Antti Rostedt

On-line measurement of size distribution and effective density of submicron aerosol particles

Abstract An on-line method is presented for simultaneous size distribution and particle density measurement, based on parallel measurements made by SMPS and ELPI. The measured SMPS number distribution is integrated with the ELPI response functions to produce calculated current response. By varying the density value, the best fit is sought between the calculated and measured current response. Simulation tests made showed relatively good stability against small uncertainties in the distribution and the response functions. Test measurements of well-defined aerosols with known density were conducted. Density values of 0.86, 1.1, and 1.9 g / cm 3 were measured for liquid particles of DOS, Santovac vacuum oil, and Fomblin vacuum oil, respectively. These values are within 8% of the accepted bulk values. For solid particles of NaCl, Zn, and Ag, slightly larger experimental errors in the range of 4–18.2% were found.

Instrumentation for measuring fluorescence cross sections from airborne microsized particles

An experimental instrument for measuring a laser-induced fluorescence spectrum from a single aerosol particle is described. As a demonstration of instrument capabilities, the results of monodisperse 4.7 microm sodium chloride particles doped with fluorescent riboflavin, produced with an inkjet aerosol generator, are presented. The fluorescence of the aerosol particles is excited in the wide range from 210 to 419 nm using a pulsed, tunable optical parametric oscillator laser. The maximum of the fluorescence emission of separately measured particles is detected at 560 nm. The dependence of the fluorescence on the excitation wavelength is studied and fluorescence cross sections are estimated. Agreement between the measured fluorescence data and the literature data for riboflavin is observed.

Fluorescence cross sections of bioaerosols and suspended biological agents

Laser-induced fluorescence is used to investigate fluorescence properties of unwashed Bacillus thuringiensis and Bacillus subtilis spores, ovalbumin, and washed bacteriophage MS2. A fluorescence detector is calibrated to obtain absolute fluorescence cross sections. Fluorescence maps of biological aerosols and suspensions are measured at a wide excitation range from 210 to 419 nm and a wide detection range from 315 to 650 nm. The dominant features of the measured spectra are the amino acid peaks, having excitation maxima at 220 and 280 nm. The peaks are similar for the bacterial spores, both for aerosols and suspensions, whereas the peaks are shifted toward the shorter emission wavelengths for the suspended ovalbumin and MS2. Moreover, the fluorescence emission, excited above 320 nm is more intensive for the aerosols than the suspensions.

Improved laser-induced fluorescence method for bio-attack early warning detection system

Laser Induced Fluorescence (LIF) could permit fast early warning systems either for point or stand-off detection if a reliable classification of warfare biological agents versus biological or non-biological fluorescing background can be achieved. In order to improve LIF discrimination capability, a new system is described in which the fluorescence pattern is enriched by the use of multiple wavelength delayed excitation while usual spectral fluorescence analysis is extended to time domain to use both aspects as criteria for classification. General considerations and guidelines for the system design are given as well as results showing good discrimination between background and simulants.

Liquid flame spray for generating metal and metal oxide nanoparticle test aerosol

A flame-based method for generating nanoparticles with production rate in the order of g/min is presented to be used in a variety of applied studies concerning nanoparticle measurements and toxicological tests. In this study, ferric oxide, titanium dioxide, and silver nanoparticles were produced by this technique, as an example of the variety of producible compounds, and number and surface area were measured by state-of-art aerosol instruments. In the primary experiments of this study, the generator was used in a conventional way, in a fume cupboard, and the aerosol was measured from the exhaust duct of the cupboard. It has been shown that this steady, turbulent flame generator is also suitable for producing high-concentration aerosols in a wider concept. The generated aerosol was measured by variety of aerosol instrumentation to show the applicability of the generator. When using the generator intentionally as a source of aerosol in the flame processing room, mean nanoparticle sizes of 5—60 nm and active surface area concentration ranges of 1—10,000 μm2/cm 3 were covered for the room aerosol.

Traffic is a major source of atmospheric nanocluster aerosol

Significance We report the significant presence of traffic-originated nanocluster aerosol (NCA) particles in a particle diameter range of 1.3–3.0 nm of urban air, determine the emission factors for the NCA, and evaluate its global importance. Our findings are important because they significantly update the current understanding of atmospheric aerosol in urban areas. They demonstrate that in urban air, extremely small particles form a significant fraction of the total particle number and are a direct result of anthropogenic emissions, that is, the emissions from road traffic. Thus, our findings also imply that in urban areas, an atmospheric nucleation process is not necessary for the formation of a large number of particles that affect population health and climate. In densely populated areas, traffic is a significant source of atmospheric aerosol particles. Owing to their small size and complicated chemical and physical characteristics, atmospheric particles resulting from traffic emissions pose a significant risk to human health and also contribute to anthropogenic forcing of climate. Previous research has established that vehicles directly emit primary aerosol particles and also contribute to secondary aerosol particle formation by emitting aerosol precursors. Here, we extend the urban atmospheric aerosol characterization to cover nanocluster aerosol (NCA) particles and show that a major fraction of particles emitted by road transportation are in a previously unmeasured size range of 1.3–3.0 nm. For instance, in a semiurban roadside environment, the NCA represented 20–54% of the total particle concentration in ambient air. The observed NCA concentrations varied significantly depending on the traffic rate and wind direction. The emission factors of NCA for traffic were 2.4·1015 (kgfuel)−1 in a roadside environment, 2.6·1015 (kgfuel)−1 in a street canyon, and 2.9·1015 (kgfuel)−1 in an on-road study throughout Europe. Interestingly, these emissions were not associated with all vehicles. In engine laboratory experiments, the emission factor of exhaust NCA varied from a relatively low value of 1.6·1012 (kgfuel)−1 to a high value of 4.3·1015 (kgfuel)−1. These NCA emissions directly affect particle concentrations and human exposure to nanosized aerosol in urban areas, and potentially may act as nanosized condensation nuclei for the condensation of atmospheric low-volatile organic compounds.

Characterization and Response Model of the PPS-M Aerosol Sensor

The Pegasor PPS-M sensor is an electrical aerosol sensor based on diffusion charging and current measurement without particle collection. In this study, the role and effect of each component in the instrument is discussed shortly and the results from a thorough calibration measurements are presented. A comprehensive response model for the operation of the PPS-M sensor was developed based on the calibration results and computational fluid dynamics (CFD) modeling results. The obtained response model, covering the effects of the particle charger, the mobility analyzer, and both diffusion and inertial losses, was tested in the laboratory measurements with polydisperse test aerosols, where a good correlation between the model and the measured results was found. Copyright 2014 American Association for Aerosol Research

Study of the PM Gas-Phase Filter Artifact Using a Setup for Mixing Diesel-Like Soot and Hydrocarbons

The filter artifact is a significant source of error in gravimetric measurements of particulate matter (PM) exhaust. However, only a few studies on the subject exist. Results from these studies show a large discrepancy mainly because the experiments were performed using real diesel vehicle exhaust with varying exhaust composition. In this study, a setup for mixing diesel-like soot and hydrocarbon vapor was constructed for generating a stable exhaust aerosol with adjustable composition. The particle size distribution of the diesel-fueled soot generator (GMD [geometric mean diameter] adjustable between 27 and 164 nm) was found to represent “real” exhaust particulate emission. This setup was applied for studying the filter artifact on Teflon-coated glass fiber filters using pentadecane as the hydrocarbon vapor. Experiments were performed using particle and hydrocarbon concentrations of 130–700 μg/m3 and 10–12 ppm, respectively. It was found that the particle concentration of the aerosol affects the filter artifact. At lower particle concentrations, more hydrocarbon adsorption was detected. In the absence of particles, the adsorption was highest. Furthermore, filter soot load, corresponding to 0.13%–0.66% of the clean filter mass, was found to affect adsorption. Sooty filters adsorbed less vapor than clean filters. However, increasing the soot load resulted in more adsorption. Moreover, it was found that the backup filter serves as a reasonable estimate of the filter artifact only for low particle concentrations and filter soot loads. These results indicate that the filter soot load is an important parameter influencing the filter artifact, and therefore, it should be considered when performing gravimetric sampling. The setup was proven to be a unique tool for quantitative studies of the filter artifact. Copyright 2012 American Association for Aerosol Research

Validating the single charged aerosol reference (SCAR) as a traceable particle number concentration standard for 10 nm to 500 nm aerosol particles

Measurement of nanometre-sized aerosol particles is based on particle number concentration measurements. The commonly used method for providing traceability for these measurements involves charging and electrical counting of aerosol particles. This method requires that the particles are singly charged or that the average charge is exactly known, neither of which is easy to ensure. In the device called a single charged aerosol reference (SCAR), the fraction of multiply charged particles is minimal due to the novel operating principle of electrical charging and subsequent growth. In this study the SCAR was validated as a primary particle number concentration standard. The average charge of the output aerosol was evaluated for the whole operational particle size range. For this, the effect of the size distribution of the primary nanoaerosol and the output number concentration on the fraction of doubly charged and neutral particles was measured. It was found that the uncertainty caused by assuming singly charged particles is only 0.16%. A full uncertainty analysis was carried out for a condensation particle counter (CPC) calibration. According to the results, the relative expanded uncertainty of calibration was 3.0%. This represents a typical uncertainty level achieved in CPC calibrations performed with SCAR. As a result of this study, SCAR was validated as a particle number concentration standard suitable for traceable calibration of particle counting instruments in the particle size range from 10 nm to 500 nm.

Optical chamber design for aerosol particle fluorescent measurement

Optical chamber for aerosol particle fluorescence measurements is designed. With the designed chamber, UV-induced fluorescent spectrum of single particles can be measured. The design includes two-nozzle flow system, with sheath air flow and virtual impactor concentrator integrated into the chamber. The operation of the flow system was verified with computational fluid dynamics (CFD). The chamber is intended to be used with pulsed UV-laser source, and it includes triggering of the laser pulse to hit individual particles.