Chen Yueyue, Liu Jia, Shang Jing, Zhu Tong
College of Environmental Science and Engineering, Peking University, Beijing 100081, China.
College of Environmental Science and Engineering, Peking University, Beijing 100081, China.
J Environ Sci (China). 2017 Jun;56:45-51. doi: 10.1016/j.jes.2016.08.018. Epub 2016 Oct 3.
The reaction of HCHO with Beijing winter's real ambient particulate matter (PM) inside a 3.3m Teflon Chamber was conducted in this study. NO, O and HO gases were removed from the ambient aerosol before entering into the chamber. The decays of HCHO were monitored (acetylacetone spectrophotometry method) during the reactions at different PM number concentrations (N) and relative humidities (RHs), and the formed particulate formate was detected by IC and XPS techniques. The results showed that when RH was 10%-15%, the decay rate of HCHO in the chamber was higher with the existence of PM from relatively clean days (with number concentration (N)<200,000particle/L, 0.35-22.5μm) compared to dirty days (N>200,000particle/L, 0.35-22.5μm). When RH increased to 30%-45%, PM can hardly have significant influences on the decay of HCHO. The formations of formate on the reacted PM were consistent with the HCHO decay rates at different ambient PM N and RH conditions. This is a first study related to the "real" ambient PM reacted with HCHO and suggested that in the clean and low RH days, PM could be an effective medium for the conversion of HCHO to formate.
本研究在一个3.3米的特氟龙反应室内进行了甲醛与北京冬季实际环境颗粒物(PM)的反应。在进入反应室之前,从环境气溶胶中去除了一氧化氮、氧气和羟基气体。在不同的颗粒物数量浓度(N)和相对湿度(RH)下,通过乙酰丙酮分光光度法监测反应过程中甲醛的衰减,并通过离子色谱和X射线光电子能谱技术检测生成的颗粒状甲酸盐。结果表明,当相对湿度为10%-15%时,与污染日(N>200,000颗粒/升,0.35-22.5微米)相比,存在来自相对清洁日(数量浓度(N)<200,000颗粒/升,0.35-22.5微米)的颗粒物时,反应室内甲醛的衰减率更高。当相对湿度增加到30%-45%时,颗粒物对甲醛的衰减几乎没有显著影响。在不同环境颗粒物N和相对湿度条件下,反应后颗粒物上甲酸盐的形成与甲醛衰减率一致。这是第一项关于“实际”环境颗粒物与甲醛反应的研究,表明在清洁和低相对湿度的日子里,颗粒物可能是甲醛转化为甲酸盐的有效介质。