博碩士論文 91223021 詳細資訊




以作者查詢圖書館館藏 以作者查詢臺灣博碩士 以作者查詢全國書目 勘誤回報 、線上人數:54 、訪客IP:18.222.117.136
姓名 歐雅雯(Ya-Wei Ou)  查詢紙本館藏   畢業系所 化學學系
論文名稱 以VOC測站網探討中台灣臭氧成因
(Use as VOC measure stand to probe into ozone formation at center Taiwan)
相關論文
★ 有機薄膜電晶體材料三併環及四併環噻吩衍生物之開發★ 以逆吹式氣相層析法分析氣體成份
★ 氣相層析法應用於工業排放連續監測★ 煙道氣揮發性有機化合物連續監測方法開發
★ 自製新型除水及熱脫附濃縮裝置用於GC/MS線上分析揮發性有機汙染物★ 觸媒式非甲烷總碳氫分析儀開發與驗證
★ 自製除水器及熱脫附儀用於線上GC/MS/FID揮發性有機污染物之分析★ 大氣及水樣中揮發性有機氣體自動化分析技術之建立及應用
★ VOC前濃縮與預警系統之建構★ 建立自動化甲烷連續量測系統與其在指示大氣輻射冷卻之應用
★ 臭氧前趨物連續監測與臭氧生成之光化學探討★ 以近連續方式量測空氣中甲烷與異戊二烯及其生成之季節性探討
★ 自行架設光化學測站與商業化儀器平行比對及所得資料初步分析★ 近地表臭氧前驅物分析之前濃縮技術改良
★ 自動化噴霧捕捉分析系統之建立與研究★ 大體積固相微萃取水中揮發性有機污染物
檔案 [Endnote RIS 格式]    [Bibtex 格式]    [相關文章]   [文章引用]   [完整記錄]   [館藏目錄]   [檢視]  [下載]
  1. 本電子論文使用權限為同意立即開放。
  2. 已達開放權限電子全文僅授權使用者為學術研究之目的,進行個人非營利性質之檢索、閱讀、列印。
  3. 請遵守中華民國著作權法之相關規定,切勿任意重製、散佈、改作、轉貼、播送,以免觸法。

摘要(中) 地表臭氧污染問題在台灣已日益嚴重,由於臭氧為前驅物經由
光化反應所產生之二次污染物,因此試圖嘗試利用中部三測站(崇倫測站、草屯測站與竹山測站)所構成之監測網數據量測之逐時前驅物數據,配合逆溫儀及物種對方法,進而釐清台灣中部臭氧成因。
本論文首先將56種VOCs排放源分三類,分別為瓦斯燃料洩漏、植物排放與移動污染物質排放,討論一次污染物的日夜以及月平均濃度變化,發現除了植物排放其他排放濃度皆有早晚高中午低的現象,日夜變化主要受光化學及逆溫影響發,季節性變化主要受逆溫影響。而isoprene濃度在冬天與汽機車排放有一樣早晚高中午低的現象,但是靠近越夏天時,呈現中午濃度最高現象。
本論文利用物種光化反應速率不一樣,建立了兩組VOC氣團老化指標分別為ethylbenzene/m,p-xylene以及pentane/t-2-pentene,與臭氧濃度有極高的相關性,兩對物種對在指示臭氧靈敏度上有很大的差異,顯示做為指標的可靠性;兩物種對皆為汽機車排放,因此汽機車排放物質對於發生在竹山高臭氧有很大之貢獻。
本論文充分把崇倫、草屯與竹山三測站利用物種對方法,顯示其老化程度不一,將其三站之上、下風處特質表現出來;而在兩下風處竹山與草屯兩站相關性好,因此竹山可代表整個南投縣下風處研究臭氧適合場所之ㄧ。
最後釐清竹山臭氧原因為風速風向將移動污染物帶到竹山而造成竹山高臭氧成因,而植物性排放為春秋為墊高臭氧基礎值濃度之角色。
摘要(英) Surface ozone has become a series pollution problem in Taiwan as well as in other major developing urban environments. While the average concentration of particular matter showed a decreasing trend, ozone on the other hand, showed an increasing trend over the past decade. To elucidate ozone formation mechanism in certain ozone plagued areas of Taiwan, in-situ VOC monitoring station network, equivalent to the US PAMS (photochemical assessment monitoring stations) program, was adopted with the first 3 station network established in central Taiwan in both urban and rural areas. Monitoring data of 2003 and 2004 was examined for their diurnal and monthly variation and three types of VOCs with different origins, namely LPG leakage, vehicular exhaust, and biogenic emissions, are discussed. While all of the VOCs have similar diurnal profile with maximum appeared in the morning and evening due largely to emissions, the change of mixing height, and photochemistry, isoprene however showed similar profile with tailpipe type of species in winter but gradually shifted its peak emission towards noon as the time progressed into later spring (May).
Our investigation has led to the development of 2 VOC indicators of air masses’ age due to photochemistry with drastic difference in indication sensitivity. Excellent agreement between ozone concentrations and ratios of ethylbenzene/xylene and pentane/t-2-pentene suggests ozone is the photochemical product of VOCs and that the car exhaust compounds control the downwind ozone peak values. Difference in the age of air parcels received at the 3 stations was also clearly revealed, based on which the Chushan (竹山) station in general received more aged air masses than the other two upwind Chunlun (崇倫) and Choaton (草屯) stations. The similarity between Choaton and Chushan proves that Chushan station can be a suitable site for representing most area of Nantou county for studying ozone formation in downwind environment.
Although biogenic emissions with isoprene being the dominant species did not appear to control the downwind ozone peak values, at least not to the same degree as the car exhaust compounds, it is shown to exert more reactivity towards ozone formation potential than other types of precursors. Production of isoprene at noon in the warm seasons synchronizes in time with the ozone peak further creates a greater possibility for ozone to exceed dangerous levels should car exhaust VOCs also been brought down to the site of observation.
關鍵字(中) ★ 臭氧 關鍵字(英) ★ ozone
論文目次 摘要 I
目錄 V
表目錄 VII
圖目錄 VIII
第一章 前言 1
1-1臭氧簡介 4
1-2對流層臭氧形成之光化反應整理 8
1-3氫氧自由基的角色與重要性 12
1-4 VOCs對臭氧生成之貢獻潛能 15
1-5臭氧控制策略 25
1-6臭氧研究文獻回顧 27
第二章 研究目的與研究方法 36
2-1研究目的 36
2-2光化測站的設立 36
2-3光化學測站網部署策略 39
2-4中部光化學監測網環境及系統描述 42
2-6中部逆溫儀簡介 55
第三章 結果與討論 58
3-1以來源區分VOCs的類別與各種類別物質季節性變化 58
3-1-1瓦斯燃料洩漏物質 59
3-1-2植物排放物質 62
3-1-3移動污染排放物質 69
3-2氣象中的逆溫效應對前驅物的濃度影響 72
3-3前驅物光化現象與臭氧之關係 83
3-3-1光化指標意義 83
3-3-2崇倫、草屯、竹山三站上下風關係 87
3-3-3崇倫站與竹山站之老化與新鮮度 92
3-3-4兩物種對(ethylbenzene/m,p-xylene,n-pentane/t-2-pentene)
與臭氧相關性 100
3-3-5釐清竹山臭氧之成因 107
第四章 結論與未來展望 114
參考文獻 115
參考文獻 1. Atkinson, R.(1989);Kinetics and mechanisms of the gas-phase reactions of the hydroxyl radical with organic compounds. Journal of Physical and Chemical Reference Data, Monograph. 1, 1-246.
2. Atkinson, R.(1991);Kinetics and mechanisms of the gas-phase reactions of the NO3 radical with organic compounds. Journal of Physical and Chemical Reference Data .20, 459-507.
3. Atkinson(1990), R. “Gas-phase tropospheric chemistry organic compounds: a review.” Atmos. Environ.24A ,1.
4. Atkinson, R.(2000);Atmospheric chemistry of VOCs and NOx Atmospheric Environment. 34, 2063-2101.
5. Arey, J.;Corchnoy, S. B.;Atkinson, R(1991). Emission of linalool from Valencia orange blossoms and its observation in ambient air. Atmos. Environ. 25A, 1377-1381.
6. Baxter, R. A. (1991) Determination of mixing heights from data collected during the 1985 SCCCAMP field program. Journal of Applied meteorology,30, 598-606.
7. Beyrich, F., Gryning, S. E., Jofire, S., Rasmussen, A., Seibert, P. and Tercier, P.(1996a) On the determination of mixing height- a review. Proceedings of the 4th workshop on harmonization within atmospheric dispersion modeling for regulatory purposes, Oostende, 155-162.
8. Beyrich, F., (1997) Mixing height estimation from sodar data-a critical discussion. Atmos. Environ.31, 3941-3953.
9. Bidleman, T. F.(1988);Atmospheric processes. Environmental Science and Technology. 22, 361-367.
10. Blanchard, C. L., (2000)“Ozone process insights from field experiments – Part III:extent of reaction and ozone formation ”, Atmospheric Environment, 34, 2035-2043.
11. Bower, J.S,. Stevenson, K.J,. J.Broughton, G.F. Lampert, J.E, Sweeney, B.P, And Wilken,J, (1994)“Assessing recent surface ozone concentrations in the U.K.,” Atmospheric Envionment,28,461-465.
12. Carter, W. P. L. (1994) Development of Ozone Reactivity Scales for Volatile Organic Compounds, J. Air & Waste Manage. Assoc. 44: 881-899
13. Chang, T. Y. and M. J. Suzio,(1995)“Assessing Ozone-Precursor Relationships Based on a Smog Production Model and Ambient Data”, Air & Waste Management Association.45, 20-28.
14. Chen,C.-L, Tsuang, B.-J,. Tu, C.-Y, Cheng, W.-L, Lin, M.-D (2002) “Wintertime vertical profiles of air pollutants over a suburban area in central Taiwan” Atmos. Environ. 36 ,2049-2059
15. Doran, J.C., Berkowitz, C. M., Coulter, R.L., Shaw, W. J., Spicer, C. W. (2003) The 2001 Phoenix Sunrise experiment: vertical mixing and chemistry during the morning transition in Phoenix, Atmos. Environ. 37, 2365-2377
16. Fuhrer, J., et.al., (1997)Critical levels for ozone effects on vegetation in Europe, Environmental Pollution, 97, 91~106,
17. Holzworth, C. G., (1967) Mixing depths, wind speeds, and air pollution potential for selected locations in the United States. Journal of Applied meteorology, 6, 1039-1044.
18. John, H. Seinfeld(1989), Urban Air Pollution:State of the Science, Science, 243.
19. Kleinman, L. I. , (2000)“Ozone process insights from field experiments – part II:Observation-based analysis for ozone production”, Atmospheric Environment.34, 2023-2033.
20. Lu, C. H., (1998) “On the Indicator-based Approach to Assess Ozone Sensitivities and Emission Feaures,” J. Geophys. Res.,. 103, 3453-3462.
21. [Milford, J. B., D. Gao, S. Sillman, P. Blosse, and A. G. Russell, (1994) “Total reactivity nitrogen (NOy) as an indicator for the sensitivity of ozone to NOX and hydrocarbons”, Journal of Geophysical Research,.99, 3533-3542
22. Office of Technology Assessment (OTA), Catching our breath: Next steps for reducing urban ozone, Washington, D.C., 1989
23. Placet, M.;Mann C.,; Gilbert, R. O.(2000); Niefer, M.; Emissions from stationary sources. Atmos. Environ. in press. .
24. Rethinking the Ozone in Urban and Regional Air Pollution(National Academy od Sciences,Washington, DC, 1991)
25. Reimann, S., Calanca, P. and Hofer, P. (2000), The anthropogenic contribution to isoprene concentrations in a rural atmosphere. Atmospheric Environment 34 109-115
26. Russell, A., J. Milford, M. S. Bergin, S. McBride, L. McNair, Y. Yang, W. R. stockwell, and B. Croes, (1995) “Urban ozone control and atmospheric reactivity of organic gases”, American Assoc. for the Advencement of Science, p.491
27. Ryerson, T. B.; Trainer, M.; Holloway, J. S.; Parrish, D. D.; Huey, L. G.; Sueper, D. T.; Frost, G. J.; Donnelly, S. G.; Schauffler, S.; Atlas, E.
L.; Kuster, W. C.; Goldan, P. D.; Hubler, G.; Meagher, J. F.;Fehsenfeld, F.C.,
(2001). Observations of Ozone Formation in Power Plant Plumes and
Implications for Ozone Control Strategies. Science,292 ,719-723.
28. Sawyer, R. F.;Harley, R. A.;Cadle, S. H.;Norbeck, J. M.;Slott, R.;Bravo, H. A. Mobile sources critical review: 1998 NARSTO assessment., Atmos. Environ. 2000, 34, 2161-2181.
29. Seibert, P., Beyrich, F., Gryning, S.E., Joffire, S., Rasmussen. A., Tercier, P.,(2000) Review and intercomparsion of operational methods for the determination of the mixing height. Atmos. Environ, 34 (7), 1001-1027
30. Sharkey T. D., and Singsaas E. L., (1995). Why plants emit isoprene. Nature 374:769
31. Sharkey, T.D. (1996) Isoprene synthesis in plants and animals. Endeavor 20,74-78
32. Shinji Wakamatsu Toshimasa Ihara and Itsushi Uno, ”Recent trends inprecursor concentrations and oxidant distributions in the Tokyo and Osaka areas(1996),” Atmos Environment,30, 715-721
33. Sillman, S., (1998) “Evaluating the Relation Between Ozone, NOX and hydrocarbons: The Method of Photochemical Incators”, EPA/600/R-98/022, USEPA, Research Triangle Park, NC.
34. Sillman, S., J. A. Logan, and S. C. Wofsy, (1995). “The Sensitivity of Ozone to Nitrogen and Hydrocarbons in Regional Ozone Episodes.” , J. of Geophysical Research, V100,N.D7,14175-14188,
35. Snyder B. J. and Strawbridge K. B. (2004) Meteorological analysis of the Pacific 2001 air quality field study. Atmos. Environ.38, 5733-5743
36. Ryerson T. B., Trainer. M, Holloway .J. S, Parrish D. D., Huey L. G., Sueper D. T., Frost G. J., Donnelly S. G., Schauffler S., Atlas E. L., Kuster W. C., Goldan P. D., Hubler G., Meagher J. F., Fehsenfeld F. C. (2001) “Observations of Ozone Formation in Power Plant Plumes and Implications for Ozone Control Strategies” Science .292. 719-723
37. Ulke, A. G. and Mazzeo, A. N.,(1998) Climatological aspects of the daytime mixing height in Buenos aires city, Argentina. Atmos. Environ. 32, 1615-1622.
38. United Nations Environmental Programme (UNEP). Montreal Protocol on substances that deplete the ozone layer. September 16, Montreal, 1987.
39. Yiwei D. and Yuegang Z., 1999, “Factors Affecting the Levels of Hydrogen Peroxide in Rainwater”, Atmospheric Environment, 33, 1469~1478.
40. Yang, K.L., Ting, C.C. and Wang, J. L. Diural and seasonal cycles of ozone precursors observed from continuous measurement at an urban site in Taiwan, Atmos. Environ. in press.
41. 美國PAMS網站http://www.epa.gov/airprogm/oar/oaqps/pams/
42. 環保署空保處網站,http://www.epa.gov.tw/F/index.htm
43. 蔡政雄 「臭氧前驅物連續監測與臭氧生成之光化研究」中央大學碩士論文2001.
44. 黃宗仁「利用類神經網路預測台中都會區臭氧趨勢之研究」中興大學碩士論文 2002
45. 張劭勳、張劭評、林秀娟,「Spss For Window 統計分析—初等統計與高等統計」,松岡電腦圖書資料股份有限公司,2001
46. 蔡詠安「氣象條件與臭氧事件日相關性之探討:以高高屏地區為例」中山大學碩士論文 2002
47. 陳幸芬「台南縣臭氧敏感性物種之調查研究」成功大學碩士論文 2002
48. 黃星富「南投地區高臭氧空氣污染事件探討」台灣大學碩士論文 2003
49. 陳德鈞、季延安、林肇信,1991,[大氣污染化學],科技圖書股份有限公司
50. 丁建中「自行架設光化學測站與商業化儀器平行比對及所得資料初步分析」中央大學碩士論文2002
指導教授 王家麟(Jia-Lin Wang) 審核日期 2005-1-26
推文 facebook   plurk   twitter   funp   google   live   udn   HD   myshare   reddit   netvibes   friend   youpush   delicious   baidu   
網路書籤 Google bookmarks   del.icio.us   hemidemi   myshare   

若有論文相關問題,請聯絡國立中央大學圖書館推廣服務組 TEL:(03)422-7151轉57407,或E-mail聯絡  - 隱私權政策聲明