Urban oxidising capacity measurements using inert and reactive tracers

使用惰性和反应性示踪剂测量城市氧化能力

基本信息

  • 批准号:
    NE/K014811/1
  • 负责人:
  • 金额:
    $ 33.32万
  • 依托单位:
  • 依托单位国家:
    英国
  • 项目类别:
    Research Grant
  • 财政年份:
    2014
  • 资助国家:
    英国
  • 起止时间:
    2014 至 无数据
  • 项目状态:
    已结题

项目摘要

By definition, the urban environment is one where many people either live or work. During the course of a day, people will be outdoors for varying lengths of time and be exposed to different levels of air pollutants. During daytime, sunlight can provide the energy needed to produce the hydroxyl radical (written as HO), which is an extremely reactive species that acts like a detergent in the atmosphere, reacting with air pollutants. Therefore, we want to know how much HO there is in the urban atmosphere and how its level changes over the course of a day and from day to day as a function of time of the year. It is possible to measure HO directly using an instrument called FAGE and this has been carried out for some cities in the UK (e.g. Birmingham and London). These data have helped us to understand how HO varies in one location but the instrument FAGE is too expensive to replicate to allow us to make measurements across a city. HO is made and destroyed very rapidly, so a measurement of HO also tells us the ratio of the rate of its production to the rate of its removal and indeed FAGE can also tell us about the rate of its removal. Therefore, we can calculate the rate of production from these measurements, but these other measurements from a number of cities suggest that the rate of production of HO is underestimated based on our current understanding. One possibility is that there are missing sources that we don't know about? Given the importance of HO and other oxidants to urban air quality it is vital to try to work out what these missing sources are.With this in mind we have developed a new technique to allow us to measure the amount of HO (and other detergents) pollutants encounter as they move through the urban environment. In this way we will be able to build up a picture of how removal rates for pollutants varies across a City as a function of time of day, season, pollution loading etc. We will also be able to estimate how rapidly particles are made in the urban environment and begin to understand what controls their production. Particles can be released into the atmosphere directly, e.g. from car exhausts, (called primary particles) but can also be made in the atmosphere, a so called secondary particles. We want to know more about the sources of secondary particles as we can make reasonable estimates of primary particle sources. Particles are known to be bad for air quality and a reduction in levels would be of great benefit. In order to make these measurements we will release small amounts of organic molecules that react with oxidants such as HO and some molecules that don't react with anything. We have tagged the reactive molecules so we can tell them apart from ones that are there already into the city and will measure the levels of both reactive and inert species downwind of the release point. As these molecules disperse their level will drop because of dilution and the inert species will tell us the dilution rate, the reactive ones will drop even more as they will not only disperse but also react. By using these two pieces of information we can estimate their chemical removal rates and hence the amount of HO present. Other measurements of pollutants and meteorology will be made at the same time and we will then be able to estimate how quickly these pollutants are removed. Computer models that contain our current knowledge of urban air quality will be compared with all the measurement data and we will then be able to test a number of hypotheses for the missing source of HO and other oxidants. We will also carry out studies at night where HO levels are very low and a different oxidant called the nitrate radical (NO3) takes over. We have an instrument that can make measurements of NO3 and so we can compare the measurement of NO3 in one location with the NO3 experienced by pollutants as they pass through the city. In this way a detailed comparison can be made
根据定义,城市环境是许多人居住或工作的环境。在一天的过程中,人们将在户外停留不同的时间,并暴露在不同程度的空气污染物中。在白天,阳光可以提供产生羟基自由基(写作HO)所需的能量,这是一种非常活跃的物种,在大气中就像洗涤剂一样,与空气污染物反应。因此,我们想知道城市大气中有多少HO,以及它的水平如何在一天的过程中变化,以及作为一年中时间的函数每天变化。可以使用称为FAGE的仪器直接测量HO,并且已经在英国的一些城市(例如伯明翰和伦敦)进行了测量。这些数据帮助我们了解HO在一个位置的变化,但FAGE仪器太昂贵,无法复制,无法让我们在整个城市进行测量。HO的生成和破坏都非常迅速,因此对HO的测量也可以告诉我们其生成速率与其去除速率的比率,事实上,FAGE也可以告诉我们其去除速率。因此,我们可以从这些测量中计算出生产率,但来自一些城市的其他测量表明,根据我们目前的理解,HO的生产率被低估了。一种可能性是有我们不知道的缺失的来源?考虑到HO和其他氧化剂对城市空气质量的重要性,尝试找出这些缺失的来源是至关重要的。考虑到这一点,我们开发了一种新技术,使我们能够测量HO(和其他清洁剂)污染物在城市环境中移动时遇到的数量。通过这种方式,我们将能够建立一幅关于污染物的去除率如何在城市中作为一天中的时间、季节、污染负荷等的函数而变化的图像。我们还将能够估计颗粒在城市环境中产生的速度,并开始了解是什么控制着它们的产生。颗粒物可以直接释放到大气中,例如从汽车尾气中释放出来(称为初级颗粒物),但也可以在大气中产生,称为次级颗粒物。我们想知道更多关于次级粒子的来源,因为我们可以对初级粒子的来源做出合理的估计。众所周知,颗粒物对空气质量有害,减少颗粒物的含量将有很大好处。为了进行这些测量,我们将释放少量的有机分子,这些分子与氧化剂(如HO)和一些不与任何物质反应的分子发生反应。我们已经标记了活性分子,这样我们就可以把它们和已经进入城市的分子区分开来,并将测量释放点顺风处的活性和惰性物质的水平。当这些分子分散时,它们的水平会因为稀释而下降,惰性物质会告诉我们稀释率,反应性物质会下降得更多,因为它们不仅会分散,而且还会反应。通过使用这两条信息,我们可以估计它们的化学去除率,从而估计HO的含量。同时,我们亦会测量其他污染物和气象数据,然后便可估计这些污染物的清除速度。包含我们目前对城市空气质量的了解的计算机模型将与所有测量数据进行比较,然后我们将能够测试一些关于HO和其他氧化剂缺失来源的假设。我们还将在夜间进行研究,在那里HO水平非常低,一种称为硝酸根(NO3)的不同氧化剂接管。我们有一个可以测量NO3的仪器,所以我们可以将一个位置的NO3测量值与污染物穿过城市时所经历的NO3进行比较。这样可以进行详细的比较

项目成果

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Carl Percival其他文献

Carl Percival的其他文献

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{{ truncateString('Carl Percival', 18)}}的其他基金

An Integrated Study of AIR Pollution PROcesses in Beijing (AIRPRO)
北京空气污染过程综合研究(AIRPRO)
  • 批准号:
    NE/N00695X/1
  • 财政年份:
    2016
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
Gas phase studies of the kinetics of Criegee Intermediates
Criegee 中间体动力学的气相研究
  • 批准号:
    NE/K005316/1
  • 财政年份:
    2013
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
Isoprene oxidation and OH recycling
异戊二烯氧化和OH回收
  • 批准号:
    NE/J009210/1
  • 财政年份:
    2012
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
Laboratory studies of Criegee radical reactions
Criegee自由基反应的实验室研究
  • 批准号:
    NE/I010505/1
  • 财政年份:
    2011
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
The development of a Lithium-attachment chemical ionization mass spectrometer for studies in the atmosphere
开发用于大气研究的锂附着化学电离质谱仪
  • 批准号:
    NE/H003061/1
  • 财政年份:
    2010
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
The gas phase atmospheric photolysis and reactions of key alkyl nitrates and their role in NOy partitioning.
关键硝酸烷基酯的气相大气光解和反应及其在 NOy 分配中的作用。
  • 批准号:
    NE/G017352/1
  • 财政年份:
    2009
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
A Laboratory Study of the Photolysis of the ClO Dimer
ClO二聚体光解的实验室研究
  • 批准号:
    NE/F018045/1
  • 财政年份:
    2009
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
An airborne dual ionisation Chemical Ionisation Mass Spectrometer
机载双电离化学电离质谱仪
  • 批准号:
    NE/E018505/1
  • 财政年份:
    2008
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
Laboratory and modelling studies of the reactions of peroxy radicals with XO (where X = Cl, Br or I).
过氧自由基与 XO(其中 X = Cl、Br 或 I)反应的实验室和模型研究。
  • 批准号:
    NE/E005268/1
  • 财政年份:
    2007
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant
An airborne dual ionisation Chemical Ionisation Mass Spectrometer
机载双电离化学电离质谱仪
  • 批准号:
    NE/E018092/1
  • 财政年份:
    2007
  • 资助金额:
    $ 33.32万
  • 项目类别:
    Research Grant

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甲烷氧化细菌中磷限制的综合生态生理学和组学研究(EcoMacet)
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