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Ozone formation in the Houston-Galveston area: A regional chemical transport model study.

机译:休斯顿-加尔维斯顿地区的臭氧形成:区域化学迁移模型研究。

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An episodic simulation (during September 7–11, 1993) is conducted to characterize ozone (O3) formation and to investigate the dependence of O3 formation on precursors in the Houston-Galveston (HG) area using a regional chemical transport model. The model reproduces the observed temporal and spatial distributions of O3 concentrations. Ground level O3 exhibits an extraordinary diurnal variation in the HG area. Midday O3 reaches a very high level due to rapid and efficient photochemical production, whereas at night there exists a shallow urban-scale O3 deficit with near-zero concentrations due to high nighttime NOx. The simulated net photochemical production rates of O3 (P(O3)) in the Houston area are much higher than those in most other U.S. urban cities, reaching 30–40 ppb hr −1 for typical daytime NOx levels. Furthermore, the NOx reversal value (the NOx concentration at which P(O 3) reaches maximum) is much larger than that in most other U.S. cities. The large abundance and high reactivity of anthropogenic volatile organic compounds (AVOCs), and the coexistence of abundant AVOCs and NOx in this area as well, are responsible for the high O3 production rates and the NOx reversal value. The simulated O3 production efficiency is typically 3–10 O3 molecules per NOx molecule emitted in midday hours in Houston. Heterogeneous conversion of NO 2 to HONO on the surfaces of soot aerosol accelerates the O3 production by about one hour in the morning, and leads to an appreciable increase of O3 level with a midday average of 7 ppb. The model study suggests that the chemistry over most of the Houston metropolitan area is in or close to the transit regime of NOx-VOC sensitivity, therefore the response of O3 production to emission reductions of either VOC or NO x is not very sensitive. Doubling AVOC emissions in the base case does not significantly affect the response of O3 production to the reduction in AVOC emissions, but greatly impacts the response of O3 production to the reduction in NOx emissions. Biogenic VOCs do not contribute significantly to the O3 pollution in the Houston area, but distant BVOC sources still can affect urban O3 through long-range transport.
机译:进行了情景模拟(1993年9月7日至11日),以表征臭氧(O 3 )的形成并研究O 3 的形成对休斯顿前体的依赖性-加尔维斯顿(HG)地区,使用区域化学品运输模型。该模型再现了观测到的O 3 浓度的时空分布。地面O 3 在HG区表现出极大的昼夜变化。由于快速有效的光化学生产,午间的O 3 达到了很高的水平,而在夜间,由于以下原因,城市范围内的O 3 浅层赤字浓度接近零。夜间NO x 。休斯敦地区模拟的O 3 (P(O 3 ))的净光化学生产率远高于美国大多数其他城市,达到30–40 ppb hr -1 对于典型的白天NO x 水平。此外,NO x 的反转值(P(O 3 )达到最大值时的NO x 浓度)比大多数情况下要大得多。美国其他城市。人为的挥发性有机化合物(AVOCs)的丰度高和高反应性,以及该地区丰富的AVOCs和NO x 的共存也是造成高O 3 生产率和NO x 反转值。在休斯顿,模拟的O 3 生产效率通常是在午间时段每NO x 分子排放3–10 O 3 分子。烟尘气溶胶表面NO 2 向HONO的非均相转化将O 3 的产生加速了大约一小时,导致O 3明显增加。 > 3 水平,中午平均值为7 ppb。该模型研究表明,休斯敦大部分都会区的化学反应处于或接近NO x -VOC敏感性的迁移方式,因此O 3 产生的反应对VOC或NO x 的减排量不是很敏感。在基本情况下,将AVOC排放量增加一倍不会显着影响O 3 产量对减少AVOC排放的反应,但会大大影响O 3 产量对减少排放的反应NO x 的排放量。在休斯顿地区,生物源挥发性有机化合物对O 3 的污染贡献不大,但遥远的BVOC来源仍可通过远程运输影响城市O 3

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