伯胺N_(1923)萃淋树脂吸萃汞(Ⅱ)的性能及萃合物组成的研究

本文研究了N_(1923)萃淋树脂对汞(Ⅱ)吸萃的性能、溶液的酸效应、吸附等温线、吸附速率及体系温度等对吸萃分配比的影响.用饱和容量法、等摩尔系列法、斜率法等对吸萃物组成进行了探讨.并用红外光谱法、核磁共振谱法对吸萃机理进行了分析.     

封闭垃圾填埋场通过地表向大气释放汞的测定

利用动力学通量箱及自动测汞仪联用技术,于2004年3月中旬对贵阳市的一座封闭生活垃圾填埋场汞通过地表向大气释放的过程进行了研究。3个采样点的汞释放通量日均值分别为559.1、88.2、53.6ng·m-2·h-1,汞释放通量强度与表层基质中的汞含量密切相关,该测定值高于世界背景地区通量的1~2个数量级,说明封闭垃圾填埋场也是大气汞的潜在来源。汞释放通量呈现明显的昼夜变化规律,白天较高并在午间前后达到最大,而夜间降至最低。气相因子中光照强度与汞的释放过程相关性最高,其次分别是气温、相对湿度、地温和风速。氧化态汞的光致还原作用是可能垃圾填埋场Hg0生成的主要途径,降雨初期能促进地表汞的释放。     

A model of mercury contamination in a woodland stream

A model for the accumulation of mercury in four compartments of woodland stream has been set up. The four components considered are sediments, detritus, invertebrates and fish. The model inputs are concentrations of dissolved monomethyl mercury and dissolved inorganic mercury (Hg²⁺) in the water. The model predicts that some reevaluation of current safe mercury concentrations in water may be needed in order to keep mercury concentrations in fish below current actions levels.     

Organochlorines and PCBs in Tilapia zillii from Lake El-Manzala,Egypt

Abstract

The mercury content has been determined in samples of fumarolic gases, phreatic waters, soil and vegetation collected at Vulcano, Aeolian Islands, Italy. Volcanic activity is demonstrated as a source of natural mercury pollution whose extent has been evaluated here by studying the contribution of different components of the surface environment. The possible influences for living organisms are examined.     

Mercury pollution in a mining area of Guizhou,China: Fluxes over contaminated surfaces and concentrations in air,biological and geological samples

A dynamic flux chamber has been used to estimate fluxes of mercury over different types of surfaces in an abandoned open‐cut mine of Tongren prefecture, Guizhou province, China during spring and summer of 1996. The highest fluxes were obtained over cinnabar slag and contaminated soils, whereas the emissions above cinnabar ore were substantially lower. These fluxes was scaled up to estimate the contribution of mercury emissions to air from mercury wastes, compared to anthropogenic activities in the province of Guizhou, China. Atmospheric mercury concentrations measured were enhanced in the mining area (<1.3 μg m^‐3) compared to regional background sites (1.8–5.1 ng m^‐3). The spreading of mercury was estimated by using biological and geological samples. Moss bags have been employed to estimate long‐time dry‐ and wet‐deposition to this area.     

Hepatoprotective effects of taurine against mercury induced toxicity in rats

An attempt has been made to study the influence of taurine on mercury intoxicated rats. The animals were treated with sublethal dose of mercuric chloride (2 mg/kg body wt.) for 30 days. During the mercury treatment, the level ofAspartate transaminase(AST), Alanine transaminase (ALT) and Alkaline phosphatase(ALP) in serum and lipid peroxidation (LPO) in liver tissue significantly increased whereas Glutathione (GSH), Glutathione peroxidase(GPx), Catalase (CAT) and Superoxide dismutase (SOD) were simultaneously decreased in the liver tissue. Present results indicate that the liver tissue was completely damaged, after mercury treatment. In another group of animals, taurine (5 mg/kg body wt.) was administrated for another 15 days. Taurine administration was observed to improve the liver function in mercury intoxicated animal as indicated by the decline in increased levels of AST, ALT and ALP in serum and LPO content in liver tissue. The decreased level of antioxidant system (GSH, GPx, CATand SOD) has been promoted Results suggested that taurine played a vital role in reducing the mercury toxicity in intoxicated animals.     

Mercury Contamination of Fish and Its Implications for Other Wildlife of the Tapajós Basin, Brazilian Amazon

Abstract: Since 1979 the gold rush in the Brazilian Amazon has caused serious environmental damage to one of the most complex ecosystems on Earth. Mainly due to the toxicity of mercury to humans, this problem has received wide public attention and prompted many studies. Although these studies have involved sampling of fish, the negative effect of mercury contamination to fish themselves and other wildlife has been largely ignored. To assess the present level of mercury contamination of fish, and its implication for fish and other animals, we collected and examined data on mercury concentration in fish of the Brazilian Amazon, especially for the Tapajós basin, between 1991 and 1996. We conclude that omnivores and piscivores that live nearer to gold mining areas in the Tapajós basin are already at high risk of mercury toxification, especially reproductive failure. Mercury concentrations in these fish are also high enough to have detrimental effects on animals at higher trophic levels. The same conclusion applies to other mercury-contaminated areas in the Brazilian Amazon. Because most Amazonian rivers or their tributaries have favorable conditions for mercury contamination, we can expect the problem to persist in the Amazon for a long time, and the consequences are likely to become more significant in the future. These conclusions have important implications for all tropical rainforests where gold mining operations have caused extensive mercury pollution.     

Distribution of mercury in the atmosphere over Idrija, Slovenia

Idrija mine, the second largest mercury mine in the world, was in use since 1490. More than 107 000 tons of Hg were produced in its five centuries of history until 1990 when production was reduced to a few hundred kilos per year. The average recovery rate of mercury has been estimated to 73%; much of the remaining 27% was dissipated into the environment. In spite of present minimal levels of production, and only a few days of smelter operation per year, a real time survey with a mercury Zeeman analyser in a car showed relatively high mercury concentrations in the air. Amounts of 300--4000 ng Hg ^m-3 have been found around both the major sources of mercury vapour, the smelter and mine ventilation shaft -- while the amounts at the Old Place, at the City Museum, and near the Nikova-Idrijca confluence are of the order of 50 ng m^-3. Polluted air will be transported from those sources to a degree which depends on the weather conditions, mainly the direction and intensity of the wind. The high mercury contents in the air are not only due to anthropogenic sources (smelter and the ventilation shaft, dumps and smelter slag used in construction), but may also partly be natural as in the Pront area, where the outcropping bedrock contains native mercury.     

A 1955�C2004 record of Hg contamination in Dianshan Lake sediments, Shanghai

Measuring Hg levels of water sediments is one of the primary routes to assess the trend of the contamination. Little work has been carried out in the Yangtze Delta to track the trend of mercury contamination caused by Shanghai, which is one of the fastest growing economies in the world today. The mercury concentration in the sedimentary cores from Dianshan Lake, Shanghai is studied here. Results show that mercury transported to Dianshan Lake from emissions of coal combustion and non-coal sources in the Yangtze Delta was greater after 1979. We found also that before 1979 mercury levels changed less with time than after 1979. Before 1967 Hg levels were more variable than in the 1970s. Moreover, the mercury dissolved in river water and bound to particles of water that flow past downtown Shanghai is different from that observed in Dianshan Lake, which is located in upper Shanghai. This indicates that atmospheric Hg deposition is probably the main source of mercury in Dianshan Lake. These results are important for the establishment of environmental protections and pollution treatment proposals for mercury in similar areas of the world, as well as in Shanghai.     

Quecksilbergasfeinreinigung mittels metall- und salzpartikelbelegter Trägermaterialien (G/S-Reaktor) Ökotoxizität von Quecksilber und seiner Verbindungen

Waste and process gases from thermal power and metallurgical plants or such products from alkali-chloride industries contain metallic, inorganic and organic mercury. Widespread processes applied to remove the greatest amount of mercury are absorption and adsorption. Caused by the lowering of the emission limit from 200 to 50 μg/m³ [STP] by national and European legislators, considerable efforts have been made to enhance the efficiency of the main separation units of flue gas cleaning plants by applying the appropriate technological measures. This article is focused on the removal of mercury from waste gases. The state of engineering is described, especially with regard to enhancing the efficiency of separation in the raw gas, in wet, dry and quasi-dry processes as well as in tail-end process units. Specially impregnated ceramic carriers can be used for the selective separation of metallic, inorganic and organic mercury. Amalgamation has been investigated as a possible separation mechanism both experimentally and in theory. Using the ceramic reactor, removal rates for gaseous mercury and its compounds can be achieved which are even lower than 50 μg/m³ [STP]. The technology, the separation mechanisms and the ecological advantages through the use of ceramic reactors are presented in the article as well.     

Quecksilbergasfeinreinigung mittels metall- und salzpartikelbelegter Trägermaterialien (G/S-Reaktor) Ökotoxizität von Quecksilber und seiner Verbindungen

Waste and process gases from thermal power and metallurgical plants or such products from alkali-chloride industries contain metallic, inorganic and organic mercury. Widespread processes applied to remove the greatest amount of mercury are absorption and adsorption. Caused by the lowering of the emission limit from 200 to 50 µg/m³ [STP] by national and European legislators, considerable efforts have been made to enhance the efficiency of the main separation units of flue gas cleaning plants by applying the appropriate technological measures. This article is focused on the removal of mercury from waste gases. The state of engineering is described, especially with regard to enhancing the efficiency of separation in the raw gas, in wet, dry and quasi-dry processes as well as in tail-end process units. Specially impregnated ceramic carriers can be used for the selective separation of metallic, inorganic and organic mercury. Amalgamation has been investigated as a possible separation mechanism both experimentally and in theory. Using the ceramic reactor, removal rates for gaseous mercury and its compounds can be achieved which are even lower than 50 µg/m³ [STP]. The technology, the separation mechanisms and the ecological advantages through the use of ceramic reactors are presented in the article as well.     

中国城市汞污染及防治对策

简要综述了当前中国城市的汞污染状况。中国许多工业城市大气中的汞含量是纽约市大气中汞含量的数倍，甚至上百倍，在采暖期城市大气的汞污染更加严重；城市土壤中的汞含量是土壤环境背景值的数倍；河流的城市河段河水中汞质量浓度普遍很高，水质多在Ⅲ-V类；城市中的植物均有不同程度地受到汞污染，其汞含量高于国外城市的植物的汞含量；城市居民膳食中鱼的汞含量很高，对城市居民的健康产生了危害；城市居民头发中的汞质量分数大多低于1rng~kg。分析了我国城市中汞的来源并提出了防治城市汞污染的对策。     

Atmospheric mercury at mediterranean coastal stations

Mercury in air has been measured at five coastal Mediterranean sites, involving measurements in Spain, France, Italy, Slovenia and Israel. Four two-weeks long measurements campaigns were performed at the five sites. The measurements were carried out during autumn 2003 and winter, spring and summer 2004. Total gaseous mercury/elemental gaseous mercury, particulate mercury and divalent gaseous mercury were measured in parallel at the five sites. The activities constituted a subtask of the EU funded MERCYMS research project, which also included Mediterranean Sea cruises where both mercury in air and water were measured. The result from an evaluation of all the coastal air data is presented. Mercury concentrations from the different sites are compared with similar data obtained in northern Europe and elsewhere. The result shows that the background concentration of mercury in Mediterranean coastal air is lower than earlier anticipated. Background concentrations of TGM, RGM and TPM corresponded to 1.75–1.80 ng m⁻³, 1–13 and 3–23 pg m⁻³, respectively. The measurements also showed that the mercury concentration occasionally can be very high in some areas due to local anthropogenic emissions. It is proposed that diurnal variation in RGM concentrations observed during situation with nocturnal inversion merely is an effect of meteorology rather than due to local photochemistry.     

Determination of mercury and arsenic levels in fish caught in the Beheshtabad River,Chaharmahal and Bakhtiari Province,Iran

Mercury and arsenic pollution has been recognized as a potential environmental and public health problem for over 40 years. The major source of exposure to mercury for humans is the ingestion of fish. This study was conducted with the aim of determining the levels of mercury and arsenic in the muscles of four fish species caught in the Beheshtabad River and comparing the results with the maximum tolerance levels for mercury and arsenic. The samples of 90 fish were used for the determination of both the metals by graphite furnace atomic absorption spectrometry. The results showed that the concentrations ranged from 1.5 to 3.8 µg kg^?1 for mercury and from 35 to 70 µg kg^?1 for arsenic, with means of 2.7 ± 0.5 and 57 ± 12 µg kg^?1, respectively. Both mean levels were lower than the threshold limits acceptable by WHO standards.     

Research progress on occurrence forms and microbial transformation of mercury北大核心CSCD

汞是一种高毒性且具有持久性的重金属污染物,汞污染的治理与修复在近几十年一直是国内外研究热点.了解微生物对汞赋存形态的转化作用,对汞污染的治理与修复具有重要意义.总结汞的不同赋存形态、毒性及对应的常用分析方法,其中甲基汞(methyl mercury,MeHg)是毒性最强的汞形态之一.环境中汞的化学形态能发生转化,尤其以微生物驱动的汞的甲基化、MeHg的去甲基化和汞的氧化还原最为常见.依据汞转化类型将汞转化相关微生物分为汞甲基化、MeHg去甲基化、汞还原、汞氧化等类群,将对应的汞转化作用机制分为基于hgcAB基因的汞甲基化、基于mer操纵子基因的MeHg去甲基化和Hg2+还原、胞内过氧化氢酶介导的Hg0氧化.微生物汞转化过程不仅受到pH和温度的显著影响,而且还受到汞的赋存形态和游离汞的浓度、微生物种/群结构与功能、矿物种类、中间体和次生产物及其交互作用的影响,基于此,提出正确客观表征汞的微生物转化过程需要综合分析微生物组和矿物组的变化规律及其交互作用的综合效应.针对酸性矿山废水(AMD)极端环境微生物汞转化研究的不足,未来的工作将聚焦结合多组学手段、同步辐射谱学和密度泛函理论(DFT)计算等分析技术研究汞赋存形态的微生物转化过程,分析和阐明汞转化中间体的键合作用方式和转化机制,从而为AMD汞污染的预防、治理和修复提供依据.(图2表2参107)     

Preliminary study on health risk from mercury exposure to residents of Wujiazhan town on the Di’er Songhua river, Northeast China

Mercury concentrations in hair are typically used as a biomarker to assess exposure to mercury. A total of 108 hair samples were collected from residents (age range 5–73 years) of Wujiazhan town, northeast China, to determine total mercury concentrations. Hair mercury concentrations ranged from 0.16 to 199 mg kg^–1 with an average value of 3.41 mg kg⁻¹. The relationships between mercury concentration and gender and between hair mercury concentration and age were not significant. Overall, 16.7% of all samples were above the RfD value published by the United States Environmental Protection agency. The results indicate that there may be some been health risk from mercury exposure to the residents in the study area.     

Efficient mercury recovery from mercuric-thiosulfate solutions by ultraviolet photolysis

Mercury-containing wastes are hazardous due to the high toxicity and bio-accumulative effect of mercury. Examples of mercury-containing wastes include fluorescent light bulbs, thermostats, and thermometers. Recently, several aqueous-phase methods have been developed to extract mercury from mercury-containing wastes. However, the slow kinetics of mercury recovery limits the application of the aqueous-based technology. Here we designed a method of mercury recovery from a mercuric-thiosulfate solution assisted by ultraviolet photolysis. We evaluated the effect of initial pH, thiosulfate concentration and temperature on ultraviolet photolysis. The precipitation products were characterized by X-ray diffraction and X-ray photoelectron spectroscopy (XPS). Results show a mercury recovery ratio of 87.94% after ultraviolet photolysis during 240 min. We conclude that mercury can be efficiently recovered from mercuric-thiosulfate complex solutions by ultraviolet photolysis.     

Acute toxicity of mercury to the fingerlings of Indian major carps (catla, rohu and mrigal) in relation to water hardness and temperature

In the present study short-term (96 hr) toxicity of mercury in relation to water hardness (270 and 560 mg/l) and temperature (16 degrees C and 35 degrees C) to the fingerlings of Indian major carps, i.e. catla, rohu and mrigal has been evaluated using static bioassay. The LC5o indicates that both water hardness and temperature played significant role in mercury toxicity. The test fishes were found most resistant with water hardness of 560 mg/l at 16 degrees C as compared to that of water hardness of 560 mg/l at 35 degrees C and water hardness of 270 mg/l at both the temperatures, i.e. 35 and 16 degrees C. Whereas the order of relative sensitivities of these fishes for mercury ions were recorded as catla>rohu>mrigal. The safe concentrations of mercury were ranged in between 12.133 to 19.689 microg/l for catla; 64.039 to 82.555 microg/l for rohu and 73.510 to 89.585 microg/l for mrigal for both the water hardness and temperature.     

Mercury budget estimates for the State of New York

The development of two comprehensive modelling systems and a test application to estimate the mercury budget for the State of New York is discussed in the present study. The modelling tools developed are based on two well known meteorological modelling systems namely, RAMS and SKIRON/Eta. Both models have been modified and the developed modules describing the physico-chemical processes of mercury have been incorporated in each modelling system. Model calculations and measurements have been compared during the 14 to 26 August 1997 simulation period. Two different simulations were performed, scenario1 where all available sources of mercury were used and scenario2 where the New York State mercury sources were excluded. An attempt was made to identify and quantify critical gaps in the current understanding of regional scale transport deposition and fate of mercury in New York State, improving modelling capabilities and understanding of mercury as an air pollutant, and provide a tool for policy makers in mitigating the impacts of mercury pollution.     

广东柘林湾养殖海域沉积物中汞的分布、累积及其生态风险

柘林湾是广东省养殖规模最大的海湾之一,为了解养殖海域沉积物中汞的分布、累积及其可能产生的生态风险,于2008年1月在柘林湾海域采集了5个站位的柱状沉积物和3个站位的表层沉积物,对其中的总汞含量进行了测定,并对其含量分布、累积特征进行了分析.结果表明,柘林湾海域表层沉积物中总汞平均含量为0.0645μg·g-1,径流输入是其空间分布特征的主要影响因素;柱状沉积物表层部分总汞含量相对较低,但不同采样区域柱样中总汞含量的垂直分布却有着显著的差异,网箱养殖区主要是由于汞近40年来来源变小导致沉积物表层部分中的总汞含量较底层低,而贝类养殖区则由于沉积后的再迁移作用使汞在氧化还原边界层富集累积;利用潜在生态危害指数法和沉积物质量基准法对此次调查的沉积物中汞的潜在生态风险进行的评价表明,汞虽对底栖生物基本无负面效应,但其潜在生态风险程度达到了中等水平,尤其是养殖区2号站位28～36cm、4号站位20～32cm和48～56cm以及6号站位36～56cm柱样中的汞甚至达到了高的潜在生态风险程度.因此,养殖区次表层沉积物中较高含量的汞应当引起足够重视.