Automatic weighing system vs. manual weighing precision comparison in PM-loaded filter measurements under different humidity conditions.

Currently, there is a lack of research directly comparing the precision of automatic weighing systems and manual weighing in the context of particulate matter (PM) filter equilibration and measurements under different humidity conditions. During experimental measurements, three different types of PM-loaded filters were weighed using manual and automatic balances. During manual weighing, every filter was weighed twice in three different relative humidity conditions. The same procedure was done using an automated weighing system. In most cases, it was found that under relative humidities in the range of 30-55% RH, the manual and automated methods can be treated as referential. Regarding device stability, very slight but overall better precision was found for 30% RH, suggesting that 40 CFR Part 50, Appendix L requirements regarding conditioning humidity (30-40% RH) seem more suitable than those presented in the PN-EN 12341:2014 standard (45-50% RH). Understanding the effects of the influence of the RH% on PM mass measurements is a matter of great importance, because water vapor condensed on a filter can affect the particulate matter concentrations. This is especially important in areas where regulatory limits are exceeded. Calculation of uncertainty in the PM mass measurements is therefore crucial for determining the actual sample mass and improving air monitoring practices. In a nutshell, the experimental results obtained clearly describe how changing RH% conditions affect the PM weighing precision during manual and automated measurements.

Particulate Matter Concentration in Selected Facilities as an Indicator of Exposure to Their Service Activities.

In recent years, the correlation between the concentration of pollutants in the atmosphere and inside buildings has been reported as high. The air inside living quarters and public utility buildings or the interiors of public transport vehicles, as well as the relationship between the internal and external sources of particulate matter (PM) and gaseous pollutants, have underwent sufficient research. On the other hand, non-production rooms, i.e., offices, restaurants, beauty salons, etc. remain very poorly recognized in this respect. For the above reasons, the aim of this work is to determine the difference in the total dust (TSP) and respirable PM (PM4) concentrations in selected rooms, i.e., offices and beauty centers, in relation to their outdoor concentrations. They were measured at six locations in accordance with the standard for the conditions at workplaces by means of PM aspirators. Indoor concentrations of TSP and PM4 were much higher than those in the external surroundings of the facilities. There were no significant relationships between the TSP and PM4 concentrations inside and outside tested rooms. Although the characteristic of the internal PM essentially depends on the characteristics of the external PM migrating to the interior of the premises, considering some types of non-production premises, internal emissions fundamentally changed the characteristics of PM.

New insights into submicron particles impact on visibility.

The aim of the study was to analyze the impact of very fine atmospheric particles (submicron particulate matter; PM1) on visibility deterioration. Taking into consideration not only their entirely different physio-chemical properties in comparison to a well-recognized PM10 but also the origin and a growing environmental awareness of PM1, the main research problem has been solved in few steps. At first, the chemical composition of PM1 was determined in two selected urban areas in Poland. Measurements of meteorological parameters, i.e., air temperature and humidity, precipitation, atmospheric pressure, wind speed, and visibility, were also conducted. The next step of the work was the analysis of (1) seasonal changes of the concentration of PM1 and its main components, (2) the influence of chemical components of PM1 on light extinction, and (3) the influence of PM1 and humidity on visibility. Hierarchical cluster analysis, correlation matrixes and a heat map, and classification and regression tree analysis were used. The light extinction coefficient is influenced mainly by coarse mass of PM, and PM1-bound ammonium nitrate, organic matter, and by Rayleigh scattering. The less important in the light extinction coefficient shaping has PM1-bound ammonium sulfate, elemental carbon, and soil. In this way, the secondary origin PM1 components were proved to most significantly influence the visibility. The obtained results confirmed the possibility of the use of statistical agglomeration techniques to identify ranges of variation of visibility, including independent variables adopted to analyses (meteorological conditions, chemical composition of PM1, etc.).

Characteristics of Particles Emitted from Waste Fires-A Construction Materials Case Study.

This study aimed to determine the relative densities of populations of particles emitted in fire experiments of selected materials through direct measurement and parametrization of size distribution as number (NSD), volume (VSD), and mass (MSD). As objects of investigation, four typical materials used in construction and furniture were chosen: pinewood (PINE), laminated particle board (LPB), polyurethane (PUR), and poly(methyl methacrylate) (PMMA). The NSD and VSD were measured using an electric low-pressure impactor, while MSD was measured by weighing filters from the impactor using a microbalance. The parametrization of distributions was made assuming that each distribution can be expressed as the sum of an arbitrary number of log-normal distributions. In all materials, except PINE, the distributions of the particles emitted in fire experiments were the sum of two log-normal distributions; in PINE, the distribution was accounted for by only one log-normal distribution. The parametrization facilitated the determination of volume and mass abundances, and therefore, the relative density. The VSDs of particles generated in PINE, LPB, and PUR fires have similar location parameters, with a median volume diameter of 0.2-0.3 µm, whereas that of particles generated during PMMA burning is 0.7 µm. To validate the presented method, we burned samples made of the four materials in similar proportions and compared the measured VSD with the VSD predicted based on the weighted sum of VSD of raw materials. The measured VSD shifted toward smaller diameters than the predicted ones due to thermal decomposition at higher temperatures.

Submicron particle-bound polycyclic aromatic hydrocarbons in the Polish teaching rooms: Concentrations, origin and health hazard.

The goal of the work was to investigate the concentrations of the 16 US EPA priority polycyclic aromatic hydrocarbons (PAH) bound to submicrometer particles (particulate matter, PM1) suspended in the air of university teaching rooms and in the atmospheric air outside. Two teaching rooms were selected in two Polish cities, Gliwice, southern Poland, and Warsaw, central Poland, differing with regard to the ambient concentrations and major sources of PM and PAH. The variabilities of indoor and outdoor 24-hr concentrations of PM1-bound PAH, the ratio (I/O) of the indoor to outdoor 24-hr concentrations of PM1-bound PAH, probable sources of PAH and the level of the hazard from the mixture of the 16 PAH (ΣPAH) to humans at both sites were analyzed. In both Warsaw and Gliwice, the mean concentrations of PM1-bound ΣPAH were slightly higher in the atmospheric air than in the rooms. The indoor and outdoor concentrations of individual PAH in Gliwice were correlated, in Warsaw - they were not. Most probably, the lack of the correlations in Warsaw was due to the existence of an unidentified indoor source of gaseous PAH enriching PM1 in phenanthrene, fluorene, and pyrene. Although the ambient concentrations of PM1-bound PAH were low compared to the ones observed earlier at both sites, they were much higher than in other urbanized European areas. However, because of low mass share of heavy PAH in ΣPAH, the various indicators of the health hazard from the 16 PAH mixture were low compared to other regions.

PM Origin or Exposure Duration? Health Hazards from PM-Bound Mercury and PM-Bound PAHs among Students and Lecturers.

This study assessed inhalation exposure to particulate matter (PM1)-bound mercury (Hgp) and PM1-bound polycyclic aromatic hydrocarbons (PAHs) among university students. For this purpose, simultaneous indoor (I) and outdoor (O) measurements were taken from two Polish technical universities (in Gliwice and Warsaw) located in distinct areas with respect to ambient concentrations and major sources of PM. The indoor geometric mean concentrations of Hgp were found to be 1.46 pg·m-3 and 6.38 pg·m-3 in Warsaw and Gliwice, while the corresponding outdoor concentrations were slightly lower at 1.38 pg·m-3 and 3.03 pg·m-3, respectively. A distinct pattern was found with respect to PAH concentrations with estimated I/O values of 22.2 ng·m-3/22.5 ng·m-3 in Gliwice and 10.9 ng·m-3/11.12 ng·m-3 in Warsaw. Hazard quotients (HQs) as a result of exposure to Hgp for students aged 21 ranged from 3.47 × 10-5 (Warsaw) to 1.3 × 10-4 (Gliwice) in terms of reasonable maximum exposure (RME). The non-cancer human health risk value related to Hgp exposure was thus found to be below the acceptable risk level value of 1.0 given by the US EPA. Daily exposure values for lecture hall occupants, adjusted to the benzo(a)pyrene (BaP) toxicity equivalent (BaPeq), were 2.9 and 1.02 ng·m-3 for the Gliwice and Warsaw students, respectively. The incremental lifetime cancer risk (ILCR) values with respect to exposure to PM1-bound PAHs during the students' time of study were 5.49 × 10-8 (Warsaw) and 1.43 × 10-7 (Gliwice). Thus, students' exposure to indoor PAHs does not lead to increased risk of lung cancer.

Particulate Matter in the Air of the Underground Chamber Complex of the Wieliczka Salt Mine Health Resort.

This study evaluates the mass concentration and chemical composition of particulate matter (PM), collected in the chamber complex of the underground health resort located in the Wieliczka Salt Mine in southern Poland. Physical and chemical properties of PM were examined from the standpoint of their possible connection with therapeutic effects of the subterranean air in the mine. We found that in three underground spots we measured the average concentration of PM did not exceed 30 µg/m3. Chemical composition of PM was dominated by sodium chloride, making up 88 % of its mass, on average. It was shown that the underground ambient concentration of PM and its chemical composition depended mostly on the nature of the rock material present in the ventilation tunnel of the health resort, filtering the incoming air. The presence and effect of external sources of PM, including patients' activity, also had an impact on the underground PM concentration.

Origin-Oriented Elemental Profile of Fine Ambient Particulate Matter in Central European Suburban Conditions.

Twenty-four-hour samples of fine ambient particulate matter (PM2.5; particles with aerodynamic diameters ≤2.5 µm) were collected in a suburban (quasi-rural) area in Racibórz (Poland) between 1 January 2011 and 26 December 2012. The samples were analyzed for the contents of 28 elements. Sources of PM2.5 were identified and the contribution of each source to the PM2.5 concentration was assessed using an enrichment factor (EF) analysis, a principal component analysis (PCA), and multi-linear regression analysis (MLRA). In the cold season (January-March and October-December 2011-2012), the mean ambient concentration of PM2.5 in Racibórz was 48.7 ± 39.4 µg·m(-3), which was much higher than at other suburban or rural sites in Europe. Additionally the ambient concentrations of some toxic PM2.5-bound elements were also high, i.e., the mean ambient concentrations of PM2.5-bound As, Cd, and Pb were 11.3 ± 11.5, 5.2 ± 2.5, and 34.0 ± 34.2 ng·m(-3), respectively. In the warm season (April-September 2011-2012), the PM2.5 and PM2.5-bound element concentrations in Racibórz were comparable to the concentrations noted at other suburban (or rural) sites in Europe. Our findings suggest that elemental composition and concentrations of PM2.5 in Racibórz are mainly influenced by anthropogenic emissions, i.e., the energy production based on coal and biomass combustion, traffic, and industry.

Spatial and seasonal variability of the mass concentration and chemical composition of PM2.5 in Poland.

The seasonal changes in ambient mass concentrations and chemical composition of fine particulate matter (PM2.5) were investigated in three locations in Poland. The analyses included PM2.5-bound hazardous benzo(a)pyrene (BaP), As, Ni, Cd, and Pb. The samples of PM2.5 were collected daily in Katowice (southern Poland, urban background site), Gdansk, and Diabla Góra (northern Poland, urban and regional background sites, respectively) during 1-year-long campaign in 2010. Based on monthly ambient concentrations of PM2.5-bound carbon (organic and elemental), water-soluble ions (Na+, NH4+, K+, Mg2+, Ca2+, Cl-, NO3-, SO42-), and elements As, Ni, Cd, Pb, Ti, Al, Fe, the chemical mass closure of PM2.5 was checked for each of the four seasons of the year and for the heating and non-heating periods at each site. Also, the annual concentrations of PM2.5 were determined and the annual PM2.5 mass closure checked. At each measuring point, the PM2.5 concentrations were high compared to its Polish yearly permissible value, 25 µg/m3, and its concentrations elsewhere in Europe. The highest annual PM2.5 concentration, 43 µg/m3, occurred in Katowice; it was twice the annual PM2.5 concentration in Gdansk, and thrice the one in Diabla Góra. The high annual averages were due to very high monthly concentrations in the heating period, which were highest in the winter. PM2.5 consisted mainly of carbonaceous matter (elemental carbon (EC) + organic matter (OM), the sum of elemental carbon, EC, and organic matter, OM; its annual mass contributions to PM2.5 were 43, 31, and 33 % in Katowice, Gdansk, and Diabla Góra, respectively), secondary inorganic aerosol (SIA), the Na_Cl group, and crustal matter (CM)-in the decreasing order of their yearly mass contributions to PM2.5. OM, EC, SIA, Na_Cl, and CM accounted for almost 81 % of the PM2.5 mass in Katowice, 74 % in Gdansk, and 90 % in Diabla Góra. The annual average toxic metal contribution to the PM2.5 mass was not greater than 0.2 % at each site. In Katowice and Gdansk, the yearly ambient BaP concentrations were high (15.4 and 3.2 ng/m3, respectively); in rural Diabla Góra, the concentrations of BaP were almost equal to 1 ng/m3, the Polish BaP annual limit. The great seasonal fluctuations of the shares of the component groups in PM2.5 and of the concentrations of PM2.5 and its components are due to the seasonal fluctuations of the emissions of PM and its precursors from hard and brown coal combustion for energy production, growing in a heating season, reaching maximum in winter, and decreasing in a non-heating period. In Gdansk, northern Poland, especially in the spring and autumn, sea spray might have affected the chemical composition of PM2.5. The greatest hazard from PM2.5 occurs in Katowice, southern Poland, in winter, when very high concentrations of PM2.5 and PM2.5-related carbonaceous matter, including BaP, are maintained by poor natural ventilation in cities, weather conditions, and the highest level of industrialization in Poland. In less industrialized northern Poland, where the aeration in cities is better and rather gaseous than solid fuels are used, the health hazard from ambient PM2.5 is much lower.

A study on the seasonal mass closure of ambient fine and coarse dusts in Zabrze, Poland.

Diurnal samples of PM(2.5) and PM(2.5-10) were taken in an urban background area in Zabrze (Upper Silesia in southern Poland) in the winter (January-March) and summer (July-September) of 2009. The samples were analyzed for carbon (organic and elemental), water soluble ions (Na(+), NH(4) (+), K(+), Mg(2+), Ca(2+), F(-), Cl(-), NO(3) (-), PO(4) (3-), SO(4) (2-)) and concentrations of 27 elements by using, respectively, a Behr C50 IRF carbon analyzer, a Herisau Metrohm AG ion chromatograph, and a PANalitycal EPSILON 5 X-ray fluorescence spectrometer. To perform the mass closure calculations for both dust fractions in the two periods, the particulate matter (PM) chemical components were categorized into organic matter, elemental carbon, secondary inorganic aerosol, crustal matter, marine components and unidentified matter. The chemical composition of the two dust fractions and the element enrichment coefficients in the two seasons, referred to proper emission profiles, proved about 80% of PM(2.5) and more than 50% (in winter 65%) of PM(2.5-10) mass coming from anthropogenic sources, mainly from fuel combustion and specific municipal emission shaping the winter emission of ambient dust in the area.