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|Title:||Study of photochemical ozone pollution in Hong Kong||Authors:||So, King-lung||Keywords:||Hong Kong Polytechnic University -- Dissertations
Ozone -- Environmental aspects -- China -- Hong Kong
Air -- Pollution -- China -- Hong Kong
|Issue Date:||2007||Publisher:||The Hong Kong Polytechnic University||Abstract:||The Pearl River Delta (PRD) of China has experienced serious air pollution along with the astonishing economic and industrial developments in the past two decades. Large emissions of pollutants like respirable suspended particulates, sulphur dioxides (SO₂), nitrogen oxides (NOₓ) and volatile organic compounds (VOC), coupled with the subtropical climate, have resulted in photochemical ozone (O₃) pollution and visibility degradation in the region, including Hong Kong (HK) which is situated in the southern part of the PRD. Photochemical theory and overseas experience show that control of O₃ pollution is a very challenging undertaking because of the non-linear dependency of O₃ on its precursors, VOC and NOₓ. Such O₃-O₃ precursors' relationship is often site specific and the O₃ migration strategy is effective only should there be an in-depth understanding of the sources, patterns, and formation of photochemical O₃ and its precursors, as well as their relationship in the region. However, as the information on the above aspects is very limited in the PRD (including HK), efforts to formulate an effective O₃control strategy has been hindered. This research is therefore aimed at filling our knowledge gap and improving our understanding of the spatio-temporal distribution of O₃ and O₃ precursors in HK, the roles of O₃ precursors in O₃ production, and the fast O₃ chemistry in the subtropical region. Measurement data from Environmental Protection Department (EPD) of HK and by researchers of the Hong Kong Polytechnic University were analyzed using various statistical and modelling tools. The results are summarized in the following sections. O₃ and regularly monitored gaseous air-quality data collected from June 1999 to May 2000 at three EPD's sites (rural, urban and suburban) were analyzed in order to obtain the information on the seasonal and spatial distribution of O₃ and the relationship with other gas pollutants. The highest average O₃ level was found at a rural site (Tap Mun) in northeastern HK which had increased levels of carbon monoxide (CO) and SO₂ (relative to NOₓ) indicating frequent influences of regional air masses from the inland region. The lowest concentration of O₃ was found at the urban site (Tsuen Wan). The southwestern suburban site (Tung Chung) showed intermediate O₃ levels on average, and analysis of CO/NOₓ and SO2/NOₓ ratios suggests this site was impacted by both local and regional pollution. Principal component analysis further elucidated that the O₃ variation in the northeastern rural area was largely determined by regional chemical and transport processes, while the O₃ variability in the southwestern suburban and urban sites were more influenced by local emissions. High O₃ episodes were also found to correlate with an enhanced ratio of SO₂ to NOₓ, further suggesting the influence of regional emissions from the PRD. The results indicated that it is imperative to consider regional scale emissions and dynamic transport in managing O₃pollution in HK.
VOC data collected by the EPD at the rural, urban and roadside sites from November 2000 to October 2001 and September 2002 to August 2003 were examined for their spatial distribution, seasonal variation, source-receptor relationships and photochemical reactivity. As expected, the roadside site showed the highest VOC level owing to the vehicular emissions and the rural site was characterized by the aged air mass with the lowest VOC level. Ratios of VOC with different photochemical reactivities indicated the mix of emission sources and increased atmospheric processing from urban to rural areas. Ratios of VOC to NOₓ were about 2-3 in the urban areas and 10 at the rural site, suggesting that the formation of O₃ in HK is generally sensitive to VOC. Among the VOC, toluene was the most abundant species on a carbon basis and also a leading contributor to O₃ production, especially in the urban areas. Isoprene, despite having a low mass concentration compared to other VOC, had a high reactivity value and was a key precursor contributing to O₃ formation especially in the rural area. To further quantify the roles of O₃ precursors in the O₃ formation, an observation-based model (OBM) and measurement indicators method were employed using the data collected in autumn 2002 and summer 2004 at two suburban/rural sites in HK (Tai O) and the PRD (Wan Qing Sha), respectively. Photochemical O₃ production was calculated to be limited by VOC at both sites. Nitric oxide (NO) tended to suppress the O₃ formation, and CO was found to be negligible in the O₃ formation. Among different VOC, reactive aromatic compounds such as toluene and xylenes dominated the O₃ production in most cases, but naturally emitted isoprene could be important on warm days. This result is consistent with that from previous analysis of urban datasets. Model results revealed that O₃ formation at Tai O was most sensitive to stationary hydrocarbons but a stronger influence of mobile hydrocarbons was found at Wan Qing Sha. The results were in line with the corresponding emission patterns in HK and the PRD. The OBM, which is a time-dependent photochemical model using the Carbon Bond (IV) mechanism, was used to infer the O₃ chemistry and elucidate the processes (in-situ production versus transport) that control the variation of O₃ at the sites. About half of the O₃ episodes at Tai O were indicative of an impact from long-range transport but the O₃ episodes at Wan Qing Sha were mainly attributable to local production. Photochemistry of two O₃ episodes was further investigated in detail. It shows that in-situ O₃ production accounted for most of the observed increase in O₃ concentrations at the PRD site (1-hour O₃ = 178 ppbv) indicating the importance of local sources, while for the case of HK (1-hour O₃ = 203 ppbv), local production accounted for only 50% suggesting the importance of transport of regional pollution in this case. In both cases, conversion of NO to NO₂ by HO₂ was the major reaction for photochemical O₃ production. The photochemical O₃ loss rate was dominated by the reaction between NO₂ and OH at Tai O while the reaction of O₃ and HO₂ was the major O₃ destruction pathway at Wan Qing Sha. The O₃ production efficiency and partition of reactive nitrogen compounds were also estimated with the calculated concentrations of NO₂, PAN, HNO₃ and measured values of NO and NOy during the two O₃ episodes. The results showed that three to four O₃ molecules were formed per NOₓ molecule oxidized while PAN and HNO₃ were the most significant reactive nitrogen compounds in the afternoon.
|Description:||222 leaves : ill. ; 31 cm.
PolyU Library Call No.: [THS] LG51 .H577P CSE 2007 So
|URI:||http://hdl.handle.net/10397/2812||Rights:||All rights reserved.|
|Appears in Collections:||Thesis|
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