北京地区某高校教室细菌气溶胶浓度随季节变化特性实测调研

为探究高校教室细菌气溶胶浓度水平与粒径分布特性随季节的变化规律,对北京地区某高校教室室内外环境中的细菌气溶胶浓度、环境参数(温度、湿度、颗粒物浓度)进行了实测调研.结果表明:室外细菌气溶胶浓度为7?1 237 cfu/m3,平均最高浓度出现在秋季,最低浓度出现在夏季;教室无人时,室内细菌气溶胶主要源自室外,通过门窗缝隙...     

Source apportionment of ambient fine particle size distribution using positive matrix factorization in Erfurt, Germany

Particle size distribution data collected between September 1997 and August 2001 in Erfurt, Germany were used to investigate the sources of ambient particulate matter by positive matrix factorization (PMF). A total of 29,313 hourly averaged particle size distribution measurements covering the size range of 0.01 to 3.0 microm were included in the analysis. The particle number concentrations (cm(-3)) for the 9 channels in the ultrafine range, and mass concentrations (ng m(-3)) for the 41 size bins in the accumulation mode and particle up to 3 microm in aerodynamic diameter were used in the PMF. The analysis was performed separately for each season. Additional analyses were performed including calculations of the correlations of factor contributions with gaseous pollutants (O(3), NO, NO(2), CO and SO(2)) and particle composition data (sulfate, organic carbon and elemental carbon), estimating the contributions of each factor to the total number and mass concentration, identifying the directional locations of the sources using the conditional probability function, and examining the diurnal patterns of factor scores. These results were used to assist in the interpretation of the factors. Five factors representing particles from airborne soil, ultrafine particles from local traffic, secondary aerosols from local fuel combustion, particles from remote traffic sources, and secondary aerosols from multiple sources were identified in all seasons.     

The chemistry of precipitation in relation to precipitation type

Collections have been made of several types of wet deposition and of aerosols in various particle size ranges. The chemical composition of the precipitation changes significantly from one precipitation type to another. The forms of deposition, diffusionally-grown ice for example, compared with accretionally-grown ice, appear to be important factors controlling the concentrations and ratios of the several elements which have been measured.The aerosol samples show significant changes in chemical composition with particle size, consistent with other observers' results. It is hypothesized that these changes in aerosol chemistry and those of the wet deposition are related, and that this information, combined with the theoretically supported processes of nucleation, Brownian capture, phoretic processes and impaction, provide a better insight to the physical processes involved in the removal of chemical impurities from the atmosphere.     

Particle size distribution and composition in a mechanically ventilated school building during air pollution episodes

Particle count-based size distribution and PM(2.5) mass were monitored inside and outside an elementary school in Salt Lake City (UT, USA) during the winter atmospheric inversion season. The site is influenced by urban traffic and the airshed is subject to periods of high PM(2.5) concentration that is mainly submicron ammonium and nitrate. The school building has mechanical ventilation with filtration and variable-volume makeup air. Comparison of the indoor and outdoor particle size distribution on the five cleanest and five most polluted school days during the study showed that the ambient submicron particulate matter (PM) penetrated the building, but indoor concentrations were about one-eighth of outdoor levels. The indoor:outdoor PM(2.5) mass ratio averaged 0.12 and particle number ratio for sizes smaller than 1 microm averaged 0.13. The indoor submicron particle count and indoor PM(2.5) mass increased slightly during pollution episodes but remained well below outdoor levels. When the building was occupied the indoor coarse particle count was much higher than ambient levels. These results contribute to understanding the relationship between ambient monitoring station data and the actual human exposure inside institutional buildings. The study confirms that staying inside a mechanically ventilated building reduces exposure to outdoor submicron particles. PRACTICAL IMPLICATIONS: This study supports the premise that remaining inside buildings during particulate matter (PM) pollution episodes reduces exposure to submicron PM. New data on a mechanically ventilated institutional building supplements similar studies made in residences.     

Factors influencing particle number concentrations, size distributions and modal parameters at a roof-level and roadside site in Leicester, UK

Measurements of urban particle number concentrations and size distributions in the range 5-1000 nm were taken at elevated (roof-level) and roadside sampling sites on Narborough Road in Leicester, UK, along with simultaneous measurements of traffic, NO(x), CO and 1,3-butadiene concentrations and meteorological parameters. A fitting program was used to determine the characteristics of up to five modal groups present in the particle size distributions. All particle modal concentrations peaked during the morning and evening rush hours. Additional events associated with the smallest mode, that were not observed to be connected to primary emissions, were also present suggesting that this mode consisted of newly formed secondary particles. These events included peaks in concentration which coincided with peaks in solar radiation, and lower concentrations of the larger modes. Investigation into the relationships between traffic flow and occupancy indicated three flow regimes; free-flow, unstable and congested. During free-flow conditions, positive linear relationships existed between traffic flow and particle modal number concentrations. However, during unstable and congested periods, this relationship was shown to break-down. Similar trends were observed for concentrations of the gas phase pollutants NO(x), CO and 1,3-butadiene. Strong linear relationships existed between NO(x), CO, 1,3-butadiene concentrations, nucleation and Aitken mode concentrations at both sampling locations, indicating a local traffic related emission source. At the roadside, both nucleation and Aitken mode are best represented by a decreasing exponential function with wind speed, whereas at the roof-level this relationship only occurred for Aitken mode particles. The differing relationships at the two sampling locations are most likely due to a combination of meteorological factors and distance from the local emission source.     

Secondary organic aerosol in residences: predicting its fraction of fine particle mass and determinants of formation strength

Indoor secondary organic aerosol (SOA) formation may contribute to particle concentrations within residences, but little systematic work has investigated its magnitude or the determinants of its formation. This work uses a time‐averaged modeling approach to predict the indoor SOA mass formed in residences due to the oxidation of 66 reactive organic compounds by ozone or the hydroxyl radical, parameterizing SOA formation with the aerosol mass fraction. Other organic and inorganic aerosols owing to outdoor and indoor sources were also predicted. Model inputs were represented as distributions within a Monte Carlo analysis, so that result distributions and sensitivity of results to inputs could be quantified, using a dataset developed from the study of Relationships between Indoor, Outdoor and Personal Air and other sources. SOA comprised a large amount of indoor organic and total fine particles for a subset of the results (e.g., >47% of indoor organic and >30% of fine aerosol for 10% of the modeled cases), but was often a small fraction. The sensitivity analysis revealed that SOA formation is driven by high terpene emission rates (particularly by d‐limonene) and outdoor ozone, along with low air exchange and ozone and particle deposition rates.     

Analysis of indoor particle size distributions in an occupied townhouse using positive matrix factorization

From late 1999 to early March 2000, measurements of particle number (particles 0.01-20 microm in aerodynamic diameter) concentrations were made inside of a townhouse occupied by two non-smoking adults and located in Reston, VA (approximately 25 miles northwest of Washington, DC). The particle size measurements were made using an SMPS and an APS as well as a Climet optical scattering instrument. In this study, positive matrix factorization (PMF) was used to study the indoor particle size distributions. The size distributions or profiles obtained were identified by relating the obtained source contributions to the source information provided by the occupants. Nine particle sources were identified, including two sources associated with gas burner use: boiling water and frying tortillas. Boiling water for tea or coffee was found to be associated only with the smallest particles, with a number mode close to the detection limit of the SMPS (i.e., 0.01 microm). Frying tortillas produced particles with a number mode at about 0.09 microm while broiling fish produced particles with a number mode at about 0.05 microm. A citronella candle was often burned during the study period, and this practice was found to produce a 0.2-microm modal number distribution. Other indoor particle sources identified included sweeping/vacuuming (volume mode at 2 microm); use of the electric toaster oven (number mode at 0.03 microm); and pouring of kitty litter (volume mode over 10 microm). Two outdoor sources were also resolved: traffic (number mode at about 0.15 microm) and wood smoke (major number mode at about 0.07 microm). The volume distributions showed presence of coarse particles in most of the resolved indoor sources probably caused by personal cloud emissions as the residents performed the various indoor activities. PRACTICAL IMPLICATIONS: This study has shown that continuous measurements of indoor particle number and volume concentrations together with records of personal activities are useful for indoor source apportionment models. Each of the particle sources identified in this study produces distinct size distributions that may be useful in studying the mortality and morbidity effects of airborne particulate matter because they will have different penetrability and deposition patterns.     

The effect of ventilation on soiling by particles of outdoor and indoor origin in historical churches

The particle concentrations outside and inside two historical churches were monitored for at least ten months. The highest levels of outdoor concentrations were recorded in winter. This was caused by high levels of particle emissions from the burning of predominantly solid fuel for domestic heating in premises around the two churches monitored. These high levels of particle concentrations declined over the warmer periods of the year with the lowest concentrations occurring in the summer months. Owing to the marked winter–summer pattern for outdoor concentrations, the particles of outdoor origin accounted for 80%–90% of the overall indoor particle concentrations in the period of predominantly cold weather conditions (December to March) and for 50%–60% in the warm period (June to September). Reducing air exchange between the external space and the church interiors by keeping windows and doors closed had a limited effect on the reduction of average particle concentrations indoors (by less than 10%). A controlled air exchange system, which would increase the ventilation of a church when the particle concentration outdoors is lower than indoors and reduce ventilation when the outdoor air is polluted, would produce a further reduction of 10% in the indoor average particle concentration. The general conclusion is that the protection of the interiors of historical churches against soiling is primarily achieved by the improved particle filtering capacity of building envelopes and the gradual reduction of the overall outdoor particle concentration. Use of air cleaning systems with particle filtration may be a viable long-term option.     

Relationship between indoor and outdoor bio-aerosols collected with a button inhalable aerosol sampler in urban homes

This field study investigated the relationship between indoor and outdoor concentrations of airborne actinomycetes, fungal spores, and pollen. Air samples were collected for 24 h with a button inhalable aerosol sampler inside and outside of six single-family homes located in the Cincinnati area (overall, 15 pairs of samples were taken in each home). The measurements were conducted during three seasons - spring and fall 2004, and winter 2005. The concentration of culturable actinomycetes was mostly below the detection limit. The median indoor/outdoor ratio (I/O) for actinomycetes was the highest: 2.857. The indoor of fungal and pollen concentrations followed the outdoor concentrations while indoor levels were mostly lower than the outdoor ones. The I/O ratio of total fungal spores (median=0.345) in six homes was greater than that of pollen grains (median=0.025). The low I/O ratios obtained for pollen during the peak ambient pollination season (spring) suggest that only a small fraction penetrated from outdoor to indoor environment. This is attributed to the larger size of pollen grains. Higher indoor concentration levels and variability in the I/O ratio observed for airborne fungi may be associated with indoor sources and/or higher outdoor-to-indoor penetration of fungal spores compared to pollen grains. Practical Implication This study addresses the relationship between indoor and outdoor concentrations of three different types of bio-aerosols, namely actinomycetes, fungal spores, and pollen grains. The results show that actinomycetes are rare in indoor and outdoor air in Midwest, USA. Exposure to pollen occurs mainly in the outdoor air even during peak pollen season. Unexpectedly high fungal spore concentrations were measured outdoors during winter. The presented pilot database on the inhalable levels of indoor and outdoor bio-aerosols can help apportion and better characterize the inhalation exposure to these bio-aerosols. Furthermore, the data can be incorporated into existing models to quantify the penetration of biological particles into indoor environments from outdoors.     

Quantification of the impact of cooking processes on indoor concentrations of volatile organic species and primary and secondary organic aerosols

Cooking is recognized as an important source of particulate pollution in indoor and outdoor environments. We conducted more than 100 individual experiments to characterize the particulate and non‐methane organic gas emissions from various cooking processes, their reaction rates, and their secondary organic aerosol yields. We used this emission data to develop a box model, for simulating the cooking emission concentrations in a typical European home and the indoor gas‐phase reactions leading to secondary organic aerosol production. Our results suggest that about half of the indoor primary organic aerosol emission rates can be explained by cooking. Emission rates of larger and unsaturated aldehydes likely are dominated by cooking while the emission rates of terpenes are negligible. We found that cooking dominates the particulate and gas‐phase air pollution in non‐smoking European households exceeding 1000 μg m^?3. While frying processes are the main driver of aldehyde emissions, terpenes are mostly emitted due to the use of condiments. The secondary aerosol production is negligible with around 2 μg m^?3. Our results further show that ambient cooking organic aerosol concentrations can only be explained by super‐polluters like restaurants. The model offers a comprehensive framework for identifying the main parameters controlling indoor gas‐ and particle‐phase concentrations.     

Lung deposition of fine and ultrafine particles outdoors and indoors during a cooking event and a no activity period

Some indoor activities increase the number concentration of small particles and, hence, enhance the dose delivered to the lungs. The received particle dose indoors may exceed noticeably the dose from ambient air under routine in-house activities like cooking. In the present work, the internal dose by inhalation of ultrafine and fine particles is assessed, using an appropriate mechanistic model of lung deposition, accommodating aerosol, and inhalation dynamics. The analysis is based on size distribution measurements (10-350 nm) of indoor and outdoor aerosol number concentrations in a typical residence in Athens, Greece. Four different cases are examined, namely, a cooking event, a no activity period indoors and the equivalent time periods outdoors. When the cooking event (frying of bacon-eggs with a gas fire) occurred, the amount of deposited particles deep into the lung of an individual indoors exceeded by up to 10 times the amount received by an individual at the same time period outdoors. The fine particle deposition depends on the level of physical exertion and the hygroscopic properties of the inhaled aerosol. The dose is not found linearly dependant on the indoor/outdoor concentrations during the cooking event, whereas it is during the no activity period. PRACTICAL IMPLICATIONS: The necessity for determining the dose in specific regions of the human lung, as well as the non-linear relationship between aerosol concentration and internal dose makes the application of dosimetry models important. Lung dose of fine and ultrafine particles, during a cooking event, is compared with the dose at no indoor activity and the dose received under outdoor exposure conditions. The dose is expressed in terms of number or surface of deposited particles. This permits to address the dosimetry of very small particles, which are released by many indoor sources but represent a slight fraction of the particulate matter mass. The enhancement of the internal dose resulting from fine and ultrafine particles generated during the cooking event vs. the dose when no indoor source is active is assessed. The results for those cases are also compared with the dose calculated for the measured aerosol outdoors.     

Real-time characterization of aerosol particle composition,sources and influences of increased ventilation and humidity in an office

Most of human exposure to atmospheric pollutants occurs indoors, and the components of outdoor aerosols may have been changed in the way before reaching indoor spaces. Here we conducted real-time online measurements of mass concentrations and chemical composition of black carbon and the non-refractory species in PM_2.5 in an occupied office for approximately one month. The open-close windows and controlled dampness experiments were also performed. Our results show that indoor aerosol species primarily originate from outdoors with indoor/outdoor ratio of these species typically less than unity except for certain organic aerosol (OA) factors. All aerosol species went through filtration upon transport indoors. Ammonium nitrate and fossil fuel OA underwent evaporation or particle-to-gas partitioning, while less oxidized secondary OA (SOA) underwent secondary formation and cooking OA might have indoor sources. With higher particulate matter (PM) mass concentration outdoors than in the office, elevated natural ventilation increased PM exposure indoors and this increased exposure was prolonged when outdoor PM was scavenged. We found that increasing humidity in the office led to higher indoor PM mass concentration particularly more oxidized SOA. Overall, our results highlight that indoor exposure of occupants is substantially different from outdoor in terms of mass concentrations and chemical species.     

混合通风空调房间中粒子谱的空间变化

根据成都市夏季室外颗粒物浓度的实测结果,利用数值流体力学方法对混合通风空调房间的粒子进行了模拟,分析了室内粒子的空间演化及其与室外粒子的浓度关系。结果表明,室内粒子浓度对室外粒子浓度具有直接的依赖性,其中进风携带的小粒子浓度在室内下降较为明显。因此,在研究室内空气品质的同时,应考虑室外背景粒子浓度变化的影响。     

Vertical variations of particle number concentration and size distribution in a street canyon in Shanghai, China

Measurements of particle number size distribution in the range of 10-487 nm were made at four heights on one side of an asymmetric street canyon on Beijing East Road in Shanghai, China. The result showed that the number size distributions were bimodal or trimodal and lognormal in form. Within a certain height from 1.5 to 20 m, the particle size distributions significantly changed with increasing height. The particle number concentrations in the nucleation mode and in the Aitken mode significantly dropped, and the peaking diameter in the Aitken mode shifted to larger sizes. The variations of the particle number size distributions in the accumulation mode were less significant than those in the nucleation and Aitken modes. The particle number size distributions slightly changed with increasing height ranging from 20 to 38 m. The particle number concentrations in the street canyon showed a stronger association with the pre-existing particle concentrations and the intensity of the solar radiation when the traffic flow was stable. The particle number concentrations were observed higher in Test I than in Test II, probably because the small pre-existing particle concentrations and the intense solar radiation promoted the formation of new particles. The pollutant concentrations in the street canyon showed a stronger association with wind speed and direction. For example, the concentrations of total particle surface area, total particle volume, PM2.5 and CO were lower in Test I (high wind speed and step-up canyon) than in Test II (low wind speed and wind blowing parallel to the canyon). The equations for the normalized concentration curves of the total particle number, CO and PM2.5 in Test I and Test II were derived. A power functions was found to be a good estimator for predicting the concentrations of total particle number, CO and PM2.5 at different heights. The decay rates of PM2.5 and CO concentrations were lower in Test I than in Test II. However, the decay rate of the total particle number concentration in Test I was similar to that in Test II. No matter how the wind direction changed, for example, in the step-up case or wind blowing parallel to the canyon, the decay rates of the total particle number concentration were larger than those of PM2.5 and CO concentrations. For example, CO concentrations decreased by 0.33 and 0.69 at the heights ranging from 1.5 to 38 m in Test I and Test II, while the total particle number concentrations decreased by 0.72 and 0.85 within the same height ranges in Test I and Test II. It is concluded that the coagulation process, besides the dilution process, affected the total particle number concentration.     

Chemical characterization of indoor and outdoor fine particulate matter in an occupied apartment in Rome,Italy

The daily concentration and chemical composition of PM_2.5 was determined in indoor and outdoor 24‐h samples simultaneously collected for a total of 5 weeks during a winter and a summer period in an apartment sited in Rome, Italy. The use of a specifically developed very quiet sampler (<35 dB) allowed the execution of the study while the family living in the apartment led its normal life. The indoor concentration of PM_2.5 showed a small seasonal variation, while outdoor values were much higher during the winter study. Outdoor sources were found to contribute significantly to indoor PM concentration especially during the summer, when the apartment was naturally ventilated by opening the windows. During the winter the infiltration of outdoor PM components was lower and mostly regulated by the particle dimensions. Organics displayed In/Out ratios higher than unity during both periods; their indoor production increased significantly during the weekends, where the family stayed mostly at home. PM components were grouped into macrosources (soil, sea, secondary inorganics, traffic, organics). During the summer the main contributions to outdoor PM_2.5 came from soil (30%), secondary inorganics (29%) and organics (22%). Organics dominated both indoor PM_2.5 during the summer (60%) and outdoor and indoor PM_2.5 during the winter (51% and 66%, respectively).     

The effectiveness of stand alone air cleaners for shelter-in-place

Stand-alone air cleaners may be efficient for rapid removal of indoor fine particles and have potential use for shelter-in-place (SIP) strategies following acts of bioterrorism. A screening model was employed to ascertain the potential significance of size-resolved particle (0.1-2 microm) removal using portable high efficiency particle arresting (HEPA) air cleaners in residential buildings following an outdoor release of particles. The number of stand-alone air cleaners, air exchange rate, volumetric flow rate through the heating, ventilating and air-conditioning (HVAC) system, and size-resolved particle removal efficiency in the HVAC filter were varied. The effectiveness of air cleaners for SIP was evaluated in terms of the outdoor and the indoor particle concentration with air cleaner(s) relative to the indoor concentration without air cleaners. Through transient and steady-state analysis of the model it was determined that one to three portable HEPA air cleaners can be effective for SIP following outdoor bioaerosol releases, with maximum reductions in particle concentrations as high as 90% relative to conditions in which an air cleaner is not employed. The relative effectiveness of HEPA air cleaners vs. other removal mechanisms was predicted to decrease with increasing particle size, because of increasing competition by particle deposition with indoor surfaces and removal to HVAC filters. However, the effect of particle size was relatively small for most scenarios considered here. PRACTICAL IMPLICATIONS: The results of a screening analysis suggest that stand-alone (portable) air cleaners that contain high efficiency particle arresting (HEPA) filters can be effective for reducing indoor fine particle concentrations in residential dwellings during outdoor releases of biological warfare agents. The relative effectiveness of stand-alone air cleaners for reducing occupants' exposure to particles of outdoor origin depends on several factors, including the type of heating, ventilating and air-conditioning (HVAC) filter, HVAC operation, building air exchange rate, particle size, and duration of elevated outdoor particle concentration. Maximum particle reductions, relative to no stand-alone air cleaners, of 90% are predicted when three stand-alone air cleaners are employed.     

An experimental study of aerosol distribution over a Mediterranean urban area

In this study an attempt is made to investigate the aerosol spatial and size distributions at different heights over the Greater Athens Area (GAA), Greece, under sea breeze conditions and clear sky and to further discuss possible implications for aerosol characteristics. The data used are airborne measurements of aerosol collected during two flights that were performed within the context of the 1997 STAAARTE experimental campaign. The aerosol measurements cover particle diameters from 0.1 to 45.5 microm. The horizontal and vertical distribution revealed that higher concentrations exist within or just above the atmospheric boundary layer, while greater concentrations are observed over the sea compared to land at high altitudes. At all altitudes the number size distributions show dominant diameter ranges between 0.1 and 0.3 microm at all altitudes. The volume distributions are characterised by two modes, one in the accumulation and the other in the coarse particle regime. At lower altitudes, fresh combustion emissions more likely cause the predominance of the size range 0.1-0.3 microm while enhanced physical and chemical processes that favour the growth of smaller particles to larger sizes could also act. The relative humidity does not seem to affect the observed number size distributions at low altitudes, where relative humidity is below 70% while at 4000 m the distributions seem to change over the sea where the humidity increases.     

Urban air quality and carboxyhemoglobin levels in a group of traffic policemen

Toxicological potential of carbon monoxide (CO) on humans is well known. Nevertheless, CO is still considered as a useful marker to detect some environmental and occupational human risk factors typical of cities. The role played by traffic pollution, indoor air quality in offices and tobacco smoke on the expression of carboxyhemoglobin (COHb%) levels was investigated in a large group of traffic policemen in Torino city (North-Western Italy). At the end of the working shift, 228 policemen responded to a questionnaire, weight and height recorded, urine spot samples collected to measure cotinine as biomarker of tobacco smoke exposure, and an arterial blood sample was taken to measure COHb levels. Data of outdoor urban air-CO were collected and to each subject a "CO outdoor air measurement" was related to his/her COHb level. Considering the annual trend of air-CO pollution from 2002 to 2004, one can assume that a general improvement of air quality in Torino was evident. Taking into account the environments where policemen work (urban outdoor and indoor), and analyzing their COHb% content, the traffic-congested areas, and, in general, the outdoor urban environment were equally risky as offices. Furthermore, if compared to CO arising from traffic-congested areas or other outdoor environments, the traffic policemen in Torino city demonstrate COHb% levels largely due to smoking habits.     

Experimental investigation of two-stage indirect/direct evaporative cooling system in various climatic conditions

Cooling performance of two-stage indirect/direct evaporative cooling system is experimentally investigated in the various simulated climatic conditions. For this purpose, a two-stage evaporative cooling experimental setup consisting of an indirect evaporative cooling stage (IEC) followed by a direct evaporative cooling stage (DEC) was designed, constructed and tested. Due to the wide variety of climatic conditions in Iran, two air simulators were provided to simulate outdoor design condition of different cities in primary and secondary air streams. Results show that under various outdoor conditions, the effectiveness of IEC stage varies over a range of 55–61% and the effectiveness of IEC/DEC unit varies over a range of 108–111%. Aspects of achieving comfort conditions and power saving have been investigated with related excess water consumption. Considering the evaporative comfort zone, this system can provide comfort condition in a vast region in Iran where direct evaporative alone is not able to provide summer comfort condition. More than 60% power saving could be obtained by this system in comparison with mechanical vapor compression systems with just 55% increase in water consumption with respect to direct evaporative cooling systems. This system can fill the gap between direct evaporative cooling systems and mechanical vapor compression systems as an energy efficient and environmentally clean alternate.     

气溶胶颗粒在风管系统中沉降的实验研究

气溶胶颗粒是室内外空气中存在的一类重要污染物。为了研究气溶胶颗粒在风管系统中分布和沉降的规律,本文以滑石粉为代表,通过在接近实际工程的矩形镀锌钢板风管系统中释放气溶胶颗粒对其在风管系统中的沉降进行了初步实验研究。实验在不同风速下共进行了两次,并主要在风管系统中的水平直段和局部构件处测量了滑石粉的沉降量。根据滑石粉的沉降量计算出滑石粉的沉降速度,并且对比和分析了不同风速下,风管系统中不同位置的滑石粉的沉降速度。实验表明,气溶胶颗粒在水平直段的底面上的沉降速度最大,侧面上的其次,顶面上的最小;并且气溶胶颗粒的沉降速度随着风速的减小而减小。根据实验数据,分析了影响气溶胶颗粒沉降速的主要因素,包括:风速、沉降面的朝向、局部构件的形状、管道漏风。