大气环境中有机污染物的研究

本文采用聚氨基甲酸乙酯泡沫和玻璃纤维滤膜，同时采集大气中气态和颗粒物样，用高效液相色谱和气相色谱分别测定了蒽、、、芘、苯并（ａ）、二苯并（ａ、ｈ）葱、苯并（ｇｈｉ）与Ｃ＿（１６）～Ｃ＿（３３）正构烷烃等有机污染物的含量。并得到了冬夏两季颗粒物和气态中有机污染物的分布规律。     

中国食品中苯并［a］芘的污染和控制

总结了近十几年来我国城市蔬菜等食品中苯并［ａ］芘污染的调查结果,表明随着大气污染的加剧以及工业“三废”排放的增大等,苯并［ａ］芘在食品中的残留污染已不容忽视。具有面源污染的特点。探讨了蔬菜等食品受苯并［ａ］芘污染的影响因素,提出了食品中苯并［ａ］芘污染的控制方法。     

尿中芘、苯并(k)萤蒽和苯并(a)芘的鉴别与测定

本文用高压液相色谱结合荧光分光光度技术定性鉴别了尿样中芘、苯并(k)萤蒽和苯并(a)芘的存在,并用标样进行了定量测定的研究。芘、苯并(k)萤蒽和笨并(a)芘在尿样中的回收率分别为60％、90％和80％;标准偏差为4.7％、17％,检测限为0.77ng、0.05ng和0.06ng。对吸烟者尿中这三种多环芳烃进行了定量测定,结果为芘53.3ng,苯并(k)萤蒽3.7ng、苯并(a)芘4.7ng;而对照组的尿样中,苯并(k)萤蒽和苯并(a)芘的含量均在检测限以下。     

蔬菜主要污染问题

根据国内外有关资料及杭州市菜区调查结果，讨论了重金属、硝酸盐、农药、氟化物、苯并（ａ）芘在及塑料薄膜等对蔬菜污染的途径和危害，阐述了目前我国蔬菜所面临的主要污染问题。     

蔬菜主要污染问题

根据国内外有关资料及杭州市菜区调查结果，讨论了重金属、硝酸盐、农药、氟化物、苯并（ａ）芘及塑料薄膜等对蔬菜污染的途径和危害，阐述了目前我国蔬菜所面临的主要污染问题。     

徐州市区大气颗粒物中多环芳烃的污染特征

采用高效液相色谱技术（HPLC）对徐州市大气颗粒物中优控的16种多环芳烃（PAHs）进行定量研究。结果表明：萘、芴、苊等低分子量芳烃的含量相对较低;苯并（g,h,i）苝、茚并（1,2,3-cd）芘、苯并（k）荧蒽、苯并（a）芘等高分子量芳烃的含量相对较高;含量最高的单体为荧蒽,占待检的16种PAHs的19%以上。不同环数多环芳烃含量大小顺序为：4环〉5环〉6环〉3环〉2环。可吸入颗粒物（PM10）中苯并（a）芘和∑PAHs在不同功能区的分布特征大体上一致,并呈现一定规律性：交通干线区〉工业区〉风景文化区〉居民区〉新城区。由此可以初步认为徐州市区PM10中的PAHs主要来源于燃煤和汽车尾气。     

大同市空气中多环芳烃与人尿中1—羟基芘的分析

用ＧＣ＾２／ＭＳ和ＨＰＬＣ鉴定出大同市空气中的多环芳烃化合物３５种，对大同市不同功能区空气中苯并（ａ）芘（ＢａＰ）和人尿中１－羟基芘同步采样分析。结果表明，不同功能区ＢａＰ浓度有显著差别：采暖期浓度急剧增加，城区浓度为对照点的１７倍，日均值达３３０ｎｇ／ｍ＾３。人尿中１－羟基芘的浓度与空气中ＢａＰ的浓度显著相关。采暖期城区尿中１－羟基芘的几何均值为１．８６μｍｏｌ／ｍｏｌ肌酐，非采暖期为１．１４μ     

煤矸石堆放场周围玉米作物中苯并(a)芘污染特征

以焦作矿区演马矿煤矸石堆放场周围农田玉米为研究对象,对玉米中苯并(a)芘污染特征进行了分析研究.在矸石堆周围布设三条采样线采集玉米样品,玉米样品经提取、浓缩、净化处理后采用高效液相色谱(HPLc)法对其中苯并(a)芘含量进行检测分析.结果表明,研究区玉米作物叶子中苯并(a)芘污染水平较高,达46.7%,茎和籽均未出现苯并(a)芘污染现象,且玉米各部位苯并(a)芘含量与距矸石堆距离呈反比.进一步指出矿区企业应加强对周围环境生态的预防保护,以确保企业的可持续发展.     

苯并（a）芘对罗非鱼（GIFT Oreochromis niloticus）肝细胞DNA损伤的影响

苯并（a）芘（Benzo（a）pyrene,BaP）是一种含有5个苯环的多环芳烃,是环境中广泛存在的一类有机污染物,苯并（a）芘可引起多种形式的DNA损伤。彗星试验,又称为单细胞凝胶电泳（Single Cell Gel Electrophoresis,SCGE）,是一项灵敏、快速的在单细胞水平检测DNA链断裂的技术,已经广泛应用于水环境的生物监测中。污染物的毒性监测与评估一直是环境科学研究的热点问题之一。本文通过生态毒理学试验,利用单细胞凝胶电泳技术,研究不同浓度苯并（a）芘暴露对罗非鱼（GIFT Oreochromis niloticus）肝细胞DNA的损伤情况。试验将罗非鱼在0.1、1、10、50μg·L-14个苯并（a）芘（BaP）浓度下分别暴露4、7、14 d,利用彗星试验研究BaP对罗非鱼肝细胞DNA的损伤情况,以尾部DNA含量、尾长、尾矩及Olive尾矩为评价指标,结果表明,BaP会对肝细胞DNA造成不同程度的损伤：在0.1、1、10μg·L-13个浓度组,DNA损伤随着BaP暴露浓度的增加而增加,呈现一定的剂量效应关系,50μg·L-1组DNA损伤有所下降。在时间上,除1μg·L-1剂量组的尾部DNA含量、10μg·L-1组的尾部DNA含量及Olive尾矩外,其他指标有在第7天降低之后又升高的趋势,这意味着肝细胞DNA损伤可在一定程度上反映水体中BaP的污染情况。该实验为进一步探讨苯并（a）芘的致癌机制及环境中苯并（a）芘的监测提供一定的科学依据。     

毛细管气相色谱—负离子化学电离源质谱法测定空气颗粒物中的硝基？…

本文用毛细管气相色谱－负离子化学电离源质谱法（ＧＣ－ＮＩＣＩＭＳ）测定了空气颗粒物中的硝基多环芳烃（ＮＯ２－ＰＡＨ）,通过与标准的保留时间和质谱图的比较,确定了空气颗粒物中含有四种ＮＯ２－ＰＡＨ,它们是２９－硝基芴,９－硝基蒽,１－硝基芘和２－硝基萤蒽。用同一样品进行了毛细管气相色谱正离子电子轰击源质谱分析,并与ＧＣ－ＮＩＣＩＭＳ进行比较     

固相微萃取-气相色谱/质谱联用法测定饮用水中苯类化合物

用固相微苹取(ＳＰＭＥ)－气相色谱/质谱联用法测定饮用水中苯类化合物,以１００μｍ ＰＤＭＳ(聚二甲基硅氧烷)萃取针提取、浓缩、分离与测定九种目标化合物．萃取时间经优化选定为８ｍｉｎ,而热解析时间设定为２ｍｉｎ． 本方法的相对标准偏差小于５%,线性范围宽(２０ｎｇ·ｍｌ－１－１００００ｎｇ·ｍｌ－１),多数化合物的检测限低于５μｇ·ｌ－１．饮用水样品检测显示,样品加标回收率范围在８４%至１１０%内．     

城市水样中首次检出痕量硝基多环芳烃（NO2—PAH）

本文利用还原衍生化高分辨ＧＣ－ＥＣＤ法，采用双柱定性首次在城市地表水样中检出环境潜在致癌物－硝基多环芳烃（ＮＯ２－ＰＡＨ），结果表明，在不同的水样中共检出包括动物致癌物２－硝基萘在内的八种ＮＯ２－ＰＡＨ。河水和饮用水中均有ｐｐｔ级ＮＯ２－ＰＡＨ存在，其中溶解度较大的两环硝基多环芳烃的含量高于三环以上的。饮用水中ＮＯ２－ＰＡＨ的浓度低于与其相邻的河水中相应硝基多环芳烃的含量，经煮沸处理后，饮用水中Ｎ     

基于umu遗传毒性效应的饮用水致癌风险评价的尝试

化学物质暴露是导致癌症发生的重要诱因,通过饮用水暴露导致的人类致癌风险在饮用水处理技术中日益引起重视.由于水中化学物质种类繁多、组成复杂,准确地检测每个致癌物质的浓度和毒性非常困难.为了控制饮用水的安全,根据DNA损伤诱导SOS反应而表达umuC基因这一基本原理建立的SOS/umu测试法,已经广泛应用于饮用水遗传毒性的检测.论文建立了基于umu遗传毒性效应的饮用水致癌风险评价方法,并对北方某水厂饮用水的遗传毒性进行了umu测试,计算了该地区饮用水的致癌风险,提出了可能的饮用水遗传毒性基准值.结果表明,该水厂常规工艺出水的致癌风险均值为1.55×10-6,存在一定的安全隐患;而深度处理工艺能有效地削减出水致癌风险均值至5.3×10-7,达到目前先进国家水质管理的要求,保障了饮用水的安全.样品中4-硝基喹啉-1-氧化物(4-NQO)的等当量浓度(TEQ4-NQO)0.0948μg·L-1可作为饮用水遗传毒性基准值。     

Determination of selected semi-volatile organic compounds in water using automated online solid-phase extraction with large-volume injection/gas chromatography/mass spectrometry

A rapid, sensitive, and cost-effective analytical method was developed for the analysis of selected semi-volatile organic compounds in water. The method used an automated online solid-phase extraction technique coupled with programmed-temperature vaporization large-volume injection gas chromatography/mass spectrometry. The water samples were extracted by using a fully automated mobile rack system based on x-y-z robotic techniques using syringes and disposable 96-well extraction plates. The method was validated for the analysis of 30 semivolatile analytes in drinking water, groundwater, and surface water. For a sample volume of 10 mL, the linear calibrations ranged from 0.01 or 0.05 to 2.5 ??g·L^?1, and the method detection limits were less than 0.1 ??g·L^?1. For the reagent water samples fortified at 1.0 ??g·L^?1 and 2.0 ??g·L^?1, the obtained mean absolute recoveries were 70%?C130% with relative standard deviations of less than 20% for most analytes. For the drinking water, groundwater, and surface water samples fortified at 1.0 ??g·L^?1, the obtained mean absolute recoveries were 50%?C130% with relative standard deviations of less than 20% for most analytes. The new method demonstrated three advantages: 1) no manipulation except the fortification of surrogate standards prior to extraction; 2) significant cost reduction associated with sample collection, shipping, storage, and preparation; and 3) reduced exposure to hazardous solvents and other chemicals. As a result, this new automated method can be used as an effective approach for screening and/or compliance monitoring of selected semi-volatile organic compounds in water.     

斑马鱼幼鱼运动行为测试评价饮用水安全

饮用水安全直接关乎人类的健康与安全,当前迫切需要全新的毒性测试方法对饮用水的潜在人类健康风险进行全面、准确和灵敏的评估和预警。本研究以反渗透技术(RO)取代常用的固相萃取,分别浓缩饮用水厂的进厂水、出厂水和管网水进行毒性试验水样的前处理。反渗透技术前处理方法可以避免传统固相萃取方法中使用的有机溶剂对行为学测试体系的干扰。RO浓缩后的饮用水对斑马鱼胚胎进行持续暴露,采用Viewpoint行为测试软件量化分析出生后第6天(6 dpf)斑马鱼幼鱼的运动行为,选择运动距离和转向行为作为测试终点,分析进厂水、出厂水及管网水的潜在毒性及可能变化。结果表明,暴露在进厂水的幼鱼出现了明显的行为变化,尤其在较高浓度(20倍浓缩)暴露时,运动距离相比对照组显著减少,同时伴有剧烈的转向等异常行为;管网水对斑马鱼幼鱼行为存在一定程度的影响,而出厂水对幼鱼的运动行为没有显著影响。研究结果反映出当前饮用水厂深度处理工艺可以有效降低进厂水的潜在毒性和健康风险,但是经供水管网输送后,其水质可能发生了改变,导致管网水可能存在潜在的毒性。本研究所采用的反渗透技术前处理技术及斑马鱼幼鱼的运动行为学测试方法,可用于未来建立评估饮用水水质安全的早期预警系统。     

Daily dietary fluoride intake in rural villages of the Ethiopian Rift Valley

Dental and skeletal fluorosis is widespread in the Ethiopian Rift Valley region. Drinking water has been considered the main reason for the development of fluorosis, but dietary intake may also be a contributor in areas with high concentration of fluoride in water, soil, and biota. The purpose of this study is to assess the total daily dietary fluoride intake by adults in a rural part of the Ethiopian Rift Valley. The food, beverage, and water samples were collected from selected households of three neighboring villages with similar dietary pattern, but with different fluoride content in their water sources. Village A uses water with 1.0 mg L^?1 fluoride, village B uses water with 3.0 mg L^?1 fluoride, and village C uses water with 11.5 mg L^?1 fluoride both for food preparation and for drinking. The level of fluoride was determined in all food ingredients, in the prepared food, beverages, and in the water used for food preparation and drinking. Recipe and food frequency questionnaires were used to gather household food preparation and consumption patterns. An alkali fusion method was used for digestion of food samples and for subsequent determination of fluoride with ion-selective electrode. The daily fluoride intake varied depending on its concentration in the water used for cooking and drinking. In households using water with 1 mg L^?1, 3 mg L^?1, and 11.5 mg L^?1 fluoride, the total personal intake was found to be 10.5, 16.6, and 35.3 mg d^?1, respectively. Contribution of the water to the daily fluoride intake was 33%, 58%, and 86%, respectively. Even in households using water containing fluoride at a concentration of 1 mg L^?1, the daily intake was higher than the recommended safe intake of 1.5–4.0 mg d^?1 for adults, which indicates that the fluoride intake through food may cause health risks. Minimizing the fluoride concentration in water to the lowest possible level will greatly reduce the daily intake. The form of fluorine (organic or inorganic) in the food items and the associated health risk factors need further investigation.     

Distribution and Risk Assessment of Fluoride in Drinking Water in the West Plain Region of Jilin Province, China

The west plain region of Jilin province of northeast China is one of the typical endemic fluorosis areas caused by drinking water for many years. Investigations of hydrogeological and ecoenvironmental conditions as well as endemic fluorosis were conducted in 1998. Results show that the ground water, especially, the water in the unconfined aquifer is the main source of drinking water for local residents. The fluoride concentration in groundwater in the unconfined aquifers is higher than that in the confined aquifer in the west plain of Jilin province. The fluoride concentration in the unconfined aquifer can be used to classify the plain into fluoride deficient area, optimum area and excess area, which trend from west to east. High fluoride (>1.0 mg L(-1)) in drinking water resulted in dental and skeletal fluorosis in local residents (children and pregnant women). There exists a positive correlation between fluoride concentration in the drinking water and the morbidities of endemic fluorosis disease (r1 = 0.781, r2 = 0.872). Health risks associated with fluoride concentration in drinking water are assessed. It has been determined that fluoride concentration in excess of 1.0 mg L(-1) exposes residents to high health risks based on risk identification. The study area is classified into five health risk classes as shown in Figure 4. The risk indexes of this area more than 1.0 are accounted for 68% of the total west plain region.     

建立适合我国国情的饮用水水质指数

目前一般利用各指标合格率评价饮用水水质，由于指标繁杂，不利于消费者了解水质整体概况，也不利于对外发布公报。本文建议采用水质指数法来对饮用水水质进行综合评价。本文介绍了目前采用的水质指数的不同评价方法，综述了不同的水质指数的原理和计算方法，根据我国国情，对我国城市供水的饮用水水质指数进行了修正，首次在水质指数中增加了超标项目“惩罚项”。修正后的饮用水水质指数具有很强的科学性和可操作性，可以从整体上对饮用水水质进行综合评价。     

Arsenic in Drinking Water and Bladder Cancer: Comparison between Studies Based on Cancer Registry and Death Certificates

Associations between arsenic in drinking water and bladder cancer in an area along the southwest coast of Taiwan have been documented for decades. Several ecologic studies were conducted to assess the dose-response relationships. Some of them used the National Cancer Registry Program to identify cancer cases, and some used death certificates. Whereas the cancer registry collects information on all patients no matter if they died of bladder cancer or not, the case ascertainment might be incomplete due to the fact that reporting of cases is not mandatory. Reporting of death, on the other hand, is strictly enforced by law, but patients who did not die of bladder cancer might not be identified. In order to assess the problems with both approaches, we conducted a study using both case identification mechanisms. A total of 243 townships with measurements of arsenic in drinking water were included in the analysis of cancer registry data, and death certificates were collected from 10 of those townships. In both analyses, the same measurements of arsenic made by the mercuric bromide stain method were adopted. Due to limitation of the method, all levels below 0.04mg L^–1 were combined as a single exposure category. The results were very much alike; both approaches detected statistically significant associations between high arsenic levels in drinking water (above 0.64mg L^–1) and occurrence of bladder cancer but did not find such associations for arsenic exposures at lower levels.     

Voltammetric determination of the herbicide Bifenox in drinking and river water using a silver solid amalgam electrode

A new method for the determination of submicromolar and nanomolar concentrations of herbicide Bifenox using differential pulse voltammetry at a mercury meniscus modified silver solid amalgam electrode is described. This new type of working electrode is non-toxic, environmentally friendly, and compatible with principles of green analytical chemistry, and its surface can be easily electrochemically renewed in the case of passivation. The newly developed direct differential pulse voltammetric determination of Bifenox gives limit of determination 6.7·10^?7 and 6.9·10^?7?M in drinking and river water, respectively. Both the selectivity and the sensitivity can be further increased by preliminary separation and preconcentration using solid phase extraction. This combination enables to reach limit of determination 0.9?×?10^?9 and 1.5?×?10^?9?M for drinking and river water, respectively. Because of lower running and investment costs, this electroanalytical method can be used for large scale monitoring of possible water contamination with tested herbicide.