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Measured saturation vapour pressures of phenolic and nitro-aromatic compounds

机译:测量酚类和硝基芳族化合物的饱和蒸气压

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摘要

Phenolic and nitro-aromatic compounds are extremely toxic components of atmospheric aerosol that are currently not well understood. In this Article, solid and subcooled-liquid-state saturation vapor pressures of phenolic and nitro-aromatic compounds are measured using Knudsen Effusion Mass Spectrometry (KEMS) over a range of temperatures (298–318 K). Vapor pressure estimation methods, assessed in this study, do not replicate the observed dependency on the relative positions of functional groups. With a few exceptions, the estimates are biased toward predicting saturation vapor pressures that are too high, by 5–6 orders of magnitude in some cases. Basic partitioning theory comparisons indicate that overestimation of vapor pressures in such cases would cause us to expect these compounds to be present in the gas state, whereas measurements in this study suggest these phenolic and nitro-aromatic will partition into the condensed state for a wide range of ambient conditions if absorptive partitioning plays a dominant role. While these techniques might have both structural and parametric uncertainties, the new data presented here should support studies trying to ascertain the role of nitrogen containing organics on aerosol growth and human health impacts.
机译:酚和硝基芳族化合物是目前尚不清楚的大气气溶胶的剧毒成分。在本文中,使用Knudsen扩散质谱法(KEMS)在一定温度(298–318 K)范围内测量了酚类和硝基芳族化合物的固态和过冷液态饱和蒸汽压。在这项研究中评估的蒸气压估算方法不能复制观察到的对官能团相对位置的依赖性。除少数例外,估计值偏向于预测过高的饱和蒸气压,在某些情况下,饱和蒸气压降低了5-6个数量级。基本分配理论的比较表明,在这种情况下,高估了蒸气压会使我们期望这些化合物以气态存在,而本研究中的测量表明,这些酚和硝基芳族化合物将在很宽的范围内分配为冷凝态如果吸收性分区起主导作用,则取决于环境条件。尽管这些技术可能在结构和参数上都具有不确定性,但此处提供的新数据应支持试图确定含氮有机物对气溶胶生长和人类健康影响的研究。

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