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141.
Background, Aims and Scope Secondary inorganic aerosol (SIA), i.e. particulate sulphate (S(VI)), ammonium and nitrate (N(V)) is formed from gaseous
precursors i.e., sulfur dioxide (S(IV)), ammonia and nitrogen oxides, in polluted air on the time-scale of hours to days.
Besides particulate ammonium and nitrate, the respective gaseous species ammonia and nitric acid can be formed, too. SIA contributes
significantly to elevated levels of respirable particulate matter in urban areas and in strongly anthropogenically influenced
air in general.
Methods The near-ground aerosol chemical composition was studied at two stationary sites in the vicinity of Berlin during a field
campaign in summer 1998. By means of analysis of the wind field, two episodes were identified which allow to study changes
within individual air masses during transport i.e., a Lagrangian type of experiment, with one station being upwind and the
other downwind of the city. By reference to a passive tracer (Na+) and estimates on dry depositional losses, the influences
of dispersion and mixing on concentration changes can be eliminated from the data analysis.
Results and Discussion Chemical changes in N(-III), N(V) and S(VI) species were observed. SIA i.e., N(V) and S(VI), was formed from emissions in
the city within a few hours. The significance of emissions in the city was furthermore confirmed by missing SIA formation
in the case of transport around the city. For the two episodes, SIA formation rates could be derived, albeit not more precise
than by an order of magnitude. N(V) formation rates were between 1.4 and 20 and between 1.9 and 59 % h-1 on the two days,
respectively, and S(VI) formation rates were > 17 and > 10 % h-1. The area south of the city was identified as a source of
ammonia.
Conclusion The probability of occurrence of situations during which the downwind site (50 km downwind of Berlin) would be hit by an
urban plume is > 7.4%. Furthermore, for the general case of rural areas in Germany it is estimated that for more than half
of these there is a significant probability to be hit by an urban plume (> 8%). The S(VI) formation rates are higher than
explainable by homogeneous gas-phase chemistry and suggest the involvement of heterogeneous reactions of aerosol particles.
Recommendation and Outlook The possible contribution of heterogeneous processes to S(VI) formation should be addressed in laboratory studies. Measurements
at more than two sites could improve the potential of Lagrangian field experiments for the quantification of atmospheric chemical
transformations, if a second downwind site is chosen in such a way that, at least under particular stability conditions, measurements
there are representative for the source area. 相似文献
142.
Jeffrey R. Brook Alan H. Wiebe Sandra A. Woodhouse Celine V. Audette Tom F. Dann Sandra Callaghan Maria Piechowski Ewa Dabek-Zlotorzynska Joseph F. Dloughy 《Atmospheric environment (Oxford, England : 1994)》1997,31(24):4223-4236
The Canadian Acid Aerosol Measurement Program (CAAMP) was established in 1992 to gain a better understanding of the atmospheric behaviour of fine particle strong acidity (“acid aerosols”) and to facilitate an assessment of the potential health risks associated with acid aerosols and particles in general. During 1992. 1993 and 1994, annular denuder and filter measurements were taken at four sites in Ontario, two in Quebec, three in the Atlantic Provinces and one in the greater Vancouver area. Mean fine particle sulphate concentrations (SO42−) were highest in southern Ontario (annual average ranged from 40–70 nmol m−3), lowest at a site in the Vancouver area (average = 16 nmol m−3) and second lowest in rural Nova Scotia. However, mean fine particle strong acid concentrations (H+) were geographically different. The highest mean concentrations were at the east coast sites (annual average of up to 30 nmol m−3). Acidities were lower in areas where the fine particle acidity experienced greater neutralization from reaction with ammonia. This included the major urban centres (i.e. Toronto and Montréal) and areas with greater amounts of agricultural activity, as in rural southern Ontario. On average, ambient concentrations of fine and coarse particle mass were larger in the urban areas and also in areas where SO42− levels were higher. All the particle components were episodic. However, compared to SO42− and fine particles (PM2.5 or PM2.1, depending upon inlet design), episodes of H+ tended to be less frequent and of shorter duration, particularly in Ontario. Saint John, New Brunswick, had the highest mean annual H+ concentration, which was 30 nmol m−3. H+ episodes (24 h concentration > 100 nmol m−3) were also the most frequent at this location. The high levels in Saint John were partially due to local sulphur dioxide sources and heterogeneous chemistry occurring in fog, which, on average, led to a 50% enhancement in sulphate, relative to upwind conditions.There was a substantial amount of intersite correlation in the day to day variations in H+, SO42− , PM2.5 and PM10 (fine + coarse particles) concentrations, which is due to the influence of synoptic-scale meteorology and the relatively long atmospheric lifetime of fine particles. Sulphate was the most regionally homogenous species. Pearson correlation coefficients comparing SO42− between sites ranged from 0.6 to 0.9, depending on site separation and lag time. In many cases, particle episodes were observed to move across the entire eastern portion of Canada with about a two-day lag between the SO42− levels in southern Ontario and in southern Nova Scotia. 相似文献
143.
144.
Vione D Maurino V Minero C Vincenti M Pelizzetti E 《Environmental science and pollution research international》2003,10(5):321-324
This work describes the nitration of aromatics upon near-UV photolysis of nitrate and nitrite in aqueous solution and upon photocatalytic oxidation of nitrite in TiO2 suspensions. Phenol is used in this work as a model aromatic molecule and as a probe for *NO2/N2O4. The photoinduced nitration of phenol in aqueous systems occurs upon the reaction between phenol and *NO2 or N2O4, and is enhanced by the photocatalytic oxidation of nitrite to *NO2 by TiO2. Aromatic photonitration in the liquid phase can play a relevant role in the formation of nitroaromatics in natural waters and atmospheric hydrometeors, thus being a potential pathway for the condensed-phase nitration of aromatics. Furthermore, the photoinduced oxidation of nitrite to nitrogen dioxide suggests a completely new role for nitrite in natural waters and atmospheric aerosols. 相似文献
145.
Brett C. Singer Alfred T. Hodgson William W Nazaroff 《Atmospheric environment (Oxford, England : 1994)》2003,37(39-40):5551
Sorption of emitted gas-phase organic compounds onto material surfaces affects environmental tobacco smoke (ETS) composition and exposures indoors. We have introduced a new metric, the exposure relevant emission factor (EREF) that accounts for sorptive uptake and reemission to give the mass of individual ETS constituents available for exposure over a day in which smoking occurs. This paper describes month-long experiments to investigate sorption effects on EREFs and potential ETS exposures under habitual smoking conditions. Cigarettes were smoked in a 50-m3 furnished room over a 3-h period 6–7 days per week, with continuous ventilation at 0.3, 0.6, or 2.1 h−1. Organic gas concentrations were measured every few days over 4-h “smoking”, 10-h “post-smoking” and 10-h “background” periods. Concentration patterns of volatile ETS components including 1,3-butadiene, benzene and acrolein were similar to those calculated for a theoretical non-sorbing tracer, indicating limited sorption. Concentrations of ETS tracers, e.g. 3-ethenylpyridine (3-EP) and nicotine, and lower volatility toxic air contaminants including phenol, cresols, and naphthalene increased as experiments progressed, indicating mass accumulation on surfaces and higher desorption rates. Daily patterns stabilized after week 2, yielding a steady daily cycle of ETS concentrations associated with habitual smoking. EREFs for sorbing compounds were higher under steady cycle versus single-day smoking conditions by 50% for 3-EP, and by 2–3 times for nicotine, phenol, cresols, naphthalene, and methylnaphthalenes. Our results provide relevant information about potential indirect exposures from residual ETS (non-smoker enters room shortly after smoker finishes) and from reemission, and their importance relative to direct exposures (non-smoker present during smoking). Under the conditions examined, indirect exposures accounted for a larger fraction of total potential exposures for sorbing versus non-sorbing compounds, and at lower versus higher ventilation rates. Increasing ventilation can reduce indirect exposures to very low levels for non-sorbing ETS components, but indirect routes accounted for 50% of potential nicotine exposures during non-smoking periods at all ventilation rates. 相似文献
146.
城市生活垃圾处置过程中环境污染防治 总被引:2,自引:0,他引:2
对我国城市生活垃圾处置技术发展现状进行了综述,着重阐述了垃圾处置过程中存在的废塑料、废电池、焚烧炉烟气等二次污染问题,指出应高度重视垃圾处置过程中环境污染防治问题。 相似文献
147.
石灰乳平均脱硫率达83%,但应用中存在一次进料量大、液气比波动大、PH值控制不严和设备不配套、管理不严等问题。应加强监督、加强管理,以充分发挥其作用。 相似文献
148.
中小型水泥企业粉尘治理的几项措施 总被引:1,自引:0,他引:1
水泥生产的粉尘污染是一个重大的环保问题,特别是我区一些中、小型水泥生产企业,只从自身的利益因素考虑而对这一问题没有引起足够的重视。本文针对水泥生产的粉尘治理问题提出了一些经济、可行的措施,从而使其降低粉尘的排放量,达到环保要求。 相似文献
149.
150.
该文叙述了合成氨生产造气工段吹风气烟尘治理的技术措施与注意事项 ,指出在改进工况操作、减少吹风带出物的同时 ,设置干式旋风除尘与水膜除尘 ,可取得很好的治理效果 ,烟尘达标排放 ,经济效益显著 相似文献