北京市机动车尾气排放PM10组分特征研究

为提高机动车尾气排放可吸入颗粒物PM10成分谱的代表性和准确性,提出并采用在机动车尾气检测线上采用稀释通道采样器随机采集机动车排出PM10的采样方法。采集了591辆轻、重型汽油车和柴油车尾气排放PM10,测试并分析了颗粒物的27种组分。数据表明:机动车排放颗粒物PM10中含量丰富的组分为OC、EC、NH+4、NO-3和SO2-4;柴油车排放PM10中OC和EC的质量分数为49.08%,是汽油车(38.38%)的1.3倍,汽油车的OC/EC(2.36)是柴油车(0.78)的3倍;汽油车排放PM10中的二次转化产物(SO42-+NH4++NO3-)的质量分数为19.37%,是柴油车(3.57%)的5.4倍;汽油车排放NH+4是柴油车的5.3倍。     

沈阳市机动车大气污染物排放清单的研究

基于机动车主要污染物排放量计算方法,对主要污染物排放因子进行识别与修正,建立沈阳市机动车污染物排放清单。结果表明:沈阳市机动车污染物的排放总量为206 804. 3 t,CO、NOx、HC和PM10的排放量分别为128 500. 4 t、44 206. 3 t、32 104. 8 t和1 992. 8 t;机动车排放的各污染物二环以内的排放量占总量70. 0%以上,和平区、沈河区和铁西区是该市机动车污染物高排放区域;小型客车和出租车对CO、HC的排放分担率较高,重型货车和轻型货车是NOx、PM10的主要排放源;沈阳市机动车污染物主要来自汽油车和柴油车,新能源机动车排放量较低。     

春季广州城区空气中VOCs来源解析

2013年4月在广州市区对大气中挥发性有机化合物(VOCs)进行了观测,对其变化特征和来源进行了分析。结果表明,观测期间测得的VOC总平均混合比为41.35×10~(-9),表现为烷烃芳香烃烯烃炔烃;利用PMF解析出观测时段内影响广州市区的9个VOCs主要来源,各源占比情况依次为:LPG排放老化VOC汽油挥发石化、未知源汽油车排放油漆溶剂柴油车排放天然源;与机动车相关和工业相关的来源分别占到了大气VOCs的46.8%和21.0%。     

不同类型机动车尾气挥发性有机化合物排放特征研究

机动车尾气主要成分包括一氧化碳、氮氧化物、碳氢化合物、铅及苯并[a]芘等.其中,挥发性有机化合物由于其对光化学烟雾的贡献及对人体健康的影响而成为近年来大气化学研究的热点.文章首次对北京市9种车辆、5种燃料在不同工况下排放挥发性有机化合物特征进行了定量研究.结果表明,车型、燃料、净化器及工况等因素对排放量产生影响,电喷车比化油器车排放低,其中,夏利比富康与奥迪排放量高;LPG与汽油车排放量最高,柴油车与CNG车排放最低.其中,-10#柴油车比0#柴油车排放更低;使用净化器可以降低挥发性有机化合物排放量;不同工况对排放量的影响随车型、燃料类型的不同而不同.因此,使用清洁燃料、安装净化器和使用电喷装置,可减少尾气中挥发性有机化合物含量.     

基于硫碳同位素研究南京北郊冬季霾事件中PM2.5来源

2015年12月27日—2016年1月6日,针对南京北郊地区一次霾事件所采PM_(2.5)样品,测定样品中水溶性离子、硫同位素与碳同位素组分含量。水溶性离子研究结果表明:该次霾事件以二次污染为主且移动源占主要地位。硫同位素分析结果表明:硫酸盐的δ~(34)S(SO_4~(2-))值的范围为4.4‰~6.8‰,平均值为5.7‰±0.7‰(n=11),结合该地潜在硫源可知,此次霾事件中硫酸盐气溶胶主要来源为机动车尾气及煤炭燃烧。PM_(2.5)中的δ~(13)C值变化范围为-28.43‰~-24.94‰,平均值为-26.62‰±1.11‰,说明碳质污染物来源主要为机动车尾气、燃煤。此外,硫、碳同位素具有较好的负相关性,结合潜在硫源、碳源可知,2016年1月1日之前,南京北郊地区大气污染源以汽油车尾气排放为主;1月1日之后大气污染源以柴油车尾气和燃煤排放为主。     

珠江三角洲某乡镇气溶胶中有机污染物的研究

通过对珠江三角洲某一乡镇的城区及三个乡村气溶胶有机污染物研究 ,发现烷烃类有机物高分子部分具有明显分不开的鼓包 ,污染较为显著 ;所有样品均含有多种多环芳烃 (PAHs) ,化合物种类比广州多 4～ 8种 ,并均含有机动车尾气排放的标志化合物烷基苯 (M Z91 ,92 )和塑料增塑剂等来源的邻苯二甲酸酯类 (M Z1 49)。表明该镇各区域均已明显受到机动车尾气排放和企业废气排放的污染。     

大连市秋冬季环境空气中VOCs特征及臭氧生成潜势分析

对大连市2015年秋冬季环境空气中VOCs进行采样分析,获得其组成、含量、昼夜和季节变化规律,分析不同类别VOCs的来源,并计算不同VOCs物种的臭氧生成潜势（OFP）。结果表明：大连市环境空气中秋季VOCs平均体积浓度（55.81×10^-9）略高于冬季（42.66×10^-9）;秋季VOCs以羰基化合物和烷烃为主,而冬季VOCs以烷烃和烯炔烃为主。大连环境空气中光化学反应的主要VOCs类别为羰基化合物、烯炔烃和芳香烃,主要物种为丙烷、乙烷、正丁烷和乙烯。羰基化合物含量高与机动车尾气及医院大量试剂的使用有关,烷烃主要来源于汽油车与液化石油气（LPG）燃烧排放,芳香烃主要由机动车排放贡献。各类别VOCs的组分含量与其OFP并不一致,大连市环境空气中各类VOCs的OFP由高到低依次为羰基化合物>芳香烃>烯炔烃>烷烃。     

南京市机动车排气监测与评价

通过对南京市机动车排气污染物的年检监测,表明南京市的汽油车、柴油车、摩托车排气合格率总体呈上升趋势,2002年全市机动车排气监测总合格率为99.9%,比1993年上升了8.6个百分点;汽车尾气达标率也呈上升趋势,2002年达83.8%,比1993年上升了2.6个百分点。对机动车排气路检结果表明,CO超标的车辆占84.4%,CO、HC两项指标都超标的车辆占31.1%。对各类汽油助力车排气监测结果表明,二冲程汽油助力车尾气中CO、HC排放量要高于四冲程汽油助力车的排放量。对各类正三轮摩托车排气抽检结果表明,大部分四冲程正三轮摩托车尾气排放污染物能达标,且排气管无碳烟;二冲程正三轮摩托车尾气中HC值偏高,排气管碳烟明显。     

国内外VOCs排放管理控制历程

介绍了挥发性有机污染物(VOCs)的定义、来源和危害,回顾了国内外VOCs监测技术、观测浓度、排放标准及规范,概括了欧美等发达国家宏观层面上的VOCs排放管理控制战略、经验及效果.建议我国建立VOCs在线监测网络,开展VOCs排放清单计算工作,进一步加强机动车尾气排放VOCs控制,初步制定宏观层面的VOCs总体控制战略...     

典型化工园区大气中挥发性有机物污染调查

对常州市某典型化工园区大气中挥发性有机物(VOCs)污染状况进行了调查。结果表明,该化工园区大气中检出挥发性有机物共有58种,组分有芳香烃、饱和烷烃、卤代烃、烯烃、醛酯类化合物及其他类;苯、甲苯、乙苯、二甲苯为主要挥发性有机污染物,质量浓度为1.0~194μg/m~3;均未超出参考标准的限值。背景点位和园区点位大气中主要ρ总(VOCs)在秋冬季最高,敏感点大气VOCs随季节变化也较为明显;园区T1和T2ρ总(VOCs)年均值高于敏感点位,背景点位年均值最低;园区点位除了汽车尾气排放之外,溶剂的挥发和生产工艺中污染物的排放也增加了大气中苯系物的浓度,同时也对敏感点位和对照点位的大气质量产生了一定的影响。     

机动车排放细颗粒物精细化源谱构建及应用

利用真空瓶现场采样并结合单颗粒气溶胶质谱（SPAMS）技术,对主流品牌汽油车和柴油车排放细颗粒物进行组分分析和源谱构建。结果表明：汽、柴油车尾气源谱特征整体较为相似,相似度均值达到0.88,均以碳和钙为主要特征组分;部分柴油车特征源谱中硫酸盐特征较为明显,碳组分中OC特征突出;汽油车源谱特征中磷酸盐特征相对突出,且碳组分中短链元素碳占比较高。根据建立的源谱进行实际道路观测,结合风速、风向等气象要素分析,2021年2月1日—24日观测点位对应的移动源占比为33.5%,其中汽油车贡献21.0%,柴油车贡献12.5%。     

2020年江苏省机动车排放污染分布特征及与大气质量耦合性研究

依据生态环境部2021年6月发布的《排放源统计调查产排污核算方法和系数手册》,结合本地实测数据,在对汽油车颗粒物(PM)排放系数进行测算的基础上,核算了2020年江苏省机动车PM、氮氧化物(NO_(X))、挥发性有机物(VOC_(S))的排放总量,分析了机动车排放污染分布特征及与大气质量的耦合关系。结果表明:2020年江苏省机动车PM、NO_(X)、VOC_(S)排放量分别为0.5×10^(4),3.71×10^(5),1.17×10^(5) t。从区域分布来看,苏州、南京、无锡3市的3项污染物排放总量及NO_(X)、VOC_(S)排放量均位列前3位,PM排放量位列前3位的是苏州、徐州、无锡。从车型、燃料类型和排放阶段来看,国Ⅳ及以下排放标准的汽油小型客车是机动车VOC_(S)排放控制的重点,国Ⅲ排放标准的重型柴油货车是机动车PM和NO_(X)排放控制的重点。分析区域机动车PM排放量与大气中PM_(2.5)来源解析结果的耦合关系,其间存在不同程度的正相关性,控制机动车污染对改善大气环境会产生积极成效,南京、徐州和盐城3市的成效会尤为明显。     

Assessment of Air Quality After the Implementation of Compressed Natural Gas (CNG) as Fuel in Public Transport in Delhi, India

Public transport in Delhi was amended by the Supreme Court of India to use Compressed Natural Gas (CNG) instead of diesel or petrol. After the implementation of CNG since April 2001, Delhi has the highest fraction of CNG-run public vehicles in the world and most of them were introduced within 20 months. In the present study, the concentrations of various criteria air pollutants (SPM, PM₁₀, CO, SO₂ and NO_x) and organic pollutants such as benzene, toluene, xylene (BTX) and polycyclic aromatic hydrocarbons (PAHs) were assessed before and after the implementation of CNG. A decreasing trend was found for PAHs, SO₂ and CO concentrations, while the NO_x level was increased in comparison to those before the implementation of CNG. Further, SPM, PM₁₀, and BTX concentrations showed no significant change after the implementation of CNG. However, the BTX concentration demonstrated a clear relation with the benzene content of gasoline. In addition to the impact of the introduction of CNG the daily variation in PAHs levels was also studied and the PAHs concentrations were observed to be relatively high between 10 pm to 6 am, which gives a proof of a relation with the limited day entry and movement of heavy vehicles in Delhi.     

Characteristics of atmospheric non-methane hydrocarbons during haze episode in Beijing, China

This study firstly focused on non-methane hydrocarbons (NMHCs) during three successive days with haze episode (16–18 August 2006) in Beijing. Concentrations of alkanes, alkenes, aromatic hydrocarbons, and ethyne all peaked at traffic rush hour, implying vehicular emission; and alkanes also peaked at non-traffic rush hour in the daytime, implying additional source. Especially, alkanes and aromatics clearly showed higher levels in the nighttime than that in the daytime, implying their active photochemical reactions in the daytime. Correlation coefficients (R ²) showed that propane, n-butane, i-butane, ethene, propene, and benzene correlated with ethyne (R ²?=?0.61–0.66), suggesting that their main source is vehicular emission; 2-methylpentane and n-hexane correlated with i-pentane (R ²?=?0.61–0.64), suggesting that gasoline evaporation is their main source; and ethylbezene, m-/p-xylene, and o-xylene correlated with toluene (R ²?=?0.60–0.79), suggesting that their main source is similar to that of toluene (e.g., solvent usage). The R ² of ethyne, i-pentane, and toluene with total NMHCs were 0.58, 0.76, and 0.60, respectively, indicating that ambient hydrocarbons are associated with vehicular emission, gasoline evaporation, and solvent usage. The sources of other hydrocarbons (e.g., ethane) might be natural gas leakage, biogenic emission, or long-range transport of air pollutants. Measured higher mean B/T ratio (0.78?±?0.27) was caused by the more intensive photochemical activity of toluene than benzene, still indicating the dominant emission from vehicles.     

Assessment of New Vehicles Emissions Certification Standards in the Metropolitan Area of Mexico City

Light duty gasoline vehicles account for most of CO hydrocarbons and NOx emissions at the Metropolitan Area of Mexico City (MAMC). In order to ameliorate air pollution from the beginning of 2001, Tier 1 emission standards became mandatory for all new model year sold in the country. Car manufacturers in Mexico do not guarantee the performance of their exhaust emissions systems for a given mileage. The purpose of this study was to assess whether the Tier 1 vehicles will stand the certification values for at least 162000 km with the regular fuel available at the MAMC. Mileage accumulation and deterioration show that certified carbon monoxide emissions will stand for the useful life of the vehicles but in the case of non-methane hydrocarbons will be shorter by 40%, and nitrogen oxides emissions above the standard will be reached at one third of the accumulated kilometers. The effect of gasoline sulfur content, on the current in use Tier 1 vehicles of the MAMC and the impact on the emissions inventory in year 2010 showed that 31000 extra tons of NOx could be added to the inventory caused by the failure of the vehicles to control this pollutant at the useful life of vehicles.     

In vitro genotoxicity of exhaust emissions of diesel and gasoline engine vehicles operated on a unified driving cycle

Acetone extracts of engine exhaust particulate matter (PM) and of vapor-phase semi-volatile organic compounds (SVOCs) collected from a set of 1998-2000 model year normal emitter diesel engine automobile or light trucks and from a set of 1982-1996 normal emitter gasoline engine automobiles or light trucks operated on the California Unified Driving Cycle at 22 [degree]C were assayed for in vitro genotoxic activities. Gasoline and diesel PM were comparably positive mutagens for Salmonella typhimurium strains YG1024 and YG1029 on a mass of PM extract basis with diesel higher on a mileage basis; gasoline SVOC was more active than diesel on an extracted-mass basis, with diesel SVOC more active on a mileage basis. For chromosomal damage indicated by micronucleus induction in Chinese hamster lung fibroblasts (V79 cells), diesel PM expressed about one-tenth that of gasoline PM on a mass of extract basis, but was comparably active on a mileage basis; diesel SVOC was inactive. For DNA damage in V79 cells indicated by the single cell gel electrophoresis (SCGE) assay, gasoline PM was positive while diesel PM was active at the higher doses; gasoline SVOC was active with toxicity preventing measurement at high doses, while diesel SVOC was inactive at all but the highest dose.     

Application and Quality Assessment of an Instantaneous Vehicle Emission Model at Fleet Level

A developed instantaneous emission model is applied to predict emission factors for small vehicle fleets for quality assessment. Extensive vehicle measurements of pre-Euro-1 gasoline, Euro-3 gasoline, and Euro-2 diesel vehicles are available. The data were used to develop individual vehicle emission models for each car. The prediction quality for each vehicle category was determined by averaging the results obtained from the individual vehicle models. The results show that the prediction quality is improved in comparison with the individual vehicles, even with a small number of vehicles in a specific category. This indicates that the errors in the individual models are mainly random and that prediction quality, when applied to fleets of cars, is exceptionally high.     

Impact of urbanization on the concentrations and distribution of organic contaminants in boreal lake sediments

The main goal of this study was to evaluate the impacts of a middle-sized Finnish urban area on the quality of sediments in an adjacent boreal lake. We investigated the sources and distribution of organic pollutants (polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs)) in the sediments from urban stormwater traps and from Lake Vesijärvi. Grab surface sediment samples were taken from Lake Vesijärvi at various distances (25–2,000 m) from four major stormwater drainage outlets and at 15 urban stormwater traps in areas with different degrees of urbanization. These samples were analysed for 16 PAHs and 28 PCBs with gas chromatography–mass spectrometry. The concentrations of pollutants in the lake sediments were elevated in the vicinity of the urban shore (∑PAH 3–16, ∑PCB up to 0.02–0.3 mg/kg dw) and decreased as a function of distance (∑PAH 0.1–2.5, ∑PCB 0.01–0.3 mg/kg dw at a distance of more than 500 m from the shore), whereas contamination levels in suburban areas were notably lower (∑PAH 0.1–3, ∑PCB?<?LOQ–0.03 mg/kg dw; did not decline with distance). Possible sources and pathways of contamination were also investigated. The majority of stormwater trap sediments contained predominantly asphalt-derived PAHs due to pulverized pavement. PAHs in lake sediments were of pyrogenic origin, including the combustion of gasoline, diesel and coal. Suggested pathways of lake contamination are urban runoff discharge, boat traffic and atmospheric deposition.     

The contribution of evaporative emissions from gasoline vehicles to the volatile organic compound inventory in Mexico City

The strategy for decreasing volatile organic compound emissions in Mexico has been focused much more on tailpipe emissions than on evaporative emissions, so there is very little information on the contribution of evaporative emissions to the total volatile organic compound inventory. We examined the magnitudes of exhaust and evaporative volatile organic compound emissions, and the species emitted, in a representative fleet of light-duty gasoline vehicles in the Metropolitan Area of Mexico City. The US “FTP-75” test protocol was used to estimate volatile organic compound emissions associated with diurnal evaporative losses, and when the engine is started and a journey begins. The amount and nature of the volatile organic compounds emitted under these conditions have not previously been accounted in the official inventory of the area. Evaporative emissions from light-duty vehicles in the Metropolitan Area of Mexico City were estimated to be 39 % of the total annual amount of hydrocarbons emitted. Vehicles built before 1992 (16 % of the fleet) were found to be responsible for 43 % of the total hydrocarbon emissions from exhausts and 31 % of the evaporative emissions of organic compounds. The relatively high amounts of volatile organic compounds emitted from older vehicles found in this study show that strong emission controls need to be implemented in order to decrease the contribution of evaporative emissions of this fraction of the fleet.