松花江三岔河—哈尔滨江段汞污染分布状况的探讨

通过对松花江三岔河—哈尔滨江段水体、底泥、水生生物中总汞和甲基汞污染的研究,基本查清了三岔河—哈尔滨江段水体、底泥、水生生物中总汞和甲基汞含量范围;掌握了此江段汞的污染分布状况;“一松”江水对来自“二松”汞的净化情况;水生生物的汞污染水平与底质和江水汞含量之间的相关性、江水和水生生物含汞量的季节变化;甲基汞与总汞之间的变化关系。为松花江汞污染的防治途径,汞污染分布状况深入研究提供了必要的基础资料。     

确定环境中汞污染的来源

科学家现在用新手段追踪环境中的汞,它们是两种不同类型的汞稳定同位素分配。鱼类汞污染是一个全球范围的人群健康威胁,因为积聚在鱼中的甲基汞毒性非常大。但是由于汞通过大气输送分布到全球,所以难以区分当地源和全球源,也难以区分自然源和人为源。     

工业污染场地土壤中汞的化学形态及其环境限值探讨

汞是中国工业污染场地土壤中常见的重金属污染物,汞的常见形态包括单质汞、无机汞和甲基汞。比较了不同形态的汞及其化合物在物化性质、环境行为、毒性效应及致毒机制上的差异,还以美国、英国为例,探讨了针对不同形态的汞分别制定土壤环境限值的方法。最后指出,中国现有的土壤环境质量相关标准以及污染场地风险评估导则中均尚未区分汞的形态,仅给出总汞含量的限值。因此,在未来的相关标准制定中,应考虑按汞的各种形态制定不同的标准,这将更有利于客观准确评价工业污染场地土壤中汞的污染程度和环境风险。     

混汞法采金地区的汞污染研究进展

混汞法是一种设备简单、操作简便且应用历史悠久的提金方法，在世界范围内得到了普遍使用，同时也导致了严重的汞污染。本文介绍了混汞法的流程以及汞的释放过程和释放因子；综述了应用混汞法提金的不同国家和地区，对由此引发的大气、水体、生物(包括人体)和土壤汞污染的研究现状，并讨论了采金地区的环境管理政策。     

人发中甲基汞、无机汞和总汞的分别测定

本文根据选择性还原的原理,提出一种分别测定人发中甲基汞、无机汞和总汞的简易方法,并实际测定了50例没有职业性汞接触的工人和山区农民头发中的甲基汞,无机汞和总汞的含量水平。现将方法介绍如下。一、测定方法 (一) 主要仪器 1.10毫升具塞比色管 2.CH7601型汞分析仪 (二) 主要试剂 1.百花牌洗衣粉;2.10当量氢氧化钠溶液(优级纯);3.2当量氢氧化钠溶     

成都东郊稻田土中汞的分布特征研究

选取成都东郊唯一的火力发电厂周围的稻田土为研究对象,对稻田土中各种形态汞的分布特征进行了调查与研究,探讨稻田土中汞的分布规律,为分析和判断稻田土中汞的迁移和转化行为及该区汞污染土壤的修复提供重要依据。结果表明,处于火力发电厂烟尘排污口下风向的1#、2#、3#、4#采样点土样受到了严重的汞污染,呈现出高含汞特征,总汞平均质量浓度在9～41mg/kg,平均值为24.546mg/kg,远远超出《土壤环境质量标准》(GB 15618—1995)二级标准所规定的限值(0.5mg/kg),而处于排污口上风向的5#、6#、7#、8#土样没有受到明显的汞污染,大部分土样的总汞含量与成都市土壤汞平均含量接近;1#、2#、3#、4#土样中5种形态汞的垂直分布均呈现出随着土壤深度增加而减少的特征;1#、2#、3#、4#土样中的各形态汞平均百分比为有机结合态汞>硝酸溶汞>残渣态汞>铁锰氧化态汞>水溶和可交换态汞,土壤中含有的大部分汞化学性质比较稳定,难以被植物吸收利用,而易被植物吸收利用的水溶和可交换态汞虽然仅占极小一部分,但含量还是高于成都市土壤中水溶和可交换态汞的背景值。     

混汞法采金地区的汞污染研究进展

混汞法是一种设备简单、操作简便且应用历史悠久的提金方法 ,在世界范围内得到了普遍使用 ,同时也导致了严重的汞污染。本文介绍了混汞法的流程以及汞的释放过程和释放因子 ;综述了应用混汞法提金的不同国家和地区 ,对由此引发的大气、水体、生物 (包括人体 )和土壤汞污染的研究现状 ,并讨论了采金地区的环境管理政策     

环境样品中甲基汞的气相色谱分析

五十年代末期,震惊世界的“水俣病”爆发以来,环境汞污染问题引起了世界各国的普遍重视,相继开展了大量的汞污染调查,汞污染毒理学研究和迁移转化研究。经大量研究表明.环境中的无机汞可以通过各种途径转化为剧毒的甲基汞,进而通过食物网链累积危害人体健康。 甲基汞比较广泛地分布在各化学地理环境中,特别是受汞污染的水生生态系和土壤中。二者具有环境“汞库”之称,又     

氯碱厂(汞极法)中甲基汞来源的模拟实验研究

本文在氯碱厂甲基汞污染调查研究工作的基础上,通过模拟实验,进一步证明了氯碱工艺过程中具有合成甲基汞的条件,揭示出氯碱厂类型的汞污染可直接向环境中提供甲基汞污染的现象。     

汞污染前后的对比调查研究

氧化汞和氧化亚汞生产过程中造成严重的汞污染，由于气型污染，被土壤吸附，蓄积形成１４７ｍ污染半径，汞污染前后调查研究对比，土壤、蔬菜、鱼、地面水中汞残留超过正常范围。对汞污染后危害特点进行讨论，提出相应的建议。     

Mercury in the stomach contents of dab (Limanda limanda) from the North East Irish Sea and Mersey Estuary

A study of mercury concentrations in the stomach contents of fish from the north-east Irish Sea and Mersey Estuary has been shown to provide a means for surveillance of geographical and time-based changes in environmental exposure of fish biota to mercury in marine and estuarine ecosystems. This paper describes data for the flatfish dab (Limanda limanda), caught during the period 1986-1988. The low degree of variability in the data enables confirmation of clear trends in mercury concentration in stomach contents over time. As the inputs of mercury to the sewage sludge dumping ground in Liverpool Bay have decreased, there has been a corresponding decrease in mercury in fish food items. The mean mercury value in stomach contents around the dump site has declined to 100 microg kg(-1) (wet weight) which now predominates over the whole of Liverpool Bay. In 1986, mercury concentrations in stomach contents of fish ranged to over 750 microg kg(-1) although the majority of values were below 200 microg kg(-1). Most of the sites within the Mersey Estuary produced mean concentrations which were similar to those in the open sea, except for Garston which is the site closest to an inland, and principal alternative, source of mercury.     

Long‐term mercury accumulation in the presence of cadmium and lead in oseochromis aureus (Steindachner)

Abstract

The effects of cadmium and lead on chronic mercury accumulation were investigated in O. aureus. After 140 days’ exposure the accumulation of mercury in the liver, brain, gill filaments, intestine, caudal muscle, spleen, trunk kidney and eye was analysed. The exposure concentrations were 0.05, 0.10 and 0.20 mg/L for mercury alone. O. aureus was also exposed to mixtures of 0.05 mg/L mercury with lead (0.05 mg/L and 0.50 mg/L or cadmium (0.05 mg/L) and 0.10 mg/L mercury with 0.10 mg/L cadmium. In food fish, a knowledge of toxic metal accumulation patterns is of great importance because of their contribution to the human diet and, as fishmeal, to the diet of agricultural animals. The trunk kidney consistently accumulated higher concentrations of mercury than any of the other tissues investigated.     

Blood mercury levels among fish consumers residing in areas with high environmental burden

Mercury is a ubiquitous, persistent toxicant found in the environment. In water, mercury bioaccumulates up the food chain and leads to high concentrations in fish. Consumption of contaminated fish is the major source of exposure to mercury in the US. The objective of this study was to enroll persons living in areas selected by the Environmental Protection Agency (EPA) to have high mercury concentrations and who consume at least 6 oz of locally caught fish per week to determine the feasibility of monitoring future trends among a population identified as highly exposed. Blood samples were collected at time of interview and analyzed for mercury. Participants (n = 287) were enrolled from North Carolina, Maryland, and South Dakota. Participants reported eating an average of five servings of fish per week. The overall geometric mean for total mercury was 0.75 μg L⁻¹, with North Carolina having the highest mean level (2.02 μg L⁻¹). Overall, 42% of the study population had levels greater than the US geometric mean 0.83 μg L⁻¹. The number of servings of fish consumed was not found to be associated with blood mercury levels. We were able to identify some persons with elevated mercury concentrations living in areas identified by EPA; however, identifying and monitoring a highly exposed population over time would be challenging.     

Periphyton as a bioindicator of mercury pollution in a temperate torrential river ecosystem

Mercury presents a potential risk to the environment and humans, especially in its methylated form. It is among the highest priority environmental pollutants. River Idrijca (Slovenia) is highly contaminated with mercury due to past mercury mining. The aim of this work was to investigate whether the periphyton community in rivers such as Idrijca is a suitable indicator of Hg pollution and of changes in mercury methylation and could serve as an early warning system of increased input of MeHg in the food chain. Periphyton is the only site of primary production in temperate torrential rivers such as Idrijca and is therefore an important link in the food chain. It is also a potential site of Hg accumulation and its introduction to higher trophic levels. Our aim was to assess the response of the periphyton to seasonal and spatial variations in mercury levels and to evaluate its potential as an early warning system of changes in mercury reactivity and mobilization The results indicate that periphyton in a torrential river is too complex and unpredictable to be used as a sole indicator of mercury concentrations and changes in the river. Nevertheless, it can complement environmental measurements due to its importance in the riverine food web.     

Recent trends of biocides in pikes of the Lake Päijänne

Pikes were sampled in May 1980 from three areas of the Lake Päijänne, Finland and analyzed for their contents of total mercury, methyl mercury, hexachlorobenzene (HCB), DDE, PCB and chlorophenolic residues. An improved method for methyl mercury determination was applied and 82–84 % methylation of mercury in pikes regardless of area or biological variation was observed. Statistical analysis with previous results from the same areas gave a very significant decreasing trend of mercury levels at all three areas from 1970 to 1980. Future levels of mercury in fish to be consumed as food could be estimated from the trend regression. The very low levels of DDE and PCB showed some increasing trend when the influence of fat contents was eliminated by covariance analysis. General appearance of HCB at sub-ppb level was observed. Also pentachlorophenol occured at 10–70 ppb (fresh weight) levels at all areas, but the other chlorophenols were abundant only at Tiirinselkä which is most contaminated by pulp bleaching effluents.     

Bioaccumulation of mercury in the trophic chain of flatfish from the Baltic Sea

Mercury concentrations in three flatfish species - flounder (Platichtys flesus), plaice (Pleuronectes platessa), and Baltic turbot (Scophthalmus maximus), netted in the southern Baltic Sea were assessed and compared to concentrations of this metal in sediments, sea water, and flatfish food - bivalve Macoma balthica, isopod Saduria entomon, and sprat (Sprattus sprattus). Collected simultaneously with flatfish in 2009 and 2010. Different concentrations of mercury depending on species, tissue or organ, sex, individual length, kind of food, and region were determined. The muscle tissues of turbot had the highest concentrations of the metal. The bioaccumulation (BF) and biomagnification (BMF) factors has been counted showing that the muscle tissues of turbot have maximum affinity for mercury, and thus best reflected the metal contamination of the Baltic Sea environment. The data suggest that the common Baltic turbot (S. maximus) is an important model species, suitable and cost-effective to biomonitor environmental mercury pollution for ecological research.     

高温载硫活性炭的制备及脱汞能力研究

研究了载硫温度、硫炭比(简称S/C),吸附温度等因素对载硫活性炭的硫含量、脱汞能力以及硫损失的影响,探讨载硫活性炭制备的工艺条件优化。结果表明,不同载硫温度下制备的载硫活性炭的气态Hg0吸附能力远强于原料活性炭;载硫温度不同时,负载到活性炭孔隙或表面上的硫的形态不同,导致了脱汞能力的差异,较合适的载硫温度为350℃;S/C为5%(质量分数,下同)时,随着吸附温度的升高,载硫活性炭的气态Hg0吸附量降低;在一定的载硫温度下,原料中S/C越高时,制备的载硫活性炭的硫含量越高、气态Hg0吸附能力越强,但其硫损失率也越高,从实际的使用效果来看,较合适的S/C为10%。     

Measurement of Particulate Bound Mercury,Gaseous Elemental Mercury,and Reactive Gaseous Mercury Concentrations by Using an Ambient Air Mercury Collection System

In this investigation, the concentrations of gaseous elemental mercury (GEM), reactive gaseous mercury (RGM) and particulate bound mercury (PBM) in ambient air were measured at the Hung Kuang (traffic) sampling site during September 27 to October 6, 2014. An ambient air mercury collection system (AAMCS) was utilized to measure simultaneously PBM, GEM, and RGM concentrations in ambient air. The results thus obtained demonstrate that the mean concentrations of PBM, GEM, and RGM were 38.57 ± 11.4 (pg/m³), 17.67 ± 5.56 (ng/m³) and 10.78 ± 2.8 (pg/m³), respectively, at this traffic-sampling site. The mean GEM/PBM and GEM/RGM concentration ratios were 458 and 1639, respectively. The results obtained herein demonstrate that AAMCS can be utilized to collect three phases of mercury simultaneously. The mean PBM, GEM, and RGM concentrations herein were compared with others found in Asia, America, Europe and Antarctica. The mean PBM, GEM, and RGM concentrations were found to be lowest in Asia and Antarctica. The mean PBM concentration in Europe was approximately eight times that in this investigation. The mean GEM and RGM concentrations in this study were 1.21 and 170 times those found in the United States.     

Routine, automated determination of inorganic and total mercury in multimedia using cold vapour atomic absorption spectrometry

A routine, automated analytical method for simultaneous determination of total and inorganic mercury by cold vapour atomic absorption spectrometry in multimedia is described. Excellent accuracy and precision results were obtained with human hair certified reference materials namely, BCR-397 and IAEA-086. The reproducibility relative standard deviation for total mercury was 4% and 22%, respectively. The limit of detection for total and inorganic mercury was 0.2 μg/g hair. The described method has been successfully applied in determination of total and inorganic mercury as well as organic mercury in human hair, urine and fish tissue samples.     

Method validation for control determination of mercury in fresh fish and shrimp samples by solid sampling thermal decomposition/amalgamation atomic absorption spectrometry

A method for the determination of total mercury in fresh fish and shrimp samples by solid sampling thermal decomposition/amalgamation atomic absorption spectrometry (TDA AAS) has been validated following international foodstuff protocols in order to fulfill the Brazilian National Residue Control Plan. The experimental parameters have been previously studied and optimized according to specific legislation on validation and inorganic contaminants in foodstuff. Linearity, sensitivity, specificity, detection and quantification limits, precision (repeatability and within-laboratory reproducibility), robustness as well as accuracy of the method have been evaluated. Linearity of response was satisfactory for the two range concentrations available on the TDA AAS equipment, between approximately 25.0 and 200.0 μg kg^?1 (square regression) and 250.0 and 2000.0 μg kg^?1 (linear regression) of mercury. The residues for both ranges were homoscedastic and independent, with normal distribution. Correlation coefficients obtained for these ranges were higher than 0.995. Limits of quantification (LOQ) and of detection of the method (LDM), based on signal standard deviation (SD) for a low-in-mercury sample, were 3.0 and 1.0 μg kg^?1, respectively. Repeatability of the method was better than 4%. Within-laboratory reproducibility achieved a relative SD better than 6%. Robustness of the current method was evaluated and pointed sample mass as a significant factor. Accuracy (assessed as the analyte recovery) was calculated on basis of the repeatability, and ranged from 89% to 99%. The obtained results showed the suitability of the present method for direct mercury measurement in fresh fish and shrimp samples and the importance of monitoring the analysis conditions for food control purposes. Additionally, the competence of this method was recognized by accreditation under the standard ISO/IEC 17025.