Characteristics of traffic-induced fugitive dust from unpaved roads

The characteristics of fugitive dust emitted from vehicles traveling on unpaved dirt roads were measured using a suite of instruments including a real-time fugitive dust sampler. The fugitive dust sampler is formed from a combination of a large particle inlet and an optical particle spectrometer that reports particle sizes from 6 to 75 µm. The large particle inlet permits the sampling of particles up to 75 µm with only a moderate dependence of sampling efficiency on wind-speed. Measurements made with the sampler showed that particles as large as ～50 µm were suspended from vehicular movement on the dirt roads, with the mode of the fugitive dust particle number size distribution ～2 µm, while the mass distribution mode was ～7 µm. A comparison of the fugitive dust sampler measurements with those made using standard PM instruments showed that the conventional instruments have a wind-direction bias that can result in under-sampling of large particles. The current measurements suggest that particles suspended from dirt roadways are of importance for local air quality within the near-road environment.

Copyright © 2017 American Association for Aerosol Research     

Experimental investigations of particle formation from propellant and solvent droplets using a monodisperse spray dryer

Experimental studies of particle formation from solution droplets were conducted using a newly developed monodisperse spray drying process. Solutes beclomethasone dipropionate and caffeine were dissolved in ethanol, pressurized hydrofluoroalkane propellant 134a, and mixtures thereof. Solutions were atomized into monodisperse microdroplets using a custom droplet generator installed in a laboratory scale spray dryer, enabling drying and collection of the resulting monodisperse microparticles. The effects of droplet diameter, solution concentration, solvent composition, and drying rate on the physical properties of the dried particles were evaluated. Particle morphology and size were assessed using ultramicroscopy and image analysis of micrographs. Extent of crystallinity and polymorphism were investigated using Raman spectroscopy. The drying temperature was found to have a large effect on the morphology of amorphous beclomethasone dipropionate particles. Particles dried near room temperature were spheroidal to ellipsoidal with prevalent surface concavities and evidence of shell buckling; increasing the drying temperature for fixed droplet size and composition resulted in a transition to more spherical, smooth-surfaced particle morphologies. Crystalline caffeine microparticles were made up of assemblies of multiple crystallites. The measured length and breadth of these crystallites was found to be correlated with the time available for crystal nucleation and growth as calculated using a particle formation model. The results highlight the abilities and limitations of currently available particle formation models in elucidating the relationships between the size, composition, and evaporation rate of drying solution droplets and the physical properties of the resulting particles. The work demonstrates the suitability of monodisperse spray drying as an experimental technique for investigating the fundamentals of particle formation from solution droplets.

© 2018 American Association for Aerosol Research     

Effect of crystallization kinetics on the properties of spray dried microparticles

A droplet chain technique was used to study the influence of the crystallization process on the morphology of spray dried microparticles. A piezoceramic dispenser produced a chain of monodisperse solution droplets with an initial diameter in the range of 60–80 µm. Aqueous solutions of sodium nitrate were prepared in concentrations ranging from 5 mg/ml to 5?10^?5 mg/ml. The solution droplets were injected into a laminar flow with gas temperatures varying from 25 to 150°C, affecting the droplet temperature and the evaporation rate, accordingly. Dried particles with diameters between 0.3 and 18 µm were collected. The properties of the collected microparticles were studied and correlated with a particle formation model which predicted the onset of saturation and crystallization. The model accounted for the dependence of the diffusion coefficient of sodium nitrate in water on droplet viscosity. The viscosity trend for sodium nitrate solutions was determined by studying the relaxation time observed during coalescence of two aqueous sodium nitrate droplets levitated in optical tweezers. The combination of theoretical derivations and experimental results showed that longer time available for crystallization correlates with larger crystal size and higher degrees of crystallinity in the final microparticles.

© 2016 American Association for Aerosol Research     

Assessment of indoor bioaerosols using a lab-made virtual impactor

To assess indoor bioaerosols, a virtual impactor having 1 µm cutoff diameter was designed, fabricated, and evaluated with computational fluid dynamics simulation and also with laboratory test using polystyrene latex particles. Two other cutoff diameters of 635 nm and 1.5 µm were obtained by changing the inlet flow rate and the ratio of minor channel-to-inlet flow rates. In field test, the virtual impactor was operated with varying cutoff diameter and field-emission scanning electron microscope (FE-SEM) analysis was performed for each cutoff diameter to observe morphologies of indoor aerosol particles sampled at the major and minor outlet channels. Particles were sampled at both outlet channels using the SKC Button Aerosol sampler and subsequently cultured. By colony counting, it was found that 56% of cultured fungal particles and 63% of cultured bacterial particles had aerodynamic sizes smaller than 1 µm. MALDI-TOF analysis and visual inspection of culture samples were used to identify indoor bacterial and fungal species, respectively. Nearly same species of bacteria and fungi were detected both in the major and minor flow channels.

© 2017 American Association for Aerosol Research     

Particulate matter characteristics,dynamics, and sources in an underground mine

Particulate matter (PM) from mining operations, engines, and ore processing may have adverse effects on health and well-being of workers and population living nearby. In this study, the characteristics of PM in an underground chrome mine were investigated in Kemi, Northern Finland. The concentrations and chemical composition of PM in size ranges from 2.5 nm to 10 µm were explored in order to identify sources, formation mechanisms, and post-emission processes of particles in the mine air. This was done by using several online instruments with high time-resolution and offline particulate sampling followed by elemental and ionic analyses. A majority of sub-micrometer particles (<1 µm in diameter, PM₁) originated from diesel engine emissions that were responsible for a rather stable composition of PM₁ in the mine air. Another sub-micrometer particle type originated from the combustion products of explosives (e.g., nitrate and ammonium). On average, PM₁ in the mine was composed of 62%, 30%, and 8% of organic matter, black carbon, and major inorganic species, respectively. Regarding the analyzed elements (e.g., Al, Si, Fe, Ca), many of them peaked at >1 µm indicating mineral dust origin. The average particle number concentration in the mine was (2.3 ± 1.4)*10⁴ #/cm³. The maximum of particle number size distribution was between 30 and 200 nm for most of the time but there was frequently a distinct mode <30 nm. The potential origin of nano-size particles remained as challenge for future studies.

Copyright © 2018 The Authors. Published with license by Taylor & Francis     

Optimization of centrifugally spun thermoplastic polyurethane nanofibers for air filtration applications

While our knowledge of fiber formation by using conventional nanofiber spinning techniques has increased to a considerable extent, there are still few studies on centrifugal spinning either in academia or in the industry. Centrifugal spinning is a comparatively new method of producing fibers having nano- or microscale diameters. In this study, three main parameters (nozzle orifice diameter, rotational speed, polymer concentration) of centrifugal spinning were optimized to produce air filter media from thermoplastic polyurethane nanofibers. The effect of concentration of polymer solution was found to be a major contributor in TPU fibers optimization estimating 77.5%. After the optimization studies, the average fiber diameter of nanofiber sample produced at optimum conditions (22G needle as an orifice, 4000 rpm, and 10 wt% concentration of polymer solution) was 205 ± 84 nm. Aerosol filtration performance of the produced webs was analyzed. Filtration efficiency of the optimized sample was found to be 99.4% for 0.3 µm particle size at an expense of 98 Pa pressure drop.

Copyright © 2018 American Association for Aerosol Research     

Aerosol Generation by a Spray-Drying Technique Under Coulomb Explosion and Rapid Evaporation for the Preparation of Aerosol Particles for Inhalation Tests

In this study, nanosized (<100 nm) aerosol particles with high mass concentrations for inhalation tests were generated by a spray-drying technique with combining Coulomb explosion and rapid evaporation of the droplets. Under typical spray-drying conditions, aerosol particles with average diameter of 50–150 nm were prepared from a suspension of NiO nanoparticles with a primary diameter of 15–30 nm. Under the Coulomb explosion method, the sprayed droplets were charged by being mixed with unipolar ions to break up the droplets, which resulted in the generation of smaller aerosol particles with diameters of 15–30 nm and high number concentrations. Under the rapid evaporation method, the droplets were heated immediately after being sprayed to avoid inertial impaction on the flow path due to shrinkage of the droplet, which increased the mass concentration of the aerosol particles. The combination of the Coulomb explosion and rapid evaporation of droplets resulted in the generation of aerosol particles with sizes less than 100 nm and mass concentrations greater than 1 mg/m³; these values are often necessary for inhalation tests. The aerosols generated under the combined method exhibited good long-term stability for inhalation tests. The techniques developed in this study were also applied to other metal oxide nanoparticle materials and to fibrous multiwalled carbon nanotubes.

Copyright 2014 American Association for Aerosol Research     

Mathematical modeling and numerical simulation of surfactant delivery within a physical model of the neonatal trachea for different aerosol characteristics

Surfactant aerosol delivery in conjunction with a noninvasive respiratory support holds the potential to treat neonatal respiratory distress syndrome in a safe manner. The objective of the present study was to gain knowledge in order to optimize the geometry of an intracorporeal inhalation catheter and improve surfactant aerosol delivery effectiveness in neonates. Initially, a mathematical model capable of predicting the aerosol flow generated by this inhalation catheter within a physical model of the neonatal trachea was implemented and validated. Subsequently, a numerical study was performed to analyze the effect of the aerosol liquid droplet size and mass flow rate on surfactant delivery and on the required aerosolization time period. Experimental validation of the mathematical model showed a close prediction of the air axial velocity at the distal end of the physical model, with an absolute error between 0.01 and 0.15 m/s. Furthermore, an admissible absolute error between 0.2 and 2 µm was attained in the prediction of the aerosol mean aerodynamic diameter and mass median aerodynamic diameter in this region. The numerical study highlighted the beneficial effects of generating an intracorporeal aerosol with a mass median aerodynamic diameter higher than 4 µm and a surfactant mass flow rate above 8.93 mg/s in order to obtain effective surfactant delivery in neonates with minimal airway manipulation.

Copyright © 2017 American Association for Aerosol Research     

Water-based single-flow mixing condensation particle counter

A novel water-based condensation particle counter has been developed using a patented, single-flow mixing (SFM) condenser that permits a conventional thermal approach of using a hot saturator followed by a cold condenser to activate and grow particles for counting with an optical detector. A computational fluid dynamics (CFD) model of the internal flow, temperature, and vapor profiles was used to predict the effectiveness of the SFM condenser. Using the results from the CFD model, the counting efficiency was numerically calculated for pure water droplets, and the CPC cut-point (i.e., 50% counting efficiency) was predicted to be 8.3 nm. The experimental performance of the new CPC was measured with differential mobility analyzer-classified, monodisperse particles. The measured cut-points were 8.2 nm for Ag particles and 3.9 nm for NaCl particles. The reduction in the cut-point for NaCl is the result of a compound effect: water uptake by NaCl particles, which increases their size before entering into the growth section (condenser), and the reduction of the equilibrium vapor pressure of water over NaCl-water droplets, resulting in a decrease of the activation diameter.

Copyright © 2016 American Association for Aerosol Research     

Design and evaluation of an aerodynamic focusing micro-well aerosol collector

Aerosol sampling and identification is vital for the assessment and control of particulate matter pollution, airborne pathogens, allergens, and toxins and their effect on air quality, human health, and climate change. In situ analysis of chemical and biological airborne components of aerosols on a conventional filter is challenging due to dilute samples in a large collection region. We present the design and evaluation of a micro-well (µ-well) aerosol collector for the assessment of airborne particulate matter (PM) in the 0.5–3 µm size range. The design minimizes particle collection areas allowing for in situ optical analysis and provides an increased limit of detection for liquid-based assays due to the high concentrations of analytes in the elution/analysis volume. The design of the collector is guided by computational fluid dynamics (CFD) modeling; it combines an aerodynamic concentrator inlet that focuses the aspirated aerosol into a narrow beam and a µ-well collector that limits the particle collection area to the µ-well volume. The optimization of the collector geometry and the operational conditions result in high concentrations of collected PM in the submillimeter region inside the µ-well. Collection efficiency experiments are performed in the aerosol chamber using fluorescent polystyrene microspheres to determine the performance of the collector as a function of particle size and sampling flow rate. The collector has the maximum collection efficiency of about 75% for 1 µm particles for the flow rate of 1 slpm. Particles bigger than 1 µm have lower collection efficiencies because of particle bounce and particle loss in the aerodynamic focusing inlet. Collected samples can be eluted from the device using standard pipettes, with an elution volume of 10–20 µL. The transparent collection substrate and the distinct collection region, independent of particle size, allows for in situ optical analysis of the collected PM.

© 2017 American Association for Aerosol Research     

Evaluation of the Alphasense optical particle counter (OPC-N2) and the Grimm portable aerosol spectrometer (PAS-1.108)

We compared the performance of a low-cost (～$500), compact optical particle counter (OPC, OPC-N2, Alphasense) to another OPC (PAS-1.108, Grimm Technologies) and reference instruments. We measured the detection efficiency of the OPCs by size from 0.5 to 5 µm for monodispersed, polystyrene latex (PSL) spheres. We then compared number and mass concentrations measured with the OPCs to those measured with reference instruments for three aerosols: salt, welding fume, and Arizona road dust. The OPC-N2 detection efficiency was similar to the PAS-1.108 for particles larger than 0.8 µm (minimum of 79% at 1 µm and maximum of 101% at 3 µm). For 0.5-µm particles, the detection efficiency of the OPC-N2 was underestimated at 78%, whereas PAS-1.108 overestimated concentrations by 183%. The mass concentrations from the OPCs were linear (r ≥ 0.97) with those from the reference instruments for all aerosols, although the slope and intercept were different. The mass concentrations were overestimated for dust (OPC-N2, slope = 1.6; PAS-1.108, slope = 2.7) and underestimated for welding fume (OPC-N2, slope = 0.05; PAS-1.108, slope = 0.4). The coefficient of variation (CV, precision) for OPC-N2 for all experiments was between 4.2% and 16%. These findings suggest that, given site-specific calibrations, the OPC-N2 can provide number and mass concentrations similar to the PAS-1.108 for particles larger than 1 µm.

Copyright © 2016 American Association for Aerosol Research     

Droplet-based microfluidics detector for bioaerosol detection

Detection of bioaerosols is important in fields ranging from environmental health monitoring to biosurveillance, and current detector weaknesses have motivated the development of new technologies. In this work, a detector was built, which applies the principles of droplet microfluidics to bioaerosol detection. Droplet microfluidics is a subfield of microfluidics based on the creation of monodisperse microdroplets with compartmentalized reagents and supports enhanced assays and fluidic manipulations. The bioaerosol detector operates by aerodynamically focusing aerosols directly into these droplets to harness the benefits of the microreactor environment. A breadboard detector system, which consisted of an aerodynamic focusing lens, aerosol-focusing capillary, microfluidic droplet chip, and optical microscope, was constructed. Computational fluid dynamic simulations and Lagrangian particle tracking modeling were conducted to identify the optimal conditions for focusing. Preliminary experiments, where aerosols were deposited onto a solid substrate, demonstrated sub 200-µm spot diameters for aerodynamic diameters of 2–5 µm. Test aerosols were then generated, and collected into the microfluidic liquid interface on the chip as verified by microscopy. Recovery efficiency of the aerosols was dependent on aerosol size and ranged from about 27% to nearly 100%. Finally, to prove bioaerosol collection and detection, a droplet propidium iodide (PI) assay was performed: the system distinguished between E. coli and non-biological aerosols within 20 s. Overall, this work established the technique of direct collection of bioaerosols into a convenient droplet microfluidic platform for detection.

Copyright © 2017 The Johns Hopkins University Applied Physics Laboratory     

Modeling the thermodynamics and kinetics of sulfuric acid-dimethylamine-water nanoparticle growth in the CLOUD chamber

Dimethylamine (DMA) has a stabilizing effect on sulfuric acid (SA) clusters, and the SA and DMA molecules and clusters likely play important roles in both aerosol particle formation and growth in the atmosphere. We use the monodisperse particle growth model for acid-base chemistry in nanoparticle growth (MABNAG) together with direct and indirect observations from the CLOUD4 and CLOUD7 experiments in the cosmics leaving outdoor droplets (CLOUD) chamber at CERN to investigate the size and composition evolution of freshly formed particles consisting of SA, DMA, and water as they grow to 20 nm in dry diameter. Hygroscopic growth factors are measured using a nano-hygroscopicity tandem differential mobility analyzer (nano-HTDMA), which combined with simulations of particle water uptake using the thermodynamic extended-aerosol inorganics model (E-AIM) constrain the chemical composition. MABNAG predicts a particle-phase ratio between DMA and SA molecules of 1.1–1.3 for a 2 nm particle and DMA gas-phase mixing ratios between 3.5 and 80 pptv. These ratios agree well with observations by an atmospheric-pressure interface time-of-flight (APi-TOF) mass spectrometer. Simulations with MABNAG, direct observations of the composition of clusters <2 nm, and indirect observations of the particle composition indicate that the acidity of the nucleated particles decreases as they grow from ～1 to 20 nm. However, MABNAG predicts less acidic particles than suggested by the indirect estimates at 10 nm diameter using the nano-HTDMA measurements, and less acidic particles than observed by a thermal desorption chemical ionization mass spectrometer (TDCIMS) at 10–30 nm. Possible explanations for these discrepancies are discussed.

Copyright © 2016 American Association for Aerosol Research     

Using silver as a surrogate for plutonium: An experimental study of the explosive silver aerosol source term

An experimental method is developed for the purpose of simulating plutonium aerosol source terms with conventional metals in laboratory. In this method, metal samples are aerosolized by high explosive detonation in a containment vessel. Aerosols having aerodynamic diameter (AD) less than 10 µm are then collected by a cascade impactor and analyzed by atomic absorption spectroscopy. Two sets of experiments were conducted. In the first set, five candidate metal samples (Ag, W, Sn, Ce, and V) were tested. It is found that the cumulative mass distribution of silver under certain conditions was in good agreement with that of plutonium from the Operation Roller Coaster-Double Track experiment. Thus, silver is chosen as a surrogate to simulate the plutonium aerosol source term. In the second set, silver aerosol source term was studied in detail with different test configurations. The results demonstrate that the peak of the mass-size distribution of silver is in the AD range 1.1–3.3 µm. The amount and fraction of relatively small silver aerosols decrease significantly with time due to coagulation and deposition. Interestingly, the amount of silver in aerosols could be expressed as a quadratic function of the peak detonation pressure.

© 2016 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     

Anisokinetic Shrouded Nozzle System for Constant Low-Flow Rate Aerosol Sampling from Turbulent Duct Flow

An anisokinetic shrouded nozzle system was designed for sampling particles at a constant low flow rate from a ventilation duct to an aerodynamic particle sizer (APS). Shrouded anisokinetic nozzles are a means for sampling from a moving airstream with higher particle transmission than with unshrouded isokinetic nozzles. This shrouded nozzle sampling system was evaluated in an experimental ventilation duct system. Aspiration and transport efficiency measurements were made for five particle sizes in the range 1–13 μm at each of three duct air speeds in the range 2.2–8.8 m/s. Under these conditions, the shrouded nozzle system showed improved performance compared to buttonhook isokinetic nozzles, especially for larger particles and higher air speeds. Measured transmission efficiencies through the shrouded nozzle sampling system were generally higher and more reliably predictable than those through buttonhook isokinetic nozzles. Model predictions of transport and aspiration efficiencies of the shrouded nozzle system showed good agreement with measurements over the entire range of experimental conditions. The shrouded nozzle sampling system could be used to measure concentrations in ventilation ducts with an APS for particles in the diameter range 1–13 μm.

Copyright 2014 American Association for Aerosol Research     

Modification and laboratory evaluation of a TSI ultrafine condensation particle counter (Model 3776) for airborne measurements

A butanol-type ultrafine condensation particle counter (UCPC, Model 3776, TSI, Inc., Shoreview, MN, USA), which can achieve a 50% detection efficiency diameter (d₅₀) of 2.5 nm using a capillary-sheath structure, was modified and tested in the laboratory for airborne measurements. The aerosol flow rate through the capillary is a key factor affecting the quantification of aerosol particle number concentrations. A pressure-dependent correction factor for the aerosol flow rate was determined using a newly added mass flow meter for the sheath flow and the external calibration system. The effect of particle coincidence in the optical sensing volume was evaluated using an aerosol electrometer (AE, Model 3068B, TSI, Inc.) as a reference. An additional correction factor for the coincidence effect was derived to improve the quantification accuracy at higher concentrations. The particle detection efficiency relative to the AE was measured for mobility diameters of 3.1–50 nm and inlet absolute pressures of 101–40 kPa. The pressure dependence of the d₅₀ value, asymptotic detection efficiency, and shape of the particle detection efficiency curve is discussed, along with simple theoretical calculations for the diffusion loss of particles and the butanol saturation ratio in the condenser.

© 2017 American Association for Aerosol Science     

Physical performances and kinetics of evaporation of the CIP 10-M personal sampler's rotating cup containing aqueous or viscous collection fluid

The CIP 10-M personal sampler measures worker exposure to airborne particles by collecting particles in a rotating metal cup containing a few milliliters of a collection fluid. This device is mainly used to sample microorganisms or microbial components to measure bioaerosol concentrations in various occupational environments. Aqueous liquids are generally used, but their rapid evaporation limits the duration of sampling; alternative collection fluids could alleviate this problem. Indeed, the particle-collection efficiency of the rotating cup has not been extensively studied, and the only data available relate to a discontinued model. This study aimed to measure the collection efficiency of the current rotating cup model containing an aqueous (water) or viscous (ViaTrap mineral oil) collection fluid. The kinetics of evaporation confirmed that ViaTrap does not evaporate, making 8-h sampling campaigns in constant volumes feasible. Particles with a wide range of aerodynamic diameters (between around 0.1 and 10 µm) were produced using various test rigs and mono- or polydisperse test aerosols. Both new and older cup models performed similarly, with a collection efficiency of >80% for larger particles (aerodynamic diameters >2.8 µm), progressively decreasing to around 50% for aerodynamic diameters of 2.1 µm; with aerodynamic diameters of <1 µm, the collection efficiency was generally <10%. In physical terms, collection efficiency was unaffected by the type (aqueous or viscous) or volume (between 0 and 3 mL) of collection fluid used. Bias maps indicated that the inhalable fraction may be underestimated in occupational settings, particularly with aerosols mainly composed of particles with aerodynamic diameters of less than around 3 µm.

Copyright © 2016 American Association for Aerosol Research     

Development of a High-Pressure Aerodynamic Lens for Focusing Large Particles (4–10 μm) into the Aerosol Time-of-Flight Mass Spectrometer

A new aerodynamic lens system for an online aerosol time-of-flight mass spectrometer (ATOFMS) has been designed and constructed to transmit and allow the analysis of individual particles in the 4–10-μm-size range. Modeling was used to help design the lens within the bounds of ATOFMS instrumental constraints. The aerodynamic lens operates at a high inlet pressure, 3066 Pa (23 Torr), with a unique tapered relaxation region to improve large particle transmission. Every stage of the lens was tested empirically using a combination of particle deposition and light scattering experiments. The critical orifice was found to significantly impact large particle transmission, with orifices <200 μm in diameter completely suppressing large particle transmission. The addition of a virtual impactor allowed for the use of large orifices without any loss of functionality in the ATOFMS. The detection efficiency of the ATOFMS was >10% for particles from 4–10 μm with a peak efficiency of 74 ± 9% for 6-μm particles. With the extended size range provided by this inlet, the ATOFMS can now be extended to investigate single cell metabolomics.

Copyright 2014 American Association for Aerosol Research     

Spatial aerosol flow maldistribution: A design flaw confounding the proper calibration and data interpretation of stages “0” and “1” of the Andersen eight-stage nonviable cascade impactor

We introduced monodisperse calibrant particles into an eight-stage non-viable Andersen cascade impactor (ACI) operated at 28.3 L/min and separately quantified the particle mass captured under each of the four concentric rings of nozzles on stages 0 and 1, the entry and succeeding stages of this impactor. On both stages, we found that each ring of nozzles has a particle capture efficiency behavior that differs from the others, and the fraction of calibrant particles deposited under each of the individual rings of nozzles depended on the particle size. We believe this behavior derives primarily from a radial flow velocity non-uniformity associated with recirculation zones introduced by the 110° expansion angle of the inlet cone. Because of these recirculation zones, the inertia of particles larger than about 5 µm aerodynamic diameter will cause their point-wise local concentration to differ from the concentration at the inlet entry. This concentration maldistribution continues to stage 1 primarily because of the annular collection plate at stage 0. The influence of the inlet cone aerodynamics on the performance of both stages means that the size of particles deposited on these plates will be uncertain unless the aerosol transport entering the impactor associated with calibration using monodisperse particles exactly simulates the in-use aerosol flow conditions. The degree of realism necessary in the calibration method has heretofore not been discussed in published calibrations of the ACI, introducing uncertainty in the size interpretation of the particle mass collected on stages 0 and 1 in practical applications of this impactor.

Copyright © 2017 American Association for Aerosol Research