物料下落过程中可吸入颗粒物产生特性及控制技术

利用实验室新设计开发的一套装置,研究物料自由下落过程影响可吸入颗粒物产生的因素.通过实验分别测定不同物料、质量流量、含水量、粒径组成和下垫面5个因素对可吸入颗粒物产生的影响.实验结果表明,不同物料可吸入颗粒物产生率不同;随着质量流量和物料含水量的增加,可吸入颗粒物产生率减小,加水是减少可吸入颗粒物排放的最有效方法之一;不同粒径组成和不同下垫面对可吸入颗粒物产生也有影响,但作用并不显著.     

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.     

Design scenario for the radioisotopic estimation of the biogenic component of airborne particles

An experimental design is described to estimate the fraction of secondary fine particle from the biogenic component of volatile organic compounds (VOCs) in the atmosphere using radiocarbon isotopic abundance ratios. The method distinguishes between "modern" carbon (C), and "old" C of primary and secondary origins based on three components, condensed-phase organic carbon (OC), semi-volatile particulate compounds (SVOCs), and VOCs. The method depends on interpretation of diurnal and seasonal variation in OC, SVOC, and VOC concentrations. Sampling employs a filter-denuder unit, which collects the three C components for isotopic analysis. The samples are collected repetitively for a daily sequence of the same hourly intervals covering diurnal periods with similar meteorological conditions. Collected C is thermally treated to separate OC from black carbon on filters and VOCs or SVOCs from adsorbents, with all four fractions individually oxidized to carbon dioxide to determine the radiocarbon content by accelerator mass spectrometry. Using C isotope abundance, the data are interpreted for fractions of primary modern C and secondary modern C as estimated from averaging diurnal and seasonal variations in the concentration data. As support for interpretation, samples of OC, SVOCs, and VOCs would be analyzed for speciation to identify source indicator species present.     

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.     

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.     

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.     

Comparison of sampling collection strategies for assessing airborne trichloramine levels in indoor swimming pools

Environmental Science and Pollution Research - Since 1995, Hery’s trichloramine sampling procedure has been widely used to determine trichloramine exposure in indoor swimming pools. This...     

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...     

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.     

Ultrafine particles at three different sampling locations in Taiwan

Atmospheric ultrafine particles (UPs or PM_0.1) were investigated at the roadside of Syuefu road in Hsinchu city, in the Syueshan highway tunnel in Taipei and in the NTU Experimental Forest in Nantou, Taiwan. A SMPS (TSI 3936) and three MOUDIs (MSP 110) were collocated to determine the number and mass concentrations of the PM_0.1 simultaneously. The filter samples were further analyzed for organic carbon (OC), element carbon (EC), water-soluble ions and trace elements. Taking into account the OC artifact of PM_0.1, good chemical mass closure (ratio of the reconstructed chemical mass to the gravimetrical mass of PMs) was obtained with an unknown percentage of 10.6, 26.2 and 37.2% at the roadside, tunnel and forest, respectively. The unexplained mass was attributed to aerosol water in this study. The artifact at the roadside, tunnel and the forest PM_0.1 mass was found to be as high as 51.6 ± 10.7%, 20.0 ± 5.4% and 85.6 ± 18.4%, respectively. Finally, the effective density of the roadside, tunnel and forest PM_0.1 was calculated based on the results of chemical speciation and found to be 1.45, 1.29 and 1.22 g cm^?3, respectively, which was in good agreement with that obtained by using the method of Spencer et al. (2007). Based on these results, it is foreseeable that the number concentration of the SMPS can be converted using the effective density determined by Spencer et al. (2007) for the real time measurement of the PM_0.1 concentration.     

杭州城市可吸入颗粒物污染与气象条件关系的分级评价和BP神经网络评估

为了解杭州城市环境空气质量与气象条件之间的关系,利用杭州市区2003-2007年的可吸入颗粒物(PM10)浓度数据和气象资料,通过分级评价的方法和基于BP神经网络的污染物浓度评估模型,得到PM10浓度与气象条件的对应关系.结果表明,随着日降水量的增大,PM10浓度减小;风速与PM10浓度呈明显的负相关,随着风速的增大,PM10浓度明显减小;气象因素与PM10浓度之间呈非线性关系,大气能见度对PM10和相对湿度的变化极为敏感.随着PM10浓度的增大,大气能见度迅速降低,相对湿度越高,大气能见度则越低;近几年杭州市气象条件不利于大气污染物的扩散和清洗,是杭州城市环境空气质量上升缓慢的主要原因之一.