Speciation and temporal characterization of dicarboxylic acids in PM2.5 during a PM episode and a period of non-episodic pollution

被引:59
作者
Hsieh, Li-Ying [2 ]
Chen, Chien-Lung [3 ]
Wan, Meng-Wei [1 ]
Tsai, Cheng-Hsien [4 ]
Tsai, Ying I. [1 ,5 ]
机构
[1] Chia Nan Univ Pharm & Sci, Dept Environm Engn & Sci, Tainan 717, Taiwan
[2] Natl Cheng Kung Univ, Dept Chem, Tainan 701, Taiwan
[3] Fortune Inst Technol, Dept Finance, Kaohsiung 831, Taiwan
[4] Natl Kaohsiung Univ Appl Sci, Dept Chem & Mat Engn, Kaohsiung 807, Taiwan
[5] Natl Cheng Kung Univ, Sustainable Environm Res Ctr, Tainan 701, Taiwan
关键词
Sampling artifacts; Diurnal variations; Oxalic acid; Malonic acid; Succinic acid; Tartaric acid; Inorganic salts;
D O I
10.1016/j.atmosenv.2008.05.021
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
PM2.5 aerosol was collected during a PM episode and a non-episodic pollution period between September and November 2004 in suburban southern Taiwan and dicarboxylic acid and inorganic species content and provenance were investigated. Oxalic acid was the dominant dicarboxylic acid species, followed by succinic acid and malonic acid. Tartaric acid concentrations were the lowest. There was 49.3% more dicarboxylic acid in PM episode aerosol than in non-episodic aerosol. However, daily oxalic acid concentration increased 72.7% in PM episode aerosol, while succinic acid fell 20.9% and malonic acid fell 21.6%, indicating higher conversion of these acids into oxalic acid in PM episode aerosol. Dicarboxyllic acid concentrations, particularly oxalic acid, peaked at night during the PM episode, due to accumulation of daytime oxalic acid combined with low wind velocity and low mixing layer height at this time. So(4)(2-), NO3- and NH4+ were the dominant ionic species in both PM episode and non-episodic aerosols. NO3- concentration increased 106% during the PM episode, while HNO3, a gaseous precursor of NO3-, fell 57%, indicating a large conversion of HNO3 to aerosol phase NO3- in PM episode aerosol. Backward trajectory data indicate that burning of paddy fields may also contribute to oxalic acid content in PM episode aerosol in the study area, especially during nighttime. Principal component analyses showed that succinic acid, malonic acid and oxalic acid were important factors in both pollution periods and also that there was high correlation between tartaric acid and NOx or HNO2, indicative of vehicle emissions. The mass ratio of oxalic acid to sulfate in this aerosol was as high as 60.3 parts per thousand, 35.5% higher than in non-episodic aerosol. Principal component analyses showed that photochemical aerosols contributed by succinic acid, malonic acid and oxalic acid were important factors in both periods. There was high correlation between tartaric acid and NOx or HN02, indicative of vehicle emissions. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6836 / 6850
页数:15
相关论文
共 55 条
  • [1] Case study of cloud physical and chemical processes in low clouds at Mt. Brocken
    Acker, K
    Mertes, S
    Möller, D
    Wieprecht, W
    Auel, R
    Kalass, D
    [J]. ATMOSPHERIC RESEARCH, 2002, 64 (1-4) : 41 - 51
  • [2] Sources of sampling error for field measurement of nitric acid gas by a denuder system
    Bai, H
    Lu, C
    Chang, KF
    Fang, GC
    [J]. ATMOSPHERIC ENVIRONMENT, 2003, 37 (07) : 941 - 947
  • [3] Measurements of gaseous HONO, HNO3,SO2, HCl, NH3, particulate sulfate and PM2.5 in New York, NY
    Bari, A
    Ferraro, V
    Wilson, LR
    Luttinger, D
    Husain, L
    [J]. ATMOSPHERIC ENVIRONMENT, 2003, 37 (20) : 2825 - 2835
  • [4] Regional sources of particulate sulfate, SO2, PM2.5, HCl, and HNO3, in New York, NY
    Bari, A
    Dutkiewicz, VA
    Judd, CD
    Wilson, LR
    Luttinger, D
    Husain, L
    [J]. ATMOSPHERIC ENVIRONMENT, 2003, 37 (20) : 2837 - 2844
  • [5] Thermodynamics of the formation of atmospheric organic particulate matter by accretion reactions - Part 3: Carboxylic and dicarboxylic acids
    Barsanti, Kelley C.
    Pankow, James F.
    [J]. ATMOSPHERIC ENVIRONMENT, 2006, 40 (34) : 6676 - 6686
  • [6] Atmospheric science - Reshaping the theory of cloud formation
    Charlson, RJ
    Seinfeld, JH
    Nenes, A
    Kulmala, M
    Laaksonen, A
    Facchini, MC
    [J]. SCIENCE, 2001, 292 (5524) : 2025 - 2026
  • [7] Carboxylic acids in the troposphere, occurrence, sources, and sinks: A review
    Chebbi, A
    Carlier, P
    [J]. ATMOSPHERIC ENVIRONMENT, 1996, 30 (24) : 4233 - 4249
  • [8] Evaporation loss of ammonium nitrate particles during filter sampling
    Cheng, YH
    Tsai, CJ
    [J]. JOURNAL OF AEROSOL SCIENCE, 1997, 28 (08) : 1553 - 1567
  • [9] Determination of low-molecular-mass carboxylic acids in atmospheric aerosol and vehicle emission samples by capillary electrophoresis
    Dabek-Zlotorzynska, E
    Piechowski, M
    McGrath, M
    Lai, EPC
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2001, 910 (02) : 331 - 345
  • [10] Sources of fine particulate sulfate in New York
    Dutkiewicz, VA
    Qureshi, S
    Khan, AR
    Ferraro, V
    Schwab, J
    Demerjian, K
    Husain, L
    [J]. ATMOSPHERIC ENVIRONMENT, 2004, 38 (20) : 3179 - 3189