中国环境科学
中國環境科學
중국배경과학
CHINA ENVIRONMENTAL SCIENCE
2014年
10期
2593-2601
,共9页
史兵方%吴启琳%欧阳辉祥%刘细祥%张金磊%左卫元
史兵方%吳啟琳%歐暘輝祥%劉細祥%張金磊%左衛元
사병방%오계림%구양휘상%류세상%장금뢰%좌위원
工业土壤%多环芳烃%污染特征%来源分析
工業土壤%多環芳烴%汙染特徵%來源分析
공업토양%다배방경%오염특정%래원분석
industrial soil%polycyclic aromatic hydrocarbons (PAHs)%pollution characteristics%source apportionment
为完善我国实地的不同的PAHs污染特征数据库,系统采集了百色市5个工业区表层土壤样品,利用HPLC分析了16种US EPA 优控 PAHs 的含量和组分特征,运用同分异构体比率法和主成分因子载荷法揭示其污染来源.结果表明,工业区土壤中 PAHs 总含量范围在18.7~6437μg/kg之间,电厂2土壤中PAHs平均含量最高,达1923.4μg/kg.与国内外相关研究比较,处于中高等污染水平.5个工业区表层土壤样品中PAHs的残留大小顺序为:电厂2>电厂1>炼油厂>润滑油厂>水泥厂;电厂2、电厂1、炼油厂和润滑油厂4个工业区土壤中PAHs污染以4环为主,毒性较高的4环和5环PAHs均高于其他环数PAHs;水泥厂附近土壤中PAHs污染以2、3环为主.研究区域内土壤中Baa、Bkf、Chr 和 Fla 等单体超标严重.工业区土壤中 PAHs 污染主要来自于燃烧源、石油源及石油源和燃烧源的混合源,燃烧源贡献最大(占45.0%),石油源和燃烧源混合贡献率为36.8%,而石油源所占比例相对较小(占18.2%).
為完善我國實地的不同的PAHs汙染特徵數據庫,繫統採集瞭百色市5箇工業區錶層土壤樣品,利用HPLC分析瞭16種US EPA 優控 PAHs 的含量和組分特徵,運用同分異構體比率法和主成分因子載荷法揭示其汙染來源.結果錶明,工業區土壤中 PAHs 總含量範圍在18.7~6437μg/kg之間,電廠2土壤中PAHs平均含量最高,達1923.4μg/kg.與國內外相關研究比較,處于中高等汙染水平.5箇工業區錶層土壤樣品中PAHs的殘留大小順序為:電廠2>電廠1>煉油廠>潤滑油廠>水泥廠;電廠2、電廠1、煉油廠和潤滑油廠4箇工業區土壤中PAHs汙染以4環為主,毒性較高的4環和5環PAHs均高于其他環數PAHs;水泥廠附近土壤中PAHs汙染以2、3環為主.研究區域內土壤中Baa、Bkf、Chr 和 Fla 等單體超標嚴重.工業區土壤中 PAHs 汙染主要來自于燃燒源、石油源及石油源和燃燒源的混閤源,燃燒源貢獻最大(佔45.0%),石油源和燃燒源混閤貢獻率為36.8%,而石油源所佔比例相對較小(佔18.2%).
위완선아국실지적불동적PAHs오염특정수거고,계통채집료백색시5개공업구표층토양양품,이용HPLC분석료16충US EPA 우공 PAHs 적함량화조분특정,운용동분이구체비솔법화주성분인자재하법게시기오염래원.결과표명,공업구토양중 PAHs 총함량범위재18.7~6437μg/kg지간,전엄2토양중PAHs평균함량최고,체1923.4μg/kg.여국내외상관연구비교,처우중고등오염수평.5개공업구표층토양양품중PAHs적잔류대소순서위:전엄2>전엄1>련유엄>윤활유엄>수니엄;전엄2、전엄1、련유엄화윤활유엄4개공업구토양중PAHs오염이4배위주,독성교고적4배화5배PAHs균고우기타배수PAHs;수니엄부근토양중PAHs오염이2、3배위주.연구구역내토양중Baa、Bkf、Chr 화 Fla 등단체초표엄중.공업구토양중 PAHs 오염주요래자우연소원、석유원급석유원화연소원적혼합원,연소원공헌최대(점45.0%),석유원화연소원혼합공헌솔위36.8%,이석유원소점비례상대교소(점18.2%).
To expand and improve the database of polycyclic aromatic hydrocarbon (PAH) pollution signatures in different environmental samples from sites in China, surface soil samples were collected from five industrial areas of Baise, a prefecture-level city of the Guangxi Zhuang Autonomous Region. The concentration and composition of 16 PAHs listed for prior control by the US EPA were determined using high performance liquid chromatography. Selected diagnostic ratios and principal component analysis were used to identify possible sources of soil PAHs. Concentrations of∑16 PAHs in the present study were shown to vary greatly, and ranged from 18.7 to 6347 μg/kg, depending on the sampling location. The highest concentrations ofΣ16 PAHs were observed in Power plant 2 soils with a value of 1923.4μg/kg. Compared with domestic and foreign research, PAH pollution in the five Baise industrial areas reached medium to high levels. Soil PAH concentrations showed a strong Power plant 2-Power plant 1-Refinery-Lubricants plant-Cement plant gradient. Four-and five-ring PAHs, which have strong carcinogenic mutagenicity and distortion, dominated in the industrial areas with power plants and lubricant plants, while two-and three-ring PAHs dominated the surface soil near cement plants. Among the PAHs detected in the study-area soil, benz[a]anthracene (BaA), benzo[k]fluoranthene (BkF), chrysene (Chr), and fluoranthene (Fla) were the major pollutants occurring above standard levels. The study also suggested that the major sources of soil PAHs in Baise were coal and petroleum combustion (45.0%) and petroleum leakage (18.2%), or a combination of the two (36.8%).