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1.
固体电解质SO_2(SO_3)传感器测定烟道气中的SO_2   总被引:2,自引:0,他引:2  
本文论述了利用北京科技大学研制的固体电解质SO2(SO3)传感器对测定烟道气中的SO2进行的研究。利用该传感器测定烟道气中的SO2,其测量范围为:50—17000mg/m3,相对标准偏差小于4.0%。因而具有测量范围宽,精确度高以及稳定性好的特点。设计的试验样机的总体噪声和漂移小于1.0mg/m3,同时具有体积小.重量轻和操作简单的特点。  相似文献   

2.
Personal monitoring methods for the determination of hourly integrated concentrations of NO2 and SO2 in ambient air have been developed. Triethanolamine (TEA)-impregnated C18 Sep-Pak cartridges were used to collect NO2 and SO2 simultaneously. After sampling, NO2 and SO2 as their nitrite, nitrate, sulfite and sulfate analogues were stripped from the cartridges with a solution of 5% methanol in distilled, deionized water (DDW) and then determined by ion chromatography. Laboratory tests were conducted to evaluate the sampling rate, collection and recovery efficiencies, breakthrough volumes, absorption capacity, interference and sample stability on the cartridge during storage. NO2 and SO2 detection limits of 0.3 and 0.4 ppb respectively for 1 h samples were obtained. Recoveries for both NO2 and SO2 exceeded 85%.  相似文献   

3.
A field campaign on aerosol chemical properties and trace gases measurements was carried out along the Delhi-Hyderabad-Delhi road corridor (spanning about 3,200 km) in India, during February 1-29, 2004. Aerosol particles were collected on quartz and cellulose filters using high volume (PM(10)) sampler at various locations along the route (i.e., urban, semi-urban, rural, and forest areas) and have been characterized for major cations (Na(+), Ca(2+), Mg(2+), K(+), and NH (4) (+)), anions (Cl(-), NO (3)(-), and SO (4)(2-)), and heavy metals (Cu, Cd, Fe, Zn, Mn, and Pb). Simultaneously, we measured NO(2) and SO(2) gases. These species show large spatial and temporal variations. The ambient PM(10) concentration has been observed to be the highest (55 ± 4 μg m(-3)) near semi-urban areas followed by forest areas (48 ± 2 μg m(-3)) and in rural areas (44 ± 22 μg m(-3)). The concentrations of NO( x ) (NO(2)+NO) and SO(2) ranged from 16 to 69 μg m(-3) and 4 to 11 μg m(-3), respectively. Among anions, NO(3)(-) and SO(4) (2-) are the major constituents of PM(10). The urban and semi-urban sites showed enhanced concentrations of Fe, Zn, Mn, Cd, and Pb. This study provide information about atmospheric concentrations of various species in the northern to central India, which may be important for policy makers to better understand the air quality of the region.  相似文献   

4.
为了探讨厦门金砖会晤期间的排放控制措施以及天气形势对大气颗粒物污染特征的影响,于2017年8月10日至9月10日对厦门气态污染物、细颗粒物(PM2.5)中的水溶性离子以及有机碳(OC)、元素碳(EC)等主要化学成分开展了高时间分辨率的在线监测。根据空气质量管控措施和天气形势将研究期分为6个阶段。管控前、管控期Ⅰ(非台风)和管控期Ⅱ(非台风) PM2.5质量浓度分别为(33. 12±9. 48)、(30. 30±17. 00)、(16. 01±4. 71)μg/m^3。管控期Ⅰ(台风)和管控期Ⅱ(台风) PM2.5质量浓度分别为(12. 40±3. 73)、(12. 45±3. 28)μg/m^3。结果表明:管控期Ⅰ(非台风)阶段受静稳天气的影响,管控效果削弱,PM2.5质量浓度下降幅度小;台风对颗粒物质量浓度下降的影响比管控更显著。管控初期,PM2.5中二次无机离子的质量浓度下降明显;台风对碳质组分质量浓度的影响不如无机组分显著。PMF源解析结果表明,二次无机源是PM2.5主要来源,随着管控措施的实行,扬尘源的贡献从21%降低到6%,而机动车源的贡献降幅不明显。台风期间SO4^2-、NO3^-、SO2、NO2以及硫酸盐氧化比值(SOR)均明显低于非台风期间,氮氧化比值(NOR)反而升高。台风和非台风期间NOR的日变化特征一致,NOR与阳离子的相关性分析结果表明,台风或高风速海风期间NOR与Na^+呈现很强的正相关性,说明海盐粒子可促进NO2非均相反应生成NO3-。  相似文献   

5.
对南通市2016年12月-2018年10月大气污染季节分布特征进行了分析。结果表明,南通市ρ(PM2.5)和ρ(水溶性离子)为冬、春季高,夏、秋季低。春夏秋冬四季ρ(水溶性离子)占ρ(PM2.5)百分比分别为68.2%,70.6%,64.5%和74.5%,其中二次离子SNA(NO3-、SO42-和NH4+)占ρ(PM2.5)的百分比分别为63.1%,67.0%,59.3%和66.8%;ρ(NO3-)/ρ(SO42-)表明,移动源已成为南通市春、秋、冬季的主要污染源,四季均存在不同程度的二次转化,且SO2的转化率均大于NO2,NO2冬季转化率最大、夏季最小,SO2夏季转化率最大、秋季最小。南通市NO2转化为硝酸盐的主要形式是气相均相反应,非均相反应和均相反应对SO2转化为硫酸盐的贡献差异不大。  相似文献   

6.
Total suspended particulate (TSP) samples were collected during wintertime from November 24, 1998 to February 12, 1999 in Beijing. Ionic species including Cl-, NO3(-), SO4(2-), Na+, NH4(+), K+, Mg2+ and Ca2+ were determined by Ion Chromatography (IC). The sum average concentration of all the determined ions accounted for 18.9% of the TSP concentration, and SO4(2-) appeared the dominant ion with an average concentration of 30.84 microg m(-3); the sum mass concentration of SO4(2-), NO3(-), Ca2+ and NH4(+) accounted for about 83.2% of all the eight ions measured. The study indicated that the chemical form of sulfate and ammonium varies with TSP concentration levels. During heavy pollution periods, the average TSP concentration was 0.66 mg m(-3), and the NH4(+)/SO4(2-) molar ratio was low (0.58). It indicated that sulfate may present as CaSO4 and (NH4)2SO4 x CaSO4 x 2H2O. When TSP concentration (average 0.186 mg m(-3)) was relatively low, the NH4(+)/SO4(2-) molar ratio was 1.94, close to the theoretical ratio of 2 of (NH4)2SO4. Under this condition (NH4)2SO4 is expected to exist as the major form of sulfate. When the TSP concentration level was medium (average 0.35 mg m(-3)), the NH4+/SO4(2-) molar ratio appeared an average value (1.27), (NH4)2SO4, (NH4)2SO4 x CaSO4 x 2H2O and CaSO4 are expected to be present in those aerosol particles. Meteorological conditions including wind speed and wind direction were related to the TSP concentration level.  相似文献   

7.
通过现场监测和调研数据,分析燃用蔗髓锅炉的硫平衡及SO 2排放情况。结果显示,烟气排放的SO 2主要来源于鲜蔗和回用洗布水中含有的硫。8个锅炉硫排放在线监测均值与手工监测均值相对偏差为3.76%~14.9%,表明结果一致性较好。蔗髓硫质量分数为0.01%~0.04%,蔗髓含硫折算后的SO 2值和在线监测SO 2值分别为22.1 mg/m 3~49.9 mg/m 3和43.9 mg/m 3~114.5 mg/m 3,说明鲜蔗和制糖工艺流程的共同影响使得燃用蔗髓锅炉排放烟气SO 2值偏高。  相似文献   

8.
The objective of this work was to develop a novel wet-scrubbing process using Fe(VI) for the simultaneous removal of gaseous NO and SO(2). The oxidation of SO(2) and NO with Fe(VI) was studied in aqueous solution at alkaline pH (9.0-11.0). A stoichiometric molar ratio for NO and SO(2) oxidation with Fe(VI) was determined to be nearly 3.0. Sulfate and nitrate was identified as final products by ion chromatography from the reaction at pH 9.0-11.0. The feasibility of simultaneous removal of multiple gas pollutants with the continuous feeding of ferrate in lab-scale was investigated from the view of industrial application. It was found that the removal efficiency of NO and SO(2) was enhanced with the increase of Fe(VI) concentration, more than 90% NO removal efficiency and 100% SO(2) removal efficiency were achieved by wet-scrubbing process using Fe(VI) at room temperature and ambient atmosphere. The results demonstrate that Fe(VI) could be an effective wet-scrubbing agent for the simultaneous removal of NO and SO(2).  相似文献   

9.
The Helsinki Metropolitan Area Council (YTV) is responsible for air quality monitoring in the Helsinki area. Air quality has been monitored periodically since the late 1950s. An automatic SO2 monitoring network was constructed in 1975 and TSP measurements were added in 1978. Since then the network has been expanded and currently five automatic multicomponent stations form the basis of the network monitoring SO2, NO, NO2, CO, PM10 and O3 concentrations. Manual TSP and PM10 measurements are also conducted. Mobile monitoring units are also being used as well as special measurement campaigns. The effects of air pollution on nature are studied in bioindicator monitoring. An air quality index is used in order to inform the public of the current air quality situation. Changes in air quality are reflected in monitoring strategy. SO2 concentrations have decreased in the past two decades. Annual averages in 1995 were at or below 5 µg/m3. Traffic is the major source for pollutants even though catalytic converters have lowered traffic emissions somewhat. The highest annual average NO2 concentration at an urban site was 49 µg/m3 in 1995, and there has been no clear change in NO2 levels. There has been a decreasing trend in CO concentrations. Maximum annual TSP and PM10 averages in 1995 were 92 and 32 µg/m3, respectively. The highest average lead concentration was 0.01 µg/m3. Elevated concentrations are experienced from time to time. During the spring daily TSP and PM10 concentrations can go up to around 300 and 150 µg/m3, respectively. This is caused by resuspension mainly due to street sanding. Also a major winter NO2 episode occurred in December 1995. The highest hourly NO2 concentrations reached 400 µg/m3.  相似文献   

10.
The emission of nitrogen compounds from power plants accounts for a significant proportion of the total emissions of nitrogen to the atmosphere. This study seeks to understand the nature of chemical reactions in the atmosphere involving nitrogen, which is important in undertaking quantitative assessments of the contribution of such reactions to local and regional air pollution. The slant column density (SCD) of power-plant-generated NO(2) was derived using imaging differential optical absorption spectroscopy (I-DOAS) with scattered sunlight as a light source. The vertical structure of NO(2) SCD from power plant stacks was simultaneously probed using a pushbroom sensor. Measured SCDs were converted to mixing ratios in calculating the rate of NO(2) increase at the center of the plume. This study presents quantitative measurements of the rate of NO(2) increase in a rising plume. An understanding of the rate of NO(2) increase is important because SO(2) and NO(x) compete for the same oxidizing radicals, and the amount of NO(x) is related to the rates of SO(2) oxidation and sulfate formation. This study is the first to directly obtain the rate of NO(2) increase in power plant plumes using the I-DOAS technique. NO(2) increase rates of 60 and 70 ppb s(-1) were observed at distances of about 45 m from the two stacks of the Pyeongtaek Power Plant, northwest South Korea.  相似文献   

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