HCI in Rocket Exhaust Clouds: Atmospheric Dispersion,Acid Aerosol Characteristics,and Acid Rain Deposition

NASA is examining Space Shuttle launch impacts. Solid rocket exhaust includes ?60 tons HCL and ?87 tons alumina particles emitted below 2.5 km, of which 50-80% forms an altitude stabilized exhaust cloud (EC). Several 60% smaller Titan-Ill EC were sampled by aircraft for this study. Three distinct features are presented: (a) An analysis of HCL (gaseous plus aqueous) data traces. Total range of peak HCL was 25-0.5 ppm (3-300 min) for 8 EC. Power-law decays of peak HCL applied. Calculated HCL dispersions for 7 standard meteorologies are also shown, (b) An analysis of simultaneous HCL (g), HCL (g + aq) data for 2 EC. Vapor-liquid HCL/H₂O equilibria were calculated for a flat surface aqueous aerosol. HCL partitioning varied with EC dilution and H₂O content. HCL (aq) and aqueous mass fraction maximized early at >3 molal and >0.1 mg/g air. Calculated H₂O (g + aq) compared favorably with independent EC measurements, (c) An analysis of wet deposition after EC interception at ?30 min by a convective storm. A 28 km² acid chloride (1 < pH < 3) footprint was defined. In conclusion, (a) HCL dispersion in large EC tends to follow power-law decay, but HCL concentration may vary widely (100 times after 1 h) with meteorology, (b) HCL (g/aq) and H₂O (g/aq) partitioning is consistent with equilibrated acid aerosol compositions, and (c) localized deposition of highly acidic rain may occur sometimes.     

Environmental Appraisal-Particulate Matter,Oxides of Sulfur,and Sulfuric Acid

The role of particulate matter and oxides of sulfur in degradation of the atmospheric environment is discussed. The Federal Air Quality Criteria for these pollutants are analyzed for their conformance with the requirement of the Clean Air Act of 1967 that they reflect the latest scientific knowledge pertinent to the indication of their effects on health and welfare. Visibility reduction by suspended particulate matter is treated and the bases for the criteria issued in the documents “Air Quality Criteria for Particulate Matter” and “Air Quality Criteria for Sulfur Oxides” are examined. The reactions between particulate matter and gaseous pollutants are discussed, along with the Impact of particulate matter on modifications of weather processes. Local effects, such as precipitation, are considered. The relationship between pollution by particulate matter and cloud formation is discussed, as are persistence of fog and the observation that certain sources of particulate pollution are also sources of ice nuclei.     

Ammonium Nitrate,Nitric Acid,and Ammonia Equilibrium in Wintertime Phoenix,Arizona

A secondary aerosol equilibrium model, SEQUILIB, is applied to evaluate the effects of emissions reductions from precursor species on ambient concentrations during the winter in Phoenix, Arizona. The model partitions total nitrate and total ammonia to gas-phase nitric acid and ammonia and to particle-phase ammonium nitrate. Agreement between these partitions and ambient measures of these species was found to be satisfactory. Equilibrium isopleths were generated for various ammonium nitrate concentrations corresponding to high and low humidity periods which occurred during sampling. These diagrams show that ammonia is so abundant in Phoenix that massive reductions in its ambient concentrations would be needed before significant reductions in particulate ammonium nitrate would be observed. When total nitrate is reduced by reductions in its nitrogen oxides precursor, proportional reductions in particulate nitrate are expected. Many of the complex reactions in SEQUILIB do not apply to Phoenix, and its ability to reproduce ambient data in this study does not guarantee that it will be as effective in areas with more complex chemistry. Nevertheless, the nitrate chemistry in SEQUILIB appears to be sound, and it is a useful model for addressing the difficult apportionment of secondary aerosol to its precursors.     

Toxicologic Appraisal of Particulate Matter,Oxides of Sulfur,and Sulfuric Acid

An examination of the available toxicological literature indicates that sulfur dioxide itself would be properly classified as a mild respiratory irritant, the main portion of which is absorbed in the upper respiratory tract. The reported industrial experience of symptoms of mild chronic respiratory irritation from exposures at or above 5 ppm is compatible with what would have been predicted on the basis of available toxicological data. The basic physiological response to inhalation of pure SO₂ appears to be a mild degree of bronchoconstriction reflected in a measurable increase in flow resistance. Although the response is highly variable, most individuals tested have responded to 5 ppm and levels of 5 to 10 ppm have upon occasion produced severe bronchospasm in sensitive individuals. This serves to point up the fact that experience with the industrial Threshold Limit Value (5 ppm) is not applicable as a guide for the general population. Although the majority of individuals tested have shown no detectable response to levels of 1 ppm, there are again sensitive individuals who have responded. It is not known whether these individuals would have responded to concentrations lower than this. The response of these more sensitive individuals to 1 ppm would be classified as detectable response, not as severe bronchospasm. An examination of the available toxicological literature also indicates that sulfuric acid and irritant sulfates, to the extent that the latter have been examined, are more potent irritants than sulfur dioxide. This has been demonstrated in studies using morality and lung pathology as criteria as well as in studies using alterations in pulmonary function in experimental animals and human subjects. The irritant potency of these substances is affected by particle size and by relative humidity, which factors are probably interrelated. It is unfortunate that these substances have not been as yet studied in as great detail as has the less irritant sulfur dioxide. There is evidence which cannot be ignored, even though it is based entirely on animal experiments of one investigator, indicating that the presence of particulate material capable of oxidizing sulfur dioxide to sulfuric acid caused a three to fourfold potentiation of the irritant response. The aerosols causing this potentiation were soluble salts of ferrous iron, manganese and vanadium all of which would become droplets upon inhalation. Insoluble aerosols such as carbon, iron oxide fume, triphenylphosphate or fly ash did not cause a potentiation of the irritant action of SO₂ even when used at higher concentrations. The concentrations of SO₂ used in these various experiments were in some cases as low as 0.16 ppm. The catalytic aerosols were used at concentrations of 0.7 to 1 mg/m³ which is above any reported levels of these metals in urban air. If the SO₂ present as an air pollutant remained unaltered until removed by dilution, there would be no evidence in the toxicological literature suggesting that it would be likely to have any effects on man at prevailing levels. Studies of atmospheric chemistry have shown that SO₂ does not remain unaltered in the atmosphere, especially under onditions of high humidity and in the presence of particulate material, but is converted to H₂SO₄. Such a conversion increases its irritant potency. On this basis the toxicological literature combined with the literature of atmospheric chemistry suggest that sulfur dioxide levels be controlled in terms of the potential formation of irritant particles. This means that control measures as far as feasible should be aimed at both SO₂ and particulate material and not against either alone.     

Particulate,Carbon Monoxide,and Acid Emission Factors for Residential Wood Burning Stoves

Emissions from residential wood burning stoves are of Increasing concern in many areas. This concern is due to the magnitude of the emissions and the toxic and chemical characteristics of the pollutants. Recent testing of standard and new technology woodstoves has provided data for developing a family of particulate and carbon monoxide emission factor curves. This testing has also provided data illustrating the acidity of woodstove emissions. The particulate and carbon monoxide curves relate the actual stove emissions to the stove size and operating parameters of burn rate, fuel loading, and fuel moisture. Curves relating stove types to the acidity of emissions have also been constructed.

Test data show actual emissions vary from 3 to 50 grams per kilogram for particles and from 50 to 300 grams per kilogram for carbon monoxide. Since woodstove emissions are the largest single category of particulate emissions in many areas, it Is essential that these emissions be quantified specifically for geographic regions, allowing meaningful impact analysis modeling to be accomplished. Emission factors for particles and carbon monoxide are presented from several stove sizes and burn rates.

The acidic nature of woodstove emissions has been clearly demonstrated. Tests indicate woodstove flue gas condensate solutions to be predominantly in the 2.8 to 4.2 pH range. Condensate solutions from conventional woodstoves exhibited the characteristic buffering capacity of carboxylic acids when titrations were performed with a strong base. The environmental impact of buffered acidic woodstove emissions is not currently well understood; however, it is possible with the data presented here to make semi-quantitative estimates of acid emissions from particulate and carbon monoxide emission factors and wood use inventories.     

Acid waters in upland Wales: causes, effects and remedies

Although situated on the western seaboard of the UK, and hence in the path of predominantly maritime air masses arriving directly from the Atlantic, Wales receives acidic deposition when winds are from the east. In conjunction with the highly base-poor rocks and soils found in the region, significant acidification of surface waters has occurred. Extensive afforestation in the Welsh uplands in the last 40 years has exacerbated acidification effects by elevating the loading of acidic anions received by catchments, thus increasing the concentrations of aluminium in watercourses. In considering possible remedial strategies, results of liming investigations from the Llyn Brianne Project in mid-Wales are presented. These studies have mainly involved liming small streams by a variety of catchment liming techniques. The most effective catchment treatments were those where finely ground CaCO3 was applied to the hydrological source areas at rates of up to 25 tonnes ha(-1). Possible drawbacks with such liming are discussed, although it is emphasized that liming is likely to be a component of any remedial strategy in the next 30 years until emissions reductions greater than those proposed in the forthcoming EC Directive are implemented.     

空气与废气中的正丁烷、丁酮、醋酸异丙酯的快速测定法

采用活性炭吸附，二硫化碳解析，毛细管气相色谱法同时测定空气与废气中的正丁烷、丁酮、醋酸异丙酯，采样体积以45L计，方法最低检出限分别为：正丁烷0．002mg／m^3，丁酮0.0024mg／m^3，醋酸异丙酯0．0028mg／m^3。     

Measurement and Analysis of the Relationship between Ammonia,Acid Gases,and Fine Particles in Eastern North Carolina

Abstract

An annular denuder system, which consisted of a cyclone separator; two diffusion denuders coated with sodium carbonate and citric acid, respectively; and a filter pack consisting of Teflon and nylon filters in series, was used to measure acid gases, ammonia (NH₃), and fine particles in the atmosphere from April 1998 to March 1999 in eastern North Carolina (i.e., an NH₃?rich environment). The sodium carbonate denuders yielded average acid gas concentrations of 0.23 μg/m³ hydrochloric acid (standard deviation [SD] ± 0.2 μg/m³); 1.14 μg/m³ nitric acid (SD ± 0.81 μg/m³), and 1.61 μg/m³ sulfuric acid (SD ± 1.58 μg/m³). The citric acid denuders yielded an average concentration of 17.89 μg/m³ NH₃ (SD ± 15.03 μg/m³). The filters yielded average fine aerosol concentrations of 1.64 μg/m³ ammonium (NH₄ ⁺;SD ± 1.26 μg/m³); 0.26 μg/m³ chloride (SD ± 0.69 μg/m³), 1.92 μg/m³ nitrate (SD ± 1.09 μg/m³), and 3.18 μg/m³ sulfate (SO₄ ^2?; SD ± 3.12 μg/m³). From seasonal variation, the measured particulates (NH₄ ⁺,SO₄ ^2?, and nitrate) showed larger peak concentrations during summer, suggesting that the gas-to-particle conversion was efficient during summer. The aerosol fraction in this study area indicated the domination of ammonium sulfate particles because of the local abundance of NH₃, and the long-range transport of SO₄ ^2? based on back trajectory analysis. Relative humidity effects on gas-to-particle conversion processes were analyzed by particulate NH₄ ⁺ concentration originally formed from the neutralization processes with the secondary pollutants in the atmosphere.     

Acid rain: chemistry and transport

This review describes the more important features of the emission, chemistry, transport and deposition of pollutants involved in acid deposition. Global emissions, both natural and man-made, of sulphur and nitrogen oxides are discussed and examples of spatial distributions and trends over the last century presented. The more significant chemical and physical processes involved in the transformation of the primary emissions into their acidic end products are described, including a summary of the approximate timescales of the processes involved. Measurements and modelled calculations of spatial and temporal patterns in the deposition of acidic pollutants by both wet and dry pathways are presented.     

Acid mine drainage arising from gold mining activity in Johannesburg,South Africa and environs

The Witwatersrand region of South Africa is famous for its gold production and a major conurbation, centred on Johannesburg, has developed as a result of mining activity. A study was undertaken of surface and ground water in a drainage system in this area. Soils were also analysed from a site within the mining district. This study revealed that the ground water within the mining district is heavily contaminated and acidified as a result of oxidation of pyrite (FeS2) contained within mine tailings dumps, and has elevated concentrations of heavy metals. Where the water table is close to surface, the upper 20 cm of soil profiles are severely contaminated by heavy metals due to capillary rise and evaporation of the ground water. The polluted ground water is discharging into streams in the area and contributes up to 20% of stream discharge, causing a lowering of pH of the stream water. Much of the metal load is precipitated in the stream: Fe and Mn precipitate as a consequence of oxidation, while other heavy metals are being removed by co-precipitation. The oxidation of iron has created a redox buffer which controls the pH of the stream water. The rate of oxidation and of dilution is slow and the deleterious effect of the addition of contaminated water persists for more than 10 km beyond the source.     

Characterization of Several Integrative Sampling Methods for Nitric Acid,Sulphur Dioxide and Atmospheric Particles

Laboratory and field experiments were performed to evaluate integrative measurement methods for atmospheric nitrates, sulphate and sulphur dioxide. Denuder tubes and several filter media were tested under laboratory and field conditions. Effects of sampling variables such as temperature and relative humidity, flow rates, concentration, loading capacity and artifacts due to NO, NO₂ and SO₂ were also evaluated. The integrative filter sampling method and the ion chromatographic analytical procedure gave a measurement precision (relative standard deviation) of ±11.5 percent for particulate NO₃ ^? on Teflon and ±15.6 percent for gaseous HNO₃ on nylon; for both these constituents, the detection limit was about 0.1 μ m^?3.     

Acid violet 7 and its biodegradation products induce chromosome aberrations,lipid peroxidation,and cholinesterase inhibition in mouse bone marrow

Introduction  

Acid violet 7 (AV7), mostly used in food, paper, cosmetic, and especially in textile industries, was degraded by Pseudomonas putida mt-2 at concentrations up to 200 mg/l.     

Acid rain, storm period chemistry and their potential impact on stream communities in Hong Kong

Hong Kong experiences acid deposition, however, little is known about the potential impact upon aquatic ecosystems. In a small drainage basin observations reveal that despite acid rain runoff, both baseflow and stormflow, was close to neutral in terms of pH. During storm events chemical analysis reveals that calcium (Ca) concentrations tended to rise. It also appears that the input of acid rain may increase aluminium (Al) levels in the stream. Due to the increased levels of Ca and only slight changes in pH acid deposition may not be generating problems in this stream. The presence of mayflies reported elsewhere may further support the results of the chemical study.     

Acid rain and pollen germination in corn

The properties of an acid rain episode that could influence the germination of pollen in corn, Zea mays L., were evaluated by treating silks with a simulated acid rain and measuring the subsequent germination of pollen on the silks. The data indicated that acid rain creates an inhospitable environment for pollen germination on the silk surface. Reduced germination appeared directly related to the acidity of the rain, but not the sulphate concentration. Rinsing silks with a pH 5.6 rain after treatment with a pH 2.6 rain did not increase pollen germination above that on silks treated only with a pH 2.6 rain, suggesting the reduced germination was due to physical and/or chemical modifications of the silk surface and not to residual acid on the tissue. Pollen germination on silks was inhibited even when silk tissue was exposed to a simulated rain of pH 2.6 for <1.5min.     

Reduced Adsorption of Ametryn in Clay,Humic Acid,and Soil by Interaction with Ferric Ion Under Fenton Treatment Conditions

Previous work in our laboratory indicated a weak interaction between ferric ion and several triazine/triazinone herbicides during a Fenton treatment process, and the intensity of the interaction was calculated. To further support the existence of this weak interaction, the adsorption of ametryn, a triazine herbicide, was investigated in kaolinite clay, humic acid, and soil under pseudo-Fenton conditions. At a low addition rate of ferric ion, the adsorption of ametryn in clay, humic acid, and soil was enhanced due to the decreased pH resulting from the hydrolysis of ferric ion. But the pH effect was totally neutralized and the adsorption of ametryn was significantly reduced by further addition of ferric ion, demonstrating the existence of the weak interaction between ametryn and ferric acid. Further study showed that the adsorption-reduction effect of ferric ion existed not only with ametryn but also with several other triazine/triazinone herbicides. This weak interaction may accelerate the desorption process during the remediation of triazine/triazinone herbicide-contaminated soil using a Fenton/Fenton-like treatment, but it may also impede the degradation of these herbicides.     

Studies on Sulfuric Acid Mist Downwind from a Sulfuric Acid Manufacturing Plant

Air pollution downstream from a sulfuric acid manufacturing plant is comprised of two aspects, the amount of acid mist fallout and the concentration in the atmosphere. This investigation shows that it is desirable to determine each of these by an independent method of collection. Pans of distilled water were used to collect and determine the sulfuric acid mist fallout and an electrostatic precipitator was used to determine the sulfuric acid mist concentration in the atmosphere. The use of Stokes’ Law to convert the results obtained by one method to those obtained by the other requires a knowledge of the particle size of the sulfuric acid mist droplets. Data presented show that tho uso of an average particle size can yield a picture of pollution which is in error by many orders of magnitude. The study shows that areas adjacent to a plant may be subjected to fallout of rather large particle size when there are not adequate methods for removal from the emission or byproduct gases.     

A Comparison of Phenoldisulfonic Acid,Nondispersive Infrared,and Saltzman Methods for the Determination of Oxides of Nitrogen in Automotive Exhaust

The Saltzman Phenoldisulfonic Acid and Nondispersive Infrared methods have been compared for the determination of oxides of nitrogen in automobile exhaust. The main purpose of this investigation was to determine whether the Nondispersive Infrared method could be used as a possible replacement for the Saltzman method. Results show that the Nondispersive Infrared analyzer can be used to measure NO_x in exhaust gases with advantages over both the Saltzman and Phenoldisulfonic Acid methods. These advantages include simplicity, speed, less complicated analytical technique, and the fact that it is better adapted to be carried out by technicians at the test site.     

酸回收的扩散渗析技术及其发展现状

介绍了扩散渗析酸回收技术的应用领域、产生过程和工作原理,着重列举了当前国内外对扩散渗析技术的研究和应用现状,展望了该技术的发展前景。该技术几乎不耗能源,是其他膜过程不可取代的,在资源日益紧张的今天,其应用前景十分乐观。