东部沿海城市与西部半干旱地区近地层臭氧浓度观测研究

利用东部沿海城市天津大气边界层观测站(以下简称天津站)和西部兰州大学半干旱气候与环境观测站(SACOL)一年的臭氧和NOx体积浓度观测资料,对比分析了两观测站点近地层臭氧浓度的逐月变化、频率分布、日变化特征以及与NOx之间的相关关系.结果表明,两观测站点臭氧浓度月均值变化呈现出很好的一致性,均在4-7月出现高值,12月至次年2月出现低值,SACOL臭氧浓度月均值的最大值和最小值出现时间要比天津站推迟一个月.天津站臭氧体积浓度主要分布在10～50μL/m3,SACOL则集中在10～70 μL/m3,春、夏季两观测站点臭氧体积浓度低于10 μL/m3的频率均很小,秋、冬季两观测站点臭氧浓度频率分布特征类似.两观测站点臭氧浓度日变化在4个季节均呈现典型的单峰型分布,SACOL臭氧浓度日最大值出现时刻要比天津站晚2h.两观测站点臭氧浓度与NOx、NO2、NO的浓度之间均呈显著的负相关关系.天津站与臭氧浓度的相关性最强的为NO,而SACOL则是NOx.     

化学发光法和Saltzman法测定环境空气中二氧化氮的对比研究

分别采用化学发光法和GB／T15439—1995 Saltzman法平行测定环境空气中NO2浓度的日均值，并进行对比研究。实验结果表明，上述两种方法测得的NO2浓度的日均值基本一致，说明2108型化学发光法氮氧化物分析仪测得的NO2浓度的日均值与本站在建立环境空气质量自动监测系统前使用Saltzman法测得的NO2浓度的日均值具有连续性和可比性。     

电弧放电产生NOx及其对亚硫酸铵的氧化

将脱硫塔产生的高浓度亚硫酸铵氧化为硫酸铵是氨法脱硫研究的一个难点.利用二氧化氮(NO2)的氧化性,可以有效氧化高浓度的亚硫酸铵.空气中电弧放电可以产生氮氧化物(NOx),本研究采用高频交流电源,不锈钢针-针电极,研究了放电间距、气体流量、湿度和O2含量等参数对产物NOx的浓度和NO2/NOx比值的影响,并对产物气体做了红外分析和光谱分析.实验结果表明,放电间距增大有利于NOx浓度和NO2/NOx的提高,气体流量和湿度的增大使NOx浓度和NO2/NOx降低,O2含量为50％和60％时NO2浓度和NO2/NOx分别达到最大值.产物NOx对亚硫酸铵的氧化速率最高可达0.0264 mol/(L·min).     

南京北郊春季地面臭氧与氮氧化物浓度特征

2009年3—5月,采用NO-NO2-NH3分析仪和O3分析仪对南京市北郊大气O3、NO、NO2和NOx浓度进行连续观测,研究南京北郊春季大气臭氧与氮氧化物浓度变化特征。结果表明:O3浓度的日变化呈单峰型结构,白天较高,夜晚较低,在06:00左右出现最低值,14:00左右出现峰值,且工作日的O3浓度值明显高于周末的O3浓度值。NOx的日变化呈现双峰型变化规律,早上07:00左右出现第1个峰值,下午14:00—15:00左右达到最低值,午夜23:00左右出现第2个峰值。从3—5月份,NO浓度明显下降,3月份的变化幅度比较大;NO2浓度则明显上升,5月份变化幅度较大。3—5月NO与O3之间呈显著的负相关关系,4—5月NO2、NOx与O3呈显著的负相关关系。     

DOC系统催化性能的仿真和分析

以Langmuire Hinshelwood机理为理论依据,基于MATLAB/Simulink建立DOC系统的数值计算模型,研究不同参数(如空速、氧气浓度、NO2/NOx比例)对氮氧化物(NOx)、一氧化碳(CO)、碳氢化合物(HC)转化效率的影响,并对部分工况进行了实验研究,从而验证数值模型的准确性。结果表明,空速的降低可以增大DOC对CO、HC、NO的氧化性能,这是由于排气在催化器内的反应时间增长。当排气温度为225~300℃时,减小空速对增大HC的氧化效率效果明显,当排气温度在175~450℃范围内,减小空速对增大NO的氧化效率影响明显;当O2浓度低于1%,排气温度在175~250℃时,CO转化效率增大,在250℃之后均接近100%。当O2浓度为10%时,温度的变化对CO的转化效率影响很小。当O2浓度大于1%时,温度的变化对NO的氧化效率影响较大;当排气温度在300~550℃时,NO2/NOx比例的变化对NO的转化效率影响较大。降低排气中NO2/NOx比例,能够在排气温度高于300℃时,明显提高NO的转化效率。     

用活性填料催化氧化-硝酸吸收法脱除氮氧化物的研究

为了提高硝酸吸收氮氧化物的效率,对活性填料催化氧化-硝酸吸收NOx进行了研究.结果表明:活性填料能明显提高NOx的吸收效率;当NOx中NO2体积百分含量增加,其吸收效率增加;随进气浓度和液气比的增大,NOx吸收效率增加;随NO2浓度的增加,NO的吸收效率先增加后减少,在NO/NO2为3时,NO吸收效率最高;随NO的增加NO2的吸收效率先增加后减少,在NO/NO2为0.6～1之间,NO2的吸收效果较好.     

带CrO_3氧化管的库仑法测定NO_x总量

程祖良等建立了库仑法测定NO_2的方法。由于一般废气同时含有NO和NO_2,上述方法不能测定NOx总量。我们在库仑仪电解池前加一个CrO_3氧化管,预先将废气中的NO氧化成NO_2,然后将分析气样通入电解池进行测定。关于CrO_3氧化管氧化NO的应用虽已比较成熟,国内外也不少报导,但都是测定大气中NOx,NOx浓度较低时使用。对污染源中用CrO_3氧化管氧化NO的工作国内外都没     

机动车尾气中氮氧化物的分析检测技术

为了分析机动车尾气氮氧化物净化催化剂的催化性能 ,建立了一套尾气模拟评价体系 ,分别使用电化学法、化学发光法和比色法 3种氮氧化物分析手段进行检测。结果表明 ,3种方法都能在一定精度范围内测量机动车尾气中的氮氧化物 ,化学发光法测量精度高 ,响应时间短 ,能够及时地反映发动机运转过程中的氮氧化物浓度变化情况 ,是一种较好的分析手段。电化学法随着使用时间推移 ,响应时间变长 ,灵敏度降低 ,需要及时更换传感器。比色法通过化学吸收可以测定氮氧化物的浓度 ,不能实现连续在线分析 ,只能采样测量。在分析中 ,还尝试利用一些辅助设备 ,将尾气中的NO和NO2转化后再通入测量仪器 ,实现测量总氮氧化物或其中某一气体的功能     

机动车尾气中氮氧化物的分析检测技术

为了分析机动车尾气氮氧化物净化催化剂的催化性能，建立了一套尾气模拟评价体系，分别使用电化学法、化学发光法和比色法3种氮氧化物分析手段进行检测。结果表明，3种方法都能在一定精度范围内测量机动车尾气中的氮氧化物，化学发光法测量精度高，响应时间短，能够及时地反映发动机运转过程中的氮氧化物浓度变化情况，是一种较好的分析手段。电化学法随着使用时间推移，响应时间变长，灵敏度降低，需要及时更换传感器。比色法通过化学吸收可以测定氮氧化物的浓度，不能实现连续在线分析，只能采样测量。在分析中，还尝试利用一些辅助设备，将尾气中的NO和NO2转化后再通人测量仪器，实现测量总氮氧化物或其中某一气体的功能。     

生物法处理NOx废气的研究进展

氮氧化物 (NOx)是主要的大气污染物之一 ,是治理大气污染的一大难题。对当前国内外生物处理NOx 的研究现状进行了系统的论述 ,介绍了生物过滤法处理氮氧化物的基本原理 ,分析了生物过滤法处理氮氧化物存在的问题 ,并预测该技术的未来发展趋势     

基于人工神经网络的街道峡谷NO_x浓度的数值模型研究

通过对反向传播人工神经网络的算法和网络结构的研究,发现拟牛顿算法训练速度较快,能够较好地接近误差目标值,同时建立了包括输入层、隐含层、输出层的人工神经网络三层拓扑结构。通过对街道峡谷人工神经网络的训练,模拟计算了街道峡谷NOx浓度分布值。结果显示,训练误差和测试误差比为1.11,训练样本的模拟值与实测值的相关系数为0.93,测试样本的模拟值与实测值的相关系数为0.87,模拟值与实测值的相关系数均高于显著水平为α=0.05与α=0.01所对应检验性表的相关系数临界值。该模型能够用于街道峡谷污染物浓度的模拟计算,具有较好的泛化能力。     

中小型燃用烟煤层燃炉NO_x排放特征分析

以86台中小型燃烟煤层燃炉(≤65 MW)的燃料特性分析数据和NOx排放实测数据为基础,通过统计分析方法,研究了锅炉出力、过量空气系数、燃煤挥发分、燃煤氮含量对NOx排放浓度的影响,分析了我国中小型燃烟煤层燃炉NOx的排放与管理控制现状。结果表明,中小型燃用烟煤层燃炉NOx平均排放浓度为324.6 mg/m3;锅炉出力对NOx排放浓度不具有显著影响;燃煤挥发分增高,NOx排放浓度降低;过量空气系数和燃煤氮含量增大,NOx排放浓度增高;并建议在国家层面上尽快制订燃煤锅炉NOx排放标准限值。     

Simultaneous DOAS and mist-chamber IC measurements of HONO in Houston,TX

Nitrous acid is an important component of nighttime N-oxide chemistry, and provides a significant source of both OH and NO in polluted urban air masses shortly after sunrise. Several recent studies have called for new sources of HONO to account for daytime levels much higher than are consistent with current understanding. However, measurement of HONO is problematic, with most in-situ techniques reporting higher values than simultaneous optical measurements by long-path DOAS, especially during daytime. The discrepancy has been attributed to positive interference in the in-situ techniques, negative interference in DOAS retrievals, the difficulty of comparing the different air masses sampled by the methods, or combinations of these.During August and September 2006, HONO mixing ratios from collocated long-path DOAS and automated mist-chamber/ion chromatograph (MC/IC) systems ranged from several ppbv during morning rush hour to daytime minima near 100 pptv. Agreement between the two techniques was excellent across this entire range during many days, showing that both instruments accurately measured HONO during this campaign. A small bias towards higher LP-DOAS observations at night can be attributed to slow vertical mixing leading to pronounced HONO profiles. A positive daytime bias of the MC/IC instrument during several days in late August/early September was correlated with photochemically produced compounds such as ozone, HNO₃ and HCHO, but not with NO₂, NO_x, HO₂NO₂, or the NO₂ photolysis rate. While an interferant could not be identified organic nitrites appear a possible explanation for our observations.     

An evaluation of the tapered element oscillating microbalance method for measuring diesel particulate emissions

We determined the usefulness of tapered element oscillating microbalances (TEOMs) for researchers and engineers involved with measuring diesel particulate mass. Two different test facilities were used for generating diesel particulates and comparing the TEOM to the commonly used U.S. Environmental Protection Agency (EPA) manual filter method. The EPA method is very labor-intensive and requires long periods of time to complete. The TEOM is an attractive approach because it has the potential to reduce the amount of time and labor required in diesel testing, as well as to provide real-time particulate-mass data that are not obtainable with the EPA method. It was found that the TEOM was a precise and easy-to-operate instrument that could measure the mass concentration (MC) of diesel particulate emissions in real time. Although the TEOM diesel particulate MC measurements were highly correlated with the manual filter measurements, the two techniques were not equivalent because the TEOM consistently reported MC results that were 20-25% lower than those obtained using the manual filter technique. In conclusion, the TEOM can be used to increase test-cell throughput and to measure transient values of diesel particulate emissions at sites performing diesel-engine testing. However, unless EPA is able to certify the TEOM as an equivalent method, it cannot replace the manual filter method for diesel certification work.     

An Evaluation of the Tapered Element Oscillating Microbalance Method for Measuring Diesel Particulate Emissions

Abstract

We determined the usefulness of tapered element oscillating microbalances (TEOMs) for researchers and engineers involved with measuring diesel particulate mass. Two different test facilities were used for generating diesel particulates and comparing the TEOM to the commonly used U.S. Environmental Protection Agency (EPA) manual filter method. The EPA method is very labor-intensive and requires long periods of time to complete. The TEOM is an attractive approach because it has the potential to reduce the amount of time and labor required in diesel testing, as well as to provide real-time particulate-mass data that are not obtainable with the EPA method. It was found that the TEOM was a precise and easy-to-operate instrument that could measure the mass concentration (MC) of diesel particulate emissions in real time. Although the TEOM diesel particulate MC measurements were highly correlated with the manual filter measurements, the two techniques were not equivalent because the TEOM consistently reported MC results that were 20–25% lower than those obtained using the manual filter technique. In conclusion, the TEOM can be used to increase test-cell throughput and to measure transient values of diesel par-ticulate emissions at sites performing diesel-engine testing. However, unless EPA is able to certify the TEOM as an equivalent method, it cannot replace the manual filter method for diesel certification work.     

Do laboratory salinity tolerances of freshwater animals correspond with their field salinity?

The degree to which laboratory derived measures of salinity tolerance reflect the field distributions of freshwater biota is uncertain. In this paper we compare laboratory-derived acute salinity tolerance (LC(50) values) of freshwater macroinvertebrates (range 5.5-76 mS/cm) and fish (range 2.7-82 mS/cm) from southeastern Australia with the salinity from which they have been collected in the field. Only 4% of the macroinvertebrates were collected at salinity levels substantially higher than their 72-h LC(50) obtained from directly transferring animals from low salinity water to the water they were tested (direct transfer LC(50)). This LC(50) value was correlated with the maximum salinity at which a species had been collected. For common macroinvertebrates, the maximum field salinity was approximated by the direct transfer 72-h LC(50). For adult freshwater fish, 21% of species were collected at salinities substantially greater than their acute direct transfer LC(50) and there was a weak relationship between these two variables. Although there was a weak correlation between the direct transfer LC(50) of early life stages of freshwater fish and the maximum field salinity, 58% of the field distribution were in higher than their LC(50) values. In contrast, LC(50) determined from experiments that acclimated adult fish to higher salinity (slow acclimation) provided a better indication of the field distribution: with only one fish species (7%) being in conflict with their maximum field salinity and a strong positive relationship between these variables. This study shows that laboratory measures of acute salinity tolerance can reflect the maximum salinity that macroinvertebrate and fish species inhabit and are consistent with some anecdotal observations from other studies.     

北京市燃煤的空气质量影响及其控制研究

建立了2005年北京市燃煤污染源排放清单,利用MM5-CMAQ模型计算了各区县各行业燃煤对北京市空气质量的影响。研究表明,2005年1月北京市燃煤源对各监测站点SO_2浓度的贡献在70%以上,对PM_(10)和NO_x浓度的贡献约为20%～40%和10%～30%;7月本地燃煤源对SO_2浓度的贡献在40%～50%左右。1月采暖锅炉对空气质量影响最大,占50%～70%;7月电厂的影响最大。依据北京市奥运空气质量保障方案以及"十一五"期间能源规划,建立了2010年燃煤污染源大气排放的规划情景,并模拟了各规划措施对大气质量的改善效果。通过实施电厂脱硫脱硝除尘、炼焦工业停产、钢铁行业和水泥行业搬迁减产、供热锅炉改造、平房用煤改造等措施,与2005年相比,SO_2平均浓度下降30%左右,NO_x和PM_(10)浓度的下降幅度15%。     

小型燃油锅炉NO_x的排放特征与管理控制

以68台燃油锅炉(≤10.5 MW)NO_x排放实测数据为基础,通过统计分析方法,研究了NO_x的排放特征;通过对比分析,探讨了我国燃油锅炉NO_x排放控制与管理现状,讨论了进一步加强我国燃油锅炉NO_x排放管理控制的可能性与可行性,并提出了相应的管理控制建议。结果表明,NO_x平均排放浓度为318.2 mg/m~3,基于燃料消耗量的平均排放因子为4.4 kg/t,基于燃料发热量的平均排放因子为102.8 ng/J,基于燃料氮含量的平均排放因子为2.1 mg/mg;建议采取分阶段控制的方式,逐步提高NO_x排放限制,从而实现控源减排目标。     

Exposure of the marine deposit feeder Hydrobia ulvae to sediment associated LAS

Linear Alkylbenzene Sulfonates (LAS) effects (mortality, egestion rate, behaviour) on the marine deposit feeder Hydrobia ulvae were assessed in whole-sediment and water-only systems. The results were combined with a bioenergetic-based kinetic model of exposure pathways to account for the observed toxicity. The 10-d LC50 value based on the freely dissolved fraction was 9.3 times lower in spiked sediment (0.152 ± 0.001 (95% CI) mg/L) than in water-only (1.390 ± 0.020 (95% CI) mg/L). Consequently, the actual 10-d LC50 value (208 mg/kg) was overestimated by the Equilibrium Partitioning calculation (1629 mg/kg). This suggests that the sediment associated LAS fraction was bioavailable to the snails. It could also be due to modifications in physiological parameters in absence of sediment, the organism natural substrate.