Soiling Potential—A New Method for Measuring Smoke Emission

There is a growing interest in effects of sub-micron, nonsettling particles in the atmosphere among air pollution control agencies throughout the country. This type of pollution, generally referred to as the “soiling index” of the atmosphere, is produced primarily by the incomplete combustion of fuels. The measurement procedure has been fairly well standardized, the values being reported as Cohs or Ruds per 1000 linear feet of air. Using a similar technique, a method of quantitating smoke emission in objective terms first demonstrated by W. C. L. Hemeon in 1953, has been applied to source testing at several operating plants by the Cincinnati Division of Air Pollution Control. The source strength will be called “soiling potential” while the effect in the general atmosphere is termed “soiling index.” The soiling potential unit is Rud-ft² per cubic foot exhaust gases or Rud-ft² per unit of fuel input. The “Soiling Potential” sampler is described and results of tests are given. Included is the use of soiling potential in quantitating smoke emission from single sources and for constructing area wide inventory of smoke emission. The use of an area wide smoke emission inventory in Rudft2 in a simple diffusion model for calculating the soiling index (Rud-ft²/1000 cu ft) in the general atmosphere at a given point is explored.     

Problems in Judging Plume Opacity—A Simple Device for Measuring Opacity of Wet Plumes

The discoloration of exterior paint, has been shown to occur when H₂S in the air reacts with heavy metal salts used as pigments or fungicides in the paint. Simple field tests can give an indication whether H₂S was involved. An electron diffraction technique is described to identify the discolored compound in paint samples. Field experience in Jacksonville using this method is described.     

Corrosion on cultural heritage buildings in Italy: A role for ozone?

Because of climatic reasons and of reduced concentrations of SO₂, ground-level ozone (O₃) is one of the main air pollutants in Southern Europe. Ozone levels are very high both in rural and urban locations. In the cities, O₃ can affect human health and materials. Regarding materials, most relevant is the exposure to pollutants of cultural heritage buildings. In particular, monuments registered on UNESCO's list of the world heritage require special monitoring. In Italy 34% and 97% of the territory is exposed to corrosion risk higher than the tolerable level for limestone and copper, respectively. The tolerable corrosion level for limestone and copper was also exceeded in the central area of Milan. In this area the tolerable O₃ concentration for copper was calculated. These concentrations (ranging between 30 and 40 μg/m³) cannot be exceeded at unchanged concentration of other pollutants to maintain corrosion levels below the tolerable ones.     

The Impact of Migration on Air Quality Dose-Response Functions: A Case Study of Jacksonville,Florida

The purpose of this study was to analyze quantitative relationships between air pollution and mortality, and to examine the impact of migration on pollution-related mortality functions. Dose-response functions were estimated for intra-urban variations in ambient air quality for the city of Jacksonville, Florida. Indices of air pollution used in this study were sulfur dioxide (SO₂) and total suspended particulates (TSP). Ambient air quality was measured by the dispersion of TSP and SO₂ across census tracts using the SYMAP dispersion model in conjunction with air quality monitoring stations.

Holding other things constant, TSP apeared to have no statistically significant association with mortality rates. By contrast, the significance of the estimated coefficient for the pollution variable, SO₂, supported the contention that there is a positive and statistically significant relationship between air pollution and mortality rates. However, after making a limited test of the impact of migration on dose-response functions, the SO₂ pollution variable was no longer statistically significant. That is, recent migrants may have limited exposure to the existing level of SO₂ in Jacksonville, Florida, but carry with them long term exposure to more heavily polluted areas in the Northern United States. The results of this study suggest that further epidemiological studies and economic analysis of the health effects on air pollution should make some attempt to control the migration effect.     

Atmospheric corrosion effects of HNO3—Influence of temperature and relative humidity on laboratory-exposed copper

The effect of HNO₃ on the atmospheric corrosion of copper has been investigated at varied temperature (15–35 °C) and relative humidity (0–85% RH). Fourier transform infrared (FT-IR) spectroscopy and X-ray diffraction (XRD) confirmed the existence of cuprite and gerhardtite as the two main corrosion products on the exposed copper surface. For determination of the corrosion rate and for estimation of the deposition velocity (V_d) of HNO₃ on copper, gravimetry and ion chromatography has been employed. Temperature had a low effect on the corrosion of copper. A minor decrease in the mass gain was observed as the temperature was increased to 35 °C, possibly as an effect of lower amount of cuprite due to a thinner adlayer on the metal surface at 35 °C. The V_d of HNO₃ on copper, however, was unaffected by temperature. The corrosion rate and V_d of HNO₃ on copper was the lowest at 0% RH, i. e. dry condition, and increased considerably when changing to 40% RH. A maximum was reached at 65% RH and the mass gain remained constant when the RH was increased to 85% RH. The V_d of HNO₃ on copper at ⩾65% RH, 25 °C and 0.03 cm s⁻¹ air velocity was as high as 0.15±0.03 cm s⁻¹ to be compared with the value obtained for an ideal absorbent, 0.19±0.02 cm s⁻¹. At sub-ppm levels of HNO₃, the corrosion rate of copper decreased after 14 d and the growth of the oxide levelled off after 7 d of exposure.     

A Multivariable Model for Atmospheric Dispersion Predictions

In conjunction with a 15-month air quality survey of Jacksonville, Fia., a mathematical model has been developed to describe the dispersion of atmospheric pollutants. The source inventory used with the model was compiled, in part, from the data obtained from the sampling of all major sources within the area. The major sources were considered separately from the one-mile square area sources which accounted for the remainder of the emissions. Meteorological data was recorded continuously in the city including vertical temperature observations to 750 ft. The model was compiled in FORTRAN and can be used for both gaseous and particulate pollutants, by utilizing proper decay rates. The variant nature of meteorological parameters and emission rates are considered. The ground level concentrations of several pollutants which were determined for 24 hr periods at 11 sites and continuously at two other sites were used to check the model. A limited tracer study was carried out in conjunction with the project.     

Atmospheric corrosion effects of HNO3—Comparison of laboratory-exposed copper,zinc and carbon steel

The influence of nitric acid (HNO₃) on the atmospheric corrosion of copper, zinc and carbon steel was investigated in laboratory exposures at 65% relative humidity (RH), 25 °C and 0.03 cm s⁻¹ air velocity. The deposition velocity (V_d) of HNO₃ on the specimens, the corrosion rates and corrosion products were determined by gravimetry, ion chromatography, X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) microspectroscopy. Comparisons were also made with literature data on the corrosion effects of sulfur dioxide (SO₂), nitrogen dioxide (NO₂) and ozone (O₃).At 65% RH, the V_d of HNO₃ on all metals was at least 70% of that of an ideal absorbent, i.e., an impregnated filter with perfect absorption for HNO₃. The V_d of HNO₃ was much higher than that of SO₂, NO₂ or O₃, which is mainly attributed to the relatively high sticking coefficient, high solubility and high reactivity of HNO₃ compared to the other gases. During identical exposures to HNO₃, the corrosion rate of carbon steel was nearly three times higher than that of copper or zinc. However, when comparing the corrosion effects induced by HNO₃ with those induced by SO₂ alone or in combination with either NO₂ or O₃, HNO₃ turned out to be far more aggressive than SO₂. Relative to SO₂, zinc is the metal most sensitive to HNO₃, followed by copper and with carbon steel least sensitive to HNO₃.     

Evaluation of total particulate matter emission factors for copper slag in dry abrasive blasting

Abrasive blasting was performed in enclosed conditions to evaluate the effect of blast pressure, feed rate and surface contamination on Total Particulate Matter (TPM) emission factors for copper slag. Stack sampling methods were used to collect uncontrolled TPM. Emission factors were calculated as grams of TPM emitted per pound of copper slag used (g/lb) and grams of TPM emitted per square foot of area cleaned (g/sq.ft). Emission factor models were developed to study variation of TPM emission factors with pressure, feed rate and surface contamination. These models can be used to reduce emissions by selecting optimum operating condition as well as to determine emission factors at any operating conditions, within the tested range, for copper slag.     

Effects of initial iron corrosion rate on long-term performance of iron permeable reactive barriers: Column experiments and numerical simulation

Column experiments and numerical simulation were conducted to test the hypothesis that iron material having a high corrosion rate is not beneficial for the long-term performance of iron permeable reactive barriers (PRBs) because of faster passivation of iron and greater porosity loss close to the influent face of the PRBs. Four iron materials (Connelly, Gotthart-Maier, Peerless, and ISPAT) were used for the column experiments, and the changes in reactivity toward cis-dichloroethene (cis-DCE) degradation in the presence of dissolved CaCO₃ were evaluated. The experimental results showed that the difference in distribution of the accumulated precipitates, resulting from differences in iron corrosion rate, caused a difference in the migration rate of the cis-DCE profiles and a significant difference in the pattern of passivation, indicating a faster passivation in the region close to the influent end for the material having a higher corrosion rate. For the numerical simulation, the accumulation of secondary minerals and reactivity loss of iron were coupled using an empirically-derived relationship that was incorporated into a multi-component reactive transport model. The simulation results provided a reasonable representation of the evolution of iron reactivity toward cis-DCE treatment and the changes in geochemical conditions for each material, consistent with the observed data. The simulations for long-term performance were also conducted to further test the hypothesis and predict the differences in performance over a period of 40 years under typical groundwater conditions. The predictions showed that the cases of higher iron corrosion rates had earlier cis-DCE breakthrough and more reduction in porosity starting from near the influent face, due to more accumulation of carbonate minerals in that region. Therefore, both the experimental and simulation results appear to support the hypothesis and suggest that reactivity changes of iron materials resulting from evolution of geochemical conditions should be considered in the design of iron PRBs.     

New Fe-immobilized natural bentonite plate used as photo-Fenton catalyst for organic pollutant degradation

Novel photo-Fenton catalysts were prepared by immobilizing iron species on commercial bentonite plates via two methods: (1) ion exchange reaction (Fe³⁺ vs. Na⁺) by aqueous suspension powder-clay/FeCl₃ followed by plate preparation, and (2) forced hydrolysis of Fe(NO₃)₃ onto a prefabricated clay plate. The last method led to a more photo-active Fe-oxide/bentonite plate. This material allowed, at a non-adjusted initial pH of 5.5 and in the presence of H₂O₂, the total degradation of resorcinol and 55% mineralization in 80 and 100 min of irradiation, respectively. The reached degradation percentages were correlated to the presence of dissolved iron, demonstrating that in these processes, the homogeneous photo-Fenton reactions were mainly responsible for the resorcinol elimination.Likewise, in slurry system, where clay has normally an increased surface area, there was no increase in activity because of a reduced leached iron probably due to the diminished light penetration in the suspension. Despite the lower surface area, in comparison to that of the slurry, the clay plates have the advantage, as heterogeneous photo-catalysts, that separation of the reaction media after treatment is not needed, and thus, a potential use for batch and continuous reaction systems is proposed.     

Supply Curves for Using Powder River Basin Coal to Reduce Sulfur Emissions

Abstract

Supply curves were prepared for coal-fired power plants in the contiguous United States switching to Wyoming's Powder River Basin (PRB) low-sulfur coal. Up to 625 plants, representing ～44% of the nameplate capacity of all coal-fired plants, could switch. If all switched, more than $8.8 billion additional capital would be required and the cost of electricity would increase by up to $5.9 billion per year, depending on levels of plant derating. Coal switching would result in sulfur dioxide (SO₂) emissions reduction of 4.5 million t/yr. Increase in cost of electricity would be in the range of 0.31-0.73 cents per kilowatt-hour. Average cost of S emissions reduction could be as high as $1298 per t of SO₂. Up to 367 plants, or 59% of selected plants with 32% of 44% nameplate capacity, could have marginal cost in excess of $1000 per t of SO₂. Up to 73 plants would appear to benefit from both a lowering of the annual cost and a lowering of SO₂ emissions by switching to the PRB coal.     

Development of a low-cost air sensor package and indoor air quality monitoring in a California middle school: Detection of a distant wildfire

A low-cost air sensor package was used to monitor indoor air quality (IAQ) in a classroom at the Albany Middle School in the San Francisco Bay Area of California. A rapid increase in carbon dioxide (CO₂) was observed in the classroom as soon as it is occupied. When the classroom is unoccupied, the CO₂ levels decay slowly toward the outdoor background level. All high CO₂ concentrations observed inside the classroom, above the outdoor background, was due to exhaling of the occupants. The CO₂ concentrations generally exceed the recommended level of 1000 ppb towards the end of the school day. The exceedances and slow decay may suggest that the ventilation rate in this school is not sufficient. The particulate level in the classroom was low until a distant wildfire advected large amount of particulate matter to the San Francisco Bay Area. Very high (10–15 times compared to the background) particle numbers (per m³ of particles with diameter >0.3 µm) were observed in the classroom during the wildfire. These particles were relatively small (0.3–1.0 µm) and the filters (MERV 8) of the ventilation system were unable to filter them out. Therefore, the measurements made by low-cost particle counters can inform the school administrators of adverse IAQ during future wildfire (or other combustion) events. The particle number was independent of the occupation before and during the wildfire suggesting that all observed particles were infiltrated into the classroom from outside. Consistent with previous studies, no appreciable increase in the local ambient CO₂ background was observed during this distant wildfire event.

Implications: Low-cost air sensors are effective in monitoring indoor air quality in classrooms. The CO₂ levels in classrooms are mainly generated indoors due to exhalation of occupants. Concentration of CO₂ generally exceed the recommended level of 1000 ppb towards the end of the school day. In contrast, the particulate matter mostly comes from outdoors and small particles penetrate though the filters normally used at schools. Distant wildfires do not increase the local CO₂ background appreciably, but significantly increase the particulate matter concentrations both indoors and outdoors. Further investigations are needed to assure that ventilation rates in classrooms are sufficiently health protective.     

The Behavior of Buoyant Merging Plumes in The Rocky Mountain Foothills

Natural gas often contains high concentrations of hydrogen sulfide which must be removed before the gas can be transmitted by pipeline. Sour gas plants extract the sulfur, by converting it to elemental sulfur through a modified Claus process. The sulfur recovery is 93% for small plants (10–100 tonnes of sulfur per day) to 99% for large plants (1000–4000 tonnes of sulfur per day). The unrecovered sulfur is Incinerated giving rise to relatively small emissions of SO₂ characterized by high buoyancy and low momentum.

Using a unique aerial probing methodology, plume dispersion studies were conducted on two plants located fn the foothills of southwestern Alberta, Canada. These studies were generally conducted under neutral conditions and with westerly air flows typical of Chinook conditions. Notable variations of the plume dispersion parameters from accepted predictive values were found, indicating that such values cannot be used with confidence to estimate plume rise and dispersion in the mountain foothills.     

Impact of Toll Removal on Air Particulate Concentration in Jacksonville,Florida

The concentration of total suspended particulate (TSP) matter was determined at commercial, residential, rural and industrial sites in metropolitan Jacksonville during the summers of 1989 and 1990. These data were compared to samples taken at the Mathews Bridge Toll Plaza in 1989 and at a similar location one year later, after removal of the toll facility. All samples were analyzed by reflectance analysis and the approximate elemental carbon content used to estimate the contribution of vehicular traffic at the roadway. The results indicate a significant improvement in air quality at the location of the previous toll facility, but did not show that a widespread improvement resulted from the removal of tolls in Jacksonville, Florida.     

The C02 Pulse Technique for Determining the Condition of Adsorbent Charcoal Beds

Activated charcoal is widely used for the purification of air. Charcoal has a large surface area (ca. 1000 square meters per gram) and acts to purify air by adsorbing gaseous pollutants on its surface. When the capacity of the surface is exhausted, the charcoal is no longer effective and must be replaced.

The carbon dioxide (CO₂) pulse technique, developed at NRL, is a non-destructive method by which one can determine the remaining capacity, or the residual life of a charcoal bed before it has become exhausted. A dose of CO₂ is injected into the air stream ahead of the charcoal bed and is eluted through the bed. The shape of the emerging CO₂ elution peak is determined by the condition of the charcoal bed. For a new, unused charcoal bed the CO₂ elution peak is considerably dispersed (flattened and broadened) due to adsorption and desorption at the charcoal surface. For a partially spent bed the elution peak is dispersed to a degree proportional to the remaining capacity of the bed. For a fully spent bed the CO₂ elution peak is little affected by passage through the bed.

The carbon dioxide puise technique has been shown to be indicative of charcoal capacity for a wide range of non-polar materials (such as hydrocarbons, alcohols, etc.), which are taken up primarily by physical adsorption. The method is essentially insensitive to relative humidity in the range between 10 and 70%. An adaptation of the method has been used for detection of leaks in a charcoal bed, such as those caused by channeling, faulty packing, etc.     

Economic Comparison of Selected Scenarios for Electrostatic Precipitators and Fabric Filters

Compliance with particulate standards for utility boilers burning low sulfur western coal has resulted in the installation and proposed installation of several fabric filter collectors where cold or hot electrostatic precipitators would have traditionally been applied. Recently, SO3 conditioning has been used to improve cold precipitator performance resulting in considerable reduction in specific collection area (SCA). All this suggests that trade-offs exist indicating ranges of SCA, A/C ratio, and power plant size (Mw) where fabric filters become competitive with electrostatic precipitators. Conceptual cost models are presented which indicate total capital investment and annual costs for the control devices. Precipitator costs are correlated with collecting area, gas flow rate, and power input and are presented as functions of SCA and Mw. Fabric filter costs are keyed to gross filter area, pressure drop, and gas flow rate. Fabric filters become competitive when a cold precipitator requires SCAs in excess of 600 to 800 and competitive when a hot precipitator requires equivalent cold precipitator SCAs in excess of 600 to 1000 depending on A/C ratio, Mw, and hot precipitator SCA credit allowance. The S0₃ conditioned precipitator scenario is shown to be economically competitive with fabric filters.     

Atmospheric Particulate Emissions from Dry Abrasive Blasting Using Coal Slag

Abstract

Coal slag is one of the widely used abrasives in dry abrasive blasting. Atmospheric emissions from this process include particulate matter (PM) and heavy metals, such as chromium, lead, manganese, nickel. Quantities and characteristics of PM emissions depend on abrasive characteristics and process parameters. Emission factors are key inputs to estimate emissions. Experiments were conducted to study the effect of blast pressure, abrasive feed rate, and initial surface contamination on total PM (TPM) emission factors for coal slag. Rusted and painted mild steel surfaces were used as base plates. Blasting was carried out in an enclosed chamber, and PM was collected from an exhaust duct using U.S. Environment Protection Agency source sampling methods for stationary sources. Results showed that there is significant effect of blast pressure, feed rate, and surface contamination on TPM emissions. Mathematical equations were developed to estimate emission factors in terms of mass of emissions per unit mass of abrasive used, as well as mass of emissions per unit of surface area cleaned. These equations will help industries in estimating PM emissions based on blast pressure and abrasive feed rate. In addition, emissions can be reduced by choosing optimum operating conditions.     

Effect of global climatic change on carbonation progress of concrete

In the recent years, global warming has dramatically increased the atmospheric carbon-dioxide (CO₂) concentration and temperature. As a consequence of this, carbonation has become one of the most critical durability issues for concrete structures in urban environment.In this study, the climate scenario IS92a recommended by Intergovernmental Panel on Climate Change (IPCC) is used for evaluating the effect of CO₂ concentration on carbonation of concrete. A modified mathematical equation, based on Fick's 1st law of diffusion, is used to evaluate CO₂ diffusion coefficient of concrete. The required cover depth of concrete is estimated by using the applicative methods of reliability and stochastic concepts to take microclimatic conditions into consideration.The tolerance of cover depth should be considered in order to prevent carbonation-induced corrosion. From the relationship between the weight loss of reinforcement and corrosion current density for a given time, the tolerance of cover depth to prevent carbonation-induced corrosion is suggested. It was observed that corrosion occurs when the distance between carbonation front and reinforcement bar surface (the uncarbonated depth) is <5 mm.     

Effects of droplet density and concentration on the efficacy of bacillus thuringiensis and carbaryl against gypsy moth larvae (Lymantria dispar L.)

Abstract

The feeding behavior of gypsy moth larvae exposed to two pesticide deposits (Bt and carbaryl) on oak leaf disks was monitored to determine the relationships between its efficacy and application parameters (droplet density and pesticide concentration). A range of pesticide concentrations and droplet densities (from 9 to 149 droplets/cm²) was used to simulate high and low application rates produced by different methods of application in the field.

The LD₅₀ and the LC₅₀, appeared to be affected by the spatial distribution of the deposit on the leaf surface. Both Bt and carbaryl showed a decreasing LD₅₀ at increasing time after spray. The LD₅₀ of Bt decreased from 14.1 BIU/liter to 3.1 BIU/Iiter between 48 and 144 hours after spray. The results show that feeding inhibition by Bt is more closely related to concentration than to droplet density and dose per unit area with the highest feeding inhibition occurring at 10 BIU/liter at 9 droplets/cm². With carbaryl, an increase in both concentration and droplet density was necessary to cause a decrease in leaf area eaten by larvae.     

The Hygienic Aspects of the Production and Use of Lead Antiknock Compounds

Hydrogen sulfide and other sulfides can be determined in the part per billion range in air if the air is bubbled through an absorption mixture of an alkaline suspension of cadmium hydroxide contained in a macro impinger. Rates as high as 1 cubic foot per minute can be used, or 0.1 cubic foot per minute with a midget impinger. The concentration of the trapped sulfides is then estimated by the methylene blue method. A colorimetric method and a spectrophotometric method are described.