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Atmospheric polycyclic aromatic hydrocarbons observed over the North Pacific Ocean and the Arctic area: Spatial distribution and source identification

机译:在北太平洋和北极地区观测到的大气多环芳烃:空间分布和来源识别

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During the 2003 Chinese Arctic Research Expedition from the Bohai Sea to the high Arctic (37-80°N) aboard the icebreaker Xuelong (Snow Dragon), air samples were collected using a modified high-volume sampler that pulls air through a quartz filter and a polyurethane foam plug (PUF). These filters and PUFs were analyzed for particulate phase and gas phase polycyclic aromatic hydrocarbons (PAHs), respectively, in the North Pacific Ocean and adjacent Arctic region. The ΣPAHs (where Σ = 15 compounds) ranged from undetectable level to 4380 pgm~(-3) in the particulate phase and 928-92 600 pgm~(-3) in the gas phase, respectively. A decreasing latitudinal trend was observed for gas-phase PAHs, probably resulting from temperature effects, dilution and decomposition processes; particulate-phase PAHs, however, showed poor latitudinal trends, because the effects of temperature, dilution and photochemistry played different roles in different regions from middle-latitude source areas to the high latitudes. The ratios of PAH isomer pairs, either conservative or sensitive to degradation during long-range transport, were employed to interpret sources and chemical aging of PAHs in ocean air. In this present study the fluoranthene/pyrene and indeno[123-cd]pyrene/benzo[ghi]pyrene isomer pairs, whose ratios are conservative to photo-degradation, implies that biomass or coal burning might be the major sources of PAHs observed over the North Pacific Ocean and the Arctic region in the summer. The isomer ratios of 1,7/ (1,7 + 2,6)-DMP (dimethylphenanthrene) and anthracene/phenanthrene, which are sensitive to aging of air masses, not only imply chemical evolving of PAHs over the North Pacific Ocean were different from those over the Arctic, but reveal that PAHs over the Arctic were mainly related to coal burning, and biomass burning might have a larger contribution to the PAHs over the North pacific ocean.
机译:在2003年的中国北极研究探险队从渤海到极高的北极(37-80°N)登上破冰船雪龙(雪龙)的过程中,使用改良的大容量采样器收集了空气样本,该采样器将空气通过石英过滤器并通过聚氨酯泡沫塞(PUF)。在北太平洋和邻近北极地区,分别对这些过滤器和PUF进行了颗粒相和气相多环芳烃(PAH)分析。 ΣPAHs(其中Σ= 15种化合物)在颗粒相中的检测水平为4380 pgm〜(-3),在气相中为928-92 600 pgm〜(-3)。气相PAHs的经纬度趋势有所降低,这可能是由于温度影响,稀释和分解过程引起的。然而,颗粒相多环芳烃表现出较差的纬向变化趋势,因为温度,稀释和光化学的影响在从中纬度源区到高纬度的不同区域发挥了不同的作用。 PAH异构体对的比例(无论是保守的还是对远程运输过程中的降解敏感)均用于解释海洋空气中PAHs的来源和化学老化。在本研究中,荧蒽/ py和茚并[123-cd] py /苯并gpy异构体对与光降解的比率呈保守性,这表明生物量或燃煤可能是整个过程中观察到的PAHs的主要来源。夏季是北太平洋和北极地区。 1,7 /(1,7 + 2,6)-DMP(二甲基菲)和蒽/菲的异构体比率对空气质量的老化敏感,不仅意味着北太平洋上多环芳烃的化学演化不同北极地区的多环芳烃主要与燃煤有关,而生物质燃烧可能对北太平洋的多环芳烃贡献更大。

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