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11.
Alexander Goetz Ph.D. Rudolf F. Pueschel M.S. 《Journal of the Air & Waste Management Association (1995)》2013,63(3):90-95
The role of nucleating particulates in the formation of photochemical aerosols has been studied in a steady, laminar flow of ultrafiltered air containing NO2 and octene-1 in the concentration range of (30 to 170 ppm) when subjected to intense irradiation under isothermal conditions. The particulates consisted of monodisperse polystyrene latex (d = 0.36 μ.) in concentrations similar to those in the atmosphere (6 × 101 to 3 × 103 cm–3); the irradiation intensity varied between (6 to 40 × 103 lumen/liter) and the mean exposure duration between 30 and 180 sec. Samples of the flow prior to and after its photoactivation were withdrawn either by an Aerosol Spectrometer (AS) or by a Royco Aerosol Photometer (PH). While these indications refer thus to the same system, they differ, because the photometric data include all colloidal components in the airborne state, whereas the counts obtained from the AS deposits refer only to the nucleated latex particles. The following pattern becomes evident: The photochemical reaction yields fractional products (less than three percent) which have the tendency to agglomerate (or polymerize) due to their relatively low volatility—independent of the presence or absence of nucleating particulates. In their presence, this reaction becomes kinetically more probable and thus faster, hence the accumulant formation occurs preferably on the nuclei and causes their growth such that, e.g., a 10-fold higher nuclei concentration will produce under the same conditions 10 times the accumulant mass while autonucleation is suppressed. The growth process appears thus principally different from that of fog formation by H2O-condensation, whereas for identical super saturation it is inversely proportional to the nuclear concentration. In the absence of nuclei autonucleation, i.e., self-agglomeration, occurs at a much lesser reaction rate and higher photon demand. The growth rate of the nuclei, when present, depends on the concentration of the oxidation catalyst (NO2), its interaction with the nuclei surface is indicated. Under identical conditions the mass of nuclear accumulant is directly proportional to the concentration of the reactive hydrocarbon, while the growth rate depends on the light intensity and the exposure duration. The findings indicate that density and nature of particulate matter present in an air mass prior or during photo-activation are—aside from the chemical reactant levels—of major significance in aerosol formation. 相似文献
12.
Lawrence Demaio Morton Corn Ph.D. 《Journal of the Air & Waste Management Association (1995)》2013,63(2):67-71
Pittsburgh air was sampled continuously at one site for 886 hrs./sample at 45 cfm with a high volume sampler equipped with a horizontal elutriator as a first stage of separation, and an MSA 1106B glass fiber filter as a final particulate collection stage. The horizontal elutriator was designed to simulate the particulate deposition characteristics of the human respiratory tract. Samples were collected during the period June 1964 to February 1965. Respirable and non-respirable particulate samples were analyzed for polynuclear aromatic hydrocarbon content by a new technique which utilized dual column, flame ionization gas chromatography. It was possible to quantitatively analyze a concentrated benzene extract of the particulate sample for the following individual components: 1, 2 benzanthracene; chrysene; pyrene; 3,4 benzofloranthene; 1, 12 benzoperylene. It was not possible to distinguish between 3,4 benzopyrene, 1,2 benzopyrene and perylene; only the total quantity of these compounds present was detected. This analytical technique is comparable in sensitivity to formerly reported, more time-consuming methods and is very rapid, requiring less than one hour to perform after benzene extraction. Amounts of the above compounds associated with the two particulate fractions collected are reported and discussed. 相似文献
13.
G. Van Houte B. Delmon J.C. Maon Ph. Dumont 《Journal of the Air & Waste Management Association (1995)》2013,63(10):1030-1033
This publication concerns the dry removal of SO2 from gases using limestone absorbents. It reports bench-scale experiments made with commercial samples of powdered limestone (CaCO3) activated by addition of a cheap substance, namely CaCl2. The absorption was carried out in a fluidized bed traversed by the flue gases, between 600° and 900° C. The degree and rate of transformation of CaCO3 to CaSO4 in the presence of SO2 and air have been compared for unmodified and modified absorbents. Initial rates of reaction, and the variation of the rate of absorption with time have been measured. The influence of the SO2 content of the gas has been assessed. At 700° C, the maximum degree of transformation of activated limestone to sulfate exceeds 90%, whereas untreated CaCO3 transforms only to 16–20%. At the same temperature, more than 90% of SO2 contained In a gas carrying 0.35% SO2 is removed. Because of the much smaller quantity of solid absorbent required, dry absorption processes based on the modified absorbents might get renewed interest. The modified absorbents might also be used for in situ absorption in fluidized bed combustion, in which the temperatures are in the range studied in the present paper. 相似文献
14.
Morris Katz Ph.D. D.Sc. 《Journal of the Air & Waste Management Association (1995)》2013,63(5):528-557
Atmospheric pollution attributed to increased combustion of fossil fuels has been implicated as a likely contributing factor in observed changes to forests in North America and Europe. Uncertainties surrounding the mechanisms and specific causes for these changes have prompted intensified interest in research on air pollution effects on forests. Major objectives of this review are 1) to provide a conceptual and historical perspective against which today's problems, concerns, and approaches can be evaluated; 2) to evaluate evidence of changes in growth and vitality of some tree species in today's forests; 3) to compare levels of principal atmospheric pollutants in Europe and the U.S.; 4) to describe mechanisms, pathways, and concentration thresholds for effects of principal pollutants on tree growth and physiology; 5) to summarize current evidence for the role of pollution in observed forest declines; and 6) to provide some perspectives on future research in this area. Evidence from laboratory and field research is examined to provide a basis for evaluating the role of atmospheric pollution in present and potential future forest responses. 相似文献
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Tendergreen bean plants were grown from seeding to seed maturity under continuous exposure to HF gas at fairly uniform concentrations averaging 0.58, 2.1, 9.1, and 10.5 µg F/m3. Progeny of these plants and of comparable control plants were grown in a clean atmosphere to determine if subsequent generations were affected by HF treatment of the parents. No effects of HF were found among the progeny of the plants grown at 0.58 µg F/m3. The F1 generation progeny of the other HF treated plants were less vigorous than control plant progeny, as shown by later emergence, smaller primary leaves, and slower stem growth. This probably was a consequence of the lower starch content of the seed of the HF treated plants. The primary leaves of some F1 progeny of the plants grown in the three highest HF treatments were severely stunted and distorted. This also may have been due to the low starch content of the seed, or perhaps it resulted from damage to the plumules in shriveled, distorted seed produced in these treatments. Some of the early trifoliate leaves of many F1 generation progeny of the plants grown at 2.1 µg F/m3 and higher were abnormal in the separation and number of their leaflets. This abnormality apparently was heritable, for in the next (F2) generation it occurred most frequently among plants whose parents were abnormal. However, considerably fewer F3 generation plants had abnormal trifoliate leaves, indicating rapid reversal to the normal form. 相似文献
17.
Amos Turk Ph.D. 《Journal of the Air & Waste Management Association (1995)》2013,63(3):157-159
In the Municipality of Metropolitan Toronto which covers 240 square miles there are over 600,000 automobiles, 350,000 domestic and industrial oil and coal-burning installations, 5000 apartment and industrial incinerators, and other numerous sources of air pollution, many of which create serious problems and contribute to the total air pollution level. The area includes 13 municipalities comprising Metropolitan Toronto and 13 additional surrounding urban and rural localities in an area of 720 square miles. The population of the planning area is 1,965,000 and is expected to increase to 2,800,000 by 1980. The Planning Board showed its recognition of the problem by a statement of policy designed to reduce pollution from fuel-burning equipment and incinerators, to develop a coordinated transportation system, to encourage central heating plants, and to control apartment development in mixed commercial areas. The Board advises and assists the individual planning boards, and building and property departments. 相似文献
18.
Ralph I. Larsen Ph.D. William W. Stalker Charles R. Claydon 《Journal of the Air & Waste Management Association (1995)》2013,63(11):529-534
This progress report describes the National Air Pollution Technical Information Center currently under development in the Division of Air Pollution, Public Health Service. It briefly reviews the report "Science, Government, and Information" (Weinberg Report) and the White House delegation of responsibility to the Department of Health, Education, and Welfare for handling air pollution technical information. 相似文献
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