Warren Bethany, Song Chen, Cocker David R
Department of Chemical and Environmental Engineering, Bourns College of Engineering, Center for Environmental Research and Technology (CE-CERT), University of California, Riverside, California 92521, USA.
Environ Sci Technol. 2008 Aug 1;42(15):5461-6. doi: 10.1021/es702985n.
A series of m-xylene/NO(x) photooxidation experiments were conducted to determine the influence of light intensity and radiation spectrum on secondary organic aerosol (SOA) formation within the UC Riverside/CE-CERT environmental chamber. The environmental chamber is equipped with 80 115-W black lights and a variable voltage 200 kW argon arc lamp that emits a wavelength spectrum more similar to natural light. SOA formation increased significantly with light intensity, measured as the photolysis rate of NO2 to NO (k1), increased from 0.09 to 0.26 min(-1). The argon arc lamp produced approximately 20% more SOA than black lights at a k1 of 0.09 min(-1) for similar amounts of m-xylene consumed. These results may help explain the variation of SOA formation between environmental chambers and the differences between measured SOA in the ambient atmosphere versus environmental chamber predictions.
进行了一系列间二甲苯/氮氧化物光氧化实验,以确定光强和辐射光谱对加州大学河滨分校/CE-CERT环境舱内二次有机气溶胶(SOA)形成的影响。该环境舱配备了80盏115瓦的黑光灯和一盏可变电压的200千瓦氩弧灯,后者发射的波长光谱更接近自然光。随着光强的增加,SOA的形成显著增加,光强以二氧化氮到一氧化氮的光解速率(k1)衡量,从0.09增加到0.26分钟-1。在消耗相似量的间二甲苯时,对于k1为0.09分钟-1的情况,氩弧灯产生的SOA比黑光灯大约多20%。这些结果可能有助于解释不同环境舱之间SOA形成的差异,以及环境大气中测量的SOA与环境舱预测值之间的差异。