PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “PM2.5”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 127 records · Page 7Linked to original sources

PM2.5 and PM10 concentrations from the Qalabotjha low-smoke fuels macro-scale experiment in South Africa.

This article presents results from the particulate monitoring campaign conducted at Qalabotjha in South Africa during the winter of 1997. Combustion of D-grade domestic coal and low-smoke fuels were compared in a residential neighborhood to evaluate the extent of air quality improvement by switching household cooking and heating fuels. Comparisons are drawn between the gravimetric results from the two types of filter substrates (Teflon-membrane and quartz-fiber) as well as between the integrated and continuous samplers. It is demonstrated that the quartz-fiber filters reported 5 to 10% greater particulate mass than the Teflon-membrane filters, mainly due to the adsorption of organic gases onto the quartz-fiber filters. Due to heating of sampling stream to 50 degrees C in the TEOM continuous sampler and the high volatile content of the samples, approximately 15% of the particulate mass was lost during sampling. The USEPA 24-hr PM2.5 and PM10 National Ambient Air Quality Standards (NAAQS) of 65 microg m(-3) and 150 microg m(-3), respectively, were exceeded on several occasions during the 30-day field campaign. Average PM concentrations are highest when D-grade domestic coal was used, and lowest between day 11 and day 20 of the experiment when a majority of the low-smoke fuels were phased in. Source impacts from residential coal combustion are also found to be influenced by changes in meteorology, especially wind velocity. PM2.5 and PM10 mass, elements, water-soluble cations (sodium, potassium, and ammonium), anions (chloride, nitrate, and sulfate), as well as organic and elemental carbon were measured on 15 selected days during the field campaign. PM2.5 constituted more than 85% of PM10 at three Qalabotjha residential sites, and more than 70% of PM10 at the gradient site in the adjacent community of Villiers. Carbonaceous aerosol is by far the most abundant component, accounting for more than half of PM mass at the three Qalabotjha sites, and for more than a third of PM mass at the gradient site. Secondary aerosols such as sulfate, nitrate, and ammonium are also significant, constituting 8 to 12% of PM mass at the three Qalabotjha sites and 15 to 20% at the Villiers gradient site.

Aerosols↗

Oxalic acid in PM2.5 particulate matter in California.

Ambient air monitoring for organic acids in PM2.5 was conducted at several locations in California. During the study, it was found that oxalic acid (ethanedioc acid) was the most abundant organic acid found in the PM2.5 fraction. Samples from Azuza (in southern California), San Jose (in the San Francisco Bay area), and Fresno (in central California), a PM2.5 Super Site, were collected in 1999 and analyzed. The results for oxalic acid concentrations during this monitoring effort are presented.

Air↗

Levoglucosan in PM2.5 at the Fresno supersite.

Ambient air monitoring for PM2.5 has been conducted on a daily basis at the Fresno, CA, supersite since 1999. It has been found that PM2.5 concentrations routinely exceed the National Ambient Air Quality Standards during the winter months. In an effort to determine the effect of biomass burning on PM2.5 concentrations, samples during 2000 were analyzed for levoglucosan, palmitic acid, and stearic acid. The results of this study are presented.

Air Pollutants↗

The regional nature of PM2.5 episodes in the upper Ohio River Valley.

From October 1999 through September 2000, particulate matter (PM) with aerodynamic diameter > or =2.5 microm (PM2.5) mass and composition were measured at the National Energy Technology Laboratory Pittsburgh site, with a particle concentrator Brigham Young University-organic sampling system and a tapered element oscillating microbalance (TEOM) monitor. PM2.5 measurements had also been obtained with TEOM monitors located in the Pittsburgh, PA, area, and at sites in Ohio, including Steubenville, Columbus, and Athens. The PM data from all these sites were analyzed on high PM days; PM2.5 TEOM particulate mass at all sites was generally associated with transitions from locally high barometric pressure to lower pressure. Elevated concentrations occurred with transport of PM from outside the local region in advance of frontal passages as the local pressure decreased. During high-pressure periods, concentrations at the study sites were generally low throughout the study region. Further details related to this transport were obtained from surface weather maps and estimated back-trajectories using the hybrid single-particle Lagrangian integrated trajectory model associated with these time periods. These analyses indicated that transport of pollutants to the Pittsburgh site was generally from the west to the southwest. These results suggest that the Ohio River Valley and possible regions beyond act as a significant source of PM and its precursors in the Pittsburgh area and at the other regional sites included in this study.

Air Movements↗

Source apportionment of indoor, outdoor, and personal PM2.5 in Seattle, Washington, using positive matrix factorization.

As part of a large exposure assessment and health-effects panel study, 33 trace elements and light-absorbing carbon were measured on 24-hr fixed-site filter samples for particulate matter with an aerodynamic diameter <2.5 microm (PM2.5) collected between September 26, 2000, and May 25, 2001, at a central outdoor site, immediately outside each subject's residence, inside each residence, and on each subject (personal sample). Both two-way (PMF2) and three-way (PMF3) positive matrix factorization were used to deduce the sources contributing to PM2.5. Five sources contributing to the indoor and outdoor samples were identified: vegetative burning, mobile emissions, secondary sulfate, a source rich in chlorine, and a source of crustal-derived material. Vegetative burning contributed more PM2.5 mass on average than any other source in all microenvironments, with average values estimated by PMF2 and PMF3, respectively, of 7.6 and 8.7 microg/m3 for the outdoor samples, 4 and 5.3 microg/m3 for the indoor samples, and 3.8 and 3.4 microg/m3 for the personal samples. Personal exposure to the combustion-related particles was correlated with outdoor sources, whereas exposure to the crustal and chlorine-rich particles was not. Personal exposures to crustal sources were strongly associated with personal activities, especially time spent at school among the child subjects.

Air Pollutants↗

Chemical speciation of PM2.5 collected during prescribed fires of the Coconino National Forest near Flagstaff, Arizona.

The use of prescribed fire is expected to increase in an effort to reduce the risk of catastrophic fire, particularly at urban/forest interfaces. Fire is a well-known source of particulate matter (PM) with particle sizes < or =2.5 microm (PM2.5), small diameter PM known to affect climate, visibility, and human health. In this work, PM2.5 was collected during seven first-entry burns (flaming and smoldering stages) and one maintenance burn of the Coconino National Forest. Samples were analyzed for organic and elemental carbon, cations (sodium, potassium [K+], and ammonium [NH4+]), anions (nitrate [NO3-] and sulfate), and 48 elements (with atomic weights between sodium and lead). The PM2.5 contained high organic carbon levels (typically >90% by mass), commonly observed ions (K+, NH4+, and NO3-) and elements (K+, chlorine, sulfur, and silicon), as well as titanium and chromium. Flaming produced higher K+ and NH4+ levels than smoldering, and the elemental signature was more complex (20 versus 7 elements). Average organic carbon x 1.4 mass fractions (+/-standard deviation) were lower during flaming (92+/-14%) than during smoldering (124+/-24%). The maintenance (grassland) burn produced lower particle concentrations, lower NH4+ and NO3- levels, and higher K and chlorine levels than did the first-entry fires.

Air Pollutants↗

Exposure to PM2.5 and PAHs from the Tong Liang, China epidemiological study.

Chemically speciated PM2.5 and particle-bound polycyclic aromatic hydrocarbon (PAH) measurements were made at three sites near urban Tong Liang, Chongqing, a Chinese inland city where coal combustion is used for electricity generation and residential purposes outside of the central city. Ambient sampling was based on 72-hr averages between 3/2/2002 and 2/26/2003. Elevated PM2.5 and PAH concentrations were observed at all three sites, with the highest concentrations found in winter and the lowest in summer. This reflects a coupling effect of source variability and meteorological conditions. The PM2.5 mass estimated from sulfate, nitrate, ammonium, organics, elemental carbon, crustal material, and salt corresponded with the annual average gravimetric mass within +/-10%. Carbonaceous aerosol was the dominant species, while positive correlations between organic carbon and trace elements (e.g., As, Se, Br, Pb, and Zn) were consistent with coal-burning and motor vehicle contributions. Ambient particle-bound PAHs of molecular weight 168-266 were enriched by 1.5 to 3.5 times during the coal-fired power plant operational period. However, further investigation is needed to determine the relative contribution from residential and utility coal combustion and vehicular activities.

Air Pollutants↗

Reduction potential of urban PM2.5 mortality risk using modern ventilation systems in buildings.

UNLABELLED: Urban PM2.5 (particulate matter with aerodynamic diameter smaller than 2.5 microm) is associated with excess mortality and other health effects. Stationary sources are regulated and considerable effort is being put into developing low-pollution vehicles and environment-friendly transportation systems. While waiting for technological breakthroughs in emission controls, the current work assesses the exposure reductions achievable by a complementary means: efficient filtration of supply air in buildings. For this purpose infiltration factors for buildings of different ages are quantified using Exposures of Adult Urban Populations in Europe Study (EXPOLIS) measurements of indoor and outdoor concentrations in a population-based probability sample of residential and occupational buildings in Helsinki, Finland. These are entered as inputs into an evaluated simulation model to compare exposures in the current scenario with an alternative scenario, where the distribution of ambient PM2.5 infiltration factors in all residential and occupational buildings are assumed to be similar to the subset of existing occupational buildings using supply air filters. In the alternative scenario exposures to ambient PM2.5 were reduced by 27%. Compared with source controls, a significant additional benefit is that infiltration affects particles from all outdoor sources. The large fraction of time spent indoors makes the reduction larger than what probably can be achieved by local transport policies or other emission controls in the near future. PRACTICAL IMPLICATIONS: It has been suggested that indoor concentrations of ambient particles and the associated health risks can be reduced by using mechanical ventilation systems with supply air filtering in buildings. The current work quantifies the effects of these concentration reductions on population exposures using population-based data from Helsinki and an exposure model. The estimated exposure reductions suggest that correctly defined building codes may reduce annual premature mortality by hundreds in Finland and by tens of thousands in the developed world altogether.

Adult↗

[Concentrations of PM10 and PM2.5 particulate material in the atmosphere of Rome].

Starting from 1993, various monitoring campaigns were carried out in Rome to determine PM10 and PM2.5. Their results are presented here cumulatively, with the aim of obtaining preliminary information on relationships among these size fractions, in various seasonal periods and in two sites with different characteristics (a road site and an urban background site in a public park). Particles were collected on filter and gravimetrically determined. Both PM10 and PM2.5 concentrations show temporal fluctuations with higher values during winter months. Background concentrations are lower than those contemporaneously measured at the road site only to a limited extent (10-17%). The contribution of PM2.5 to PM10 during the winter semester is higher than during the summer one (67 vs. 52%), with no substantial intersite differences.

Air Pollutants↗

GC/ITMS measurement of carbonyls and multifunctional carbonyls in PM2.5 particles emitted from motor vehicles.

A method was developed and tested to identify and quantitate carbonyls and multifunctional carbonyls in fine particulate matter (PM2.5; <2.5 microm aerodynamic diameter). The method relies on ultrasonic extraction of particulate matter on filters at -8 degrees C; derivatization with O-(2,3,4,5,6-pentafluorobenzyl) hydroxylamine (PFBHA), and PFBHA along with bis (trimethylsilyl) trifluoroacetamide (BSTFA); and detection of the derivatives by gas chromatography/ion trap mass spectrometry. Ultrasonic extraction of model compounds from enriched particles was affected by solvent polarity (water > methylene chloride > toluene-isopropanol (2 + 1, v/v). Water provided the highest recovery for dihydroxy acetone, pyruvic acid, and hydroxy acetone, compared to methylene chloride, and toluene-isopropanol. Lowering the ultrasonication bath temperature from 0 degrees to -8 degrees C improved the recoveries of the less water soluble and more volatile species-methacrolein, methyl vinyl ketone, 2,3-butanedione, and tolualdehyde. The power of the method was demonstrated by identification and quantitation of carbonyls and multifunctional carbonyls in sample extracts of fine particulate matter (PM2.5) collected in the Caldecott tunnel, CA. The identities of crotonaldehyde, 2,3-butanedione, glyoxal, 9H-fluoren-9-one, glycolaldehyde, glyoxylic acid, levulinic acid, and 3-hydroxybenzaldehyde were confirmed by comparing the relative retention time and mass spectra of the analyte in the sample extract with an authentic standard. Quantitation of crotonaldehyde, glyoxal, 2,3-butanedione, glyoxylic acid, and levulinic acid was accomplished. This is the first report of glyoxylic acid, levulinic acid, and 3-hydroxybenzaldheyde in PM2.5 particles sampled in a roadway tunnel. It is also the first report of a C10 carbonyl with the molecular formula of C10H16O2, a hydroxy carbonyl with the molecular formula of C17H21NO2, and a hydroxy or dihydroxy carbonyl with the molecular formula of C16H14O2 or C9H10O3. The high-molecular weight hydroxy carbonyls, which were found only in the heavy-duty (diesel) bore, may be tracers of diesel emissions in air.

Air Pollutants↗

[Characteristics and sources of trace elements in ambient PM2.5 in Beijing].

To understand concentration levels and sources of trace elements in PM2.5(particulate matter with aerodynamic diameters less than 2.5 microns) concentration and composition in the ambient air of Beijing, weekly samples were simultaneously collected for one year in Chegongzhuang and Qinghuayuan. Trace elements exhibited similar significant weekly variations. The strongest weekly shift occurred in winter, which reached as high as a factor of 1.6 for two consecutive weeks. No obvious seasonal pattern was found for trace elements except for that their average concentrations were much higher in winter. The EFs of trace elements were lowest in spring, probably due to frequent dust storms resulting in reduced contribution of anthropogenic sources and increased contribution of soil dust. The ambient concentrations of Se, Br, and Pb were about 1000-8000 times higher than those expected from the crustal soil in Beijing. Se was most enriched in PM2.5, reflecting the characteristics of fine particles from coal burning in Beijing. The annual mean concentration of Pb of 0.31 microgram.m-3 did not exceeded the WHO annual standard, but was at very high level compared to those measured in Los Angles and Brisbane. Comparison analysis of Pb with Br and Se shows that coal burning is probably another major source of Pb in PM2.5 other than vehicle emission.

Air↗

[Advances on the immunotoxicity of airborne fine particulate matter (PM2.5)].

Exposure to airborne fine particulate matter (PM2.5) is an health risk factor, and immune system is one of the target tissues. Fine particulate matter had an effect on the host specific immune and nonspecific immune. The immune effect has two side, it can cause the damage to body, on the other hand it can also clean up the particulate matter. Immunotoxicity of PM2.5 is also associated with the other biological effect such as genotoxicity. Damage of fine particulate is through oxidant stress, inflammation and neurogenic inflammation and so on, but the detail of the mechanism for them is lacking. This review describes the immunotoxicity of PM2.5 from different aspects and levels.

Air Pollutants↗

Chemical fractionation of elements in airborne particulate matter: primary results on PM10 and PM2.5 samples in the Lazio region (central Italy).

This paper describes how a two-step chemical fractionation method that allows the determination of 17 elements in airborne particulate matter, has been applied to a monitoring campaign of PM10 and PM2.5 in the Lazio region (Italy). This method involved an extraction in a pH buffered aqueous solution followed by a microwave-assisted acid digestion of the residue. With respect to the determination of the total elemental contents, the evaluation of a soluble fraction provides more reliable information on the presence and of the destiny of heavy metals in the environment. Furthermore, the pH buffered extraction conditions chosen, rendered the results independent of the intrinsic acidity of the collected samples and, although the chemical fractionation has a purely operational function, it facilitates the study of the relationship between the distribution of solubility and the different emission sources. Results are discussed in relation to the different concentration and the different degrees of solubility of the elements observed in two sampling sites; one in an urban and one in a rural environment. Since in-parallel sampling of PM2.5 and PM10 were performed in both sites, the influence of particle size is also discussed. Behaviour of some tracers deriving from both vehicular traffic, with particular attention to re-suspended road dusts, and naturally generated particulate matter, such as marine aerosol and Saharian dust, are discussed.

Air Pollutants↗

Cytotoxicity and induction of proinflammatory cytokines from human monocytes exposed to fine (PM2.5) and coarse particles (PM10-2.5) in outdoor and indoor air.

Increased incidence of mortality and morbidity due to cardiopulmonary complications has been found to associate with elevated levels of particulate air pollution (particulate matter with an aerodynamic diameter < 10 microm, PM10 and <2.5 microm, PM2. 5). Lung injury and an imbalance of inflammatory mediators are proposed causative mechanisms, while the toxic constituents may be acidity, transition metals, organic, and biogenic materials. To compare the ability of inhalable fine particles (PM2.5), and coarse particles (PM10-2.5) to cause cell injury and cytokine production in monocytes, dichotomous Andersen samplers were used to collect size-fractionated PM10 for in vitro testing of the particle extracts. Particles from both outdoor and indoor air were collected onto Teflon filters, on nine separate occasions. Each filter was water extracted and each extract assessed for ability to cause cell death, as well as interleukin (IL)-6 and IL-8 production in human monocytes. Significant toxicity and cytokine production was induced by outdoor PM10-2.5, but not by outdoor PM2.5 or the particles collected indoors. Outdoor PM10-2.5 induced 20 times the amounts of IL-6 and IL-8 than the fine particles. Cytotoxicity was inhibited by deferoxamine, a chelator of transition metals, while cytokine production was not. On the other hand, lipopolysaccharide binding protein (LBP) completely inhibited cytokine induction by PM10-2.5, suggesting that gram-negative bacteria and/or endotoxins are components of PM10-2.5. The effective proinflammatory effects of endotoxin on macrophages may upset lung homeostasis while metals-induced cytotoxicity/necrosis may set up inflammation independent of macrophage-derived cytokines.

Acute-Phase Proteins↗

Evaluation of a sampling strategy for estimation of long-term PM2.5 exposure for epidemiological studies.

As part of the European Community Respiratory Health Survey (ECRHS) PM2.5 (particles collected with an upper 50% cut point of 2.5 microm aerodynamic diameter) was measured using an EPA-WINS (Environmental Protection Agency Well Impactor Ninety-six) sampler. The monitoring schedule was restricted to 7 days per month for one year. Simultaneously, during this one year study period a collocated Harvard Impactor (HI) was run on a daily basis in Erfurt, Germany. Here we validated the reliability of annual, seasonal and monthly means estimated using the ECRHS scheme (measurements taken less than 25% of the whole study period) with the 'true' long-term averages, which were estimated using all available daily means. The daily PM2.5 means, obtained by both instruments operated in parallel, were only slightly different (the mean difference between EPA-WINS and HI was 1.8 microg m(-3) and 2.8 microg m(-3) for the winter means). The values obtained by the two instruments were highly correlated (r = 0.95). In view of that negligible difference, no additional bias was seen with respect to the annual and the winter means estimated by the two different sampling strategies (the difference was 1.7 microg m(-3) and 2.7 microg m(-3), respectively). Monthly means, however, can only be considered to be a crude estimate that may substantially under- or overestimate the true monthly mean value.

Air Pollutants↗

Polycyclic aromatic hydrocarbons in bulk PM2.5 and size-segregated aerosol particle samples measured in an urban environment.

To analyze polycyclic aromatic hydrocarbons (PAHs) at an urban site in Seoul, South Korea, 24-hr ambient air PM2.5 samples were collected during five intensive sampling periods between November 1998 and December 1999. To determine the PAH size distribution, 3-day size-segregated aerosol samples were also collected in December 1999. Concentrations of the 16 PAHs in the PM2.5 particles ranged from 3.9 to 119.9 ng m(-3) with a mean of 24.3 ng m(-3). An exceptionally high concentration of PAHs( approximately 120 ng m(-3)) observed during a haze event in December 1999 was likely influenced more by diesel vehicle exhaust than by gasoline exhaust, as well as air stagnation, as evidenced by the low carbon monoxide/elemental carbon (CO/EC) ratio of 205 found in this study and results reported by previous studies. The total PAHs associated with the size-segregated particles showed unimodal distributions. Compared to the unimodal size distributions of PAHs with modal peaks at < 0.12 microm measured in highway tunnels in Los Angeles (Venkataraman and Friedlander, 1994), four- to six-ring PAHs in our study had unimodal size distributions, peaking at the larger size range of 0.28-0.53 microm, suggesting the coagulation of freshly emitted ultrafine particles during transport to the sampling site. Further, the fraction of PAHs associated with coarse particles(> 1.8 microm) increased as the molecular weight of the PAHs decreased due to volatilization of fine particles followed by condensation onto coarse particles.

Aerosols↗

Application of capillary electrophoresis combined with a modified BCR sequential extraction for estimating of distribution of selected trace metals in PM2.5 fractions of urban airborne particulate matter.

The capillary electrophoresis (CE) method combined with a sequential extraction was applied to determine the distribution of Fe, Zn, Cu, Mn and Cd in urban ambient air PM2.5 samples. PM2.5 was collected on Teflon filters with dichotomous sampler, and the modified extraction procedure following the BCR leaching procedure was used to chemically fractionate metals into "easily exchangeable" with water, "acid extractable" with 0.11 mol/l acetic acid, "reducible" with 0.1 mol/l hydroxylamine hydrochloride acidified to pH 2.0 with nitric acid, and "oxidisable" with oxidation by 8.8 mol/l hydrogen peroxide (H2O2) followed by extraction with 1.0 mol/l ammonium acetate. Based on the obtained results it was concluded that the application of the studied methodology provides chemical fractionation data that reflect the general sources and potential health hazards of the studied metals.

Air Pollutants↗

Optimization and improvement of PM2.5 thermophoretic deposition efficiency in turbulent gas flowing over tube surfaces.

PM2.5 thermophoretic deposition efficiency in turbulent gas flowing over tube surfaces is analyzed using the new concept of potential capacity and potential capacity variation. According to Romay's model, a thermophoretic deposition efficiency model in turbulent gas flowing over tube surfaces is built up based on the potential capacity. Through computing and analyzing thermophoretic deposition efficiency, PM2.5 thermophoretic deposition efficiency in turbulent gas flowing over tube surfaces in direct ratio to the potential capacity variation and in inverse ratio to the temperature ratio of tube wall to entrance gas-particle mixture. And the imprecise notion of thermophoretic deposition efficiency direct ratio to the temperature difference between tube wall and entrance gas-particle mixture is reviewed. There are credible foundations to be provided for improving and researching thermophoretic deposition efficiency in theory and experiment.

Journal Article↗