High-volume Sampler Research Articles

Passive Sampling as a Tool to Assess Atmospheric Pesticide Contamination Related to Vineyard Land Use

The massive use of pesticides in agriculture has led to widespread contamination of the environment, particularly the atmospheric compartment. Thirty-six pesticides, most used in viticulture, were monitored in ambient air using polyurethane foams as passive air samplers (PUF-PAS). Spatiotemporal data were collected from the samplers for 10 months (February–December 2013), using two different sampling times (1 and 2 months) at two different sites in a chateau vineyard in Gironde (France). A high-volume active air sampler was also deployed in June. Samples were extracted with dichloromethane using accelerated solvent extraction (ASE) (PUFs from both passive and active) or microwave-assisted extraction (MAE) (filters from active sampling). Extracts were analyzed by both gas and liquid chromatography coupled with tandem mass spectrometry. A total of 23 airborne pesticides were detected at least once. Concentrations in PUF exposed one month ranged from below the limits of quantification (LOQs) to 23,481 ng PUF−1. The highest concentrations were for folpet, boscalid, chlorpyrifos-methyl, and metalaxyl-m—23,481, 17,615, 3931, and 3324 ng PUF−1. Clear seasonal trends were observed for most of the pesticides detected, the highest levels (in the ng m−3 range or the µg PUF−1 range) being measured during their application period. Impregnation levels at both sites were heterogeneous, but the same pesticides were involved. Sampling rates (Rs) were also estimated using a high-volume active air sampler and varied significantly from one pesticide to another. These results provide preliminary information on the seasonality of pesticide concentrations in vineyard areas and evidence for the effectiveness of PUF-PAS to monitor pesticides in ambient air.

Comparison of atmospheric polycyclic aromatic hydrocarbons (PAHs) over six years at a CAWNET background site in central China: Changes of seasonal variations and potential sources

Total suspended particles (TSP) and gaseous samples were collected by using a high-volume sampler from March 2012 to March 2013 and January 2018 to January 2019 at a background site (Jinsha, JSH) in central China to study the chemical characteristics, seasonal variations, and potential sources of polycyclic aromatic hydrocarbons (PAHs). The average concentrations of ∑15PAHs were 24.55 ± 9.19 ng m−3 in 2012/2013 and 20.98 ± 9.77 ng m−3 in 2018/2019. Low-ring PAHs were more concentrated in gas phase while high-ring PAHs were prone into particle phase. The concentrations of PAHs in the two sampling years were high in winter but low in summer and autumn. The relationships between the gas concentrations of PAHs and temperature indicated that most PAHs were influenced by long-range atmospheric transport (LRAT) in 2012/2013 and in 2018/2019, excluding anthracene (Ant) and pyrene (Pyr) were partially affected by air-surface re-volatilization in 2012/2013. The source of atmospheric PAHs at JSH was similar in 2012/2013 and 2018/2019,which was mainly due to the LRAT of PAHs emitted from biomass/fossil fuel combustion in the northern area of JSH. From 2012/2013 to 2018/2019, there was no significant difference between the concentrations of PAHs in spring and winter, whereas the concentrations of PAHs decreased from 2012/2013 to 2018/2019 in summer. In all, the control of PAHs at the source region was partially effective from 2012/2013 to 2018/2019.

Neutron Activation Analysis of PM10 for Air Quality of an Industrial Region in the Czech Republic: A Case Study

This work was conducted to focus on pollutant transmission between Poland and Czechia at the most polluted area in the Czech Republic, the Moravian Silesian region. Instrumental neutron activation analysis (INAA) and multivariate statistical analyses were used to determine the mass fractions of inorganic air pollutants accumulated on filters. Particle matters of sizes smaller than 10 µm (PM10) were collected using a high-volume sampler (SAM Hi 30 AUTO WIND). Pollutants PM10 were collected on Whatman QM-A Quartz Microfiber Filters of 150 mm in diameter based on various wind conditions. These filters were irradiated by neutron flux at the experimental reactor IBR-2 at the Joint Institute of Nuclear Research in Dubna, RF. Irradiated samples were measured by gamma spectrometry techniques using HPGe detectors. In total, results are shown for 49 samples (from March to July 2021) and five field blank filters. The mass fractions of 24 elements (Sc, Cr, Fe, Ni, Co, Zn, Se, As, Br, Rb, Mo, Sb, Ba, Cs, La, Ce, Sm, Eu, Tb, Yb, Hf, Au, Th, and U) were determined. The sources of pollution were specified using correlation and exploratory factor analyses and including meteorological conditions. A strong positive correlation was shown between the elements Cr, As, Br, Co, Fe, Sc, Se, Sm, Th, La, and Ce. Elemental exposure to PM10 can be divided based on the factor loadings of common chemical components into three main pollution sources. According to the wind rose, the pollution came from the southeast/west direction; therefore, we can assume that the pollution most likely originated from the metallurgic complex (steel and iron production in the southeast, and a coking plant, metal foundry, and generation plant in the west).

Atmospheric resuspension of insoluble radioactive cesium-bearing particles found in the difficult-to-return area in Fukushima

The deposition of insoluble radiocesium-bearing microparticles (CsMPs), which were released from the Fukushima Daiichi Nuclear Power Plant (F1NPP) accident in March 2011, has resulted in the widespread contamination of eastern Japan. Obviously, these deposited insoluble CsMPs may become the secondary contamination sources by atmospheric migration or other environmental transferring process; however, the understanding of the transport mechanism remains non-elucidation, and the relevant evidence has not been directly provided. This study, for the first time, provides the direct evidence for the resuspension of these insoluble CsMPs to the atmosphere from (1) proximity of 137Cs radioactivity and resemblance of the morphology and the elemental compositions of CsMPs in the samples of soil and aerosol derived from the same sampling site, (2) the special characteristics of the resuspended CsMPs of which the ratios of Na/Si, K/Si and/or Cs/Si were smaller than those from the initially released CsMPs collected at either long distance or near F1NPP, which can be ascribed to the slowly natural corrosion of CsMPs by the loss of the small amount of soluble contents in CsMPs, and (3) high CsMPs concentration of 10 granules/g in the surface soil of our sampling site and high resuspension frequency of CsMPs in spring when predominant suspended particles were soil dust. Specifically, 15 single CsMPs were successfully isolated from the aerosol filters collected by unmanned high-volume air samplers at a severely polluted area in Fukushima Prefecture, about 25 km away from F1NPP, from January 2015 to September 2019. The mean diameter of these CsMPs was 1.8 ± 0.5 μm, and the average 137Cs radioactivity was 0.35 ± 0.23 Bq/granule. The contribution rate of the resuspended CsMPs to the atmospheric radiocesium was estimated from the ratio of 137Cs radioactivity of a single CsMP to that of the aerosol filter to be of 23.9 ± 15.3%. There has been no considerable decreasing trend in the annual CsMP resuspension frequency.

Distribution and sources of SVOCs in fine and coarse aerosols in the megacity of Istanbul

Approximately 15.4 million people are continuously exposed to various air pollutants in the megacity of Istanbul. Anthropogenic activities in Istanbul generate emissions from mobile sources (i.e., vehicles, aircraft, ships, etc.) and stationary sources such as industrial and residential heating emissions. Biogenic emissions and long-range transport such as desert dust from Sahara and pollutants from Balkan countries also contribute to the local air pollution in Istanbul. In this work, fine (Dp < 2.5 μm) and coarse (Dp > 2.5 μm) particles were collected with a high-volume sampler during four seasons of the period Jan 2017 - Jan 2018. A total of 15 PAHs and 28 n-alkanes were identified and quantified with a newly developed thermal desorption – gas chromatography with mass spectrometry method (TD-GC–MS). Source analysis was performed with PAH and n-alkane diagnostic ratios, and source apportionment was performed with principal component analysis. The yearly averages of PAHs and n-alkanes in the fine fraction were 21.6 ng m−3 and 103.8 ng m−3, with daily averages of 7.1–80.8 ng m−3 and 55.3–204.2 ng m−3, respectively. Approximately 90% of the PAHs and n-alkanes were found in the fine PM fraction in this traffic site. The BaP carcinogenic (BaP-TEQ) and mutagenic (BaP-MEQ) equivalents were on average 5.47 ± 0.64 and 4.72 ± 0.8 ng m−3 in the fine fraction, respectively, and were approximately 6–7 times lower in the coarse fraction. This has important implications due to the respirable nature of fine aerosols and their longer lifetimes in the atmosphere. Multivariate analysis coupled with principal component analysis led to an important result that the organic aerosol mainly originates from two local sources: road traffic (50.4%) and shipping emissions (26.6%). The results found in this work indicate the urgent need for the application of mitigation measures to control road traffic and minimize the emissions from ships passing through the İstanbul Bosphorus.

Elemental composition of airborne particulate matter from coastal South Florida area influenced by African dust events

• The elements Pb, Zn, V, Ni, Cd, As, Cr, and Cu presented the highest EFs. • As, Ni, Cd and Pb levels were below the maximum levels set by EU and USEPA. • REE were used to identify African dust contributions to the local APM. • The oil-fired Port Everglades Power Plant played an important role in the APM. • Road dust and waste incineration emissions were the second APM source of importance. Airborne particulate matter (APM) is a complex mixture of dust, dirt, soot and smoke containing both organic and inorganic components as well as biological particles. APM below 10 µm can enter the respiratory track and are known to cause adverse health effects. African dust storms are responsible for the transport of large amount of APM across the Atlantic Ocean during summer months. Anthropogenic activities are also responsible for APM pollution contribution in coastal areas and could have potential effects on sensitive ecosystems. The present study evaluates the elemental composition of APM collected from a coastal area in South Florida. In this study, a high-volume air sampler equipped with Versapor filters and located near the Port of Fort Lauderdale was employed for APM collection from 2005 to 2010. APM chemical composition was analyzed for multiple elements by ICP-MS. Seven of the eleven metals listed by the EPA as hazardous air pollutants (Mn, Cd, Cr, Ni, Pb, As, Co and Se) were detected in the samples. Iron and aluminum were the most abundant elements found in all samples, followed by V and Ni, which are usually associated with anthropogenic pollution coming from fossil fuel combustion. Specific sources of APM pollution were identified by principal component analysis and using the U.S. EPA UNMIX model for environmental data analyses. Rare earth elements were used to identify contributions of geological material to the APM and African dust influence during the summer months.

Airborne Alt a 1 Dynamic and Its Relationship with the Airborne Dynamics of Alternaria Conidia and Pleosporales Spores.

Fungal spores are universal atmospheric components associated to allergic reactions. Alternaria (Ascomycota) is considered the most allergenic spore taxa. Alt a 1 is the major allergen of Alternaria and is present also in other Pleosporales. In this study, standard Hirst-based sampling and analyzing methods for measuring spore daily concentrations of Alternaria, Curvularia, Drechslera-Helminthosporium, Epicoccum, Leptosphaeria, Pithomyces, Pleospora and Stemphylium (all included in the taxon Pleosporales) have been used as well as two high-volume samplers, Burkard Cyclone (2017) and MCV CAV-A/mb (2019–2020), and ELISA kits for measuring the allergen. The detection and quantification of Alt a 1 was only possible in the samples from the MCV sampler. Although Alt a 1 was better correlated with Alternaria spores than with Pleosporales spores, the three of them showed high correlations. It is shown that there is a high and significant correlation of Alt a 1 with temperature, a negative correlation with relative humidity and no correlation with precipitation. The aerobiological monitoring of these three elements ensures the best information for understanding the affectation to allergy sufferers, but, if this is not possible, as a minimum public health service aimed at the detection, treatment and prevention of allergies, the study of the airborne Alternaria spores should be ensured.

List mode data acquisition technique for Compton suppression and minimum detectable activity (MDA) reduction in standard high-volume air samples

The Minimum Detectable Activity (MDA) reduction and Compton continuum suppression were performed using portable High-purity Germanium (HPGe) and annular NaI(TI) detectors. In this research, instead of using timing and coincidence electronic modules, the list mode data acquisition was used. This method was very simple but the results was attractive. In the list mode data acquisition technique, the Multiparameter Analyzer (MPA) recorded the time stamp of each event, and the coincidence spectrum can be replayed for a specific coincidence window. Using this method, there is no need for the further data acquisition and by one-time data acquisition, we can replay data for another coincidence time. The suppression factor (SF) for the high-volume standard air filter sample was estimated to be 2.9 while the amount of MDA reduction for this sample was about 30%.

Assessment of Atmospheric PM2.5 and PCDD/Fs Collected by Different High-volume Ambient Air Sampling Systems

To evaluate the difference in hazardous air pollutants in PM2.5 between reference method (National Institute of Environmental Analysis; NIEA A205) and high-volume air sampler (European standard:EN14907 and Japan method), we set up a sampling station on the campus of National Yang-Ming Chiao Tung University, northern Taiwan, during 2014-2015. Both vapor and solid phases of dioxins were collected using high-volume samplers, according to EN14907 and Japan method. The flow rate was set at 500 L min-1 and 1000 L min-1, respectively. To compare the difference with the high-volume air sampler, we simultaneously used the reference air sampler based on Taiwan NIEA A205.11C, at the flow rate of 16.7 L min-1 (BGI PQ200-FRM). The mass concentrations of PM2.5 measured with NIEA A205, EN14907, and Japan method were 20.2 ± 8.79, 25.4 ± 10.5 and 28.6 ± 13.9 μg m-3, respectively. The difference of the mass concentration of PM2.5 obtained from two different methods was lower than 3.9%. Moreover, the concentrations of PCDD/F between solid and vapor phases were 56.9-1,090 and 38.6-67.1 fg m-3 via EN14907 and 51.1-1,150 and 18.4-81.8 fg m-3 via Japan method, respectively. Obviously, there is no significant difference between these two samplers. Compared to the method of NIEA, high volume air sampling method not only provided equivalently good quality data but offer a higher sample quantity for analyzing the trace level chemical component of hazardous air pollutants and the toxicity in different areas.

PM10 Source Identification: A Case of a Coastal City in Colombia

This paper assesses the spatial variation of EC, OC, major, and trace elements in an industrialized coastal city, allowing identification and tracers of PM10 emission sources. 83 samples (24h average) were collected on quartz filters during the dry season using high-volume samplers. Major and trace elements were analyzed using ICP-AES and ICP-MS, whereas a thermal/optical carbon analyzer was used to determine OC and EC. Chemical characterization of major elements, SiO2, SO42-, MgO, and CaO, showed high spatial variation between sites. The abundance of these major elements and OC confirmed the effect of exposed land resuspension and road dust; mutually with the production of secondary organic aerosol (SOA). Trace elements showed high values of Cu, Pb, Mn, and V, indicating the influence of road traffic and some industries (Cu) and oil burning (V and Mn). Enrichment Factor analysis revealed that Mg, P, S, Cu, and Pb were highly/moderately enriched indicating the substantial contribution of anthropogenic sources. Results of diagnostic ratios and PMF receptor model of the spatially obtained data suggested major sources of PM10 as traffic-related emissions, heavy fuel oil combustion, biomass burning, and industrial processes. Back trajectory analysis (HYSPLIT) indicated air masses were coming from the North-East region of the Atlantic Ocean as the principal origin.

A preliminary investigation comparing high-volume and low-volume air samplers for measurement of PAHs, NPAHs and airborne bacterial communities in atmospheric particulate matter

Exposure to atmospheric particulate matter (PM) constitutes a severe public health threat in African countries' urban areas.

Identification of sites with elevated PM levels along an urban cycle path using a mobile platform and the analysis of 48 particle bound PAH

Using a multidisciplinary approach, this study provides insight into everyday exposure scenarios of urban commuters to aerosol particles and their associated polycyclic aromatic hydrocarbons. It combines high spatiotemporal resolution particle measurements, used to determine the distribution of particulate matter in the urban environment, with the chemical analysis of the health-relevant particle fraction (< 2.5 μm) at higher polluted sites. In September 2019, multiple test rides were conducted using a mobile platform along an urban cycle path in Aachen, Germany. With this, particle number and mass concentrations were recorded. Based on this data, five sites with elevated levels of particulate matter concentrations were identified. At these locations, the airborne respirable particles (PM2.5) were collected using a high-volume sampler. These were then quantified for an extended set of PAH and alkylated PAH by GC-MS. The alkylated distribution pattern of PAH in the samples all exhibited a typical pyrogenic pattern. A more detailed assessment of toxicity was possible because PAH such as dibenzo[a,l]pyrene or 7H-benzo[c]fluorene could be taken into account. The non-EPA PAH contributed up to 81% to the total toxicity of the particles expressed in toxic equivalents. The measurement of an extended set of PAH was beneficial and is highly recommended for future studies.

Antibiotic resistance genes and antibiotic sensitivity in bacterial aerosols and their comparisons with known respiratory pathogens

Airborne transmission of antibiotic resistance genes (ARGs) has emerged as a global health threat, while their hosts’ resistance phenotype remains largely unknown. Here, culturable bacterial aerosol samples were collected from polluted air in Beijing using a portable high volume sampler (1000 L/min). Antimicrobial susceptibility testing was conducted to explore the antibiotic sensitivity of culturable bacterial aerosols to seven widely used antibiotics. As a comparison, ARG distribution and expression in two human respiratory pathogenic bacterial strains (Pseudomonas aeruginosa and Methicillin-resistant Staphylococcus aureus) and a non-pathogenic bacterial strain (Pseudomonas fluorescens) were also studied. Relative abundances of 39 ARG subtypes in three bacterial strains including Haemophilus influenzae were investigated by high throughput real-time qPCR platform. Surprisingly, 24.66% of the culturable bacterial aerosols in polluted air were resistant to vancomycin-the most powerful antibiotics to date, while 53.05% of airborne culturable bacteria were susceptible to ampicillin (β-lactams). Different bacteria demonstrated very different ARG distribution patterns of more or less skewed toward certain one ARG type. On the other hand, the vancomycin resistance gene vanB was detected both in H. influenza and P. fluorescens, however these bacteria did not exhibit anti-vancomycin phenotype. Furthermore, the resistance to ciprofloxacin (quinolones) was not observed in P. aeruginosa and P. fluorescens although these bacteria harbor abundant quinolone resistance gene qepA. Experimental data from this work show that air represents an important active reservoir of diverse ARGs, and some bacterial aerosols are harboring vancomycin resistance gene though not expressed. Results from human respiratory pathogens have further demonstrated similar findings. This work underscores the serious concern of airborne dissemination of ARBs including those resistant to vancomycin in polluted ambient environments, while revealing abundances and patterns of various ARGs in both pathogenic and non-pathogenic bacteria.

Seasonal characteristics of atmospheric water-soluble organic nitrogen in PM2.5 in Seoul, Korea: Source and atmospheric processes of free amino acids and aliphatic amines

The seasonal characteristics of atmospheric water-soluble organic nitrogen (WSON) in particulate matter with a diameter of 2.5 μm or smaller (PM2.5) were analyzed focusing on sources and atmospheric processing. Daily collected samples over 23 h (10:00–9:00) from 7 August 2018 to 31 December 2019 on quartz filters with a high-volume sampler at the Korea Institute of Science and Technology (KIST) in Seoul were considered. The most common species in the Seoul atmosphere included Glycine (5.45 ± 9.81 ng/m3) among free amino acids (FAAs) and trimethylamine (TMA) (5.35 ± 3.80 ng/m3) among aliphatic amines (AAs). The top 10 WSON species (93.6% of all WSON species) were categorized into three groups based on correlation analysis considering meteorological data, (e.g., temperature, rainfall, relative humidity (RH), wind speed) gaseous pollutants (e.g., SO2, CO, NO2) and mass concentration of PM10 and PM2.5. Those three groups are G1 (Glycine, Alanine, and Threonine), G2 (Gln Glutamine, Lys Lysine, and Glutamic acid) and G3 (Trimethylamine (TMA), dimethylamine (DMA), and methylamine (MA)), where G1, G2 and G3 accounted for 31.1%, 8.8% and 51.1%, respectively, of the total species. Among these three groups, G1 and G3 are from combustion sources, and G2 shows secondary features generated by photochemical reactions involving ozone. Although both G1 and G3 exhibited features influenced by combustion sources, the AA species (TMA, DMA, and MA) in G3 demonstrated typical features enhanced under high-humidity conditions, suggesting not only primary sources but also secondary formation at the local scale influence to the AA in G3 group. Based on long-term measurements more than a year, our findings suggest that complex and diverse sources of atmospheric WSON are in Seoul, Korea both from primary and secondary, which may affect its environmental, climate and health.

The oxidative and neurotoxic potentials of the ambient PM2.5 extracts: The efficient multi-solvent extraction method

The health effects of ambient air particulate matter with a diameter of ≤2.5 μm (PM2.5) on the central nervous system are well known and the induced oxidative stress has been shown as their main neuropathologic outcome. Ambient air PM2.5 sampling methods mostly use air sampler systems that collect PM2.5 on filters, which is followed by a PM2.5 extraction approach. Inefficient extraction may lead to compositional bias and unreal interpretation of the results. This study aimed to compare our proposed multi-solvent extraction (MSE) approach for PM2.5 extraction with a conventional aqueous extraction (AqE) method using the analysis of oxidative effects and cytotoxicity in the human neuroblastoma SH-SY5Y cell line. Ambient PM2.5 samples were collected from an urban traffic location in Tehran city, the capital of Iran, using a high-volume sampler. The developed MSE method was proved to have superior advantages over the AqE method including an increased extraction efficiency (as much as 96 against 48% for PMms and PMaq, respectively), and decreased artifacts and compositional biases. Ambient PM2.5, besides PMms and PMaq were analyzed for water-soluble ions, metals, and major elements. Dithiothreitol, ascorbic acid, lipid peroxidation, and cell viability assays on SH-SY5Y cells represented the significantly higher oxidative potential for PMms compared to PMaq. The increased cytotoxicity may occur because of the increased oxidative potential of PMms and possibly is associated with higher efficiency of the MSE over the AqE method for removal of total redox-active PM components.

Collection of Bacterial Community Associated with Size Fractionated Aerosols from Kuwait

Airborne particles play a significant role in the spread of bacterial communities. The prevalence of both pathogenic and non-pathogenic forms in the inhalable fractions of aerosols is known. The abundance of microorganisms in the aerosols heightens the likely health hazards due to inhalation since they serve as carriers for pathogens and allergens, often acting as a vector for pulmonary/respiratory infections. Not much information is available on the occurrence and prevalence of bacterial communities in different size-fractionated aerosols in Kuwait. A high-volume air sampler with a six-stage cascade impactor was deployed for sample collection at two sites representing a remote and an urban site. A total volume of 815 ± 5 m3 of air was passed through the filters to trap the particulate matter ranging from 0.39 to &gt;10.2 μm in size (Stage 1 to Stage 5 and base filter). Aeromonas dominated all the stages at the urban site and Stage 5 at the remote site, whereas Sphingobium was prevalent at Stages, 2, 3 and 4 at the remote site. Brevundimonas were found at Stages 1 and 5, and the base filter at the remote site. These results show that the bacterial community is altered in different size fractions of aerosols. Stages 1–4 form the respirable fraction, whereas Stage 5 and particles on the base filter are the inhalable fractions. Many species of Aeromonas cause disease, and hence their presence in inhalable fractions is a health concern, meaning that species-level identification is warranted.

Feasibility of a High-Volume Filter Sampler for Detecting SARS-CoV-2 RNA in COVID-19 Patient Rooms.

Aerosolization of SARS-CoV-2 by COVID-19 patients can put healthcare workers and susceptible individuals at risk of infection. Air sampling for SARS-CoV-2 has been conducted in healthcare settings, but methods vary widely and there is need for improvement. The objective of this study was to evaluate the feasibility of using a high-volume filter sampler, BioCapture z720, to detect SARS-CoV-2 in COVID-19 patient rooms in a medical intensive care unit, a dedicated COVID-19 ward, and at nurses’ stations. In some locations, the BioSpot-VIVAS, known for high efficiency in the collection of virus-containing bioaerosols, was also operated. The samples were processed for SARS-CoV-2 RNA with multi-plex nested polymerase chain reaction. One of 28 samples collected with the high-volume filter sampler was positive for SARS-CoV-2; all 6 samples collected with BioSpot-VIVAS were negative for SARS-CoV-2. The high-volume filter sampler was more portable and less intrusive in patient rooms than the BioSpot-VIVAS, but limits of detection remain unknown for this device. This study will inform future work to evaluate the reliability of these types of instruments and inform best practices for their use in healthcare environments for SARS-CoV-2 air sampling.

Airborne SARS-CoV-2 in home and hospital environments investigated with a high-powered air sampler

BackgroundThe initial aim was to study the effects of face masks worn by recently infected individuals on the airborne spread of SARS-CoV-2, but findings motivated us to proceed with comparing the presence of SARS-CoV-2 in air samples near infected individuals at home with those near infected intensive care unit (ICU) patients.AimTo assess the presence of SARS-CoV-2 in the air of homes of infected individuals and in ICU rooms of critically ill patients with COVID-19 who were undergoing different forms of potential aerosol-generating medical procedures.MethodsA high-volume air sampler method was developed that used a household vacuum cleaner with surgical face masks serving as sample filters. SARS-CoV-2 RNA was harvested from these filters and analysed by polymerase chain reaction. Fog experiments were performed to visualize the airflow around the air sampler. Air samples were acquired in close proximity of infected individuals, with or without wearing face masks, in their homes. Environmental air samples remote from these infected individuals were also obtained, plus samples near patients in the ICU undergoing potential aerosol-generating medical procedures.FindingsWearing a face mask resulted in a delayed and reduced flow of the fog into the air sampler. Face masks worn by infected individuals were found to contain SARS-CoV-2 RNA in 71% of cases. SARS-CoV-2 was detected in air samples regardless of mask experiments. The proportion of positive air samples was higher in the homes (29/41; 70.7%) than in the ICU (4/17; 23.5%) (P < 0.01).ConclusionSARS-CoV-2 RNA could be detected in air samples by using a vacuum cleaner based air sampler method. Air samples in the home environment of recently infected individuals contained SARS-CoV-2 RNA nearly three times more frequently by comparison with those obtained in ICU rooms during potential aerosol-generating medical procedures.

Potential noise annoyance from ambient air quality measurement using high volume air sampler (HVAS)

One of the benchmarks in air pollution is the quality of ambient air consisting of gas and particulate matter. Measurement of particulates in ambient air can be done using a High-Volume Air Sampler (HVAS). However, in the measurement process it sometimes causes noise annoyance to the community where the measuring instrument is operated, considering that the operating time of the instrument is 24 consecutive hours. This research identifies the value of the sound power level emitted from the several types of HVAS to the surrounding environment. There are two types of HVAS measured in this study consisting of one unit of HVAS with analogue flow control made by Indonesian manufacturer and two units of HVAS with digital flow control made by Japan and United States of America manufacturers. Sound power level is determined using ISO 9614 method with a sound intensity analyzer as the main instrument. The sound power level data for each HVAS were than compared and frequency spectrum distributions are evaluated. Based on the research results, it was found that some sample units emitted sound power levels of more than 90 dBA with dominant noise being at high frequencies starting from 4000 Hz. The results of the research can be used as an early information in the development of the HVAS regarding noise mitigation, because there is different approach for controlling noise specifics in low, mid and high frequencies noise source.

Development of a high-volume ambient aerosol sampling inlet with an adjustable cutoff size and its performance evaluation using road dust

Aerosol samplers are generally classified into particulate matter (PM2.5 or PM10) and total suspended particle (TSP) samplers. As changing the cutoff size is cumbersome, it necessitates either replacing the particle size separator or adjusting the sampling flow rate. In this study, a novel high-volume aerosol-sampling inlet with an adjustable cutoff size was developed. Its performance was evaluated at a sampling flow rate of 1000 L/min of road dust. The cyclone separator installed with the newly developed inlet absorbed airflow from all directions. The cutoff size of this inlet was easily adjustable using the guide vane angle. For the guide vane angles of 29°, 42°, and 90° (at a 2 km/h freestream velocity), the cutoff sizes were 2.59, 9.92, and 26.2 μm, respectively. At the 90° angle of the guide vanes and the free stream velocity of 2 km/h, no rotational airflow occurred inside the cyclone separator to allow TSP sampling. Increasing the freestream velocity to 16 km/h at angles of 29° and 42° decreased the cutoff size by 0.12 and 0.45 μm, respectively; finely adjusting these angles further reduced the cutoff size to 0.04 and 0.07 μm, respectively. Thus, an almost constant cutoff size was possible. The developed inlet allowed sampling of PM2.5, PM10, or TSP using a single device.