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Analysis of the Dynamic Interaction Between SVOCs and Airborne Particles

机译:SVOC与机载颗粒之间的动态相互作用分析

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A proper quantitative understanding of the dynamic interaction between gas-phase semivolatile organic compounds (SVOCs) and airborne particles is important for human exposure assessment and risk evaluation. Questions regarding how to properly address gas/particle interactions have introduced uncertainty when predicting SVOC concentrations and assessing exposures to these compounds. In this study, we have developed a dimensionless description for the dynamic interaction between SVOCs and organic particles. A better criterion to judge whether the internal resistance (diffusion in and out of aerosols) is negligible compared with the external one (from bulk air to aerosol surfaces) is presented. The analysis is applicable regardless of the phase state of particles (either liquid or amorphous semisolid/solid). It is found that for both porous and nonporous particles, the internal resistance can be reasonably neglected for particles with diameters between 0.01 and 10 μm if the particulate organic matter is in the liquid phase. A lumped description therefore can be applied to determine, with greater accuracy than in previous studies, the timescale required to attain gas/particle equilibrium for such particles. The instantaneous equilibrium assumption is found to be reasonable for relatively volatile species such as pyrene, but not for the less volatile species such as di-(2-ethylhexyl)-phthalate (DEHP). For DEHP and 2.5 μm diameter particles, the instantaneous gas/particle equilibrium assumption can cause a two orders of magnitude error in the estimation of the gas-phase concentration and a factor of two error in the estimation of the particle-phase concentration.
机译:正确定量了解气相半挥发性有机化合物(SVOC)与空气传播颗粒之间的动态相互作用,对于人体暴露评估和风险评估非常重要。有关如何正确解决气体/粒子相互作用的问题,在预测SVOC浓度和评估这些化合物的暴露量时引入了不确定性。在这项研究中,我们为SVOC与有机颗粒之间的动态相互作用建立了无量纲的描述。提出了一个更好的标准来判断内部阻力(从气溶胶中扩散出来和从外部扩散到气溶胶表面)是否可以忽略不计。无论颗粒的相态(液体或无定形半固体/固体),该分析均适用。发现对于多孔和无孔颗粒,如果颗粒有机物为液相,则对于直径在0.01μm和10μm之间的颗粒,内部电阻可以被合理地忽略。因此,与以前的研究相比,可以使用集总描述来更准确地确定实现此类粒子的气体/粒子平衡所需的时间尺度。发现瞬时平衡假设对于相对挥发性的物质(例如pyr)是合理的,但对于较低挥发性的物质(例如邻苯二甲酸二-(2-乙基己基)酯(DEHP))则不合理。对于DEHP和直径为2.5μm的颗粒,瞬时气体/颗粒平衡假设可能会导致气相浓度估算出现两个数量级的误差,而导致颗粒相浓度估算出现两个误差。

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