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371.
Hans-Karl Petzel Heinrich Igelbuscher Michael Esche Charles Leivo 《Journal of the Air & Waste Management Association (1995)》2013,63(5):658-662
When the 230-MW Volklingen power plant entered service in August 1982, it became the first power plant in Europe to desulfurize 100 percent of the flue gas without bypass. The FGD system forms an integral part of the cooling tower, and the flue gas is discharged through the tower. There is no stack. Mathematical models for the dispersal of the mixed emissions from the cooling tower have now been confirmed by readings of ground level concentrations. The dispersion pattern was recorded as part of exhaustive emission readings, which included measurements from powered gliders. It was shown that the dispersal of the desulfurized flue gas encounters more favorable atmospheric conditions than would be the case if it were discharged separately from a stack. One major element is the thermal thrust of the exhaust from the cooling tower. This approach to flue gas discharge reduces costs considerably, eliminating the need for reheating the gases to the 72° C required in West Germany for conventional FGD systems discharging through a stack. 相似文献
372.
373.
Charles D. Kolstad 《Journal of the Air & Waste Management Association (1995)》2013,63(2):177-184
Air pollution regulation in the United States has come under repeated attack over the years for a number of reasons. Early in the past decade, prevention of significant deterioration (PSD) legislation, which protects currently clean areas, came into conflict with domestic energy production goals. This paper presents an applied analysis of present and alternative regulations for achievement of PSD air quality goals. A model of the Four Corners region of the Southwest is developed, and several policy alternatives tested in terms of economic efficiency and ability to achieve air quality goals. Alternatives examined include emission fees, marketable emission permits, and technological standards. 相似文献
374.
Charles L. Blanchard Shelley J. Tanenbaum 《Journal of the Air & Waste Management Association (1995)》2013,63(7):816-828
Abstract Ambient air quality data were analyzed to empirically evaluate the effects of reductions of volatile organic compounds (VOCs) and oxides of nitrogen (NOx) emissions on weekday and weekend levels of ozone (O3; 1991–1998) and particulate NO3 - (1980–1999) in southern California. Despite significantly lower O3 precursor levels on weekends, 20 of 28 South Coast Air Basin (SoCAB) sites (28 of all 78 southern California sites) showed statistically significant higher mean O3 levels on Sundays than on weekdays (p < 0.01); 49 of the remaining 50 sites showed no significant differences between mean weekday and Sunday peak O3 levels. We also observed no statistically significant differences between mean weekday and weekend concentrations of particulate NO3 - or nitric acid (HNO3, the precursor of particulate NO3 -). Averaged over sites, the mean Sunday NOx and nonmethane hydrocarbon concentrations were 25–41% and 16–30% lower, respectively, than on weekdays. Site-to-site differences between weekend and weekday mean peak hourly O3 levels were related to whether O3 formation was limited by the availability of NOx. A thermodynamic equilibrium model predicts that particulate NO3 - levels would decrease in response to a reduction of HNO3, and that particulate ammonium NO3 - formation was not limited by the availability of ammonia. The similarity of mean weekday and weekend levels of NO3 - therefore did not result from limitations on the formation of particulate NO3 - from its precursor, HNO3. 相似文献
375.
Steven D. Reynolds Charles L. Blanchard Stephen D. Ziman 《Journal of the Air & Waste Management Association (1995)》2013,63(11):1452-1470
Abstract Analyses of ozone (O3) measurements in conjunction with photochemical modeling were used to assess the feasibility of attaining the federal 8-hr O3 standard in the eastern United States. Various combinations of volatile organic compound (VOC) and oxides of nitrogen (NOx) emission reductions were effective in lowering modeled peak 1-hr O3 concentrations. VOC emissions reductions alone had only a modest impact on modeled peak 8-hr O3 concentrations. Anthropogenic NOx emissions reductions of 46–86% of 1996 base case values were needed to reach the level of the 8-hr standard in some areas. As NOx emissions are reduced, O3 production efficiency increases, which accounts for the less than proportional response of calculated 8-hr O3 levels. Such increases in O3 production efficiency also were noted in previous modeling work for central California. O3 production in some urban core areas, such as New York City and Chicago, IL, was found to be VOC-limited. In these areas, moderate NOx emissions reductions may be accompanied by increases in peak 8-hr O3 levels. The findings help to explain differences in historical trends in 1- and 8-hr O3 levels and have serious implications for the feasibility of attaining the 8-hr O3 standard in several areas of the eastern United States. 相似文献
376.
Wendy S. Goliff Dennis R. Fitz Kathy Cocker Kurt Bumiller Charles Bufalino Dylan Switzer 《Journal of the Air & Waste Management Association (1995)》2013,63(6):680-685
2,2,4-trimethyl, 1,3-pentanediol monoisobutyrate (TPM) is a widely used solvent found in water-based coatings. Ambient measurements of TPM are reported here for the first time. Although this compound has been previously measured in indoor air, this study illustrates successful detection and quantification of TPM in ambient air at three locations in Southern California: Pico Rivera, Azusa, and Riverside. TPM was detected in every sample collected, with concentrations ranging from 0.7 to 49.5 parts per trillion (ppt). Collections took place during summer 2009, fall 2009, winter 2009/2010, and spring 2010, for 5–7 days during each season. The highest mean concentrations were observed during the summer months for each city, when coating activities are typically at their highest.
Implications 2,2,4-Trimethyl, 1,3-pentanediol monoisobutyrate (TPM) is a widely used solvent found in water-based coatings. Ambient measurements of TPM are reported here for the first time. The highest mean concentrations were observed during the summer months for each city, when coating activities are typically at their highest. Unreacted TPM constitutes approximately 0.01% of the total nonmethane hydrocarbon (NMHC) concentrations in the Los Angeles air basin and given its slow reactivity rate in forming ozone, this would be an approximate upper limit for the fraction of ozone that it is responsible for forming. 相似文献
377.
Charles W. Gruber George A. Jutze Norman A. Huey 《Journal of the Air & Waste Management Association (1995)》2013,63(4):327-330
Abstract An airborne lidar was used to study the smoke plume from the burning of a controlled oil spill on the ocean. The ratio of the amount of light (at a wavelength, λ, of 0.532 u.m) backscattered by the smoke to the amount of light extinguished by the smoke was determined by measuring the strength of a laser beam after it had passed through the smoke plume, been reflected from the ocean, and passed through the smoke plume again, and comparing this to the strength of the laser beam reflected directly from the ocean. The optical depth of the smoke (at λ = 0.532 µm) was typically between 0.2 and 0.5. The mass fluxes of smoke particles that passed through four vertical cross sections of the (nonsteady state) smoke plume were estimated from lidar measurements to be 142, 175, 423, and 414 g s-1, compared to an average smoke mass production rate of ~770 g s-1. The spatial distribution of smoke mass along the long axis of the plume was also estimated from the lidar measurements; derived smoke mass concentrations were generally <300 µg m-3, with a few isolated values up to ~800 µg m-3. 相似文献
378.
Donald M. Keagy William W. Stalker Charles E. Zimmer Richard C. Dickerson 《Journal of the Air & Waste Management Association (1995)》2013,63(6):270-280
A diffusion flame burner was operated to determine the effect of several parameters on the quantity of NOx and unburned hydrocarbons produced. The statistical analysis indicated the unburned hydrocarbon emissions to be dependent upon the rate of heat release in the system, the amount of excess combustion air, the fuel molecular structure, and the interaction between the fuel structure and the amount of excess air. Analysis of the NOx emissions, after an adjustment to a common temperature to eliminate the temperature effect, showed them to be dependent upon the fuel molecular structure and the amount of excess air. The NOx emissions reached a maximum at the conditions which yielded minimum unburned hydrocarbon emissions. Multiple regressions were made which yielded predicting equations for both the unburned hydrocarbon and the NOx for the apparatus used. 相似文献
379.
George M. Hidy Charles L. Blanchard 《Journal of the Air & Waste Management Association (1995)》2013,63(10):1261-1282
Numerous papers analyze ground-level ozone (O3) trends since the 1980s, but few have linked O3 trends with observed changes in nitrogen oxide (NOx) and volatile organic compound (VOC) emissions and ambient concentrations. This analysis of emissions and ambient measurements examines this linkage across the United States on multiple spatial scales from continental to urban. O3 concentrations follow the general decreases in both NOx and VOC emissions and ambient concentrations of precursors (nitrogen dioxide, NO2; nonmethane organic compounds, NMOCs). Annual fourth-highest daily peak 8-hr average ozone and annual average or 98th percentile daily maximum hourly NO2 concentrations show a statistically significant (p < 0.05) linear fit whose slope is less than 1:1 and intercept is in the 30 to >50 ppbv range. This empirical relationship is consistent with current understanding of O3 photochemistry. The linear O3–NO2 relationships found from our multispatial scale analysis can be used to extrapolate the rate of change of O3 with projected NOx emission reductions, which suggests that future declines in annual fourth-highest daily average 8-hr maximum O3 concentrations are unlikely to reach 65 ppbv or lower everywhere in the next decade. Measurements do not indicate increased annual reduction rates in (high) O3 concentrations beyond the multidecadal precursor proportionality, since aggressive measures for NOx and VOC reduction are in place and have not produced an accelerated O3 reduction rate beyond that prior to the mid-2000s. Empirically estimated changes in O3 with emissions suggest that O3 is less sensitive to precursor reductions than is found by the CAMx (v. 6.1) photochemical model. Options for increasing the rate of O3 change are limited by photochemical factors, including the increase in NOx sensitivity with time (NMOC/NOx ratio increase), increase in O3 production efficiency at lower NOx concentrations (higher O3/NOy ratio), and the presence of natural NOx and NMOC precursors and background O3.Implications:?This analysis demonstrates empirical relations between O3 and precursors based on long term trends in U.S. locations. The results indicate that ground-level O3 concentrations have responded predictably to reductions in VOC and NOx since the 1980s. The analysis reveals linear relations between the highest O3 and NO2 concentrations. Extrapolation of the historic trends to the future with expected continued precursor reductions suggest that achieving the 2014 proposed reduction in the U.S. National Ambient Air Quality Standard to a level between 65 and 70 ppbv is unlikely within the next decade. Comparison of measurements with national results from a regulatory photochemical model, CAMx, v. 6.1, suggests that model predictions are more sensitive to emissions changes than the observations would support. 相似文献
380.
Steven W. Chapman Beth L. Parker John A. Cherry Shane D. McDonald Kenneth J. Goldstein Jeffrey J. Frederick Daniel J. St. Germain Diana M. Cutt Charles E. Williams 《补救:环境净化治理成本、技术与工艺杂志》2013,23(3):7-35
Detailed field investigations and numerical modeling were conducted to evaluate transport and fate of chlorinated solvent contamination in a fractured sedimentary bedrock aquifer (sandstone/siltstone/mudstone) at a Superfund site in central New Jersey. Field investigations provided information on the fractured rock system hydrogeology, including hydraulic gradients, bulk hydraulic conductivity, fracture network, and rock matrix, and on depth discrete contaminant distribution in fractures (via groundwater sampling) and matrix (via detailed subsampling of continuous cores). The numerical modeling endeavor involved application of both an equivalent porous media (EPM) model for flow and a discrete fracture network (DFN) model for transport. This combination of complementary models, informed by appropriate field data, allowed a quantitative representation of the conceptual site model (CSM) to assess relative importance of various processes, and to examine efficacy of remedial alternatives. Modeling progressed in two stages: first a large‐scale (20 km x 25 km domain) 3‐D EPM flow model (MODFLOW) was used to evaluate the bulk groundwater flow system and contaminant transport pathways under historic and current aquifer stress conditions and current stresses. Then, results of the flow model informed a 2‐D DFN transport model (FRACTRAN) to evaluate transport along a 1,000‐m flowpath from the source represented as a 2‐D vertical cross‐section. The combined model results were used to interpret and estimate the current and potential future extent of rock matrix and aqueous‐phase contaminant conditions and evaluate remedial strategies. Results of this study show strong effects of matrix diffusion and other processes on attenuating the plume such that future impacts on downgradient well fields under the hydraulic stresses modeled should be negligible. Results also showed futility of source remediation efforts in the fractured rock, and supported a technical impracticability (TI) waiver for the site. © 2013 Wiley Periodicals, Inc. 相似文献