Photodegradation Reactions Mono and Dinitro PAHs

单硝基多环芳烃和二硝基多环芳烃光降解反应

• 批准号: 7924640
• 负责人: RAFAEL ARCE
• 金额: $ 25.38万
• 依托单位: UNIVERSITY OF PUERTO RICO RIO PIEDRAS
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-09-01 至 2012-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7924640
• 关键词: 1-Nitropyrene; 2,4-Dinitrophenol; Aerosols; Affect; Air; Air Pollutants; Air Pollution; Area; Aromatic Polycyclic Hydrocarbons; Automobile Exhaust; Benzo(a)pyrene; Biological Assay; Breathing; Caliber; Carbon; Cardiopulmonary; Cardiovascular system; Chemicals; Classification; Coal; Complex; DNA Sequence Rearrangement; Data; Death Rate; Diesel Exhaust; Dissociation; Environment; Environmental Exposure; Environmental Health; Environmental Risk Factor; Evaluation; Excision; Exposure to; Film; Gases; Genetic Recombination; Goals; Health; Human; Hydrogen; Inorganic Sulfates; Kinetics; Knowledge; Laboratories; Lasers; Link; Liquid substance; Lung; Malignant neoplasm of lung; Mechanics; Modeling; Mono-S; Motor Vehicles; Movement; Nature; Nitrites; Oxides; Oxygen; Parents; Particulate; Particulate Matter; Photochemistry; Power Plants; Process; Property; Reaction; Relative (related person); Reporting; Research; Research Personnel; Risk; Risk Assessment; Route; Salts; Smoke; Solid; Solutions; Solvents; Source; Structure; Surface; Surface Properties; System; Techniques; Temperature; Testing; Time; Toxic effect; Triplet Multiple Birth; Unspecified or Sulfate Ion Sulfates; Water; Wood material; Work; base; chemical property; design; fly ash; irradiation; mortality; particle; physical property; physical state; planetary Atmosphere; pollutant; quantum; residence; respiratory; triplet state

DESCRIPTION (provided by applicant): Particulate matter (PM2.5) has been linked to a range of serious respiratory and cardiovascular health problems. The nitroPAHs found in the (PM2.5) are formed during combustion processes or by either chemical or photochemical reactions of polycyclic aromatic hydrocarbon in polluted atmospheres. NitroPAHs have been identified in extracts of respirable particles collected from polluted urban air, diesel exhaust particles, automobile exhaust, coal fly ash and wood smoke. The nitroPAHs are typically less abundant in ambient air than PAHs and are found at concentrations in the range of pg/m3 to ng/m3. Nonetheless, some of them could be more mutagenic or carcinogenic in laboratory bioassays than the parent PAH. Thus, it is of great significance to understand their sources and transformations in the atmosphere in assessing environmental exposure and risks. Specifically, their transformations at the solid/air interface or in the liquid-like environment of the organic fraction of the combustion derived aerosols can have a significant impact on controlling their residence time in the environment. It is important to study the photochemistry in these two environments because their photodegradation can proceed by entirely different mechanisms depending on the reaction medium. We are proposing to utilize techniques, already developed in our laboratory, to study the photochemical transformation mechanisms of nitroPAHs adsorbed or absorbed into models of atmospheric particulate matter in order to provide some understanding of the fate of these contaminants in the atmosphere. As we have found with PAHs, that phototransformations at the solid/air interface can have a significant impact in controlling their residence time in the environment, and are thus important in the evaluation of the potential risks of these contaminants, as well as in the possible design of systems for their removal. The working hypothesis is that the physical and chemical properties of the particulate matter are determining factors in the reactivity of the excited states and intermediates participating in the photochemical transformations of these pollutants in that environment. In order to understand the phototransformation mechanism of adsorbed or absorbed nitroPAHs we will: (1) isolate/and characterize the principal stable photoproducts and determine their quantum yields and the effect of the nature of the solvent (polar, non polar, polar aprotic, hydrogen abstraction easiness), and of organic compounds found in the atmospheric aerosols on the product yields, (2) isolate and characterize the principal stable photoproducts produced on adsorbents that mimic the atmospheric particle matter such as inorganic oxides, and sulfate salts, and determine the effect of the physical and chemical properties of the surfaces of these solids (such as composition average pore diameter, surface coverage) on the products relative yields, and to compare their relative yields and distribution with those obtained in the different solvents. The effect of coadsorbed water and oxygen on the yields will also be examined and (3) identify and characterize the participating excited states and reactive intermediates in the phototransformation process occurring in solution and on the surfaces. Related to this aim is the determination of the effect of organic cosolutes encountered in the atmospheric aerosol on the reaction kinetics of the intermediates. The physical properties of the participating excited states and reactive intermediates will be supported by quantum mechanical calculations.

描述（由申请人提供）：颗粒物 (PM2.5) 与一系列严重的呼吸系统和心血管健康问题有关。 (PM2.5) 中发现的硝基多环芳烃是在污染大气中的燃烧过程中或多环芳烃的化学或光化学反应中形成的。从污染的城市空气、柴油机尾气颗粒、汽车尾气、煤飞灰和木烟中收集的可吸入颗粒的提取物中已鉴定出硝基多环芳烃。硝基多环芳烃在环境空气中的含量通常低于多环芳烃，浓度范围为 pg/m3 至 ng/m3。尽管如此，在实验室生物测定中，其中一些可能比母体多环芳烃更具致突变性或致癌性。因此，了解它们的来源和在大气中的转化对于评估环境暴露和风险具有重要意义。具体而言，它们在固体/空气界面或燃烧产生的气溶胶的有机部分的类液体环境中的转化可以对控制它们在环境中的停留时间产生重大影响。研究这两种环境中的光化学非常重要，因为根据反应介质的不同，它们的光降解可以通过完全不同的机制进行。 我们建议利用我们实验室已经开发的技术来研究硝基多环芳烃被吸附或吸收到大气颗粒物模型中的光化学转化机制，以便对这些污染物在大气中的命运有一定的了解。正如我们在多环芳烃方面发现的那样，固体/空气界面处的光转化可以对控制其在环境中的停留时间产生重大影响，因此对于评估这些污染物的潜在风险以及可能发生的风险非常重要。设计去除它们的系统。工作假设是，颗粒物的物理和化学性质是参与该环境中这些污染物的光化学转化的激发态和中间体的反应性的决定因素。为了了解吸附或吸收的硝基多环芳烃的光转化机制，我们将：（1）分离/和表征主要的稳定光产物，并确定它们的量子产率和溶剂性质的影响（极性、非极性、极性非质子、氢）提取容易性），以及大气气溶胶中发现的有机化合物对产品产率的影响，（2）分离并表征在模拟大气颗粒物（例如无机物）的吸附剂上产生的主要稳定光产品氧化物、硫酸盐等，测定这些固体表面的物理化学性质（如组成平均孔径、表面覆盖度）对产物相对收率的影响，并与所得结果进行比较。在不同的溶剂中。还将检查共吸附的水和氧对产率的影响，并且（3）识别和表征溶液中和表面上发生的光转化过程中参与的激发态和反应中间体。与此目标相关的是确定大气气溶胶中遇到的有机共溶质对中间体反应动力学的影响。参与的激发态和反应中间体的物理性质将得到量子力学计算的支持。