首页> 外文OA文献 >Insights into aerosol chemistry during the 2015 China Victory Day parade: results from simultaneous measurements at ground level and 260 m in Beijing
【2h】

Insights into aerosol chemistry during the 2015 China Victory Day parade: results from simultaneous measurements at ground level and 260 m in Beijing

机译:2015年中国胜利纪念日游行期间对气溶胶化学的见解:北京地面和260 m的同时测量结果

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Strict emission controls were implemented in Beijing and adjacentprovinces to ensure good air quality during the 2015 China Victory Dayparade. Here, we conducted synchronous measurements of submicron aerosols(PM) at ground level and 260 m on a meteorological tower by using ahigh-resolution aerosol mass spectrometer and an aerosol chemical speciationmonitor, respectively, in Beijing from 22 August to 30 September. Ourresults showed that the average PM concentrations are 19.3 and 14.8 µg m at ground level and 260 m, respectively, during thecontrol period (20 August–3 September), which are 57 and 50 % lowerthan those after the control period (4–30 September). Organic aerosols(OAs) dominated PM during the control period at both ground level and260 m (55 and 53 %, respectively), while their contribution showedsubstantial decreases (∼  40 %) associated with an increasein secondary inorganic aerosols (SIAs) after the parade, indicating a largerimpact of emission controls on SIA than OA. Positive matrix factorization ofOA further illustrated that primary OA (POA) showed similar decreases assecondary OA (SOA) at both ground level (40 % vs. 42 %) and 260 m(35 % vs. 36 %). However, we also observed significant changes in SOAcomposition at ground level. While the more oxidized SOA showed a large decrease by 75 %,the less oxidized SOA was comparable during (5.6 µg m) andafter the control periods (6.5 µg m). Our results demonstratedthat the changes in meteorological conditions and PM loadings have affectedSOA formation mechanisms, and the photochemical production of fresh SOA wasmore important during the control period. By isolating the influences ofmeteorological conditions and footprint regions in polluted episodes, wefound that regional emission controls on average reduced PM levels by 44–45 %, and the reductions were close among SIA, SOA and POA at 260 m,whereas primary species showed relatively more reductions (55–67 %)than secondary aerosol species (33–44 %) at ground level.
机译:北京及邻近省份实施了严格的排放控制,以确保在2015年“中国胜利日”游行期间的良好空气质量。在这里,我们分别在8月22日至9月30日在北京分别使用高分辨率气溶胶质谱仪和气溶胶化学形态监测仪在气象塔上对地面和260 m处的亚微米气溶胶(PM)进行了同步测量。我们的结果表明,在控制期内(8月20日至9月20日),地面平均PM浓度分别为19.3和14.8μg/ m2和260μm,分别比控制期(9月4-30日)低57%和50%。 )。在控制期内,有机气溶胶(OAs)在地面和260 m处均占主导地位(分别为55%和53%),而游行后,其次生无机气溶胶(SIA)的增加则显着降低(约decreases40(%),表明排放控制对SIA的影响大于OA。 OA的正矩阵因式分解进一步说明,初级OA(POA)在两个地面水平(40 %%对42 %%)和260μm(35 %%对36%)处的次要OA(SOA)都有相似的下降。但是,我们还观察到了地面SOA组成的重大变化。虽然氧化程度更高的SOA降低了75%,但在控制期间(5.6μg/ m)和氧化后的SOA含量较低(6.5μg/ m)。我们的结果表明,气象条件和PM含量的变化已经影响了SOA的形成机理,并且在控制期内,新鲜SOA的光化学生产更为重要。通过隔离污染事件中的气象条件和足迹区域的影响,我们发现区域排放控制使PM水平平均降低了44–45%,SIA,SOA和POA在260µm时的减少幅度接近,而原始物种相对较多在地面水平上比第二气溶胶种类(33-44%)减少(55-67%)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号