliguan were inline with measurements from sites located between 30° and 60°N. There were variations observed in the CH 4 annual increase patterns at Waliguan that were slightly different from the global pattern. The mean CH 4 annual cycle at Waliguan shows an unusual pattern of two gentle peaks in summer and February along with two small valleys in early winter and spring and a mean peak-to-peak amplitude of ∼11 ppb, much smaller than amplitudes observed at most other mid- and high-northern latitude sites. The Waliguan CH 4 data are strongly influenced by continental Asian CH 4 emissions and provide key information for global atmospheric CH 4 models.

Variability and repeatability of olfactometric results of n-butanol, pig odour and a synthetic gas mixture

For the purposes of a research project for the Flemish authorities, olfactometric measurements were carried out at six closed pig farms and six fattener farms. The results of these olfactometric measurements were compared with the olfactometric results of n-butanol samples and samples of a synthetic gas mixture of ethanethiol, methylacetate and 2-propanol in nitrogen, both analysed on the same days as the air samples from the pig farms. The results of the n-butanol tests for all panellists showed that nobody was qualified according to the CEN criteria, and that, consequently, these criteria are rather stringent. Comparing the variability of the results for the three different odours showed that the mean and standard deviation of the mean variance were not significantly different for the three odour types, which means that the repeatability of the panellist results was equal for the examined odour types. The principle of traceability was checked by comparing the variance of the n-butanol, pig odour and synthetic mixture ratio. For the complete dataset, the principle of traceability could not been proven for n-butanol. For the restricted dataset, the principle of traceability was more valid for n-butanol than for the mixture, but differences were small. Finally, normalization was looked for with regard to olfactometric measurements of air samples from pig arms based either on n-butanol or on the synthetic mixture. Both models had low determination coefficients, but the model based on the synthetic mixture gave better results than the one based on n-butanol.

Comprehensive two-dimensional gas chromatography (GC × GC) measurements of volatile organic compounds in the atmosphere

Abstract. During the MINOS campaign in August 2001 comprehensive two-dimensional gas chromatography (GC x GC) was applied to the in situ measurements of atmospheric volatile organic compounds (VOCs) at the Finokalia ground station, Crete. The measurement system employs a thermal desorption unit for on-line sampling and injection, and a GC x GC separation system equipped with a flame ionization detector (FID) for detection. The system was optimized to resolve C7-C14 organic components. Two-dimensional chromatograms from measurements of Finokalia air samples show several hundred well-separated peaks. To facilitate peak identification, cartridge samples collected at Finokalia were analyzed using the same GC x GC system coupled with a time-of-flight mass spectrometer (TOF-MS). The resulting mass spectra were deconvoluted and compared to spectra from a database for tentative peak identification. About 650 peaks have been identified in the two-dimensional plane, with significant signal/noise ratios (&gt;100) and high spectra similarities (&gt;800). By comparing observed retention indices with those found in the literature, 235 of the identifications have been confirmed. 150 of the confirmed compounds show up in the C7-C14 range of the chromatogram from the in situ measurement. However, at least as many peaks remain unidentified. For quantification of the GC x GC measurements, peak volumes of measured compounds have been integrated and externally calibrated using a standard gas mixture.

Interannual growth rate variations of atmospheric CO2 and its δ13C, H2, CH4, and CO between 1992 and 1999 linked to biomass burning

High‐precision, multispecies measurements of flask air samples since 1992 from CSIRO's global sampling network reveal strong correlation among interannual growth rate variations of CO2 and its δ13C, H2, CH4, and CO. We show that a major fraction of the variability is consistent with two emission pulses coinciding with large biomass burning events in 1994/1995 and 1997/1998 in tropical and boreal regions, and observations of unusually high levels of combustion products in the overlying troposphere at these times. Implied pulse strengths and multispecies emission ratios are not consistent with any other single process, but do not exclude possible contributions from covarying processes that are linked through climatic forcing. Comparison of CO2 with its δ13C indicates that most of the CO2 variation is from terrestrial exchange, but does not distinguish forcing by biomass burning from imbalance in photosynthesis/respiration of terrestrial ecosystems. Partitioning of terrestrial CO2 fluxes is constrained by H2, CH4, and CO, all of which are products of biomass burning but which have no direct link to net respiration of CO2. While CO is a strong indicator of biomass burning, its short lifetime prevents it from usefully constraining the magnitude of CO2 emissions. If the H2 and CH4 variations were dominated by biomass burning, they would imply associated carbon emissions in excess of mean annual levels of other years, of 0.6–3.5 and 0.8–3.7 Pg C for 1994/1995 and 1997/1998, respectively. The large range in emission estimates mainly reflects uncertainty in H2/CO2 and CH4/CO2 emission ratios of fires in these years.

In situ measurements of atmospheric methane at GAGE/AGAGE sites during 1985–2000 and resulting source inferences

Continuous measurements of methane since 1986 at the Global Atmospherics Gases Experiment/Advanced Global Atmospherics Gases Experiment (GAGE/AGAGE) surface sites are described. The precisions range from approximately 10 ppb at Mace Head, Ireland, during GAGE to better than 2 ppb at Cape Grim, Tasmania, during AGAGE (i.e., since 1993). The measurements exhibit good agreement with coincident measurements of air samples from the same locations analyzed by Climate Monitoring and Diagnostics Laboratory (CMDL) except for differences of approximately 5 ppb before 1989 (GAGE lower) and about 4 ppb from 1991 to 1995 (GAGE higher). These results are obtained before applying a factor of 1.0119 to the GAGE/AGAGE values to place them on the Tohoku University scale. The measurements combined with a 12‐box atmospheric model and an assumed atmospheric lifetime of 9.1 years indicates net annual emissions (emissions minus soil sinks) of 545 Tg CH4 with a variability of only ±20 Tg from 1985 to 1997 but an increase in the emissions in 1998 of 37 ± 10 Tg. The effect of OH changes inferred by Prinn et al. [2001] is to increase the estimated methane emissions by approximately 20 Tg in the mid‐1980s and to reduce them by 20 Tg in 1997 and by more thereafter. Using a two‐dimensional (2‐D), 12‐box model with transport constrained by the GAGE/AGAGE chlorofluorocarbon measurements, we calculate that the proportion of the emissions coming from the Northern Hemisphere is between 73 and 81%, depending on the OH distribution used. However, this result includes an adjustment of 5% derived from a simulation of the 2‐D estimation procedure using the 3‐D MOZART model. This adjustment is needed because of the very different spatial emission distributions of the chlorofluorocarbons and methane which makes chlorofluorocarbons derived transport rates inaccurate for the 2‐D simulation of methane. The 2‐D model combined with the annual cycle in OH from Spivakovsky et al. [2000] provide an acceptable fit to the observed 12‐month cycles in methane. The trend in the amplitude of the annual cycle of methane at Cape Grim is used to infer a trend in OH in 30°–90°S of 0 ± 5% per decade from 1985 to 2000, in qualitative agreement with Prinn et al. [2001] for the Southern Hemisphere.

Summary of stationary and personal air sampling measurements made during a plutonium glovebox decommissioning project.

Workplace air sampling was performed during the decommissioning of a previously active plutonium glovebox facility located at Argonne National Laboratory. Personal air samplers (PAS) were used to measure breathing zone activity concentrations of workers engaged in size-reducing contaminated gloveboxes. Stationary air samplers (SAS) were used to measure the work area activity concentrations and test their application in providing representative sampling of breathing zone activity concentrations. The relative response of these samplers (PAS:SAS) was tracked during the course of the decommissioning work, with results yielding favorable agreement to within a factor of +/-5. A cascade impactor was used to determine the particle size distribution of workplace aerosols. The average activity median aerodynamic diameter (AMAD) was estimated to be 3.0 microm, with a corresponding geometric standard deviation of 2.4. A gas-flow proportional counter was utilized to measure the gross alpha activity collected on both the SAS glass fiber and the PAS cellulose fiber filters. A subset of this filter group was subsequently analyzed using an alpha spectrometer post radiochemical processing and isotopic separation. The quantity of alpha activity measured on the SAS filters was generally within +/-30% of the alpha spectrometry measurements. However, measurements made of the activity present on the PAS cellulose fiber filters were consistently underestimated using a gas-flow proportional counter, suggesting a small correction factor of 15-20% to account for the absorption of alpha particle emissions.

Determinants of Exposure to Respirable Quartz Dust in the Construction Industry

Because most masonry building materials contain quartz and because these materials are subjected to a variety of treatments during the building process, quartz is encountered everywhere in building operations. The level of exposure to respirable quartz has been measured for some highly exposed groups of employees. At 30 construction sites personal air sampling (PAS) measurements of respirable dust and quartz have been performed and 171 samples have been taken. Both respirable dust and quartz levels were high. Respirable quartz exposures of more than ten times the Dutch limit value of 0.075 mg/m(3) TWA were common, but exposures up to 200 times the Dutch limit value were also found. The measurements were task oriented. By statistical analysis the contribution of the different determinants to the total exposure has been identified. With this approach, directions for an effective control measures programme can be given.

Determinants of exposure to respirable quartz dust in the construction industry

Because most masonry building materials contain quartz and because these materials are subjected to a variety of treatments during the building process, quartz is encountered everywhere in building operations. The level of exposure to respirable quartz has been measured for some highly exposed groups of employees. At 30 construction sites personal air sampling (PAS) measurements of respirable dust and quartz have been performed and 171 samples have been taken. Both respirable dust and quartz levels were high. Respirable quartz exposures of more than ten times the Dutch limit value of 0.075 mg/m3 TWA were common, but exposures up to 200 times the Dutch limit value were also found. The measurements were task oriented.By statistical analysis the contribution of the different determinants to the total exposure has been identified. With this approach, directions for an effective control measures programme can be given.

Biological monitoring of workers exposed to dimethylformamide in a textile polyurethane unit.

Dimethylformamide (DMF) is a universal solvent noted for its solubility in both aqueous and lipid media. It is hepatotoxic, and there are concerns about its carcinogenicity. Our objective was to determine the correlation between air monitoring measurements and biological measurements of a suitable metabolite of DMF in a cohort of operatives in a polyurethane production unit. This was done with a view to assessing how much the inhalation route contributed to total DMF exposure, mainly for control purposes. We investigated the relationship between personal air sample measurements of DMF and biological measurements of N-methylformamide (NMF) in nine adult subjects, recruited across the shifts, with varying levels of exposure to DMF. Personal exposure monitoring was carried out with a low-flow-rate Model 222-4 SKC pump, while post-shift urine samples were obtained for further analysis. Operatives were asked to abstain from consuming alcohol for 24 h before the designated shift, as advised by the laboratory responsible for the analysis of urine samples. We found a very strong statistical association between air sample measurements of DMF and NMF in the urine of the sample population (R(2) = 0.95, P < 0.0001). This study suggests that airborne exposure contributes significantly to elevated levels of NMF and, therefore, indicates that efforts should be concentrated on engineering controls in reducing workplace DMF exposure.