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Photoacoustic optical properties at UV, VIS, and near IR wavelengths for laboratory generated and winter time ambient urban aerosols

机译:紫外光,可见光和近红外波长下的光声光学性质,用于实验室产生的和冬季的城市环境气溶胶

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We present the laboratory and ambient photoacoustic (PA) measurement ofaerosol light absorption coefficients at ultraviolet wavelength (i.e., 355 nm) and compare with measurements at 405, 532, 870, and 1047 nm.Simultaneous measurements of aerosol light scattering coefficients wereachieved by the integrating reciprocal nephelometer within the PA's acousticresonator. Absorption and scattering measurements were carried out forvarious laboratory-generated aerosols, including salt, incense, and kerosenesoot to evaluate the instrument calibration and gain insight on the spectraldependence of aerosol light absorption and scattering. Ambient measurementswere obtained in Reno, Nevada, between 18 December 2009 and 18 January 2010.The measurement period included days with and without strong ground leveltemperature inversions, corresponding to highly polluted (freshly emittedaerosols) and relatively clean (aged aerosols) conditions. Particulatematter (PM) concentrations were measured and analyzed with other tracers oftraffic emissions. The temperature inversion episodes caused very highconcentration of PM2.5 and PM10 (particulate matter withaerodynamic diameters less than 2.5 μm and 10 μm, respectively)and gaseous pollutants: carbon monoxide (CO), nitric oxide (NO), andnitrogen dioxide (NO2). The diurnal change of absorption and scatteringcoefficients during the polluted (inversion) days increased approximately bya factor of two for all wavelengths compared to the clean days. The spectralvariation in aerosol absorption coefficients indicated a significant amountof absorbing aerosol from traffic emissions and residential wood burning.The analysis of single scattering albedo (SSA), ?ngstr?m exponent ofabsorption (AEA), and ?ngstr?m exponent of scattering (AES) forclean and polluted days provides evidences that the aerosol aging andcoating process is suppressed by strong temperature inversion under cloudyconditions. In general, measured UV absorption coefficients were found to bemuch larger for biomass burning aerosol than for typical ambient aerosols.
机译:我们介绍了实验室和环境光声(PA)在紫外波长(即355 nm)下对气溶胶光吸收系数的测量结果,并与在405、532、870和1047 nm处的测量结果进行了比较。通过积分可以同时测量气溶胶光散射系数PA的声学谐振器中的往复式浊度计。对各种实验室产生的气溶胶(包括盐,香和煤油)进行了吸收和散射测量,以评估仪器的校准并深入了解气溶胶光吸收和散射的光谱依赖性。环境测量是在内华达州里诺市于2009年12月18日至2010年1月18日之间进行的,测量期间包括有或没有强烈的地面温度反演的天,这对应于高度污染的(新鲜散发的浮质)和相对清洁的(老化的浮质)条件。测量了颗粒物(PM)浓度,并与其他交通排放示踪剂进行了分析。温度反转事件导致PM 2.5 和PM 10 (空气动力学直径分别小于2.5μm和10μm的颗粒物)和气态污染物的浓度非常高。 ),一氧化氮(NO)和二氧化氮(NO 2 )。与干净天数相比,在所有污染波长下,污染(反转)天的吸收系数和散射系数的日变化大约增加了两倍。气溶胶吸收系数的光谱变化表明从交通排放和住宅木材燃烧中吸收了大量的气溶胶。单散射反照率(SSA),吸收指数(AEA)和散射指数(AES)的分析)在无尘和污染的日子提供了证据,证明在多云条件下强烈的温度反转抑制了气溶胶的老化和涂覆过程。通常,发现生物质燃烧气溶胶的测量紫外线吸收系数比典型的环境气溶胶的紫外线吸收系数大得多。

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