The Use of Nonlinear Acoustics as an Energy-Efficient Technique for Aerosol Removal

This article is a feasibility study on using nonlinear acoustic effects, acoustic streaming and acoustic radiation pressure, for aerosol removal in an air duct. Unlike previous research, which used acoustics solely to cause aerosol agglomeration prior to aerosol removal in traditional duct collection systems, this article considers the acoustic streaming effect, which is significant but was previously neglected. Monodispersed polystyrene spheres with diameters ranging from 0.3 to 6 μm were tested. The proposed system removed 12–20% of the submicron aerosols and 25–32% of the micron aerosols when the airflow rate was approximately 90 L/min. Acoustic streaming introduces stagnation points on the surface of the air duct and removes the aerosols by deposition. Acoustic radiation pressure causes aerosols to form agglomerates. This enhances inertial impaction and/or gravitational sedimentation, which further enhances the removal efficiency of micron aerosols. The particle-removal efficiency is proportional to the duration that the aerosols are exposed to the acoustic field. The pressure drop due to the nonlinear acoustic effects is negligible; thus, power consumption is minimal. This system has the potential to be developed into an energy-efficient technique for aerosol removal.

Copyright 2014 American Association for Aerosol Research     

Opto-aerodynamic focusing of aerosol particles

We describe a new method for focusing and concentrating a stream of moving micron-sized aerosol particles in air. The focusing and concentrating process is carried out by the combined drag force and optical force that is generated by a double-layer co-axial nozzle and a focused doughnut-shaped hollow laser beam, respectively. This method should supply a new tool for aerosol science and related research.

Copyright © 2018 American Association for Aerosol Research     

Assessing the accuracy of complex refractive index retrievals from single aerosol particle cavity ring-down spectroscopy

Cavity ring-down spectroscopy (CRDS) of single, optically manipulated aerosol particles affords quantitative retrieval of refractive indices for particles of fixed or evolving composition with high precision. Here, we quantify the accuracy with which refractive index determinations can be made by CRDS for single particles confined within the core of a Bessel laser beam and how that accuracy is degraded as the particle size is progressively reduced from the coarse mode (>1 μm radius) to the accumulation mode (<500 nm radius) regime. We apply generalized Lorenz–Mie theory to the intra-cavity standing wave to explore the effect of particle absorption on the distribution of extinction cross section determinations resulting from stochastic particle motion in the Bessel beam trap. The analysis provides an assessment of the accuracy with which the real, n, and imaginary, κ, components of the refractive index can be determined for a single aerosol particle.

Published with license by American Association for Aerosol Research     

Modeling of submicron particle filtration in an electret monolith filter with rectangular cross-section microchannels

Electret monolith filters have the advantage of low pressure drop and high filtration efficiency. In such filters, the filtration of submicron aerosol particles occurs as air passes through millions of microchannels. This article investigates the flow and filtration mechanisms in a representative rectangular microchannel of an electret monolith filter. An improved incompressible lattice Boltzmann method with Bhatnagar–Gross–Krook (traditionally shortened as LBGK) and lattice velocity D3Q15 model is employed to simulate no-slip and slip flows in the rectangular microchannels of a monolith filter. We considered mono-disperse submicron particles and one-way coupling (particle motion was affected by the flow, but the presence of particles did not affect the flow). Based on flow computations, the effects of key dimensionless parameters (Reynolds number, Knudsen number, Stokes number and the dimensionless length of the channel) on the total capture efficiency of mono-disperse submicron particles were investigated. Our results indicate that the optimal monolith filter should be characterized by a Knudsen number between 0.022 and 0.044, and that the dimensionless length of the channel should be between 4 and 8.

Copyright © 2016 American Association for Aerosol Research     

Numerical investigation of spatially nonhomogeneous acoustic agglomeration using sectional algorithm

In the simulation of acoustic agglomeration, the conventional temporal model assumes spatial homogeneity in aerosol properties and sound field, which is often not the case in real applications. In this article, we investigated the effects of spatial nonhomogeneity of sound field on the acoustic agglomeration process through a one-dimensional spatial sectional model. The spatial sectional model is validated against existing experimental data and results indicate lower requirements on the number of sections and better accuracy. Two typical cases of spatial nonhomogeneous acoustic agglomeration are studied by the established model. The first case involves acoustic agglomeration in a standing wave field with spatial alternation of acoustic kernels from nodes to antinodes. The good agreement between the simulation and experiments demonstrates the predictive capability of the present spatial sectional model for the standing-conditioned agglomeration. The second case incorporates sound attenuation in the particulate medium into acoustic agglomeration. Results indicate that sound attenuation can influence acoustic agglomeration significantly, particularly at high frequencies, and neglecting the effects of sound attenuation can cause overprediction of agglomeration rates. The present investigation demonstrates that the spatial sectional method is capable of simulating the spatially nonhomogeneous acoustic agglomeration with high computation efficiency and numerical robustness and the coupling with flow dynamics will be the goal of future work.

Copyright © 2018 American Association for Aerosol Research     

Loss processes affecting submicrometer particles in a house heavily affected by road traffic emissions

The fraction of outdoor aerosol that penetrates into indoor environments plays an important role in determining the contribution of outdoor particles to the total lung dose of particles in human exposure. The objective of this study was to investigate the physical processes affecting migration of outdoor traffic particles into indoor environments. Particle number size distributions were measured by a fast mobility particle sizer system in both indoor and outdoor environments of a house located in close proximity to a busy street in Bologna (Italy) in the period February–April 2012. Indoor to outdoor (I/O) ratios for submicron particle number concentrations showed strong dependence on particle size and meteorological conditions. The loss rates of particles due to deposition, coagulation, and evaporation were determined using dynamic mass balance and coagulation models. Higher loss rates were found for small particles (nucleation and Aitken mode) indoors than for larger particles (accumulation mode). The coagulation and evaporation processes made a significant contribution to the loss of traffic nanoparticles indoors, especially during the day time. Application of positive matrix factorization to the indoor and outdoor particle size distributions showed a substantial loss of traffic-generated nucleation mode particles in the indoor environment, with evaporation playing a major role.

Copyright © 2017 American Association for Aerosol Research     

Visualization of submicron aerosol agglomeration by laser-induced fluorescence

A new experimental technique is reported to visualize agglomeration of submicron aerosol particles by laser-induced fluorescence (LIF). The basic idea is to produce or activate the fluorescent tracer material by a chemical reaction triggered by the agglomeration between two chemically different primary particles. Different types of chemical reactions are able to fulfil this task, among others acid–base reactions or molecule solvation. In this work, we demonstrate the feasibility of the fluorescent tracer activation by means of solvation. The fluorescence is activated almost instantaneously when the dry fluorescent material (Fluorescein or Rhodamine B) contained in the dye aerosol is dissolved by a water/glycerol mixture constituting the particles of the solvent aerosol. Estimations of the timescale for diffusional mixing suggest that the fluorescence is activated within 1 ms. Agglomerates can be detected as single particles or in bulk quantities depending on the available laser excitation energy and light sensitivity. In order to enhance agglomeration in the validation experiments, two aerosol streams were electrostatically charged with opposite polarity. Finally, potential variations and applications of the newly introduced technique are briefly discussed, mentioning the detection of humidity among others.

© 2017 American Association for Aerosol Research     

Application of centrifugal filter to aerosol size distribution measurement

In the present work, the centrifugal filter proposed by the authors was applied to classify aerosol particles followed by the detection of total mass or number concentrations so as to measure the size distribution of aerosol particles. The structure and operating condition of the centrifugal filter were optimized in order to attain sharp separation curves with various cut-off sizes between 0.3 and 10 μm. The aerosol penetrating the centrifugal filter at various rotation speeds was measured with a photometer to determine the total mass concentration. The virtue of this system is that the cut-off size is varied just by scanning the rotation speed of filter and that it can be applied to the measurement of high concentration aerosols without dilution by choosing an appropriate filter medium. As a result, the centrifugal filter was successfully applied to measure the size distribution of solid particles in size ranging from 0.3 to 10 μm.

Copyright © 2017 American Association for Aerosol Research     

The First Combined Thermal Desorption Aerosol Gas Chromatograph—Aerosol Mass Spectrometer (TAG-AMS)

To address the critical need for improving the chemical characterization of the organic composition of ambient particulate matter, we introduce a combined thermal desorption aerosol gas chromatograph—aerosol mass spectrometer (TAG-AMS). The TAG system provides in-situ speciation of organic chemicals in ambient aerosol particles with hourly time resolution for marker compounds indicative of sources and transformation processes. However, by itself the TAG cannot separate by particle size and it typically speciates and quantifies only a fraction of the organic aerosol (OA) mass. The AMS is a real-time, in-situ instrument that provides quantitative size distributions and mass loadings for ambient fine OA and major inorganic fractions; however, by itself the AMS has limited ability for identification of individual organic compounds due to the electron impact ionization detection scheme used without prior molecular separation.

The combined TAG-AMS system provides real-time detection by AMS followed by semicontinuous analysis of the TAG sample that was acquired during AMS operation, achieving simultaneous and complementary measurements of quantitative organic mass loading and detailed organic speciation. We have employed a high-resolution time-of-flight mass spectrometer (HR-ToF-MS) to enable elemental-level determination of OA oxidation state as measured on the AMS, and to allow improved compound identification and separation of unresolved complex mixtures (UCM) measured on the TAG. The TAG-AMS interface has been developed as an upgrade for existing AMS systems. Such measurements will improve the identification of organic constituents of ambient aerosol and contribute to the ability of atmospheric chemistry models to predict ambient aerosol composition and loadings.

Copyright 2014 American Association for Aerosol Research     

Differential diffusion analyzer

In this article, a proof of concept of a new measurement instrument, differential diffusion analyzer (DDA), is established. The DDA enables the measurement of the size distribution of sub-10 nm aerosol particles, and it can also be used as a size classifier to separate a certain particle size from a size distribution for subsequent analysis. The developed technique is based on the diffusion separation of different size particles. Thus, the main advantage of the DDA compared to other methods is that particle charging is not required. Simulated and experimentally measured transmission efficiencies show that the diffusion-based differential size classification is a feasible concept, and moreover, shows that particle size is inversely proportional to the square root of the total flow rate.

Copyright © 2017 American Association for Aerosol Research     

An artifact-minimizing method for total dust sampling and chemical characterization of industrial high-temperature aerosols

Conventional methods for total dust sampling from industrial high-temperature aerosols containing condensable species, e.g., in boilers of municipal solid waste incinerators (MSWI), are always influenced by condensation artifacts. Therefore, we extended the scope of a previously developed probe intended for size-fractionated aerosol sampling with reduced artifacts and employed it for total dust measurements. The dust is collected on quartz fiber filters, which are gravimetrically evaluated and chemically analyzed by energy dispersive X-ray spectroscopy and wet-chemical methods. First measurements in the boiler of an MSWI confirm that the probe is also suitable for artifact-minimized total dust sampling. The data are consistent with results from measurements with the size-fractionating method conducted in parallel. By combining the results of both sampling methods, we reveal the average chemical composition of the submicron particles in the aerosol, which is not accessible by one of the two methods alone.

© 2017 American Association for Aerosol Research     

Sensitivity of Aerosol Refractive Index Retrievals Using Optical Spectroscopy

Accurate refractive index values are required to determine the effects of aerosol particles on direct radiative forcing. Theoretical retrievals using extinction data alone or extinction plus absorption data have been simulated to determine the sensitivity of each retrieval. A range of aerosol types with a range of different refractive indices were considered. The simulations showed that the extinction-only retrieval was not able to accurately or precisely retrieve refractive index values, even for purely scattering compounds, but the addition of a simulated absorption measurement greatly improved the retrieval.

Copyright 2014 American Association for Aerosol Research     

Aerosol Measurement by Induced Currents

We introduce a new electrical measurement technique for aerosol detection, based on pulsed unipolar charging followed by a non-contact measurement of the rate of change of the aerosol space charge in a Faraday cage. This technique, which we call “aerosol measurement with induced currents,” has some advantages compared to the traditional method of collecting the charged particles on either an electrode or with a particle filter. We describe the method and illustrate it with a simple and miniature (shirt-pocket-sized) instrument to measure lung-deposited surface area. Aerosol measurement by induced currents can also be applied to more complex devices.

Copyright 2014 American Association for Aerosol Research     

Generation of monodisperse aerosols by combining aerodynamic flow-focusing and mechanical perturbation

A novel instrument has been developed for generating highly monodisperse aerosol particles with a geometrical standard deviation of 1.05 or less. This aerosol generator applies a periodic mechanical excitation to a micro-liquid jet obtained by aerodynamic flow-focusing. The jet diameter and its fastest growth wavelength have been optimized as a function of the flow-focusing pressure drop and the liquid flow rate. The monodisperse aerosol generated by this instrument is also charge neutralized with bipolar ions produced by a non-radioactive, corona discharge device. Monodisperse droplet generation in the 15- to 72-μm diameter range from a single 100-micron nozzle has been demonstrated. Both liquid and solid monodisperse particles can be generated from 0.7- to 15-μm diameter by varying solution concentration, liquid flow rate, and excitation frequency. The calculated monodisperse particle diameter agrees well with independent measurements. The operation of this new monodisperse aerosol generator is stable and reliable without nozzle clogging, typical of other aerosol generators at the lower end of the operating particle size ranges.

Copyright © 2016 American Association for Aerosol Research     

Extension of the Smoluchowski Theory to Transitions from Dilute to Dense Regime of Brownian Coagulation: Triple Collisions

In order to study the transition from dilute (controlled by binary collisions) to dense (controlled by multiple collisions) regime of coagulation of colloidal or aerosol suspensions, the Smoluchowski equation is generalized by consideration of triple collisions in the kinetic approach, recently proposed by the authors for coagulation of comparable size particles. A good agreement of the new model predictions with more general results of the direct numerical simulations by Langevin dynamics (from the literature) is attained in a relatively wide range of the fractional volume, corresponding to the transition from dilute to dense regime of coagulation dynamics, in which multiple collisions among more than three particles can be neglected.

Copyright 2014 American Association for Aerosol Research     

Influence of surfactants on growth of individual aqueous coarse mode aerosol particles

Understanding the links between aerosol and cloud and radiative properties remains a large uncertainty in predicting Earth's changing energy budget. Surfactants are observed in ambient atmospheric aerosol particles, and their effect on cloud droplet growth is a mechanism that was, until recently, neglected in model calculations of particle activation and droplet growth. In this study, coarse mode aqueous aerosol particles were created containing the surfactant Igepal CA-630 and NaCl. The evaporation and condensation of these individual aqueous particles were investigated using an aerosol optical trap combined with Raman spectroscopy. For a relative humidity (RH) change from 70% to 80%, droplets containing both Igepal and NaCl at atmospheric concentrations exhibited on average more than 4% larger changes in droplet radii, compared to droplets containing NaCl only. This indicates enhanced water uptake in the presence of surfactants, but this result is unexpected based on the standard calculation of the effect of surfactants, using surface tension reduction and/or hygroscopicity changes, for particles of this size. One implication of these results is that in periods with increasing RH, surfactant-containing aqueous particles may grow larger than similarly sized aqueous NaCl particles without surfactants, thus shifting atmospheric particle size distributions, influencing particle growth, and affecting aerosol loading, visibility, and radiative forcing.

Copyright © 2018 American Association for Aerosol Research     

Unique DNA-barcoded aerosol test particles for studying aerosol transport

Data are presented for the first use of novel DNA-barcoded aerosol test particles that have been developed to track the fate of airborne contaminants in populated environments. Until DNATrax (DNA Tagged Reagents for Aerosol eXperiments) particles were developed, there was no way to rapidly validate air transport models with realistic particles in the respirable range of 1–10 μm in diameter. The DNATrax particles, developed at Lawrence Livermore National Laboratory (LLNL) and tested with the assistance of the Pentagon Force Protection Agency, are the first safe and effective materials for aerosol transport studies that are identified by DNA molecules. The use of unique synthetic DNA barcodes overcomes the challenges of discerning the test material from pre-existing environmental or background contaminants (either naturally occurring or previously released). The DNATrax particle properties are demonstrated to have appropriate size range (approximately 1–4.5 μm in diameter) to accurately simulate bacterial spore transport. Here, we describe details of the first field test of the DNATrax aerosol test particles in a large indoor facility.

Copyright © 2016 American Association for Aerosol Research     

Intercomparison of a portable and two stationary mobility particle sizers for nanoscale aerosol measurements

During occupational exposure studies, the use of conventional scanning mobility particle sizers (SMPS) provides high quality data but may convey transport and application limitations. New instruments aiming to overcome these limitations are being currently developed. The purpose of the present study was to compare the performance of the novel portable NanoScan SMPS TSI 3910 with that of two stationary SMPS instruments and one ultrafine condensation particle counter (UCPC) in a controlled atmosphere and for different particle types and concentrations.

The results show that NanoScan tends to overestimate particle number concentrations with regard to the UCPC, particularly for agglomerated particles (ZnO, spark generated soot and diesel soot particles) with relative differences >20%. The best agreements between the internal reference values and measured number concentrations were obtained when measuring compact and spherical particles (NaCl and DEHS particles). With regard to particle diameter (modal size), results from NanoScan were comparable < [± 20%] to those measured by SMPSs for most of the aerosols measured.

The findings of this study show that mobility particle sizers using unipolar and bipolar charging may be affected differently by particle size, morphologies, particle composition and concentration. While the sizing accuracy of the NanoScan SMPS was mostly within ±25%, it may miscount total particle number concentration by more than 50% (especially for agglomerated particles), thus making it unsuitable for occupational exposure assessments where high degree of accuracy is required (e.g., in tier 3). However, can be a useful instrument to obtain an estimate of the aerosol size distribution in indoor and workplace air, e.g., in tier 2.     

The correlation between acoustic streaming patterns and aerosol removal efficiencies in an acoustic aerosol removal system

Recently, researchers proposed that a second-order effect, acoustic streaming, induced aerosol depositions as a noninvasive aerosol removal technique. However, the acoustic streaming patterns, which determined the deposition efficiencies, were merely observed but not investigated. This article studied this correlation by both experimental and numerical methods. By keeping the sound frequency and sound pressure level constant, the acoustic streaming field was varied by the dimensions of the air duct and ultrasonic radiating plate. The numerical model was validated by the experimental results on three accounts, acoustic streaming patterns, velocity vectors, and deposition trends. Two new parameters, acoustic deposition ratio and near wall vorticity magnitude, were introduced to measure and predict the correlation between variation of the acoustic fields and deposition efficiencies. It was found that the geometry that produced a high vorticity magnitude near the deposition surfaces provided the condition to induced high occurrence for aerosols depositions (up to 3.5 times the rate caused by nature deposition). The finding in this study provided a method to quantify acoustic streaming fields, and the correlation between such quantity and the related deposition performance. This provides a guideline for designing acoustic aerosol manipulation devices, which aims to cause deposit with a noninvasive method.

Copyright © 2016 American Association for Aerosol Research