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Indoor secondary organic aerosol formation: Influence of particle controls, mixtures, and surfaces.

机译:室内二次有机气溶胶形成:颗粒物控制,混合物和表面的影响。

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摘要

Ozone (O3) and terpenoids react to produce secondary organic aerosol (SOA). This work explored novel ways that these reactions form SOA indoors, with five investigations, in two categories: investigations of (i) the impacts of particle controls on indoor SOA formation, and (ii) two fundamental aspects of indoor SOA formation.;For category (i), two investigations examined the particle control devices of ion generators, which are air purifiers that are ineffective at removing particles and emit ozone during operation. With a terpenoid source present (an air freshener), ion generators acted as steady-state SOA generators, both in a 15 m3 chamber and 27 m3 room. The final investigation in category (i) modeled how heating, ventilating, and air-conditioning (HVAC) systems influence SOA formation. Influential HVAC parameters were flow rates, particle filtration, and indoor temperature for residential and commercial models, as well as ozone removal by particle-laden filters for the commercial model.;For category (ii), the first investigation measured SOA formation from ozone reactions with single terpenoids and terpenoid mixtures in a 90 L Teflon-film chamber, at low and high ozone concentrations. For low ozone, experiments with only d-limonene yielded the largest SOA number formation, relative to other mixtures, some of which had three times the effective amount of reactive terpenoids. This trend was not observed for high ozone experiments, and these results imply that ozone-limited reactions with d-limonene form byproducts with high nucleation potential.;The second investigation in category (ii) explored SOA formation from ozone reactions with surface-adsorbed terpenoids. A model framework was developed to describe SOA formation due to ozone/terpenoid surface reactions, and experiments in a 283 L chamber determined the SOA yield for ozone/d-limonene surface reactions. The observed molar yields were 0.14--0.16 over a range of relative humidities, and lower relative humidity led to higher SOA number formation from surface reactions. Building materials on which ozone/d-limonene surface reactions are predicted to lead to substantial SOA formation are those with initially low surface reactivity, such as glass, sealed materials, or metals. The results from category (ii) suggest significant, previously unexplored mechanisms of SOA number formation indoors.
机译:臭氧(O3)和萜类化合物反应生成二次有机气溶胶(SOA)。这项工作探索了这些反应在室内形成SOA的新颖方式,分为五类进行了两类调查:(i)颗粒控制对室内SOA形成的影响;以及(ii)室内SOA形成的两个基本方面的调查。 (i),两项研究检查了离子发生器的颗粒控制装置,这些装置是空气净化器,在操作过程中不能有效去除颗粒并排放臭氧。在存在萜类化合物源(空气清新剂)的情况下,离子发生器在15 m3的房间和27 m3的房间中充当稳态SOA发生器。 (i)类中的最终调查模拟了采暖,通风和空调(HVAC)系统如何影响SOA的形成。影响HVAC的参数包括民用和商用型号的流速,颗粒过滤和室内温度,以及商用型号的装有颗粒过滤器的臭氧去除量;对于(ii)类,首次调查测量了臭氧反应中SOA的形成在低和高臭氧浓度下,在90 L特富龙薄膜腔中使用单个萜类化合物和萜类化合物混合物。对于低臭氧,相对于其他混合物,仅用d-柠檬烯进行的实验会形成最大的SOA数,其中一些混合物的有效萜烯有效量是其三倍。在高强度的臭氧实验中未观察到这种趋势,这些结果表明,与d-柠檬烯进行臭氧限制的反应会形成具有高成核潜能的副产物。 。开发了模型框架来描述由于臭氧/类萜表面反应而形成的SOA,并在283 L的室内进行实验确定了臭氧/ d-柠檬烯表面反应的SOA收率。在一定的相对湿度范围内,观察到的摩尔产率为0.14--0.16,较低的相对湿度导致较高的表面反应形成SOA数。预计在其上臭氧/ d-柠檬烯表面反应会导致大量SOA形成的建筑材料是最初具有低表面反应性的建筑材料,例如玻璃,密封材料或金属。 (ii)类的结果表明,室内SOA号码形成的重要机制是以前尚未探索的。

著录项

  • 作者

    Waring, Michael Shannon.;

  • 作者单位

    The University of Texas at Austin.;

  • 授予单位 The University of Texas at Austin.;
  • 学科 Environmental Health.;Engineering Civil.;Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 199 p.
  • 总页数 199
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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