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Chemical composition of ambient PM2.?5 over China and relationship to precursor emissions during 2005–2012

机译:环境PM2的化学成分。2005 - 2012年期间与中国的关系与前体排放的关系

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In this work, we presented the characteristics of PM2.?5 chemical composition over China for the period of 2005–2012 by synthesis of in situ measurement data collected from literatures and satellite-based estimates using aerosol optical depth (AOD) data and the GEOS-Chem chemical transport model. We revealed the spatiotemporal variations in PM2.?5 composition during 2005–2012 and investigated the driving forces behind the variations by examining the changes in precursor emissions using a bottom-up emission inventory. Both in situ observations and satellite-based estimates identified that secondary inorganic aerosols (i.e., sulfate, nitrate, and ammonium; SNA) ranked as the highest fraction of dust-free PM2.?5 concentrations, followed by organic matter (OM) and black carbon (BC). For instance, satellite-based estimates found that SNA, OM, and BC contributed to 59, 33, and 8?%, respectively, of national population-weighted mean dust-free PM2.?5 concentrations during 2005–2012. National population-weighted mean PM2.?5 concentration increased from 63.9?μg?m?3 in 2005 to 75.2?μg?m?3 in 2007 and subsequently decreased to 66.9?μg?m?3 from 2007 to 2012. Variations in PM2.?5 concentrations are mainly driven by the decrease in sulfate and the increase in nitrate. Population-weighted mean sulfate concentration decreased by 2.4?%?yr?1 during 2005–2012 (from 14.4 to 12.9?μg?m?3), while population-weighted mean nitrate concentration increased by 3.4?%?yr?1 during 2005–2012 (from 9.8 to 12.2?μg?m?3), largely offsetting the decrease in sulfate concentrations. By examining the emission data from the Multi-resolution Emission Inventory for China (MEIC), we found that the changes in sulfate and nitrate concentrations were in line with the decrease in SO2 emissions and the increase in NOx emissions during the same period. The desulfurization regulation in power plants enforced around 2005 has been the primary contributor to the SO2 emission reduction since 2006. In contrast, growth of energy consumption and lack of control measures for NOx resulted in a persistent increase in NOx emissions until the installation of denitrification devices on power plants late in 2011, which began to take effect in 2012. The results of this work indicate that the synchronized abatement of emissions for multipollutants is necessary for reducing ambient PM2.?5 concentrations over China.
机译:在这项工作中,我们通过使用气溶胶光学深度(AOD)数据和地球机构的原位测量数据,通过合成来自文献和基于卫星的估计的原位测量数据来提出PM2.5的化学成分的特点。 -Chem化学传输模型。我们在2005 - 2012年期间揭示了PM2.5组成的时空变化,并通过从自下而上排放清单检查前体排放的变化来研究变化背后的驱动力。原位观察和基于卫星的估计均确定二次无机气溶胶(即硫酸盐,硝酸盐和铵; SNA)排名为无尘PM2的最高分数,其次是有机物质(OM)和黑色碳(BC)。例如,基于卫星的估计发现,在2005 - 2012年期间,SNA,OM和BC分别为国家人群加权的平均无尘PM2.?5浓度贡献为59,33和8μl%。国家人口加权平均PM2.5浓度从63.9〜μg?m?3在2005中增加到75.2?μg?m?3在2007年,随后从2007到2012年下降到66.9?μg?3。PM2的变化。?5浓度主要由硫酸盐的降低和硝酸盐的增加驱动。人口加权平均硫酸盐浓度在2005-2012期间减少了2.4?%?1(从14.4-12.9≤m≤3),而群体加权平均硝酸盐浓度增加3.4?%?1 -2012(从9.8至12.2?μg?m≤3),在很大程度上抵消硫酸盐浓度的降低。通过研究来自中国(MEIC)的多分辨率排放库存的排放数据,我们发现硫酸盐和硝酸盐浓度的变化符合SO2排放的降低和同期NOx排放的增加。 2005年左右强制执行的发电厂的脱硫调节是自2006年以来的SO2排放减排的主要因素。相反,能耗的增长和NOx的控制措施导致NOx排放持续增加,直到安装脱硝设备在2011年晚些时候发电厂,在2012年开始生效。这项工作的结果表明,多体塑料排放的同步减少对中国的环境PM2浓度是必要的。

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