Assessment of environmental tobacco smoke contamination in public premises: significance of 2,5-dimethylfuran as an effective marker

Contamination by environmental tobacco smoke (ETS) on premises where smoking is permitted is evaluated. Although all target VOCs evaluated show significant differences between smoking and nonsmoking indoors, the results obtained indicate that 2,5-dimethylfuran is the most appropriate and effective marker of ETS contamination given that this compound is only detected in environments where people have smoked and so the detection of this compound cannot be attributed to other contamination sources such as traffic. Moreover, the air levels of this compound due to coffee aroma are below the detection limits for this methodology. A preliminary study is performed to evaluate whether 2,5-dimethylfuran, a smoking breath biomarker, can be detected in passive smokers working in smoking environments. The compound was continuously detected in the breath of nonsmoking employees after being in direct contact with ETS for just a few hours. The Tedlar gas sampling bags had 5% loss of 2,5-dimethylfuran after 3 h of storage, which we took as the maximum recommended period for air sample storage.     

Calibration of a passive sampler for both gaseous and particulate phase polycyclic aromatic hydrocarbons

A novel passive air sampler was designed and tested that individually collects the gaseous and particulate phase polycyclic aromatic hydrocarbons (PAHs) in air. The sampler was calibrated against a conventional active sampler in an indoor environment. A PUF (polyurethane foam) disk and a piece of GFF (glass fiber filter) were installed in a sampling shelter for collecting gaseous and particulate phase PAHs, respectively. The passive samplers were deployed in seven indoor locations for 86 days. Six times during this period, 24-h conventional active sampling was conducted for calibration at an average interval of 17-days. Principle component analysis showed that the measured congener profile compositions were totally different between the gaseous and particulate phase PAHs, but similar between the passive and the active samples. This suggested that gaseous and particulate phase PAHs were primarily trapped by the PUF disk and GFF, respectively. Linear relationships between the passively and the actively measured and log-transformed concentrations were derived for calibration of both gaseous and particulate phase PAHs. The uptake rates of the sampler were 0.10 +/- 0.014 m3/d and 0.007 +/- 0.001 m3/d for gaseous and particulate phase PAHs, respectively. The rates were significantly lower than those reported in the literature using similar PUF samplers, mainly because of the special design with limited air circulation.     

Field testing passive air samplers for current use pesticides in a tropical environment

Air was sampled for one year in the central valley of Costa Rica using an active high-volume sampler as well as passive samplers (PAS) based on polyurethane foam (PUF) disks and XAD-resin filled mesh cylinders. Extracts were analyzed for pesticides that are either banned or currently used in Costa Rican agriculture. Sampling rates for PUF-based passive air samplers, determined from the loss of depuration compounds spiked on the disks prior to deployment averaged 5.9 +/- 0.9 m3 x d(-1) and were higher during the windier dry season than during the rainy season. Sampling rates for the XAD-based passive sampler were determined from the slopes of linear relationships that were observed between the amount of pesticide sequestered in the resin and the length of deployment, which varied from 4 months to 1 year. Those sampling rates increased with decreasing molecular size of a pesticide, and their average of 2.1 +/- 1.5 m3 x d(-1) is higher than rates previously reported for temperate and polar sampling sites. Even though the trends of the sampling rate with molecular size and temperature are consistent with the hypothesis that molecular diffusion controls uptake in passive samplers, the trends are much more pronounced than a direct proportionality between sampling rate and molecular diffusivity would suggest. Air concentrations derived by the three sampling methods are within a factor of 2 of each other, suggesting that properly calibrated PAS can be effective tools for monitoring levels of pesticides in the tropical atmosphere. In particular, HiVol samplers, PUF-disk samplers, and XAD-based passive samplers are suitable for obtaining information on air concentration variability on the time scale of days, seasons and years, respectively. This study represents the first calibration study for the uptake of current use pesticides by passive air samplers.     

Adaptation of an osmotically pumped continuous in situ water sampler for application in riverine environments

We present the design of an osmotic water sampler that is adapted to and validated in freshwater. The sample is drawn into and stored in a continuous narrow bore tube. This geometry and slow pump rate (which is temperature dependent: 0.8 mL/d at 4 °C to 2.0 mL/d at 28 °C) minimizes sample dispersion. We have implemented in situ time-stamping which enables accurate study of pump rates and sample time defining procedures in field deployments and comparison with laboratory measurements. Temperature variations are common in rivers, and without an accurate time-stamping, or other defining procedure, time of sampling is ambiguous. The sampler was deployed for one month in a river, and its performance was evaluated by comparison with manually collected samples. Samples were analyzed for major ions using Ion Chromatography and collision reaction Inductively Couple Mass Spectrometry. Despite the differences of the two sampling methods (osmotic sampler averages, while manual samples provide snapshots), the two data sets show good agreement (average R(2) ≈ 0.7), indicating the reliability of the sampler and at the same time highlighting the advantages of high frequency sampling in dynamic environments.     

The dog as a passive smoker: effects of exposure to environmental cigarette smoke on domestic dogs.

Of the few studies available regarding the effects of smoking on animals, most of them involve animals actively smoking through the use of a mask or tracheostomy. The present study investigated the effects of passive smoke exposure on domestic dogs. The sample comprised 30 Yorkshire terriers (18 males) ranging in age from 27 to 106 months (M = 38.6+/-15.8) and weighing 1.9-4.0 kg (M = 3.04+/-0.48). Half of the dogs came from homes where residents smoked at least 20 cigarettes/day for a minimum of 24 months, and the other half were from homes without smokers. All animals were subjected to bronchoalveolar lavage to determine cell populations and the presence of anthracosis in macrophage cytoplasm; in addition, a carinal biopsy was obtained. To characterize environmental cigarette smoke exposure, urinary cotinine was determined by an immunochromatographic assay. Cotinine was not detected in the urine of dogs not exposed to cigarette smoke, whereas exposed dogs tested positive. In dogs exposed to cigarette smoke, macrophage and lymphocyte populations were significantly increased (p<.05) and anthracosis was present in the cytoplasm of macrophages. The measurement of urinary cotinine by an immunochromatographic assay is an effective method that can be used to confirm environmental tobacco exposure. Cytological analysis of bronchoalveolar lavage fluid demonstrated airway alterations triggered by passive exposure to tobacco smoke in domestic animals.     

Automated sampler for the measurement of non-methane organic compounds

An automated sampler has been constructed for the unattended collection of whole-air samples in Summa passivated stainless steel canisters. The sampler consists of a Viton diaphragm pump; a differential-pressure flow controller; a 2-position, 3-port valve; a 10-port multiposition valve; and a digital valve sequence programmer that controls the sequence and timing of the electrically actuated valves. All connecting tubing was constructed from Silcosteel tubing. Two configurations of the automated sampler and a passive collection system were evaluated by comparing the combined sampling precisions of the three systems with the analytic precision, derived from replicate analyses of an ambient air sample. The analytic precision was generally < +/- 5%, with higher values observed for analytes with mixing ratios in the tens of pptv. However, analytic precision values for methanol and ethanol were poor, greater than +/- 20%. Values for sampling precision were greater by about a factor of 2 than the analytic precision. The poor results for the light oxygenated hydrocarbons could be caused by sorption of the analytes in the preconcentration and sampling systems and difficulties in peak integration.     

与环境烟气相关的挥发性有机物的特性

本项研究测定了环境烟气(ETS)中的多种挥发性有机物,在环境实验室中目标化合物的唯一来源就是ETS。实验室中的ETS是由燃吸肯塔基参考卷烟和其他8种市售卷烟产生的。在12轮试验中同时测定了30多种化合物。目标化合物分为3类,即:气相ETS标识物3乙基吡啶(简称3-EP)与烟碱、羰基化合物(包括甲醛)和挥发性有机化合物(简称VOCs)。利用环境实验室研究结果可以确定各种VOCs与3-EP(气相ETS标记物)的特征比率,另外还可以用来估测与ETS相关的VOCs的散发因子。总体说来,本项研究测得的特征比率与以往已经发表的实验室研究数据是一致的,这意味着,"真实"室内环境受多种来源的复杂的混合物影响。本项研究测定的特征比值也可以用于ETS目标化合物的定性和定量分析      

A passive sampler for the determination of airborne ammonia concentrations near large-scale animal facilities

Few data are available on the ammonia emissions of large-scale outdoor animal facilities in arid climates such as those found in California's San Joaquin Valley. Passive samplers provide an ideal tool for studying such large and heterogeneous area sources, because they are inexpensive, portable, and fully self-contained. UC Davis passive ammonia samplers incorporate modifications on a previous design, the Willems Badge, for ease of analysis. Citric acid was chosen as a coating medium though it performed as well as oxalic, sulfuric, and tartaric acids. Zefluor PTFE prefilters were used instead of Teflo though both showed the same resistance to diffusion. Citric acid-coated filters were stable for up to 10 weeks, though more so if stored in Petri dishes rather than in the sampling cassettes themselves. The most effective sampler position was found to be in a face-down configuration fixed into the wind to avoid debris and sensitivity to wind shifts. A new method of rinsing the filters within the cassettes by dropwise elution proved highly effective, with 85% of the ammonium being removed in the first 3 mL of the 10-mL rinse volume. Application of the sampler at a dairy in the Joaquin Valley revealed large variations in concentrations at different locations along the downwind fenceline, which correlated with animal populations and activities directly upwind. In addition, large variations in ammonia concentrations were observed in relation to time of day and animal activity. Field blank loadings were of 1.40 microg NH4-N/filter (SD = 0.74 microg NH4-N/filter). Replicate passive samplers placed side-by-side during sampling episodes agreed with a slope of 1.010 (standard error = 0.028). Impingers were used as a reference method to obtain the correlation between filter loadings and air concentrations, yielding an "effective sampling rate" for the passive samplers of 6.18 L/h (error = 0.23 L/h). Using a theoretical calculation, that "effective flow rate" was calculated to be 6.29 L/h. The method's limit of detection was found to be 82.5 microg NH4-N/m3. Wind speed was found to theoretically affect linearity of sampler response only for speeds less than 0.92 m/s.     

Rapidly equilibrating micrometer film sampler for priority pollutants in air

Modified polymer-coated glass samplers (POGs), termed EVA samplers, consist of micrometer-thin layers of ethylene vinyl acetate (EVA) coated onto a glass fiber filter or aluminum foil substrate. These samplers were designed to equilibrate rapidly with priority pollutants in air, making them ideal for short-term spatial studies in ambient or indoor air. The EVA sampler was calibrated by measuring the uptake of polychlorinated biphenyls (PCBs) over 8 weeks in an indoor environment, and four different film thicknesses were monitored that ranged from 0.1 to 30 μm. The results were used to calculate the average mass transfer coefficient (50.5 m/day) and generate contour maps that provide guidance in choosing an appropriate EVA sampler for a particular study based on film thickness, deployment time, and the log K(OA) of the anlayte. A range of air pollutant classes was also added to the EVA sampler prior to deployment to assess depuration rates. These included polychlorinated biphenyls (PCBs), current-use pesticides (CUPs), perfluorinated compounds (PFCs), and polybrominated diphenyl ethers (PBDEs). On the basis of the depuration profiles, the EVA sampler was a suitable equilibrium sampler for several CUPs and PCBs; however, for the high molecular weight PCBs and PBDEs, the EVA sampler operates as a linear uptake sampler. Samplers were also evaluated for their use as a rapid screening tool for assessing concentrations of siloxanes in indoor air. The EVA sampler was used to estimate air concentrations for D4 and D5 in laboratory air to be 118 and 89 ng/m(3), respectively. Analyses were performed directly using thermal desorption gas chromatography/mass spectrometry (TDS-GC-MS). EVA samplers show promise due to their relatively low cost and ease of deployment and applicability to a wide range of priority chemicals. The ability to alter the film thickness, and hence the sorption capacity and performance of the EVA sampler, allows for a versatile sampler that can be used under varying sampling conditions and deployment times.     

Characterization and comparison of three passive air samplers for persistent organic pollutants

The accumulation of persistent organic pollutants by three passive sampling media--semipermeable membrane devices (SPMDs), polyurethane foam (PUF) disks, and an organic-rich soil--was investigated. The media were exposed to contaminated indoor air over a period of 450 days, and concentrations in the air and in the media were monitored for individual polychlorinated biphenyl (PCB) congeners and polychlorinated naphthalene homologue groups. Uptake was initially linear and governed by the surface area of the sampler and the boundary layer airside mass transfer coefficient (MTC). Mean values of the MTC were 0.13, 0.11, and 0.26 cm s-1 for SPMD, PUF, and soil, respectively. As the study progressed, equilibrium was established between ambient air and the passive sampling media for the lower molecular weight PCB congeners. This information was used to calculate passive sampler-air partition coefficients, KPSM-A. These were correlated to the octanol-air partition coefficient, and the resulting regressions were used to predict KPSM-A for the full suite of PCBs. Information on MTC, KPSM-A, surface area, and effective thickness of each sampler was used to estimate times to equilibrium for each medium. These ranged from tens of days for the lower molecular weight congeners to tens of years for the higher molecular weight PCBs. Expressions were also developed to relate the amount of chemical accumulated by the passive sampling media to average ambient air concentrations over the integration period of the sample.     

Assessing the influence of meteorological parameters on the performance of polyurethane foam-based passive air samplers

Polyurethane foam (PUF) disk passive air samplers were evaluated under field conditionsto assessthe effect of temperature and wind speed on the sampling rate for polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and organochlorine pesticides (OCPs). Passive samples integrated over 28-day periods were compared to high-volume air samples collected for 24 h, every 7 days. This provided a large data set of 42 passive sampling events and 168 high-volume samples over a 3-year period, starting in October 2003. Average PUF disk sampling rates for gas-phase chemicals was approximately 7 m3 d(-1) and comparable to previous reports. The high molecular weight PAHs, which are mainly particle-bound, experienced much lower sampling rates of approximately 0.7 m3 d(-1). This small rate was attributed to the ability of the sampling chamber to filter out coarse particles with only the fine/ultrafine fraction capable of penetration and collection on the PUF disk. Passive sampler-derived data were converted to equivalent air volumes (V(EQ), m3) using the high-volume air measurement results. Correlations of V(EQ) against meteorological data collected on-site yielded different behavior for gas- and particle-associated compounds. For gas-phase chemicals, sampling rates varied by about a factor of 2 with temperature and wind speed. The higher sampling rates at colder temperatures were explained bythe wind effecton sampling rates. Temperature and wind were strongly correlated with the greatest winds at coldertemperatures. Mainly particle-phase compounds (namely, the high molecular weight PAHs) had more variable sampling rates. Sampling rates increased greatly atwarmertemperatures as the high molecular weight PAH burden was shifted toward the gas phase and subject to higher gas-phase sampling rates. At colder temperatures, sampling rates were reduced as the partitioning of the high molecular weight PAHs was shifted toward the particle phase. The observed wind effect on sampling for the particle-phase compounds is believed to be tied to this strong temperature dependence on phase partitioning and hence sampling rate. For purposes of comparing passive sampler derived data for persistent organic pollutants, the factor of 2 variability observed for mainly gas-phase compounds is deemed to be acceptable in many instances for semiquantitative analysis. Depuration compounds may be used to improve accuracy and provide site-specific sampling rates, although this adds a level of complexity to the analysis. More research is needed to develop and test passive air samplers for particle-associated chemicals.     

A flow-through sampler for semivolatile organic compounds in air

A widely acknowledged limitation of current passive air sampling designs for semivolatile organic chemicals is their relatively low sampling rate, severely constraining the temporal resolution that can be achieved. Addressing the need for an improved sampling design which achieves significantly faster uptake while maintaining the capability of providing quantitative information, a new sampler has been developed that provides greatly increased sampling rates by forcing the wind to blow through the sampling medium. The sampler consists of a horizontally oriented, aerodynamically shaped, stainless steel flow tube mounted on a post with ball bearings, which turns into the wind with the help of vanes. A series of polyurethane foam (PUF) discs with relatively large porosity mounted inside the flow tube serve as the sampling medium. The sampled air volume is calculated from wind speed, which is measured outside the sampler and after passage through the sampling medium using precalibrated vortex rotor and turbine anemometers mounted on top of the sampler and at the exit of the flow tube, respectively. Small battery-operated data loggers are used for data storage. Under typical wind speed conditions, the sampler can collect 100 m(3)/ day, which is approaching the sampling rates of conventional high volume samplers. Controlled experiments in the laboratory and frontal chromatography theory yield the theoretical plate number and breakthrough volumes for polychlorinated biphenyls and polycyclic aromatic hydrocarbons in the PUF plugs and allow for the estimation of breakthrough levels for relatively volatile organic chemicals. After correction for breakthrough, the air concentration obtained with the new flow-through sampler are independent of sampling length and volume and compare favorably with those obtained from conventional pumped high volume samples.     

Integrated sampling and analytical approach for common groundwater dissolved gases

A novel passive gas diffusion sampler (PGDS) combines sampling, storage and direct injection into a single gas chromatograph (GC). The sampler has a 4.5 mL internal volume when deployed, is easy to operate, and eliminates sample-partitioning. The associated GC method analyzes for a large, dynamic sampling range from a single, small volume injection. Dissolved gases were separated on parallel Rt-Molsieve 5A and Rt-Q-PLOT columns and eluted solutes were quantified using a pulse discharge helium ionization detector (PD-HID). The combined sampling and analytical method appears to be less prone to systematic bias than conventional sampling and headspace partitioning and analysis. Total dissolved gas pressure used in tandem with the PGDS improved the accuracy of dissolved gas concentrations. The incorporation of routine measurements of dissolved biogeochemical and permanent gases into groundwater investigations will provide increased insight into chemical and biological processes in groundwater and improve chemical mass balance accuracy.     

Gas-phase organics in environmental tobacco smoke. 1. Effects of smoking rate, ventilation, and furnishing level on emission factors

We measured the emissions of 26 gas-phase organic compounds in environmental tobacco smoke (ETS) using a model room that simulates realistic conditions in residences and offices. Exposure-relevant emission factors (EREFs), which include the effects of sorption and re-emission over a 24-h period, were calculated by mass balance from measured compound concentrations and chamber ventilation rates in a 50-m3 room constructed and furnished with typical materials. Experiments were conducted at three smoking rates (5, 10, and 20 cigarettes day(-1)), three ventilation rates (0.3, 0.6, and 2 h(-1)), and three furnishing levels (wallboard with aluminum flooring, wallboard with carpet, and full furnishings). Smoking rate did not affect EREFs, suggesting that sorption was linearly related to gas-phase concentration. Furnishing level and ventilation rate in the model room had little effect on EREFs of several ETS compounds including 1,3-butadiene, acrolein, acrylonitrile, benzene, toluene, and styrene. However, sorptive losses at low ventilation with full furnishings reduced EREFs for the ETS tracers nicotine and 3-ethenylpyridine by as much as 90 and 65% as compared to high ventilation, wallboard/aluminum experiments. Likewise, sorptive losses were 40-70% for phenol, cresols, naphthalene, and methylnaphthalenes. Sorption persisted for many compounds; for example, almost all of the sorbed nicotine and most of the sorbed cresol remained sorbed 3 days after smoking. EREFs can be used in models and with ETS tracer-based methods to refine and improve estimates of exposures to ETS constituents.     

Evaluation of passive samplers for assessment of community exposure to toxic air contaminants and related pollutants

The precision, accuracy, and sampling rates of Radiello and Ogawa passive samplers were evaluated in the laboratory using a flow-through chamber and under field conditions prior to their use in the 2007 Harbor Community Monitoring Study (HCMS), a saturation monitoring campaign in the communities adjacent to the Ports of Los Angeles and Long Beach. Passive methods included Radiello samplers for volatile organic compounds (benzene, toluene, ethylbenzene, xylenes, 1,3-butadiene), aldehydes (formaldehyde, acetaldehyde, acrolein) and hydrogen sulfide, and Ogawa samplers for nitrogen oxides and sulfur dioxide. Additional experiments were conducted to study the robustness of the passive sampling methods under variable ambient wind speed, sampling duration, and storage time before analysis. Our experimentally determined sampling rates were in agreement with the rates published by Radiello and Ogawa with the following exceptions: we observed a diffusion rate of 22.4 ± 0.1 mL/min for benzene and 37.4 ± 1.5 mL/min for ethylbenzene compared to the Radiello published values of 27.8 and 25.7 mL/min, respectively. With few exceptions, the passive monitoring methods measured one-week average ambient concentrations of selected pollutants with sensitivity and precision comparable to conventional monitoring methods averaged over the same period. Radiello Carbograph 4 VOC sampler is not suitable for the collection of 1,3-butadiene due to backdiffusion. Results for the Radiello aldehyde sampler were inconclusive due to lack of reliable reference methods for all carbonyl compounds of interest.     

Environmental tobacco smoke as a source of polycyclic aromatic hydrocarbons in settled household dust

Environmental tobacco smoke is a major contributor to indoor air pollution. Dust and surfaces may remain contaminated long after active smoking has ceased (called 'thirdhand' smoke). Polycyclic aromatic hydrocarbons (PAHs) are known carcinogenic components of tobacco smoke found in settled house dust (SHD). We investigated whether tobacco smoke is a source of PAHs in SHD. House dust was collected from 132 homes in urban areas of Southern California. Total PAHs were significantly higher in smoker homes than nonsmoker homes (by concentration: 990 ng/g vs 756 ng/g, p = 0.025; by loading: 1650 ng/m(2) vs 796 ng/m(2), p = 0.012). We also found significant linear correlations between nicotine and total PAH levels in SHD (concentration, R(2) = 0.105; loading, R(2) = 0.385). Dust collected per square meter (g/m(2)) was significantly greater in smoker homes and might dilute PAH concentration in SHD inconsistently. Therefore, dust PAH loading (ng PAH/m(2)) is a better indicator of PAH content in SHD. House dust PAH loadings in the bedroom and living room in the same home were significantly correlated (R(2) = 0.468, p < 0.001) suggesting PAHs are distributed by tobacco smoke throughout a home. In conclusion, tobacco smoke is a source of PAHs in SHD, and tobacco smoke generated PAHs are a component of thirdhand smoke.     

Passive sampling screening method using thin-layer chromatography plates

An in situ solid-phase extraction method, thin-layer chromatography (TLC) passive sampling, was investigated as a screening method for determining the presence of organic compounds in water using laboratory experiments and field applications. The TLC passive sampler developed in this research enables the spatial and temporal distributions of organic compounds to be determined qualitatively with little expense. The materials for the sampler developed here cost dollar 1.60 each. By first identifying the areas where a pollutant is present using the TLC passive sampling screening method, total analytical costs for monitoring programs may be reduced by eliminating unnecessary conventional analyses for locations where the pollutant is not present. Two organophosphorus pesticides, diazinon and chlorpyrifos, were used as a model for the development and as a potential application of the TLC passive sampling method. Passive sampler adsorption kinetics, enrichment factors, and extraction efficiencies were determined from batch experiments with exposure times ranging from 1 h to 4 weeks. In field applications, TLC passive sampling was conducted in natural and engineered systems with two silica gel extraction media, C2 and C18. Diazinon and chlorpyrifos were detected by analyzing the adsorbed compounds by high-performance liquid chromatography with ultraviolet detection.     

Passive air sampling using semipermeable membrane devices at different wind-speeds in situ calibrated by performance reference compounds

Semipermeable membrane devices (SPMDs) are passive samplers used to measure the vapor phase of organic pollutants in air. This study tested whether extremely high wind-speeds during a 21-day sampling increased the sampling rates of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), and whether the release of performance reference compounds (PRCs) was related to the uptakes at different wind-speeds. Five samplers were deployed in an indoor, unheated, and dark wind tunnel with different wind-speeds at each site (6-50 m s(-1)). In addition, one sampler was deployed outside the wind tunnel and one outside the building. To test whether a sampler, designed to reduce the wind-speeds, decreased the uptake and release rates, each sampler in the wind tunnel included two SPMDs positioned inside a protective device and one unprotected SPMD outside the device. The highest amounts of PAHs and PCBs were found in the SPMDs exposed to the assumed highest wind-speeds. Thus, the SPMD sampling rates increased with increasing wind-speeds, indicating that the uptake was largely controlled by the boundary layer at the membrane-air interface. The coefficient of variance (introduced by the 21-day sampling and the chemical analysis) for the air concentrations of three PAHs and three PCBs, calculated using the PRC data, was 28-46%. Thus, the PRCs had a high ability to predict site effects of wind and assess the actual sampling situation. Comparison between protected and unprotected SPMDs showed that the sampler design reduced the wind-speed inside the devices and thereby the uptake and release rates.     

基于CFD-DEM的打叶后烟叶风分运动特性分析与试验

为研究打叶后烟叶在离心风分仓内的运动特性及受力变化，基于CFD-DEM耦合方法分析了不同进风风速下，物料在风分仓内的运动过程及受力变化规律。仿真结果表明:随着进风风速增大，风分仓内压力逐渐增大，片烟间碰撞次数增加，流场均匀性变化较小；当进风风速为11、13、15 m/s时，片烟与仓体壁面产生的最大平均碰撞力分别为0.155、0.164、0.378 N，叶含梗率分别为2.46%、2.37%、3.12%。以叶含梗率作为风分效率评价指标进行试验，结果表明:当进风风速为11、13、15 m/s时，叶含梗率分别为2.27%、1.84%、2.54%，试验结果与仿真结果误差 < 1百分点，验证了仿真模拟的合理性。该研究可为优化风分仓结构和工艺参数提供理论支持。      

Sampling atmospheric carbonaceous aerosols using an integrated organic gas and particle sampler

Measurement of particle-bound organic carbon (OC) may be complicated by sampling artifacts such as adsorption of gas-phase species onto particles or filters or evaporation of semivolatile compounds off the particles. A denuder-based integrated organic gas and particle sampler (IOGAPS), specifically designed to minimize sampling artifacts, has been developed to sample atmospheric carbonaceous aerosols. IOGAPS is designed to first remove gas-phase chemicals via sorption to the XAD-coated denuder, and subsequently particles are trapped on a quartz filter. A backup sorbent system consisting of sorbent- (XAD-4 resin) impregnated filters (SIFs) was used to capture the semivolatile OC that evaporates from the particles accumulated on the upstream quartz filter. A traditional filter pack (FP) air sampler, which uses a single quartz filter to collect the particles, was employed for comparison in this study. Elemental and organic carbon were determined from filter punches by a thermal optical transmittance aerosol carbon analyzer. Field measurements show that there was no significant difference between the elemental carbon concentrations determined by the FP and IOGAPS, indicating that particle loss during the transit through the denuder tube was negligible. Compared with the OC determined by FP (3.9-12.6 microg of C/m3), the lower OC observed on the quartz filter in the IOGAPS (2.2-6.0 microg of C/m3) was expected because of the removal of gas-phase organics by the denuder. Higher semivolatile organic carbon (SVOC) on the backup SIFs during the night (1.24-8.43 microg of C/m3) suggests that more SVOC, emitted from primary sources or formed as secondary organic compounds, partitions onto the particles during the night because of the decreased ambient temperature. These data illustrate the utility of an IOGAPS system to more accurately determine the particle-bound OC in comparison to FP-based systems.