淮南矿区煤中12种微量元素的赋存状态及环境效应

为研究淮南矿区煤中微量元素的赋存状态和环境效应,在淮南矿区7个矿井共采集17个样品,采用电感耦合等离子质谱仪（ICP-MS）测定了12种微量元素的含量,分别利用聚类分析和因子分析,结合其地球化学性质,讨论了它们的赋存状态,并采用静态燃烧实验研究其挥发性。结果表明:研究的元素没有异常富集;Zn和Cu赋存于闪锌矿中,Cr、Pb和Cd被粘土矿物吸附,Ba可能赋存于铁白云石和方解石中,Ni、Mo、Co和As主要赋存于黄铁矿中,Be和Se以有机结合态存在;研究的元素大多不易挥发,但Zn和Pb易挥发,且含量较高,环境危害较大,Zn和Pb分别赋存于闪锌矿和粘土矿物中,可通过洗选脱除减小其危害。      

Abundances and modes of occurrence of trace elements in the Çan coals (Miocene), Çanakkale-Turkey

This study presents the concentrations and modes of occurrence of trace elements in 81 coal samples from the Çan basin of northwestern Turkey. The concentration of trace elements in coal were determined by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry. Additionally, traditional coal parameters were studied by proximate, ultimate, X-ray diffraction, and petrographic analyses. Twenty trace elements, including As, B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se Sn, Th, Tl, U, V, and Zn, receive much attention due to their related environmental and human health concerns. The Çan coals investigated in this study are lignite to sub-bituminous coal, with a broad range of ash yields and sulphur contents. The trace element concentrations show variety within the coal seams in the basin, and the affinities vary among locations. The concentrations of B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se, Sn, Tl, and Zn in Çan coals are within the Swaine's worldwide concentration range, with the exception of As, Th, U, and V. On the other hand, compared with world coals, the Çan basin coals have higher contents of As, B, Cu, Co, Mo, Pb, Th, U, V, and Zn. Based on statistical analyses, most of the trace elements, except for U, show an affinity to ash yield. Elements including As, Cd, Hg, Se, Cu, Mo, Ni, and Zn, show a possible association with pyrite; however, the elements Se, B, and Mo can be have both organic and inorganic associations.     

电感耦合等离子体发射光谱-逐级化学提取法研究低硫煤矸石中微量元素的赋存状态及其环境效应

煤矸石是我国堆存量最大的工业固体废物,本文应用电感耦合等离子体发射光谱法、逐级化学提取法和相关性分析研究了淮北临涣矿区低硫煤矸石中10种微量元素的含量及赋存状态,并运用风险评价指数法评价其环境效应。结果表明,低硫煤矸石中Ba、Co、Cr、Mn、Ni、Pb、V含量均高于淮北煤和中国煤均值,Mn、V的富集系数大于1,有一定迁移风险。微量元素主要以残渣态和铁锰氧化物结合态存在,两者质量分数之和为68.87%~92.93%,其中Cd、Co、Cr、Cu、Ni、Pb、Zn赋存于硫化物矿物中,V赋存于黏土矿物中,Mn赋存于碳酸盐矿物和硫化物矿物中。10种微量元素对环境的危害性大小为:MnZnNiPbCdCuBaVCrCo,表明低硫煤矸石堆存过程中活性态Mn对生态环境造成危害的可能性最大,由Mn可能引起的煤矸石山周边地区土壤及水体污染应当重视。     

Pyrite trace element geochemistry of mafic granulite xenoliths from Xikeer: implications for the source of Cu in the sediment-hosted mineralization in the northwestern Tarim Basin (Northwest China)

The Xikeer mafic granulite xenoliths are hosted by a Cenozoic basanite sill (∼20 Ma) in the northwest Tarim Basin, northwest China. Sulfides, identified in these xenoliths consist mainly of pyrite. Two groups of pyrite (types A and B) can be distinguished based on petrography and trace element geochemistry, as determined by laser-ablation ICP-MS analysis. Type A pyrite is subhedral and in general has lower trace element abundance than type B pyrite. Type B pyrite is fractured with ragged anhedral morphology and has extremely high Cu, Tl, Ni, and Co abundance. The low Co and Ni contents combined with a positive correlation between Cu, Cr, and Pb all indicate that the type A pyrite may have formed from a high-temperature magmatic hydrothermal fluid. In contrast, the Cu-, Tl-, Ni-, and Co-rich type B pyrite was probably formed in a relatively low-temperature basinal environment. The Cu mineralization at Xikeer can be explained when Cu, Tl, Ni, and Co were leached from the intruded basanites and subsequently enriched in circulating basin brines. Such enrichment of Cu in basin brines could provide an important Cu source for the Cu mineralization in the Xikeer district and other Cenozoic sub-basins in the Tarim Basin.     

Adsorption of Heavy Metal Cations by Base Metal Sulfides in the Broken Spur and TAG Hydrothermal Fields,Atlantic Ocean

Data on the mineral and chemical composition of samples of sulfide deposits from the Broken Spur and TAG (Mid-Atlantic Ridge) are presented. The main minerals in the Broken Spur field are marcasite, pyrrhotite, pyrite, chalcopyrite, and sphalerite; in sample from TAG: chalcopyrite, pyrite, and marcasite. It has been established that these sulfide minerals of Fe, Cu, and Zn are natural ion exchangers and belong to the class of adsorbents. Exchange capacity of sulfide minerals in terms of heavy metal cations (Ni2+, Co2+, Cd2+, and Pb2+) is 0.022–0.32 mg-equiv/g. In the exchange reaction products, the mineral composition of sulfide deposits is retained, and new phases do not appear. It is suggested that the adsorbed heavy metal cations populate either vacant cationic or interstitial defect sites in the structures of sulfide minerals. Bond strength of the adsorbed heavy metal cations with the main structural elements of minerals is low, which is confirmed by their high extraction in an acid medium. The results of adsorption-desorption experiments indicate two forms of heavy metal cations in sulfide minerals: adsorbed (basic) and chemically bound.     

吉尔吉斯斯坦Taldybulak Levoberezhny(左岸)金矿地质特征及金属矿物学研究

Taldybulak Levoberezhny(又称左岸)矿床位于吉尔吉斯斯坦北天山东段,是区内第三大金矿(金储量130 t,平均品位6.9 g/t)。长期以来,该矿床矿物学研究薄弱,成因类型存在争议,已有观点包括斑岩型、造山型、多阶段叠加成矿等。野外地质调查及室内岩相学鉴定发现：金矿化同时受韧性剪切带和岩体控制,局部显示一定的顺层特征;常见矿石类型包括浸染细脉浸染型、石英电气石硫化物型、块状硫化物型、稀疏浸染型、方解石硫化物脉型等;相关围岩蚀变以硅化、绢云母化、电气石化、碳酸盐化最为强烈,可见绿泥石化、绿帘石化、泥化等。电子探针分析发现,左岸金矿同时发育可见金和不可见金。前者包括银金矿(w(Au)=67.90%~80.86%,w(Ag)=14.24%~30.76%)、含银自然金(w(Au)=88.95%,w(Ag)=8.09%)等,以包体金、裂隙金或粒间金形式赋存于黄铁矿中。后者可赋存于黄铁矿和黄铜矿中(w(Au)=0.16%~0.33%)。不同类型矿石中黄铁矿的形态、结构、成分存在一定差异,显示了叠加成矿的可能性。浸染状细脉浸染型矿石中黄铁矿以中粗粒(30~1 300 μm,多数>200 μm)、半自形自形立方体为主,基本无碎裂或碎裂不明显,可含有自然金、银金矿或硅酸盐包体;成分上具有中等的As(0.03%~1.72%,平均0.66%)、Co(0.06%~0.19%,平均0.13%)、Te(0.03%~0.06%,平均0.04%)含量和As/S、Fe/S、Co/As比值,基本不含Cu、Pb、Zn、Ag。石英电气石硫化物型矿石中黄铁矿多呈中粗粒(30~2 000 μm)、半自形它形粒状,往往发生碎裂,并被黄铜矿、方铅矿等矿物交代;部分颗粒可含有银金矿或硅酸盐包体;总体具有较高的As(0.05%~2.05%,平均0.97%)、Co(0.05%~0.34%,平均0.15%)含量和As/S、Fe/S比值,Co/As比值较低。块状硫化物型矿石中黄铁矿多呈半自形它形粒状产出,但粒度变化较大(250~3 000 μm或者30~300 μm);化学成分上以较高的As(0.05%~2.20%,平均1.21%)、Te(0.04%~0.09%,平均0.06%)含量,高的As/S、Fe/S比值和低的Co/As比值为特征。稀疏浸染型矿石中黄铁矿呈中粒(集中于50~200 μm)、半自形它形粒状产出,内部可含有硫化物、硅酸盐、银金矿、自然金等包体;可发生碎裂并被黄铜矿等沿裂隙充填交代;化学成分变化较大,总体具有较高的Co(0.08%~1.04%,平均0.35%)含量和Co/As比值,几乎不含Te、Cu、Zn。方解石硫化物脉型矿石中黄铁矿呈中粗粒(40~480 μm)、半自形它形粒状产出,内部往往含硅酸盐等包体;黄铁矿以显著低的As(0.04%~0.08%,平均0.06%)、Co含量(0.04%~0.20%,平均0.10%)以及As/S、Fe/S比值为特征,Co/As比值较高,且不含Zn。从上述左岸金矿的控矿构造、矿化类型、围岩蚀变以及不同类型矿石中黄铁矿形态、结构、成分的差异等4方面特征显示,左岸金矿可能存在多期次矿化、叠加成矿。     

安徽铜陵新桥Cu-Au-S矿床黄铁矿微量元素LA-ICP-MS原位测定及其对矿床成因的制约

激光剥蚀电感耦合等离子体质谱(LA-ICP-MS)是一种固体微区分析新技术。用该技术来分析矿床中硫化物的微量元素组成可以为研究成矿流体特征、矿床成因及找矿勘探提供有关的科学信息。文中以安徽铜陵矿集区内新桥Cu-Au-S矿床中的黄铁矿为研究对象,在详细的野外观察和室内鉴定的基础上,将矿床中的黄铁矿分为具有沉积特征的胶状黄铁矿(PyⅠ)、具有变形重结晶和热液叠加作用特征的细粒他形黄铁矿(PyⅡ)和具热液成因特征的中—粗粒自形黄铁矿(PyⅢ)3种类型。LA-ICP-MS原位微量元素测定结果显示,PyⅠ中相对富含Ti、Co、Ni、As、Se、Te;PyⅡ继承了PyⅠ中富含Ti、Co、Ni、As、Se、Te、Bi的特征,同时还含有不均匀分布的少量成矿元素(Cu、Pb、Zn、Au、Ag);PyⅢ中成矿元素Cu、Pb、Zn、Ag、Au以及Bi元素的含量较高,Co、Ni、As的含量较低。在元素赋存状态方面,Co、Ni、As、Se和Te均以类质同象的形式进入到了黄铁矿的晶格中;Bi在PyⅡ中主要以含Bi矿物的微细包裹体形式存在,而在PyⅢ中的Bi还部分取代了Fe而占据了晶格;Cu、Pb、Zn、Au、Ag这些成矿元素中,Cu和Zn分别以黄铜矿和闪锌矿的矿物包裹体存在于黄铁矿中;PyⅡ中所含的少量Au、Ag,可能分别以自然金和自然银的形式存在,而在PyⅢ中Au可能主要以银金矿的形式存在,Ag除了以银金矿的形式存在以外还可能赋存于黄铁矿中含铋的矿物包裹体内;Pb主要赋存于黄铁矿中的方铅矿或含铋矿物的包裹体中。在综合分析黄铁矿的结构形态和微量元素组成特征的基础上认为,PyⅠ型黄铁矿可能形成于前人提出的晚古生代海底沉积或喷流沉积环境,PyⅡ和PyⅢ型黄铁矿分别形成于中生代区域构造变形-热液叠加改造的过渡环境和热液环境,PyⅡ和PyⅢ的形成时间相近。新桥矿床的形成可能经历了晚古生代海底沉积或喷流沉积期和燕山期热液期,胶黄铁矿主要形成于沉积成矿期,而矿床中成矿物质Cu、Pb、Zn、Au、Ag等主要来自燕山期岩浆侵入作用形成的热液成矿系统。     

The determination of minor and trace element associations in coal using a sequential microwave digestion procedure

A sequential extraction procedure, using acid digestion in a CEM MDS-81D® microwave system, is reported for the investigation of trace and minor element associations in coal in (1) mineral phases other than pyrite, (2) pyrite and (3) the organic matrix. The concentrations of sulphate, pyrite and organic sulphur can also be determined by this method. The extract solutions from each stage are rapidly analysed by ICP-AES. The association of major, minor and trace elements with mineral and organic phases is suggested for a suite of certified reference coal samples. In stage 1, a significant percentage of the total Ba, Co, Cr, Cu, Mn, Ni, Pb and Sr was extracted suggesting an association with silicate, carbonate, sulphate and phosphate minerals for these elements. In stage 2, a proportion of the Cu, Mn, Ni, Pb and Zn was dissolved implying the occurrence of these elements in pyrite. An association with the organic matrix is suggested for Cr and also for Ba and Sr in lower rank coals.     

云浮黄铁矿利用过程中微量毒害元素的环境化学活动性

为了解云浮黄铁矿利用过程中微量毒害元素的环境地球化学行为，客观评价它们对环境质量的影响，利用元素结合形态的连续提取实验方法，分析了云浮黄铁矿及其工业废渣中Co,Ni,Cu,Zn,As,Se,Cd,Sn,Sb,Pb和Tl等11种毒害元素的形态及化学活动性。结果表明，黄铁矿中大部分微量毒害元素都有着极强的化学活动性，各元素活动态浸出比例依次为Co96.3%,Se91.9%,Cu90.3%,Cd90.0%,Pb89.7%,Zn88.6%,Sb82.5%,Ni80.6%，Sn70%,Tl55.1%和As31.9％，元素As和Tl主要赋存于硫化物和硅酸盐矿物相中，另有少量的Cu,Pb和Sb可能赋存于碳酸盐矿物相中，其他元素则主要赋存于硫化物矿物相中。与黄铁矿相比，飞灰和灰渣中各元素可交换态和碳酸盐结合态所占的比例明显减少。废渣中各元素的化学活动性表现出很大的差别，其中Cu,Zn和Cd的化学活动性最强，活性态浸出比例在90％以上；其次是Co,Ni,Se,Pb和Tl，浸出比例在50％左右；Sb,As和Sn的稳定性较高，浸出比例分别为1％、5％和14％左右；飞灰中微量毒害元素的活动性均高于灰渣。     

Experimental modeling of the immobilization of heavy metals at the carbonate adsorption–precipitation geochemical barrier

Experimental data obtained on the adsorption–precipitation immobilization of heavy metals (Cu, Zn, Pb, Cd, Co, and Ni) from acidic and neutral solutions by calcite and dolomite demonstrate that interaction of solutions of heavy metals with these minerals at pH > 7.8–8.1 leads to a significant decrease in the concentrations of the metals because of the crystallization of carbonates of these metals. Except Pb, which is equally removed from solutions by both minerals, the immobilization efficiency of the metals on dolomite is greater than on calculate at the same pH. Residual Zn, Cd, Co, and Ni concentrations are immobilized by chemosorption, which is the most efficient for Cd and less significant for Co, Ni, and Zn. It is proved that artificial geochemical barriers on the basis of carbonate rocks can be efficiently applied to protect environment from contamination with heavy metals.     

Concentration and association of minor and trace elements in Mukah coal from Sarawak, Malaysia, with emphasis on the potentially hazardous trace elements

The ash yield and concentrations of twenty-four minor and trace elements, including twelve potentially hazardous trace elements were determined in Mukah coal from Sarawak, Malaysia. Comparisons made to the Clarke values show that Mukah coal is depleted in Ag, Ba, Be, Cd, Co, Mn, Ni, Se, U, and V. On the other hand, it is enriched in As, Cr, Cu, Pb, Sb, Th, and Zn. Among the trace elements studied, V and Ba are associated predominantly with the clay minerals. Manganese, Cr, Cu, Th, and Ni are mostly bound within the aluminosilicate, sulphide and/or carbonate minerals in varying proportions, though a portion of these elements are also organically bound. Arsenic, Pb and Sb are mostly organically bound, though some of these elements are also associated with the sulphide minerals. Zinc is associated with both the organic and inorganic contents of the coal. Among the potentially hazardous trace elements, Be, Cd, Co, Mn, Ni, Se, and U may be of little or no health and environmental concerns, whereas As, Cr, Pb, Sb and Th require further examination for their potential health and environmental concerns. Of particular concern are the elements As, Pb and Sb, which are mostly organically bound and hence cannot be removed by physical cleaning technologies. They escape during coal combustion, either released as vapours to the atmosphere or are adsorbed onto the fine fly ash particles.     

Geochemistry of trace metals associated with reduced sulfur in freshwater sediments

Porewater concentration profiles were determined for Fe, trace elements (As, Cd, Co, Cu, Mn, Ni, Pb, Zn), sulfide, SO₄ and pH in two Canadian Shield lakes (Chevreuil and Clearwater). Profiles of pyrite, sedimentary trace elements associated with pyrite and AVS were also obtained at the same sites. Thermodynamic calculations are used, for the anoxic porewaters where sulfide was measured, to characterize diagenetic processes involving sulfide and trace elements and to illustrate the importance of sulfide, and possibly polysulfides and thiols, in binding trace elements. The ion activity products (IAP) of Fe sulfide agree with the solubility products (K_s) of greigite or mackinawite. For Co, Ni and Zn, IAP values are close to the K_S values of their sulfide precipitates; for Cu and Pb, IAP/K_s indicate large oversaturations, which can be explained by the presence of other ligands (not measured) such as polysulfides (Cu) and thiols (Pb). Cobalt, Cu, Ni and Zn porewater profiles generally display a decrease in concentration with increasing ΣH₂S, as expected for transition metals, whereas Cd, Pb and Zn show an increase (mobilisation). The results suggest that removal of trace elements from anoxic porewaters occurs by coprecipitation (As and Mn) with FeS(s) and/or adsorption (As and Mn) on FeS(s), and by formation of discrete solid sulfides (Cd, Cu, Ni, Pb, Zn and Co). Reactive Fe is extensively sulfidized (51–65%) in both lakes, mostly as pyrite, but also as AVS. Similarities between As, Co, Cu and Ni to Fe ratios in pyrite and their corresponding mean diffusive flux ratios suggest that pyrite is an important sink at depth for these trace elements. High molar ratios of trace elements to Fe in pyrite from Clearwater Lake correspond chronologically to the onset of smelting activities. AVS can be an important reservoir of reactive As, Cd and Ni and, to a lesser extent, of Co, Cu and Pb. Overall, the trace elements most extensively sulfidized were Ni, Cd and As (maximum of 100%, 81% and 49% of the reactive fraction, respectively), whereas Co, Cu, Mn, Pb and Zn were only moderately sulfidized (11–16%).     

An attempt to use LA-ICP-SMS to quantify enrichment of trace elements on pyrite surfaces in oxidizing mine tailings

Metals released from oxidation and weathering of sulphide minerals in mine tailings are to a high degree retained at deeper levels within the tailings themselves. To be able to predict what could happen in the future with these secondarily retained metals, it is important to understand the retention mechanisms. In this study an attempt to use laser ablation high-resolution ICP-MS (LA-ICP-SMS) to quantify enrichment of trace elements on pyrite surfaces in mine tailings was performed. Pyrite grains were collected from a profile through the pyrite-rich tailings at the Kristineberg mine in northern Sweden. At each spot hit by the laser, the surface layer was analyzed in the first shot, and a second shot on the same spot gave the chemical composition of the pyrite immediately below. The crater diameter for a laser shot was known, and by estimating the crater depth and total pyrite surface, the total enrichment on pyrite grains was calculated. Results are presented for As, Cd, Co, Cu, Ni and Zn. The results clearly show that there was an enrichment of As, Cd, Cu and Zn on the pyrite surfaces below the oxidation front in the tailings, but not of Co and Ni. Arsenic was also enriched on the pyrite grains that survived in the oxidized zone. Copper has been enriched on pyrite surfaces in unoxidized tailings in the largest amount, followed by Zn and As. However, only 1.4 to 3.1% of the Cd and Zn released by sulphide oxidation in the oxidized zone have been enriched on the pyrite surfaces in the unoxidized tailings, but for As and Cu corresponding figures are about 64 and 43%, respectively. There were many uncertainties in these calculations, and the results shall not be taken too literally but allowed the conclusion that enrichment on pyrite surfaces is an important process for retention of As and Cu below the oxidation front in pyrite rich tailings. Laser ablation is not a surface analysis technique, but more of a thin layer method, and gives no information on the type of processes resulting in enrichment on the pyrite surfaces. Although only pyrite grains that appeared to be fresh and without surface coatings were used in this study, the possibility that a thin layer of Fe-hydroxides occurred must be considered. Both adsorption to the pyrite directly or to Fe-oxyhydroxides may explain the enrichment of As, Cd, Cu and Zn on the pyrite surfaces, and, in the case of Cu, also the replacement of Fe(II) by Cu(II) in pyrite.     

Enrichment characteristics and its geological significance of dispersed elements within sulfide minerals from the VI ore belt in the Maoping Pb-Zn deposit,Yunnan Province,ChinaSCIEI北大核心CSCD

作为华南大面积低温成矿域的重要组成部分,川滇黔铅锌矿集区是我国重要的铅锌银等资源基地之一,同时该矿集区也是Ge、Cd、Ga和In等稀散元素的超常富集区域。毛坪矿床是该矿集区内第二大铅锌矿床,累计探明铅锌金属储量超过3Mt(Pb+Zn平均品位≥18%),锗(Ge)保有储量182t。本文以新发现的Ⅵ矿带(铅锌金属已探明储量≥60万t,Pb+Zn平均品位≥20%)为研究对象,利用LA-ICPMS对主要矿石矿物闪锌矿和黄铁矿进行了微区原位微量元素组成和Mapping分析。研究结果显示Ⅵ矿带闪锌矿普遍富集Ge(最高580×10^(-6),均值81.1×10^(-6))、Cd(最高3486×10^(-6),均值1613×10^(-6))和Ga(最高190×10^(-6),均值44.4×10^(-6));黄铁矿普遍富集Mn、As、Pb、Cu、Ag和Sb。与Ⅰ和Ⅱ号矿带闪锌矿相比,Ⅵ号矿带闪锌矿更富集Ge和Ga。闪锌矿中Fe和Pb以类质同象为主,偶见黄铁矿和方铅矿显微包体;Cu、Ge、Ag和As赋存形式主要为类质同象,替代方式为Ge^(4+)+2(Cu+,Ag+,As+)↔3Zn^(2+);Cd以类质同象方式赋存为主,替代机制为Cd^(2+)↔Zn^(2+);Ga和In可能主要以类质同象方式存在。黄铁矿中Pb和Mn主要以方铅矿和碳酸盐矿物显微包体为主;Cu、As和Sb以类质同象形式存在于黄铁矿中;Ag和Zn可能以独立矿物形式赋存;Co和Ni以类质同象方式替代Fe进入黄铁矿晶格中,替代方式为Ni^(2+)+Co^(2+)↔2Fe^(2+)。毛坪矿床新发现Ⅵ矿带硫化物相比典型MVT矿床硫化物具有不同的In和Ge含量以及Cd/Fe比值,结合矿床地质特征和其他证据,表明毛坪矿床成因类型特殊,有别于经典MVT铅锌矿床,属于川滇黔型铅锌矿床。     

Metal source of gold deposits in the Jiaoxibei area,Eastern China: Insights from trace element analysis of gold and pyrite

The metal source of gold deposits in the Jiaoxibei area, eastern China, has been investigated by many researchers, but no consensus has been reached so far. In this study, three typical gold deposits, the Xinli, Jiaojia, and Dayingezhuang deposits, were selected for trace element analysis of gold and pyrite to constrain the metal source. Pyrite from these three deposits has similar morphological and compositional characteristics, and can be divided into three types: Py1 with euhedral to subhedral textures, Py2 with subhedral to anhedral textures with micro-fractures, and Py3 with subhedral to anhedral textures and intergrowing polymetallic sulfides. Among them, Py2 and Py3 were formed in the main ore-forming stage and they are the dominant host minerals of visible gold. In these deposits, visible gold occurs mainly in micro-fractures or as inclusions in Py2 and Py3. Most of the pyrite has extremely low concentration of invisible gold, indicating that visible gold in the Jiaoxibei district is not a product of the remobilization of invisible gold from earlier pyrite. Both Py2 and Py3 are characterized by low Co concentration of <100 ppm and Co/Ni ratio of <1, which are similar to those of pyrite in sedimentary rocks. Therefore, ore-forming metals of these gold deposits in the Jiaoxibei district may originate mainly from a sediment-related metal source.     

Concentrations and solubility of heavy metals in muck sediments from the St. Lucie Estuary,U.S.A.

To evaluate muck sediments as a potential soil amendment, total and Mehlich III-extractable concentrations of Cd, Cu, Cr, Ni, Pb, Zn, and Co in 59 muck sediment samples from the St. Lucie Estuary were analyzed. A seven-step chemical fractionation procedure was used to assess the potential mobility of heavy metals. Except for Cd, the average total concentrations of the metals are lower than the reported average concentrations of these elements in municipal composts in the U.S.A. The concentrations were also below critical levels for the safe use of wastes and byproducts in agriculture, as established by the United States Environmental Protection Agency. The Cd, Cu, Cr, Ni, Pb, Zn and Co in the sediments were predominantly associated with silicate minerals in the residual form. Most metals in the muck sediments occur predominantly in weakly mobile or nonbioavailable forms. Use of mucks in neutral pH upland soils should not pose any significant hazards or risk to the environment. However, Cd, Cu, Cr, Ni, Pb, Zn, and Co, especially Zn, Cu, and Pb, could be more readily released from the muck sediments under acidic soil conditions.     

Sulfide minerals in Coal Bed V,minnehaha mine,Sullivan County,Indiana

Polished and thin section examinations of samples from Indiana Coal Bed V (Springfield) have shown three sulfides to be present; namely pyrite, marcasite and sphalerite. Pyrite and marcasite are dominant forms whereas sphalerite is very minor. These sulfides appear to have formed in four distinct stages as judged on the basis of mineralogy and mineral texture. Pyrite occurs as framboids throughout the coal seam, as fibrous crystals in two horizons of the coal and in massive form as cleat fillings and cell fillings in fusinite and semi-fusinite. Marcasite occurs in spherical polycrystalline and twinned grains, as polycrystalline overgrowths on framboids, as cementing material for clusters of framboids, as blocky polycrystalline grains and with pyrite as cell fillings in fusinite and semi-fusinite. Sphalerite occurs exclusively as cell fillings in semi-fusinite. The paragenetic sequence indicates fluctuations in the overall coal bed chemistry. Individual sections display evidence of chemical variation on the micro scale.     

甘肃寨上金矿床矿物组成特征与矿质沉淀机理

位于西秦岭礼(县)—岷(县)成矿带西段的寨上金矿床,是近年发现的一个大型微细浸染型金矿。笔者通过显微镜观察、电子探针和扫描分析等综合分析技术,确认金矿床中矿物组成相当丰富,既有大量硫化物、硫盐、氧化物、硫酸盐、碳酸盐、钨酸盐,又有碲化物、自然金属及多金属互化物。除常见矿物为自然金、黄铁矿、黄铜矿、黝铜矿、方铅矿、闪锌矿、辉锑矿、石英、白钨矿、方解石、菱铁矿、铁白云石和重晶石外,笔者还鉴定出在卡林型金矿床较少见的一些矿物,如硫铜锑矿、车轮矿、辉锑铅矿、辉钼矿、碲汞矿、碲镍矿、Cu-Zn-Ni-Sn-Fe的金属互化物和白钨矿等。矿石中矿物种类较多,组成较复杂以及存在显微自然金,构成寨上金矿床的一大特色。赋矿围岩中含Fe碳酸盐矿物溶解释放Fe以及溶解Fe的大量硫化物化,是寨上金矿床中存在显微可见自然金的最重要因素和金沉淀富集的有利条件。     

兰坪盆地白秧坪银铜多金属矿集区中银、钴、铋、镍的赋存状态与成因意义

白秧坪银铜多金属矿集区位于兰坪盆地北部。矿集区可分为东、西两个成矿带。赋矿地层主要为上三叠统三合洞组碳酸盐岩、第三系始新统保相寺组碎屑岩和下白垩统景星组碎屑岩。矿体主要以脉状、网脉状及透镜状形式产出。作者通过显微镜观察、电子探针和扫描分析等综合分析技术,确认白秧坪银铜多金属矿集区中矿物组成相当丰富,已鉴定出的矿物超过50种,既有大量硫化物、硫盐、氧化物、硫酸盐、碳酸盐,又有自然金属及金属互化物、卤化物等。除常见矿物为黄铁矿、毒砂、白铁矿、黄铜矿、方铅矿、闪锌矿、黝铜矿、砷黝铜矿、铜蓝、斑铜矿、辉铜矿、雌黄、菱铁矿、方解石、铁白云石、重晶石、天青石和石英外,作者还鉴定出一些银、钴、铋、镍、砷、锑的矿物,如自然铋、辉铋矿、辉银矿、辉砷钴矿、硫钴镍矿、硫铜铋矿、硫铋铜矿、辉砷镍矿、车轮矿、硫砷铜矿、单斜硫砷铅矿、灰硫砷铅矿等。矿石中矿物种类较多,组成较复杂,存在Co,Bi,Ni等元素的矿物,构成白秧坪银铜多金属矿集区的一大特色。在兰坪盆地白秧坪银铜多金属矿集区各矿段内,除了Cu、Pb、Zn构成工业矿体外,矿石中Ag、Co、Ni、Bi及As、Sb、Ba等元素的含量也相当高,可作为Cu-Pb-Zn-Ag-Co-Ni-Bi矿石来综合开发利用。白秧坪银铜多金属矿集区中Ag、Co、Ni、Bi等元素富集条件为低温、中低盐度,形成压力较小的浅成环境;成矿流体是一种富含CO2的Ca2+-Na+-SO24-Cl-类型、由大气降水演化而成的盆地热卤水。成矿物质主要来源于含有基性火山岩的兰坪盆地基底变质岩系。     

Mineralogy and the release of trace elements from slag from the Hegeler Zinc smelter,Illinois (USA)

Slag from the former Hegeler Zn-smelting facility in Illinois (USA) is mainly composed of spinifex Ca-rich plagioclase, fine-grained dendritic or coarse-grained subhedral to anhedral clinopyroxenes, euhedral to subhedral spinels, spherical blebs of Fe sulfides, silicate glass, and less commonly fayalitic olivine. Mullite and quartz were also identified in one sample as representing remnants of the furnace lining. Secondary phases such as goethite, hematite and gypsum are significant in some samples and reflect surficial weathering of the dump piles or represent byproducts of roasting. A relatively rare Zn-rich material contains anhedral willemite, subhedral gahnite, massive zincite, hardystonite and a Zn sulfate (brianyoungite), among other phases, and likely represents the molten content of the smelting furnace before Zn extraction. The bulk major-element chemistry of most slag samples is dominated by SiO₂, Al₂O₃, Fe₂O₃ and CaO. The bulk composition of the slag suggests a high viscosity of the melt and the mineralogy suggests a high silica content of the melt. Bulk slag trace-element chemistry shows that the dominant metal is Zn with >28.4 wt.% in the Zn-rich material and between 212 and 14,900 mg/kg in the other slags. The concentrations of other trace elements reach the following: 45 mg/kg As, 1170 mg/kg Ba, 191 mg/kg Cd, 242 mg/kg Co, 103 mg/kg Cr, 6360 mg/kg Cu, 107 mg/kg Ni, and 711 mg/kg Pb.