Abstract

Semi-volatile (SV) aerosols still represent an important challenge to occupational hygienists due to toxicological and sampling issues. Particularly problematic is the sampling of hazardous SV that are present in both particulate and vapour phases at a workplace. In this study we investigate the potential evaporation losses of SV aerosols when using off-line filter-adsorber personal samplers. Furthermore, we provide experimental data showing the extent of the evaporation loss that can bias the workplace risk assessment. An experimental apparatus consisting of an aerosol generator, a flow tube and an aerosol monitoring and sampling system was set up inside a temperature controlled chamber. Aerosols from three n-alkanes were generated, diluted with nitrogen and sampled using on-line and off-line filter-adsorber methods. Parallel measurements using the on-line and off-line methods were conducted to quantify the bias induced by filter sampling. Additionally, two mineral oils of different volatility were spiked on filters and monitored for evaporation depending on the samplers flow rate. No significant differences between the on-line and off-line methods were detected for the sum of particles and vapour. The filter-adsorber method however tended to underestimate up to 100% of the particle mass, especially for the more volatile compounds and lower concentrations. The off-line sampling method systematically returned lower particle and higher vapour values, an indication for particle evaporation losses. We conclude that using only filter sampling for the assessment of semi-volatiles may considerably underestimate the presence of the particulate phase due to evaporation. Thus, this underestimation can have a negative impact on the occupational risk assessment if the evaporated particle mass is no longer quantified.

Highlights

  • The sampling of hazardous semi-volatile (SV) compounds in workplace air can prove to be difficult for occupational hygienists when confronted with substances that are present as aerosols, partitioned between the particulate and the gaseous phases.[1,2,3,4,5]

  • The usage of mineral oils in workplaces can lead to the formation of hazardous oil mists/aerosols through physical dispersion and evaporation followed by re-condensation.[24,25]

  • The method used as reference in this paper (FID for total hydrocarbon mass and white light particle sizer for particle mass)[7] is not in uenced by evaporation as the aerosol characteristics are not changed in the sensor of the optical particle counters (OPCs) and as all droplets are vaporized in the transfer line to the Flame ionization detectors (FID)

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Summary

Introduction

The sampling of hazardous semi-volatile (SV) compounds in workplace air can prove to be difficult for occupational hygienists when confronted with substances that are present as aerosols, partitioned between the particulate and the gaseous phases (oil mists, PAHs, inorganic acids, alkanolamines, bitumen etc.).[1,2,3,4,5] The European norm EN 13936 de nes semivolatiles as substances with vapour pressures between 100 and 0.001 Pa at room temperature.[6]. The authors noted that the lter sampling method may not be appropriate for semi-volatiles as the evaporative losses can lead to an exposure underestimation These studies did not provide a non-biased method that accurately differentiates between particles and vapours but compared the existing measurement techniques between themselves without being able to measure the actual particle–vapour distribution. The method used as reference in this paper (FID for total hydrocarbon mass and white light particle sizer for particle mass)[7] is not in uenced by evaporation as the aerosol characteristics are not changed in the sensor of the OPC and as all droplets are vaporized in the transfer line to the FID This setup minimizes artefacts and allows it to be used to determine particle–vapour fractionation while sampling oil mists. The focus of the present study was to accurately quantify the sampling bias due to volatilization of oil mist from a “GGP” lter-adsorber personal sampler, which is used for oil mist sampling at workplaces in Germany, under temperaturecontrolled laboratory conditions

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