三峡库区神女溪水华成因初探

通过对神女溪大规模水华进行现场监测和调查,结合当地水文、气象、污染源调查资料,并运用对比、相关分析等方法对神女溪水华原因进行了综合分析,认为叶绿素a与溶解氧、氧化还原电位、总氮、总磷、高锰酸钾指数均存在正相关关系,与pH和电导率呈负相关关系,总磷是此次水华的限制因子.     

土壤和河流沉积物中六六六和滴滴涕残留的测定

采用密闭微波提取、超声波提取、索氏提取对土壤和河流沉积物进行前处理,提取液经弗罗里硅土柱净化或浓硫酸净化.通过回收率实验和精密度实验对三种提取方法和两种净化方法进行比较,建立了微波提取土壤和河流沉积物中六六六和滴滴涕,浓硫酸净化,气相色谱一质谱测定的分析方法,方法回收率在84%～110%之间,精密度(RSD)在2.8%～9.9%之间.采用该方法对阜阳市废弃农药厂周围的土壤和河流沉积物中六六六和滴滴涕进行了监测.     

抑制型电导-离子色谱法测定水中无机阴离子

采用抑制型电导-离子色谱法测定生活饮用水、污水和地表水中F-、Cl-、NO2-、Br-、NO3-、PO43-、SO42-等7种无机阴离子,对清洁水样过滤后直接测定,浑浊样品离心后取上清液过滤测定。F-在0.100 mg/L~1.20 mg/L范围内、其余6种阴离子在1.00 mg/L~12.0 mg/L范围内线性良好,方法检出限为0.031 mg/L~0.47 mg/L,水样平行测定的RSD为0.9%~1.8%,加标回收率为82.6%~110%。     

Polycyclic aromatic hydrocarbons in surface sediments from drinking water sources of Taihu Lake, China: sources, partitioning and toxicological risk

Sources, partitioning and toxicological risk of 15 priority polycyclic aromatic hydrocarbons (PAHs) in surface sediments from drinking water sources of Taihu Lake, with an area of 2428 km(2) located in the most developed and populated area of China, were studied, and the results were compared with those in other lakes of China and the USA. Concentrations of the 15 PAHs in sediments ranged from 436.6 to 1334.9 ng g(-1) (dw). Gasoline combustion, coal combustion, diesel combustion from shipping and spillage of petroleum were apportioned to be the main sources of PAHs in this area by principal component analysis, which contributed 35.19%, 26.43%, 25.41% and 12.97% to the PAH sources estimated by further multiple linear regression. Levels of PAHs in sediments were negatively correlated with contents of clay and fine silt (<16 μm), while positively with contents of medium silt, coarse silt and sand (>16 μm). Humin with size larger than 16 μm contained the largest part of the burden of PAHs in sediments, but the specific partitioning domain (bound humic acid, lipid or insoluble residue) depended on properties of organic matter reflected by optical absorbance at 465 and 665 nm. Total toxic benzo[a]pyrene equivalent (TEQ(carc)) of the carcinogenic PAHs in sediments varied from 31.8 to 209.3 ngTEQ(carc) g(-1). Benzo[a]pyrene and dibenzo[a,h]anthracene contributed 45.36 and 25.31% to total TEQ(carc), posing high toxicological risk to this area.     

Distribution characteristics of polycyclic aromatic hydrocarbons in sediments and biota from the Zha Long Wetland, China

In this paper, the concentrations of polycyclic aromatic hydrocarbons (PAHs) were measured in biota (reed, grass, mussel, fish, and red-crowned crane) and sediments collected from seven locations in the Zha Long Wetland. PAHs were recovered from the sediments and biota by ultrasonic extraction and then analyzed by means of gas chromatography-mass spectrometry. The total PAH concentrations were 244–713 ng/g dw in sediments, 82.8–415 ng/g dw in plants and 207–4,780 ng/g dw in animals. The total sediment PAH concentrations were categorized as lower to moderate contamination compared with other regions of China and the world. In the plant samples, the accumulation abilities of reed roots and stems for PAHs were higher than those of grass roots. In addition, the concentration of individual PAHs in mussel muscles was the highest in all of the animal samples, followed by fish, feeding crane fetuses, and wild crane fetuses. Compositional analysis suggests that the PAHs in the sediments from the Zha Long Wetland were derived from incomplete biomass combustion. Risk assessment shows that the levels of PAHs in sediments are mostly lower than the effects range mean value (effects range mean), whereas only naphthalene in all sample sites was higher than the effects range low value. It is worthwhile to note that benzo(b)fluoranthene, benzo(k)fluoranthene, indeno(1,2,3-cd)pyrene and benzo(ghi)perylene were detected in crane fetal, which have potential carcinogenicity for organisms from the Zha Long Wetland.     

城市大气中挥发性有机化合物监测技术进展

挥发性有机物(VOCs)是臭氧及二次有机颗粒物(SOA)的主要前体物。近年来,我国逐步将VOCs纳入大气污染物控制体系。准确可靠的监测技术是大气VOCs研究及控制的重要前提保障。按照采样方法、分析方法 2个方面介绍并讨论了城市大气中VOCs的现有监测方法,较为详细地介绍了几类广泛采用的离线及在线监测技术,简要讨论了目前VOCs监测中存在的一些问题,展望了今后的发展趋势。     

徐州市生活垃圾填埋场地下水典型金属污染物研究

在对徐州地区生活垃圾填埋场调查分析的基础上,根据填埋特征和地质状况选取4座典型填埋场为调查对象,采用ICP-MS对垃圾渗滤液及地下水中26种重金属进行监测分析。结果表明,在4个垃圾填埋场地下水及渗滤液中ρ(Sr)均相对较高(700μg/L);地下水中金属元素均正在以Ca,Mg为主向Na,Mg为主转化;地下水中Al,B质量浓度大小顺序为Y场(雁群)S场(睢宁)C场(翠屏山)P场(邳州);4个垃圾填埋场共同典型重金属污染物为Mn,Fe,Zn,Ba;除上述污染物外,Y场地下水潜在典型重金属污染物为Pb和Mo;S场为Mo和As;C场为Tl和Co;P场为As。     

碱片-离子色谱法测定硫酸盐化速率影响因素

采用碱片-离子色谱法测定空气的硫酸盐化速率,方法在硫酸盐质量浓度为1.00~20.0 mg/L范围内线性良好(r≥0.999 0);碱片剪碎或不剪碎对空白碱片中硫酸根离子质量浓度的测定无明显影响,且高低两种加标浓度的回收率均在80.0%~120%之间;对于碱片实际样品,碱片剪碎更有利于硫酸根离子的快速溶出;随浸泡时间的延长,碱片中溶出的硫酸根离子质量浓度呈上升趋势,7 h硫酸根离子基本溶出完全,从保证结果质量和节省时间的角度考虑,确定最佳浸泡时间为3.5 h,建议碱片全部采取剪碎处理。