Dasgupta Purnendu K, Li Jianzhong, Zhang Genfa, Luke Winston T, McClenny William A, Stutz Jochen, Fried Alan
Department of Chemistry, Texas Tech University, Lubbock, Texas 79409-1061, USA.
Environ Sci Technol. 2005 Jul 1;39(13):4767-83. doi: 10.1021/es048327d.
First, we briefly review the atmospheric chemistry and previous intercomparison measurements for HCHO, with special reference to the diffusion scrubber Hantzsch reaction based fluorescence instrument used in the field studies reported herein. Then we discuss summertime HCHO levels in five major U.S. cities measured over 1999-2002, primarily from ground-based measurements. Land-sea breeze circulations play a major role in observed concentrations in coastal cities. Very high HCHO peak mixing ratios were observed in Houston (>47 ppb) where the overall median mixing ratio was 3.3 ppb; the corresponding values in Atlanta were approximately >18 and 7.9 ppb, respectively. The peak and median mixing ratios (9.3 and 2.3 ppb) were the lowest for Tampa, where the land-sea breeze also played an important role. In several cities, replicate HCHO measurements were made by direct spectroscopic instruments; the instruments were located kilometers from each other and addressed very different heights (e.g., 106 vs 10 m). Even under these conditions, there was remarkable qualitative and often quantitative agreement between the different instruments, when they were all sampling the same air mass within a short period of each other. Local chemistry dominates how HCHO is formed and dissipated. The high concentrations in Houston resulted from emissions near the ship channel; the same formaldehyde plume was measured at two sites and clearly ranged over tens of kilometers. Local micrometeorology is another factor. HCHO patterns measured at a high-rise site in downtown Nashville were very much in synchrony with other ground sites 12 km away until July 4 celebrations whence HCHO concentrations at the downtown site remained elevated for several days and nights. The formation and dissipation of HCHO in the different cities are discussed in terms of other concurrently measured species and meteorological vectors. The vertical profiles of HCHO in and around Tampa under several different atmospheric conditions are presented. The extensive data set represented in this paper underscores that urban HCHO measurements can now be made easily; the agreement between disparate instruments (that are independently calibrated or rely on the absolute absorption cross section) further indicates that such measurements can be done reliably and accurately for this very important atmospheric species. The data set presented here can be used as a benchmark for future measurements if the use of formaldehyde precursors such as methanol or methyl tert-butyl ether (MTBE) as oxygenated fuel additives increases in the future.
首先,我们简要回顾一下大气化学以及先前针对甲醛(HCHO)的相互比较测量,特别提及本文所报道的实地研究中使用的基于扩散洗涤器汉茨希反应的荧光仪器。然后我们讨论1999 - 2002年期间在美国五个主要城市测量到的夏季甲醛水平,主要基于地面测量数据。海陆风环流在沿海城市观测到的浓度中起主要作用。在休斯顿观测到非常高的甲醛峰值混合比(>47 ppb),其总体中位数混合比为3.3 ppb;在亚特兰大,相应的值分别约为>18 ppb和7.9 ppb。对于坦帕,峰值和中位数混合比(9.3 ppb和2.3 ppb)最低,在那里海陆风也起到了重要作用。在几个城市,通过直接光谱仪器进行了重复的甲醛测量;这些仪器彼此相距数公里,且测量高度差异很大(例如,106米与10米)。即使在这些条件下,当不同仪器在短时间内对同一气团进行采样时,它们之间在定性上往往有显著一致性,在定量上也常常如此。当地的化学过程主导着甲醛的形成和消散。休斯顿的高浓度是由船舶航道附近的排放造成的;在两个地点测量到了相同的甲醛羽流,其明显延伸了数十公里。当地的微气象学是另一个因素。在纳什维尔市中心一个高层建筑站点测量到的甲醛模式与12公里外的其他地面站点非常同步,直到7月4日庆祝活动期间,市中心站点的甲醛浓度在数天和数夜内一直保持在较高水平。根据同时测量的其他物种和气象向量,讨论了不同城市中甲醛的形成和消散情况。展示了在几种不同大气条件下坦帕及其周边地区甲醛的垂直剖面。本文所呈现的大量数据集强调,现在可以轻松地进行城市甲醛测量;不同仪器(独立校准或依赖绝对吸收截面)之间的一致性进一步表明,对于这种非常重要的大气物种,可以可靠且准确地进行此类测量。如果未来作为含氧燃料添加剂的甲醇或甲基叔丁基醚(MTBE)等甲醛前体的使用增加,这里呈现的数据集可作为未来测量的基准。