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.     

Performance Audit Results for Volatile POHC Measurements

Audit materials containing principal organic hazardous constituents (POHCs) have been developed by EPA for use by federal, state, and local agencies or their contractors to assess the accuracy of measurement methods used during RCRA trial burn tests. Audit materials are currently available for 27gaseous organics in five, six, seven, and nine-component mixtures at parts-per-billion levels (7 to 10,000 ppb) in compressed gas cylinders in a balance gas of nitrogen. The criteria used for the selection of 27 gaseous organic compounds is described.

Stability studies indicate that all of the organics tested (with the exception of ethylene oxide and propylene oxide below 10 ppb levels) are stable enough to be used as reliable audit materials.

Subsequent to completion of the stability studies, 89 performance audits have been conducted with the audit materials to assess the accuracy of the Volatile Organic Sampling Train (VOST) and bag measurement methods during or prior to RCRA trial burn tests. A summary of the audits conducted for each POHC and the measurement system audited is shown in this paper. The audit results obtained with audit gases during RCRA trial burn tests are generally within ±50 percent of the audit concentrations.     

A New Audit Technique for EPA Method 25

A simple, inexpensive, and accurate technique for evaluating or auditing the sampling, recovery, and analytical phases of EPA Source Reference Method 25 has been developed. The technique involves spiking a U-shaped stainless steel cartridge containing Tenax® with known quantities of selected organic compounds and thermally desorbing them at temperatures from 160°C to 180°C to generate organic vapors quantitatively. The major advantages of this technique are that no other measurement methods can be used to determine the generated organic concentrations in lieu of Method 25; and that the cartridge can easily be taken to the field for evaluation. The organic compounds generated in test runs are collected and analyzed using the Method 25 procedure. The generation of organics is quantitative and recoveries were found to be 100 ± 10%. The time required for desorption of the majority of organics is generally less than forty-five minutes at a flow rate of 100 mL/min; however, based on laboratory experience the recommended sampling time is sixty minutes. These spiked cartridges are stable at room temperature over a two-month period. Results of interlaboratory studies showed close agreement with the expected concentrations based on calculations from the mass loadings and sample volumes.     

Calibration of Sharp Cut Impactors for Indoor and Outdoor Particle Sampling

ABSTRACT

A low-flow rate, sharp cut point inertial impaction sampler was developed in 1986 that has been widely used in PM exposure studies in the United States and several other countries. Although sold commercially as the MS&T Area Sampler, this sampler is widely referred to as the Harvard Impactor, since the initial use was at the Harvard School of Public Health. Impactor nozzles for this sampler have been designed and characterized for flows of 4,10, 20, and 23 L/min and cut points of 1, 2, 5, and 10 |im. An improved method for determining the actual collecting efficiency curve was developed and used for the recent impactor calibrations reported here. It consists of placing a multiplet reduction impactor inline just downstream of the vibrating orifice aerosol generator to remove the multiplets, thus allowing only the singlet particle s to penetrate through to the impactor being calibrated.

This paper documents the techniques and results of recent nozzle calibrations for this sampler and compares it with other size-selective inertial impactors. In general, the impactors were found to have sharp cutoff characteristics. Particle interstage losses for all of the impactors were very low, with the exception of the 10-|im cut size 20 L/ min impactor, which had greater losses due to the higher flow rate. All of the cut nozzle laboratory calibrations compare favorably to the U.S. Environmental Protection Agency (EPA) WINS-96 fine particle mass (PM_{2 5}) impactor calibration data.     

Calibration of sharp cut impactors for indoor and outdoor particle sampling

A low-flow rate, sharp cut point inertial impaction sampler was developed in 1986 that has been widely used in PM exposure studies in the United States and several other countries. Although sold commercially as the MS&T Area Sampler, this sampler is widely referred to as the Harvard Impactor, since the initial use was at the Harvard School of Public Health. Impactor nozzles for this sampler have been designed and characterized for flows of 4, 10, 20, and 23 L/min and cut points of 1, 2, 5, and 10 microns. An improved method for determining the actual collecting efficiency curve was developed and used for the recent impactor calibrations reported here. It consists of placing a multiplet reduction impactor inline just downstream of the vibrating orifice aerosol generator to remove the multiplets, thus allowing only the singlet particle s to penetrate through to the impactor being calibrated This paper documents the techniques and results of recent nozzle calibrations for this sampler and compares it with other size-selective inertial impactors. In general, the impactors were found to have sharp cutoff characteristics. Particle interstage losses for all of the impactors were very low, with the exception of the 10-micron cut size 20 L/min impactor, which had greater losses due to the higher flow rate. All of the 2.5-micron cut nozzle laboratory calibrations compare favorably to the U.S. Environmental Protection Agency (EPA) WINS-96 fine particle mass (PM2.5) impactor calibration data.     

Characterization of Sonic Devices Used for Cleaning Fabric Filters

ABSTRACT

Ozone reactivity scales play an important role in selecting which chemical compounds are used in products ranging from gasoline to pesticides to hairspray in California, across the United States and around the world. The California Statewide Air Pollution Research Center (SAPRC) box model that calculates ozone reactivity uses a representative urban atmosphere to predict how much additional ozone forms for each kilogram of compound emission. This representative urban atmosphere has remained constant since 1988, even though more than 25 years of emissions controls have greatly reduced ambient ozone concentrations across the United States during this time period. Here we explore the effects of updating the representative urban atmosphere used for ozone reactivity calculations from 1988 to 2010 conditions by updating the meteorology, emission rates, concentration of initial conditions, concentration of background species, and composition of volatile organic compound (VOC) profiles. Box model scenarios are explored for 39 cities across the United States to calculate the Maximum Incremental Reactivity (MIR) scale for 1,233 individual compounds and compound-mixtures. Median MIR values across the cities decreased by approximately 20.3% when model conditions were updated. The decrease is primarily due to changes in atmospheric composition ultimately attributable to emissions control programs between 1998 and 2010. Further effects were caused by changes in meteorological variables stemming from shifting seasons for peak ozone events (summer versus early fall). Lumped model species with the highest MIR values in 1988 experienced the greatest decrease in MIR values when conditions were updated to 2010. Despite the reduction in the absolute reactivity in the updated 2010 atmosphere, the relative ranking of the VOCs according to their reactivity did not change strongly compared to the original 1988 atmosphere. These findings indicate that past decisions about ozone control programs remain valid today, and the ozone reactivity scale continues to provide relevant guidance for future policy decisions even as new products are developed.

Implications: Updating the representative urban atmosphere used for the Maximum Incremental Reactivity (MIR) scale from 1988 to 2010 conditions caused the reactivity of 1223 individual compounds and combined mixtures to decrease by an average of 20.3% but the relative ranking of the VOCs was not strongly affected. This means that previous guidance about preferred chemical formulations to reduce ozone formation in cities across the United States remain valid today, and the MIR scale continues to provide relevant guidance for future policy decisions even as new products are developed.     

Calibration and error analysis of multiwavelength telephotometers

In preparation for the EPA-VISTTA summer 1979 field program, 12 multiwavelength telephotometers were tested and calibrated. A standard light source was used in the calibration process, and the linearity of the instruments was checked using neutral density filters. Calibration of the telephotometers was performed before and after this experiment to determine individual instrument response and drift. Results of the calibration indicated that the instruments had an average inherent error of approximately 1 per cent when operating in the contrast (or ratio) mode. The degree of error is less if a correction is made. In the absolute radiance mode, the instrument was estimated to have an average inherent error of approximately 10 per cent.Results of two of the telephotometer comparisons performed during the VISTTA program are shown to illustrate the problems of target selection and inhomogeneity. A comparison of the extinction coefficients determined from the telephotometers and the scattering coefficients measured by nephelometers showed reasonable agreement for the first example.A more comprehensive, side-by-side comparison showed that results from the two telephotometers agreed within 2 per cent in the ratio mode. However, the uncertainty in the extinction coefficient is between 10 and 15 per cent. This uncertainty can be reduced by eliminating the low contrast cases.     

Evaluation of Absorption Sampling Devices

The information presented in this paper is directed to those with the responsibility of designing and operating air quality monitoring networks. An analytical model for location of monitor sites based upon maximizing a sum of coverage factors for each source is developed. An heuristic solution method from the facilities location analysis literature is used for solution of the model. Results of an example problem are presented and compared with the monitoring network currently In place. The model is shown to be a valuable addition to the methods available to the air quality monitor network designer. Needs for further research are pointed out.     

水质总氮在线检测的光谱数据校正方法

由于受光纤灯源光能波动和一些外界干扰的影响,微型光谱仪检测到的光谱数据存在波动现象,这将直接影响水质总氮在线检测的精确性。在采用均值法去除随机噪声干扰的基础上,针对光能波动的问题基于支持向量机提出了一种光谱数据校正方法,并建立了吸光度与浓度的线性关系。实验结果表明,该方法提高了光谱数据的稳定性,检测相对误差从校正前的12%提高到5%以内,满足水质总氮的分析测试要求。     

Certification of a long-term sampling system for PCDFs and PCDDs in the flue gas from industrial facilities

AMESA (adsorption method for sampling of dioxins) is a fully automatic system for long term monitoring of dioxin emissions from industrial processes based on the adsorption method. The system has been tested and undergoing a certification procedure according to the German guidelines for certification of systems for continuous monitoring of special substances. The certification covered parameters such as disposability of the system, reproducibility of the results and comparability of the sampling method with German and European standard methods. Furthermore break through, blanks and sample storability were investigated. The results prove that AMESA is a state of the art sampling system for continuous monitoring of dioxin/furan emissions.     

New Kinds of Fabric Filtration Devices

New kinds of fabric filtration devices are reviewed in this paper. The industry is on the threshold of a period of innovation and development in this field which should see the advancement of new concepts of the way filters function.     

Design and Calibration of A High Volume Cascade Impactor

The purpose of this study was to develop an air sampling device capable of classifying large quantities of airborne particulate matter into discrete size fractions. Such frac-tionation will facilitate chemical analysis of the various particulate pollutants and thereby provide a more realistic assessment of the effects of particulate matter on human beings.

A 30 cfm, 5 stage cascade impactor of the slit-type has been constructed and calibrated. The calibration aerosol consisted of six different sizes of monodispersed methylene blue produced with a spinning disc generator. The test aerosol sizes varied from 1.35 to 14 μm. The calibration was challenged with heterodispersed aerosols of methylene blue, Arizona road dust, and DOP.     

Dynamic Calibration and Data Interpretation of a Light-Scattering Instrument

Size distributions of sulfate aerosol in Cincinnati and Chicago show MMD’s of 0.4 and 0.3μ. Eighty to 90 percent of the sulfate measured was in the respirable size range (below 3.5 mμ), whereas about 50 percent of the total aerosol was in the respirable range. Two sampling trains were used: one, a cascade impactor followed by a filter, gave seven stages of size and sampled at one cfm. The other, a cyclone-type sampler followed by a filter, sampled at 40 cfm. The smaller samples were analyzed nephelometrically and the larger, turbidimetrically.     

Low Flow Rate Sharp Cut Impactors for Indoor Air Sampling: Design and Calibration

Two single round nozzle impactors have been developed for use in Harvard’s indoor air pollution health study. Both impactors operate at flow rates of 4 L/m and are nearly identical, differing only in their cut sizes of 2.5 μm and 10 μm aerodynamic diameters. Two identical cascaded stages of the same cut size are used to obtain sharp cut-off characteristics. The particles are deposited on impaction plates made of oil impregnated, porous material to reduce particle bounce and are discarded. Only the particles collected on the afterfilter are analyzed. Special care has been taken to collect the particles uniformly on the afterfilter to aid in particle analysis.

The jmpactors were calibrated with a vibrating orifice monodisperse aerosol generator. However, due to the sharp cut of the impactors, doublets and triplets in the calibration aerosols, even in small quantities, gave erroneous calibration curves. Therefore, the number of doublets and triplets in the challenging aerosols were measured and appropriate corrections made to the calibration curves.     

Calibration and testing of a dynamic flow-through chamber for field determination of methyl bromide volatilization flux

Accurate emission measurement of highly volatile chemicals such as methyl bromide (MeBr) is a crucial step in assessing their potential for environmental contamination. Use of flux chambers is a simple method for measuring emission rate under field conditions. To validate the applicability of a dynamic flow-through chamber for measuring MeBr emission, we provide a complete presentation of calibration and testing of the chamber. The calibration was made under a controlled system subject to ambient temperature changes. Two field experiments were conducted to test the chamber for measuring MeBr flux under conditions similar to commercial soil fumigation practices. In both the calibration and the two field experiments, the chamber provided accurate emission estimates. The maximum mass balance error was < 10% which is comparable to the micrometerological method. Because of its simplicity, we believe this dynamic flux chamber can be used reliably in quantifying the emission dynamics of highly volatile chemicals such as MeBr.