Laser Aerosol Spectrometer Research Articles

Investigation of the Influence of Data Collection and Analysis Procedures on Aerosol Filtration Model Development

Fibrous air filters are common devices used to remove airborne particles. Their performance is typically measured through their resistance to airflow and captured particle mass. Models describing the evolution of filter performance have been heavily researched; however, the need for improvement remains. Experimental work is irreplaceable in the development of high-fidelity models, yet the estimation of necessary variables is not trivial and may be influenced by selected measurement instruments and analysis methodologies. Therefore, the purpose of this work is to propose a framework to investigate the response of common aerosol measurement instruments, their corresponding analysis methodologies, and the application of their data. A Scanning Mobility Particle Sizer (SMPS) and Laser Aerosol Spectrometer (LAS) were selected for consideration, and their recorded data were compared against baseline measurements. The results of the experiments indicated that the SMPS and LAS yielded a ratio of estimated mass concentrations to the baseline mass concentrations of approximately 1.175 and 0.749, respectively. Regarding the SMPS, it was suggested that the measurable size range, application of a coverage factor, dynamic shape factor, and association between the curve fits and histograms were influential in the final estimates. For the LAS, the application of a curve fit, its association to the histograms, and the selection of the sampling periods were influential. Considering the results, the impact of these factors may not be considered negligible and may skew reproducibility between studies and fossilize confounding factors. Therefore, the proposed methodologies are useful in addressing potential errors in data collection and analysis.

Size Distribution as a Forensic Tool to Source Apportion Ambient PM

The particulate matter (PM) emitted from multiple sources contribute to air pollution near highways, affecting, mainly the commuters on road, dwellers and shopkeepers nearby. In this study, the size distribution of the PM near a highway, obtained using real time laser aerosol spectrometer, was used to apportion the contributions from vehicular traffic and road dust. Data on vehicle count and type were obtained for the selected highway stretch. The size distribution of emission from petrol and diesel vehicles and the size distribution of re-suspended dust were obtained through independent studies. Size based distribution of PM in the study area contributed by vehicles, were modelled using AERMOD using the vehicle emissions and vehicle count data. Aggregation of the modelled concentrations of PM of various size ranges with the contribution from re-suspended dust gave size based concentration distributions closely matching with that of PM in ambient air. The size based PM analyses showed that in the study area, 47.36%, 15.74%, and 15.46% of PM2.5, were contributed by diesel vehicles, petrol vehicles and suspended dust, respectively. The corresponding contributions to PM10 were, 14.42%, 10.59% and 68.35%. The emission studies on vehicles showed diesel vehicles contributing significantly higher concentration of PM to ambient air than petrol vehicles, with condition of vehicle influencing the amount of PM emitted. The use of particle size distribution pattern for preliminary source apportionment, demonstrated in this study, has promising environmental forensic applications as it provides a cheap and fast corroborative evidence for responsibility allocation.

The Structural Influence of Airborne Particles on their Toxicity

This paper studies human exposure to microplastics in real-life situations. The concentration of the polyamide nano/microplastics in the proximity of textile workplaces was made by the device Laser Aerosol Spectrometer. The descriptive statistical analysis was elaborated for: variables TSC (total concentration µg/m3), PM10 (µg/m3), PM2.5 (µg/m3), PM1 (µg/m3) and TC (total number of particles, 1/l). The histograms of each variable highlight the asymmetry of the distribution, with the predominance of frequencies or variables; representation of level indicators (average, median) and dispersion-box-plot graphs were obtained. Collection of the particle made with TECORA-SKYPORT PM-HV and GilAirPlus pumps, by using Quartz and Nucleopore filters with different diameters highlighted that the highest mass (683µg) was collected by using GilAir Plus pump and Quartz filter 37mm. A strong correlation was obtained between the variable: "Collected mass/ Air concentration": r = 0997775 ÷ 0,999477 and "Collected mass/ Air volume", r = -0,97473 ÷ 0.80064. The prediction of the value of the collected mass as a function of the diameter of the filters, particle concentration, airflow, and total air volume was made by obtaining the regression equations. Optic microscope analyses highlighted the dimension of microfibres (50% are <10µm) and SEM the dimension: 25% < 68.47 nm and the spherical shape of particles. FT-IR, µRaman and TG-DSC analyses showed the presence of PA particles in the collected particles.

Discrepancy of particle passage in 101 mask batches during the first year of the Covid-19 pandemic in Germany

During the first wave of Covid-19 infections in Germany in April 2020, clinics reported a shortage of filtering face masks with aerosol retention> 94% (FFP2 & 3, KN95, N95). Companies all over the world increased their production capacities, but quality control of once-certified materials and masks came up short. To help identify falsely labeled masks and ensure safe protection equipment, we tested 101 different batches of masks in 993 measurements with a self-made setup based on DIN standards. An aerosol generator provided a NaCl test aerosol which was applied to the mask. A laser aerosol spectrometer measured the aerosol concentration in a range from 90 to 500 nm to quantify the masks’ retention. Of 101 tested mask batches, only 31 batches kept what their label promised. Especially in the initial phase of the pandemic in Germany, we observed fluctuating mask qualities. Many batches show very high variability in aerosol retention. In addition, by measuring with a laser aerosol spectrometer, we were able to show that not all masks filter small and large particles equally well. In this study we demonstrate how important internal and independent quality controls are, especially in times of need and shortage of personal protection equipment.

Investigation of Particulate Matter (PM10) Pollution in Ipoh City, Malaysia

Air pollution is one of the phenomena that adversely affect the environment and negatively impact human health. Air pollution occurs when there are excessive air pollutants in the atmosphere. This study aims to identify and discuss the sources of PM10 emissions according to land use around Ipoh using descriptive and boxplot analysis. There are five areas selected as a sampling location for this study: Ipoh, Lahat, Chemor, Tanjung Rambutan, and Simpang Pulai that located in Hulu Kinta and Sungai Raya district. This sampling location's primary focus is located around Ipoh city, concentrated in the industrial area. Ten land use-based sampling stations are selected to measure. PM10 data were recorded for one week during working and non-working days in July 2020 on 10 sampling stations around Ipoh. The result shows PM10 concentrations consist of industrial, infrastructure and utility, commercial, residential, and recreational areas, as shown PM10 values were recorded for one week during working days and non-working days on 10 observation stations using Portable Laser Aerosol Spectrometer and Dust Monitor Model 1.108. Based on the observations, two stations show the daily average mean of PM10 exceeding 100 μg/m3 outlined in the Malaysian Ambient Air Quality Standard (MAAQS) at S6 (175.78 μg/m3) and S10 (103.79 μg/m3). This situation is driven by the presence of limestone-based industrial areas as well as quarrying activities. The findings also show that PM10 concentration is higher during working days rather than non-working days. Overall, PM10 concentrations that exceed the limit will have a detrimental effect on the environment and human health.

Sizing response of the Ultra-High Sensitivity Aerosol Spectrometer (UHSAS) and Laser Aerosol Spectrometer (LAS) to changes in submicron aerosol composition and refractive index

Abstract. We evaluate the sensitivity of the size calibrations of two commercially available, high-resolution optical particle sizers to changes in aerosol composition and complex refractive index (RI). The Droplet Measurement Technologies Ultra-High Sensitivity Aerosol Spectrometer (UHSAS) and the TSI, Inc. Laser Aerosol Spectrometer (LAS) are two commonly used instruments for measuring the portion of the aerosol size distribution with diameters larger than nominally 60–90 nm. Both instruments illuminate particles with a laser and relate the single-particle light scattering intensity and count rate measured over a wide range of angles to the size-dependent particle concentration. While the optical block geometry and flow system are similar for each instrument, a significant difference between the two models is the laser wavelength (1054 nm for the UHSAS and 633 nm for the LAS) and intensity (about 100 times higher for the UHSAS), which may affect the way each instrument sizes non-spherical or absorbing aerosols. Here, we challenge the UHSAS and LAS with laboratory-generated, mobility-size-classified aerosols of known chemical composition to quantify changes in the optical size response relative to that of ammonium sulfate (RI of 1.52+0i at 532 nm) and NIST-traceable polystyrene latex spheres (PSLs with RI of 1.59+0i at 589 nm). Aerosol inorganic salt species are chosen to cover the real refractive index range of 1.32 to 1.78, while chosen light-absorbing carbonaceous aerosols include fullerene soot, nigrosine dye, humic acid, and fulvic acid standards. The instrument response is generally in good agreement with the electrical mobility diameter. However, large undersizing deviations are observed for the low-refractive-index fluoride salts and the strongly absorbing nigrosine dye and fullerene soot particles. Polydisperse size distributions for both fresh and aged wildfire smoke aerosols from the recent Fire Influence on Regional to Global Environments Experiment and Air Quality (FIREX-AQ) and the Cloud, Aerosol, and Monsoon Processes Philippines Experiment (CAMP2Ex) airborne campaigns show good agreement between both optical sizers and contemporaneous electrical mobility sizing and particle time-of-flight mass spectrometric measurements. We assess the instrument uncertainties by interpolating the laboratory response curves using previously reported RIs and size distributions for multiple aerosol type classifications. These results suggest that, while the optical sizers may underperform for strongly absorbing laboratory compounds and fresh tailpipe emissions measurements, sampling aerosols within the atmospherically relevant range of refractive indices are likely to be sized to better than ±10 %–20 % uncertainty over the submicron aerosol size range when using instruments calibrated with ammonium sulfate.

Aerosol generation with various approaches to oxygenation in healthy volunteers in the emergency department.

ObjectivesHealth care workers experience an uncertain risk of aerosol exposure during patient oxygenation. To improve our understanding of these risks, we sought to measure aerosol production during various approaches to oxygenation in healthy volunteers in an emergency department.MethodsThis was a prospective study conducted in an empty patient room in an academic ED. The room was 10 ft. long x 10 ft. wide x 9 ft. tall (total volume 900 ft3) with positive pressure airflow (1 complete turnover of air every 10 minutes). Five oxygenation conditions were used: humidified high‐flow nasal cannula (HFNC) at 3 flow rates [15, 30, and 60 liters per minute (LPM)], non‐rebreather mask (NRB) at 1 flow rate (15 LPM), and closed‐circuit continuous positive airway pressure (CPAP) using the ED ventilator; in all cases a simple procedural mask was used. The NRB and HFNC at 30 LPM maneuvers were also repeated without the procedural mask, and CPAP was applied both with and without a filter. Each subject then sequentially underwent 8 total oxygenation conditions, always in the same order. Each oxygenation condition was performed with the participant on a standard ED bed. Particles were measured by laser aerosol spectrometer, with the detector sampling port positioned directly over the center of the bed, 0.35 meters away and at a 45‐degree angle from the subject's mouth. Each approach to oxygenation was performed for 10 minutes, followed by a 20‐minute room washout (≈ 2 complete room air turnovers). Particle counts were summated for 2 size ranges (150–300 nm and 0.5–2.0 μm) and compared before, during, and after each of the 8 oxygenation conditions.ResultsEight adult subjects were enrolled (mean age 42 years, body mass index 25). All subjects completed 8 oxygenation procedures (64 total). Mean particle counts per minute across all oxygenation procedures was 379 ± 112 (mean ± SD) for smaller aerosols (150–300 nm) and 9.3 ± 4.6 for larger aerosols (0.5–2.0 μm). HFNC exhibited a flow‐dependent increase in particulate matter (PM) generation—at 60 LPM, HFNC had a substantial generation of small (55% increase) and large particles (70% increase) compared to 15 LPM. CPAP was associated with lowered small and large particle generation (≈ 10–15% below baseline for both sizes of PM). A patient mask limited particle generation with the NRB, where it was associated with a reduction in small and large particulates (average 40% and 20% lower, respectively).ConclusionAmong 3 standard oxygenation procedures, higher flow rates generally were associated with greater production of both small and large aerosols. A patient mask lowered aerosol counts in the NRB only. Protocol development for oxygenation application should consider these factors to increase health care worker safety.

P0736 / #1895: EVALUATION OF SPLASHGUARDCG PREVENTION OF AEROSOLISED PARTICLE DISPERSION IN A PAEDIATRIC MODEL OF SPONTANEOUS AND NON-INVASIVE VENTILATION

AIMS & OBJECTIVES: The Splashguard (SG) is a plexiglass enclosure placed around the patient's head to limit the risk of transmission of COVID-19 during care. The SG was designed to prevent droplet transmission, but can concentrate aerosolized particles inside the SG. The objective was to evaluate the effectiveness of adding suction to prevent the risk of dispersal of aerosolized particles (AP) from critically ill patients on spontaneous ventilation (SV) and non-invasive ventilation (NIV). METHODS: The Topas Aerosol Generator (ATM-220) was connected to the airways of a high-fidelity manikin (SimBabyTM) with a breathing simulator (ASL 5000 tm), to generate a stable concentration of di-ethyl-hexyl-sebacat aerosol particles for 40 s within the SG. The NIV was applied using a Servo-I ventilator with a full-face mask (Figure). The temporal variation of the particle number density and size distribution was measured using a laser aerosol spectrometer (GRIMM 11-R) over the 0.5 μm to 1.0 mm range inside the SG, just above the manikin's head, with and without suction (92 L/min) inside the enclosure. RESULTS: While the aerosol generator is supplying aerosol to the Simbaby airways, the particle concentration increases steadily in the enclosure, with a larger peak in SV than in NIV. The PA peak was greater in SV than in NIV (1.4x106 vs 6.0x105, respectively). Aspiration decreased both the PA peak in SV and NIV, and the time to achieve a 50% reduction in AP concentration. CONCLUSIONS: The application of suction reduced the aerosol concentration inside the SG and may reduce the risk of airborne transmission when handling the SG.

Particulate matter emissions of less harmful-looking super-slim size cigarettes appealing to women: a laser spectrometric analysis of second-hand smoke.

Slim tobacco products shall appear by their look less harmful. In 2013, the European Union ministers discussed to ban them. However, only a ban on small package sizes was realized. To add more data for exposure risk assessment of slim tobacco products, the particulate matter (PM) amount in second-hand smoke (SHS) of super-slim size cigarettes compared with a king size brand was investigated. PM amount of four super-slim size cigarette types of the brand Couture was analysed in comparison with the king-size reference cigarette. Therefore, SHS was produced in an enclosed space with a volume of 2.88m3 by an automatic environmental tobacco smoke emitter. PM size fractions PM10, PM2.5 and PM1 were measured in real time using a laser aerosol spectrometer. SHS of Couture Gold contained about 36% and Couture Purple about 28% more PM than the reference cigarette. In contrast, Couture Green emitted about 37% and Couture Silver about 53% less PM than the reference cigarette. Depending on the brand, the PM2.5 mean concentrations increased up to 1538μg/m3. This exceeds the 24-h mean concentration of at most 25μg/m3 according to the WHO Air quality guidelines about 62-fold. Smoking in enclosed rooms leads to a massive increase of PM. The PM pollution by slim-size tobacco products are substantial and sometimes higher than by king size tobacco products. Therefore, SHS exposure from slim-size tobacco products is not less harmful to health. Decision makers should take this aspect in consideration.

Environmental forensic investigation of the air pollution from a cement manufacturing unit

Cement manufacturing is a process that results in the emission of significant quantities of suspended particulate matter (SPM) to the ambient air. An environmental forensic investigation was carried out in the surroundings of a major cement manufacturing unit at a place called Coimbatore in the southern Indian state of Tamil Nadu. The investigation was carried out to identify the contribution of the cement manufacturing unit to the SPM concentration of the surrounding air environment. The sampling points’ selection and sample collection were done following the principles outlined in the INTERPOL Manual for Pollution Crime Forensic Investigation. On-site monitoring of the air samples was carried out using Mini Laser Aerosol Spectrometer (GRIMM, Mini-LAS Model 11R). The instrument was capable of measuring particles ranging from 0.25 to 32 µm and classifying them into 31 size channels. The test results at majority of the monitoring locations were well above the limits specified in the National Ambient Air Quality Standards of India. Microscopic studies of the dust samples were carried out for surface texture and particle shape. The spatial distribution of particles was analysed using geographic information system (GIS) for the visual identification of the extent of the pollution by keeping the cement factory as the focal point. The results from the GIS and microscopic analysis established the role of the cement factory in the particulate matter pollution of its surroundings, specifically in the areas North-West of the factory. The successfully adopted procedure can serve as a guideline for the environmental forensic investigation of similar pollution incidences.

One year of aerosol refractive index measurement from a coastal Antarctic site

Abstract. Though the environmental conditions of the Weddell Sea region and Dronning Maud Land are still relatively stable compared to the fast-changing Antarctic Peninsula, we may suspect pronounced effects of global climate change for the near future (Thompson et al., 2011). Reducing the uncertainties in climate change modeling requires a better understanding of the aerosol optical properties, and for this we need accurate data on the aerosol refractive index (RI). Due to the remoteness of Antarctica only very few RI data are available from this region (Hogan et al., 1979; Virkkula et al., 2006; Shepherd et al., 2018). We calculate the real refractive index of natural atmospheric aerosols from number size distribution measurements at the German coastal Antarctic station Neumayer III. Given the high average scattering albedo of 0.992 (Weller et al., 2013), we assumed that the imaginary part of the RI is zero. Our method uses the overlapping size range (particle diameter D between 120 and 340 nm) of a scanning mobility particle sizer (SMPS), which sizes the particles by their electrical mobility, and a laser aerosol spectrometer (LAS), which sizes the particles by their optical scattering signal at the 633 nm wavelength. Based on almost a complete year of measurement, the average effective refractive index (RIeff, as we call our retrieved RI because of the used assumptions) for the dry aerosol particles turned out to be 1.44 with a standard deviation of 0.08, in a good agreement with the RI value of 1.47, which we derived from the chemical composition of bulk aerosol sampling measurements. At Neumayer the aerosol shows a pronounced seasonal pattern in both number concentration and chemical composition. Despite this, the variability of the monthly averaged RIeff values remained between 1.40 and 1.50. Compared to the annual mean, two austral winter months (July and September) showed slightly but significantly increased values (1.50 and 1.47, respectively). The size dependency of the RIeff could be determined from time-averaged LAS and SMPS number size distributions measured between December 2017 and January 2018. Here we calculated RIeff for four different particle size ranges and observed a slight decrease from 1.47 (D range 116–168 nm) to 1.37 (D range 346–478 nm). We find no significant dependence of the derived RIeff values on the wind direction. Thus we conclude that RIeff is largely independent of the general weather situation, roughly classified as (i) advection of marine boundary layer air masses during easterly winds caused by passing cyclones in contrast to (ii) air mass transport from continental Antarctica under southern katabatic winds. Neumayer, the only relevant contamination source, is located 1.5 km north of the air chemistry observatory, where the measurements were performed. Given that northerly winds are almost absent, the potential impact of local contamination is minimized in general. Indeed our data show no impact of local contamination on RIeff. Just in one case a temporary high-contamination episode with diesel engines operating right next to the measurement site resulted in an unusual high RIeff of 1.59, probably caused by the high black carbon content of the exhaust fumes. To conclude, our study revealed largely constant RIeff values throughout the year without any sign of seasonality. Therefore, it seems reasonable to use a single, constant RIeff value of 1.44 for modeling optical properties of natural, coastal Antarctic sub-micrometer aerosol.

Aerosol size distributions during the Atmospheric Tomography Mission (ATom): methods, uncertainties, and data products

Abstract. From 2016 to 2018 a DC-8 aircraft operated by the US National Aeronautics and Space Administration (NASA) made four series of flights, profiling the atmosphere from 180 m to ∼12 km above sea level (km a.s.l.) from the Arctic to the Antarctic over both the Pacific and Atlantic oceans. This program, the Atmospheric Tomography Mission (ATom), sought to sample the troposphere in a representative manner, making measurements of atmospheric composition in each season. This paper describes the aerosol microphysical measurements and derived quantities obtained during this mission. Dry size distributions from 2.7 nm to 4.8 µm in diameter were measured in situ at 1 Hz using a battery of instruments: 10 condensation particle counters with different nucleation diameters, two ultra-high-sensitivity aerosol size spectrometers (UHSASs), one of which measured particles surviving heating to 300 ∘C, and a laser aerosol spectrometer (LAS). The dry aerosol measurements were complemented by size distribution measurements from 0.5 to 930 µm diameter at near-ambient conditions using a cloud, aerosol, and precipitation spectrometer (CAPS) mounted under the wing of the DC-8. Dry aerosol number, surface area, and volume, and optical scattering and asymmetry parameters at several wavelengths from the near-UV to the near-IR ranges were calculated from the measured dry size distributions (2.7 nm to 4.8 µm). Dry aerosol mass was estimated by combining the size distribution data with particle density estimated from independent measurements of aerosol composition with a high-resolution aerosol mass spectrometer and a single-particle soot photometer. We describe the instrumentation and fully document the aircraft inlet and flow distribution system, the derivation of uncertainties, and the calculation of data products from combined size distributions. Comparisons between the instruments and direct measurements of some aerosol properties confirm that in-flight performance was consistent with calibrations and within stated uncertainties for the two deployments analyzed. The unique ATom dataset contains accurate, precise, high-resolution in situ measurements of dry aerosol size distributions, and integral parameters, and estimates and measurements of optical properties, for particles &lt; 4.8 µm in diameter that can be used to evaluate aerosol abundance and processes in global models.

Particulate matter emissions of four types of one cigarette brand with and without additives: a laser spectrometric particulate matter analysis of secondhand smoke

ObjectiveInhaled particulate matter (PM) in secondhand smoke (SHS) is deleterious for smokers and non-smokers. Different additives in cigarettes might effect the amount of PM. This study aimed to assess the...

Particulate Matter Emissions of Four Different Cigarette Types of One Popular Brand: Influence of Tobacco Strength and Additives

The inhalation of particulate matter (PM) in second-hand smoke (SHS) is hazardous to health of smokers and non-smokers. Tobacco strength (amount of tar, nicotine, and carbon monoxide) and different additives might have an effect on the amount of PM. This study aimed to investigate the influence of tobacco strength or additives on PM. Four cigarette types of the brand Marlboro with different strengths and with or without additives were analyzed in comparison to the 3R4F reference cigarette. SHS was generated by an automatic environmental tobacco smoke emitter (AETSE) in an enclosed space with a volume of 2.88 m³. PM concentrations (PM10, PM2.5, PM1) were measured with a laser aerosol spectrometer followed by statistical analysis. The two strongest Marlboro brands (Red and Red without additives) showed the highest PM concentrations of all tested cigarettes. The measured mean concentrations Cmean of PM10 increased up to 1458 µg/m³ for the Marlboro Red without additives (PM2.5: 1452 µg/m³, PM1: 1263 µg/m³). The similarly strong Marlboro Red showed very similar PM values. The second strongest type Marlboro Gold showed 36% (PM10, PM2.5) and 32% (PM1) lower values, respectively. The “lightest” type Marlboro Silver Blue showed 54% (PM10, PM2.5) or 50% (PM1) lower PM values. The results indicate that the lower the tar, nicotine, and carbon monoxide amounts, as well as the longer the cigarette filter, the lower are the PM levels. An influence of additives could not be determined.

Evaluation of correlation between PM2.5 and radon-progeny equilibrium factor in radon chamber

The dosage of environmental radon progeny is typically estimated according to the environmental radon exposure and the recommended radon-progeny equilibrium factor, F. To investigate the relationship between PM2.5 and the radon-progeny equilibrium factor, cigarettes are used to simulate the haze–fog in a multi-functional radon chamber to achieve a stable radon concentration environment. A radon detector and a portable laser aerosol spectrometer are used to obtain the values for Cmean PM2.5, CRn, and Cp. The results show that the mean values of F conform with the typical value recommended by the United Nations Scientific Committee on the Effects of Atomic Radiation and are within the reasonable range of 0.1–0.9. In this study, a positive correlation is observed between the F values and PM2.5 concentrations.

Emission factors for PM2.5, CO, CO2, NOx, SO2 and particle size distributions from the combustion of wood species using a new controlled combustion chamber 3CE.

The objective of this research was to determine emission factors (EF) for particulate matter (PM2.5), combustion gases and particle size distribution generated by the combustion of Eucalyptus globulus (EG), Nothofagus obliqua (NO), both hardwoods, and Pinus radiata (PR), softwood, using a controlled combustion chamber (3CE). Additionally, the contribution of the different emissions stages associated with the combustion of these wood samples was also determined. Combustion experiments were performed using shaving size dried wood (0% humidity). The emission samples were collected with a tedlar bag and sampling cartridges containing quartz fiber filters. High reproducibility was achieved between experiment repetitions (CV<10%, n=3). The EF for PM2.5 was 1.06gkg-1 for EG, 1.33gkg-1 for NO, and 0.84gkg-1 for PR. Using a laser aerosol spectrometer (0.25-34μm), the contribution of particle emissions (PM2.5) in each stage of emission process (SEP) was sampled in real time. Particle size of 0.265μm were predominant during all stages, and the percentages emitted were PR (33%), EG (29%), and NO (21%). The distributions of EF for PM2.5 in pre-ignition, flame and smoldering stage varied from predominance of the flame stage for PR (77%) to predominance of the smoldering stage for NO (60%). These results prove that flame phase is not the only stage contributing to emissions and on the contrary, pre-ignition and in especial post-combustion smoldering have also very significant contributions. This demonstrates that particle concentrations measured only in stationary state during flame stage may cause underestimation of emissions.

A scattering methodology for droplet sizing of e-cigarette aerosols

Context: Knowledge of the droplet size distribution of inhalable aerosols is important to predict aerosol deposition yield at various respiratory tract locations in human. Optical methodologies are usually preferred over the multi-stage cascade impactor for high-throughput measurements of aerosol particle/droplet size distributions.Objective: Evaluate the Laser Aerosol Spectrometer technology based on Polystyrene Sphere Latex (PSL) calibration curve applied for the experimental determination of droplet size distributions in the diameter range typical of commercial e-cigarette aerosols (147–1361 nm).Materials and methods: This calibration procedure was tested for a TSI Laser Aerosol Spectrometer (LAS) operating at a wavelength of 633 nm and assessed against model di-ethyl-hexyl-sebacat (DEHS) droplets and e-cigarette aerosols. The PSL size response was measured, and intra- and between-day standard deviations calculated.Results: DEHS droplet sizes were underestimated by 15–20% by the LAS when the PSL calibration curve was used; however, the intra- and between-day relative standard deviations were < 3%. This bias is attributed to the fact that the index of refraction of PSL calibrated particles is different in comparison to test aerosols. This 15–20% does not include the droplet evaporation component, which may reduce droplet size prior a measurement is performed. Aerosol concentration was measured accurately with a maximum uncertainty of 20%. Count median diameters and mass median aerodynamic diameters of selected e-cigarette aerosols ranged from 130–191 nm to 225–293 nm, respectively, similar to published values.Discussion and conclusion: The LAS instrument can be used to measure e-cigarette aerosol droplet size distributions with a bias underestimating the expected value by 15–20% when using a precise PSL calibration curve. Controlled variability of DEHS size measurements can be achieved with the LAS system; however, this method can only be applied to test aerosols having a refractive index close to that of PSL particles used for calibration.

2014 iAREA campaign on aerosol in Spitsbergen – Part 1: Study of physical and chemical properties

This paper presents the results of measurements of aerosol physical and chemical properties during iAREA2014 campaign that took place on Svalbard between 15th of Mar and 4th of May 2014. With respect to field area, the experiment consisted of two sites: Ny–Ålesund (78°55′N, 11°56′E) and Longyearbyen (78°13′N, 15°33′E) with further integration of Aerosol Robotic Network (AERONET) station in Hornsund (77°00′N, 15°33′E). The subject of this study is to investigate the in–situ, passive and active remote sensing observations as well as numerical simulations to describe the temporal variability of aerosol single–scattering properties during spring season on Spitsbergen. The retrieval of the data indicates several event days with enhanced single–scattering properties due to the existence of sulphate and additional sea–salt load in the atmosphere which is possibly caused by relatively high wind speed. Optical results were confirmed by numerical simulations made by the GEM–AQ model and by chemical observations that indicated up to 45% contribution of the sea–salt to a PM10 total aerosol mass concentration. An agreement between the in-situ optical and microphysical properties was found, namely: the positive correlation between aerosol scattering coefficient measured by the nephelometer and effective radius obtained from laser aerosol spectrometer as well as negative correlation between aerosol scattering coefficient and the Ångstrom exponent indicated that slightly larger particles dominated during special events. The in–situ surface observations do not show any significant enhancement of the absorption coefficient as well as the black carbon concentration which might occur during spring. All of extensive single–scattering properties indicate a diurnal cycle in Longyearbyen, where 21:00–5:00 data stays at the background level, however increasing during the day by the factor of 3–4. It is considered to be highly connected with local emissions originating in combustion, traffic and harbour activities. On the other hand, no daily fluctuations in Ny–Ålesund are observed. Mean values in Ny–Ålesund are equal to 8.2, 0.8 Mm−1 and 103 ng/m3 for scattering, absorption coefficients and black carbon concentration; however in Longyearbyen (only data from 21:00–05:00 UTC) they reach 7.9, 0.6 Mm−1 as well as 83 ng/m3 respectively. Overall, the spring 2014 was considerably clean and sea–salt was the major aerosol component.

Deposition of intranasal glucocorticoids--preliminary study.

Intranasal glucocorticoids are the treatment of choice in the therapy of rhinitis. The differences in efficiency of particular medications proven by therapeutic index may result from differences in composition of particular formulations as well as from diverse deposition in nasal cavities. Intranasal formulations of glucocorticoids differ in volume of a single dose in addition to variety in density, viscosity and dispenser nozzle structure. The aim of this report was to analyze the deposition of most often used intranasal glucocorticoids in the nasal cavity and assessment of the usefulness of a nose model from a 3D printer reflecting anatomical features of a concrete patient. Three newest and most often used in Poland intranasal glucocorticoids were chosen to analysis; mometasone furoate (MF), fluticasone propionate (FP) and fluticasone furoate (FF). Droplet size distribution obtained from the tested formulations was determined by use of a laser aerosol spectrometer Spraytec (Malvern Instruments, UK). The model of the nasal cavity was obtained using a 3D printer. The printout was based upon a tridimensional reconstruction of nasal cavity created on the basis of digital processing of computed tomography of paranasal sinuses. The deposition of examined medications was established by a method of visualization combined with image analysis using commercial substance which colored itself intensively under the influence of water being the dominant ingredient of all tested preparations. On the basis of obtained results regions of dominating deposition of droplets of intranasal medication on the wall and septum of the nasal cavity were compared. Droplet size of aerosol of tested intranasal medications typically lies within the range of 25-150 µm. All tested medications deposited mainly on the anterior part of inferior turbinate. FP preparation deposited also on the anterior part of the middle nasal turbinate, marginally embracing a fragment of the central part of this turbinate as well together with deposition in the middle and superior nasal meatus reaching the region of nasal ceiling and olfactory field. MF preparation deposited on the anterior part of the inferior turbinate and central part of this turbinate alike. The area of mucous membrane of lateral wall of nasal cavity on which MF deposited was similar to the area achieved after the application of FP preparation but much greater than in the case of FF preparation. FF drug deposition concentrates only on the anterior part of the inferior turbinate. Despite directing the drug to the lateral wall of the nasal cavity a great proportion of examined preparations deposit also on the nasal septum. The practical application of tridimensional representation (3D printout) of actual geometry of nasal cavity to establish the deposition of inGKS was proven. Droplet size and the geometry of the aerosol cloud introduced into the nostril determine the significant deposition of medication droplets in the anterior part of the nasal cavity. Both physical properties of the drug as well as spraying system applied influence spatial distribution of the drug. The interaction of the air flow with the layer of deposited fluid plays a major role in the deposition of the drug in the nasal cavity, therefore it is so important that the drug does not drain by gravity but remains at the site of deposition which may be reinforced by thixotropic properties of the preparation.

Charge distribution of welding fume particles after charging by corona ionizer

An experimental technique, including the differential mobility analyzer and laser aerosol spectrometer, is proposed for determining the aerosol particles charge distribution, charged by the corona discharge. Experimental data processing procedure for determining the polydisperse welding fume particles charge distribution is proposed. Unipolar particle charging process in the environment saturated by ions is studied. Proposed theoretical model of unipolar charging in approximation of the dust–ion plasma demonstrates good correlation with experimental data. The two-dimensional size and charge distributions of welding fume particles are demonstrated.