环境监测中确定最佳点位的关键技术

环境监测网络设计的关键问题是确定最佳的环境监测点位 ,而最优的监测点位必须既能代表所在区域环境质量的平均水平 ,又能反映该区域环境质量的变化状况。为此提出一个兼容样本贴近与相似程度的统计量——近似度 ,不仅在理论上证明了其合理性 ,而且在厦门的应用中得到满意的结果 ,从而解决了如何确定环境监测中最佳点位的问题     

广佛公路(盐步段)两侧挥发性有机物(VOC)污染研究

选取广佛公路盐步路段作机动车尾气污染研究 ,结果表明 :污染物主要由烷烃、苯系物和氯代烃组成 ,主要是毒害性 VOC;污染随着与公路距离的增加而降低 ;污染源除机动车以外 ,还有大量的工业企业     

生态工程治理玄武湖水污染效果的监测与评价

选取总磷、总氮、叶绿素a、浮游生物、浮游植物等多项环境监测指标,对利用生态工程治疗玄武湖水环境污染的效果进行了环境监测与评价。指出生态工程治理玄武湖水环境污染效果显著,经过治理使湖水中生物多样性大大增加,浮游植物大幅减少,湖水透明度增加,总磷、总氮等主要指标大幅下降,生态工程区中的水环境已从高度富营养化降到中度富营养化。     

伊犁河水质中CODCr和CODMn的相关性探讨

对伊犁河水质中CODCr与CODMn的相关性进行了讨论。     

Size and resin fractionations of dissolved organic matter and trihalomethane precursors from four typical source waters in China

Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during drinking water treatment raise challenges to water quality control. Understanding both chemical and physical characteristics of DOM in source waters is key to better water treatment. In this study, the DOM from four typical source waters in China was fractionated by XAD resin adsorption (RA) and ultrafiltration (UF) techniques. The trihalomethane formation potential (THMFP) of all fractions in the DOM were investigated to reveal the major THM precursors. The fraction distributions of DOM could be related to their geographical origins in a certain extent. The dominant chemical fraction as THM precursors in the DOM from south waters (East-Lake reservoir in Shenzhen and Peal rivers in Guangzhou) was hydrophobic acid (HoA). The size fraction with molecular weight (MW) <1 kDa in both south waters had the highest THMFP. The results of cluster analysis showed that the parameters of fractions including DOC percentage (DOC%), UV₂₅₄%, SUVA₂₅₄ (specific UV₂₅₄ absorbance) and THMFP were better for representing the differences of DOM from the studied waters than specific THMFP (STHMFP). The weak correlation between SUVA₂₅₄ and STHMFP for either size or XAD fractions suggests that whether SUVA₂₅₄ can be used as an indicator for the reactivity of THM formation is highly dependent on the nature of organic matter.     

Regional differences and sources of organochlorine pesticides in soils surrounding chemical industrial parks

Concentrations of organochlorine pesticides (OCPs; dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB)) were investigated in 105 soil samples collected in vicinity of the chemical industrial parks in Tianjin, China. OCP concentrations significantly varied in the study area, high HCH and DDT levels were found close to the chemical industrial parks. The intensity of agricultural activity and distance from the potential OCP emitters have important influences on the OCP residue distributions. Principal component analysis indicates that HCH pollution is a mix of historical technical HCH and current lindane pollution and DDT pollution input is only due to technical DDT sources. The significant correlations of OCP compounds reveal that HCHs, DDTs and HCB could have some similar sources of origin.     

Distribution and sources of mercury in soils from former industrialized urban areas of Beijing, China

Fifty-seven typical surface soils and 108 deeper soils were collected from five former industrial sites in Beijing and concentrations of total Hg (SigmaHg) as well as pH, total carbon (TC), total nitrogen (TN), total sulfur, and dissolved organic carbon concentrations determined. The mean concentration of SigmaHg in surface soils was significantly greater than background concentrations in the vicinity of Beijing. Forty-eight percent of the samples exceeded the "critical" concentration of 1.0 mg Hg/kg, dry weight in soils, which has been established by the Chinese government. At depths of 0-80 cm in the soil, profile concentrations of SigmaHg also exceeded the background value. There were significant correlations between concentrations of SigmaHg, TC, and TN in the industrial soils. The greater concentration of SigmaHg in most soils could have been due in part to combustion of coal and leakage from industrial processes.     

水浴消解-原子荧光法测定土壤中的砷汞

建立了王水水浴消解-原子荧光法测定土壤中砷汞的方法,确定还原剂为硼氢化钾,测砷和汞时硼氢化钾的最优质量分数分别为2%和0.05%,载流为5%盐酸。该法砷和汞分别在质量浓度0.0~40.0μg/L和0.00~4.00μg/L范围内线性良好,相关系数均0.999 5,砷和汞的检出限分别为0.009和0.001 mg/kg,相对标准偏差分别为3.90%和2.67%,加标回收率分别为94.1%~107.6%和92.0%~104.0%。采用本法对国家标准土壤样品和东海县部分农田土壤样品进行测定分析,结果良好,表明该法操作简单、灵敏度高、实用性好,适用于土壤中砷和汞的测定。