簡易檢索 / 詳目顯示

研究生: 林龍富
Lin, Long-Full
論文名稱: 污染源及環境介質中戴奧辛/呋喃之特徵
Characteristics of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans from Emission Sources and in the Environmental Media
指導教授: 李文智
Lee, Wen-Jhy
學位類別: 博士
Doctor
系所名稱: 工學院 - 環境工程學系
Department of Environmental Engineering
論文出版年: 2007
畢業學年度: 95
語文別: 英文
論文頁數: 125
中文關鍵詞: 乾沉降氣固相分佈濕沉降排放清單活動強度排放係數戴奧辛呋喃
外文關鍵詞: Gas/particle partitioning, Dry deposition, Wet deposition, Emission inventory, Activity rate, Dioxins, Furans, Emission factors
相關次數: 點閱:198下載:2
分享至:
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報
  • 本研究之目的為建立:(1) 不同工業污染源戴奧辛/呋喃之排放係數;(2) 台灣及高雄縣(KC地區)戴奧辛/呋喃排放清單;(3) 榕樹葉中戴奧辛/呋喃成分與大氣戴奧辛/呋喃濃度之關係;(4) 岡山及仁武垃圾焚化廠周圍戴奧辛/呋喃乾/溼沉降通量;及(5) 釐清乾/溼沉降對土壤戴奧辛/呋喃成分之影響。為達成這些目的,本研究從17個工業污染源共採取51個煙道樣品以建立其排放係數。另外,從20個污染源,包括燃煤火力發電廠,稻草、蓮霧枝及金紙露天燃燒,及柴油引擎等共採取95個煙道樣品藉以建立排放清單。此外,在都市垃圾焚化廠周圍分別採取56個大氣、植物及土壤樣品以得知大氣戴奧辛/呋喃濃度,據以推估乾/溼沉降通量,並釐清大氣濃度對植物及乾/溼沉降對土壤戴奧辛/呋喃成分之影響。

    研究結果顯示,工業污染源中,鋅及銅二級冶煉廠煙道廢氣平均濃度為2.44 ng I-TEQ Nm-3 (at 11% O2),遠高於工業廢棄物焚化爐(平均濃度為0.15 ng I-TEQ Nm-3),顯示金屬二級冶煉在戴奧辛/呋喃的減量上比工業廢棄物焚化爐更重要。

    此外,燃煤火力發電廠之排放係數 (620 ng I-TEQ ton-1) 遠高於國外文獻值(2.34 ng I-TEQ ton-1),顯示國內燃煤火力發電廠空氣污染防治設備去除戴奧辛/呋喃之效率有待提升。KC地區及台灣戴奧辛/呋喃年排放量分別為6.1及95 g I-TEQ,KC地區之主要汙染源為燃煤火力發電、鋁二級冶煉、電弧爐煉鋼及稻草露天燃燒,其貢獻分別佔總排放量之56, 17, 13, 及3.3%,而台灣之主要汙染源則為鐵礦燒結製程、燃煤火力發電、電弧爐煉鋼及稻草露天燃燒,其貢獻分別佔總排放量之32, 28, 23, 及 8.1%。

    另外,榕樹葉中戴奧辛/呋喃成分與長期大氣採樣分析結果成高度正相關,此ㄧ結果顯示,長期大氣採樣分析結果(一季以上),可用以推估植物中戴奧辛/呋喃成分。

    另由岡山及仁武垃圾焚化廠周界大氣乾/溼沉降模擬結果顯示,其總乾/溼沉降通量分別為8.59及10.1 ng I-TEQ m-2 year-1,溼沉降貢獻量分別佔42及34%,顯示乾沉降比溼沉降更重要。最後,藉由乾/溼沉降所去除之戴奧辛/呋喃,其特徵剖面與土壤之特徵剖面頗為相似,但在土壤中,部分物種已經消失,特別是低氯數之戴奧辛/呋喃,可能經由揮發、生物分解或光分解而從土壤中消失。

    上述研究結果顯示燃煤火力發電廠為一非常重要之戴奧辛/呋喃污染排放源,結合本研究所提供之各種戴奧辛/呋喃排放源之排放濃度、排放係數、年排放量及貢獻百分比資料庫,可做為環保單位決策之參考,亦可做為進一步學術研究之寶貴資訊。

    The objectives of the present study were to develop (1) emission factors of polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF) for various industrial sources which seldom being investigated; (2) the overall PCDD/F emission inventory in Taiwan as well as in the KC area; (3) correlation between banyan leaf compositions and ambient air concentration of PCDD/Fs; (4) dry and wet deposition fluxes of PCDD/Fs in the ambient air of two municipal solid waste incinerators (MSWIs); and (5) to clarify the influence of deposition on the soil content of PCDD/Fs. To achieve these goals, a total of 51 flue gas samples from seventeen industrial sources were collected to develop emission factors. In addition, a total of 95 flue gas samples from 20 sources including coal-fired power plants, open burning of rice straw, wax apples, and ritual paper, and diesel engines et al., were collected and analyzed for 17 PCDD/Fs to develop emission inventory. Furthermore, a total of 56 samples for each environment media including air, vegetation, and soil, were collected from the environment media of two MSWIs to establish atmospheric level and to estimate deposition fluxes.

    The results of this study show that mean PCDD/F concentration of the secondary zinc smelter (Zn-S) and secondary copper smelter (Cu-S) is 2.44 ng I-TEQ Nm-3 (at 11% O2), which was found to be greater than that of industrial waste incinerators (mean concentration = 0.15 ng I-TEQ Nm-3). These results imply that the controlling of secondary metallic melting processes is more important for the reduction of PCDD/F emissions than industrial waste incineration.

    In addition, the emission factor of PCDD/Fs from coal-fired power plants (620 ng I-TEQ ton-1) obtained in this study is greatly higher than the value of previous study (2.34 ng I-TEQ ton-1). It means that in Taiwan the air pollution control devices for PCDD/F removal in certain power plants need to be more efficient. The emission data showed that there is a total annual release to air of 6.1 and 95 g I-TEQ from major sources in the KC area and Taiwan, respectively. The dominant sources of PCDD/Fs in the KC area are the coal-fired power plants, secondary aluminum smelting, electric arc furnaces, and open burning of rice straw, which contributed about 56, 17, 13, and 3.3% to the total, respectively. However, in Taiwan, the dominant sources of PCDD/Fs are the iron ore sintering, coal-fired power plants, electric arc furnaces, and open burning of rice straw, which contributed about 32, 28, 23, and 8.1% to the total, respectively.

    Furthermore, there is a good correlation between banyan leaf compositions and ambient air concentration of PCDD/Fs using an average data of individual measurement for each sampling location. This implies that an ambient data for long period monitoring (longer than three months) can be used to predict the composition in vegetation.

    In the vicinity of MSWI-GS and MSWI-RW, the annual deposition fluxes of PCDD/Fs are about 8.59 and 10.1 ng I-TEQ m-2 year-1, respectively, and wet deposition contributed 42% and 34% to the total, respectively, it reveals that dry deposition is more important than wet deposition. Finally, the dominant congeners of PCDD/Fs in ambient air of MSWIs removed by dry and wet deposition are very similar to that of soil in the vicinity of MSWIs, but some congeners removed by deposition disappeared in the soil, especially the congeners with lower chlorine number. This can be explained as vaporization, biodegradation or photodecomposition.

    The results of this study showed that coal-fired power plants are very significant sources of PCDD/Fs, the results also provide important database to assist the decision makers for formulating policies to alleviate dioxin concerns.

    中文摘要 I 英文摘要 III 致謝 VII Table of Contents IX List of Tables XIII List of Figures XVII 1. Introduction 1 2. Literature review 4 2.1. Chemical properties of PCDD/Fs 5 2.2. Toxic equivalency factors for PCDD/Fs 7 2.3. Formation mechanism of PCDD/Fs 11 2.4. Direct releases of PCDD/Fs from sources 12 2.5. Gas/particle partitioning 13 2.6. Dry deposition processes of PCDD/Fs 15 2.7. Wet deposition processes of PCDD/Fs 16 3. Experimental section 21 3.1. Emissions of PCDD/Fs from various industrial sources 21 3.1.1. Concentrations of PCDD/Fs in flue gases from various industrial sources 26 3.1.2. Congener profiles of PCDD/Fs in flue gases from various industrial sources 26 3.1.3. Indicatory PCDD/Fs of various industrial sources 26 3.1.4. Emission factors of PCDD/Fs from various industrial sources 27 3.2. Emission inventory of PCDD/Fs in Taiwan as well as in the KC area 27 3.2.1. Emission factors of PCDD/Fs from major sources in Taiwan 27 3.2.2. Annual releases to air of PCDD/Fs from major sources in Taiwan 29 3.3. Sampling of PCDD/Fs 31 3.3.1. Sampling of PCDD/Fs from the stack flue gases 31 3.3.2. Sampling of PCDD/Fs from the ambient air 31 3.3.3. Sampling of PCDD/Fs from the banyan leaves 32 3.3.4. Sampling of PCDD/Fs from the soils 37 3.4. Analyses of PCDD/Fs 37 4. Results and discussion 41 4.1. Emissions of PCDD/Fs from various industrial sources 41 4.1.1. Concentrations of PCDD/Fs in flue gases of various industrial sources 41 4.1.2. Congener profiles of PCDD/Fs in various industrial flue gases 46 4.1.3. Indicatory PCDD/Fs of various industrial flue gases 46 4.1.4. Emission Factors of various industrial sources 50 4.2. Emission inventory of PCDD/Fs in Taiwan as well as in the KC area 56 4.2.1. Concentrations of PCDD/Fs in the stack flue gases of coal-fired power plants 56 4.2.2. Congener profiles of PCDD/Fs in the stack flue gases of coal-fired power plants 58 4.2.3. Emission factors of major dioxin sources 60 4.2.4. Annual releases of PCDD/Fs to air from major sources in Taiwan as well as in the KC area 63 4.3. The relationship between air concentration and banyan leaf content of PCDD/Fs 66 4.4. Dry and wet deposition of PCDD/Fs in the ambient air of MSWIs 73 4.4.1. Concentrations of PCDD/Fs in the ambient air in the vicinity of MSWIs 73 4.4.2. Gas-particle partitioning 76 4.4.3. Dry deposition of PCDD/Fs 86 4.4.4. Wet deposition of PCDD/Fs 91 4.4.5. Annual dry and wet deposition flux of PCDD/Fs 99 4.5. Influence of deposition on soil content of PCDD/Fs 103 5. Conclusions and suggestions 107 5.1. Conclusions 107 5.2. Suggestions 109 References 111

    Agriculture and Food Agency, Council of Agriculture, http://www.afa.gov.tw/, 2006.
    Buekens, A., Cornelis, E., Huang, H., Dewettinck T. “Fingerprints of dioxin from thermal industrial processes.” Chemosphere 40, 1021-1024, 2000.
    Bureau of Energy, Ministry of Economic Affairs, http://www.moeaboe.gov.tw/, 2006.
    Chao, M.R., Hu, C.W., Chen, Y.L., Chang-Chien, G.P., Lee, W.J., Chang, L.W., Lee, W.S., Wu, K.Y. “Approaching gas-particle partitioning equilibrium of atmospheric PCDD/Fs with increasing distance from an incinerator: measurements and observations on modeling.” Atmospheric Environment 38, 1501-1510, 2004.
    Department of Statistics, Ministry of the Interior, http://www.moi.gov.tw/stat/, 2006.
    Domingo, J.L., Granero, S., Schuhmacher, M. “Congener profiles of PCDD/Fs in soil and vegetation samples collected near to a municipal waste incinerator.” Chemosphere 43, 517-524, 2001.
    Donnelly, J.R., Munslow, W.D., Mitchum, R.K., Sovocool, G.W. “Correlation of structure with retention index for chlorinated dibenzo-p-dioxins.” Journal of Chromatography 392, 51-63, 1987.
    Economic Daily News, Economic Yearbook of the Republic of China. Taipei, Taiwan, ROC, 2005.
    Eduljee, G.H., Dyke, P. “An updated inventory of potential PCDD and PCDF emission sources in the UK.” The Science of the Total Environment 177, 303-321, 1996.
    Eitzer, B.D., Hites, R.A. “Vapor pressures of chlorinated dioxins and dibenzofurans.” Environmental Science and Technology 22, 1362–1364, 1988. (Erratum 1998, 32, 2804).
    Eitzer, B.D., Hites, R.A. “Atmospheric transport and deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans.” Environmental Science and Technology 23, 1396–1401, 1989.
    Everaert, K., Baeyens, J. “The formation and emission of dioxins in large scale thermal processes.” Chemosphere 46, 439-448, 2002.
    Fabrellas, B., Larrazabal, D., Martinez, M.A., Sanz, P., Ruiz, M.L., Abad, E., Rivera, J. “Global assessment of PCDD/F emissions from the spanish cement sector: Effect of conventional/alternative fuels.” Organohalogen Compounds 66, 905-911, 2004.
    Fernández-Martínez, G., López-Vilariño, J.M., López-Mahía, P., Muniategui-Lorenzo, S., Prada-Rodríguez, D., Abad, E., Rivera, J. “First assessment of dioxin emissions from coal-fired power stations in Spain.” Chemosphere 57, 67-71, 2004.
    Fiedler, H. “Thermal formation of PCDD/PCDF: A survey.” Environmental Engineering Science 15, 49-58, 1998.
    Fiedler, H. “First results of release inventories of PCDD/PCDF under the Stockholm Convention.” Organohalogen Compounds 63, 1-4, 2003.
    Hale, M.D., Hileman, F.D., Mazer, T., Shell, T.L., Noble, R.W., Brooks, J.J. “Mathematical modeling of temperature programmed capillary gas chromatographic retention indexes for polychlorinated dibenzofurans.” Analytical Chemistry 57, 640-648, 1985.
    Huang, H., Buckens, A. “On the mechanisms of dioxin formation in combustion processes.” Chemosphere 31, 4099-4117, 1995.
    Hung, H., Blanchard P., Poole G., Thibert B., Chiu C.H. “Measurement of particle-bound polychlorinated dibenzo- p-dioxins and dibenzofurans (PCDD/Fs) in Arctic air at Alert, Nunavut, Canada.” Atmospheric Environment 36, 1041-1050, 2002.
    Jones, K.C., de Vooge, P. “Persistent organic pollutants (POPs): state of the science.” Environmental Pollution 100, 209-221, 1999.
    Kim, B.H., Lee, S.J., Mun, S.J., Chang, Y.S. “A case study of dioxin monitoring in and around an industrial waste incinerator in Korea.” Chemosphere 58, 1589-1599, 2005.
    Kim, S.C., Na, J.G., Choe, S.H., Lee, J.H., Kim, Y.H., Hwang, S.R., Joo, C.H., Jung, D.H., You, J.C., Lee, S.W., Jeon, S.E. “PCDDs/PCDFs emission from nonferrous metal industry.” Organohalogen Compounds 63, 77-80, 2003.
    Lee, W.J., Lin Lewis, S.J., Chen, Y.Y., Wang, Y.F., Sheu, H.L., Su, C.C., Fan, Y.C. “Polychlorinated biphenyls in the ambient air of petroleum refinery, urban and rural areas.” Atmospheric Environment 30, 2371-2378, 1996.
    Lee, W. S., Chang-Chien, G. P., Wang, L.C., Lee, W.J., Tsai, P.J., Wu, K.Y., Lin, C. “Source identification of PCDD/Fs for various atmospheric environments in a highly industrialized city.” Environ. Sci. Technol. 38, 4937-4944, 2004 .
    Lee, W.S., Chang-Chien, G.P., Wang, L.C., Lee, W.J., Tsai, P.J., Chen, C.K. “Emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans from the incinerations of both medical and municipal solid wastes.” Aerosol Air Qual. Res. 3, 1-6, 2003.
    Lee, W.S., Chang-Chien, G.P., Wang, L.C., Lee, W.J., Wu, K.Y., Tsai, P.J. “Emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans from stack flue gases of electric arc furnaces and secondary aluminum smelters.” J. of the Air & Waste Management Association 55, 219-226, 2005.
    Ligocki, M.P., Leuenberger, C., Pankow, J.F. “Trace organic compounds in rain-II. Gas scavenging of neutral organic compounds.” Atmospheric Environment 19, 1609-1617, 1985a.
    Ligocki, M.P., Leuenberger, C., Pankow, J.F. “Trace organic compounds in rain-III. Particle scavenging of neutral organic compounds.” Atmospheric Environment 19, 1619-1626, 1985b.
    Lin, L.F., Lee W.J., Chang-Chien G.P. “Emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans from various industrial sources.” J. Air Waste Manage., in press, 2006.
    Lohmann, R., Jones K.C. “Dioxins and furans in air and deposition - a review of levels, behaviour and processes.” Science of the Total Environment 219, 53-81, 1998.
    Mackay, D., Shiu, W.Y., Ma, K.C. Polynuclear Aromatic Hydrocarbon, Polychlorinated Dioxins, and Dibenzofurans in: Illustrated Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, Volume 2, Lewis Publishers, Michigan, 1992.
    McKay, G. “Dioxin characterisation, formation and minimisation during municipal solid waste (MSW) incineration: review.” Chemical Engineering Journal 86, 343-368, 2002.
    NATO/CCMS, International Toxicity Equivalency Factor (I-TEF) Method of Risk Assessment for Complex Mixtures of Dioxins and Related Compounds. Pilot Study on International Information Exchange on Dioxins and Related Compounds, Report Number 176, North Atlantic Treaty Organization, Committee on Challenges of Modern Society, 1988.
    Olie, K., Vermeulen, P.L., Hutzinger, O. “Chlorodibenzo-p-dioxins and chlorodibenzofurans are trace components of fly ash and flue gas of some municipal incinerators in the Netherlands.” Chemosphere 6, 455-459, 1977.
    Pankow, J.F. “Common y-intercept and single compound regressions of gas-particle partitioning data vs. 1/T.” Atmospheric Environment 25A, 2229-2239, 1991.
    Pankow, J.F. “An absorption model of gas/particle partitioning of organic compounds in the atmosphere.” Atmospheric Environment 28, 185-188, 1994.
    Pankow, J.F., Bidleman, T.F. “Interdependence of the slopes and intercepts from log-log correlations of measured gas-particle partitioning and vapor pressure-Ι. Theory and analysis of available data.” Atmospheric Environment 26A, 1071-1080, 1992.
    Quass, U., Pulles, T., Kok, H. “The DG environment project “Dioxin Emissions in Candidate Countries”: Scope, approach and first results.” Organohalogen Compounds 66, 878-883, 2004.
    Schröder, J. Welsch-Pausch, K., McLachlan, M.S. “Measurement of atmospheric deposition of polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) to a soil.” Atmospheric Environment 31, 2983-2989, 1997.
    Schuhmacher, M., Bocio, A., Agramunt, M.C., Domingo, J.L., de Kok, H.A.M. “PCDD/F and metal concentrations in soil and herbage samples collected in the vicinity of a cement plant”. Chemosphere 48, 209-217, 2002.
    Schuhmacher, M., Domingo, J.L., Garreta, J. “Pollutants emitted by a cement plant: Health risks for the population living in the neighbourhood.” Environmental Research 95, 198-206, 2004.
    Sheu, H.L., Lee, W.J., Su, C.C., Chao, H.R., Fan, Y.C. “Dry deposition of polycyclic aromatic hydrocarbons in ambient air.” Journal of Environmental Engineering 122, 1101-1109, 1996.
    Shih, Minliang, Lee, Wei-Shan, Chang-Chien, Guo-Ping, Wang, Lin-Chi, Hung, Chia-Yang, Lin, Kuo-Ching. “Dry deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in ambient air.” Chemosphere 62, 411-416, 2006.
    Slinn W.G.N., Hasse, L., Hicks, B.B., Hogan, A.W., Lal, D., Liss, P.S., Munnich, K.O., Sehmel, G.A., Vittori, O. “Some aspects of the transfer of atmospheric trace constituents past the air-sea interface.” Atmospheric Environment 12, 2055-2087, 1978.
    Stieglitz, L., Zwick, G., Beck, J. “Carbonaceous particles in fly ash--a source for the de novo synthesis of organochlorocompounds.” Chemosphere 19, 283-290. 1989.
    Stockholm Convention, Stockholm Convention on Persistent Organic Pollutants (POPs). UNEP Chemicals, Geneva, Switzerland. Text for download at http://www.pops.int/, 2001.
    Taiwan EPA, http://edb.epa.gov.tw/, 2006.
    U.S. EPA, Database of Sources of Environmental Releases of Dioxin-Like Compounds in the United States. EPA/600/C-01/012, 2001.
    UNEP Chemicals, Standardized Toolkit for Identification and Quantification of Dioxin and Furan Releases. 2nd edition, Geneva, Switzerland, http://www.chem.unep.ch/pops/newlayout/repdocs.html, 2005.
    UNEP, Dioxin and Furan Inventory, National and Regional Emissions of PCDD/Fs. UNEP Chemicals, Geneva, Switzerland, http://www.chem.unep.ch/pops/newlayout/repdocs.html, 1999.
    UNEP, Standardized Toolkit for Identification and Quantification of Dioxin and Furan Releases. 2nd Ed., Geneva, Switzerland, http://www.chem.unep.ch/pops/newlayout/repdocs.html, 2005.
    US EPA, Database of Sources of Environmental Releases of Dioxin-Like Compounds in the United States. EPA/600/C-01/012, Washington, DC, 2001.
    US EPA, The Inventory of Sources of Dioxin in the United States (External Review Draft 2005). EPA/600/p-03/002a, 2005.
    Van den Berg, M., Birnbaum, L., Bosveld, A.T.C., Brunstrom, B., Cook, P., Feeley, M., Giesy, J.P., Hanberg, A., Hasegawa, R., Kennedy, S.W., Kubiak, T., Larsen, J.C., van Leeuwen, F.X.R., Liem, A.K.D., Nolt, C., Peterson, R.E., Poellinger, L., Safe, S., Schrenk, D., Tillit, D., Tyskland, M., Younes, M., Waern, F., Zacharewski, T. “Toxic equivalency factors (TEFs) for PCBs, PCDDs, PCDFs for humans and wildlife.” Environmental Health Perspectives, 106, 775-792, 1998
    van Leeuwen, F.X.R., Feeley, M., Schrenk, D., Larsen, J.C. “Farland, W. Younes, M. Dioxins: WHO’s tolerable daily intake (TDI) revisited.” Chemosphere 40, 1095-1101, 2000.
    Wang, L.C., Lee, W.J., Lee, W.S., Chang-Chien, G. P., Tsai, P.J. “Characterizing the emission of polychlorinated dibenzo-p-dioxins and dibenzofurans from crematories and their impacts to the surrounding environment.” Environ. Sci. Technol. 37, 62-67, 2003a.
    Wang, L.C., Lee, W.J., Tsai, P.J., Lee, W.S. “Chang-Chien, G.P. Emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans from stack flue gases of sinter plants.” Chemosphere 50, 1123-1129, 2003b.
    Yamasaki, H., Kuwata, K., Miyamoto, H. “Effects of ambient temperature on aspects of airbone polycyclic aromatic hydrocarbons.” Environmental Science and Technology 16, 189-194, 1982.
    Yang, H.H., Lee, W.J., Chen, S.J., Lai, S.O. “PAH emission from various industrial stacks.” J. Hazard. Mater. 60, 159-174, 1998.
    Yu, B.W., Moon, Y.H., Kim, M.K., Kyoung, J.D., Chang, Y.S. “Inventory study of PCDD/Fs for metal industries in south korea.” Organohalogen Compounds 63, 94-97, 2003.
    王琳麒, “污染源及大氣中戴奧辛/呋喃之特徵”,國立成功大學環境工程學系博士論文,2003。
    臺北市環境保護局,臺北市垃圾焚化廠-北投廠和木柵廠區內外環境中的戴奧辛、重金屬污染風險評估與管理,2002。
    台東縣環境保護局,台東市地區垃圾焚化廠周界空氣中及植物、土壤戴奧辛含量濃度調查及分析計畫,2002。
    台灣省自來水股份有限公司總管理處工程處:雲林縣BOO垃圾焚化廠興建對林內淨水廠影響評估,2003。
    行政院環境保護署,電弧爐煉鋼廠乙座與四座大型垃圾焚化廠周界空氣,植物及土壤中戴奧辛含量調查計畫,2002。
    行政院環境保護署,大型垃圾焚化廠周界空氣、植物及土壤中戴奧辛含量調查計畫,2003。
    行政院環境保護署,大型垃圾焚化廠周界空氣、植物及土壤中戴奧辛含量調查計畫,2004。
    行政院環境保護署,大型垃圾焚化廠周界空氣、植物及土壤中戴奧辛含量調查計畫,2005。

    下載圖示 校內:2009-10-14公開
    校外:2009-10-14公開
    QR CODE