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Gas-particle partitioning of primary organic aerosol emissions: (1) Gasoline vehicle exhaust

机译:主要有机气溶胶排放物的气体颗粒分配:(1)汽油车尾气

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The gas-particle partitioning of the primary organic aerosol (POA) emissions from fifty-one light-duty gasoline vehicles (model years 1987-2012) was investigated at the California Air Resources Board Haagen-Smit Laboratory. Each vehicle was operated over the cold-start unified cycle on a chassis dynamometer and its emissions were sampled using a constant volume sampler. Four independent yet complementary approaches were used to investigate POA gas-particle partitioning: sampling artifact correction of quartz filter data, dilution from the constant volume sampler into a portable environmental chamber, heating in a thermodenuder, and thermal desorption/gas chromatography/mass spectrometry analysis of quartz filter samples. This combination of techniques allowed gas-particle partitioning measurements to be made across a wide range of atmospherically relevant conditions - temperatures of 25-100 ℃ and organic aerosol concentrations of <1-600 μg m~(-3). The gas-particle partitioning of the POA emissions varied continuously over this entire range of conditions and essentially none of the POA should be considered non-volatile. Furthermore, for most vehicles, the low levels of dilution used in the constant volume sampler created particle mass concentrations that were greater than a factor of 10 or higher than typical ambient levels. This resulted in large and systematic partitioning biases in the POA emission factors compared to more dilute atmospheric conditions, as the POA emission rates may be over-estimated by nearly a factor of four due to gas-particle partitioning at higher particle mass concentrations. A volatility distribution was derived to quantitatively describe the measured gas-particle partitioning data using absorptive partitioning theory. Although the POA emission factors varied by more than two orders of magnitude across the test fleet, the vehicle-to-vehicle differences in gas-particle partitioning were modest. Therefore, a single volatility distribution can be used to quantitatively describe the gas-particle partitioning of the entire test fleet. This distribution is designed to be applied to quartz filter POA emission factors in order to update emissions inventories for use in chemical transport models.
机译:加利福尼亚空气资源委员会哈根-史密特实验室研究了五十一辆轻型汽油车(1987年至2012年)的主要有机气溶胶(POA)排放物的气体颗粒分配。每辆车都在底盘测功机上以冷启动统一循环运行,并使用恒定体积采样器对排放量进行采样。四种独立但互补的方法用于研究POA气体颗粒的分配:对石英滤池数据进行采样伪影校正,从恒定体积采样器稀释到便携式环境室中,在热剥蚀仪中加热以及热脱附/气相色谱/质谱分析石英过滤器样品。这种技术的结合使得可以在与大气有关的各种条件下进行气体颗粒分配测量,温度范围为25-100℃,有机气溶胶浓度<1-600μgm〜(-3)。 POA排放物的气体颗粒分配在整个条件范围内连续变化,并且基本上没有POA应该被认为是非挥发性的。此外,对于大多数车辆而言,在恒定体积采样器中使用的低稀释水平产生的颗粒质量浓度大于典型环境水平的10倍或更高。与更稀薄的大气条件相比,这会导致POA排放因子出现较大且系统的分配偏差,因为在较高的颗粒质量浓度下,由于气体颗粒的分配,POA排放速率可能被高估了近四倍。利用吸收分配理论推导了挥发度分布,以定量描述测量的气体-颗粒分配数据。尽管在整个测试车队中,POA排放因子的变化幅度超过两个数量级,但车辆之间的气体颗粒分配差异不大。因此,单个挥发性分布可用于定量描述整个测试车队的气体颗粒分配。该分布旨在应用于石英过滤器POA排放因子,以便更新用于化学运输模型的排放清单。

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