Comparison of Predicted and Measured Concentrations for 58 Alternative models of Plume Transport in Complex Terrain

The purpose of this study was to evaluate alternative prediction models for the SO₂ concentrations produced in the vicinity of the Ohio Edison Company Sammis Power Plant. The plant is situated in the northeastern portion of the Ohio River Valley in complex terrain. Comparisons of the 16 highest predicted and measured short-term SO₂ concentrations were conducted for a one year period for 58 alternative models. Several models were found to predict reasonably accurately the 16 highest measured 24-hour SO₂ concentrations. Each of these models requires an upward adjustment in the plume centerline location as the plume is transported downwind in rising terrain. These same models overpredict by substantial margins the 16 highest measured 3-hour SO₂ concentrations. Improvements in emissions inventory data and improvements in the prediction models used are believed necessary to increase prediction accuracy further.     

A Comparison of Organic Emissions from Hazardous Waste Incinerators Versus the 1990 Toxics Release Inventory Air Releases

Incineration is often the preferred technology for disposing of hazardous waste and remediating Superfund sites. The effective implementation of this technology is frequently impeded by strong public opposition to hazardous waste incineration (HWI). One of the reasons cited for this opposition is the perception that the emission of organics pose an unreasonable threat to human health. While numerous risk assessments for these facilities have demonstrated that the risks from the inhalation of HWI emissions are very low, this has not totally allayed some of the concerns. In order to put organic emissions in perspective, the mass of these emissions from the incineration of hazardous waste on a national scale has been estimated using “reasonable worst-case” assumptions and compared to the 1990 Toxics Release Inventory (TRI) air releases. Comparisons were made for 15 carcinogenic organic compounds and 17 non-carcinogenic organic compounds. Ratios for all but one of these compound-specific HWI emissions to their corresponding TRI air releases ranged from 0.0003 to 0.678 percent. The total mass emissions (110.5 tons) of all 32 specific organics from HWIs was less than 0.03 percent of the corresponding 1990 TRI air releases (431,586 tons).     

Empirical Relationships between Observed Ozone Concentrations and Geographical Areas with Concentrations Likely to Be above 120 ppb

The extent to which existing ozone monitoring data can be used to represent concentrations outside the area immediately surrounding a monitoring station is investigated. The results should be of Interest to those who wish to define areas within which standards are likely to have been exceeded. Relationships are established between the observed second-maximum hour-average ozone concentrations and the area within which It is possible to state with reasonable probability that National Ambient Air Quality Standards (NAAQS) have or have not been exceeded. All pairs of SAROAD stations (Storage and Retrieval of Aerometric Data) separated by 500 km or less which had nearly complete annual data sets were considered for the years 1974 through 1977 to determine the probability that the NAAQS would be exceeded at one station of the pair, given station separation and the observed second-maximum hourly ozone concentration at the other station. The resulting relationship was applied to SAROAD data for 1977, and circles were drawn around each SAROAD monitoring site to show the area within which it is 90% probable that the 120 ppb NAAQS was exceeded during 1977.     

Ambient Air Hydroxyl Radical Concentrations: Measurements and Model Predictions

This review critically examines the limited number of recent near surface measurements of hydroxyl radicals in urban and rural areas. Predictions of average tropospheric, hemispheric and/or zonal concentrations of hydroxyl radicals derived from methylchloroform and carbon monoxide concentrations and models are discussed. The limitations of one- and two-dimensional model predictions of zonal and seasonal hydroxyl concentrations receive detailed consideration. Of especial concern on a regional scale are cloud cover effects on the penetration of ultraviolet radiation below 320 μm which is critical to the subsequent reactions forming hydroxyl radicals.     

Use of Packed Beds for Separation of Entrained Particles and Fumes from An Air Stream

This paper deals with packed beds in discussion of separation of entrained particles and fumes from an air stream. Packed beds develop between the gas and liquid a maximum of contact in order to get maximum mass transfer from a gas to a liquid phase, and they are considered to be one of the better methods of scrubbing contaminants from a gas stream.     

Statistical Study of Air Pollutant Concentrations via Generalized Gamma Distributions

This paper deals with modeling observed frequency distributions of air quality data measured in the area of Venice, Italy. The paper discusses the application of the generalized gamma distribution (ggd) which has not been commonly applied to air quality data notwithstanding the fact that it embodies most distribution models used for air quality analyses. The approach yields important simplifications for statistical analyses. A comparison among the ggd and other relevant models (standard gamma, Weibull, lognormal), carried out on daily sulphur dioxide concentrations in the area of Venice underlines the efficiency of ggd models in portraying experimental data.     

A Combustion Method for the Determination of Solvent Vapors at Low Concentrations in Air

The nitrogen-containing products of smog chamber reactions have been the subject of much controversy. Concern has arisen over nitrogen products because of the almost universally poor nitrogen balance reported for irradiated mixtures of hydrocarbons and nitrogen oxides. Some possible nitrogen-containing products, such as molecular nitrogen, nitrous oxide, and nitroolefins have been investigated and shown to be unimportant. The nitrogen products most often measured are peroxyacetyl nitrate and residual nitrogen dioxide. These two products rarely comprise more than 70% of the initial nitrogen at the end of an experiment, and often account for less than 50%. Previous experiments in which total nitrate was determined in the gas phase and on the vessel walls at the end of irradiation have shown very good nitrogen balances. The assumption has been made that the nitrate arises from nitric acid formed on the walls by adsorbed N₂O₅.

In the work reported here, all major nitrogen-containing compounds have been monitored continuously for the first time. Nitric oxide and nitrogen dioxide have been monitored by chemilumines-cence and automated Saltzman techniques. Methyl, ethyl, and peroxyacetyl nitrate have been determined by gas chromatogra-phy. Two methods, one continuous and one integrated, have been specially developed to measure nitric acid both in the smog chambers and in the atmosphere. Continuous determination of these compounds yields good nitrogen balances throughout the irradiations.

Profiles of the nitrogen-containing species from irradiated HC/ NO_x mixtures are discussed in terms of nitrogen products and nitrogen balance. Differences in product distribution for different hydrocarbon systems are also considered. Using rate information from the nitrogen compound profiles, important reactions leading to nitrogen-containing products are identified. Interference with the chemiluminescent technique by HON0₂, PAN, and C₂H₅ONO₂ is discussed.     

Lead Concentrations in Detroit,New York,and Los Angeles Air

Lead concentrations in air were measured at 12 sites in Detroit, New York and Los Angeles as part of a program to relate automobile emissions and polynuclear aromatic hydrocarbons in air. The information on lead is reported separately because of the current interest in lead as an air pollutant. Sampling was conducted by means of a large “absolute” filter and equipment contained in a step-van truck. A portion of the filter was macerated in nitric acid and the lead determined spectrographically. The combined annual average lead concentration for four sites in metropolitan Los Angeles was approximately 40% higher than the combined averages of either the five sites in metropolitan New York or the three sites in metropolitan Detroit. Concentrations ranged from 0.4 ug/M³ at Santa Monica, to 18.4 ug/M³ at a Los Angeles Freeway Interchange. Concentrations were generally highest in freeway areas, intermediate in commercial areas, and lowest in residential areas. They were about 40% higher in daytime than at night. Average lead concentrations were highest during autumn in New York and winter in Los Angeles reflecting an inverse relationship with wind speed. Correlation coefficients between lead and carbon monoxide, at all sites, were statistically non-zero with 99% confidence and varied from 0.75 to 0.96. Lead concentrations in this study were higher than concentrations reported by others for Detroit, New York, and Los Angeles, presumably because sampling in this study was closer to traffic. However, concentrations in this study were lower than in-traffic concentrations given in the literature.     

A Note on Comparison of Statistical and Analytical Results for Calculating Oxides of Nitrogen Concentrations

A question often asked about analytical diffusion models is “How do the analytical results for calculating pollution concentrations compare with those obtained by statistical techniques?” Miller and Holzworth (1967) have developed a simple analytical diffusion model that yields relative pollution concentrations, x/Q, as a function of afternoon mixing depth, mean transport wind speed, and city size. This analytical model may also be used in reverse to determine apparent afternoon source strengths from observed afternoon pollution concentrations. The apparent source strengths may then be used with the model on independent data to estimate pollution concentrations. It is the purpose of this note to compare results of calculating average afternoon concentrations of oxides of nitrogen (NO_x) by use of the Miller-Holzworth model with those obtained from statistical regression equations.     

Design and Verification of a Programmable Gas Dispensing System for Exposing Plants to Dynamic Concentrations of Air Pollutants

Abstract

Landfills represent a source of distributed emissions source over an irregular and heterogeneous surface. In the method termed “Other Test Method-10” (OTM-10), the U.S. Environmental Protection Agency (EPA) has proposed a method to quantify emissions from such sources by the use of vertical radial plume mapping (VRPM) techniques combined with measurement of wind speed to determine the average emission flux per unit area per time from nonpoint sources. In such application, the VRPM is used as a tool to estimate the mass of the gas of interest crossing a vertical plane. This estimation is done by fitting the field-measured concentration spatial data to a Gaussian or some other distribution to define a plume crossing the vertical plane. When this technique is applied to landfill surfaces, the VRPM plane may be within the emitting source area itself. The objective of this study was to investigate uncertainties associated with using OTM-10 for landfills. The spatial variability of emission in the emitting domain can lead to uncertainties of –34 to 190% in the measured flux value when idealistic scenarios were simulated. The level of uncertainty might be higher when the number and locations of emitting sources are not known (typical field conditions). The level of uncertainty can be reduced by improving the layout of the VRPM plane in the field in accordance with an initial survey of the emission patterns. The change in wind direction during an OTM-10 testing setup can introduce an uncertainty of 20% of the measured flux value. This study also provides estimates of the area contributing to flux (ACF) to be used in conjunction with OTM-10 procedures. The estimate of ACF is a function of the atmospheric stability class and has an uncertainty of 10–30%.     

Comparison of Air Pollutant Emissions from Vaporizing and Air Atomizing Waste Oil Heaters

Information presented in this paper is directed to individuals concerned with emissions from combustion of waste crankcase oil for space heating. Studies were performed to characterize gaseous and particulate emissions and vaporizing pot solid residues resulting from the combustion of waste crankcase oil. Two types of waste oil burners were tested. One was a vaporizing oil burner rated at 35.2 kW (120,000 Btu/h heat input), and the other was an air atomizing oil burner rated at 73.3 kW (250,000 Btu/h heat input). Except for NO_X and SO_X, gaseous emissions were similar to those from conventional distillate oil combustion. NO_X and SO_X emissions were higher due to higher fuel nitrogen and sulfur concentrations. Waste oil from automotive use showed higher inorganic levels than crankcase oil used for truck engine lubrication. Both burner types discharged high levels of metallic species, but the air atomizing unit had much higher stack emission levels than did the vaporizing pot system. Also, particulate loading levels were an order of magnitude higher for the air atomizing burner than for the vaporizing pot burner when firing the waste oils. However, the vaporizing pot burner generated a waste residue containing the majority of its elemental emissions. Elements which exceeded threshold limit values for one or both heaters were cadmium, chromium, cobalt, copper, iron, lead, nickel, phosphorus, and zinc. However, the nickel and much of chromium appeared to be a sampling artifact caused by the stainless steel sampling system.     

Measurement of Ozone Concentrations in Ambient Air Using a Badge-Type Passive Monitor

Abstract

A badge-type passive monitor was used to evaluate the effectiveness of four ozone trapping reagents for measuring O₃ concentrations in the air. These were sodium nitrite (NaNO₂), 3-methyl-2-benzothiazolinone acetone azine (MBTH), p-acetamidophenol (p-ATP), and indigo carmine. Experiments in an exposure chamber showed that only NaNO₂ and MBTH monitors gave sensitive and linear responses over realistic ranges of O₃ concentrations. When tested in ambient air, NaNO₂ and MBTH monitors with a single-layer diffusion barrier overestimated O₃ concentrations by a significant amount. This was largely canceled out in the NaNO₂ monitor by using a multi-layered diffusion barrier to combat wind turbulence effects. However it had almost no effect on the MBTH monitor, and it was found that NO₂ was a source of serious interference. We concluded that using the NaNO₂ monitor with an effective diffusion barrier can measure O₃ in ambient air with an accuracy of ±16%.     

Comparison of Different Packing Materials for the Biofiltration of Air Toxics

Abstract

Four different biofilter packing materials (two porous ceramics, perlite, and open pore polyurethane foam) were compared for the removal of toluene vapors. The focus was on evaluating performance at relatively short gas retention time (13.5 and 27 sec). The reactors were initially operated as biotrickling filters with continuous feeding and trickling of a nutrient solution. After significant plugging of the biotrickling filter beds with biomass was observed, the operation mode was switched to biofiltration with only periodic supply of mineral nutrients. This resulted in stable conditions, which allowed detailed investigations over >6 months. The reactor packed with cattle bone Porcelite (CBP), a ceramic material containing some macronutrients and micronutrients, exhibited the highest performance. The critical load (i.e., load at which 95% removal occurred) was 29 g m^?3 hr^?1 at a gas retention time of 13.5 sec and 66 g m^?3 hr^?1 at a gas retention time of 27 sec. After the long-term experiment, the packing materials were taken from the reactors and examined. The reactors were divided into three sections, top, middle, and bottom, to determine whether spatial differentiation of biomass occurred. The assays included a double-staining technique to count total and live microorganisms and determination of moisture, protein, and dry weight contents. Microbial community analysis was also conducted by denaturing gradient gel electrophoresis. The results showed that most reactors had a significant fraction of inactive biomass. Comparatively, the CBP biofilter held significantly higher densities of active biomass, which may be the reason for the higher toluene removal performance. The analyses suggest that favorable material properties and the nutrients slowly released by the CBP provided better environmental conditions for the process culture.     

Removal of Small Particles from Air by Foam in a Sieve-Plate Column

Particle collection by foam produced on sieve plate apparatus was studied in a 3 x 3 in. sq column and in a 2 in. diam circular column. Experimental data have been obtained for silica test dust, glass beads, sulfur aerosol, polystyrene beads, and extensively for methylene blue aerosol. A new technique utilizing the Goetz aerosol spectrometer was developed and was used to obtain the collection efficiency as a function of particle diameter. A correlation was developed based on inertial mechanism. In this correlation the collection efficiency is expressed as a function of inertial parameter and foam density. The pressure drop in the operating range varied from 2 to 4 in. of water.     

A Method of Predicting Point and Path- Averaged Ambient Air VOC Concentrations,Using Meteorological Data

A method of predicting point and path-averaged ambient air VOC concentrations is described. This method was developed for the case of a plume generated from a single point source, and is based on the relationship between wind directional frequency and concentration. One-minute means of wind direction and wind speed were used as inputs to a Gaussian dispersion model to develop this relationship.

Both FTIR spectrometry and a whole-air sampling method were used to monitor VOC plumes during simulated field tests. One test set was also conducted using only whole-air samplers deployed in a closely-spaced network, thus providing an evaluation of the prediction technique free of any bias that might exist between the two analytical methods.

Correlations between observed point concentrations and wind directional frequencies were significant at the 0.05 level in most cases. Predicted path-integrated concentrations, based on observed point concentrations and meteorological data, were strongly correlated with observed values. Predicted point concentrations, based on observed path-integrated concentrations and meteorological data, accurately reflected the location and magnitude of the highest concentrations from each test, as well as the shape of the concentration-versus-crosswind distance curve.