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.     

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.     

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.     

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.     

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.     

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。     

Electrostatic precipitation of airborne charged dust particles trapped in stationary or quasi-stationary vortices

In conventional industrial electrostatic dust precipitators, shielded collecting plates are commonly employed in order to minimize erosion of collected dust by the flowing gas, and thus to maintain maximum collection efficiency. It is shown that the gains in efficiency thus produced are not necessarily all due to this reduction in reentrainment losses, but that there may be enhancement of the basic initial collection process by the trapping of dust into the stationary or quasi-stationary vortices formed in the wakes of the shielding slats.     

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.     

Influence of secondary formation on atmospheric occurrences of oxygenated polycyclic aromatic hydrocarbons in airborne particles

Temporal and spatial variations in concentrations of particle-associated polycyclic aromatic hydrocarbons (PAHs) and their nitrated and oxygenated derivatives (nitro-PAHs and oxy-PAHs) were investigated to assess the influence of secondary formation on atmospheric occurrences of oxy-PAHs associated with particulate matter in downtown Tokyo, Japan. The daily variation in concentration of 1,8-naphthalic anhydride (1,8-NA) in summer 2007 was similar to that for 2-nitrofluoranthene (2-NF), a representative secondary formed nitro-PAH, while the variation for benzanthrone (BA) was similar to PAHs. In addition, the concentrations of polycyclic aromatic compounds (PACs) associated with airborne particulate matter decreased in the order of PAHs > BA > 9-fluorenone (9-FO) or 9,10-anthraquinone (9,10-AQ) > 1,8-NA with an increase in distance from the roadside, whereas 2-NF was constant. These results suggest that a considerable fraction of some oxy-PAHs such as 1,8-NA associated with airborne particulate matter in downtown Tokyo originates from atmospheric secondary formation.     

Generic scenario for the impact of cooling lubricants into the hydrosphere

According to directive 93/67/EEC of the European Commission, this paper deals with the generic exposition evaluation of the environmental concentration of cooling Lubricant chemicals from the metal working industry into the hydrosphere. After considering the relevant life-cycle steps and the selection of a representative point source for the 'reasonable worst case', the emission per day Elocal(water) is determined. It leads to the predicted environmental concentration (PEClocal(water)) for the local stage in the compartment water. In order to gain the PEClocal(water) for an example--a corrosion inhibitor as additive in a cooling lubricant--, the relevant emission paths and the corresponding representative point source are described for the reasonable worst case. For non-water-miscible cooling lubricants, none of the operations in the life cycle leads to a release into the compartment water. To evaluate the hazard potential for cooling lubricant chemicals, the complete risk assessment has to be done. Also, the assessment has to be done for all high production volume chemicals, new substances and existing hazard chemicals. This means that even industrial categories like chemicals used in the textile industry or biocides and others have to be evaluated.     

Application of principal component analysis for the estimation of source of heavy metal contamination in surface sediments from the Rybnik Reservoir

The concentrations of metals, loss of ignition and nutrient (N, P) were determined in the bottom sediments of the Rybnik Reservoir (southern Poland). The mean concentrations of the metals in the bottom sediments were: Cd 25.8 microgram/g, Cu 451.7 microgram/g, Zn 1583.4 microgram/g, Ni 71.1 microgram/g, Pb 118.6 microgram/g, Cr 129.8 microgram/g, Fe 38782 microgram/g and Mn 2018.7 microgram/g. The bottom sediments are very heavily loaded with zinc, manganese, copper, nickel, phosphorus and lead (percentage enrichment factor), and cadmium, phosphorus and zinc (index of geoaccumulation). The increase of cadmium, lead, nickel and zinc concentrations was connected with the inflow of the contaminated water of the river Ruda and long-range transport. The contamination of the reservoir with copper and manganese resulted mainly from atmospheric precipitation. The variability of the bottom sediment loading with metals during the investigations was affected in the first place by changes in the concentration of iron, but also those elements whose concentrations in the bottom sediment were elevated compared to the concentrations in shale--cadmium, nickel and lead.     

Detection of a carcinogen, 2-amino-1-methyl-6-phenylimidazo [4,5-b]pyridine, in airborne particles and diesel-exhaust particles

A carcinogen, 2-amino-1-methyl-6-phenylimidazo [4,5-b]-pyridine (PhIP), has been measured in airborne particles, diesel-exhaust particles, and incineration ash from garbage-burning plants. PhIP was found in all kinds of samples. In the light of the present results, together with the previous findings that PhIP was present in cooked foods and cigarette smoke, PhIP is likely to be an ubiquitous environmental pollutant. These observations also suggest that PhIP may be formed through the combustion process.     

Physicochemical characteristics,mutagenicity and genotoxicity of airborne particles under industrial and rural influences in Northern Lebanon

In this work, the main objectives were to assess the mutagenic and genotoxic effects of fine particulate matter collected in an industrial influenced site in comparison with a non-industrial influenced one (rural site) and to relate the particulate matter (PM) composition to the observed genotoxic effects. At the industrial influenced site, higher concentrations of phosphates, trace metals, and polycyclic aromatic hydrocarbons (PAHs) in particles could be related to the contributions of quarries, fertilizer producer, cement plants, and tires burning. Gasoline and diesel combustion contributions were evidenced in particles collected at both sites. Particles collected under industrial influence showed a higher mutagenic potential on three tested strains of Salmonella typhimurium (TA98, YG1041, and TA102), and especially on the YG1041, compared to particles from the rural site. Furthermore, only particles collected in the vicinity of the industrial site showed a tendency to activate the SOS responses in Escherichia coli PQ37, which is indicative of DNA damage as a result of exposure of the bacteria cells to the action of mutagenic samples. The mutagenicity and genotoxicity of the industrial PM_2.5–0.3 particulates may be attributed to its composition especially in organic compounds. This study showed that proximity of industries can affect local PM composition as well as PM genotoxic and mutagenic potential.     

Comparison of two estimation methods for surface area concentration using number concentration and mass concentration of combustion-related ultrafine particles

Recent research has suggested that the adverse health effects caused by nanoparticles are associated with their surface area (SA) concentrations. In this study, SA was estimated in two ways using number and mass concentrations and compared with SA (SA_meas) measured using a diffusion charger (DC). Aerosol measurements were made twice: once starting in October 2002 and again starting in December 2002 in Mysore, India in residences that used kerosene or liquefied petroleum gas (LPG) for cooking. Mass, number, and SA concentrations and size distributions by number were measured in each residence. The first estimation method (SA_PSD) used the size distribution by number to estimate SA. The second method (SA_INV) used a simple inversion scheme that incorporated number and mass concentrations while assuming a lognormal size distribution with a known geometrical standard deviation. SA_PSD was, on average, 2.4 times greater (range = 1.6–3.4) than SA_meas while SA_INV was, on average, 6.0 times greater (range = 4.6–7.7) than SA_meas. The logarithms of SA_PSD and SA_INV were found to be statistically significant predictors of the logarithm of SA_meas. The study showed that particle number and mass concentration measurements can be used to estimate SA with a correction factor that ranges between 2 and 6.