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动态腔室系统中α-蒎烯臭氧分解产生的二次有机气溶胶。

Secondary organic aerosol from alpha-pinene ozonolysis in dynamic chamber system.

作者信息

Chen X, Hopke P K

机构信息

Center for Air Resources Engineering and Science, Clarkson University, Potsdam, NY, USA.

出版信息

Indoor Air. 2009 Aug;19(4):335-45. doi: 10.1111/j.1600-0668.2009.00596.x. Epub 2009 Jan 19.

Abstract

UNLABELLED

The formation of secondary organic aerosol (SOA) produced from alpha-pinene ozonolysis was examined using a dynamic chamber system that allowed the simulation of ventilated indoor environments. Particle-bound reactive species (ROS) including peroxides, peroxy radicals and ions that could penetrate into the lungs and deliver oxidative stress to the tissue causing damage were quantitatively determined from filters collected from the chamber. ROS was determined using dichlorofluorescin such that resulting fluorescent intensities were converted to equivalent H(2)O(2) concentrations. Measured ROS concentrations at alpha-pinene and ozone concentrations relevant to prevailing indoor concentrations ranged from 1.1 to 7.2 nmol/m(3) of H(2)O(2). Particle density was also determined from scanning mobility particle sizer measurements and mass collected onto filters to obtain volume and mass concentration, respectively. Partitioning theory reveals the fact that with increased SOA mass loading, even for more volatile species, partitioning onto particle phase is favored relative to low SOA mass loadings. Other recent studies have found changes in composition of the SOA depending on the precursor VOC concentrations. This behavior was reflected in these experiments in terms of a change of density. Measured densities ranged from 1.07 to 1.69 g/cm(3).

PRACTICAL IMPLICATIONS

A better understanding of the formation mechanism of secondary organic aerosol generated from indoor chemistry allows us to evaluate and predict the exposure under such environments. Measurements of particle-bound reactive oxygen species (ROS) shed light on potential adverse health effect associated upon exposure to particles.

摘要

未标注

使用动态腔室系统研究了α-蒎烯臭氧分解产生的二次有机气溶胶(SOA)的形成,该系统可模拟通风的室内环境。从腔室收集的过滤器中定量测定了颗粒结合的活性物种(ROS),包括过氧化物、过氧自由基和离子,这些物质可穿透肺部并对组织造成氧化应激损伤。使用二氯荧光素测定ROS,将产生的荧光强度转换为等效的H₂O₂浓度。在与室内普遍浓度相关的α-蒎烯和臭氧浓度下,测得的ROS浓度范围为1.1至7.2 nmol/m³的H₂O₂。还通过扫描迁移率粒径分析仪测量和收集在过滤器上的质量分别测定颗粒密度,以获得体积浓度和质量浓度。分配理论表明,随着SOA质量负荷的增加,即使对于挥发性更强的物种,相对于低SOA质量负荷,其在颗粒相上的分配更受青睐。其他近期研究发现,SOA的组成会根据前体挥发性有机化合物(VOC)浓度而变化。这种行为在这些实验中通过密度变化得以体现。测得的密度范围为1.07至1.69 g/cm³。

实际意义

更好地理解室内化学反应产生的二次有机气溶胶的形成机制,有助于我们评估和预测此类环境下的暴露情况。对颗粒结合的活性氧物种(ROS)的测量揭示了暴露于颗粒时潜在的不良健康影响。

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