中和共沉淀法形成铁氧体微晶及其对重金属离子的并合

本文对中和共沉淀法Fe_3O_4生成过程中重金属离子并合程度及其影响因素进行了研究,在实验条件下,发现重金属离子在Fe_3O_4晶格中的并合与其离子半径、电负性和外层电子分布等因素有关。并合程度为:Cu~(2+),CO~(2+),Fe~(2+)>Mn~(2+),Zn~(2+)>Ni~(2+),Cd~(2+),当Fe~(2+)/Fe~(3+)=0.5,pH=9.5±0.5时,对40mgCu~(2+),总铁量(Fe~(2+)+Fe~(3+))2.5g为最小投料量,其并合率可达99.7％以上,相同条件下CO~(2+)并合率大于99.7％,其它重金属离子由于本征特性影响,并合率各不相同,工艺条件适合于污水中Cu~(2+)和Co~(2+)的有效去除,对Mn~(2+),Zn~(2+)的去除也有一定效果,从沉渣的XRD物相分析可知,重金属离子在Fe_3O_4中的并合,是以尖晶石型结构取代式固溶体组成完成的。     

海底铁锰氧化还原过程的模拟研究

本文用室内海水-沉积物平衡箱研究了沉积物间隙水中铁、锰的垂直变化分布和随时间变化的分布,Fe~(2+)随深度、时间的变化幅度大,在六个月的实验期内均是如此,而Mn~(2+)在放置三个月后即趋于稳定;Fe~(2+),Mn~(2+)产生的宏观经验动力学表明:Fe~(2+)受pH影响远比Mn~(2+)大,且随着深度的增加更为明显,Fe~(2+)在较下层产生速率大,而Mn~(2+)反之;Fe~(2+)的扩散转移是上覆海水向沉积物中转移,扩散量为-60.7ug/m~2d,Nn~(2+)转移方向相反,扩散量为1746.2ug/m~2.d。     

P204-熔融石蜡固液萃取废水中铜、钴、镍

本文研究了二-(2-乙基己基)磷酸(P204)-熔融石蜡对废水中Cu~(2+)、Co~(2+)、Ni~(2+)的固液萃取行为.探讨了水相的酸度、萃取剂P204用量及搅拌时间等对废水中Cu~(2+)、Co~(2+)、Ni~(2+)的萃取率的影响.结果表明,当p H=2.5时,Cu~(2+)萃取率几乎达到100%,远高于Co~(2+)和Ni~(2+);当P204用量为0.05 mL时,水相中Co~(2+)不被萃取,Cu~(2+)和Ni~(2+)萃取率不到60%;当搅拌时间为3 min时,Ni~(2+)萃取达到平衡,萃取完全,Cu~(2+)和Co~(2+)萃取平衡时间需要7 min.用斜率法确定其萃取机理,测定并计算出表观萃取平衡常数Kex和相关热力学参数.     

土壤理化性质对草甘膦残留检测的影响

在土壤环境中草甘膦极易被土壤颗粒吸附,并与土壤中有机质、金属氧化物等反应,对草甘膦的检测造成影响。采用磷酸钠和柠檬酸三钠混合溶液超声提取、正己烷萃取净化、氯甲酸-9-芴基甲酯(FMOC-Cl)衍生化、液相色谱-荧光检测器测定的方法,分别探究了腐殖酸含量、重金属离子含量以及土壤pH值对草甘膦检测方法的影响。结果表明,随着土壤中有机质含量增加,草甘膦的回收率逐渐降低;在土壤pH值为3~11范围内,随着pH值增加,草甘膦的回收率总体呈增加趋势,在pH值为8~9时取得最大值,当pH值9时回收率又有所降低;土壤中的重金属离子Cu~(2+)、Fe~(2+)、Fe~(3+)、Zn~(2+)和Ni~(2+)可以与草甘膦形成稳定的络合物,使回收率降低,而重金属离子Co~(2+)和Mn~(2+)对草甘膦检测没有影响。该研究建立的土壤和沉积物中草甘膦的标准检测方法能够满足各种类型土壤和沉积物的检测要求。     

胞外多聚物在氧化亚铁硫杆菌吸附Mn~(2+)、Ni~(2+)、Pb~(2+)中的作用

利用从粤北大宝山酸性矿山废水(AMD)分离的氧化亚铁硫杆菌(A.f菌),采用原子吸收分光光度技术和荧光分光光度技术,研究其胞外多聚物(EPS)对水中Mn~(2+)、Ni~(2+)、Pb~(2+)的吸附率及二者间的相互作用方式.结果表明,A.f菌对Mn~(2+)、Ni~(2+)、Pb~(2+)具有较强的耐受性;A.f菌的EPS对3种金属离子吸附率随时间的延长而升高,当EPS吸附Mn~(2+)、Ni~(2+)、Pb~(2+)后,类蛋白复合物荧光强度增强且最大发射峰位蓝移;A.f菌对Mn~(2+)、Ni~(2+)、Pb~(2+)的耐受性与其胞外有机多聚物特别是类蛋白物质的生物吸附密切相关.A.f菌的EPS的生物吸附在水中重金属的去除中可发挥重要作用.     

交联壳聚糖乙酸酯冠醚对金属离子的吸附性能研究

本文合成了二苯并-16-冠-5-氯代乙酸酯冠醚和3,5-二叔丁基-二苯并-14-冠-4-双氯代乙酸酯冠醚,然后分别将之与交联壳聚糖(简称CCTS)反应,制备了交联壳聚糖二苯并-16-冠-5-乙酸酯冠醚(简称CCTS-1)和交联壳聚糖3,5-二叔丁基-二苯并-14-冠-4-双乙酸酯冠醚(简称CCTS-2),并研究了它们对Pb~(2+),Cu~(2+),Cr~(3+),Ni~(2+),Cd~(2+)的吸附性能。结果表明:这两种吸附剂对pb~(2+),Cu~(2+)有较高的吸附选择性。     

FTIR研究非完全脱乙酰甲壳质对金属离子的吸附机理

以傅立叶交换红外光谱(FTIR)法研究了非完全脱乙酰甲壳质(NCTS)与Cu~ (2+),Ni~(2+),Co~(1+),Zn~(2+),Cd(2+),Hg~(2+),Ag~+,Pb~(2+)等八种金属离子形成的配合物的结构特征,并对各配合物在4000—400cm~(-1)范围内的主要吸收带作了经验归属.研究结果表明,在NCTS的金属离子配合物中,除—NH_2,—OH参予了配位外,羰基((?)C=O)和酰胺基(—CONH—)亦在不同程度上参予了配位;NCTS对Hg~(2+),Ag~+的吸附过程中存在着明显的氧化还原现象,Hg~(2+),Ag~+,分别被还原为Hg_2~(2+)和Ag~0,而NCTS分子中的—CH_2OH有可能被氧化成—COOH.     

亚铁活化过硫酸盐降解水中双氯芬酸钠

研究了Fe~(2+)活化过硫酸盐(PS)对水中双氯芬酸钠(DCF)的降解,调查了pH、Fe~(2+)用量、PS用量、Cl~-、常见过渡金属离子以及常见还原剂对Fe~(2+)/PS降解DCF的影响.结果表明:DCF在pH 2.0—9.0范围内均有一定的去除效果,且pH 3.0时效果最佳;Fe~(2+)与S_2O_8~(2-)的最佳投加摩尔比为1∶1,过量的Fe~(2+)可消耗部分硫酸根自由基从而抑制DCF降解;Cl~-对DCF的降解具有一定的促进作用,且Cl~-浓度越大,促进作用越大;Ce~(3+)和Co~(2+)对DCF的降解几乎没有影响,而Cu~(2+)和Mn~(2+)具有一定的促进作用;抗坏血酸和硫代硫酸钠具有双重作用,在低浓度时对DCF的降解具有促进作用,高浓度时呈现抑制作用,而盐酸羟胺和亚硫酸氢钠在研究的浓度范围内均呈现促进作用.     

水处理氧化还原过程的电动化学特性

以流动电流为参数,研究了水处理条件下氧化还原过程的电动化学特性.考察了水中KMnO_4及其与Mn~(2+),Fe~(2+)之间氧化还原作用的流动电流(SC)规律,探讨了氧化还原的初始条件、水处理环境、原水水质、氧化剂与还原剂的投加方式等对流动电流的影响.结果表明,水中约0.5mg·l~(-1)的KMnO_4可产生SC的峰值,而且当它与Mn~(2+)和Fe~(2+)经不同条件进行氧化还原作用时,可通过SC值的变化表现出更为明显的电动化学特性.     

不同菌糠生物炭对水体中Cu2+、Cd2+的吸附性能

以菌糠废弃物为原料,采用限氧裂解法在500℃条件下制备香菇菌糠、猴头菇菌糠和平菇菌糠生物炭(LEBC、HEBC和POBC).利用SEM、XRD和FTIR等方法对吸附剂进行了表征;通过吸附动力学、等温吸附、生物炭酸化实验探究了3种菌糠生物炭去除水溶液中Cu~(2+)、Cd~(2+)的效果及机理.结果表明,在溶液初始pH 2—3时,3种菌糠生物炭对溶液中Cu~(2+)、Cd~(2+)的吸附量急剧增加.LEBC、HEBC、POBC对Cu~(2+)、Cd~(2+)的吸附符合准二级动力学模型,对Cu~(2+)的吸附速率分别为10.15×10~(-3)、7.08×10~(-3)、0.69×10~(-3) mg·g~(-1)·min~(-1),对Cd~(2+)的吸附速率分别为6.53×10~(-3)、5.19×10~(-3)、0.26×10~(-3) mg·g~(-1)·min~(-1).不同浓度下LEBC、HEBC、POBC对Cu~(2+)的吸附符合Langmuir模型,最大吸附量依次为56.74、11.98、77.32 mg·g~(-1);而Cd~(2+)的吸附符合Freundlich模型,最大吸附量依次为74.26、36.49、70.2 mg·g~(-1).LEBC在较短的时间内能达到较大的吸附量,可作为去除水体中Cu~(2+)、Cd~(2+)的优质吸附剂.XRD和FTIR等分析结果表明生物炭对Cu~(2+)、Cd~(2+)的吸附机制包括物理吸附、阳离子-π作用、官能团络合及沉淀.3种生物炭经酸化处理后,对Cu~(2+)、Cd~(2+)的吸附能力显著下降,表明生物炭中碳酸盐引起的Cu~(2+)、Cd~(2+)表面沉淀在吸附过程中起重要作用.     

宝鸡城市街尘、土壤及河流沉积物重金属形态迁移特征

在宝鸡城市街尘、土壤及河流沉积物基本理化性质和重金属元素含量分析的基础上,重点研究了重金属元素在街尘、土壤及河流沉积物中的赋存形态和迁移特征.结果表明:在街尘中Cu主要以可氧化态和残余态形式存在,Pb主要以可还原态和可氧化态形式存在,Zn和Cd主要以乙酸可提取态形式存在,Mn、Fe、Co、Ni和Cr主要以残余态形式存在...     

南京城市土壤中重金属的化学形态分布

采取Tessier连续提取法，研究了南京市不同城区表层土壤中Fe,Mn,Cr,Ni,Co,V,Cu,Zn,Pb的化学形态分布。结果表明，南京城市土壤中Fe,Mn,Cr,Ni,Co,V,Zn,Pb以残渣晶格态为主，可交换态比例极低；Cu在城市道路旁的土壤中有机物结合态所占的比例最高，其他区域残渣晶格态所占的比例最高，与非城区自然土壤相比，主要来源于人为输入的Mn,Cu,Zn,Pb残渣晶格态所占的比例低，活性态比例大；Cr和主要来源于原土壤物质的Fe,Ni,Co,V在城市土壤与非城区自然土壤中各形态所占的比例相似，残渣晶格态比例大，活性态比例极低。     

Concentration of polyvalent metals by seaweeds in Vostok Bay,Sea of Japan

Spectrophotometric methods were used to measure the contents of the polyvalent metals Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Mo and Zn in 16 species of red, brown, and green seaweeds and 2 species of higher water plants collected from the intertidal and sublittoral zones of Vostok Bay, Sea of Japan. Some of the species displayed a unique capability for increased accumulation of groups of several metals. We have termed this ability specific group concentration. Thus, Ptilota filicina concentrates Ti, V, Mn, Fe, Ni, Cu, Zn, and Mo; Polysiphonia japonica Ti, V, Mn, Fe, Zn, Mo, and Cr; Rhodomela larix Ti, V, Mn, Fe, Ni, Zn, and Cr; Agarum cribrosum Ti, V, Mn, Fe, Ni, Zn, and Cr; Ulvaria splendens Ti, V, Mn, Fe, Ni, and Cu; Ulva fenestrata Mn, Fe, Ni, and Cu; Enteromorpha prolifera Mn, Co, Zn, Mo, and Cr; codium yessoensis V, Mn, Fe, Ni, and Cr; Zostera asiatica Ti, Mn, Ni, and Mo; Phyllospadix iwatensis Ti, V, Mn, Fe, and Zn. Specific group concentration makes possible a new approach to the study of active transport of polyvalent metals, physiologically significant for live organisms, through cell membranes, and the study of the formation of complex metal compounds inside the cell, i.e., the study of the processes that determine the degree of element concentration. The contents of the metals studied in sea water and the accumulation coefficients were also determined. The variation range is extremely high both for the seaweed species and metals investigated. Maximum coefficients were noted for Mn: 1.8·10⁵; Ti: 4.4·10⁴; Fe: 2.4·10⁴; Cr: 1.2·10⁶.     

pH对黄棕壤重金属解吸特征的影响

对黄棕壤在pH 4~7不同吸附量下6种典型重金属(Cu2+、Zn2+、Cd2+、Pb2+、Co2+、Ni2+)的解吸进行了测定。结果表明,6种重金属的解吸量随吸附量增加而线性增大,解吸量随pH升高而增加,但解吸量占吸附量的比例随pH升高而降低。在试验条件下,黄棕壤吸附Cu2+、Zn2+、Cd2+、Pb2+、Co2+、Ni2+的平均解吸率分别为8.6%、14.3%、74.1%、9.2%、42.1%和36.9%,表明黄棕壤对6种重金属的专性吸附选择性和亲和力顺序为Cu2+、Pb2+ > Zn2+ > Co2+ > Ni2+ > Cd2+。     

Scalp hair metal analysis in the assessment of the occupational exposure of arc welders

Eleven metals (Ca, Mg, Fe, Zn, Cu, Mn, Cd, Co, Cr, Ni and Pb) were estimated in hair samples of metal arc welders and a control group with the same socioeconomic background. Nitric acid–perchloric acid wet digestion procedure was adopted for the estimation of endogenous metal contents by ICP-AE technique. The study exhibited the following increasing order of the metal concentrations: Cd??1, dry weight, respectively. On average, the levels of Mn, Ni, Pb and Fe were found to be 1.5–2.4 times higher in the hair of welders compared with controls. Besides age and exposure which were strongly correlated, Cu–Mg, Mn–Mg, Ca–Co and Cd–Zn also showed significantly positive correlations. The identification of metal sources, done by cluster and principal component analyses, revealed four factors: age and exposure; Cu, Mg, Mn and Fe; Ca and Co; Cd, Zn, Ni and Pb. High levels of Fe were found to have a depleting impact on Co levels. The arc welders were feared to accumulate heavy metals in their bodies due to long-term endogenous exposure.     

Environmental impact of heavy metals (Fe, Ni, Cr, Co) in soils waters and plants of triada in euboea from ultrabasic rocks and nickeliferous mineralisation

Soil, water and vegetation samples were collected from the Triada area of Central Euboea and analysed for heavy metals in order to evaluate their environmental impact. The geology of the area studied includes ultrabasic rocks that are overlaid by Upper Cretaceous limestones whereas Fe–Ni mineralisation is intercalated between either the ultrabasic parent rocks or the karstified Jurassic/Triassic carbonates and the transgessive Upper Cretaceous limestones. All the samples were analysed for heavy metals by using atomic absorption spectroscopy. The heavy metal ranges (in g g^–1) for soils samples are: Ni 480–4000, Cr 240–2720, Co 40–208, Fe 24,000–380,000, Mn 46–1680, Pb 16–56, Zn 40–144, Cu 2–82. The values of soil samples of the Triada area are much higher than the values found for Ni, Cr, Co and Fe, in normal soils of the world. The heavy metal ranges (in g L^–1) for water samples are: Ni 19–24, Cr 19–476, Co <5, Fe <100, Mn <100, Mg 5.7–220.5, As 30–69, Cd <2, Pd <10, Zn 5–11, Cu 2–7. The water samples of the Triada area have Cr and Mg concentrations higher than the permittable values. The heavy metal ranges (in g g^–1) for vegetation samples are: Ni 1–135, Cr 0–24, Co 1–21.5, Fe 20–680, Mn 10–206, Cd 0–10, Pb 0–14, Zn 14–70, Cu 0–10.5. The vegetation samples of the Triada area have so high values of Ni, Cr and Co that are considered toxic. The intercorrelated elements Fe, Ni, Cr, Co of the Triada soils, waters and vegetation reflect their association with the ultrabasic rocks and with the Fe–Ni mineralisation.     

芜湖市区土壤重金属污染评价及来源分析

对芜湖市区153个土壤样品中9种重金属的含量进行测定和评价,利用多元地统计方法进行污染来源分析。结果表明：芜湖市区土壤Zn、Fe、Mn、Cu、Pb、Co、Cd、Ni、Cr的平均含量分别为96.8、30600.1、466.1、35.0、29.1、16.7、1.2、26.3、78.3mg/kg;除Fe、Mn、Ni外,其他元素均高于相应土壤背景值,Zn、Cu、Pb、Co、Cd、Cr分别是背景值的1.26、1.09、1.17、1.20、6.11、1.29倍,说明这些元素出现了一定程度的积累。单因子评价结果表明Cd污染最为严重,Zn、Cu、Pb、Co和Cr为轻度污染,Fe、Mn和Ni没有污染。综合相关性、聚类及主成分分析可知,Fe和Mn为＂自然源因子＂,不同功能区分布主要受成土母质控制;Zn、Cu、Pb和Cd为＂交通及工业活动因子＂,Cu、Cd高值区均分布在开发区,Zn和Pb的高值区分布在镜湖区;Ni、Co和Cr为＂农业活动因子＂,其空间变异受成土母质及农业活动等因素影响。     

Trace metal concentrations in cigarette brands commonly available in Turkey: relation with human health

In this study, the concentrations of Co, Ni, Fe, Cu, Mn, Pb, Cr, and Cd were determined in 15 cigarette brands from Turkey by flame atomic absorption spectrometry (FAAS). A wet digestion method was employed to cigarette samples. The mean values obtained for Co, Ni, Fe, Cu, Mn, Pb, Cr, and Cd were 1.2, 4.1, 134, 14, 66, 3.7, 5.0, and 1.1?µg?g^?1, respectively, i.e., in the order of Fe?>?Mn?>?Cu?>?Cr?>?Ni?>?Pb?>?Co?>?Cd. The results were compared with the literature values for other international cigarette brands.     

Bioaccumulation of heavy metals in Octopus vulgaris from coastal waters of Alexandria (Eastern Mediterranean)

Heavy metal concentrations (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) were determined in various tissues (hepatopancreas, branchial hearts, salivary gland, gills, genital tract, mantle, arms and skin) of Octopus vulgaris collected from three different contaminated sites in front of Alexandria (Egypt) during 2000. All collected tissues displayed high enrichment factors when compared to ambient levels. Heavy metal concentrations in most tissues displayed significant differences among sites, sizes and sex. This study suggests that hepatopancreas, and to a lesser extent branchial hearts, are better indicators of chronic Cu, Fe, Zn and Cd contamination than edible tissues. The enrichment factor (EF) for heavy metals in the hepatopancreas and in edible tissues allowed discriminating our samples into three main groups; (1) EF?>?55 (Cu), (2) EF ranging from 15 to 7.5 (Fe, Cd and Zn) and (3) EF?相似文献