Scanning Mobility Particle Sizer Research Articles

Evolution of particulate matter in the post-combustion zone of Zhundong lignite

Understanding the conversion of particulate matter (PM) in the post-combustion zone is important for controlling the emissions and ash deposition from coal combustion. In this study, the evolution of PM in the post-combustion zone of coal was investigated experimentally and numerically. The air combustion of three Zhundong lignite was performed in a drop tube furnace. PM was sampled at different flue gas temperature from 473K to 1273K. Low pressure impactor, X-ray fluorescence, scanning electron microscope, and scanning mobility particle sizer were applied to analyze mass-based particle size distribution (MPSD), elemental compositions, morphology, and number-based particle size distribution (NPSD) of PM. The results show that when the flue gas temperature decreases from 1273K to 473K, the MPSD and compositions of PM0.4-10 remain stable, while PM0.4 moves towards larger particle size. The reduction of NaCl concentration in the flue gas between 1073K and 1273K may be due to the sulfation of NaCl. The critical condensation temperature of NaCl in flue gas is between 843K and 902K. When the flue gas was sampled beyond the critical condensation temperature, NaCl vapors is converted to PM0.4 through nucleation and condensation during the cooling of the sampling system. The particle size distribution of submicron particles in the post-combustion zone is well described by an aerosol dynamics model with moment method. In the post-combustion zone of Zhundong lignite, coagulation is the dominate mechanism controlling the evolution of PM0.4 from 1273K to 473K.

An overlooked route of inhalation exposure to tap water constituents for children and adults: Aerosolized aqueous minerals from ultrasonic humidifiers

Fine particulates and aerosols emitted by commonly used, room-sized ultrasonic humidifiers may pose adverse health effects to children and adults. The literature documents adverse effects for children exposed to minerals emitted from humidifiers. This study performs novel and comprehensive characterization of bivariate particle size and element concentrations of emitted airborne aerosols and particles from ultrasonic humidifiers filled with tap water, including size distribution from 0.014 to 10 μm by scanning mobility particle sizer and AeroTrak; corresponding metal and elemental concentrations as a function of particle size by inductively coupled plasma mass spectrometer; and calculations of deposition fraction in human lungs for age-specific groups using the multi-path particle dosimetry model (MPPD). Deposition fraction is the ratio of mass deposited to total mass inhaled. When filled with tap water, water evaporated from emitted aerosols to form submicron particles that became essentially “dried tap water” with median size 146 nm and mean concentration of 211 μg-total elements/m3-air including 35 μg-calcium/m3-air in a room of 33.5 m3 and air exchange rate at ∼0.8 hr−1. Approximately 90% of emitted particles deposited in human lungs were <1 μm as shown by MPPD model. The smaller particles contained little water and higher concentration of minerals, while larger particles of >1 μm consisted of lower elemental concentrations and more water due to low evaporation. Deposition fraction in pulmonary region was ∼2-fold higher, and deposited particulate mass was 3.5-fold higher for children than adults, indicating greater inhalation exposure to children compared to adults. Modeled data of total particles mass per body weight (BW) that will deposit in adult and child lungs after 8-h humidifier exposure were respectively 2.8 μg/kg-BW and 9.8 μg/kg-BW, where calcium contributes 0.4 μg/kg-BW and 1.6 μg/kg-BW. This comprehensive study of bivariate inorganic chemical composition as a function of particle size expanded, quantified, and modeled exposure for children and adults to aerosolized calcium and other inorganic constituents in water.

Biodegradable CA/CPB electrospun nanofibers for efficient retention of airborne nanoparticles

The increase of the industrialization process brought the growth of pollutant emissions into the atmosphere. At the same time, the demand for advances in aerosol filtration is evolving towards more sustainable technologies. Electrospinning is gaining notoriety, once it enables to produce polymeric nanofibers with different additives and also the obtaining of small pore sizes and fiber diameters; desirable features for air filtration materials. Therefore, this work aims to evaluate the filtration performance of cellulose acetate (CA) nanofibers and cationic surfactant cetylpyridinium bromide (CPB) produced by electrospinning technique for retention of aerosol nanoparticles. The pressure drop and collection efficiency measurements of sodium chloride (NaCl) aerosol particles (diameters from 7 to 300 nm) were performed using Scanning Mobility Particle Sizer (SMPS). The average diameter of the electrospun nanofibers used was 239 nm, ranging from 113 to 398 nm. Experimental results indicated that the nanofibers showed good permeability (10−11 m2) and high-efficiency filtration for aerosol nanoparticles (about 100 %), which can include black carbon (BC) and the new coronavirus. The pressure drop was 1.8 kPa at 1.6 cm s-1, which is similar to reported for some high-efficiency nanofiber filters. In addition, it also retains BC particles present in air, which was about 90 % for 375 nm and about 60 % for the 880 nm wavelength. Finally, this research provided information for future designs of indoor air filters and filter media for facial masks with renewable, non-toxic biodegradable, and potential antibacterial characteristics.

Transient plasma-enhanced remediation of nanoscale particulate matter in restaurant smoke emissions via electrostatic precipitation

It is now recognized that nanoscale particulate matter (PM) represents a substantial health hazard for our society, including PM from restaurant smoke. In this study, we explored the use of a transient pulsed plasma in conjunction with an applied DC bias to treat oil aerosols that closely resemble restaurant (i.e., charbroiler) smoke emissions. For polyaromatic olefin PAO-4 and soybean oil, we found that a three-order-of-magnitude reduction in particulates (i.e., 99.9% remediation) could be achieved with this system. Here, the plasma discharge was produced in a 4-in.-diameter cylindrical reactor with a 5–10ns high voltage (30 kV) pulse generator together with applied DC bias voltages up to 10kV. The distribution of nanoparticle sizes was measured using a scanning mobility particle sizer (SMPS) with diameter centered around 225nm. Here, the main mechanism of remediation occurs in a two-step process in which the oil nanoparticles are first ionized by the free electrons and free radicals in the plasma and then the charged particles are swept out to the sidewalls of the reactor by the applied DC potential. We believe this general approach opens up new degrees of freedom in the design of electrostatic oil aerosol pollution control devices.

Morphology and size of soot from gas flares as a function of fuel and water addition

A large-scale, laboratory turbulent diffusion flame was used to study the effects of fuel composition on soot size and morphology. The burner and fuels are typical of those used in the upstream oil and gas industry for gas flaring, a practice commonly used to dispose of excess gaseous hydrocarbons. Fuels were characterized by their carbon-to-hydrogen ratio (from 0.264 to 0.369) and their volumetric higher heating value (HHVv) (from 35.8 to 75.2 MJ/m3). Transmission electron microscopy (TEM) was used to assess primary particle and aggregate size, showing that the scaling of primary particle size to aggregate size was roughly the same for all of the considered fuels (dp = 16.3(da,100 [nm]/100)0.35). However, fuels with higher HHVv produced substantially larger soot aggregates. A scanning mobility particle sizer (SMPS) was also used (i) to measure mobility diameter distributions and (ii) in tandem with a centrifugal particle mass analyzer (CPMA) to determine the two-dimensional mass-mobility and effective density-mobility distributions using a new inversion approach. The new approach was shown to improve internal consistency of inferred morphological parameters, though with a shift relative to median-based analysis of the tandem data. Raman spectroscopy was used to quantify the degree of graphitization in the soot nanostructure. The addition of water to the fuel consistently reduced the soot yields but did not affect other morphological parameters. Larger aggregates also tended to have larger primary particles and higher Raman D/G ratios suggesting larger graphitic domains.

Quantification of Non-refractory Aerosol Nitrate in Ambient Air by Thermal Dissociation Cavity Ring-Down Spectroscopy.

A thermal dissociation cavity ring-down spectrometer (TD-CRDS) for real-time quantification of non-refractory aerosol nitrate in ambient air is described. The instrument uses four parallel detection channels and heated quartz inlets to convert particulate organic nitrate (pON) (at 350 °C) and ammonium nitrate (NH4NO3) aerosol (at 540 °C) to nitrogen dioxide (NO2), whose mixing ratio is monitored via its absorption at 405 nm. Concentrations of aerosol nitrate are determined by difference relative to a parallel TD-CRDS channel in which aerosol is removed by in-line filtering. The method was validated by sampling gas streams containing laboratory-generated NH4NO3 aerosol in parallel to a scanning mobility particle sizer (SMPS). Scatter plots of TD-CRDS and SMPS data correlated (r2 > 0.9) with slopes near unity, confirming quantitative TD-CRDS response to NH4NO3 aerosol. In contrast, no response was observed when sampling (NH4)2SO4 aerosol. Instrument limits of detection (LOD; 2σ, 10 s) were 120 parts per trillion by volume (10-12, pptv) for NO2 and 148 pptv for ammonium nitrate. Partial and unsustained conversion of refractory sodium nitrate (NaNO3) was observed at the inlet temperature used for complete dissociation of HNO3 and NH4NO3, suggesting that this channel may not constitute a robust measurement of total odd nitrogen (NOy) in environments where NaNO3 particles may be present (e.g., the polluted marine boundary layer). A potential application of the TD-CRDS is the calibration of particle counters, for which convenient methods are not currently available. Sample ambient air measurements of pON and total aerosol nitrate in Calgary are presented.

Airborne reactive oxygen species (ROS) is associated with nano TiO2 concentrations in aerosolized cement particles during simulated work activities

Photocatalytic cement is self-cleaning due to the addition of titanium dioxide (TiO2) nanoparticles, which react with sunlight (UV) and produce reactive oxygen species (ROS). Construction workers using photocatalytic cement are exposed not only to cement particles that are irritants but also to nano TiO2 and UV, both carcinogens, as well as the generated ROS. Quantifying ROS generated from added nano TiO2 in photocatalytic cement is necessary to efficiently assess combined health risks. We designed and built an experimental setup to generate, under controlled environmental conditions (i.e., temperature, relative humidity, UV irradiance), both regular and photocatalytic cement aerosols. In addition, cement working activities—namely bag emptying and concrete cutting—were simulated in an exposure chamber while continuously measuring particle size distribution/concentration with a scanning mobility particle sizer (SMPS). ROS production was measured with a newly developed photonic sensing system based on a colorimetric assay. ROS production generated from the photocatalytic cement aerosol exposed to UV (3.3∙10−9 nmol/pt) was significantly higher than for regular cement aerosol, either UV-exposed (0.5∙10−9 nmol/pt) or not (1.1∙10−9 nmol/pt). Quantitatively, the level of photocatalytic activity measured for nano TiO2-containing cement aerosol was in good agreement with the one obtained with only nano TiO2 aerosol at similar experimental conditions of temperature and relative humidity (around 60%). As a consequence, we recommend that exposure reduction strategies, in addition to cement particle exposures, also consider nano TiO2 and in situ–generated ROS, in particular if the work is done in sunny environments.Graphical abstract

Application of electrospray-scanning mobility particle sizer for the measurement of sub-10 nm chemical mechanical planarization slurry abrasive size distribution.

A scanning mobility particle sizer (SMPS) was used for measuring the size of a sub-10 nm chemical mechanical planarization slurry abrasive. An atomizer and an electrospray were used for aerosolization of slurry abrasives. It was difficult to measure the exact particle size distribution using the atomizer due to the agglomeration peak generated by the relatively large droplet size. However, the electrospray-SMPS (ES-SMPS) measurement result well matched with that of the transmission electron microscopy analysis without the agglomeration peak as ES is known to generate a relatively small droplet during aerosolization. The particle size distribution of the two sub-10 nm ceria slurries was measured using the ES-SMPS. To avoid the dispersion stability issue due to the pH change, pH adjustment was required when the sample was diluted.

Comparative Performance of the NanoScan and the Classic SMPS in Determining N95 Filtering Facepiece Efficiency Against Nanoparticles

Nanoparticles are defined as particles with at least one dimension in the range of 1–100 nm. Due to the special properties of nanoparticles, they are used in many workplaces, thus leading to occupational exposure. Filtering facepieces (FFPs) are generally used in these workplaces to reduce the exposure. Many studies have measured FFP efficiency in laboratories using a scanning mobility particle sizer (SMPS). The aim of this study was to determine whether a NanoScan could be used to measure FFP efficiency against nanoparticles in workplaces for one type of N95 FFP. The results showed that the NanoScan gave maximum penetration and most penetrating particle size (MPPS) data for all configurations tested. Observations were consistent with those of previous studies: low penetration, MPPS smaller than 100 nm, and penetration increased as the airflow rate increased. The NanoScan gave a less precise MPPS and a slightly overestimated maximum penetration. These results confirm that the classic SMPS is a more precise instrument considering these two devices, whereas the NanoScan is faster to provide general information about the overall behaviour, which make it easy to use for a workplace environment. A NanoScan can thus be used as a first approach in workplaces.

Complex Aerosol Characterization by Scanning Electron Microscopy Coupled with Energy Dispersive X-ray Spectroscopy

Particulate matter (PM) air pollution is a central concern for public health. Current legislation relies on a mass concentration basis, despite broad acceptance that mass alone is insufficient to capture the complexity and toxicity of airborne PM, calling for additional and more comprehensive measurement techniques. We study to what extent scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM/EDS) can be applied for physicochemical characterization of complex aerosols, and investigate its potential for separating particle properties on a single particle basis, even for nanosized particles. SEM/EDS analysis is performed on impactor samples of laboratory generated aerosols, consisting of either NaCl, Halloysite fibers, soot-like Printex90 agglomerates, or their combination. The analysis is automated and performed as EDS maps, covering a statistically relevant number of particles, with analysis times of approximately one hour/sample. Derived size distributions are compared to scanning mobility particle sizer (SMPS) and electric low-pressure impactor (ELPI) results. A method is presented to estimate airborne number concentrations and size distributions directly from SEM results, within a factor 10 of SMPS and ELPI outcomes. A classification scheme is developed based on elemental composition, providing class-specific information with individual particle statistics on shape, size, and mixing state. This can identify primary particles for source apportionment and enables easy distinction between fibrous and dense particle classes, e.g. for targeted risk assessments. Overall, the SEM/EDS analysis provides a more detailed physicochemical characterization of PM than online measurements, e.g. SMPS and ELPI. The method has the potential to improve assessments of PM exposure and risk, and facilitates source identification, even without prior knowledge at sampling.

The Influence of Graphene Oxide on Nanoparticle Emissions during Drilling of Graphene/Epoxy Carbon-Fiber Reinforced Engineered Nanomaterials

Graphene oxide (GO) nanoparticles are increasingly being used to tailor industrial composites. However, despite the advantages, GO has shown conceivable health risks and toxicity to humans and the environment if released. This study investigates the influence that GO concentrations have on nanoparticle emissions from epoxy-reinforced carbon fiber hybrid composites (EP/CF) during a lifecycle scenario, that is, a drilling process. The mechanical properties are investigated and an automated drilling methodology in which the background noise is eliminated is used for the nanoparticle emissions measurements. Real-time measurements are collected using a condensation particle counter (CPC), a scanning mobility particle sizer spectrometer (SMPS), a real-time fast mobility particle spectrometer (DMS50) and post-test analytical methods. The results observe that all three nanoparticle reinforced samples demonstrated a statistically significant difference of up to a 243% increase in mean peak particle number concentration in comparison to the EP/CF sample. The results offer a novel set of data comparing the nanoparticle release of GO with varying filler weight concentration and correlating it the mechanical influence of the fillers. The results show that the release characteristics and the influence in particle number concentration are primarily dependent on the matrix brittleness and not necessarily the filler weight concentration within the nanocomposite.

Effects of exponentially decaying and growing concentrations on particle size distribution from a scanning mobility particle sizer

A scanning mobility particle sizer (SMPS) is one of the most widely used instruments to obtain size distribution for atmospheric particles. In an SMPS measurement, a voltage scanning process on a d...

From nano to micrometer size particles – A characterization of airborne cement particles during construction activities

Although, photocatalytic cement contains nanosized TiO2, a possibly carcinogen, no exposure assessments exist for construction workers. We characterized airborne nanoparticle exposures during construction activities simulated in an exposure chamber. We collected some construction site samples for regular cement in Switzerland and Thailand for comparison. Airborne nanoparticles were characterized using scanning mobility particle sizer (SMPS), portable aerosol spectrometer (PAS), diffusion size classifier (DiSCmini), transmission electron microscopy (TEM), scanning electron microscope energy dispersive X-ray spectroscopy (SEM-EDX), and X-ray diffraction. Bagged photocatalytic cement had 2.0 wt% (GSD ± 0.55) TiO2, while TiO2 in aerosols reached 16.5 wt% (GSD ± 1.72) during bag emptying and 9.7 wt% (GSD ± 1.36) after sweeping. The airborne photocatalytic cement particles were far smaller (approximately 50 nm) compared to regular cement. Cutting blocks made from photocatalytic cement or concrete, resulted in similar amounts of airborne nano TiO2 (2.0 wt% GSD ± 0.57) particles as in bagged material. Both photocatalytic and regular cement had a geometric mean diameter (GMD) < 3.5 μm. Main exposures for Thai workers were during sweeping and Swiss workers during drilling and polishing cement blocks. Targeted nanoparticle exposure assessments are needed as a significantly greater exposure to nano TiO2 were observed than what would have been predicted from the material's nano- TiO2 contents.

Particle and volatile organic compound emissions from a 3D printer filament extruder

Fused Deposition Modeling (FDM®), also known as Fused Filament Fabrication (FFF), 3D printers have been shown in numerous studies to emit ultrafine particles and volatile organic compounds (VOCs). Filament extruders, designed to create feedstocks for 3D printers, have recently come onto the consumer market for at-home hobbyists as an alternative to buying 3D printer filaments. These instruments allow for the creation of 3D printer filaments from raw plastic pellets. Given the similarity in processes and materials used by 3D printers and filament extruders, we hypothesized that filament extruders may also release ultrafine particle emissions and VOCs. An off-the-shelf filament extruder was operated in a 2 m3 chamber using three separate feedstocks: acrylonitrile butadiene styrene (ABS) pellets, pulverized poly-lactic acid (PLA), and PLA pellets. Ultrafine particle emissions were measured in real-time using a scanning mobility particle sizer and thermal desorption tubes were used for both non-targeted and targeted analysis of VOCs present in emissions. Ultrafine particle number emission rates were comparable to those found in 3D printer studies with the greatest to least emission rates from ABS pellets, pulverized PLA, and PLA pellets, respectively. In addition, the majority of particles released were found to be ultrafine (1–100 nm), similar to 3D printer studies. A variety of VOCs were identified using the ABS feedstock, including styrene and ethylbenzene, and PLA feedstock. Styrene average mass concentration amounts were found to be near the EPA Integrated Risk Information System Reference Concentration for Inhalation Exposure for 3 min and 5 min samples. Further studies will be needed to determine the impact on emissions of environmental volume, air exchange rate, and extruder settings such as extrusion speed and temperature. The results support the hypothesis that use of a filament extruder may present an additional exposure risk to 3D printer hobbyists.

Diffusional transfer function for the scanning electrical mobility spectrometer (SEMS)

The scanning electrical mobility spectrometer (SEMS), or scanning mobility particle sizer (SMPS), uses the differential mobility analyzer (DMA) operated in scanning mode to measure particle size di...

Nanoparticle exposure due to pyrotechnics during a football match

Abstract Use of pyrotechnic articles is a common, though forbidden practice at football matches. While the fans, especially the members of the ultras groups, view pyrotechnic displays as a part of their culture, these devices can be dangerous for the public. In addition to the risks of burning, hand flares and similar items release toxic combustion by-products, including particulate matter – inhaling of which is harmful both for the spectators and players. In order to assess the amounts and composition of the aerosol particles released at a typical event, we performed a study using both a scanning mobility particle sizer and a low-pressure cascade impactor. The number concentration of nanoparticles was clearly correlated with the burning events. Several elements were identified in the collected samples, including heavy metals, while the majority of the sample consisted of amorphous carbon. The nanoparticle number concentration increased up to 12-fold immediately after the beginning of the flares burning, with the largest contribution of particles 155 nm in diameter. The cumulative dose the players inhaled during the match was around 7 × 108 particles/kg, which is 300% higher than the dose one would get in a low-pollution environment. We discuss the results in view of similar pyrotechnical events, especially fireworks.

Investigation of the Dynamism of Nanosized SOA Particle Formation in Indoor Air by a Scanning Mobility Particle Sizer and Proton-Transfer-Reaction Mass Spectrometry

Terpenes are VOCs of particular importance, since they are emitted from a wide range of indoor sources and are considered to be precursors of Secondary Organic Aerosol (SOA) formation. It has been proven that SOA particles, especially nanosized ones, pose a threat to human health. In this research, experiments with the application of an environmental chamber and real-time measurement techniques were carried out to investigate in a complimentary way the formation of monoterpene oxidation products and nanosized SOA particles initiated by monoterpene ozonolysis. Proton-Transfer-Reaction Mass Spectrometry with a Time-Of-Flight analyzer (PTR-TOF-MS) and a Scanning Mobility Particle Sizer (SMPS) were applied to determine in real time the dynamism of the formation of the corresponding terpene ozonolysis products and submicron SOA particles. Results proved that firstly, oxidation products were formed, and then, they underwent nucleation and condensation, forming particles whose diameters grew with time. The oxidation products formed were different depending on the type of terpenes applied. The comparison of the results obtained during the experiments with gaseous standard mixtures and real samples commonly present and used in indoor air revealed that the diversified chemical composition of the emission source had implications for both the particle formation initiated by the oxidation of essential oil components and the chemical reactions occurring via the oxidation process. With the instrumentation utilized, the concentration changes at the level of a few ppbv could be monitored.

An intercomparison exercise of good laboratory practices for nano-aerosol size measurements by mobility spectrometers

An intercomparison campaign on nanoparticle size measurement was organized in the frame of the French nanoMetrology club. The aim of this study is to make an inventory of the metrological capabilities of all measurement techniques in France involved in the “nano” size range, including the SMPS (scanning mobility particle sizer) concerning aerosol metrology. For this study, four samples have been proposed, namely (1) a SiO2 colloidal suspension (FD304) consisting of a monomodal population, (2) two samples consisting of two nanoparticle populations of SiO2 having proportions to be determined, and (3) a TiO2 colloidal suspension. Ten SMPS associated with five participants around a common experimental setup were performed in link with a control SMPS to have simultaneous measurements with a same instrument in each laboratory in parallel with the SMPS used by each partner. This article presents SMPS results of this study associated with the description of the experimental setup and the sample preparation protocol with an identified schedule and comparison with SEM measurements. The present paper does not focus on the actual capability of the tested mobility spectrometers, but aims to highlight the good laboratory practices using their own but common resources in terms of aerosol generation and measurement setups.

Behavioral characteristics to airborne particles generated from commercial spray products

Commercial spray products are commonly used in daily life and airborne particles generated by these products may cause adverse health effects. Our study was aimed to characterize the behaviors of airborne particles from spray products and to determine the deposition loss rate. Four categories of spray products with highly frequent use - air fresheners, fabric deodorants, window cleaners, and a bathroom cleaner - were selected for the study. The products were applied in a cleanroom according to the instructions for use. Airborne particles (10–10,000 nm) were measured within the breathing zone of a user with a scanning mobility particle sizer and an optical particle spectrometer. Additionally, filter sampling was performed to examine the morphological characteristics of the particles using a field emission-scanning electron microscope (FE-SEM). The initial concentration and particle size distribution varied among different spray types and products. Two propellant-type air fresheners that we tested showed a high initial concentration of smaller sized particles. However, one of these and all hand-pressure type propellants showed a low initial concentration in all size ranges. We observed that particles in nucleation mode (10–31.6 nm) decreased and aggregated particles shifted to accumulation mode (100–1,000 nm) over time. The FS-SEM analysis confirmed the aggregation of nano-sized particles for all products. The deposition loss rates of various particle sizes depended on the initial concentration and distribution of particle sizes. For two air fresheners with high initial concentrations, the loss rate of small-sized particles was higher than that of the other products whereas the particle loss rate of large-sized particles was higher, regardless of initial concentration. The results of this study can give us useful information in the behaviors of airborne particles in the consumer spray products and resulting exposure assessment especially in the application to the exposure modeling of spray products.

An apparatus to synthesize ceramic nanoparticles with a precisely adjusted temperature history and a significant mass output.

For gas phase nanoparticle production, hot wall reactors are widely used. In this article, we will describe the fundamental design considerations for a hot wall reactor system able to produce oxide nanoparticles. The system is outstanding in its ability to produce mostly spherical nanoparticles at particle sizes of up to 100 nm and even larger at mass outputs in the order of grams per hour by being able to rapidly quench the aerosol. While high production rates or larger particle sizes are already easily obtained with hot wall reactors, it is very challenging to produce these spherical particles at high mass rates. We will show in this research that the temperature and the particle number concentration are the major aspects influencing the particle morphology at the end of the process. Investigation on the performance of the setup shows good control over the temperature and the particle production stability. A representative particle characterization using SEM and scanning mobility particle sizer showed that particles are mostly spherical, while the particle size distribution had a geometric standard deviation close to 1.5. In addition to the aspects mentioned above, a possibility to manipulate the aggregation downstream of the reactor is to be presented as well. We found that applying electrical charges to the aerosol particles (in opposite polarity) can significantly foster aggregation.