Particle size distribution predicts particulate phosphorus removal

Particulate phosphorus (PP) is often the largest component of the total phosphorus (P) load in stormwater. Fine-resolution measurement of particle sizes allows us to investigate the mechanisms behind the removal of PP in stormwater wetlands, since the diameter of particles influences the settling velocity and the amount of sorbed P on a particle. In this paper, we present a novel method to estimate PP, where we measure and count individual particles in stormwater and use the total surface area as a proxy for PP. Our results show a strong relationship between total particle surface area and PP, which we use to put forth a simple mechanistic model of PP removal via gravitational settling of individual mineral particles, based on a continuous particle size distribution. This information can help improve the design of stormwater Best management practices to reduce PP loading in both urban and agricultural watersheds.     

Studies on Sulfuric Acid Mist Downwind from a Sulfuric Acid Manufacturing Plant

Air pollution downstream from a sulfuric acid manufacturing plant is comprised of two aspects, the amount of acid mist fallout and the concentration in the atmosphere. This investigation shows that it is desirable to determine each of these by an independent method of collection. Pans of distilled water were used to collect and determine the sulfuric acid mist fallout and an electrostatic precipitator was used to determine the sulfuric acid mist concentration in the atmosphere. The use of Stokes’ Law to convert the results obtained by one method to those obtained by the other requires a knowledge of the particle size of the sulfuric acid mist droplets. Data presented show that tho uso of an average particle size can yield a picture of pollution which is in error by many orders of magnitude. The study shows that areas adjacent to a plant may be subjected to fallout of rather large particle size when there are not adequate methods for removal from the emission or byproduct gases.     

Size Distribution Studies with the Aerosol Spectrometer

It is shown how the Goetz Aerosol Spectrometer can be used to determine the particle size distribution of a specific component of a mixed atmospheric aerosol. The method requires no micrographic counting, but does require that sensitive quantitative chemical analysis methods be available for the compounds of interest. The accuracy of the method and the sensitivity limitations are briefly discussed.     

The potential of diffuse reflectance spectroscopy for the determination of carbon inventories in soils

Investigations have shown that near- and mid-infrared reflectance spectroscopy can accurately determine organic-C in soil. Efforts have also demonstrated that both can differentiate between organic and inorganic-C in soils, but the mid-infrared produces more accurate calibrations. Nevertheless, the greatest benefit would come with in situ determinations where factors such as particle size, sample heterogeneity and moisture can be important. While the variations in large (> 20 mesh) particle size can adversely effect calibration accuracy, efforts have demonstrated that the scanning of larger amounts of sample can overcome this, but the effects of moisture have not been fully explored. While under in situ conditions C distribution and sample heterogeneity are a problem for any analytical method, the rapid analysis possible with spectroscopic techniques will allow many more samples to be analyzed. In conclusion, near- and mid-infrared spectroscopy have great potential for providing the C values needed for C sequestration studies.     

Approximation of a radial diffusion model with a multiple-rate model for hetero-disperse particle mixtures

An innovative method is proposed for approximation of the set of radial diffusion equations governing mass exchange between aqueous bulk phase and intra-particle phase for a hetero-disperse mixture of particles such as those occurring in suspension in surface water, in riverine/estuarine sediment beds, in soils and in aquifer materials. For this purpose the temporal variation of concentration at several uniformly distributed points within a normalized representative particle with spherical, cylindrical or planar shape is fitted with a 2-domain linear reversible mass exchange model. The approximation method is then superposed in order to generalize the model to a hetero-disperse mixture of particles. The method can reduce the computational effort needed in solving the intra-particle mass exchange of a hetero-disperse mixture of particles significantly and also the error due to the approximation is shown to be relatively small. The method is applied to describe desorption batch experiment of 1,2-dichlorobenzene from four different soils with known particle size distributions and it could produce good agreement with experimental data.     

内循环厌氧反应器多相流流场的三维数值分析

利用数值模拟的方法,引入欧拉双流体多相流模型及标准k-s紊流模型,模拟计算内循环厌氧反应器的三相流三维流场,并通过改变污泥颗粒密度及进水流量,针对固相流速及固含率的变化情况,分析条件的改变对流场的影响。研究结果表明,应用数值模拟方法可以获得内循环厌氧反应器内的流场特征;污泥颗粒密度及进水流量的改变对于反应器内污泥颗粒的流速及分布的均匀性有较为明显的影响。模拟结果对反应器的应用及优化设计具有一定的参考价值。     

Resuspension of allergen-containing particles under mechanical and aerodynamic disturbances from human walking

This study presents and develops a controlled and characterized method to explore the influence of specific occupant activity on the aerosolization of allergen-containing particles. Indoor allergen-related diseases are primarily inhalation sensitized and developed, suggesting an aerobiological pathway of allergen-containing carrier particles from dust reservoir to occupant respiration. But the pathways are not well understood or quantified. The influence of occupant walking on particle aerosolization is simulated by a system in which complex floor disturbances are deconvoluted into aerodynamic and mechanical components. Time resolved particle size distributions are measured for particles resuspended from representative samples of flooring materials and different types of floor disturbances in an environmentally controlled experimental chamber. Results indicate aerodynamic disturbances, relative to mechanical, dominate the particle resuspension behavior. Dust type, dust load and floor type showed marginal influences on a normalized surface loading basis. Humidity effects were not clear since during experiments the floor samples may not have reached moisture partitioning equilibrium with the controlled air humidity. Average resuspension rates ranged from 10⁻⁷ to 10⁻³ min⁻¹, having phenomenological consistency with previous, large room or chamber investigations, suggesting the method can be utilized to develop a database for particle resuspension rates.     

Source apportionment of airborne particulate matter using organic compounds as tracers

A chemical mass balance receptor model based on organic compounds has been developed that relates source contributions to airborne fine particle mass concentrations. Source contributions to the concentrations of specific organic compounds are revealed as well. The model is applied to four air quality monitoring sites in southern California using atmospheric organic compound concentration data and source test data collected specifically for the purpose of testing this model. The contributions of up to nine primary particle source types can be separately identified in ambient samples based on this method, and approximately 85% of the organic fine aerosol is assigned to primary sources on an annual average basis. The model provides information on source contributions to fine mass concentrations, fine organic aerosol concentrations and individual organic compound concentrations. The largest primary source contributors to fine particle mass concentrations in Los Angeles are found to include diesel engine exhaust, paved road dust, gasoline-powered vehicle exhaust, plus emissions from food cooking and wood smoke, with smaller contribution from tire dust, plant fragments, natural gas combustion aerosol, and cigarette smoke. Once these primary aerosol source contributions are added to the secondary sulfates, nitrates and organics present, virtually all of the annual average fine particle mass at Los Angeles area monitoring sites can be assigned to its source.     

Identifying the effect of individual emissions sources on particulate air quality within a photochemical aerosol processes trajectory model

A procedure is demonstrated that greatly expands the number of sources whose contribution to ambient particle levels can be followed separately within an aerosol processes trajectory model without significantly increasing the computational burden of the problem. Particles emitted from different sources within the same general class can be differentiated from each other with this technique; for example particles emitted by on-road diesel vehicles can be distinguished from particles emitted by diesel railroad locomotives, and particles emitted from identical sources at different locations can be distinguished from each other as well. The method developed is illustrated by application to the air quality situation in Southern California. The contributions of more than 50 types of air pollution sources to primary particle concentrations at Claremont, CA, are separated from each other by post-processing the output from the aerosol processes trajectory model for an externally mixed aerosol developed previously by Kleeman and Cass (1998, Atmospheric Environment 32, 2803–2816; 1999 Environmental Science and Technology, 33, 177–189).     

Experimental analysis of particle concentration heterogeneity in a ventilated scale chamber

The mixing processes of the aerosol particles from an outdoor environment in a ventilated scale chamber were experimentally studied. The particles were classified into five groups by size: 0.3–0.5 μm, 0.5–1.0 μm, 1.0–3.0 μm, 3.0–5.0 μm and 5.0–10.0 μm. The developing process for the concentration of each particle group was measured in different kinds of flow fields.The results show that the flow field configuration can effectively influence the dispersion time rate of the particles at certain positions. The increase in particle diameter can decrease the dispersion time rate. When the gas flow velocity is high, the particle dispersion time rate is independent of particle size; but when the gas flow velocity is low, particle size can significantly affect the particle dispersion time rate because the turbulent diffusion becomes important in the air and particle transport. The uniformity of the particle concentration for certain positions in steady state tends to be controlled by the inflow velocity, flow field configuration and the particle diameters.     

微通道内细颗粒驻波会聚/分离过程的数值模拟

为了研究微通道内可吸入颗粒的声波会聚现象,在两相流的框架下,对三出口微通道颗粒分离元件实现了声-流场中的颗粒运动的两相流动计算;计算方法中,首次提出的颗粒方程全导数离散方法,并成功运用于两相流动颗粒轨道的计算;模拟结果表明了超声换能器的长度对颗粒会聚的影响和出口流量对颗粒分离的影响。计算结果为三出口微通道颗粒分离元件的设计和应用提供参考。     

A detailed numerical study of the evolution of soot particle size distributions in laminar premixed flames

In this work, two numerical techniques, viz. the method of moments and a discrete h-p-Galerkin method, have been applied for numerical simulation of soot formation in a laminar premixed acetylene/oxygen/argon flame. From the evolution of the PAH and the soot particle size distributions, new insight into the different processes of soot formation is provided. For this, the single submodels have been examined with respect to their influence on the PAH and the soot particle size distributions. The particle inception step was studied in detail by comparing the simulated PAH size distributions with experimental results. Additionally, an estimation of the interaction energy of layered PAH dimers was performed by quantum chemical calculations. From these results, some evidence for the particle inception model employing coalescence of PAH molecules has been found. The numerical results for the gas phase chemical species, the particle number densities and volume fractions of soot as well as for the soot particle size distributions are compared with experimental data. Thereby, the consistency of the entire model is demonstrated.     

A Comparative Study of Environmental Tobacco Smoke Particulate Mass Measurements in an Environmental Chamber

Particulate mass concentration measurements have been made on environmental tobacco smoke (ETS) for the purpose of assessing the relative accuracy of several measurement procedures. ETS over a range of concentrations was generated in an environmental chamber by three methods. Mass concentration was measured by a gravimetric/spectrophotometric collection procedure, piezoelectric particle mass monitors, two nephelometry-based mass monitors, and a particle counting and sizing system. Two-hour average mass concentrations were determined by each method for concentrations ranging from very low levels up to those achieved by smoking one entire cigarette in the chamber. Statistical comparisons were made among procedures employing the gravimetric filter measurement as the basis for comparison. One nephelometry-based procedure gave significantly higher and the other significantly lower values than the filter determination. In one case, a correction for the difference between the particle mass density of the calibrating aerosol and that of ETS brought the nephelometry-based procedure into reasonable agreement with the filter measurement, while for the other, the correction did not resolve the discrepancy between methods. Statistically significant differences between the responses of two supposedly identical piezoelectric mass monitors were found, as was some slight dependence of the nephelometry- based procedures on method of ETS generation. In summary, the results indicate that significant errors can be expected if the instruments studied are used “off the shelf,” even for ETS generated under controlled laboratory conditions. Caution should be employed in field measurements where numerous sources and types of particulate matter can be encountered.     

A fast and efficient modified sectional method for simulating multicomponent collisional kinetics

A fast and efficient method for simulating the evolution of internally mixed multicomponent particle size distributions for aerosol coagulation and droplet coalescence is developed. The technique is based upon a bin-wise sectionalization of the particle mass domain and by imposing the condition of mass conservation for each component. The distribution of each species as a function of the total particle mass is represented in each mass bin as a two-parameter exponential function. Particles of a given mass are assumed to be internally homogeneously mixed. The method is shown to be numerically stable for a wide range of time steps. The numerical solution is compared with both analytical results and results from other well-accepted numerical schemes. This comparison reveals that the proposed technique offers the advantage of being fast and accurate, even for coarse spectral resolution. The method is computationally attractive and easily allows the treatment of ten or more different chemical species in a collisionally evolving particle size distribution. The applicability of the method is demonstrated with several examples: Coalescence growth of multicomponent cloud droplet spectra, coagulation of measured multi-species aerosol particle size distributions, and the simulation of the accumulation mode due to a source of small aerosol particles. The technique is ideally suited for modelling the interaction of microphysics and chemistry in a size-bin resolving aerosol or cloud model.     

基本单分散气溶胶透过率测试中真实值的计算

通过对高效、超高效滤料透过率测试台工作原理的分析得到:利用基本单分散粒子作为气溶胶测得的透过率关系与滤料真正的透过率-粒径曲线有区别,实际上是所使用实验气溶胶的综合透过率。详细研究了真正透过率与实验透过率的关系、误差和偏离产生原因,最终提出了一种独特的计算方法,实现了根据实验得到的表观透过率-粒径关系,就可以计算出真实透过率-粒径曲线,并得到了采用较为理想的实验气溶胶测试出的真实透过率的实际验证,这将大大提高高效、超高效滤料性能测试台的精度,拓展了其应用范围,为高效滤料的过滤理论和应用研究提供了比较理想的测试手段。     

Difficulties inherent to the use of analytic solution of the condensation–evaporation equation for multicomponent aerosols

We present the analytic solution to the problem of multicomponent aerosol evolution due to condensation and/or evaporation of its components. We pose the general equation that governs the evolution of the particle size distributions of each species, and then solve it through the method of characteristic curves. The obtained solution is of interest because it permits an approximate analysis of cases of practical importance without numerical methods. Furthermore, the analytic solutions can be used to validate the numerical methods which, up to now, are only compared with mono-component cases. When all components condense, the obtained solution is valid for all time values. When some of the components evaporate the problem is more complex, due to the fact that no component exists in a negative amount. This suggests the formation of shock waves (high peaks in particle size distribution) and rare-faction waves, which are difficult to handle. Finally, we apply the method to several interesting cases.     

Modelling radionuclide transport for time varying flow in a channel network

Water flowrates and flow directions may change over time in the subsurface for a number of reasons. In fractured rocks flow takes place in channels within fractures. Solutes are carried by the advective flow. In addition, solutes may diffuse in and out of stagnant waters in the rock matrix and other stagnant water regions. Sorbing species may sorb on fracture surfaces and on the micropore surfaces in the rock matrix. We present a method by which solute particles can be traced in flowing water undergoing changes in flowrate and direction in a complex channel network where the solutes can also interact with the rock by diffusion in the rock matrix. The novelty of this paper is handling of diffusion in the rock matrix under transient flow conditions. The diffusive processes are stochastic and it is not possible to follow a particle deterministically. The method therefore utilises the properties of a probability distribution function for a tracer moving in a fracture where matrix diffusion is active. The method is incorporated in a three dimensional channel network model. Particle tracking is used to trace out a multitude of flowpaths, each of which consists of a large number of channels within fractures. Along each channel the aperture and velocity as well as the matrix sorption properties can vary. An efficient method is presented whereby a particle can be followed along the variable property flowpath. For stationary flow conditions and a network of channels with advective flow and matrix diffusion, a simple analytical solution for the residence time distribution along each pathway can be used. Only two parameter groups need to be integrated along each path. For transient flow conditions, a time stepping procedure that incorporates a stochastic Monte-Carlo like method to follow the particles along the paths when flow conditions change is used. The method is fast and an example is used for illustrative purposes. It is exemplified by a case where land rises due to glacial rebound. It is shown that the effects of changing flowrates and directions can be considerable and that the diffusive migration in the matrix can have a dominating effect on the results.     

A Comparison of Tailpipe,Dilution Tunnel,and Wind Tunnel Data in Measuring Motor Vehicle PM

ABSTRACT

Comparison between particle size distributions recorded directly at the tailpipes of both diesel and gasoline vehicles and measurements made using a conventional dilution tunnel reveals two problems incurred when using the latter method for studying particle number emissions. One is the potential for particulate matter (PM) artifacts originating from hydrocarbon material stored in the transfer hose connecting the tailpipe to the dilution tunnel, and the other is the particle coagulation (as well as condensation and chemical changes) that occurs during the transport. Both are potentially generic to current PM emissions measurement practices. The artifacts typically occur as a nanoparticle mode (10–30 nm) that is 2–4 orders of magnitude larger than what is present in the vehicle exhaust and can easily be mistaken for a similar mode that can arise from the nucleation of hydrocarbon or SO₄ ^2-components in the exhaust under appropriate dilution rates. Wind tunnel measurements are in good agreement with those made directly from the tailpipe and substantiate the potential for artifacts. They reveal PM levels for the recent model port fuel injection (PFI) gasoline vehicles tested that are small compared with the ambient background particle level during steady-state driving. The PM emissions recorded for drive cycles such as the Federal Test Procedure (FTP) and US06 occur primarily during acceleration, as has been previously noted. Light-duty diesel vehicle emissions normally exhibit a single lognormal mode centered between 55 and 80 nm, although a nonartifact nanoparticle mode in some cases appears at a 70-mph cruise up a grade.     

A comparison of tailpipe, dilution tunnel, and wind tunnel data in measuring motor vehicle PM.

Comparison between particle size distributions recorded directly at the tailpipes of both diesel and gasoline vehicles and measurements made using a conventional dilution tunnel reveals two problems incurred when using the latter method for studying particle number emissions. One is the potential for particulate matter (PM) artifacts originating from hydrocarbon material stored in the transfer hose connecting the tailpipe to the dilution tunnel, and the other is the particle coagulation (as well as condensation and chemical changes) that occurs during the transport. Both are potentially generic to current PM emissions measurement practices. The artifacts typically occur as a nanoparticle mode (10-30 nm) that is 2-4 orders of magnitude larger than what is present in the vehicle exhaust and can easily be mistaken for a similar mode that can arise from the nucleation of hydrocarbon or SO4(2-) components in the exhaust under appropriate dilution rates. Wind tunnel measurements are in good agreement with those made directly from the tailpipe and substantiate the potential for artifacts. They reveal PM levels for the recent model port fuel injection (PFI) gasoline vehicles tested that are small compared with the ambient background particle level during steady-state driving. The PM emissions recorded for drive cycles such as the Federal Test Procedure (FTP) and US06 occur primarily during acceleration, as has been previously noted. Light-duty diesel vehicle emissions normally exhibit a single lognormal mode centered between 55 and 80 nm, although a nonartifact nanoparticle mode in some cases appears at a 70-mph cruise up a grade.