中国金矿开采区环境汞污染

汞是金矿区环境的特征污染物。金汞同源性导致金矿床一般汞含量偏高,且在以混汞法为代表的提金过程影响下,导致了中国金矿区严重的环境汞污染问题。本文介绍了中国金矿分布与开采及选冶概况,研究了导致金矿区环境汞污染的原因,分析了金矿石选冶过程中汞的释放,并综述了金矿开采所致矿区土壤、水体、大气、生物体中汞污染状况,最后讨论了金矿区汞污染环境管理与生态修复。     

光氧化反应脱汞技术发展综述

燃煤电厂烟气中汞污染的控制技术研究是目前重要的环保课题之一。气相元素汞成为大气中汞污染的主要来源。文章分析了光氧化反应脱汞技术(包括光化学氧化反应和光催化氧化反应)的反应机理,认为光化学氧化反应技术脱汞均是在紫外光作用下,产生具有强氧化性的基态原子或自由基,将难以脱除的Hg0氧化为高价汞,再通过配套的电除尘器等设备将高价汞捕集,进而达到汞污染控制的目的。不同的是,在光化学氧化反应中,汞的氧化需要借助于电厂烟气中的O2、H2O等成分,而在光催化氧化反应中,反应需要在光催化剂(TiO2或TiO2负载复合物等)的催化作用下进行。阐述了光氧化反应汞脱除技术研究进展。光氧化反应脱汞技术的汞脱除率均可达到60%~70%,具备设备简单、无二次污染等优点。     

粒级、pH和有机质对汞在松花江沉积物表面吸附-解吸的影响

为进一步揭示汞在松花江沉积物表面的环境行为,通过模拟实验,研究粒级、pH和溶解性有机质(DOM)对汞在松花江沉积物表面吸附-解吸量的影响.结果表明,不同粒级沉积物的吸附能力差别较大,本实验条件下,沉积物粒级越小,其吸附能力越强.在各种浓度的实验设计组中均有:pH由3.5升高至4.5时,吸附量增加,当pH4.5时,随pH的继续升高吸附量开始降低;沉积物中汞的解吸量随pH的增加呈先下降后上升的趋势变化,各体系的最小值均出现在pH5.柠檬酸对沉积物吸附汞的影响以抑制作用为主,其抑制作用强度与吸附体系中汞浓度有关;柠檬酸对解吸量的影响也比较明显,随着柠檬酸浓度的增加,对沉积物中汞解吸作用的影响表现为促进-抑制-稳定的变化趋势.因此,以上因素对汞在沉积物表面吸附-解吸的影响较大,在进行河流汞污染控制及突发污染事件处理时,有必要充分考虑以上因素的影响.     

街区建筑物对城市交通隧道废气排放的影响

采用大气边界层模式和随机游动扩散模式相连接的模拟方法,对上海市拟建的交通隧道排气口附近街道建筑物区域的气流分布和废气排放物浓度场进行了数值模拟分析,设计了6种方案,并按不同的废气排放形式,分别分析了街区的地面污染物质量浓度分布.结果表明,在建筑物存在的情况下,排风口造成的地面污染物质量浓度的最高值会很大,可达0.44 mg/m3,若换成排风塔,则为0.13 mg/m3; 没有建筑物的情况下,由排风口和排风塔造成的地面污染物最高质量浓度分别为0.11 mg/m3,0.4 mg/m3.当风速增大,质量浓度会降低,最大值分别从0.44 mg/m3降为0.2 mg/m3,和从0.13 mg/m3降为0.1mg/m3.分析表明,建筑物附近的气流特征对污染物扩散会起引导作用: 垂直方向上,导致污染物从高空被带入地面; 水平方向上,使得污染物在下风向堆积; 当风速增大时,地面污染物质量浓度值降低.同时研究表明,对排风塔污染物散布起主要作用的是水平方向的气流结构,而对排风口的污染物散布起主要作用的则是其附近建筑物的背风侧的气流下洗效应和水平流场,因此建筑物背风侧有可能成为重污染区.     

西藏拉萨市土壤气中氡、汞环境地球化学特征

研究了拉萨市及其附近土壤气中的氡、汞地球化学特征,利用地质累计指数法评价了其环境质量.1?579个测点的测量结果表明,土壤气中氡、汞的背景值分别是7?634.9 Bq/m³、41.5 ng/m³,标准偏差分别为2.7 Bq/m³、2.2 ng/m³.土壤气氡环境质量在研究区东部和西部比较好,在中部从南向北有逐渐加重的趋势,最高达到中度污染;氡的主要污染源是山间盆地沉积物中局部富集的放射性铀元素.从拉萨郊区向市中心,土壤气汞污染程度逐渐增加,最高达到严重污染;污染源主要是废气中的汞、宗教活动中使用的汞以及含汞的垃圾和废水.     

第二松花江中下游沉积物汞的时空变化规律

将1973、1976、1983、1991年和本次的研究结果进行对比分析,得出了第二松花江中下游表层沉积物汞含量的时间变化规律.1976年以前汞含量处于增加趋势;1976～1982年汞含量有所下降;1982年汞污染源被切断,汞含量骤降;随后,汞污染浓度处于缓慢净化时期.将本次采集的沉积物样品分为3个粒度等级,最后以63 μm粒级的沉积物汞含量为代表分析了汞的水平变化规律,总体趋势是,排污口处汞含量最高;哨口至朝阳桥断面汞含量增加;朝阳桥至五家站断面,汞含量骤降,在五家站断面汞含量达到最小值;五家站至泔水缸断面汞含量又略有增加.并给出了本次研究中各断面沉积物汞的垂直变化规律.     

基于我国规范与PIARC标准的公路隧道需风量分析

以某长大高速公路隧道为例,结合我国隧道通风设计规范JTJ026.1-1999与PIARC2007标准(世界道路协会),针对不同行车速度,不同车辆更新情况、不同排放标准组合形式以及是否考虑NOx等情况,对各个不同工况的需风量分别进行计算,并从需风量计算方法、机动车排放量和污染物设计浓度三个方面对隧道需风量差异进行分析。研究结果表明:我国设计规范与PIARC2007存在较大差距,为了适应当前及今后我国交通量及机动车排放特点的发展趋势,我国现行规范应在机动车排放量、污染物设计浓度限值等方面做出必要改进以达到合理确定隧道需风量的目的。     

Transport and fate of mercury under different hydrologic regimes in polluted stream in mining area

Seepage from Hg mine wastes and calcines contains high concentrations of mercury (Hg). Hg pollution is a major environmental problem in areas with abandoned mercury mines and retorting units. This study evaluates factors, especially the hydrological and sedimentary variables, governing temporal and spatial variation in levels and state of mercury in streams impacted by Hg contaminated runo . Samples were taken during di erent flow regimes in theWanshan Hg mining area in Guizhou Province, China. In its headwaters the sampled streams/rivers pass by several mine wastes and calcines with high concentration of Hg. Seepage causes serious Hg contamination to the downstream area. Concentrations of Hg in water samples showed significant seasonal variations. Periods of higher flow showed high concentrations of total Hg (THg) in water due to more particles being re-suspended and transported. The concentrations of major anions (e.g., Cl??, F??, NO3?? and SO4 2??) were lower during higher flow due to dilution. Due to both sedimentation of particles and dilution from tributaries the concentration of THg decreased from 2100 ng/L to background levels (< 50 ng/L) within 10 km distance downstream. Sedimentation is the main reason for the fast decrease of the concentration, it accounts for 69% and 60% for higher flow and lower flow regimes respectively in the upper part of the stream. Speciation calculation of the dissolved Hg fraction (DHg) (using Visual MINTEQ) showed that Hg(OH)2 associated with dissolved organic matter is the main form of Hg in dissolved phase in surface waters in Wanshan (over 95%).     

Silver impregnated carbon for adsorption and desorption of elemental mercury vapors

The Hg0 vapor adsorption experimental results on a novel sorbent obtained by impregnating a commercially available activated carbon (Darco G60 from BDH) with silver nitrate were reported. The study was performed by using a fundamental approach, in an apparatus at laboratory scale in which a synthetic flue gas, formed by Hg0 vapors in a nitrogen gas stream, at a given temperature and mercury concentration, was flowed through a fixed bed of adsorbent material. Breakthrough curves and adsorption isotherms were obtained for bed temperatures of 90, 120 and 150°C and for Hg0 concentrations in the gas varying in the range of 0.8–5.0 mg/m3. The experimental gas-solid equilibrium data were used to evaluate the Langmuir parameters and the heat of adsorption. The experimental results showed that silver impregnated carbon was very effective to capture elemental mercury and the amount of mercury adsorbed by the carbon decreased as the bed temperature increased. In addition, to evaluate the possibility of adsorbent recovery, desorption was also studied. Desorption runs showed that both the adsorbing material and the mercury could be easily recovered, since at the end of desorption the residue on solid was almost negligible. The material balance on mercury and the constitutive equations of the adsorption phenomenon were integrated, leading to the evaluation of only one kinetic parameter which fits well both the experimentally determined breakthrough and desorption curves.