土壤、大气尘中晶体的组成及其物源指示意义——以长沙、株洲和湘潭地区为例

基于长沙、株洲和湘潭地区大气尘(可吸入颗粒和近地表积尘)和表层土壤的X-射线衍射(XRD)分析数据,采用微量相鉴定方法获得的结果显示,大气尘和表层土壤中包含石英、石膏、方解石、白云石、硫酸镉等自然矿物及SiS_2、NiTi、Cd_3As_2、FeOCl等非自然源晶体。比较了长沙、株洲、湘潭地区大气尘与表层土壤的晶体组成,分析了大气尘矿物及非自然源晶体的空间分布,探讨了其环境指示意义。     

土壤及大气尘矿物及非自然源晶体及源物指示意义——以长沙、株洲和湘潭地区为例

通过对长沙、株洲、湘潭地区近地表大气尘和土壤中矿物X-射线射弱峰的分级分析,获得其存在非自然源晶体信息,通过矿物及非自然源晶体空间分布分析,获得其环境指示意义.     

成都市近地表大气尘的矿物学特征及其环境指示意义

通过对成都市近地表大气尘X射线衍射、电镜扫描分析等研究显示:其主要由石英、长石、伊利石、绿泥石、方解石、石膏等矿物组成;就其形状看有致密的不规则粒状、片状单矿物、不规则粒状聚合体、浑圆形球状飘珠、聚合体放大观察可见片状的粘土矿物和细小的粒状单矿物,偶见藻类;矿物形貌特征及矿物组成空间分布特征的研究显示:球形状飘珠及伊利石、绿泥石、石膏的空间分布特征与工业布局和表层土壤的pH值密切相关,成都市近地表大气尘主要为地表扬尘和工业烟尘的混合物;与土壤的矿物组成比较可见,近地表大气尘重金属污染除土壤贡献外,还有其他污染贡献;石膏在本次研究中平均含量高达8.2%,推测可能成为成都市往年燃煤量大而无明显酸雨现象的原因之一。     

成都经济区近地表大气尘地球化学基线

成都经济区近地表大气尘中重金属元素含量空间分布显示,经济区中东部高于西部,北部高于中南部,重工业城市高于综合性城市和旅游城市,工矿影响区元素含量总体偏高,人口密集的平原区高于山区。通过标准极限方法确定了近地表大气尘中元素的“极限浓度”,以低于“极限浓度”值统计确定了地球化学基线值：As为28.6mg/kg 、Hg 0.63mg/kg 、Cd 2.94mg/kg、Cr 110mg/kg、Pb 281mg/kg、Ni 32mg/kg、Zn 535mg/kg。近地表大气尘中元素地球化学基线与区域地质背景和矿产开发有关,矿业活动、工业活动及居民生活是造成近地表大气尘中人为扰动元素含量偏高的主要原因。     

江苏地区大气降尘元素地球化学特征与城市地质调查有关问题研究

通过对江苏南京市等典型地区大气降尘样品微量元素分布数据的分析研究,总结了上述各地大气降尘的元素含量分布等地球化学特征,发现不同地区大气降伞的微量元素分布存在明显差异,Cd、Ph、Zn、Se、S等元素在大气降尘中呈相对寓集趋势,城市地区大气降尘污染程度总体要高于乡村,部分降尘样品中Cd、Pb、Zn、Cr、Nj等重金属元素的超量富集与人为活动有关.认为大气降尘环境地球化学调查可在城市土地资源规划利用与保护、产业合理布局、地表物质循环研究、居民健康等方面发挥独特作用,建议今后江苏城市地质调查工作增加这方面的研究内容.     

济南市大气降尘地球化学特征及污染端元研究

在济南市城区对大气降尘及不同污染端元样品进行采集,系统分析了大气降尘和污染端元元素含量特征,并对大气降尘空间分布及污染来源进行研究。结果表明:不同污染端元中元素含量差别明显,燃煤尘中As、Cd、F、Pb是汽车尾气尘的3倍以上,是交通尘、冶炼尘、建筑尘等其他端元尘的1.26~2.35倍,对环境影响较大;汽车尾气尘中Cr、Ni、S、Zn含量最高,冶炼尘中Co、Ni、Pb、F含量偏高,而建筑尘中多数元素含量为所有端元尘中最低。与土壤背景值相比,济南市大气降尘中Cr、Cu、Pb、Zn、Cd、F、S富集程度较高,受到不同程度人为污染;相关分析和因子分析结果表明,Cd、Cu、Hg、Pb、As主要来源于企业燃煤,大气降尘中这些元素高含量区与热电厂、冶炼厂、化工厂等燃煤污染源空间分布相一致;F、S可能与汽车尾气排放有关,而As、Cr主源于交通污染,这3种污染源是济南市大气降尘污染的主要来源,对降尘的贡献约占60.42%。研究表明,工业燃煤排放已逐渐代替汽车尾气成为大气降尘中Pb元素的主要来源。     

北京市春夏季大气气溶胶的单颗粒分析表征

采集了北京市2000年春夏季大气气溶胶样品5个，采用扫描电镜X射线能谱技术分析大气气溶胶单颗粒约2500个。研究结果表明，沙尘期间，矿物尘是最主要的颗粒物种类，非沙尘期间，北京市大气气溶胶中主要检出矿物尘和含硫颗粒物。夏季随着颗粒物污染的加重，含硫颗粒物的数目百分数增加。是北京市大气颗粒物污染的重要特征。重点讨论了Ca-S颗粒、K-S颗粒和Ca-K-S颗粒三类典型含硫颗粒物的化学组成和粒径分布特征。数目可观的Ca-K-S颗粒以及其他硫酸盐颗粒的生成与相对湿度和云量等气象条件相关，这些颗粒物可能是云中过程的产物。减少SO2排放，减少含硫颗粒物，对于控制北京市的大气颗粒物浓度水平具有重要意义。     

拉萨市夏季大气降尘单颗粒矿物组成及其形貌特征

应用带能谱的电子扫描电镜(SEM-EDX)对拉萨市夏季正常天气下收集的大气自然沉降气溶胶样品进行分析,研究了拉萨市大气降尘矿物组成和各种物相形貌特征信息。拉萨市大气颗粒物含有硅酸盐颗粒、富钙颗粒、富铁颗粒、富碳颗粒(燃煤飞灰颗粒和燃油飞灰颗粒)和植物残体颗粒。根据颗粒物数量统计发现拉萨市大气颗粒物以硅酸盐颗粒为主,富钙颗粒和富铁颗粒次之,需要指出的是以燃油飞灰为主的富碳颗粒已占到一定比重,说明以燃油为主的机动车尾气对拉萨大气污染在加强。研究结果表明,大气降尘矿物成分及其形貌特征可以用作判定污染物来源的重要标志,拉萨大气中颗粒来源的多样性决定了治理措施也应综合进行。     

西南典型矿业城市土壤及近地表大气尘中重金属污染特征及评价——以攀枝花市为例

以攀枝花市为研究区域,分别采用富集因子法、潜在生态危害系数法和单因子指数-内梅罗综合污染指数法有针对性地对土壤和近地表大气尘中As,Cd,Cr,Cu,V,Zn和Ni七种重金属污染状况进行了综合性评价。结果表明,攀枝花宝鼎煤矿区和攀钢片区土壤及近地表大气尘中的重金属含量较高,均超过四川省土壤背景值。富集因子指数分析表明,研究区重金属污染受到人为活动的影响较大,污染也较为严重,其中Zn和Cd的富集情况较为显著,Cd,V,Zn,Cu为主要污染因子。潜在生态危害系数结果表明,在各元素中,绝大多数元素处于轻微生态危害,Cd 8个点位处于强生态危害,7个点位处于很强生态危害,处于中等生态危害的占5%,处于强生态危害的占47%,处于很强生态危害的占41%,土壤中Cd元素的潜在生态危险最高,其余元素处于轻微生态危险状态。单因子指数-内梅罗综合污染指数分析结果表明,Cd,Cr和Ni元素在宝鼎煤矿区和攀钢片区都存在重度污染,Cd(7.70),Cr(3.38),Cu(4.49),V(3.62),Zn(3.68)和Ni(5.80)存在重度污染,As(2.07)存在中度污染。     

成都市中心城区地表沉积物中重金属分布及矿物学特征

城市地表沉积物已成为城市环境污染的重要组成部分,是城市环境中各种污染物的"源"和"汇",通过研究城市地表沉积物的物化及矿物学特征对城市环境质量的监测具有良好的指示作用。本文在成都市中心城区不同区域采集40件地表沉积物样品,利用激光粒度分析仪、扫描电镜能谱和X射线衍射等技术分析研究了地表沉积物的粒径分布特征、重金属分布特征、矿物组成特征及微区形貌特征。结果表明:地表沉积物粒径的质量和体积分布特征具有较高一致性,均以中细颗粒物为主,其中小于0. 3mm的地表沉积物占总质量或体积的70%以上,小于0. 125mm的地表沉积物占总质量或体积的40%左右; Cu、Pb、Zn、As、Hg、Cr、Cd、Ni等重金属随着沉积物粒径的减小而呈明显增加的趋势,主要存在于小于0. 125mm粒径的沉积物中,同时在成都市中心城区各方位区域和各环路区域的分布上存在一定的差异; Si、Ca、K、Na等造岩元素在不同粒径级别沉积物中都大量存在;地表沉积物矿物组成主要是石英、长石类、方解石等,且各类矿物在不同粒径级别沉积物中所占含量大致相当,但细粒径矿物表现出胶体行为,极易吸附各种微量重金属。研究认为,城市地表沉积物的粒径分布特征和矿物组成特征是影响重金属在沉积物中分布的内在因素,而人类活动是决定地表沉积物重金属污染程度的关键因素。     

贵州都匀牛角塘富镉锌矿床中镉的分布及赋存状态探讨

对贵州都匀牛角塘富镉锌矿的研究发现该矿床高度富集镉 ,矿石中镉含量一般为 2 2 84× 1 0 -6～ 9850× 1 0 -6,最高为 1 3 4 0 0× 1 0 -6,比地壳克拉克值 ( 0 .2× 1 0 -6)高 5～ 6个数量级 ,比工业品位高n× 1 0～n×1 0 2 倍 ,且其储量达到大型矿床的规模 ,在世界上十分罕见。镉主要以类质同象存在于闪锌矿中 ,少量镉以硫镉矿等独立矿物形式存在于矿床的氧化带 ,是风化淋滤过程中形成的镉的次生矿物。     

A study on the distribution characteristics and existing states of cadmium in the Jinding Pb-Zn deposit,Yunnan Province,China

The distribution characteristics and existing state of cadmium in the Jinding Pb-Zn deposit were studied. It was discovered that Cd was mainly distributed in sphalerite as an isomorphic impurity. There was a good correla-tion between Cd and Zn in the primary ore. With the oxidation and resolution of pyrite, sphalerite, sulfide, and etc., many secondary minerals, such as colloform sphalerite and smithsonite, were formed. The distribution of Cd is not symmetrical, and enrichment and dilution were observed in partial area of the oxidation zone in the deposit. Cd, except in external pore space or cracks of secondary minerals as independent minerals, such as greenockite, was mainly distributed in sphalerite as an isomorphic impurity in the secondary sphalerate and smithsonite in the oxida-tion zone. The research showed that Cd showed a very strong active transfer ability in the oxidation process, not only indicating that supergene leaching might be the main reason for Cd enrichment in some Pb-Zn deposits, but also reflecting that Cd was easily mobilizeed and transferred to pollute ore areas in the oxidation process. Furthermore, Cd in oxidation ore was more easily mobilized and transferred to induce bad hazards for ore areas with the effect from AMD which was produced from oxidation of sulfides.     

国内矿物治理重金属废水研究进展与展望

综述了我国利用天然矿物治理重金属废水方面的研究新成果。天然铁的硫化物、天然铁锰的氧化物、方解石与磷灰石等具有良好的表面吸附与氧化还原化学活性;不同介质中它们能不同程度地表现出对Cr^6 、Pb^2 、Hg^2 、Cd^2 等重金属离子的吸附作用,可广泛用于重金属废水处理。矿物吸附重金属离子机理的研究表明,矿物对重金属的吸附是矿物表面与无机重金属离子之间的表面作用过程,包括矿物表面功能基与重金属离子的配位反应、矿物表面氧化还原反应和沉淀转化作用,以及矿物表面离子交换吸附作用等。     

矿物材料与环境污染治理—以粘土矿物和沸石为例

矿物的性能，矿区地质测试和吸附能力实验表明，粘土矿物和沸石等矿物材料对于Cr,Cd,Pb,Hg,As等有害元素具有很强的吸附能力，是理想的低成本吸附剂，在废水处理中可用来取代活性炭或离子交换树脂来去除重金属等有害元素。     

常见硫化物的氧化作用及其环境效应

自然或人为采矿活动暴露的硫化物矿物的氧化作用，常产生一定范围的次生地球化学异常和严重的环境污染，在黄铁矿，方铅矿，闪锌矿，毒砂等硫化物矿物氧化过程中，S，Pb,Cd,As等有害元素将被有效释放而进入水体，并通过大气－水－土壤－植物－动物等途径危害人类。     

山西临汾盆地黄土剖面重金属分布特征及其影响因素

山西临汾盆地2条黄土剖面重金属分布特征及其影响因素研究表明,Pb、Cu和Zn的垂向变化特征非常相似,而As、Cd和Hg在剖面中的分布特征与前三者不同。各重金属元素在黄土剖面中的变化特征首先均受到黄土源区物质成分的控制,其次不同程度地受到古气候变化的影响。依据Pb、Cu、Zn与各古气候替代性指标(例如磁化率,w(SiO2)/w(Al2O3)等)均呈显著相关,As、Cd和Hg与古气候替代性指标的相关性较差,推断剖面中Cu、Pb、Zn的分布特征受古气候变化的影响,其原因可能主要是这3个金属元素易以类质同象形式赋存在磁性矿物中;而As、Cd和Hg在剖面中的分布特征与古气候无关。但各重金属元素与源区指示元素的相关性表明其在剖面中的分布特征均受黄土源区物质成分的影响和控制。     

Terrestrial geochemistry of Cd,Bi, Tl,Pb, Zn and Rb

About 2000 common magmatic, metamorphic and sedimentary rocks and rockforming minerals contained in 465 individual samples have been analyzed for 6 trace metals and potassium with high precision, mainly by combined distillation and AAS methods. Estimates of average abundances in the continental crust are: 98 ppb Cd. 82 ppb Bi. 490 ppb Tl, 14.8 ppm Pb, 77 ppm Zn and 98 ppm Rb (K/Rb: 223). These averages are close to the mean concentrations of the 6 elements in sedimentary and in low to medium grade metamorphic rocks. In relation to the upper mantle the earth's crust has very effectively accumulated Rb, Pb, Tl (and Bi). Cd and Zn are equally distributed between the upper and lower crust. Bi, Tl, Rb, Pb and K are accumulated in the upper relative to the lower continental crust by factors between 3.5 and 1.4. This is mainly due to higher concentrations in granites and lower abundances in granulites relative to gneisses and schists. The five metals form large ions with bulk coefficients less than one for the partition between metamorphic rocks and anatectic granitic melts. The major hosts of Rb, Tl, Pb and Bi in rocks are minerals with 8- to 12-coordinated sites such as mica, K-feldspar, plagioclase etc. (except for some preference of Bi for sphene and apatite). As examples of significant correlations those of Pb with Tl, K, Bi and Rb in mafic rocks and of Bi with K, Rb, Tl and Pb in sedimentary rocks can be reported. In granites and gneisses hydroxyl containing Fe²⁺-Mg-silicates are major host minerals for Zn and Cd. Except in some carbonate rocks Cd has no preference for Ca minerals.     

Sorption of heavy metal cations by low-temperature deposits of Pacific hydrothermal fields

Cation exchange reactions with participation of heavy metals Mn, Co, Ni, Cu, Zn, Cd, Ba, and Pb were studed in oceanic low-temperature hydrothermal deposits of various mineral compositions and in hydrogenic Fe-Mn crusts. Individual minerals and their assemblages differ significantly in absorptive capacity, which increases in the following order: hematite ? Si-protoferrihydrite < protoferrihydrite < geothite < nontronite ? Fe-vernadite + Mn-feroxyhyte < Fe-free vernadite < bernessite + Fe-free vernadite < bernessite; i.e., it successively increases from the mineral with a coordination type of lattice to minerals with a layer-type structure. The exchange complex of all minerals includes Na⁺, K⁺, Ca²⁺, and Mg²⁺, i.e., the main cations of seawater. In Mn minerals, Mn²⁺ is the main exchange component. The contribution of all the mentioned cations to the exchange capacity of minerals is as high as 90–98%. The highest absorptive capacity among the examined low-temperature oceanic deposits is characteristic of hydrothermal Mn minerals. Their capacity exceeds substantially that of hydrothermal oxides, hydroxides, Fe-aluminosilicates, and hydrogenic Fe-Mn minerals. The absorptive capacity of all examined Mn minerals relative to heavy metals increases in the same order: Ni < Zn < Cd < Mn < Co < Pb < Cu.     

The role of sulphide and carbonate minerals in the concentration of chalcophile elements in the bituminous coal seams of a paralic series (Upper Carboniferous) in the Upper Silesian Coal Basin (USCB), Poland

Sulphide and carbonate minerals from nine bituminous coal seams of a Paralic Series were investigated by means of polished-section microscopy, scanning electron microscopy and absorption spectral analyses. In addition to syngenetic accumulations of kaolinite, illite and quartz, diagenetic veinlets of subhedral pyrite and marcasite most often occur in vitrinite clast fissures and in post-tectonic fissures, nests and lenses with fusinite. Epigenetic anhedral and subhedral grains of ankerite, dolomite, siderite and calcite are also frequently found in post-tectonic veins. Pyrite replaced some of the marcasite grains and it dominates in older coal seams in the Flora Beds as compared with the Grodziec Beds. Occasionally there are anhedral and subhedral galena, sphalerite and chalcopyrite grains among coal macerals as well as cerussite among post-tectonic carbonate veins. They all represent the only minerals that are abundant in definite chalcophile elements (Cd, Co, Cu, Ni, Pb, Zn). In addition to the minerals just mentioned, the elements occurred in pyrite and ankerite grains, which contained inclusions of fusinite and other minerals (among others, clay and carbonate minerals in pyrite, pyrite in carbonates). Although there is a low content of minerals accumulating Cd, Co, Cu, Ni, Pb and Zn, the minerals significantly influence the average concentration of elements in the coal seams. In the Grodziec Beds, mineral matter, especially carbonates and sulphides, determines (>50%) the concentration of Cd, Cu, Pb and Zn in coal. The basic part of Cd, Co and Ni in the coal seams of the Grodziec Beds and of Co, Cu, Ni, Pb and Zn in coal seams of the Flora Beds originates from organic matter. These regularities can be important, from an ecological perspective, in stating whether the coals investigated are useful for combustion and in chemical processing.     

Geochemical Peculiarities of Galena and Sphalerite from Polymetallic Deposits of the Dal’negorskii Ore Region (Primorsky Krai,Russia)

New data on the composition of the major minerals from the skarn and vein polymetallic deposits of the Dal’negorskii ore region are reported. Analysis of galena and sphalerite was carried out by the X-ray fluorescent energy-dispersive method of synchrotron radiation for the first time. It is shown that the minor elements in major minerals of different deposits are typomorphic. Among these elements are Fe, Cu, Ni, Cd, Ag, Sn, and Sb, as well as In in sphalerite and Te in galena. The high concentrations of Ag, Cu, Te, Cd, and In in the extracted minerals indicate the complex character of mineralization. The compositional patterns of ore minerals characterize the sequence of mineral formation from the skarn to vein ores, and the sequence of deposits from the mesothermal to epithermal conditions. This provides geochemical evidence for the stage model of the formation of mineralization in the Dal’negorskii ore region.