Criteria for Certification of Motor Vehicle Pollution Control Devices in California

This investigation used an acid medium for sampling atmospheric oxidants. The acid iodide oxidant procedure was unaffected by air or oxygen, temperature variance, and reducing gases (sulfur dioxide and hydrogen sulfide.) The method possessed good color stability. The method also agreed favorably with the 1 or 2% neutral buffered iodide method when a chromium trioxide scrubber was required to remove the reducing gases from the latter procedure.

The acid oxidant absorption solution of 1 3 ml in a midget impinger contained 10 ml of 1.5% potassium iodide in a 0.1 N sodium hydroxide solution and 3 ml of acetic acid (1:5) which produced a solution of approximately 3.8 pH. Particulate matter was removed by a glass wool attachment to the midget impinger. The air was sampled with a Gelman Sequential Sampler at the rate of 1.41 liters per minute. After the oxidant sample was collected, the absorbing solution was transferred to a graduated cylinder and the volume was adjusted to 25 ml with distilled water. The absorbance was read at 355 millimicrons wavelength by a spectrophotometer in a 1 cm cell. The acid oxidant method was effective between 1 to 70 pphm of ozone.     

Tools For Evaluating New Process and Control Plans

The purpose of this paper on industrial plan evaluation is twofold: to present tools which can be used to evaluate quantitatively certain aspects of air pollution control devices, and to point up specifically two areas in which research is urgently needed. These research areas are in removing solid particles after wetting in scrubbers and use of surface active agents in scrubbing gaseous pollutants. Therefore, the body of information presented is directed to engineers in the field of evaluating the air pollution potential of new industrial plants, to scientists involved in determining the parameters and effectiveness of control devices, and to research and development scientists in the field of surfactants.

One tool presented is a chart for measuring the effectiveness of incinerator afterburners and vapor incinerators. The required inputs to the chart are the rate of flue gas flow in standard cubic feet per minute and the auxiliary fuel burner capacity in Btu per hour. The chart yields the flue gas temperature increase which will result, given in degrees F. The second tool presented is a new psychrometric graph for the humidifying and cooling of gases from processes as hot as 3000°F. Inputs into the graph are the temperature of the gases entering the sprays from the hot process and the temperature desired before they enter a control device such as a fabric filter or a scrubber. The chart yield is the amount of water needed in gallons per thousand cubic feet of gas. The only calculation needed is a correction of the hot gas volume to 70°F. Water needed to saturate the gases can be read directly also.     

Atmospheric H2O2 measurement: comparison of cold trap method with impinger bubbling method.

Collection of atmospheric H2O2 was performed by a cold trap method using dry ice-acetone as the refrigerant. The air was drawn by a pump into a glass gas trap immersed in the dry ice-acetone slush in a dewar flask at a flow rate of 2.5 l min-1 for approximately 2 h. Collection efficiency was > 99% and negligible interferences by O3, SO2 or organic matter with the collected H2O2 in the trap were observed. This method was compared with the air impinger bubbling method which has been previously described (Kok et al., 1978a, b, Envir. Sci. Technol. 12, 1072-1080). The measured total peroxide (H2O2 + organic peroxide) values in a series of aim samples collected by the impinger bubbling method (0.06-3.7 ppb) were always higher than those obtained by the cold trap method (0.02-1.2 ppb). Laboratory experiments suggest that the difference in values between the two methods probably results from the aqueous phase generation of H2O2 and organic peroxide in the impinger solution by a reaction of atmospheric O3 with olefinic and aromatic compounds. If these O3-organic compound reactions which occur in the impinger also occur in aqueous droplets in the atmosphere, the process could be very important for aqueous phase generation of H2O2 in clouds and rainwater.     

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.     

An Inertial-Type Particle Separator for Collecting Large Samples

A two-stage inertial-type particle separator has been developed for collecting large size-selective samples of particulates on filters. The sampler operates at a flow rate of 1.4 cubic feet per minute and may be run for extended periods without change in collecting efficiency. The particle size cut of the sampler is at a diameter of 1.4 microns; separation of greater than 90 percent is obtained for particles below 0.80 micron and above 2.0 microns. The sampler was calibrated with monodisperse polystyrene latexes. Data are presented to relate the separating efficiency of the sampler to its separation parameters.     

Issues related to solution chemistry in mercury sampling impingers

Analysis of Hg speciation in combustion flue gases is often accomplished in standardized sampling trains in which the sample is passed sequentially through a series of aqueous solutions to capture and separate oxidized Hg (Hg2+) and elemental Hg (Hg0). Such methods include the Ontario Hydro (OH) and the Alkaline Mercury Speciation (AMS) methods, which were investigated in the laboratory to determine whether the presence of Cl2 and other common flue gas species can bias the partitioning of Hg0 to front impingers intended to isolate Hg2+ species. Using only a single impinger to represent the front three impingers for each method, it was found that as little as 1-ppm Cl2 in a simulated flue gas mixture led to a bias of approximately 10-20% of Hg0 misreported as Hg2+ for both the OH and the AMS methods. Experiments using 100-ppm Cl2 led to a similar bias in the OH method, but to a 30-60% bias in the AMS method. These false readings are shown to be due to liquid-phase chemistry in the impinger solutions, and not necessarily to the gas-phase reactions between Cl2 and Hg as previously proposed. The pertinent solution chemistry causing the interference involves the hypochlorite ion (OCl-), which oxidizes Hg0 to soluble Hg2+. Addition of sodium thiosulfate (Na2S2O3) to the front impinger solutions eliminates this false positive measurement of Hg2+ by selectively reacting with the OCl- ion. In general, the presence of SO2 also mitigates this interference in the same way, and so this bias is not likely to be a factor for Hg speciation measurements from actual coal combustion flue gases. It might, however, be a problem for those few combustor flue gas measurements and research studies where Cl2 is present without appreciable amounts of SO2.     

Epidemiological Bases for Possible Air Quality Criteria for Lead

In at least some urban areas, population exposure to elevated atmospheric lead levels is associated with increased blood lead. No reasonable alternative explanation exists other than that the increased levels of lead pollution are causing increased lead storage in the body. The study of lead body burdens in U. S. populations indicates an increasing concentration with age in liver, spleen, pancreas, kidney, and lung. No such increase is found in samples of residents from foreign countries.

The effect of increased storage of lead on porphyrin metabolism is in urgent need of investigation. Higher levels of lead exposure may interfere with hemoglobin synthesis.

Using WHO categories for air quality guides (criteria), a level I criterion for two micrograms of lead per cubic meter of air for a long-term average can be proposed. It would apply to pollution largely derived from motor vehicular sources.     

Public Health Service National Fallout Surveillance Program

A semi-automated method for determination of fluorine in biological materials has been developed incorporating the Technicon AutoAnalyzer. One-half gram of dried, ground plant material is ashed, alkali-fused, diluted with water, and the suspension is pumped, along with H₂SO₄, at controlled rates, into the hot revolving glass helix of a digestor unit. As the acid-digest mixture passes through the heated coil, volatile fluoride and water vapor are evolved. The volatile fluoride and water vapor are pulled from the helix under reduced pressure through a tube which projects into the helix. The tube, in turn, is connected to a water-jacketed condenser and then to an impinger where the sample is continuously mixed. An aliquot of the impinger liquid is being constantly withdrawn. This sample is then air-segmented and mixed with a reagent containing alizarin complexone, pH 4 acetate buffer, lanthanum nitrate, acetone, and water. The sample-reagent combination passes through 4 full-length mixing coils where color development takes place. Upon reacting with fluoride, the wine-red alizarin complexone-La(III) reagent forms a lilac blue fluoride complex. The solution is pumped from the mixing coils through the tubular flow cell of the colorimeter. The absorbence of the solution is measured at 624 mμ, and the signal is transmitted to a recorder where the results are plotted on absorbency paper. The absorbence at the apex of the peak is proportional to the amount of fluoride in the sample between the range of 2.5-80 μg °F. Samples are analyzed at a rate of 12 per hour. Results compare favorably with those obtained by Willard-Winter distillation. Recent studies indicate that the F content of plant tissues can be estimated without prior ashing and fusion     

Recommendations on a Preferred Procedure for the Determination of Particulate in Gaseous Emissions

Studies were made over a 3 year period to evaluate the EPA Method 5 manual particulate sampling procedure in the forest products industry through laboratory and field studies. Results of the study showed that several modifications could be made to improve the performance and suitability of the method for routine source particulate measurements. Physical system changes included the use of a Teflon-lined umbilical cord to the collection system. Procedure changes included changing the isokinetic sampling rate variations to ±20% for emission sources where the particles were smaller than three micrometers in aerodynamic diameter, purging the impinger solutions with an inert gas immediately following collection, and separate evaporation of impinger organics and inorganics at 25 °C and 105°C, respectively. Calculation changes included inclusion of impinger-caught particulate and separate consideration of inorganic and organic particulates.     

Emission Standards for the Control of Solid Particles,A New Approach by New Jersey

Existing chapters of the New Jersey Air Pollution Control Code are described, followed by an explanation of a proposed new chapter to control emissions of coarse solid particles and fine solid particles from industrial processes. The chapter is designed to limit dustfall of coarse particles off the premises of the emitter to WO tons per square mile per year, and the methods used to relate this criterion to stack emissions are explained. Fine particles, suspended in the air off the premises, are limited to 0.615 milligrams per cubic meter during average weather conditions. Measures taken for the protection of buildings, where the plant property line is less than 10 stack heights from the base of the stack, are described.     

Project Engineering

Abstract

Screening of biofiltering material for treatment of volatile organic compounds was performed by using a gas stream containing methyl ethyl ketone (MEK) as a target pollutant. Filtering media (FM) for screening were prepared by blending compost (such as pig and cow manure) and filling material (such as fern chips, wheat bran, and bagasse). Results show that a blend of pig manure/fern chips = 9:1 (wt basis) was superior with respect to the stability of the pH and the water-holding capacity of the FM and in the capacity for treating the target compound. Complete removal of the target compound was obtained at an organic loading of 100 g per cubic meter of filtering media per hour. By using the screened FM for treating MEK and toluene, long-term stability (>1,200 hours) and complete removal can be obtained at an organic loading of 50 g per cubic meter of FM per hour for either compound.     

Issues Related to Solution Chemistry in Mercury Sampling Impingers

ABSTRACT

Analysis of Hg speciation in combustion flue gases is often accomplished in standardized sampling trains in which the sample is passed sequentially through a series of aqueous solutions to capture and separate oxidized Hg (Hg²⁺) and elemental Hg (Hg⁰). Such methods include the Ontario Hydro (OH) and the Alkaline Mercury Speciation (AMS) methods, which were investigated in the laboratory to determine whether the presence of Cl₂ and other common flue gas species can bias the partitioning of Hg⁰ to front impingers intended to isolate Hg²⁺ species. Using only a single impinger to represent the front three impingers for each method, it was found that as little as 1-ppm Cl₂ in a simulated flue gas mixture led to a bias of approximately 10-20% of Hg⁰ misreported as Hg²+ for both the OH and the AMS methods. Experiments using 100-ppm Cl₂ led to a similar bias in the OH method, but to a 30-60% bias in the AMS method. These false readings are shown to be due to liquid-phase chemistry in the impinger solutions, and not necessarily to the gas-phase reactions between Cl₂ and Hg as previously proposed. The pertinent solution chemistry causing the interference     

A real-time monitoring and assessment method for calculation of total amounts of indoor air pollutants emitted in subway stations

Subway systems are considered as main public transportation facility in developed countries. Time spent by people in indoors, such as underground spaces, subway stations, and indoor buildings, has gradually increased in the recent past. Especially, operators or old persons who stay in indoor environments more than 15 hr per day usually influenced a greater extent by indoor air pollutants. Hence, regulations on indoor air pollutants are needed to ensure good health of people. Therefore, in this study, a new cumulative calculation method for the estimation of total amounts of indoor air pollutants emitted inside the subway station is proposed by taking cumulative amounts of indoor air pollutants based on integration concept. Minimum concentration of individual air pollutants which naturally exist in indoor space is referred as base concentration of air pollutants and can be found from the data collected. After subtracting the value of base concentration from data point of each data set of indoor air pollutant, the primary quantity of emitted air pollutant is calculated. After integration is carried out with these values, adding the base concentration to the integration quantity gives the total amount of indoor air pollutant emitted. Moreover the values of new index for cumulative indoor air quality obtained for 1 day are calculated using the values of cumulative air quality index (CAI). Cumulative comprehensive indoor air quality index (CCIAI) is also proposed to compare the values of cumulative concentrations of indoor air pollutants. From the results, it is clear that the cumulative assessment approach of indoor air quality (IAQ) is useful for monitoring the values of total amounts of indoor air pollutants emitted, in case of exposure to indoor air pollutants for a long time. Also, the values of CCIAI are influenced more by the values of concentration of NO2, which is released due to the use of air conditioners and combustion of the fuel. The results obtained in this study confirm that the proposed method can be applied to monitor total amounts of indoor air pollutants emitted, inside apartments and hospitals as well. Implications: Nowadays, subway systems are considered as main public transportation facility in developed countries. Time spent by people in indoors, such as underground spaces, subway stations, and indoor buildings, has gradually increased in the recent past. Especially, operators or old persons who stay in the indoor environments more than 15 hr per day usually influenced a greater extent by indoor air pollutants. Hence, regulations on indoor air pollutants are needed to ensure good health of people. Therefore, this paper presents a new methodology for monitoring and assessing total amounts of indoor air pollutants emitted inside underground spaces and subway stations. A new methodology for the calculation of cumulative amounts of indoor air pollutants based on integration concept is proposed. The results suggest that the cumulative assessment approach of IAQ is useful for monitoring the values of total amounts of indoor air pollutants, if indoor air pollutants accumulated for a long time, especially NO2 pollutants. The results obtained here confirm that the proposed method can be applied to monitor total amounts of indoor air pollutants emitted, inside apartments and hospitals as well.     

Cincinnati’s Radioactive Fallout Monitoring Program

A fluoride analyzer originally designed by Wiggins, St. John, Thomas arid associates at Stanford Research Institute, has been modified to improve its operational capabilities and reliability so as to operate for periods in excess of six months with virtually no maintenance. It measures hydrogen fluoride in the atmosphere in the sub-parts per billion range. The need for the instrument, method of measuring fluoride and the modifications made to improve the SRI instrument are presented. The instrument has been operated in the field for two years beside impingers which obtain daily integrated samples. The impingers samples are subsequently titrated. Satisfactory correlation has been found between the average daily values by the automatic analyzer and the impinger.     

Hot filter/impinger and dilution sampling for fine particulate matter characterization from ferrous metal casting processes

A study using two stack-sampling methodologies for collecting particulate matter (PM) emissions was conducted using a hot filter followed by a cold impinger sampling train and a dilution sampler. Samples were collected from ferrous iron metal casting processes that included pouring molten iron into a sand mold containing an organic binder, metal cooling, removal of the sand from the cooled casting (shakeout), and postshakeout cooling. The shakeout process contributed more to PM emissions than the metal pouring and cooling processes. Particulate matter less than 2.5 microm in aerodynamic diameter (PM2.5) mass emissions for the entire casting cycle ranged from 3.4 to 4.7 lb/t of metal for the hot filter/impinger method and from 0.8 to 1.8 lb/t of metal for the dilution method. Most of the difference was due to PM captured by the impingers, much of which was probably dissolved gases rather than condensable vapors. Of the PM fraction captured by the impingers, 96-98% was organic in nature. The impinger PM fraction contributed 32-38% to the total suspended particle mass and caused a factor of 2-4 positive bias for PM2.5 emissions. For the pouring and cooling processes only, the factor increased to over seven times.     

The Gas Supply Situation in the United States

The body of information presented in this paper is directed to those individuals who require information on the present natural gas supply and demand relationship and the prospects for future changes, including individuals concerned with air quality control and the use of natural gas for combating air pollution.

If natural gas could continue to capture large shares of the energy market, as in the past when supply was not a growth inhibiting factor, annual demand for gas is projected to increase to 34.5 and 46.4 trillion cubic feet in 1980 and 1990, respectively. Annual production levels which could be supported by presently proven reserves and anticipated future reserve additions are estimated to peak in the mid-1970’s and decline to about 18 trillion cubic feet in 1990.

When viewed from the perspective of anticipated indigenous supply deficiencies, the acquisition of supplemental sources of gas becomes of paramount importance. Pipeline imports, the only substantive supplemental source presently available, could almost double by 1980 and be about 2 trillion cubic feet annually in 1990.

Available volumes of gas from Alaska could be 0.7 trillion cubic feet in 1980 and could increase to 2.3 trillion cubic feet annually by 1990. Actual initial deliveries of gas are inextricably related to construction of an oil pipeline from Prudhoe Bay. Construction delays postpone initial delivery dates for gas as well as oil.

Advancements in cryogenic transportation and storage technologies have made the heretofore largely untapped supplies of gas from several countries with limited internal markets available to the United States as LNG. Annual LNG imports could be about 0.3 trillion cubic feet in 1975 and perhaps 2 and 4 trillion cubic feet by 1980 and 1990, respectively.

Pipeline quality gas from coal presents the prospect for a supplemental source of gaseous fuel independent of foreign sources and free from balance of payments problems. The first pipeline quality gas from coal may be expected by 1976, and by 1980 perhaps 0.3 trillion cubic feet could be provided annually from this source; in 1990, 3.3 trillion cubic feet might be available. An additional, but presently unqualified, source of synthetic gas will be the conversion of liquid hydrocarbons.

In the aggregate, supplemental gas supplies are anticipated to total about 4.6 and 11.5 trillion cubic feet annually by 1980 and 1990, respectively. While demand for gas is anticipated to increase, domestic conventional gas production is projected to peak in the mid-1970’s and decrease somewhat thereafter. As a consequence, a continuing gas supply-demand imbalance is anticipated.     

Particle-Molecule Collection by Sonic Flow Impingers

The information presented in this paper is directed to those industrialists and researchers interested in molecule and near micron and submicron particle sampling by a convenient, inexpensive, and sufficiently accurate method. The use of two sonic flow impingers in series is predicted to collect 98-99% of a phosphoric acid aerosol having a mass median diameter of 0.7 p. The first impinger of a new design is shown, in field sampling, to collect simultaneously 90-98% of the aerosol and 95% of molecular fluoride compounds. On the same aerosol, the standard Greenburg-Smith impinger shows a low collection performance, less than 50% at 1 cfm and 65% at sonic velocity. The use of a first impinger at sonic flow greatly simplifies sampling procedures by eliminating the need for a test meter and associated pressure and temperature measurements. Also, for small particle sizes isokinetic sampling is not necessary and sampling line losses by deposition are shown to be less than 1%. The low initial cost of the sampling units and the low manpower requirements for setting up and supervising sampling make possible the taking of a number of samples sufficient to establish emissions over extended intervals of time. The equipment is especially suited to locations having multiple emission sources, or for locations requiring simultaneous sampling of many points.     

日本大气污染和控制技术研究进展

本文详细地介绍了日本大气污染现状及其趋势,对主要污染物的污染状况进行了分析。概述了日本几十年来大气污染防治技术研究的进展。对改善燃烧、电子束法、NO_x处理触媒研究、NO_x吸附剂的研究、活性炭法干式脱硫、利用煤炭的干式脱硫、半干式简易脱硫、静电的应用、微生物的应用、电除尘、过滤除尘等大气污染防治技术的研究,做了详细介绍。对目前人们普遍关心的含氟气体排放控制问题进行了探讨。还简要介绍了日本大阪府等地,准备偿试的汽车排气总量控制的研究状况。     

Hot Filter/Impinger and Dilution Sampling for Fine Particulate Matter Characterization from Ferrous Metal Casting Processes

Abstract

A study using two stack-sampling methodologies for collecting particulate matter (PM) emissions was conducted using a hot filter followed by a cold impinger sampling train and a dilution sampler. Samples were collected from ferrous iron metal casting processes that included pouring molten iron into a sand mold containing an organic binder, metal cooling, removal of the sand from the cooled casting (shakeout), and postshakeout cooling. The shakeout process contributed more to PM emissions than the metal pouring and cooling processes. Particulate matter less than 2.5 μm in aerodynamic diameter (PM_2.5) mass emissions for the entire casting cycle ranged from 3.4 to 4.7 lb/t of metal for the hot filter/impinger method and from 0.8 to 1.8 lb/t of metal for the dilution method. Most of the difference was due to PM captured by the impingers, much of which was probably dissolved gases rather than condensable vapors. Of the PM fraction captured by the impingers, 96–98% was organic in nature. The impinger PM fraction contributed 32–38% to the total suspended particle mass and caused a factor of 2–4 positive bias for PM_2.5 emissions. For the pouring and cooling processes only, the factor increased to over seven times.