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Speciation studies for biogenic volatile organic compounds and secondary organic aerosol generated by ozonolysis of volatile organic compound mixtures.

机译:对挥发性有机化合物混合物进行臭氧分解产生的生物挥发性有机化合物和次级有机气溶胶的形态研究。

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摘要

Aerosols are either emitted directly into the atmosphere or are generated in the atmosphere; the latter process forms secondary organic aerosol (SOA). One of the important sources for SOA is the oxidation of volatile organic compounds (VOCs) by OH radicals, NOx, and O3. Aerosol can be visualized as suspended solid or liquid particle which is in equilibrium with surrounding gases. The products of SOA formation is a mixture of semi volatile organic compounds and a fraction of the products are condensable under atmospheric conditions. The condensable portion of aerosol is called particulate matter (PM) and these suspended particles can range in diameter from a few nanometers to microns. PM can impact climate through direct and indirect radiative forcing and can degrade air quality by reducing visibility and causing detrimental health effects. SOA can also form indoors, which also contributes to the health risk of PM. The severe impact of PM on human health and climate drives the scientific community to investigate the volatile organic compounds (VOCs) and their potential to form SOA, as well as the factors that alter the efficiency of SOA generation and the type of products. In a similar pursuit, the focus of this dissertation is the investigation of the SOA precursors that are emitted from trees and how they vary as a function of insect infestation. Also, the role of mixtures of VOCs as SOA precursors are investigated; commercial and lab made VOC mixtures are studied for SOA generation, product analysis, and absorption characteristics of aged SOA.;Chapter 1 introduces PM, VOCs present in atmosphere, SOA generation, and speciation of products generated from the ozonolysis of VOCs. The impact of PM on human health and climate are summarized. A literature survey on the VOCs that are precursors to SOA and present in the outdoor and indoor environment is presented along with factors that may lead to variability in amount of VOCs. SOA generation from direct plant emissions and consumer products is surveyed. These studies show that VOC oxidation generate SOA which is important in the atmosphere due to climate and health effects and indoors due to health effects. A summary of SOA phase partitioning theories, the reaction mechanism for the formation of products from ozonolysis of the dominant biogenic SOA precursors (monoterpenes), and the factors that affect SOA generation is presented.;Chapter 2 summarizes the results obtained from a field study assessing the impact of bark beetle infestation on SOA precursor emissions from forests in the Western United States. Samples of VOCs were collected by our collaborators from healthy and bark beetle infested trees using scent traps. We solvent extracted and analyzed by gas chromatography/mass spectrometry (GC/MS) nearly four hundred scent traps. An increase in the total and the individual VOCs emitted by infested trees was measured. A statistical analysis shows significant differences between the emissions from infested and healthy trees. A perspective is provided on potential impact of bark beetle infestation on regional SOA.;The majority of the laboratory experiments for SOA generation have focused on individual VOCs as the single SOA precursor. However, as demonstrated in Chapter 2 for example, in a real environment multiple VOCs co-exist. Multiple SOA precursors undergo concurrent oxidation reactions, and it is not known if the products from concurrent oxidation of multiple precursors are the same as the sum of the products from individual SOA precursors. Mass closure analysis of field samples show that a significant fraction of the chemical identity of organic PM is unknown, but the chemistry impacts the toxicity of PM. Hence, it is important to understand SOA formation from realistic SOA mixtures. Chapter 3 describes the results of the SOA generation by ozonolysis of limonene and VOC mixtures containing limonene. We use an additive approach for building a surrogate VOC mixture close in composition to a commercially-available mixture. The yield of PM as a function of VOC precursor mixture was measured with respect to VOC composition using smog chamber SOA generation and scanning mobility particle sizing. PM in the chamber was collected onto filters and extracted, and the individual products of SOA were identified and quantified by GC/MS. The condensed-phase SOA products generated during these experiments for different VOC mixtures are compared.;In Chapter 4, condensed-phase products sampled from SOA generated by the ozonolysis of &agr; pinene and VOC mixtures containing &agr; pinene, including two fir needle essential oils, are studied by extracting filter samples and analyzing the extracts by GC/MS. The products generated from VOC mixtures are characteristic of the most dominant VOC present in the mixture i.e. either limonene or &agr; pinene. Some mixtures show the generation of new products which are not observed for corresponding individual VOC ozonolysis and hence can be used as marker for the corresponding VOC mixture. The distribution of &agr;-pinene SOA products changes as the composition of the SOA precursor mixture changes.;In Chapter 5, the UV visible absorption characteristics of ammonium ion aged SOA are discussed. Ammonium ion aging of aerosol leads impacts the radiative properties of aerosol and has the potential to impact aerosol's role in climate change. Filter samples containing SOA generated from two mixtures with different dominant monoterpenes (&agr;-pinene-based Siberian fir needle oil and a limonene-based air freshener) were extracted. The absorption coefficients of the extracts were measured as a function of ammonium ion aging time using UV-visible absorption spectrometry. The conclusions from all above chapters are summarized in Chapter 6.
机译:气溶胶直接排放到大气中或在大气中产生;后者形成二次有机气溶胶(SOA)。 SOA的重要来源之一是挥发性有机化合物(VOC)被OH自由基,NOx和O3氧化。气溶胶可视为悬浮的固体或液体颗粒,与周围的气体处于平衡状态。 SOA形成的产物是半挥发性有机化合物的混合物,一部分产物在大气条件下可冷凝。气溶胶的可冷凝部分称为颗粒物(PM),这些悬浮颗粒的直径范围可以从几纳米到微米。 PM可通过直接和间接的辐射强迫影响气候,并通过降低能见度并造成有害的健康影响而降低空气质量。 SOA也可以在室内形成,这也增加了PM的健康风险。 PM对人类健康和气候的严重影响促使科学界对挥发性有机化合物(VOC)及其形成SOA的潜力以及影响SOA产生效率和产品类型的因素进行研究。在类似的追求中,本论文的重点是对树木排放的SOA前体及其随昆虫侵染而变化的研究。此外,还研究了VOC混合物作为SOA前体的作用。对商业和实验室生产的VOC混合物进行了研究,以研究SOA的产生,产品分析以及老化的SOA的吸收特性。第1章介绍了PM,大气中存在的VOC,SOA的产生以及VOC臭氧分解产生的产品的形态。总结了PM对人类健康和气候的影响。介绍了有关SOA的前体并存在于室外和室内环境中的VOC的文献调查,以及可能导致VOC量变化的因素。对直接工厂排放和消费产品产生的SOA进行了调查。这些研究表明,VOC氧化产生SOA,由于气候和健康影响,SOA在大气中很重要;而由于健康影响,在室内则很重要。概述了SOA相分配理论,主要的生物成因SOA前体(单萜)进行臭氧分解形成产物的反应机理,以及影响SOA产生的因素。第二章总结了实地研究评估的结果树皮甲虫侵害对美国西部森林SOA前体排放的影响。我们的合作者使用气味捕捉器从健康和树皮甲虫感染的树木中收集了挥发性有机化合物的样品。我们通过气相色谱/质谱(GC / MS)提取并分析了近四百个气味阱。测量了受侵染树木排放的总VOC和单个VOC的增加。统计分析显示,出没和健康树木的排放量之间存在显着差异。提供了有关树皮甲虫侵染对区域SOA的潜在影响的观点。大多数SOA生成的实验室实验都将单个VOC作为单一SOA前体。但是,例如,如第2章所示,在实际环境中,多个VOC并存。多个SOA前体会同时发生氧化反应,尚不清楚多个前体同时发生氧化的产物是否与单个SOA前体产生的总和相同。现场样品的质量封闭分析表明,有机PM的化学特性的很大一部分是未知的,但是化学影响PM的毒性。因此,重要的是要从现实的SOA混合物中了解SOA的形成。第3章介绍了通过臭氧分解柠檬烯和含有柠檬烯的VOC混合物进行SOA生成的结果。我们使用加成法来构建替代VOC混合物,其成分与市售混合物接近。使用烟雾室SOA产生和扫描迁移率颗粒尺寸,相对于VOC组成测量了PM的产量与VOC前体混合物的关系。将室中的PM收集到过滤器上并提取,然后通过GC / MS鉴定和定量SOA的各个产物。比较了在这些实验中针对不同VOC混合物生成的冷凝相SOA产物。在第4章中,通过&agr的臭氧分解从SOA采样得到的冷凝相产物;含有&agr;的烯和VOC混合物ene烯,包括两种杉木针精油通过提取过滤器样品并通过GC / MS分析提取物来研究。由VOC混合物产生的产物是混合物中存在的最主要VOC的特征,即li烯或α-烯烃。 ene烯。一些混合物显示出新产物的生成,对于相应的单独的VOC臭氧分解而言未观察到这些产物,因此可以用作相应的VOC混合物的标记。 pine-ne烯SOA产物的分布随SOA前体混合物组成的变化而变化。在第5章中,讨论了铵离子老化SOA的紫外可见吸收特性。气溶胶的铵离子老化会影响气溶胶的辐射特性,并有可能影响气溶胶在气候变化中的作用。提取包含SOA的过滤器样品,该样品是由具有不同主要单萜的两种混合物(α-pine烯基西伯利亚冷杉针油和柠檬烯基空气清新剂)产生的。使用紫外可见吸收光谱法测量提取物的吸收系数,作为铵离子老化时间的函数。以上所有章节的结论在第6章中进行了总结。

著录项

  • 作者

    Amin, Hardik Surendra.;

  • 作者单位

    Southern Illinois University at Carbondale.;

  • 授予单位 Southern Illinois University at Carbondale.;
  • 学科 Chemistry Analytical.;Chemistry Organic.;Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 298 p.
  • 总页数 298
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:43:33

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