Sadanaga Yasuhiro, Yoshino Ayako, Kato Shungo, Kajii Yoshizumi
Japan Science and Technology Agency, 4-1-8, Honcho, Kawaguchi, Saitama 332-0012, Japan.
Environ Sci Technol. 2005 Nov 15;39(22):8847-52. doi: 10.1021/es049457p.
Measurements of OH reactivity (i.e., OH loss rates) in the troposphere are essential for discussing tropospheric OH photochemistry. In July and August 2003, we observed the total OH reactivity in a suburban area of Tokyo. More than 90% of the data of the measured OH loss rates were higher than the calculated values with simultaneously measured concentrations of various trace species even though the rate coefficient of the OH + NO2 reaction was measured by us. We concluded that this discrepancy is due to the existence of unmeasured volatile organic compounds (VOCs). We estimated the potential of the photochemical ozone production in the case of including the unknown species as VOCs and excluding the missing sink, respectively. When the unknown species were included as VOCs, the potential increases from 32% to 88%. This result indicates the photochemical production rates of ozone in the urban air are substantially greater than expected.
对流层中羟基反应活性(即羟基损失率)的测量对于探讨对流层羟基光化学至关重要。2003年7月和8月,我们在东京郊区观测了总羟基反应活性。尽管我们测量了羟基与二氧化氮反应的速率系数,但超过90%的测量羟基损失率数据高于根据同时测量的各种痕量物种浓度计算得出的值。我们得出结论,这种差异是由于存在未测量的挥发性有机化合物(VOCs)。我们分别估算了将未知物种作为挥发性有机化合物包含在内以及排除缺失汇的情况下光化学臭氧生成的潜力。当将未知物种作为挥发性有机化合物包含在内时,潜力从32%增加到88%。这一结果表明城市空气中臭氧的光化学生成速率大大高于预期。