共查询到19条相似文献，搜索用时 191 毫秒
1.
矿渣和酸性矿山废水的排放会使矿区周围的农田受到污染。为研究厌氧条件下矿区农田中氮和砷之间的联系,本文通过摇瓶实验探究了含砷水铁矿在厌氧含氮农田中释放的砷形态的变化,通过柱实验探究了水稻生长对氮、砷形态和浓度的影响。研究结果发现,在厌氧条件下,外源氮的加入促进了砷污染水稻土中As(Ⅴ)的还原,使生成的As(Ⅲ)浓度最高达396μg/L;在柱实验模拟的厌氧农田不同层位中,水稻的生长过程促进了氮和砷的还原以及砷向下层位的迁移,使装置中的As(Ⅲ)浓度最高达517μg/L;摇瓶实验和柱实验在相近的厌氧条件下,NO-3的存在能够直接参与As(Ⅴ)还原。研究结果为农田砷污染的治理提供了一定的参考价值。 相似文献
2.
北方典型内陆盆地高砷地下水的水化学特征及处理技术 总被引：1，自引：0，他引：1
我国高砷地下水分布广泛,是受砷污染最严重的地区之一,严重危害居民身体健康,开发经济、高效、环境友好的高砷地下水修复治理技术极具必要性。以大同盆地、呼包平原、河套平原和银川平原为代表性研究区域,归纳总结了北方干旱、半干旱地区典型高砷地下水区水化学特征。通常情况下,高砷地下水的pH值较高,共存阴离子(HCO-3、SO2-4和Cl-)浓度较大,溶解性有机碳含量较高,并且As(Ⅲ)为主要砷形态。开展了针对北方典型高砷地下水特定水化学环境特点(如pH值、共存阴阳离子以及溶解性有机物等)的改性天然菱铁矿除砷性能研究。结果表明,改性天然菱铁矿对溶液pH值具有良好的缓冲能力,其除砷性能基本不受pH值、共存阴离子、Ca/Mg阳离子及以腐殖酸为代表的溶解性有机物等典型高砷地下水水化学特征因素的影响,表明吸附剂对砷具有良好的吸附选择性。另外,改性天然菱铁矿对As(Ⅲ)的去除效果优于对As(V)的去除效果,因此,利用改性天然菱铁矿作为反应介质材料,将其应用于处理主要以As(Ⅲ)形式存在的高砷地下水具备良好的发展前景。 相似文献
3.
内蒙古河套平原是世界地方性砷中毒较为严重的地区之一。笔者以平原西部的重病区杭锦后旗为研究区,对高砷地下水赋存环境进行了调查研究。研究表明:高砷区沉积物中As的含量为7.7～34.6mg/kg,其中粘性土和亚粘性土中As含量相对较高。高砷地下水的pH值为7.0～8.3,平均Eh值为-155.1mV,平均矿化度为1.58g/L,主要的水化学类型包括:Cl-HCO3-Na型、Cl-Na型、HCO3-Cl-Na型,As的含量为15.5～1093μg/L,且主要以As(Ⅲ)形态存在,水中DOC(0.73～35.76mg/L)、HCO3-(283.75～1290.48mg/L)、NH4+(0.27～10.48mg/L)的浓度较高,硝酸盐和硫酸盐含量较低。研究区的氟中毒现象也较严重,高氟地下水中氟含量为1.11～6.01mg/L。绝大多数高氟水中砷含量也超标,出现了一种高砷水与高氟水并存的现象。综合判断,河套平原的高砷地下水赋存环境处于还原性环境。还原条件下,高砷区沉积物中的铁/锰氧化物的还原溶解易使吸附的砷释放到地下水中。这是研究区高砷地下水形成的主要原因。 相似文献
4.
江苏泗阳城区浅层地下水化学特征及其影响因素 总被引：2，自引：0，他引：2
根据现场取样分析,对江苏泗阳城区浅层地下水水文地质特征、水化学组分在空间上的分布特征进行了研究,并对其形成特点和影响因素进行探讨。结果表明：研究区浅层地下水水化学类型呈现明显的平面分带性,京杭运河西南侧浅层地下水阴离子中HCO-3占主导地位,溶解性总固体(TDS)多小于1 g/L,总硬度小于450 mg/L,水质一般较好;京杭运河东北侧浅层地下水阴离子以HCO-3、Cl-、SO2-4为主,TDS多介于1~3 g/L,总硬度大于450 mg/L,为微咸水,水质变差。研究区NH+4-N、NO-3-N污染较明显,空间分布具有明显的地域性差异;高浓度分布在京杭运河两岸以及泗阳农场一带,纵向上NH+4-N高浓度主要集中在小于18 m的浅层地下水,NO-3-N多在8~20 m的浅层地下水富集。研究区浅层地下水水化学组分现状特征及其差异性的形成与演化,受海陆交互相沉积环境、含水介质、地下水补径条件以及人类活动等因素的影响。 相似文献
5.
江汉平原被确认为我国南方新的饮水型砷中毒病区,目前对于江汉平原高砷地下水的成因机理研究还有待完善.综合运用水文地球化学分析与PHREEQC地球化学模拟计算,分析了地下水和沉积物中REE分异特征及其沿地下水流向形态变化规律.江汉平原地下水REE含量为0.032~0.843 μg/L,富集LREE,具显著Eu正异常,且地下水中Eu异常与As含量呈正相关关系.地下水中REE形态主要以LnCO3+及Ln(CO3)2-为主,沿地下水流向LnCO3+降低、Ln(CO3)22-升高.地下水REE浓度分布受到HCO3-的络合作用及Fe氧化物矿物的还原性解吸附过程控制,径流途径中继承沉积物矿物的REE配分模式及Fe氧化物矿物对LREE的优先解吸附可能是地下水富集LREE的原因,并且沿流向上REE形态分布受到pH控制.研究区中Eu含量及Eu正异常对地下水As富集程度具有一定的指示意义. 相似文献
6.
湖南石门雄黄矿区黄水溪砷昼夜变化及藻对砷释放影响研究 总被引：1，自引：0，他引：1
湖南石门黄水溪受历史雄黄矿区污染严重,溪流中砷昼夜变化及藻-砷矿物水岩作用昼夜规律的研究对认识该流域中砷的迁移行为和控制污染具有重要意义。本研究野外调查了砷浓度的昼夜变化及其水化学参数,实验分离出黄水溪藻种并且模拟了光合作用下藻的生长与砷矿物(雄黄)释砷动力学过程。研究结果表明,黄水溪流中砷浓度范围在0.8～1.1 mg/L之间,夜晚降低,白天上升,且湖口处砷分层效应最为明显,温度、pH值、溶解氧及碳酸根含量与砷浓度变化规律一致,但叶绿素a和碳酸氢根含量与砷浓度变化规律相反;黄水溪藻种丰富,分离获得了小球藻、水绵、栅藻等多种藻类;在实验中,相比于纯雄黄,低浓度藻能够促使每克雄黄在48 h作用后释放182.1 mg的As(Ⅲ)和459.3 mg的As(V);中浓度藻存在显著的吸收现象,且As(Ⅲ)优于As(V);高浓度藻促进雄黄释放,显著提高As(V)释放量,是纯雄黄释放的2.9倍。本文实验结果表明,昼夜变化能改变砷的浓度和价态,其中藻的存在起着重要的作用。 相似文献
7.
实验室合成制得的纳米铁BET比表面积为49.16 m2/g, 直径范围为20~40 nm.通过批实验考察纳米铁对As(Ⅲ)吸附动力学情况.结果表明, 在20℃、pH为7时, 纳米铁能够快速地去除As(Ⅲ), 在60 min内, 0.1 g纳米铁对起始浓度为910 μg/L溶液As(Ⅲ)去除率大于99%.反应遵循准一级反应动力学方程, 标准化后的As(Ⅲ)速率常数kSA为2.6 mL/(m2·min).纳米铁对As(Ⅲ)的吸附等温曲线能够很好地满足Langmuir和Freundlich方程, 相关系数R2＞0.95, 由Langmuir模型获得单层纳米铁的最大吸附量为76.3 mg/g.0.1 mol/L NaOH对吸附在纳米零价铁(NZVI)的As(Ⅲ)解吸率为21%.在竞争阴离子中, SiO32-和H2PO4-对As(Ⅲ)的去除有明显阻碍作用, 而其他离子基本上没有影响.纳米铁对As(Ⅲ)的去除机理主要是吸附和共沉淀. 相似文献
8.
为探析长江口沉积物-水界面砷的迁移转化机制,本文分析了2019年夏季长江口4个站位上覆水和间隙水中总As浓度及形态的剖面变化特征,耦合氧化还原敏感元素(Fe、Mn和S)的剖面变化剖析了沉积物-水界面砷循环的Fe-Mn-S控制机制,同时结合砷相关功能基因探讨了沉积物-水界面砷迁移转化的微生物调控过程,估算了沉积物-水界面总As的扩散通量。结果表明,除A7-4站位外,长江口其他3个站位间隙水总As以As3+为主要存在形态,且总As浓度均在上覆水中为最低值(0.748~1.57 μg·L-1),而在间隙水中随着深度增加而逐渐增加并在6~9 cm深度达到峰值(7.14~26.9 μg·L-1)。间隙水总As及As3+浓度的剖面变化趋势与溶解态Fe2+、Mn2+相似,其均在中间层出现高值,说明沉积物Fe/Mn还原带砷的释放可能是随固相Fe(Ⅲ)或Mn(Ⅳ)的还原而转移到间隙水中的。氧化层和Fe/Mn还原带过渡区间隙水砷浓度与砷异化还原菌功能基因arrA和arsC丰度存在对应关系(除A1-3站外),说明砷异化还原菌将溶解As5+或固相As5+还原为溶解As3+可能是该过渡层砷迁移转化的另一重要过程。硫酸盐还原带的间隙水总As和As3+浓度降低,但由于间隙水的低S2-浓度不利于砷硫化物生成,因此深层间隙水砷可能与铁硫矿物结合而被移除。底层环境氧化还原条件是影响沉积物-水界面砷迁移转化的重要因素,随底层水DO浓度的降低,砷迁移转化更倾向于微生物还原控制。长江口沉积物-水界面总As的扩散通量为1.18×10-7~2.07×10-7 μmol·cm-2·s-1,均表现为沉积物间隙水中总As向上覆水释放,即沉积物是研究区域水体总As的来源之一。 相似文献
9.
江汉平原高砷地下水与含水层沉积物的地球化学特征 总被引：1，自引：0，他引：1
通过采集江汉平原沙湖原种场典型高砷地下水区的27个地下水样品、6个地表水样品和不同深度的沉积物样品,采用X射线荧光光谱、离子色谱、TOC分析仪以及沉积物平行提取方法对该区含水层的水化学特征以及沉积物的地球化学特征进行了分析。结果表明:该区地下水水化学类型主要为HCO_3-Ca·Mg型,属中性偏弱碱性水;氧化还原电位较负,NH+4-N、HS-和Fe(Ⅱ)质量浓度较高,指示地下水的强还原环境;地下水As质量浓度平均值为74.39μg/L,最大值达580.77μg/L,出现在地面以下25m位置,且As(Ⅲ)质量浓度普遍高于As(V)。随深度增加,沉积物中w(As)呈先增加后减小的趋势,在17.4m(黏土层)深度处达到最大(21.15mg/kg),且w(As)随深度的变化与沉积物中TOC、Fe_2O_3、Al_2O_3质量分数以及沉积物比表面积随深度的变化呈现相同的趋势,采用SPSS软件经相关分析亦表明As与TOC、Fe_2O_3、Al_2O_3和比表面积具有较强的相关关系,相关系数分别为0.70,0.68,0.70,0.67,揭示砷在富含有机质、铁铝氧化物及比表面积大的黏土层沉积物中更易富集。沉积物平行提取实验结果表明,江汉平原沉积物中的砷主要以强结晶态铁氧化物、溶解态硫化物和反应性硅酸盐的形式存在。 相似文献
10.
江汉平原高砷含水层沉积物地球化学特征 总被引：2，自引：0，他引：2
选取江汉平原典型地下水砷中毒区仙桃市沙湖原种场为研究区,对3个长50m的钻孔沉积物砷含量与赋存形态及其他化学组成进行了分析。结果表明区内沉积物砷质量分数为1.35~107.5mg/kg(平均值为12.8mg/kg)。黏土或亚黏土层中砷含量较高,这与细粒沉积物中铁锰氧化物、黏土矿物对砷的吸附有关。地下20m左右深度内含水层沉积物中砷含量最高,相应地下水中砷质量浓度高达到1 000μg/L。草酸-草酸铵选择性提取结果指示沉积物中10%~77%(平均38%)的As与无定形铁氢氧化物结合,表明无定形铁氢氧化物还原性溶解可能是控制砷释放与还原的主要地球化学过程,并且有机质生物氧化机制极大地促进了该过程。然而,沉积物中仅1.2%~23%的铁被草酸-草酸铵提取,含水层中砷浓度主要受铁的氢氧化物还原性溶解影响,但其他形式的铁、有机物的吸附作用亦控制着砷的含量。 相似文献
11.
S. L. Wang C. Y. Lin X. Z. Cao X. Zhong 《International Journal of Environmental Science and Technology》2012,9(1):31-40
The Nansi Lake has been seriously affected by long-term intensive industrial and urban activities. The objectives of this study were to determine the content, distribution, and ecological risk of arsenic and investigate the geochemical relationships between arsenic forms and sediment mineral phases of the Nansi Lake. Twenty samples of surface sediments were collected and analyzed for arsenic contents and chemical forms. Results indicated that total content of arsenic in the sediment samples averaged 13.45?mg/kg and ranged from 8.27 to 21.75?mg/kg. The arsenic was mostly associated with iron oxides (67.3%), followed by the association with the residual fraction (19.2%). In addition, total content of arsenic was positively correlated with the organic matter and iron contents in the sediment. The molar ratios of iron oxide bound arsenic content to iron content are lower than the maximal molar ratios of arsenic to iron for natural hematite, magnetite, and goethite. The total content of arsenic in the sediment samples was usually higher than threshold effect concentration of 9.79?mg/kg, but lower than probable effect concentration of 33.0?mg/kg for arsenic in freshwater sediments. Adverse effects or toxicity to the aquatic organisms, caused by arsenic in the sediments of the Nansi Lake, will likely occur at these levels of arsenic contamination. 相似文献
12.
P. K. Govil J. E. Sorlie D. Sujatha A. K. Krishna N. N. Murthy K. Rama Mohan 《Environmental Earth Sciences》2012,66(1):121-128
Spatial distribution and temporal trends studies were carried out at Katedan Industrial Development Area (KIDA) near Hyderabad,
capital of Andhra Pradesh state, India under Indo-Norwegian Institutional Cooperation Program, to find out the extent of contamination
in streams and lake sediments from the discharge of industrial effluents. Stream and lake sediment samples were collected
from the five lakes in the study area and connecting water streams. The samples were analyzed by XRF spectrometer for toxic
elements. The studies reveal that the stream sediments with in the KIDA and the impounded Noor Mohammed Lake down stream have
high concentration of some of the toxic elements like chromium, nickel, lead, arsenic, zinc etc. The geology of the area indicates
that the study area consists of residual soil of acidic rocks, which are predominantly of Archaean gneisses and granites having
low to medium concentrations of chromium and nickel. The source of these high concentration of elements like lead 2,300 mg/kg,
copper 1,500 mg/kg, arsenic 500 mg/kg, chromium 500 mg/kg etc. cannot be derived from the surrounding acidic rocks and may
be attributed to the industrial effluents released in the ditches and random dumping of hazardous solid waste. It was observed
that the metal concentrations increased in the streams during the dry season (pre-monsoon period). After the monsoon rains,
the metal concentrations in the streams were reduced by half which may be due to dilution. The eroded sediments are deposited
in the lake where very high concentrations were encountered. Overflowing of the lake will spread the contamination further
downstream. The lake sediments will remain as a major source of contamination by desorption to the water phase regardless
of what happens to the effluent discharge in the KIDA. However, some samples showed enrichment of lead, arsenic and nickel
during post-monsoon, which were collected near the dumpsite due to the leaching of toxic elements from the dump site to the
lakes. Some of the toxic elements like nickel and copper have not shown any dilution but have increased after the rains, which
could be due to the leaching of arsenic from the dumpsite to the lake along with rainwater. Geochemical maps showing the distribution
of heavy/trace elements in streams and lakes are prepared and presented in this paper. Effect of toxic elements on the health
of the residents in the surrounding residential areas is also discussed. 相似文献
13.
青海湖沉积物中的甾醇及其演化 总被引：3，自引：0，他引：3
Ｃ２７，Ｃ２８和Ｃ２９甾醇（△５.２２，△２２，△５和△５.２４（２８）和５α－甾烷醇）在青海湖三孔近代沉积物（ＱＨ，ＱＥ和ＱＯ）中被检出。其中以Ｃ２９甾醇占优势。在ＱＥ和ＱＧ孔沉积物中还检出了低浓度的三个Ｃ３０甾醇（４α，２３，２４－三甲基－５α－胆甾－２２Ｅ－烯醇（甲藻甾醇），４α－甲基－２４－乙基－５α－胆甾－２２Ｅ－烯醇和４α－甲基－２４－乙基－５α－胆甾烷醇］。在ＱＨ和ＱＧ孔上部层段沉积物中，Ｃ２７，Ｃ２９.饱和的和不饱和的甾醇的碳数分布的平行性，甾烷醇/△５－甾醇及△２２－/△５.２２－甾醇的比值随沉积物埋深而增加提供了甾酸氢化作用的间接证据。青海湖沉积物中的甾醇主要来自湖区丰富的高等植物和湖中的藻类等。在ＱＧ孔８０～１００ｃｍ和１２０～１４０ｃｍ层段沉积物中，５ａ－胆甾烷醇浓度迅速增加可能反映特殊的生物（介形类）对该二层段沉积物中高浓度的胆甾烷醇的贡献。 相似文献
14.
采用地震约束测井、测井标定和校正地震,二者相互动态调整的方法,对冀东高尚堡油田深层地层进行了深入的层序地层学研究：将Es2+33地层划分为1个层序、2个体系域、6个准层序组和16个准层序;总结了层序界面特征,将Es23和顶部大套厚层泥岩作为目的层段层序研究的一般标志Es43层,但是陆相沉积特有的复杂性,使得其识别难度很大;探讨了地层层序特征,认为目的层有两处沉积中心,其总体延伸方向近东西向。下部湖退体系域形成于湖盆收缩期,以G35-1、G62井区和G82井区沉积为中心,地层最厚;上部湖进体系域形成于湖盆大面积扩张时期,其沉积中心（G30-28井区以及G13-13井区）相对于下部体系域两个沉积中心,分别向北和东迁移。 相似文献
15.
接触氧化技术在公园景观水体功能恢复中的运用试验研究 总被引：1，自引：0，他引：1
通过自行设计加工的试验装置,进行生物接触氧化技术在景观水体功能恢复中的试验研究。待处理的景观水体ρ(CODCr)为25~35 mg/L,ρ(NH3-N)为2.2~3 mg/L,ρ(TP)为0.55~0.85 mg/L,有机负荷低,且水质变化幅度大。试验结果表明,在合适的运行参数下,生物接触氧化技术可以使经过处理的景观水体的ρ(CODCr)、ρ(NH3-N)、ρ(TP)分别降至14.62 mg/L、0.26 mg/L、0.19 mg/L,满足地表水Ⅲ类水质标准,达到景观水体水质要求。 相似文献
16.
达则错位于班怒构造带的次级盆地中,湖水最深为36 m,平均深度为20.8 m。湖表水体矿化度17.27~20.27 g/L,平均为19.46 g/L,水化学类型为(CO3+HCO3)·SO4-Na型,属弱度碳酸盐型咸水湖;在垂向上,由浅及深矿化度略有增加,水化学类型不变。湖表水体铀浓度264~324μg/L,平均铀浓度为286μg/L,8 m、18 m和28 m深度铀浓度平均值分别为288μg/L、290μg/L和300μg/L。湖底沉积物铀含量为2.31~4.08μg/g,平均铀含量为3.16μg/g,略高于我国东海大陆架海底沉积物的铀含量。达则错湖水的铀元素来自于周边岩体和地层,通过河水迁移到湖泊中。在河口混合带,铀酰离子部分吸附于悬浮物上,到湖区以碳酸铀酰的形式存在于水体中,沉淀于湖底的悬浮物铀含量没有明显增加。 相似文献
17.
Iron transformations in a calcium carbonate rich fresh-water sediment were studied by analyzing the relevant constituents of both interstitial water and solid matter. Analysis of interstitial water shows that the observed redox sequence NO−3/NH+4, MnO2/Mn(II), FeOOH/Fe(II), SO2−4/S(−II) is roughly in agreement with that predicted by the Gibbs Free Energy for the corresponding reactions. In contrast to marine sediments, these redox transitions occur in the uppermost sediments, i.e., at depths of 0–4 cm.
Deeper in the sedimentary sequence, the depth profile for dissolved iron exhibits a steady non-linear increase up to 400 μmol dm−3. In this anoxic zone, according to thermodynamic predictions, iron (II)-minerals such as iron sulfide, siderite, and vivianite should precipitate while Fe(III) oxides should be completely dissolved. However, microscopic analysis showed that Fe(III) oxides were present throughout the studied sediment. Furthermore, scanning electron microscope/energy dispersive spectroscopy analysis suggests the presence of iron sulfide could be verified but not that of siderite or vivianite. These observations indicate kinetic control of iron transformations.
We have investigated the importance of kinetic control of iron distribution in anoxic sediments using a diagenetic model for dissolved iron(II). A rough estimate of time scales for dissolution and precipitation rates was made by imposing limiting boundary conditions. Using the calculated rate constant, we established that more than 1000 years would be required for the complete dissolution of Fe(III) oxides, which is agreement with our observations and experimental data from the literature. Calculated precipitation rates of Fe(II) for a given mineral phase such as siderite yield a maximum value of 3 μg(FeCO3) g−1(dry sediment) yr−1. Such low rates would explain the absence of siderite and vivianite.
Finally, it can be inferred from the MnT/FeT ratio in the sediments that this ratio depends on the redox conditions of the sediment-water interface at the time of deposition. Thus, this ratio can be used as “paleo-redox indicator” in lacustrine sediments. 相似文献
18.
通过对长江下游镇扬段的牛轭湖—内江的泥沙、水质、光强、藻类等进行现场监测和数据分析,探讨了内江悬浮泥沙对水下光强的衰减规律以及对藻类生长的影响。结果表明:内江水体中存在80%以上的粒径小于75μm的微细悬浮颗粒,其中不易沉降的粘土颗粒占到20%～50%左右,枯水期平均含量为40 mg/L,丰水期平均含量为70 mg/L,而藻细胞生物总量基本都在100万个/L以内,其中绿藻、硅藻为优势种。数据分析表明:泥沙对水下光强的衰减遵循指数函数衰减规律,光衰减系数与泥沙含量呈较好的线性相关性,内江的优势种绿藻、硅藻的生物量与泥沙含量呈显著的指数相关。认为,泥沙通过衰减光强间接地抑制藻类繁殖,这一抑制作用可以由泥沙含量和藻细胞密度之间的关系进行定量。 相似文献
19.
Lake sediments are integrators of watershed wide environmental information that includes bedrock geology, glacial overburden, vegetation, hydrology and land use. Lake sediments were collected from an area covering approximately 13,600 km2 from the Gowganda and Temagami regions to determine the geochemical background conditions representing different bedrock types. For the entire dataset, the median value for arsenic in lake sediment was 2.6 mg/kg, well within the prescribed limits indicating that the Canadian national objective for arsenic in sediments for the protection of aquatic life (17 mg/kg). Overall, the vast majority of lake sediment samples (97.2%) were below the 17 mg/kg Canadian objective for the protection of aquatic life, however, catchments with Nipissing Diabase had the highest background levels for arsenic (10 mg/kg) with some lakes ranging up to 30 mg/kg. The major geological controls influencing changes in lake sediment geochemistry were determined using random forest classification and principal component analysis (PCA). Random forest classification was able to identify which geological province the samples were derived from and the dominant rock types in the sample catchment with respectable accuracy. PCA revealed strong spatial relationships between lake sediment geochemistry and bedrock geology, particularly a strong relationship between Nipissing Diabase in the watershed of the lake and the cobalt-type mineralization indicator elements in the lake sediment including naturally higher levels of arsenic. Within the samples that exceeded regulatory standards, over half the samples that exceeded the regulatory objectives were located in watersheds that contained Nipissing Diabase in their catchment. This study demonstrates that unique geochemical assemblages can be associated with specific geological areas which is of interest to exploration geologists, for target generation and prospecting, and to environmental policy makers, for site-specific restoration targets. 相似文献