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首页> 外文期刊>Atmospheric Chemistry and Physics Discussions >A temporally and spatially resolved validation of emission inventories by measurements of ambient volatile organic compounds in Beijing, China
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A temporally and spatially resolved validation of emission inventories by measurements of ambient volatile organic compounds in Beijing, China

机译:通过测量北京地区环境中挥发性有机化合物对排放清单进行时空解析验证

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pstrongAbstract./strong Understanding the sources of volatile organic compounds (VOCs) is essential for ground-level ozone and secondary organic aerosol (SOA) abatement measures. We made VOC measurements at 27 sites and online observations at an urban site in Beijing from July 2009 to January 2012. Based on these measurement data, we determined the spatial and temporal distribution of VOCs, estimated their annual emission strengths based on their emission ratios relative to carbon monoxide (CO), and quantified the relative contributions of various sources using the chemical mass balance (CMB) model. These results from ambient measurements were compared with existing emission inventories to evaluate the spatial distribution, species-specific emissions, and source structure of VOCs in Beijing. The measured VOC distributions revealed a hotspot in the southern suburban area of Beijing, whereas current emission inventories suggested that VOC emissions were concentrated in downtown areas. Compared with results derived from ambient measurements, the annual inventoried emissions of oxygenated VOC (OVOC) species and C2a??C4 alkanes may be underestimated, while the emissions of styrene and 1,3-butadiene may be overestimated by current inventories. Source apportionment using the CMB model identified vehicular exhaust as the most important VOC source, with the relative contribution of 49%, in good agreement with the 40a??51% estimated by emission inventories. The relative contribution of paint and solvent utilization obtained from the CMB model was 14%, significantly lower than the value of 32% reported by one existing inventory. Meanwhile, the relative contribution of liquefied petroleum gas (LPG) usage calculated using the CMB model was 6%, whereas LPG usage contribution was not reported by current emission inventories. These results suggested that VOC emission strengths in southern suburban area of Beijing, annual emissions of C2a??C4 alkanes, OVOCs and some alkenes, and the contributions of solvent and paint utilization and LPG usage in current inventories all require significant revisions./p.
机译:> >摘要。了解挥发性有机化合物(VOC)的来源对于减少地面臭氧和二次有机气溶胶(SOA)的措施至关重要。 2009年7月至2012年1月,我们在北京的27个站点进行了VOC测量,并在一个城市站点进行了在线观测。基于这些测量数据,我们确定了VOC的时空分布,并根据相对的排放比估算了其年排放强度。一氧化碳(CO),并使用化学质量平衡(CMB)模型量化各种来源的相对贡献。将环境测量的结果与现有的排放清单进行比较,以评估北京的挥发性有机化合物的空间分布,特定物种的排放和源结构。测得的挥发性有机化合物分布揭示了北京南部郊区的一个热点,而目前的排放清单表明,挥发性有机化合物的排放集中在市区。与环境测量结果相比,含氧量的挥发性有机化合物(OVOC)和C2a ?? C4烷烃的年度清单排放量可能被低估了,而苯乙烯和1,3-丁二烯的排放量可能被当前清单高估了。使用CMB模型进行的源分配确定了汽车尾气是最重要的VOC源,相对贡献为49%,与排放清单估算的40a%〜51%吻合良好。从CMB模型获得的油漆和溶剂利用率的相对贡献为14%,大大低于一个现有库存报告的32%的值。同时,使用CMB模型计算的液化石油气(LPG)使用的相对贡献为6%,而当前的排放清单并未报告LPG使用的贡献。这些结果表明,北京南部郊区的VOC排放强度,C2a ?? C4烷烃,OVOC和某些烯烃的年排放量以及当前清单中溶剂和涂料利用率以及LPG用量的贡献都需要进行重大修订。

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