On the Feasibility of a Number Concentration Calibration Using a Wafer Surface Scanner

A new primary standard method for calibrating optical particle counters (OPC) has been developed based on quantitative gravitational deposition on a silicon wafer and accurate counting of the particles by a wafer surface scanner (WSS). The test aerosol consists of 3-μm diameter monodisperse polystyrene latex (PSL) spheres at concentrations in the range of 0.1 cm^?3 to 1 cm^?3. A key element to the calibration is the ability to generate monodisperse PSL spheres without residue particles by use of a virtual impactor and differential mobility analyzer. The use of these devices reduced the percentage of residue particles from more than 99.98% to about 5%. The expanded relative uncertainty (95% confidence level) in the number concentration determined with a WSS for a deposition of 200 particles is 17.8%. The major uncertainty component arises from the Poisson fluctuations in the aerosol concentration because of the low concentration. This methodology has advantages of a fast scanning time by the WSS of minutes compared to hours or days by microscopy and of counting every particle deposited compared to often only a small fraction via microscopy.

The WSS was used in the calibration of an OPC based on 12 depositions with concentrations ranging from 0.1 cm^?3 to 1 cm^?3 for each deposition. Make-up air was added to the aerosol entering the OPC so that the lowest achievable concentration for the OPC measurement is about 0.01 cm^?3 in this study. The detection efficiency of the OPC was measured to be 0.984 with an expanded uncertainty of 13.4%.

Copyright 2014 American Association for Aerosol Research     

Laboratory measurements of light scattering properties of kaolinite dust at 532 nm

Light scattering by kaolinite dust samples at 532 nm is studied using a newly developed laboratory apparatus. During the experiments, dust samples are suspended in water, aerosolized by a nebulizer, and then injected into the scattering zone, with or without going through a diffusion drier, to generate either dried dust particles or water droplets with dust inclusions. The light source is a dual wavelength (532 and 1064 nm) diode-pumped solid state laser. Light scattered by an ensemble of particles is collected by a charge-coupled device (CCD) camera, which is mounted on the rotating arm of a stepper motor. The stepper motor rotates the CCD to cover the scattering angle range from 3° to 177°. Polarized scattering light is measured for the horizontally and vertically polarized incident light. The apparatus is calibrated, using pure water droplets as the scattering media. The response function with respect to the scattering angle is obtained by comparing the measurements with Lorenz–Mie calculations and then used in the later data analysis. Measurements show that the backward scattering features of the water droplets are smoothened due to their dust inclusions. Numerical simulations and measurements are extensively compared and discussed. It is found that the Lorenz–Mie theory is inadequate to reproduce the scattering phase functions of either dust particles or water droplets with dust inclusions. A nonspherical aggregate model is applied to simulate the scattering phase functions. The simulation is able to reproduce the overall scattering features; however, substantial discrepancies still exist due to uncertainties in particle shape and refractive index.

Copyright © 2018 American Association for Aerosol Research     

Single Particle Measurements of the Optical Properties of Small Ice Crystals and Heterogeneous Ice Nuclei

Dust aerosol and ice crystals are two major types of nonspherical particles in the atmosphere which have significant roles in cloud-aerosol interactions and the radiative budget. The presence of dust and ice often coincide in the atmosphere because dust particles are efficient ice nuclei. The size and composition dependence of the scattering properties of dust and ice are needed to assess their individual contributions to the optical scattering of sunlight. Here we present a new measurement technique used to determine the single particle forward scattering, backscattering, and depolarization ratio (at a wavelength of 680 nm) for representative nonspherical atmospheric particles. The Texas A&M University Continuous Flow Diffusion Chamber (CFDC) was used as an ice crystal generator to produce ice crystals via both homogenous and heterogeneous nucleation mechanisms under well-controlled laboratory conditions. Optical scattering properties of mineral dusts and small ice crystals (0.6 μm to 50 μm optical diameter) were measured by the Droplet Measurement Technologies, Inc. (DMT) Cloud Aerosol Spectrometer with Polarization (CASPOL). Significant differences between the optical properties of single dusts and ice particles of the same size were observed. Differences between the optical signatures of homogeneously and heterogeneously nucleated ice crystals were not statistically significant. Our results suggest that atmospheric ice crystals can be identified and quantified independently from the dust particles on which they form based on analysis of their backscatter and depolarization signals.

Copyright 2014 American Association for Aerosol Research     

Refractive index retrievals for polystyrene latex spheres in the spectral range 220–420 nm

The recent development of an Aerosol Extinction Differential Optical Absorption Spectrometer (AE-DOAS) has allowed for the retrieval of wavelength dependent complex refractive indices for polystyrene latex spheres (PSL). The AE-DOAS is a white-type multi-pass gas cell coupled to a UV-Vis spectrometer. Refractive index values are retrieved for wavelengths between 220 and 420 nm by minimizing the χ² goodness-of-fit between measured extinction for five diameters of PSL and model Mie Theory predictions. Comparison to literature shows agreement at wavelengths >360 nm demonstrating the validity of this new instrumental approach while expanding the known refractive index range for PSLs further into the UV where it is previously unreported. In the studied wavelength range, coefficients for the general Cauchy dispersion relationship (A = 1.538(11); B = 0.0043(16) μm²; C = 0.00094(5) μm⁴) for PSLs were determined using the retrieved real portion of the refractive index and the wavelength in microns. In addition, this work indicates that the precision of retrieved values is impacted by the particle diameters chosen for the experiment where retrievals for shorter wavelengths of light benefit from the study of smaller sized particles.

Copyright © 2017 American Association for Aerosol Research     

Development of a Pulsed-Field Differential Mobility Analyzer: A Method for Measuring Shape Parameters for Nonspherical Particles

For a nonspherical particle, a standard differential mobility analyzer (DMA) measurement yields a mobility-equivalent spherical diameter, but provides no information about the degree of sphericity. However, given that the electrical mobility for nonspheres is orientation-dependent, and that orientation can be manipulated using electric fields of varying strength, one can, in principle, extract some type of shape information through a systematic measurement of mobility as a function of particle orientation. Here, we describe the development of a pulsed-field differential mobility analyzer (PFDMA) which enables one to change the peak E-field experienced by the particle to induce orientation, while still maintaining the same time-averaged field strength as a standard DMA experiment. The instrument is validated with polystyrene latex (PSL) spheres with accurately known size, and gold rods with dimensions accurately determined by transmission electron microscopy (TEM). We demonstrate how the instrument can be used for particle separation and extraction of shape information. In particular, we show how one can extract both length and diameter information for rod-like particles. This generic approach can be used to obtain dynamic shape factors or other multivariate dimensional information (e.g., length and diameter).

Copyright 2014 American Association for Aerosol Research     

Characterization of nanosized silica size standards

Nanosized silica size standards produced with a sol–gel synthesis process were evaluated for particle size, effective density, and refractive index in this study. Particle size and effective density measurements were conducted following protocol from the National Institute of Advanced Industrial Science and Technology (AIST) in Japan. Particle sizes were measured via electrical mobility analysis using a differential mobility analyzer (DMA) at sheath flow rates (Q_sh) of 3.0 and 6.0 L/min and a constant aerosol flow rate (Q_a) of 0.3 L/min. The measured mean and mode diameters agreed well with the labeled sizes in the size range 40–200 nm, with differences ranging from 0.03% to 0.8%, well within the labeled expanded uncertainties (95% confidence intervals) of 1.8%–2.2%. The coefficient of variation (CV) of the size distribution was 0.012–0.027 for 40–200 nm. Particle sizes measured for 20 nm and 30 nm standards showed size differences with respect to the certified sizes of 1.7% and 8.3% at Q_sh = 6.0 L/min, but the size distributions were narrow, with CV = 0.047–0.064. The average effective density for the range 40–200 nm measured with an aerosol particle mass analyzer (APM) was 1.9 g/cm³. The real component of the refractive index measured with an optical particle counter (OPC) was 1.41 at a wavelength of 633 nm. All properties (size, effective density, and refractive index) were stable and could be measured with good repeatability. From these evaluations, it was found that the nanosized silica size standards have good characteristics for use as size standards and constitute a feasible alternative to PSL particles.

© 2017 American Association for Aerosol Research     

Mobility Analysis of 2 nm to 11 nm Aerosol Particles with an Aspirating Drift Tube Ion Mobility Spectrometer

We describe the performance of a drift tube-ion mobility spectrometry (DT-IMS) instrument for the measurement of aerosol particles. In DT-IMS, the electrical mobility of a measured particle is inferred directly from the time required for the particle to traverse a drift region, with motion driven by an electrostatic field. Electrical mobility distributions are hence linked to arrival time distributions (ATDs) for particles reaching a detector downstream of the drift region. The developed instrument addresses two obstacles that have limited DT-IMS use for aerosol measurement previously: (1) conventional drift tubes cannot efficiently sample charged particles at ground potential and (2) the sensitivities of commonly used Faraday plate detectors are too low for most aerosols. Obstacle (1) is circumvented by creating a “sample volume” of aerosol for measurement, defined by the streamlines of fluid flow. Obstacle (2) is bypassed by interfacing the end of the drift region with a condensation particle counter. The DT-IMS prototype shows high linearity for arrival time versus inverse electrical mobility (R ² > 0.99) over the size range tested (2.2–11.1 nm), and measurements compare well with both analytical and numerical models of device performance. A dimensionless calibration curve linking drift time to inverse electrical mobility is developed. In less than 5 s, it is possible to measure 11.1 nm particles, while 2.2 nm particles are analyzable on a subsecond scale. The transmission efficiency is found to be dependent upon electrostatic deposition for short drift times and upon advective losses for long drift times.

Copyright 2014 American Association for Aerosol Research     

Distinguishing Between Spherical and Nonspherical Particles by Measuring the Variability in Azimuthal Light Scattering

Azimuthal variabilities in scattering of monochromatic, circularly polarized light by individual spherical and nonspherical particles were measured using the DAWN-A (Wyatt et al. Appl. Opt. 27:2405–2421, 1988) differential light scattering detector. Measured aerosols included polystyrene latex spheres (PSL), quartz, and sodium chloride particles of 0.576, 0.741, 0.966, and 1.250 μm diameter. Signals from eight detectors at different azimuthal angles at a polar angle of 55° showed that variabilities for nonspherical particles significantly exceeded values for the spherical PSL. The probability that a quartz or sodium chloride particle would be incorrectly identified as a sphere are less than about 5% for all sizes investigated.     

Development of laser-induced breakdown spectroscopy (LIBS) with timed ablation to improve detection efficiency

A laser-induced breakdown spectrometer (LIBS) was developed for determining the elemental composition of individual airborne particles. The system employs two lasers focused on a narrow beam of particles. A continuous wave laser placed upstream scatters light from particles, while a pulse laser downstream ablates the particles. The scattered light from the upstream laser is used to trigger the downstream pulse laser, resulting in more accurate hitting of the particles than a free-firing laser system without the triggering signal (i.e., constant pulse laser firing). Various laboratory-generated aerosols (NaCl, MgCl₂, KCl, and CaCl₂) were used to evaluate the newly developed LIBS system. Particles were tightly focused into a center line with a sheath air focusing system using an optimum aerosol-to-sheath air velocity ratio. The locations of both the scattering laser and pulse laser beams were precisely controlled by a motorized X-Y stage controller. Data showed that for the LIBS with the triggering system, the hitting efficiency (%) of particles (200–600 nm) significantly increased (e.g., 350 nm particles had more than 26 times higher hitting efficiency at 1,000 particles/cm³), and much lower limits of particle size (～200 nm) and number concentration (<100 particles/cm³) were achieved compared to the free-firing laser condition. Additionally, the hitting rate (hits/min) significantly increased with the triggering system. Our results suggest that the LIBS with the triggering system can be useful for real-time detection of elements of particles existing at low number concentrations (e.g., atmospheric particles) and for the determination of the variation of elemental composition among particles.

© 2017 American Association for Aerosol Research     

A novel miniature inverted-flame burner for the generation of soot nanoparticles

Lab-scale soot nanoparticle generators are used by the aerosol research community to study the properties of soot over a broad range of particle size distributions, and number and mass concentrations. In this study, a novel miniature inverted-flame burner is presented and its emitted soot particles were characterized. The burner consisted of two co-annular tubes for fuel and co-flow air and the flame was enclosed by the latter. The fuel used was ethylene. A scanning mobility particle sizer (SMPS) and an aerodynamic aerosol classifier (AAC) were used to measure mobility and aerodynamic size distribution of soot particles, respectively. Particle morphology was studied using transmission electron microscopy (TEM). The elemental carbon (EC) and organic carbon (OC) content of the soot were measured using thermal-optical analysis (TOA). The burner produced soot particles with mobility diameter range of 66–270?nm, aerodynamic diameter range of 56–140?nm, and total concentration range of 2?×?10⁵–1?×?10⁷?cm^?3. TEM images showed that most soot particles were sub-micron soot aggregates. Some soot superaggregates, typically larger than 2?µm in length, were observed and their abundance increased with ethylene flow rate. TOA showed that the concentration of EC in the generated soot increased with ethylene flow rate, and the soot was observed to have high EC fraction at high ethylene flow rates. The miniature inverted-flame burner was demonstrated to produce soot nanoparticles over a range of concentrations and sizes with high EC content, making it a practical device to study soot nanoparticle properties in different applications.

Copyright © 2019 American Association for Aerosol Research     

The effect of nanosilica (SiO2) and nanoalumina (Al2O3) reinforced polyester nanocomposites on aerosol nanoparticle emissions into the environment during automated drilling

The aim of this study is to investigate the effect nanosilica and nanoalumina has on nanoparticle release from industrial nanocomposites due to drilling for hazard reduction whilst simultaneously obtaining the necessary mechanical performance. This study is therefore specifically designed such that all background noise is eliminated in the measurements range of 0.01 particles/cm³ and ±10% at 10⁶ particles/cm³. The impact nano-sized SiO₂ and Al₂O₃ reinforced polyester has on nanoparticle aerosols generated due to drilling is investigated. Real-time measurement was conducted within a specially designed controlled test chamber using a condensation particle counter (CPC) and a scanning mobility particle sizer spectrometer (SMPS). The results show that the polyester nanocomposite samples displayed statistically significant differences and an increase in nanoparticle number concentration by up to 228% compared to virgin polyester. It is shown that the nanofillers adhered to the polyester matrix showing a higher concentration of larger particles released (between 20 – 100 nm). The increase in nanoparticle reinforcement weight concentration and resulting nanoparticle release vary considerably between the nanosilica and nanoalumina samples due to the nanofillers presence. This study indicates a future opportunity to safer by design strategy that reduces number of particles released concentration and sizes without compromising desired mechanical properties for engineered polymers and composites.

© 2017 American Association for Aerosol Research     

Assessment of a Cylindrical and a Rectangular Plate Differential Mobility Analyzer for Size Fractionation of Nanoparticles at High-Aerosol Flow Rates

An existing differential mobility analyzer (DMA) of cylindrical electrodes and a novel DMA of rectangular plate electrodes are demonstrated for size fractionation of nanoparticles at high-aerosol flow rates in this work. The two DMAs are capable of delivering monodisperse size selected nanoparticles (SMPS σ_g < 1.1) at gas flow rates ranging from 200 slm to 500 slm. At an aerosol flow rate of 200 slm, the maximum attainable particle mean size is of about 20 nm for the cylindrical DMA and of nearly 50 nm for the rectangular plate DMA. The number concentration of the monodisperse nanoparticles delivered by the high-flow DMAs spans from 10⁴ cm^?3 to 10⁶ cm^?3 depending upon the particle mean size and particle size dispersion.

Copyright 2014 American Association for Aerosol Research     

An Aerosol-Based Process for Electrostatic Coating of Particle Surfaces with Nanoparticles

An aerosol-based process for coating the surface of arbitrary “carrier” particles with other types of (smaller) “coating” particles via mutual electrostatic attraction is described. Its practical viability was tested by depositing negatively charged 12-nm palladium particles on 250-nm silica spheres carrying a charge of approximately +40 units each. At respective concentrations of 3 to 8 × 10⁶ particles per cm³ (with a charge fraction of about 25%) and 1 × 10⁴ particles per cm³, the deposition process runs to completion (i.e., to neutralization of the carrier particles) within less than a minute. Comparative estimates show that electrostatically enhanced deposition rates are up to 50 times higher than purely thermal collisions. Transmission electron micrographs show a fairly uniform distribution of coating particles across the surface of the carrier particles. The electrostatic coating kinetics were determined experimentally via the charge loss of the carrier particles and compared also to numerical simulations using Zebel's model for electrostatic enhancement of the collision kernel. Measured rates were generally within 10–15% of the simulations, except for the very early stages of attachment (the first 10 s), where agreement was found to be rather sensitive to the coating particle concentration, possibly due to space charge effects.

Copyright 2014 American Association for Aerosol Research     

High-Resolution Mobility and Mass Spectrometry of Negative Ions Produced in a 241Am Aerosol Charger

This work concentrates on the simultaneous mobility and mass measurement of negative ions generated by the ionizing radiation in a ²⁴¹Am aerosol charger in N₂ (5.0), a 1:1-mixture of N₂ and synthetic air, pure synthetic air (5.0), and filtered laboratory air at ～30% relative humidity. Therefore, a high-resolution mobility analyzer (UDMA) and an atmospheric pressure interface time-of-flight mass spectrometer (APi-TOF) were operated in series. Experiments with N₂ as carrier gas showed a dominating signal at an electrical mobility of 2.09 cm²/Vs with 90% of the ions being nitrate based. The ion composition was altered after a baking-out to a spectrum with three strong mobility-peaks at Z₁ = 2.34 cm²/Vs, Z₂ = 1.42 cm²/Vs, Z₃ = 1.08 cm²/Vs and a higher diversity of ions in the corresponding mass spectra. The carrier gas was gradually changed from N₂ (5.0) to a 1:1-mixture of N₂ with synthetic air and pure synthetic air (5.0), having only a minor effect on the overall pattern of the ion spectrum. Using room air leads to a domination of the nitrate based ions. The mobility-dependent transmission efficiency of the UDMA was modeled using an empirical, laminar diffusion deposition model. The data were further compared to an empirical mass-mobility relationship to evaluate the fragmentation of the ion clusters in the inlet of the mass spectrometer. This study suggests that the nitrate ion, NO₃ ^?, is found to be the dominant ion species produced in an aerosol charger, and that it may be mostly responsible for the charging of aerosol particles in negative polarity.

Copyright 2014 American Association for Aerosol Research     

Physicochemical Characterization of Simulated Welding Fumes from a Spark Discharge System

This study introduces a spark discharge system (SDS) as a way to simulate welding fumes. The SDS was developed using welding rods as electrodes with an optional coagulation chamber. The size, morphology, composition, and concentration of the fume produced and the concentration of ozone (O₃) and nitrogen oxides (NO_X) were characterized. The number median diameter (NMD) and total number concentration (TNC) of fresh fume particles were ranged 10–23 nm and 3.1×10⁷ ? 6×10⁷ particles/cm³, respectively. For fresh fume particles, the total mass concentration (TMC) measured gravimetrically ranged 85–760 μg/m³. The size distribution was stable over a period of 12 h. The NMD and TNC of aged fume particles were ranged 81–154 nm and 1.5×10⁶?2.7×10⁶ particles/cm³, respectively. The composition of the aged fume particles was dominated by Fe and O with an estimated stoichiometry between that of Fe₂O₃ and Fe₃O₄. Concentrations of O₃ and NO_X were ranged 0.07–2.2 ppm and 1–20 ppm, respectively. These results indicate that the SDS is capable of producing stable fumes over a long-period that are similar to actual welding fumes. This system may be useful in toxicological studies and evaluation of instrumentation.

Copyright 2014 American Association for Aerosol Research     

Real-time separation of aerosolized Staphylococcus epidermidis and polystyrene latex particles with similar size distributions

For rapid and effective detection of airborne microorganisms, it is preferable to remove dust particles during the air sampling process because they can reduce the detection accuracy of measurements. In this study, a methodology of real-time separation ofaerosolized Staphylococcus epidermidis (S. epidermidis) andpolystyrene latex (PSL) particles of similar size was investigated. These two species represent biological and non-biological particles, respectively. Due to their different relative permittivities, they grasp different numbers of air ions under corona discharge. After these charged particles enter a mobility analyzer with airflow, in which an electric field is applied perpendicular to the airflow, the S. epidermidis and PSL particles separate, due to the difference in their electric mobilities, and exit through two different outlets. Purities and recoveries for S. epidermidis and PSLat their respective outlets were determined with measurements of aerosol number concentrations and ATP bioluminescence intensities at the inlet and two outlets. The results were that purities for PSL and S. epidermidis were 70% and 80%, respectively. This methodology provides a rapid and simple way to increase the detection accuracy of bacterial agents in air.

Copyright © 2017 American Association for Aerosol Research     

Diffusion Sampler for Measurement of Acidic Ultrafine Particles in the Atmosphere

The adverse health effect of acidic ultrafine particles (AUFPs) has been widely recognized in scientific societies. These particles mainly deposit on the surface by diffusion and so far there is no mature method for the measurement of airborne AUFPs. The purpose of this study was to develop a diffusion sampler (DS) with iron nanofilm detectors to effectively measure the number concentration and size distribution of airborne AUFPs in indoor and outdoor environments. The developed DS was made of stainless steel with a flat and rectangular channel with 1.0 mm height, 50 mm width, and 500 mm length. The iron nanofilm detectors were deployed on rectangular recesses inside the sampler at three different locations along the length of the channel to collect the ultrafine particles. The exposed detectors were then scanned using an atomic force microscope (AFM) to numerate and distinguish the AUFPs from the nonacidic UFPs. Prior to sampling, the semi-empirical equations for the diffusive deposition efficiency of particles at the different detector locations in the sampler were obtained on the basis of theoretical diffusive mechanism and modified by the experimental data using polystyrene latex (PSL) standard particles. After calibration, the DS + AFM method and a commercially available online measurement system, i.e., scanning mobility particle sizer (SMPS) incorporated with a condensation particle counter (CPC), were simultaneously used in a 4-week field measurement. Both methods showed very good agreement in terms of total particle number concentration and size distribution. The results indicate that the diffusion sampler is effective for the quantification of ambient acidic ultrafine particles.

Copyright 2014 American Association for Aerosol Research     

A water-based fast integrated mobility spectrometer (WFIMS) with enhanced dynamic size range

A water-based fast integrated mobility spectrometer (WFIMS) with enhanced dynamic size range is developed. The WFIMS builds on two established technologies: the fast integrated mobility spectrometer and laminar flow water-based condensation methodology. Inside WFIMS, particles of differing electrical mobility are separated in a drift tube and subsequently enlarged through water condensation. Particle size and concentration are measured via digital imaging at a frame rate of 10 Hz. By measuring particles of different mobilities simultaneously, the WFIMS resolves particle diameters ranging from 8 to 580 nm within 1 s or less. The performance of WFIMS was characterized with differential mobility analyzer (DMA) classified (NH₄)₂SO₂ particles with diameters ranging from 8 to 265 nm. The mean particle diameters measured by WFIMS were found to be in excellent agreement with DMA centroid diameters. Furthermore, detection efficiency of WFIMS was characterized using a condensation particle counter as a reference and is nearly 100% for particles with diameter greater than 8 nm. In general, measured and simulated WFIMS mobility resolutions are in good agreement. However, some deviations are observed at low particle mobilities, likely due to the non-idealities of the WFIMS electric field.

Copyright © 2017 American Association for Aerosol Research     

Optical properties of black carbon in cookstove emissions coated with secondary organic aerosols: Measurements and modeling

Cookstoves are a major source of black carbon (BC) particles and associated organic compounds, which influence the atmospheric radiative balance. We present results from experiments that characterize BC emissions from a rocket stove coated with secondary organic aerosol. Optical properties, namely, BC mass absorption cross-section (MAC_BC) and mass scattering cross-section (MSC), as a function of the organic-to-black carbon ratio (OA:BC) of fresh and aged cookstove emissions were compared with Mie and Rayleigh–Debye–Gans (RDG) calculations. Mie theory reproduced the measured MAC_BC across the entire OA:BC range. However, Mie theory failed to capture the MSC at low OA:BC, where the data agreed better with RDG, consistent with a fractal morphology of fresh BC aggregates. As the OA:BC increased, the MSC approached Mie predictions indicating that BC-containing particles approach a core–shell structure as BC cores become heavily coated. To gain insight into the implications of our findings, we calculated the spectral simple forcing efficiency (dSFE) using measured and modeled optical properties as inputs. Good agreement between dSFE estimates calculated from measurements and Mie-modeled dSFE across the entire OA:BC range suggests that Mie theory can be used to simulate the optical properties of aged cookstove emissions.

Copyright © 2016 American Association for Aerosol Research     

Characteristics of secondhand electronic cigarette aerosols from active human use

The electronic cigarette (EC) is a new source of indoor airborne particles. To better understand the impacts of secondhand vaping (SHV) emissions on indoor air quality, real-time measurements of particle size distribution, particle number concentration (PNC), fine particulate matter (PM_2.5), CO₂, CO, and formaldehyde were conducted before, during, and after 10 min EC-use among 13 experienced users in an 80 m³ room. To assess particle transport in the room, multiple sampling locations were set up at 0.8, 1.5, 2.0, and 2.5 m away from the subjects. The arithmetic mean (standard deviation) of background PNC and PM_2.5 concentrations in the room were 6.39 × 10³ (1.58 × 10²) particles/cm³ and 8 (1) μg/m³, respectively. At 0.8 m away from EC users, right after initiation of puffing, the PNC and PM_2.5 concentrations can reach a peak of ～10⁵ particles/cm³ and ～3 × 10³ µg/m³, respectively, and then dropped quickly to background levels within 20 s due to dilution and evaporation. At the 0.8 m sampling location, the mean PNC and PM_2.5 concentrations during puffing were 2.48 × 10⁴ (2.14 × 10⁴) particles/cm³ and 188 (433) µg/m³, respectively. In addition, two modes of SHV particles were observed at about 15 and 85 nm. Moreover, concentrations of SHV particles were negatively correlated with the distances to EC users. At the 1.5 m location, PNC and PM_2.5 levels were 9.91 × 10³ (1.76 × 10³) particles/cm³ and 19 (14) µg/m³, respectively. Large variations of mean PNC levels exhaled per puff were observed both within and between EC users. Data presented in this study can be used for SHV particle exposure assessment.

Copyright © 2017 American Association for Aerosol Research