A system for the sampling of inhalable airborne particles

This paper describes an instrument developed for the semi-continuous measurement of aerosol mass and its classification into three classes. These classes have been chosen to evaluate the health hazards caused by inhalable particles. The instrument takes samples through three probes, each providing different cut-off points ( approximately 15 microm, approximately 4 microm, approximately 2 microm) and collects airborne particles on circular membrane filters. The increase in weight is measured by the beta-ray attenuation method.     

Relation between particle mass and number for submicrometer airborne particles

The relationship between particle mass and the number of ambient air particles for the submicrometer size range was examined using a tapered element oscillating microbalance (TEOM) to determine the mass concentration, and a scan-ning mobility particle sizer (SMPS) to determine the volume concentration and total number of particles. The techniques were validated through their application to the estimation of submicrometer particle density for two laboratory generated aerosols of known bulk density (sodium chloride and di-2-ethylhexyl-sebacate). Further evaluation was done with the submicrometer fraction of laboratory generated environmental tobacco smoke (ETS), for which the estimated density of 1.18±0.06 g/cm³ was very close to the previously reported literature value of 1.12 g cm³. Finally, ambient air particles were examined and an estimate of the average submicrometer particle densities for these aerosols was found to vary from 1.2 to 1.8 g cm^-3 depending on the time of day. This high variation in the density of the ambient air submicrometer particles, makes it hard to estimate the mass concentration from the SMPS number concentration with better than 60% uncertainty, based on an assumed density value.     

烟草烟雾对室内空气颗粒物浓度的影响

采用电称冲击低压系统(ELPI)将无烟室和吸烟室内的空气颗粒物(0.03～10.00 μm)分成12级,对其粒子数和质量浓度进行测定.结果表明,吸烟室PM0.03～10.00的日平均粒子数和质量浓度分别是无烟室的1.50、1.13倍.烟草烟雾对室内颗粒物粒子数的影响集中在0.03～1.00 μm粒径段;对室内颗粒物质量浓度的影响表现为双模态结构,峰值分别在0.20～0.70、5.00～8.20 μm粒径段.烟草烟雾颗粒物的粒子数和质量浓度随烟雾消散时间的增加而减少,粒径越小,减小的越明显;烟草烟雾颗粒物在室内消散缓慢,会在长时间内造成影响,应引起足够关注.     

Application of cluster analysis to identify sources of airborne particles

A sampling programme for determining the concentrations in particulate matter of SO₄²⁻, Fe, Pb, Zn, K, Ca, Mg, Cd, Cr and Ni was established in the city of Valladolid for 13 months. Seasonal variations and enrichment factors were determined, then source apportionment techniques were applied. A multivariate clustering Q-technique has been used to identify specific sources. Each one of the six retained clusters has been interpreted by analyzing the composition of their centroids and the common attributes of the samples belonging to each one of them. To simplify the interpretation, some external auxiliary variables were chosen: percentage of the samples corresponding to the heating season period, minimum temperature, weekends, precipitation, daily average wind speed, etc. The reliability and practical significance of the results were studied after comparing the results obtained by two different initial partitions P1 and P2.This algorithm identified a crustal source (Fe, K, Ca and Mg), residual fuel burning (SO₄²⁻, Zn, Cd and Ni) and indirect vehicle exhaust (Pb). In addition, a double source for Cr (soil and coal ashes), a pollution ‘episode’ cluster, a low pollution cluster and an average pollution cluster have been identified.     

The relationship between indoor and outdoor airborne particles in the residential environment

The relationship between indoor and outdoor airborne particles was investigated for 16 residential houses located in a suburban area of Brisbane, Australia. The submicrometer particle numbers were measured using the Scanning Mobility Particle Sizer, the larger particle numbers using the Aerodynamic Particle Sizer and an approximation of PM_2.5 was also measured using a DustTrak. The measurements were conducted for normal and minimum ventilation conditions using simultaneous and non-simultaneous measurement methods designed for the purpose of the study. Comparison of the ratios of indoor to outdoor particle concentrations revealed that while temporary values of the ratio vary in a broad range from 0.2 to 2.5 for both lower and higher ventilation conditions, average values of the ratios were very close to one regardless of ventilation conditions and of particle size range. The ratios were in the range from 0.78 to 1.07 for submicrometer particles, from 0.95 to 1.0 for supermicrometer particles and from 1.01 to 1.08 for PM_2.5 fraction. Comparison of the time series of indoor to outdoor particle concentrations shows a clear positive relationship existing for many houses under normal ventilation conditions (estimated to be about and above 2 h⁻¹), but not under minimum ventilation conditions (estimated to be about and below 1 h⁻¹). These results suggest that for normal ventilation conditions, outdoor particle concentrations could be used to predict instantaneous indoor particle concentrations but not for minimum ventilation, unless air exchange rate is known, thus allowing for estimation of the “delay constant”.     

太仓大气细颗粒物的粒径分布及来源分析

超大城市大气环境日益改善的同时,其周边卫星城市的大气环境将逐步得到关注.利用静电低压撞击器(ELPI)在线测量上海周边卫星城市太仓大气细颗粒物(PM2.5)粒子数浓度和质量浓度的粒径分布;结合太仓大气PM2.5样品中Ca、Ti、V、Cr、Mn、Fe、Co、Ni、Cu、Zn、As、Se、Sr、CA和Pb等15种元素的浓度...     

An estimation of the spatial and temporal distribution of biogenic non-methane hydrocarbon emissions in Greece

The present study presents the first detailed inventory for non-methane hydrocarbon emissions from vegetation over Greece. The emission inventory, based on a Geographic Information System (GIS), has a spatial resolution of 5×5 km² and a time resolution of 1 h. For the area under study, the calculated yearly monoterpene emissions are higher than the corresponding isoprene ones. In addition to the methodology presented here, the CORINAIR methodology was also applied for the calculation of emission rates. This resulted in orders of magnitude differences in the calculated emission rates. The CORINAIR methodology is judged to lead to unrealistically high values of biogenic NMHC emission rates. The temperature dependence of the CORINAIR correction factors seems to affect most the emissions, together with grazing land emission factors.     

Any factors influencing the dispersion and the transport of heavy hydrocarbons associated with airborne particles

Recent observations in Belgium indicated that particulate combustion residues are transported over large distances. The purpose of this paper is to examine in greater detail any factors — size distributions of heavy hydrocarbons, dynamic characteristics of the lowest atmosphere — influencing the advection of these pollutants.     

Effect of atmospheric electricity on dry deposition of airborne particles from atmosphere

The electric mechanism of dry deposition is well known in the case of unattached radon daughter clusters that are unipolar charged and of high mobility. The problematic role of the electric forces in deposition of aerosol particles is theoretically examined by comparing the fluxes of particles carried by different deposition mechanisms in a model situation. The electric mechanism of deposition appears essential for particles of diameter 10–200 nm in conditions of low wind speed. The electric flux of fine particles can be dominant on the tips of leaves and needles even in a moderate atmospheric electric field of a few hundred V m⁻¹ measured over the plane ground surface. The electric deposition is enhanced under thunderclouds and high voltage power lines. Strong wind suppresses the relative role of the electric deposition when compared with aerodynamic deposition. When compared with diffusion deposition the electric deposition appears less uniform: the precipitation particulate matter on the tips of leaves and especially on needles of top branches of conifer trees is much more intensive than on the ground surface and electrically shielded surfaces of plants. The knowledge of deposition geometry could improve our understanding of air pollution damage to plants.     

Isomer distribution of nitrotriphenylenes in airborne particles, diesel exhaust particles, and the products of gas-phase radical-initiated nitration of triphenylene

The formation of mutagenic nitro-polycyclic aromatic hydrocarbons (NPAHs) 1- and 2-nitrotriphenylene (1- and 2-NTP) via gas-phase OH or NO₃ radical-initiated reactions of triphenylene was demonstrated for the first time using a flow reaction system. In contrast with the results of conventional electrophilic nitration, 2-NTP was formed in larger yield than 1-NTP, but this is consistent with the mechanism proposed for gas-phase radical-initiated nitration of PAH. In diesel exhaust particle (DEP) samples, both 1- and 2-NTP were identified and their concentrations determined, as well as 1-nitropyrene (1-NP), which is a representative combustion-derived NPAH: the mean concentrations of 1-NTP, 2-NTP, and 1-NP were 4.7, 1.9, and 32 pmol mg_DEP^–1, respectively. The mean 2-NTP/1-NTP, 1-NTP/1-NP, and 2-NTP/1-NP ratios in samples of airborne particles collected in a residential area in Osaka, Japan, were>1.55,<0.25, and 0.37, respectively; these values are much higher than those of the DEP samples. This finding indicates that there is another source for airborne NTPs, especially 2-NTP, apart from diesel exhaust. These results strongly suggest that airborne NTPs originate from atmospheric processes such as radical-initiated reactions of triphenylene, and this has a significant influence on the atmospheric occurrence of NTPs.     

Efflorescence relative humidity of airborne sodium chloride particles: A theoretical investigation

The previously developed theoretical model [Gao, Y., Chen, S.B., Yu, L.E., 2006. Efflorescence relative humidity for ammonium sulfate particles. Journal of Physical Chemistry A, 110, 7602–7608], which has successfully predicted the efflorescence relative humidity (ERH) of ammonium sulfate ((NH₄)₂SO₄) particles at room temperature, is employed to estimate the ERH of sodium chloride (NaCl) particles in sizes ranging from 6 nm to 20 μm. The theoretical predictions well agree with the reported experimental data in literatures. When the NaCl particles are larger than 70 nm, the ERH decreases with decreasing dry particle sizes, and reach a minimum around 44% RH, otherwise the ERH increases with decreasing dry particle sizes (<70 nm) because of the Kelvin effect. Compared with (NH₄)₂SO₄ particles, the Kelvin effect on ERH is stronger for NaCl particles smaller than 30 nm, while the dry particle size exerts weaker influence on NaCl particles larger than 70 nm.     

Association of size-resolved airborne particles with foot traffic inside a carpeted hallway

The effect of foot traffic on indoor particle resuspension was evaluated by associating non-prescribed foot traffic with simultaneous size-resolved airborne particulate matter (PM) concentrations in a northern California hospital. Foot traffic and PM were measured every 15 min in a carpeted hallway over two 27-h periods. The PM concentration in the hallway was modeled based on the foot traffic intensity, including the previous PM concentration via an autocorrelation regression method based on the well-mixed box model. All 5 size ranges of PM, ranging from 0.75–1 μm to 5–7.5 μm, were highly correlated with foot traffic measurements for both monitoring periods (p < 0.001, R² = 0.87–0.90). However, correlations during daytime hours were less significant than nighttime. Coefficients found via this autoregressive analysis can be interpreted to reveal (i) time-independent contributions of walking activities on PM levels for a specific location; and (ii) size-specific characteristics of the resuspended PM.     

Cytotoxicity to alveolar macrophages of airborne particles and waste incinerator fly-ash fractions

A waste incinerator fly ash was separated into different grain-size fractions by sieving and sedimentation in butanol. The element content of each fraction was determined by atomic absorption and emission spectrometry. The fly-ash fractions, an eluted fine fly-ash fraction and an eluted airborne dust were analysed microscopically for particle size and numbers, together with standard quartz DQ 12 and three element-analysed airborne dusts. Rabbit alveolar macrophages, isolated by lung lavage, were incubated for 24 h with the particulates, the two eluates and a mixed element compound solution corresponding to the element concentrations of one airborne dust. At the end of incubation, the activities of lactate dehydrogenase, N-acetyl-beta-glucosaminidase, beta-galactosidase and acid phosphatase were determined in medium and cell lysates. Cytotoxicity was expressed as ratio of extracellular to total LDH (lactate dehydrogenase) activity. Release of N-acetyl-beta-glucosaminidase and beta-galactosidase was correlated positively with LDH release, whereas the total activity of acid phosphatase decreased with increasing LDH release. Cytotoxicity of the dusts was correlated with particle numbers, and As, Sb and Pb contents. The contribution of As to particle toxicity is discussed. Eluates of dusts did not affect rabbit alveolar macrophage viability.     

The effects of wind speed on the relative relationships between different sized-fractions of airborne particles

The concentrations of three different size fractions of particulate matter (PM) including PM2.5, PM10, and TSP were determined continuously at hourly intervals from four different sites in Seoul, Korea during the spring of 2001. To learn the effects of wind speed change on PM fractionation, the entire data sets were initially sorted into three particle fractions such as: fine (F: PM2.5), coarse (C: PM10-PM2.5), and giant (G: TSP-PM10). The inter-fraction relationships of PM were then explored by linear regression analysis of the data divided into four wind speed regimes. The results of this analysis, when examined in terms of either relative dominance between different PM fractions (i.e., in terms of their slope values) or strength of correlations, indicate the existence of diverse inter-fraction patterns. Most importantly, the physical influence of wind speed is seen to be reflected most efficiently between fine and coarse particle fractions, as the relative contribution of coarse fraction to the mass concentration of total particles (e.g., PM10) changes proportionally with changes in wind speed. However, such systematic patterns decrease noticeably between fine and giant fractions, as they can be affected more sensitively by such factors as the nature of their sources or the surrounding environmental conditions. The results of our comparative analysis thus confirm that wind speed is a useful barometer to distinguish and predict the behavior of different particle fractions in relation to each other.     

Assessment of exposure to airborne ultrafine particles in the urban environment of Lisbon, Portugal

The aim of this study was the assessment of exposure to ultrafine in the urban environment ofLisbon, Portugal, due to automobile traffic, and consisted of the determination of deposited alveolar surface area in an avenue leading to the town center during late spring. This study revealed differentiated patterns for weekdays and weekends, which could be related with the fluxes of automobile traffic. During a typical week, ultrafine particles alveolar deposited surface area varied between 35.0 and 89.2 microm2/cm3, which is comparable with levels reported for other towns such in Germany and the United States. These measurements were also complemented by measuring the electrical mobility diameter (varying from 18.3 to 128.3 nm) and number of particles that showed higher values than those previously reported for Madrid and Brisbane. Also, electron microscopy showed that the collected particles were composed of carbonaceous agglomerates, typical of particles emitted by the exhaustion of diesel vehicles.     

Natural and anthropogenic influences on heavy metals in airborne particles over the Korean Peninsula

Six monitoring stations were selected to characterize the variations in airborne concentrations of heavy metals in South Korea between 1999 and 2012. Three stations represented higher concentrations, and three represented lower concentrations. The heavy metals monitored at these stations include cadmium, chromium, copper, iron (Fe), lead, manganese (Mn), and nickel. During the study period, concentrations of heavy metals at many stations, including those around the Seoul metropolitan area, showed a decreasing trend. However, concentrations of Mn and Fe that are primarily of crustal origin increased at four of the six stations. Some stations were significantly affected by emissions from the local industrial complex (IC), and heavy metal concentrations at those stations were relatively high even in summer. Many heavy metal concentrations were higher in spring than in winter, but wintertime concentrations of Cr and Pb were higher at the stations representing lower concentrations due to the dominant influence of combustion emissions. At stations less affected by emissions from the IC, concentrations of Fe and Mn that are predominantly crustal in origin were higher in spring, when Asian dust (AD) events are most frequent. Although Mn concentrations were also high at stations within the steelmaking IC during AD periods, they were much higher during non-AD periods due to local emissions. Variations in heavy metal concentrations, which are heavily influenced by emissions from the IC, warrant individual analysis because their emission characteristics differ from those of typical cases.     

基于主成分分析法的辽河水体中溶解性金属来源分析

在测定辽河水体中几种主要的溶解性金属(包括7种重金属)的含量和分析其空间分布特征的基础上,运用主成分分析(PCA)法分析了金属的可能来源。结果表明,辽河水体中溶解性金属的平均浓度为Al>Cu>Zn>Cr>Hg>As>Pb>Cd,与欧美发达国家的主要水体相比,辽河水体的金属污染状况总体较重;辽河水体中溶解性金属的污染来源主要分两类:农业面源和工业废水污染源,工业综合污染源;根据主成分得分系数可知,采样点2(通江口)、3(三合屯)、7(朱尔山)的金属污染主要来源于农业面源和工业废水污染源;采样点6(药王庙)的金属污染主要来源于工业综合污染源;基于PCA法的金属来源分析对辽河流域水体金属污染治理对策的制定有着重要的指导意义。     

Improving estimation of indoor exposure to inhalable particles for children in the first year of life

There is growing scientific evidence linking early childhood exposure to environmental agents with asthma and other illnesses that may not appear until later in life. Unfortunately the direct measurement of personal exposures of children in the first year of life is not possible by existing methodologies. This study developed and evaluated a new methodology to better assess exposure of children to inhalable particles in the first year of life while involved in floor play in the home. We constructed the Pre-Toddler Inhalable Particulate Environmental Robotic (PIPER) sampler. Two series of measurements of inhalable particles were carried out. One collected filter samples of airborne inhalable particles and a second used a real-time total particle mass concentration monitor. Samples were collected for seven residential locations. Duplicate samples were collected with PIPER 20 cm above the floor and from an identical stationary monitor positioned at a height of 110 cm. The mean observed airborne inhalable particle concentrations measured by PIPER was 98.6 microg/ m3, whereas simultaneously collected stationary samples mean concentration was 49.8 microg/m3. The average observed ratio of PIPER samples to stationary samples was 2.4. A paired t test comparison of the two sampling methods indicated a statistically significant higher level of inhalable particle concentration measured by PIPER in comparison with the fixed sampler (P < 0.0001). Peak concentrations as measured by a real-time monitor were in excess of 3600 microg/m3. The results suggest that children playing on the floor are exposed to a higher concentration of total inhalable particles than previous methodologies estimate.