Workplace Aerosols Research Articles

1 Comparison of Ni Speciation Using Methods of Sequential Leaching and Quantitative Mineralogy for Workplace Aerosol at a Stainless Steel Plant

Abstract Based on epidemiological records of workers at Ni operations, regulatory guidelines often target specific Ni compounds for setting exposure limits. Thus, reliable methods of Ni speciation in airborne dust samples are required for effective monitoring of workplace exposure. In this study, Ni speciation of dust collected from a stainless steel operation was performed using a variety of methods: Zatka sequential leaching (original and modified protocols), soluble and insoluble Ni as described in ISO 15202, and quantitative mineralogy (QEMSCAN). Mineral characterization was also performed on bulk material collected from selected work areas at the plant. The quantitative mineralogical analysis determined that the Ni dust is composed of oxidic Ni (Ni in chromite and trevorite, > 80 % of the Ni in most samples) and metallic Ni (Ni-Fe alloy), and the results were validated against chemical assays and alternate methods of mineral characterization (Electron Probe Microanalysis, EPMA). In contrast, the original Zatka method erroneously identified soluble Ni as a major Ni contributor, whereas the modified Zatka method identified sulfidic Ni. The mineralogy identified ambient dust and grain sizes and textures of individual Ni compounds as potential factors that can affect leaching selectivity. Improving methods of sequential leaching is important because the resolution of quantitative mineralogical techniques diminishes at < 3 µm (respirable dust fraction). We recommend that quantitative mineralogy be performed in parallel with methods of sequential leaching to provide a robust system of characterization.

100 Lightweight Air Sampling Badge for Material-Specific Monitoring of Workplace Aerosol Exposure

Abstract Monitoring occupational exposure to hazardous airborne materials like carbon nanotubes (CNTs) or graphene is an inevitable element of every risk mitigation strategy to protect employees. Conventional air samplers are often bulky, need to be operated by trained personnel and results are not available on-site. Here, we address these issues and introduce the patented Stat Peel Identifier system comprised of portable, lightweight sampling badges and a fully automatized Raman spectroscopy-based bench-top reader. This presentation is focused on the characterization of our air sampling badge and its capabilities in combination with our reader. The badges feature silent micro air pumps and a series of sensors to monitor flow rate, temperature, relative humidity, TVOC and movement during sampling. Filtration slides provide the means for inertia-based particle separation and deposition onto collection membranes optimized for efficient particle retention and inspection with Raman spectroscopy. The sampling characteristic of the badges closely follows the respirable convention according to ISO 7708 with an average sampler bias below 10%. Our analytical approach to quantify the collected particles using Raman spectroscopy and in-house developed analysis routines provide unprecedented sensitivity and material-specificity enabling e.g., the unambiguous distinction between CNTs and carbon black. The Identifier system provides fast results directly on-site and facilitates continuous monitoring and recording of long-term exposure histories for locations and employees. Lastly, recent advancements in the development of our respirable sampler towards a combined respirable/thoracic sampler are discussed in the context of emerging fields of application ranging from RCS to active pharmaceutical ingredients and modern battery materials.

Correlation between Graphitic Carbon and Elemental Carbon in Diesel Particulate Matter in Workplace Atmospheres.

We investigated the suitability of the graphitic carbon (GC) content of diesel particulate matter (DPM), measured using Raman spectroscopy, as a surrogate measure of elemental carbon (EC) determined by thermal optical analysis. The Raman spectra in the range of 800-1800 cm-1 (including the D mode at ∼1322 cm-1 and the G mode at ∼1595 cm-1) were used for GC identification and quantification. Comparison of the Raman spectra for two certified DPM standards (NIST SRM 1650 and SRM 2975), two types of diesel engine exhaust soot, and three types of DPM-enriched workplace aerosols show that the uncertainty of GC quantification based on the D peak height, G peak height, and the total peak area below D and G peaks was about 6.0, 6.7, and 6.9%, respectively. The low uncertainty for different aerosol types suggested possible use of GC as a surrogate measure of EC in workplace atmospheres. A calibration curve was constructed using two laboratory-aerosolized DPM standards to describe the relationship between GC measured by a portable Raman spectrometer and the EC concentration determined by NIOSH Method 5040. The calibration curve was then applied to determine GC-based estimates of the EC contents of diesel engine exhaust samples from two vehicles and seven air samples collected at a hydraulic fracturing worksite. The GC-EC estimates obtained through Raman measurements agreed well with those found by NIOSH Method 5040 for the same samples at EC filter loadings below 2.86 μg/cm2. The study shows that using an appropriate sample collection method that avoids high filter mass loadings, onsite measurement of GC by a portable or hand-held Raman spectrometer can provide a useful indicator of EC in workplace aerosol.

Aerosol Analysis Using Handheld Raman Spectrometer: On-site Quantification of Trace Crystalline Silica in Workplace Atmospheres.

A method for aerosol chemical analysis using handheld Raman spectrometer has been developed and its application to measurement of crystalline silica concentration in workplace atmosphere is described. The approach involves collecting aerosol as a spot sample using a wearable optical aerosol monitor, followed by direct-on-filter quantitative analysis of the spot sample for crystalline silica using handheld Raman spectrometer. The filter cassette of a commercially available optical aerosol monitor (designed to collect aerosol for post-shift analysis) was modified to collect 1.5-mm-diameter spot sample, which provided adequate detection limits for short-term measurements over a few tens of minutes or hours. The method was calibrated using aerosolized α-quartz standard reference material in the laboratory. Two Raman spectrometers were evaluated, one a handheld unit (weighing less than 410 g) and the other a larger probe-based field-portable unit (weighing about 5 kg). The lowest limit of quantification for α-quartz of 16.6 μg m-3 was obtained using the handheld Raman unit at a sample collection time of 1 h at 0.4 l min-1. Short-term measurement capability and sensitivity of the Raman method were demonstrated using a transient simulated workplace aerosol. Workplace air and personal breathing zone concentrations of crystalline silica of workers at a hydraulic fracturing worksite were measured using the Raman method. The measurements showed good agreement with the co-located samples analyzed using the standard X-ray powder diffraction (XRD) method, agreeing within 0.15-23.2% of each other. This magnitude of difference was comparable to the inter- and intra-laboratory analytical precision of established XRD and infrared methods. The pilot study shows that for silica-containing materials studied in this work it is possible to obtain quantitative measurements with good analytical figures of merit using handheld or portable Raman spectrometers. Further studies will be needed to assess matrix interferences and measurement uncertainty for several other types of particle matrices to assess the broader applicability of the method.

Challenge with a Personal Cascade Impactor Sampler in a Silicon Metal Smelter

ABSTRACT Cascade impactors are useful tools in the measurement of particle size mass distribution of workplace aerosols. The application of cascade impactors, however, is sometimes challenging. Personal aerosol samples were collected by Sioutas cascade impactors and respirable cyclones in parallel in a silicon (Si) metal smelter to investigate the different particulate matter (PM) fractions. In a second campaign, nine new air samples were collected with the Sioutas personal cascade impactors using stationary sampling. It was found that wall deposition was substantial in the upper stages of the Sioutas cascade impactors, which meant that quite often more PM was deposited on the inner walls of the impactor than on the filter substrates. At the same time, wall deposition did most probably not affect the collection of the finest particles (< 0.25 µm). Besides wall deposition of the particles, the effect of high PM concentration on the impactor performance, particle bouncing and blow off, high particle mass loading and impact fragmentation of the particle agglomerates were considered for explaining the malfunctioning of the Sioutas impactors in the Si metal smelter. Furthermore, concentrations of the finest PM fraction (< 0.25 µm) and respirable fraction both collected by personal sampling are reported and discussed in the paper.

Is “Enough” Really Enough? How Protected Are Our Most Vulnerable Workers—Those That Support Our Country’s Economy and Infrastructure?

In a congressional letter sent on March 1st, 2021 addressed to the White House COVID Response Coordinator Jeff Zients, the Centers for Disease Control and Prevention Director Rochelle Walensky, and the U.S. Department of Labor’s Acting Secretary Al Stewart,1 a group of public health leaders in the fields of infectious disease and aerosol science voiced their concerns about the current CDC recommendations on workplace aerosol exposure protection and urged OSHA to use the most recent information about PPE in their upcoming March 15 promulgation of an emergency standard. With the recent SARS-CoV-2 plans, the availability of life-saving vaccines has expanded, the call for the widespread use of masks has increased, and stronger measures and guidelines to protect workers and the public have been implemented.2 But these measures are not enough. Vaccinations are not a viable short-term solution because new variants can develop rapidly, long before the majority of the population can receive the vaccination.3 Current regulations and recommendations on the types of masks people should wear are insufficient and are not regularly updated. SARS-CoV-2 infection rates and death rates recently reached record-high levels,4 which indicates that there is an urgent need for further action. There is still much to be done to prevent SARS-CoV-2 infections and deaths.

Aerosol analysis using quantum cascade laser infrared spectroscopy: Application to crystalline silica measurement

A method for trace analysis of aerosol mineral components using quantum cascade laser (QCL) based infrared absorption spectroscopy is described. The measurement approach involves: (a) collection of aerosol on a particulate filter; (b) sample treatment using low-temperature oxygenated plasma to minimize the matrix interferences; (c) redeposition of the treated sample as a dried spot for direct-on-filter analysis; and (d) infrared transmittance measurement of the dried spot using the QCL and mercury-cadmium-telluride detector. The method was applied to quantification of trace α-quartz in workplace aerosols. Infrared absorbance spectra in the range 750–1030 cm−1 were obtained using the QCL instrument; the characteristic peak of α-quartz at 798 cm−1 was used to measure its content. A correction scheme was applied to account for spectral interference from kaolinite mineral for coal dust samples. The detection limit for α-quartz was estimated to be 0.12 μg for a dried spot diameter of 1 mm. This detection limit is an order-of-magnitude lower than those attainable by the current standard X-ray diffraction (XRD) or Fourier transform infrared spectroscopy (FTIR) methods involving similar sample preparation and treatment. The QCL method was extended to the measurement of respirable α-quartz concentrations in workplace aerosols released during cutting of fiber-reinforced cement and engineered stone products (used in building construction), as well as those from various coal mine dusts. The measurements compared well with those from the standard XRD method, even for samples with matrix and mineral interferences. The results show that QCL-based IR transmission spectroscopy can offer sensitive, trace-level measurement of aerosol mineral components.

Introduction to the Feature Articles: Occupational Safety and Health Associated with Aerosols in Workplaces

Introduction to the Feature Articles: Occupational Safety and Health Associated with Aerosols in Workplaces

Technical Terms Related to the Feature Articles: Occupational Safety and Health Associated with Aerosols in Workplaces

Technical Terms Related to the Feature Articles: Occupational Safety and Health Associated with Aerosols in Workplaces

Analysis of Crystalline Silica Aerosol Using Portable Raman Spectrometry: Feasibility of Near Real-Time Measurement.

A Raman spectroscopy based method has been developed for measurement of trace airborne concentrations of respirable crystalline silica (RCS) using various aerosol sampling and analysis techniques. Three aerosol microconcentration techniques were investigated for effective coupling of collected particulate samples with micro-Raman spectroscopy: (i) direct analysis on a particulate filter after focused aerosol collection using a converging nozzle; (ii) analysis of dried particulate deposit on a filter obtained directly from the aerosol phase using the Spotsampler device; and (iii) analysis of a dried spot (∼1-3 mm diameter) obtained by redepositing the particulate sample, after low-temperature plasma ashing of the filter sample. The deposition characteristics (i.e., spot diameter, shape, and deposit uniformity) of each technique were investigated. Calibration curves were constructed and detection limits were estimated for α-quartz using the A1 Raman Si-O-Si stretching-bending phonon mode at 465 cm-1. The measurement sensitivity could be substantially improved by increasing the signal integration time and by reducing the particle deposition area. Detection limits in the range of 8-55 ng could be achieved by microconcentrating the aerosol sample over a spot measuring 400-1000 μm in diameter. These detection limits were two to three orders of magnitude lower compared to those attainable using current standardized X-ray diffraction and infrared spectroscopy methods. The low detection limits suggest that near real-time measurements of RCS could be achieved with limits of quantification ranging from 2 to 18.5 μg/m3 (at 10 min collection time and 1.2 L/min sampling flow rate), depending on microconcentration technique used. The method was successfully extended to the measurement of α-quartz air concentration in representative workplace aerosol samples. This study demonstrates the potential of portable micro-Raman spectroscopy for near-real time measurement of trace RCS in air.

Combining NSAM and CPC concentrations to determine airborne nanoparticle count median diameter: Application to various laboratory and workplace aerosols

ABSTRACTBecause nanomaterials have been increasingly developed and used in many technology and industry sectors over the last 20 years, an increasing number of workers is likely to be exposed to airborne nanoparticles. In addition, the question of the nanomaterial characteristics that should be assessed in epidemiological studies remains open. Thus, assessing occupational exposure to airborne nanoparticles will not only rely on mass concentration and chemical composition. Rather, key parameters, such as particle size, have to be included in measurement strategies.We previously proposed a methodology to estimate the Count Median Diameter (CMD) of an aerosol based on the simultaneous size-integrated measurement of two particle concentrations, lung-deposited surface area, and number, thanks to field-portable, commercially available aerosol instruments (Nanoparticle Surface Area Monitor/Condensation Particle Counter combination).In addition to previous work, this study investigates the case of various polydisperse metal oxides, organic oil, and salt particles with CMDs ranging from 16–410 nm. Once corrected, the CMDs derived from the NSAM/CPC agree within ±20% with regard to the reference electrical mobility equivalent diameter, regardless of aerosol composition, morphology, or geometric standard deviation (GSD).Furthermore, the field-applicability of the method was tested through 6 sets of experimental data stemming from workplace measurement campaigns where different materials were produced and handled (TiO2, SiO2, Ag, Multi-Walled Carbon Nanotubes—MWCNT), covering a range of CMDs between 40 and 190 nm. All situations considered, the approach based on the combination of a NSAM and a CPC leads to a satisfying estimation of particle CMD, within ±20% compared to reference CMD.

Phase identification of individual crystalline particles by combining EDX and EBSD: application to workplace aerosols.

This paper discusses the combined use of electron backscatter diffraction (EBSD) and energy dispersive X-ray microanalysis (EDX) to identify unknown phases in particulate matter from different workplace aerosols. Particles of α-silicon carbide (α-SiC), manganese oxide (MnO) and α-quartz (α-SiO2) were used to test the method. Phase identification of spherical manganese oxide particles from ferromanganese production, with diameter less than 200nm, was unambiguous, and phases of both MnO and Mn3O4 were identified in the same agglomerate. The same phases were identified by selected area electron diffraction (SAED) in transmission electron microscopy (TEM). The method was also used to identify the phases of different SiC fibres, and both β-SiC and α-SiC fibres were found. Our results clearly demonstrate that EBSD combined with EDX can be successfully applied to the characterisation of workplace aerosols. Graphical abstract Secondary electron image of an agglomerate of manganese oxide particles collected at a ferromanganese smelter (a). EDX spectrum of the particle highlighted by an arrow (b). Indexed patterns after dynamic background subtraction from three particles shown with numbers in a

Droplet Assisted Inlet Ionization for Online Analysis of Airborne Nanoparticles.

Airborne nanoparticles play a key role in climate effects as well as impacting human health. Their small mass and complex chemical composition represent significant challenges for analysis. This work introduces a new ionization method, droplet assisted inlet ionization (DAII), where aqueous droplets are produced from airborne nanoparticles. When these droplets enter the mass spectrometer through a heated inlet, rapid vaporization leads to the formation of molecular ions. The method is demonstrated with test aerosols consisting of polypropylene glycol (PPG), angiotensin II, bovine serum albumin, and the "thermometer" compound p-methoxybenzylpyridinium chloride. High-quality spectra were obtained from PPG particles down to 13 nm in diameter and sampled masses in the low pictogram range. These correspond to aerosol number and mass concentrations smaller than 1000 particles/cm3 and 100 ng/m3, respectively, and a time resolution on the order of seconds. Fragmentation of the thermometer ion using DAII was inlet temperature dependent and similar in magnitude to that observed with a conventional ESI source on the same instrument. DAII should be applicable to other types of aerosols including workplace aerosols and those produced for drug delivery by inhalation.

Comparison of nickel speciation in workplace aerosol samples using sequential extraction analysis and X-ray absorption near-edge structure spectroscopy.

There is a pressing need to further develop speciation knowledge of Ni workplace aerosols as the Zatka sequential extraction method used until now to speciate workplace Ni exposures has limitations. Here we compare the Zatka and XANES methods and evaluate XANES spectroscopy as a more appropriate and accurate technique for identifying nickel species in workplace aerosols. XANES spectroscopy is capable of identifying unique Ni species in the unaltered samples. Our findings indicate some significant departures in speciation assignment between the Zatka and XANES methods. In particular, the Zatka method can overestimate the soluble Ni fraction and it may underestimate the sulphidic and metallic fractions in some samples. Of particular importance, XANES is able to identify component sulphidic species. This information can lead to more accurate exposure matrices and more refined epidemiological analysis of respiratory cancer causation in sulphidic Ni processing.

Particle size distribution of workplace aerosols in manganese alloy smelters applying a personal sampling strategy.

Air samples were collected by personal sampling with five stage Sioutas cascade impactors and respirable cyclones in parallel among tappers and crane operators in two manganese (Mn) alloy smelters in Norway to investigate PM fractions. The mass concentrations of PM collected by using the impactors and the respirable cyclones were critically evaluated by comparing the results of the parallel measurements. The geometric mean (GM) mass concentrations of the respirable fraction and the <10 μm PM fraction were 0.18 and 0.39 mg m(-3), respectively. Particle size distributions were determined using the impactor data in the range from 0 to 10 μm and by stationary measurements by using a scanning mobility particle sizer in the range from 10 to 487 nm. On average 50% of the particulate mass in the Mn alloy smelters was in the range from 2.5 to 10 μm, while the rest was distributed between the lower stages of the impactors. On average 15% of the particulate mass was found in the <0.25 μm PM fraction. The comparisons of the different PM fraction mass concentrations related to different work tasks or different workplaces, showed in many cases statistically significant differences, however, the particle size distribution of PM in the fraction <10 μm d(ae) was independent of the plant, furnace or work task.

Phase-contrast helium-3 MRI of aerosol deposition in human airways.

One of the key challenges in the study of health-related aerosols is predicting and monitoring sites of particle deposition in the respiratory tract. The potential health risks of ambient exposure to environmental or workplace aerosols and the beneficial effects of medical aerosols are strongly influenced by the site of aerosol deposition along the respiratory tract. Nuclear medicine is the only current modality that combines quantification and regional localization of aerosol deposition, and this technique remains limited by its spatial and temporal resolutions and by patient exposure to radiation. Recent work in MRI has shed light on techniques to quantify micro-sized magnetic particles in living bodies by the measurement of associated static magnetic field variations. With regard to lung MRI, hyperpolarized helium-3 may be used as a tracer gas to compensate for the lack of MR signal in the airways, so as to allow assessment of pulmonary function and morphology. The extrathoracic region of the human respiratory system plays a critical role in determining aerosol deposition patterns, as it acts as a filter upstream from the lungs. In the present work, aerosol deposition in a mouth-throat phantom was measured using helium-3 MRI and compared with single-photon emission computed tomography. By providing high sensitivity with high spatial and temporal resolutions, phase-contrast helium-3 MRI offers new insights for the study of particle transport and deposition.

0406 Prospective monitoring of exposure and lung function among cement production workers – is drop out from the study associated with respiratory health at inclusion?

ObjectivesIn this study we aimed to estimate the associations between respiratory health at inclusion and drop-out from a 4-year longitudinal study of lung function among cement production workers in Europe...

An Occupational Exposure Assessment for Engineered Nanoparticles Used in Semiconductor Fabrication

Engineered nanoparticles of alumina, amorphous silica, and ceria are used in semiconductor device fabrication during wafer polishing steps referred to as 'chemical mechanical planarization' (CMP). Some metal oxide nanoparticles can impact the biological response of cells and organ systems and may cause adverse health effects; additional research is necessary to better understand potential risks from nanomaterial applications and occupational exposure scenarios. This study was conducted to assess potential airborne exposures to nanoparticles and agglomerates using direct-reading instruments and filter-based samples to characterize workplace aerosols by particle number, mass, size, composition, and morphology. Sampling was repeated for tasks in three work areas (fab, subfab, wastewater treatment) at a facility using engineered nanoparticles for CMP. Real-time measurements were collected using a condensation particle counter (CPC), optical particle counter, and scanning mobility particle spectrometer (SMPS). Filter-based samples were analyzed for total mass or the respirable fraction, and for specific metals of interest. Additional air sample filters were analyzed by transmission electron microscopy with energy dispersive x-ray spectroscopy (TEM/EDX) for elemental identification and to provide data on particle size, morphology, and concentration. Peak concentrations measured on the CPC ranged from 1 to 16 particles per cubic centimeter (P cm(-3)) for background and from 4 to 74 P cm(-3) during tasks sampled in the fab; from 1 to 60 P cm(-3) for background and from 3 to 84 P cm(-3) for tasks sampled in the subfab; and from 1160 to 45 894 P cm(-3) for background and from 1710 to 45 519 P cm(-3) during wastewater treatment system filter change tasks. Significant variability was seen among the repeated task measurements and among background comparisons in each area. Several data analysis methods were used to compare each set of task and background measurements. Increased concentrations of respirable particles were identified for some tasks sampled in each work area, although of relatively low magnitude and inconsistently among repeated measurements for specific tasks. Measurements with a portable SMPS indicated that nanoparticle number concentrations (channels 11.5-115.5nm) increased above background levels by 3.2 P cm(-3) during CMP tool set-up in the fab area but were not elevated when changing filters for the CMP wastewater treatment system. All results from mass concentration analysis were below the limits of detection. Characterization by TEM/EDX identified structures containing the elements of interest (Al, Si), primarily as agglomerates or aggregates in the 100-1000nm size range. Although health-based occupational exposure limits have not been established for nanoscale alumina, silica, or ceria, the measured concentrations by number and mass were below currently proposed benchmarks or reference values for poorly soluble low-toxicity nanoparticles.

A modular tool for analyzing cascade impactors data to improve exposure assessment to airborne nanomaterials

Cascade impactors are widely used to provide particle size distributions for the study of aerosols in workplaces and ambient air. In the frame of exposure assessment to airborne particles, one of their main advantages is the possibility to perform further off-line analysis (e.g. electron microscopy, physical-chemical characterization by XRD, ICP-MS, etc.) on the collected samples according to particle size. However, the large channel width makes the particle size distributions not enough size-resolved. Furthermore, in spite of the sharpness of the collection efficiency curves, the existence of an overlap between stages renders data interpretation difficult. This work aim was to develop a modular program allowing the inversion of data stemming from cascade impactors based on the mass (or any quantity) collected on each impaction stage. Through a precise description of the collection efficiency curves of the different stages, the software provides a continuous curve (from 100 to 1000 points) using the Markowski method, and more particularly the Twomey iterative algorithm, according to several publications about inverse problems in cascade impactors. An additional option consists in determining the experimental error at each point of the inverse curve, performed by realizing several consecutive inversions. The inversion procedure was first tested and optimized for the case of the SIOUTAS personal sampler. Validation of the calculation was performed considering theoretical aerosols. Then, the software was used for two sets of data obtained during field measurement campaigns.

Acid-Soluble Internal Capsules for Closed-Face Cassette Elemental Sampling and Analysis of Workplace Air

Airborne particles that are collected using closed-face filter cassettes (CFCs), which are used widely in the sampling of workplace aerosols, can deposit in places other than on the filter and thereby may not be included in the ensuing analysis. A technique for ensuring that internal non-filter deposits are included in the analysis is to collect airborne particles within an acid-soluble internal capsule that, following sampling, can be dissolved along with the filter for subsequent elemental analysis. An interlaboratory study (ILS) was carried out to evaluate the use of cellulosic CFC capsule inserts for their suitability in the determination of trace elements in airborne samples. The ILS was performed in accordance with an applicable ASTM International standard practice, ASTM E691, which describes statistical procedures for investigating interlaboratory precision. Performance evaluation materials consisted of prototype cellulose acetate capsules attached to mixed-cellulose ester filters. Batches of capsules were dosed with Pb-containing materials (standard aqueous solutions, and certified reference material soil and paint). Also, aerosol samples containing nine target analyte elements (As, Cd, Co, Cr, Cu, Fe, Pb, Mn, and Ni) were generated using a multiport sampler; various concentrations and sampling times were employed to yield samples fortified at desired loading levels. Triplicates of spiked capsules at three different loadings were conveyed to each volunteer laboratory; loading levels were unknown to the participants. The laboratories were asked to prepare the samples by acid dissolution and to analyze aliquots of extracted samples by atomic spectrometry in accordance with applicable ASTM International Standards. Participants were asked to report their results in units of μg of each target element per sample. For the elements investigated, inter-laboratory precision and recovery estimates from the participating laboratories demonstrated the utility of the cellulosic capsule inserts for the measurement of sampled trace elements.