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Direct Nsub2/subOsub5/sub reactivity measurements at a polluted coastal site

机译:在受污染的沿海地区直接进行N 2 O 5 反应性测量

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pstrongAbstract./strong Direct measurements of Nsub2/subOsub5/sub reactivity on ambient aerosol particles were made during September 2009 at the Scripps Institution of Oceanography (SIO) Pier facility located in La Jolla, CA. Nsub2/subOsub5/sub reactivity measurements were made using a custom flow reactor and the particle modulation technique alongside measurements of aerosol particle size distributions and non-refractory composition. The pseudo-first order rate coefficients derived from the particle modulation technique and the particle surface area concentrations were used to determine the population average Nsub2/subOsub5/sub reaction probability, i ?3/i(Nsub2/subOsub5/sub), approximately every 50 min. Insufficient environmental controls within the instrumentation trailer led us to restrict our analysis primarily to nighttime measurements. Within this subset of data, i ?3/i(Nsub2/subOsub5/sub) ranged from &0.001 to 0.029 and showed significant day-to-day variations. We compare these data to a recent parameterization that utilizes aerosol composition measurements and an aerosol thermodynamics model. The parameterization captures several aspects of the measurements with similar general trends over the time series. However, the parameterization persistently overestimates the measurements by a factor of 1.5a??3 and does not illustrate the same extent of variability. Assuming chloride is internally mixed across the particle population leads to the largest overestimates. Removing this assumption only partially reduces the discrepancies, suggesting that other particle characteristics that can suppressi ?3/i(Nsub2/subOsub5/sub) are important, such as organic coatings or non-aqueous particles. The largest apparent driver of day-to-day variability in the measured i ?3/i(Nsub2/subOsub5/sub) at this site was the particle nitrate loading, as inferred from both the measured particle composition and the parameterizations. The relative change in measured i ?3/i(Nsub2/subOsub5/sub) as a function of particle nitrate loading appears to be consistent with expectations based on laboratory data, providing direct support for the atmospheric importance of the so-called "nitrate effect"./p.
机译:> >摘要。2009年9月,美国斯克里普斯海洋研究所(Scripps Institution of Oceanography)直接测量了N 2 O 5 对周围气溶胶颗粒的反应性( SIO)位于加利福尼亚州拉霍亚的码头设施。使用定制的流动反应器和粒子调制技术对N 2 O 5 反应性进行了测量,同时还测量了气溶胶粒径分布和非耐火成分。利用粒子调制技术和粒子表面积浓度得出的伪一阶速率系数确定总体平均N 2 O 5 反应概率, ?3 (N 2 O 5 ),大约每50分钟一次。仪表拖车内的环境控制不足,导致我们的分析主要限于夜间测量。在此数据子集中,?3 (N 2 O 5 )的范围从<0.001到0.029,并且每天都有明显的变化变化。我们将这些数据与利用气溶胶成分测量和气溶胶热力学模型的最新参数化进行了比较。参数化捕获了在时间序列上具有相似总体趋势的测量的多个方面。然而,参数化持续高估测量值1.5a≤3,并且没有说明相同程度的可变性。假设氯化物在整个粒子总体内部混合,则会导致最大的高估。删除此假设仅能部分减少差异,这表明可以抑制?3 (N 2 O 5 )的其他粒子特性很重要,例如作为有机涂料或非水颗粒。在该位置,测量到的?3 (N 2 O 5 )的日常变化的最大表观驱动力是硝酸盐颗粒。从测量的颗粒成分和参数设置推断出的最大载荷。被测?3 (N 2 O 5 )的相对变化与硝酸盐颗粒负荷的函数似乎符合实验室的预期数据,为所谓的“硝酸盐效应”在大气中的重要性提供直接支持。

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