共存镉/铜对沉积物(生物膜)中主要组分吸附阿特拉津的影响

采用选择性萃取分离技术对沉积物(生物膜)中非残渣态组分(铁、锰氧化物和有机质)进行分离,研究阿特拉津(atrazine,AT)-Cd-Cu系中共存重金属对选择性萃取前后沉积物(生物膜)吸附AT的影响.研究结果表明:共存体系中,沉积物(生物膜)中铁氧化物对AT的吸附贡献最大,其次是有机质,而锰氧化物则抑制AT的吸附;共存镉促进了AT在沉积物(生物膜)原样及各非残渣态组分上的吸附,镉质量浓度为0.2 mg/L时,促进作用最显著,各组分对阿特拉津的吸附贡献增加了3.20%～32.31%(沉积物)和1.61%～17.10%(生物膜),但随镉质量浓度的增加,其促进作用减弱;共存铜抑制沉积物(生物膜)原样及铁氧化物、有机质对AT的吸附,铜质量浓度为75.0 mg/L时,其抑制作用最强,铁氧化物和有机质对阿特拉津的吸附贡献分别降低了29.21%、22.36%(沉积物)和9.46%、77.27%(生物膜),但同时减弱了锰氧化物对AT吸附的抑制作用,其吸附贡献分别提高了28.98%(沉积物)和17.46%(生物膜).     

溶液pH对自然水体中多种固相介质吸附铅、镉、铜影响的比较

采用实验室内模拟吸附方法,研究不同溶液pH下沉积物、悬浮颗粒物和生物膜吸附重金属的热力学特征。结果表明：在不同pH下,Langmuir方程均可以很好地描述自然水体三种固相介质吸附重金属的热力学过程。在相同pH条件下,三种固相介质对重金属的吸附能力从大到小依次为悬浮颗粒物、生物膜、沉积物,它们对重金属的吸附能力为铅>铜>镉;这三种固相介质对重金属的吸附能力都随着pH值的升高而增大,其中悬浮颗粒物对重金属的吸附能力受溶液pH影响最大;另外,相对于铜和镉,三种固相介质对铅的吸附受溶液pH影响较大。     

土壤中铅铜锌镉的吸附特性

以徐州王庄矿（WZK）、奎河（KH）、背景-1（BG-1）和背景-2（BG-2）等4个土壤样品为供试对象，加入不同浓度梯度的铅、铜、锌、镉离子，通过静态实验研究了铅、铜、锌、镉的吸附特性。结果表明，土壤对4个重金属的吸附量与加入到土壤中的重金属离子浓度呈正相关性，它们之间大部分满足线性相关关系。在4个土壤样品中加入铅、铜、锌、镉离子的初始浓度比为10：10：10：1时，平衡浓度为Czn〉Ccu〉CPh〉Ccd，吸附量为Scd〉SPh〉Scu〉Szn，4个土壤样品对铅、铜、锌、镉离子的吸附能力依次为WZK〉KH〉BG-2〉BG-1。在所选实验条件下，土壤对铅、铜、锌、镉的吸附能力受土壤中铅、铜、锌、镉的含量、土壤有机质含量、阳离子交换量、土壤饱和含水量和土壤的pH值影响较大。     

改性沸石对重金属离子竞争吸附特性研究

以钠型改性沸石为吸附剂,以含有单一的镉、锌、铅溶液以及镉、锌、铅的混合溶液为吸附质,开展了改性沸石中重金属离子的竞争吸附及其影响因素等实验研究。结果表明,当溶液中有多种二价重金属离子存在时,各离子之间存在竞争吸附,竞争能力为Pb2+>Cd2+>Zn2+;Zn2+-Cd2+表现出显著的协同吸附效应,而Zn2+-Pb2+、Cd2+-Pb2+表现出拮抗吸附。     

印染污泥中重金属形态分析及生物有效性

选取上海某印染厂的印染废水处理后的活性污泥样品,通过盆栽土培试验,用黑麦草对印染污泥进行修复,运用Tessier A连续提取法研究修复后黑麦草根际和非根际印染污泥中铅、铜、镍、锌、镉5种重金属形态的变化,以及重金属的生物有效性与植物中有效态含量之间的关系。结果表明,栽培后根际与非根际环境中各重金属元素具有典型的形态分布特征:铅主要以离子交换态和残渣态存在;铜主要以碳酸盐结合态和残渣态存在;镍由紧结合态(铁锰氧化物结合态+有机结合态)向离子交换态转移;锌的有机结合态和碳酸盐结合态有所增加;镉主要以离子交换态和铁锰氧化物结合态为主,说明镉元素较活泼,具有潜在的环境影响能力,应该给予更多的关注。印染污泥中重金属的生物有效性与重金属元素的性质有关,铜、锌的生物有效性较高,其次是铅,最低是镍、镉。     

长江口海域表层沉积物重金属元素赋存形态特征

通过长江河口地区水下表层沉积物样品多种化学元素的赋存形态分析测试数据,综合分析重金属元素的赋存形态特征。研究结果显示：镉、汞、铅残渣态所占比例均小于50%,锌、砷、铬、铜、镍残渣态占比均大于50%;8个元素的残渣态与全量呈显著正相关关系。沉积环境和沉积物粒径对重金属元素赋存形态具有重要影响。沉积物的物质来源、矿物组成特征、水动力作用与沉积物粒度和物理化学条件等是长江口地区表层沉积物重金属元素赋存形态的主要控制因素。     

湿地水环境中表层沉积物吸附铅、镉能力的研究

在选定的实验条件下,对向海自然保护区5个不同类型湿地水体的表层沉积物样品进行了铅、镉的热力学吸附实验.结果表明,沉积物样品吸附铅、镉的过程符合Langmuir和Freundlich(n=8,p= 0.01) 等温吸附曲线.在所讨论的范围内,沉积物样品吸附铅、镉的能力与样品中铁、锰氧化物及有机质含量存在着显著的相关性.表层沉积物吸附铅、镉的能力小于生物膜吸附铅、镉的能力,即在湿地水环境中,生物膜对重金属迁移转化的作用相对于表层沉积物而言更重要.     

长江武汉段冲积土壤中重金属的环境地球化学特征

长江沿江全流域的重金属元素镉异常带引发了人们对沿长江流域城市的镉及其他重金属元素的环境地球化学特征及生态效应的关注。本文以长江流域具有重要的经济发展战略意义的武汉为研究区,对长江武汉段沿岸的冲积土壤中主要重金属元素镉、铜、铅、镍、铬的含量和以BCR法分步提取的弱酸提取态、可还原态、可氧化态和残渣态等4种形态的分量进行了较系统的分析,同时,配套分析了蔬菜样品中的重金属元素镉、铜、铅、镍、铬的含量,以便了解重金属元素的环境地球化学特征。结果显示,长江武汉段沿岸的冲积土壤中,重金属镉含量超标;铅、铜、镍元素含量接近国家土壤环境质量标准二级指标,基本上对植物和环境不造成危害和污染,满足一般农田、蔬菜地、茶园、果园、牧场等土壤环境标准;铬元素含量较低,接近其背景值。长江武汉段沿岸的冲积土壤中重金属元素的含量和活动性强的弱酸提取态分量随着采样点位置距离武汉钢铁厂越近而增大,显示重金属污染的部分原因可能是工业生产造成的。重金属元素在表层土壤中存在积累效应,表现为表层土壤中重金属元素含量高于对应深层的含量。重金属元素的形态分布特征与各自的地球化学性质有关,活动性强的弱酸提取态镉和铅分量高,具有潜在的环境危害。这些土壤中种植的蔬菜中,重金属元素镉含量普遍明显超标,部分蔬菜中铅元素含量超标,铜、镍、铬元素含量正常。     

金矿区农田土壤重金属污染的环境效应分析

通过对比研究小秦岭某金矿区土壤重金属综合污染区和对比区内的小麦、玉米籽粒中重金属的含量,结果表明污染区内小麦籽粒中汞、铅、镉累积程度显著高于土壤对比区对照样,铬、砷、铜、锌与对照区几乎没有差异,汞、铅、镉、锌、铜的超标率分别为86.67%、60%、33.33%、6.67%、20%。在污染区,玉米中铅、镉、铬较对照区明显累积,但仅有汞超标,超标率为15.15%。同一采样地点,金矿区小麦籽粒比玉米更易吸收累积重金属。小麦中重金属含量与立地土壤重金属污染程度存在较好的相关性。与1990年比较,小麦中汞、镉累积效应非常显著。研究区土壤重金属污染已经造成了小麦严重污染。     

响应曲面法优化生物质炭去除水溶液中的阿特拉津

将农业废弃物大豆秆在450℃缺氧条件下热裂解制备生物质炭。采用元素分析仪、扫描电镜(SEM)、傅里叶变换红外光谱(FTIR)、光电子能谱分析(XPS)等手段对生物质炭进行理化性质分析;应用响应曲面法(RSM)下的中心合成设计(CCD)功能研究4个因素(初始pH、吸附剂质量浓度、阿特拉津质量浓度、温度)对阿特拉津去除率的影响;建立二阶模型,并通过方差分析验证二阶方程的有效性。结果表明:生物质炭表面充满孔状结构,且富含C=C、C-C、CHx、-C-OR、-COOR等官能团;吸附阿特拉津后生物质炭在羟基(-OH)的位置产生了新的吸收峰,推测羟基官能团在吸附过程中发挥了重要作用。RSM法优化最佳吸附去除阿特拉津条件为:初始阿特拉津质量浓度为5mg/L、pH=6.67,吸附剂质量浓度为7.75g/L、温度为32℃;在该条件下阿特拉津的吸附去除率达到92.18%。该研究可为评价施加生物质炭土壤中阿特拉津的迁移规律及阿特拉津污染水体修复提供参考。     

Association of trace metals with various sedimentary phases in dam reservoirs

In the present study sediment and water samples collected from Kowsar Dam reservoir in Kohkiluye and Boyerahmad Province, southwest of Iran, are subjected to bulk digestion and chemical partitioning. The concentrations of nickel, lead, zinc, copper, cobalt, cadmium, manganese and iron in water and bed sediment were determined by atomic absorption spectrometry. The concentrations of metals bounded to five sedimentary phases were estimated. On this basis, the proportions of natural and anthropogenic elements were calculated.The anthropogenic portion of elements are as follows: zinc (96 %)> cobalt (88 %)> iron (78 %)> magnesium (78 %)> nickel (78 %)> copper (66 %)> lead (63 %)> cadmium (59 %). The results show sediment contamination by nickel, cadmium and lead, according to the world aquatic sediments and mean earth crust values. Manganese and copper have strong association with organic matter and are of high portion of sulfide bounded ions. Finally, The degree of sediment contamination was evaluated using enrichment factor, geo-accumulation index (Igeo) and pollution index (IPoll). The sediments were identified to be of high cadmium and lead pollution index. The pattern of pollution intensity according to enrichment factor is as follows; manganese (1.25) < copper (1.63) < zinc (1.93) < cobalt (2.35) < nickel (3.83) < lead (12.63) < cadmium (78.32). Cluster analysis was performed in order to assess heavy metal interactions between water and sediment. Accordingly, nickel, cadmium and copper are earth originated. Zinc, copper and manganese are dominated by pH. All the elemental concentrations in water and sediment are correlated except for sedimental copper.     

Single and binary adsorption of lead and cadmium ions from aqueous solution using the clay mineral beidellite

Beidellite, a low-cost, locally available and natural mineral was used as an adsorbent for the removal of lead and cadmium ions from aqueous solutions in batch experiments. The kinetics of adsorption process was tested for the pseudo first-order, pseudo second-order reaction and intra-particle diffusion models. The rate constants of adsorption for all these kinetic models were calculated. Comparison amongst the models showed that the sorption kinetics was best described by the pseudo second-order model. Langmuir and Freundlich isotherm models were applied to the experimental equilibrium data for different temperatures. The adsorption capacities (Q°) of beidellite for lead and cadmium ions were calculated from the Langmuir isotherm. It was found that adsorption capacity was in the range of 83.3–86.9 for lead and 42–45.6 mg/g for cadmium at different temperatures. Thermodynamic studies showed that the metal uptake reaction by beidellite was endothermic in nature. Binary metal adsorption studies were also conducted to investigate the interactions and competitive effects in binary adsorption process. Based on the optimum parameters found, beidellite can be used as adsorbent for metal removal processes.     

基于BP神经网络的复合污染体系中沉积物吸附阿特拉津的规律

建立了Cu2+和阿特拉津(AT)复合污染体系中沉积物各活性组分及其交互作用对AT吸附量影响的BP神经网络模型,模型预测值和实验值的相关系数达到0.97,各集合的平均偏差均小于10%。模型显示,AT在沉积物上的主要吸附位是铁氧化物。沉积物吸附AT时铁氧化物、锰氧化物、有机质之间存在显著的交互作用,铁氧化物、锰氧化物交互作用贡献率为-130%～80%,铁氧化物、有机质交互作用贡献率为5%～28%,锰氧化物、有机质交互作用贡献率为-200%～-70%。各活性组分吸附AT的能力及其交互作用受Cu2+的影响较大,其中:Cu2+对AT在铁氧化物上的吸附表现为拮抗作用,对AT在锰氧化物上的吸附表现为协同作用,而对AT在有机质上的吸附影响不显著,同时Cu2+减弱了铁氧化物-锰氧化物和锰氧化物-有机质的交互作用影响,增强了铁氧化物-有机质的交互作用影响。     

石英尾砂对濠河上游沉积物污染的磁学响应

濠河上游沉积物和石英尾砂磁学参数及SiO₂质量分数(w(SiO₂))分析结果表明,沉积物中w(SiO₂)高达80%以上,说明沉积物已被石英尾砂严重污染。磁测结果显示,沉积物与石英尾砂的磁学特征基本相同,这2类样品中的主要磁性矿物是磁铁矿,含量较低,磁性矿物粒径较宽,主要为0.1~5 μm;这主要是大量石英尾砂进入濠河后,在其稀释作用下,沉积物磁性减弱,使磁性矿物的粒径变粗。沉积物中w(SiO₂)与磁学参数(χ、SIRM和χ_ARM)存在负相关关系(-0.83≤R≤-0.61),表明磁学参数能反映石英尾砂对沉积物的污染程度,其值越低说明石英尾砂对濠河污染越严重。     

Synthesis of nano-γ-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/chitosan beads (AlCBs) and continuous heavy metals removal from liquid solution

In this work, synthesis of chitosan beads impregnated with nano-γ-Al₂O₃ (AlCB) was carried out. The characteristics of the synthesized adsorbent were obtained by using Brunauer Emmett and Teller technique and Scanning Electron Microscopy method. The use of AlCB in continuous removal of chromium, lead, nickel and cadmium ions from liquid solution was studied using fixed-bed column system. Bed depths and flow rate effects on breakthrough and uptake capacity of the adsorbent in column were also examined. Dynamic parameters of the adsorption were calculated by using bed depth service time (BDST) and Thomas models. In both models, the data were analyzed by error analyzing and combining the values of determined coefficient (R ²) from regression analysis. The adsorption capacities of AlCB in breakthrough were 158.33, 183.33, 63.33 and 31.67 mg/g for chromium, lead, nickel and cadmium, respectively. In addition, BDST model was found to be an acceptable kinetic model to describe the experimental data.     

Heavy metals contamination in water and sediments of an urban river in a developing country

Water and sediment samples were collected from 20 location of the Buriganga river of Bangladesh during Summer and Winter 2009 to determine the spatial distribution, seasonal and temporal variation of different heavy metal contents. Sequential extraction procedure was employed in sediment samples for the geochemical partitioning of the metals. Total trace metal content in water and sediment samples were analyzed and compared with different standard and reference values. Concentration of total chromium, lead, cadmium, zinc, copper, nickel, cobalt and arsenic in water samples were greatly exceeded the toxicity reference values in both season. Concentration of chromium, lead, copper and nickel in sediment samples were mostly higher than that of severe effect level values, at which the sediment is considered heavily polluted. On average 72 % chromium, 92 % lead, 88 % zinc, 73 % copper, 63 % nickel and 68 % of total cobalt were associated with the first three labile sequential extraction phases, which portion is readily bioavailable and might be associated with frequent negative biological effects. Enrichment factor values demonstrated that the lead, cadmium, zinc, chromium and copper in most of the sediment samples were enriched sever to very severely. The pollution load index value for the total area was as high as 21.1 in Summer and 24.6 in Winter season; while values above one indicates progressive deterioration of the sites and estuarine quality. The extent of heavy metals pollution in the Buriganga river system implies that the condition is much frightening and may severely affect the aquatic ecology of the river.     

古龙南地区低阻油层胶结指数和饱和度指数影响因素实验

采用变胶结指数m和饱和度指数n的阿尔奇公式仍是目前定量评价低阻油层饱和度的主要方法之一。然而,由于不同地区低阻油层的成因不同,从而使得低阻油层m和n的影响因素随地区不同而发生变化。因此,针对不同地区低阻油层,有必要研究其阿尔奇公式m和n的影响因素及变化规律。依据古龙南地区葡萄花低电阻率油层划分标准以及考虑岩性、物性、电性变化,选取了低阻油层岩样,设计了岩样岩石物理实验。基于岩石物理实验数据,绘制m和n与物性参数、孔隙结构参数、黏土附加导电能力参数的交会图。经分析可知：低阻油层的m和n值小于常规油层的m和n值,并随孔渗综合指数、中值半径、平均半径、半径均值的增大而增大。低阻油层的m值随泥质体积分数、阳离子交换容量、微孔隙体积与可动流体体积之比的增大而减小,随核磁共振测量的T₂几何平均值的增加而增大;n值随孔隙度、孔隙度和泥质体积分数比值的增加而增大。低阻油层的m值与T₂几何平均值、微孔隙体积与可动流体体积之比关系较好,n值与孔渗综合指数、平均半径、最大半径、半径均值的相关性非常好。研究表明,低阻油层的m值受孔隙结构和泥的影响较大,而n受孔隙结构影响较大。可用T₂几何平均值或微孔隙体积与可动流体体积之比确定低阻油层的m值,可用孔渗综合指数、平均半径、最大半径、半径均值确定低阻油层的n值。     

张广才岭英城子金矿区早古生代花岗岩的元素地球化学特征、岩石成因及构造意义

系统研究了英城子金矿区内花岗岩的地质、岩相学和元素地球化学特征。研究结果显示：该类花岗岩为富硅（w(SiO₂)=71.12%～75.66%）、高分异（DI=90.53～94.42）、钾质钙碱性岩（σ=2.37～3.94）,富集大离子亲石元素（LREE/HREE=11.20～14.62,w（Rb）=（270.6～165.3）×10^-6,Na₂O/K₂O =0.18～0.67,等）,具负的铕异常,相对亏损Ba、Nb、Sr、P和Ti等元素。这种特征揭示该类花岗岩是准铝质、高分异I型花岗岩,它的母岩浆可能是I型花岗质岩浆,是母岩浆经以斜长石为主的矿物相分离结晶作用后产生的岩浆经结晶作用形成。结合锆石的年代学研究成果,进一步确立该花岗岩可能是在麻山期深变质作用过程中地壳深熔形成的岩浆经分离结晶作用形成,岩浆就位发生在麻山期陆内造山作用的挤压向伸展转换阶段,从发生到就位持续大约20 Ma。     

Trace metals in surface seawaters and sediments from various habitats of the Red Sea coast of Yemen

The purpose of this study was to determine and assess the concentrations of trace metals in surface seawaters and sediments from different coastal habitats of the Red Sea coast of Yemen. Surface seawater and sediment samples were collected, treated and analyzed for cadmium, cobalt, manganese, chromium, lead, iron, nickel, copper, zinc and vanadium by the atomic absorption spectrometric analysis. The concentrations were high for cadmium, cobalt and lead and low or consistent with the natural background concentrations for the rest of the metals. However, the coastal habitats of the Red Sea coast of Yemen are still considered unpolluted, it is concluded that the cadmium cobalt and lead levels in surface seawaters are high and could have negative effects on marine life of the sites. Further studies are needed to characterize the sources fate, biogeochemical processes and impacts of these trace metals on coastal habitats and marine life of the region.     

Nettle ash as a low cost adsorbent for the removal of nickel and cadmium from wastewater

This study was focused on nettle ash as an alternative adsorbent for the removal of nickel (II) and cadmium (II) from wastewater. Batch experiments were conducted to determine the factors affecting adsorption of nickel (II) and cadmium (II). The adsorption process is affected by various parameters such as contact time, solution pH and adsorbent dose. The optimum pH required for maximum adsorption was found to be 6. The experimental data were tested using Langmuir, Freundlich and Tempkin equations. The data were fitted well to the Langmuir isotherm with monolayer adsorption capacity of 192.3 and 142.8 mg/g for nickel and cadmium, respectively. The adsorption kinetics were best described by the pseudo second order model. The cost of removal is expected to be quite low, as the adsorbent is cheap and easily available in large quantities. The present study showed that nettle ash was capable of removing nickel and cadmium ions from aqueous solution.