Furuta Naoki, Iijima Akihiro, Kambe Akiko, Sakai Kazuhiro, Sato Keiichi
Department of Applied Chemistry, Faculty of Science and Engineering, Chuo University, 1-13-27 Kasuga, Tokyo, 112-8551, Japan.
J Environ Monit. 2005 Dec;7(12):1155-61. doi: 10.1039/b513988k. Epub 2005 Nov 9.
APM was collected and trace elements existing in the particles were monitored since May 1995 in this study. APM sample was collected separately by size (d < 2 microm, 2-11 microm and >11 microm) on the roof of the university building (45 m above ground) in the campus of Faculty of Science and Engineering, Chuo University, Tokyo, Japan, using an Anderson low volume air sampler. The collected sample was digested by HNO3, H2O2 and HF using a microwave oven, and major elements (Na, Mg, Al, K, Ca and Fe) were measured by ICP-AES, and trace elements (Li, Be, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Sb, Ba and Pb) were measured by ICP-MS. It was observed that the APM concentration was higher between the winter and the spring, compared to during the summer. The enrichment factor was calculated for each element in each set of APM (d < 2 microm, 2-11 microm and >11 microm). Seasonal trends of enrichment factors were examined, and the elements were classified into 3 groups according to the common seasonal behavior. It is likely that the elements in the same group have common origins. Toxic pollutant elements (Sb, Se, Cd, Pb and As) were found in small particles with d of <2 microm in concentrated levels. Antimony (Sb) had the highest enrichment factor, and the results suggested that Sb level in APM was extremely high. The origins of Sb were sought, and wastes from plastic incineration and brake pad wears of automobiles were suspected. Each set of APM (d < 2 microm, 2-11 microm and >11 microm) was classified by the shape, and the shape-dependent constituents of a single APM particle were quantitatively measured by SEM-EDX. High concentration of Sb was found in APM <2 microm and square particles. Particles less than 2 microm and square shaped particles were major particles produced by actual car braking experiments. From these experimental results it was concluded that the source of Sb in squared APM <2 microm is considered to be from brake pad wear.
本研究自1995年5月起收集大气颗粒物(APM)并监测其中存在的微量元素。在日本东京中央大学理工学院校园内的大学建筑屋顶(距地面45米),使用安德森低流量空气采样器按粒径(d < 2微米、2 - 11微米和> 11微米)分别采集APM样本。采集的样本用硝酸、过氧化氢和氢氟酸在微波炉中进行消解,主要元素(钠、镁、铝、钾、钙和铁)通过电感耦合等离子体发射光谱法(ICP - AES)测定,微量元素(锂、铍、钛、钒、铬、锰、钴、镍、铜、锌、砷、硒、钼、镉、锑、钡和铅)通过电感耦合等离子体质谱法(ICP - MS)测定。观察到与夏季相比,APM浓度在冬季和春季之间更高。计算了每组APM(d < 2微米、2 - 11微米和> 11微米)中各元素的富集因子。研究了富集因子的季节趋势,并根据共同的季节行为将元素分为3组。同一组中的元素可能有共同的来源。在d < 2微米的小颗粒中发现了高浓度的有毒污染物元素(锑、硒、镉、铅和砷)。锑(Sb)的富集因子最高,结果表明APM中的锑含量极高。探寻了锑的来源,怀疑是塑料焚烧废物和汽车刹车片磨损。每组APM(d < 2微米、2 - 11微米和> 11微米)按形状分类,并通过扫描电子显微镜 - 能谱仪(SEM - EDX)定量测量单个APM颗粒的形状相关成分。在<2微米的APM和方形颗粒中发现了高浓度的锑。小于2微米的颗粒和方形颗粒是实际汽车制动实验产生的主要颗粒。从这些实验结果得出结论,<2微米方形APM中锑的来源被认为是刹车片磨损。