環境資源報告成果查詢系統

臺灣大氣甲烷源匯模式評估計畫

中文摘要 本計畫旨在探討臺灣大氣甲烷源匯模式,主要工作項目包含比較分析世界先進國家CH4監測現況、校正比對測站CH4監測資料、分析CH4與其他汙染物之相關性、發展反演模式和案例應用及辦理技術研討課程。 我們彙整世界先進國家CH4監測資料,發現全球大氣監測網多著重溫室氣體和其他重要微量氣體,測站分布偏重歐美和北大西洋,其他區域監測頻度和密度較低,臺灣環保署的CH4監測系統則與日本環境省取向較相近,以空氣污染防治為主,測站密度較高,對亞洲和太平洋區域的CH4監測具有一定貢獻。 我們以光學分析儀與測站HC監測儀同步測量大氣CH4濃度,發現測值有差距,且各站差值不一,發現誤差來源是透過氣體稀釋校正器產出標準氣體的校正程序。我們以光學分析儀實測氣體稀釋校正器所產出零點和全幅CH4濃度,以修正過的校正參數重新計算測站CH4濃度修正值,大幅改善了測值的準確度。 我們分析環保署歷年監測資料中CH4與其他污染物之相關性,結果顯示相關性不高,代表汙染物各有潛在機制影響消長。大氣CH4於對流層中能與O3光反應產物羥基反應而消逸,但本案分析結果兩者相關性相當微弱,可能在測站尺度有更細緻的影響機制,如大氣擴散條件、排放源特徵、測站取樣高度、位置等。 我們分析南部空品區高CH4濃度事件時的反軌跡模式和風場資料,比對探討反軌跡通過地點與TEDS排放熱點間關聯性,發現排放源集中在舊高雄市區和鄰近舊高雄縣區域,主因可能來自點源排放,搭配適當大氣條件,而發生高濃度事件。但屏東站反軌跡通過點的排放強度較弱,無法單純從TEDS資料庫中驗證汙染源,需進一步網格模擬探討。
中文關鍵字 溫室氣體、甲烷監測系統、甲烷反演模式、源與匯

基本資訊

專案計畫編號 EPA-107-FA11-03-A031 經費年度 107 計畫經費 1950 千元
專案開始日期 2018/01/11 專案結束日期 2018/12/31 專案主持人 張世杰
主辦單位 監資處 承辦人 蔡宜君 執行單位 國立東華大學自然資源與環境學系

成果下載

類型 檔名 檔案大小 說明
期末報告 EPA-107-FA11-03-A031.pdf 24MB

The Model of Atmospheric Methane Sources and Sinks in Taiwan

英文摘要 This project aims to explore the model of atmospheric methane sources and sinks in Taiwan. Our work targets include comparative analysis of methane monitoring systems among the world's advanced countries, calibration of methane monitoring data, correlation analysis of methane and other air pollutants, developing methane inverse models with case application, and conducting a seminar. We analyzed the methane monitoring systems of the world's advanced countries and found the global atmospheric monitoring networks mostly focus on greenhouse gases and other important trace gases. The observation sites of these networks mainly distribute around Europe, North America, and the North Atlantic area, while the monitoring frequency and site density are relatively lower in other regions. Taiwan’s Environmental Protection Agency's methane monitoring system is more similar to that of Japan’s Ministry of the Environment, both focusing on air pollutants monitoring. The monitoring results from their high density of observation sites also contribute to the methane monitoring in Asia and the Pacific area. The accuracy of HC analyzers in EPA stations was verified by synchronous measurements of the ambient air using LGR UGGA infrared gas analyzer and the on-site HC system. The results showed a significant discrepancy between the two measurement systems. The extent of differences varied among stations. The on-site dilution system for the production of standard gases may have resulted this problem. We used the optical analyzer to check the zero span mode of the dilution calibrator, and recalculated the methane concentrations according to the corrected calibration parameters. The results showed great improvement in the accuracy of the measurement. We analyzed the correlations between methane and other air pollutants in the EPA's monitoring data over the years. The results showed that the correlations were weak. Atmospheric methane can react with the hydroxyl produced through the photoreaction of ozone in the troposphere, but our analysis of the correlation between the methane and ozone was quite weak. The result suggested that there might be other potential mechanisms at the site scale, such as atmospheric diffusion conditions, emission source characteristics, sampling heights and site positions. We analyzed the back-trajectory patterns and the wind field data of the high methane concentration events in Kaohsiung and Pingtung area. We compared between the back-trajectories and the TEDS emission hotspots, and found that the emission sources centered around the old Kaohsiung city area and the adjacent old Kaohsiung county area. The cause of high methane concentration events may be emissions from point sources with the favorite atmospheric conditions that facilitate the situation. However, the emission intensity of Pingtung Station’s back-trajectory was weak, and we could not identify the emission sources from the TEDS database. Further grid simulation is needed.
英文關鍵字 Greenhouse Gas, Methane Monitoring System, Inverse Modeling of Methane, Source and Sink