Toda Kei, Tokunaga Wataru, Gushiken Yosuke, Hirota Kazutoshi, Nose Teppei, Suda Daisaku, Nagai Jun, Ohira Shin-Ichi
Department of Chemistry, Kumamoto University, Kurokami 2-39-1, Kumamoto 860-8555, Japan.
J Environ Monit. 2012 May;14(5):1462-72. doi: 10.1039/c2em10935b. Epub 2012 Apr 17.
A micro-gas analysis system (μGAS) was developed for mobile monitoring and continuous measurements of atmospheric HCHO. HCHO gas was trapped into an absorbing/reaction solution continuously using a microchannel scrubber in which the microchannels were patterned in a honeycomb structure to form a wide absorbing area with a thin absorbing solution layer. Fluorescence was monitored after reaction of the collected HCHO with 2,4-pentanedione (PD) in the presence of acetic acid/ammonium acetate. The system was portable, battery-driven, highly sensitive (limit of detection = 0.01 ppbv) and had good time resolution (response time 50 s). The results revealed that the PD chemistry was subject to interference from O(3). The mechanism of this interference was investigated and the problem was addressed by incorporating a wet denuder. Mobile monitoring was performed along traffic roads, and elevated HCHO levels in a street canyon were evident upon mapping of the obtained data. The system was also applied to stationary monitoring in a forest in which HCHO formed naturally via reaction of biogenic compounds with oxidants. Concentrations of a few ppbv-HCHO and several-tens of ppbv of O(3) were then simultaneously monitored with the μGAS in forest air monitoring campaigns. The obtained 1 h average data were compared with those obtained by 1 h impinger collection and offsite GC-MS analysis after derivatization with o-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine (PFBOA). From the obtained data in the forest, daily variations of chemical HCHO production and loss are discussed.
开发了一种用于大气中甲醛移动监测和连续测量的微气体分析系统(μGAS)。使用微通道洗涤器将甲醛气体连续捕获到吸收/反应溶液中,其中微通道呈蜂窝结构图案化,以形成具有薄吸收溶液层的宽吸收区域。在乙酸/乙酸铵存在下,收集的甲醛与2,4-戊二酮(PD)反应后监测荧光。该系统便于携带,由电池驱动,灵敏度高(检测限 = 0.01 ppbv),具有良好的时间分辨率(响应时间50秒)。结果表明,PD化学受到O(3)的干扰。研究了这种干扰的机制,并通过加入湿式除雾器解决了该问题。沿交通道路进行移动监测,绘制获得的数据后,街道峡谷中甲醛水平升高明显。该系统还应用于森林中的固定监测,其中甲醛通过生物源化合物与氧化剂的反应自然形成。在森林空气监测活动中,使用μGAS同时监测了几ppbv的甲醛浓度和几十ppbv的O(3)浓度。将获得的1小时平均数据与通过1小时冲击器收集并在用邻-(2,3,4,5,6-五氟苄基)羟胺(PFBOA)衍生化后进行场外气相色谱-质谱分析获得的数据进行比较。根据在森林中获得的数据,讨论了化学甲醛产生和损失的日变化。