祁连山石—一种新的硼碳酸盐矿物

作者在鉴定青海省居红图硼矿床的矿物标本时发现了祁连山石,经系统测试确定为一种含硼的碳酸盐新矿物,并经国际新矿物及矿物命名委员会批准,现予以报道。祁连山石呈无色透明的板状或柱状晶体,多以集合体产出。矿物具玻璃光泽,硬度约等于2,D=1.706。{100}和{010}解理完全。矿物的化学分子式为NaHCO_3·H_3BO_3·2H_2O。该矿物属单斜晶系,空间群为C2。晶胞常数:a=1.6119 (8),b=0.6928 (4),c=0.6730 (3) nm;β=100.46(4)°,V=0.7390nm~3,Z=4。二轴晶(-),a=1.351(计算值),β=1.459,γ=1.486,2V=50°,光性方位x=b,y∧a=1°,z∧c=9°,中等色散r相似文献   

二溴羧基偶氮胂光度法测定钛酸铋烧结物中游离氧化铋

在0.04～0.16mol/LHClO_4介质中,Bi与二溴羧基偶氮胂发生显色反应,生成1:2的蓝色络合物,λ_(max)=625nm,ε=7.2×10~4L·mol~(-1)·cm~(-1),Bi量在0～0.5μg/ml范围内符合比耳定律。所拟方法已用于检测陶瓷电容钛酸铋烧结物中游离Bi_2O_3。     

我国首次发现的硅钾铀矿

硅钾铀矿属罕见的次生铀矿物,1986年我国首次发现于甘肃龙首山铀矿床氧化。带。对该矿物进行了多种测试工作。矿物为层状结构的铀酰硅酸盐矿物。晶胞参数a=6.62,b=7.03,c=7.06,β=105.2°。化学式:(K_(0·58) Na_(0·33)0.91(H_3O)[UO_2SiO_4]·0.8H_2O     

自然界中的辉锑矿-硒锑矿矿物系列

自然界中的辉锑矿-硒锑矿系列发现于西秦岭寒武系拉尔玛、邛莫金矿床中。与其密切共生的矿物有硒汞矿、硒铅矿、硒质块硫锑铜矿、硒镍矿、自然金以及石英、重晶石等。辉锑矿–硒锑矿系列的显微压力硬度为101.26~103 kg/mm²。主要元素的质量分数为: Sb 43.78%~73.81%,S 0.00%~28.76%,Se 0.00%~49.72%(但缺乏30.59%~43.04%之间的数据)。根据电子探针分析数据中Se/(S+Se)比值(原子比),可将所测矿物系列划分为(含硒质)辉锑矿、硒质辉锑矿、硫质硒锑矿和(含硫质)硒锑矿。矿物系列代表性的反射率(%)：(470 nm)Rg’=42.62~47.62,Rp’=30.83~40.55;(550 nm)Rg’=41.84~46.75,Rp’=31.48~38.85;(590 nm)Rg’=42.25~46.63,Rp’=30.73~39.46;(650 nm)Rg’=43.30~46.48,Rp’=30.01~41.56。两个含Se量为3%~5%含硒质辉锑矿的晶胞参数值为:a=1.120 9~1.121 2 nm,b=1.1299~1.130 3 nm,c=0.384 7~0.384 9 nm;而硫质硒锑矿、硒锑矿的晶胞参数值分别为：a=1.159 1~1.159 3 nm;b=1.172 4~1.174 7 nm;c=0.394 1~0.398 4 nm。晶胞参数的变化与矿物中硫、硒含量变化密切相关。     

东天山维权银矿床自然铋的发现及流体演化特征

为研究东天山维权银矿中呈脉状、浸染状分布的自然铋和含铋矿物特征及其形成机制,对维权矿床中含铋的银矿石中的矿物进行了矿相学、电子探针和能谱分析及流体包裹体研究。结果表明,维权银矿床中铋矿物与银矿物共生,铋矿物主要为自然金属(自然铋)、硫化物(辉铋矿)及硫盐矿物(硫铋银矿)等类型;维权矿床的热液成矿过程可分为3个阶段:(Ⅰ)石英-氧化物阶段,主要矿物组合为毒砂-黄铁矿-磁铁矿,流体温度为376~289℃;(Ⅱ)铋矿物-碳酸盐阶段,主要矿物组合为自然铋-硫铋银矿,其流体温度低于271℃;(Ⅲ)银矿物-硫化物阶段,以自然银-方解石-黄铜矿-方铅矿-闪锌矿为主,流体温度为200~160℃。     

海南乐东地区抱伦金矿矿石特征及其成因矿物学意义

抱伦金矿为大型中温热液石英脉型矿床,矿石以含金石英脉型为主,次为含金蚀变岩型。主要金属矿物为黄铁矿和磁黄铁矿,次要金属矿物20多种;脉石矿物有石英、方解石、绢云母和绿泥石等。金矿物主要为自然金,次为金、铋和银的固溶体,含Au8.20%～99.30%,Ag≤52.71%,Bi≤91.20%。铋、碲矿物有自然金属、硫化物、铋化物、硫盐和碲化物等类型。金矿石含Bi0.18×10-6～16×10-6,平均4.11×10-6,富矿石中达419×10-6。该矿床属较特殊的富铋类型,与琼西戈枕剪切带的金矿有相似之处,在琼西-粤东金矿带大陆一侧存在类似矿床,它们在成因上均应与岩浆和韧—脆性断裂活动有关。     

人工晶体(Bi38CrO60)--驾鹿矿在自然界的首次发现及矿物成因和地质意义

1983年, ZhitomirsKii等人在实验室条件下合成了四方晶体Bi16CrO27和立方晶体Bi38CrO60.它们在自然界首次发现于中国陕西省洛南县驾鹿金矿床中,分别被命名为铬铋矿(Bi16.006Cr0.997O27)和驾鹿矿(Bi38.008Cr0.996O60).驾鹿矿较铬铋矿形成较晚,其共生、伴生矿物有黄铜矿、自然金、碲金矿、含氧金矿物、石英等.常呈不规则粒状集合体,偶见＜0.05 mm立方体微晶,棕黑色,金属光泽;平均维克硬度Hv=232.78 kg/mm2 ,平均摩氏硬度Hm=4.15;实测密度D=14.10(3) g/cm3,计算密度Dx=14.08(2) g/cm3,折射率n=3.14(3).采用2种电子探针进行波谱定量分析的成分及计算的化学式分别是①EPM8100分析的结果w(Bi2O3)为98.854%、w(CrO3)为1.111%,总和为99.965%;化学式为Bi38.009Cr0.995O60;②CAMEBAX-SX51分析的结果w(Bi2O3)为98.862%,w(CrO2)为1.112%,总和为99.974%;化学式为Bi38.008Cr0.996O60.均可写为Bi38CrO60.2种仪器测定的结果非常接近,说明所测定的化学成分和计算的化学式是十分可靠的.X-射线粉晶分析主要强线d(I)(hkl)分别为0.3215(100),(310); 0.27211(72),(321); 0.17145(40),(530); 0.1696(30), (600);0.1651(30),(611);0.1608(30),(620);0.29411(25),(222);0.3596(22),(220);0.2171(20),(332);0.1503(20),(631);0.1996(18),(510);0.2401(13),(330);0.2275(13),(420);0.1217(12),(653);0.1184(12),(750);0.1858(10),(521)等轴晶系,可能的空间群为Im3m;a=1.0181(1) nm,c/a=1,晶胞体积V=1.05529(1) nm3,Z=1.1-Kp/Kc=0.019.Cr+6,Bi+3,O-2.驾鹿矿和人工晶体(Bi38CrO60)在化学成分、X-射线粉晶数据基本一致,充分证明了驾鹿矿是人工晶体(Bi38CrO60)在自然界的首次发现.新矿物--铬铋矿及驾鹿矿是在碱性高温热液条件下形成的,受体系组份浓度的影响,特别是Cr+6的影响,驾鹿矿的形成稍晚于铬铋矿.Bi在金矿物中含量较高,因此铬铋矿及驾鹿矿的发现和研究对该金矿床找矿和研究有着重要的理论和实际意义.     

盈江铀矿的新资料

本文第一次提供了由单晶X射线衍射分析测定的盈江铀矿的空间群和晶胞参数。该矿物产于广东省下庄铀矿田。斜方晶系,空间群Bmmb(63),a=15.707(3),b=17·424(3),c=13.692(2)?,V=3747?~3,Z=4。Dc=4.60g/cm~3,Dm=4.54g/cm~3。化学式:(K_2,Ca)(UO_2)_7(PO_4)_4(OH)_6·6H_2O。二轴晶,负光性。2Vc=36°,2Vm=36—38°。Ng=1.707(2),Nm=1.703(2),Np=1.666(1)。光性方位:Ng//Y,Nm//X,Np//Z。     

首次发现锰副硅灰石

锰副硅灰石是副硅灰石一个新变种矿物,为国内外首次发现。产于我国内蒙古矽卡岩型铅锌矿床中。矿物属于单斜晶系,空间群C_(2h)~5-P2_(1/c),晶胞参数a=1.47213,b=0.70489,c=0.69055nm,β=95.827°±0.03,V=0.71289nm~3,Z=12。化学分子式为(Ca_(0.75)Mn_(0.19)Fe_(0.068))_(1.00)Si_(1.00)O_3,属于硅灰石亚族矿物。     

利用扫描电镜-电子探针研究四川杨柳坪镍铜硫化物矿床铂钯的赋存状态及沉淀机制

本文利用电子探针和配备能谱分析功能的扫描电镜对四川杨柳坪镍-铜硫化物矿床中铂钯的赋存状态进行了研究。结果表明,铂以独立矿物相砷铂矿和自然铂存在;钯以碲化物、碲铋化物、碲锑化物、锑化物及自然钯独立矿物相存在,也以类质同象形式分布在碲镍矿中(钯含量约10%),另外还以锑铋钯碲矿、六方锑碲钯矿、碲钯矿独立矿物相存,并以类质同象形式分布在Vavrinite(钯含量5%)和砷铂矿(钯含量1%~5%)中。杨柳坪矿床中铂钯元素沉淀与贱金属矿物(BMS)及晚期热液蚀变矿物蛇纹石、方解石密切相关,其沉淀经历了3个阶段:1早期高温阶段(1200~900℃),铂钯元素沉淀并包裹在BMS中;2中期中高温阶段(650~250℃),分离结晶作用使铂钯元素沉淀并分布BMS矿物的边部,同时该阶段热液来源的铂钯元素沉淀于BMS粒间;3晚期热液蚀变阶段(500~300℃),热液蚀变作用引起铂钯元素沉淀在蚀变矿物中或嵌布在BMS裂隙。本文研究成果为认识该矿床及同类型镍-铜硫化物矿床的铂钯成矿过程提供了新的依据。     

The Nucleus Deposit: Superposed Au–Ag–Bi–Cu Mineralization Systems at Freegold Mountain,Yukon, Canada

In this paper we present titanite U–Pb (both single crystal CA ID‐TIMS and in situ LA ICP‐MS) data, coupled with ore and gangue mineralogy and geochemical (both lithogeochemistry and microanalysis) data from the Nucleus Au–Ag–Bi–Cu deposit, in the Yukon (Canada) portion of the Tintina Au province. Arsenic‐bearing Au–Ag–Bi–Cu mineralization at Nucleus consists of two distinct styles of mineralization including: (i) reduced Au skarn and sulfide replacement; and (ii) a relatively shallow‐emplaced (as supported by textures and temperature of formation), vein‐controlled mineralization occurring mainly as veins and veinlets of various shapes (sheeted, single, stockworks, and crustiform), breccias, and disseminations. Whereas Au, Bi, and Cu mineralization from skarn is associated with hydrous retrograde alteration phases (actinolite, ferro‐actinolite, hastingsite, cannilloite, and hornblende), numerous alteration types are associated with the vein‐controlled style of mineralization and these include: biotite, phyllic, argillic, propylitic, carbonate, and quartz (silicification) alterations. The mineralization–alteration processes took place over a wide temperature range that is bracketed between 340 and 568°C, as indicated by chlorite and arsenopyrite geothermometers. The Au‐rich Nucleus deposit is characterized by anomalously high content of As and Bi (as much as 1 %), and whereas Au moderately correlates with Bi (r = 0.40) in the skarn mineralization style (where native Au is spatially associated with native Bi and Bi‐bearing sulfides), the two elements correlate poorly (r = 0.14) in the vein‐controlled type, in which native Bi‐ and Bi‐sulfide‐bearing veins are locally observed. Sphalerite from the vein‐controlled mineralized type is Fe‐rich (9.92–10.54 mol % FeS) indicative of low sulfidation conditions, as well as high temperature, with the latter further supported by arsenopyrite geothermometry (up to 491°C), low Ag content (3–7 wt.%) in Au, and the high gold fineness (926–964). Whereas molybdenite Re–Os ages from quartz‐molybdenite veins range from 75.8 to 76.2 ± 0.3 Ma, titanite from the skarn type mineralization recorded CA ID‐TIMS and LA ICP‐MS U–Pb ages of 182.6 ± 2.4 Ma and 191.0 ± 1.5 Ma, respectively, thus precluding any genetic link between the two spatially associated styles of mineralization from the Nucleus deposit area. The Au–Ag–Bi–Cu Nucleus deposit is therefore regarded as a superposed system in which two mineralization types, without any petrogenetic relationship, overlapped, possibly with remobilization of early‐formed mineralization.     

Trace metal nanoparticles in pyrite

Hydrothermal pyrite contains significant amounts of minor and trace elements including As, Pb, Sb, Bi, Cu, Co, Ni, Zn, Au, Ag, Se and Te, which can be incorporated into nanoparticles (NPs). NP-bearing pyrite is most common in hydrothermal ore deposits that contain a wide range of trace elements, especially deposits that formed at low temperatures. In this study, we have characterized the chemical composition and structure of these NPs and their host pyrite with high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), analytical electron microscopy (AEM), and electron microprobe analysis (EMPA). Pyrite containing the NPs comes from two types of common low-temperature deposits, Carlin-type (Lone Tree, Screamer, Deep Star (Nevada, USA)), and epithermal (Pueblo Viejo (Dominican Republic) and Porgera (Papua New-Guinea)).EMPA analyses of the pyrite show maximum concentrations of As (11.2), Ni (3.04), Cu (2.99), Sb (2.24), Pb (0.99), Co (0.58), Se (0.2), Au (0.19), Hg (0.19), Ag (0.16), Zn (0.04), and Te (0.04) (in wt.%). Three types of pyrite have been investigated: “pure” or “barren” pyrite, Cu-rich pyrite and As-rich pyrite. Arsenic in pyrite from Carlin-type deposits and the Porgera epithermal deposit is negatively correlated with S, whereas some (colloform) pyrite from Pueblo Viejo shows a negative correlation between As + Cu and Fe. HRTEM observations and SAED patterns confirm that almost all NPs are crystalline and that their size varies from 5 to 100 nm (except for NPs of galena, which have diameters of up to 500 nm). NPs can be divided into three groups on the basis of their chemical composition: (i) native metals: Au, Ag, Ag–Au (electrum); (ii) sulfides and sulfosalts: PbS (galena), HgS (cinnabar), Pb–Sb–S, Ag–Pb–S, Pb–Ag–Sb–S, Pb–Sb–Bi–Ag–Te–S, Pb–Te–Sb–Au–Ag–Bi–S, Cu–Fe–S NPs, and Au–Ag–As–Ni–S; and (iii) Fe-bearing NPs: Fe–As–Ag–Ni–S, Fe–As–Sb–Pb–Ni–Au–S, all of which are in a matrix of distorted and polycrystalline pyrite. TEM-EDX spectra collected from the NPs and pyrite matrix document preferential partitioning of trace metals including Pb, Bi, Sb, Au, Ag, Ni, Te, and As into the NPs. The NPs formed due to exsolution from the pyrite matrix, most commonly for NPs less than 10 nm in size, and direct precipitation from the hydrothermal fluid and deposition into the growing pyrite, most commonly for those > 20 nm in size. NPs containing numerous heavy metals are likely to be found in pyrite and/or other sulfides in various hydrothermal, diagenetic and groundwater systems dominated by reducing conditions.     

湘西沃溪钨锑金矿床超纯自然金

湘西沃溪钨锑金矿床产有自然界中十分罕见的超纯自然金。超纯自然金的Au含量在99 %以上 ,Fisher成色接近1000。自然金中含有Ag、Pb、Zn、Cu、As、Sb、Hg、Bi等显微化学组分。与一般自然金相比 ,超纯自然金的Ag 含量显著偏低 ,而Pb、Zn、As、Sb、Hg、Bi等显微化学组分含量趋于偏高 ,且较稳定。理论分析表明 ,超纯自然金的形成与强氧化性的酸性成矿流体有关。流体中金、银主要以MeCl2-(Me=Au或Ag)的络合物形式迁移。推断矿床成矿可能与区域中酸性岩浆活动有成因联系。     

Te and Se mineralogy of the high-sulfidation Kochbulak and Kairagach epithermal gold telluride deposits (Kurama Ridge, Middle Tien Shan, Uzbekistan)

Summary The Late Paleozoic Kochbulak and Kairagach deposits are located on the northern slope of the Kurama Ridge, Middle Tien Shan, in the same volcanic structure and the same ore-forming system. Au–Ag–Cu–Bi–Te–Se mineralization is confined to veins and dissemination zones accompanied by quartz-sericite wall-rock alteration. The tellurides, calaverite, altaite, hessite, and tetradymite are widespread at both deposits; at Kairagach selenides and sulfoselenides of Bi and Pb are common, while at Kochbulak Bi and Pb telluroselenides and sulfotelluroselenides are typical. The paragenetic sequence of telluride assemblages are similar for both deposits and change from calaverite + altaite + native Au to sylvanite + Bi tellurides + native Te, Bi tellurides + native Au, and, finally, to Au + Ag tellurides with time. These mineralogical changes are accompanied by an increase in the Ag content of native gold that correlates with a decrease in temperature, fTe₂ and fO₂ and an increase in pH.     

Ore prospecting model and targets for the Dashuigou tellurium deposit,Sichuan Province,China

The Dashuigou tellurium (Te) deposit in Shimian city, Sichuan Province is the only known independent Te ore deposit in China. Samples were collected by 1/50,000 stream sediment survey and analyzed by inductively coupled plasma–mass spectrometry, X-ray fluorescence spectrometry, emission spectrometry, and atomic absorption spectroscopy. An ore prospecting model for the Dashuigou Te deposit was then established. In the Dashuigou area, bismuth (Bi), Te, and gold (Au) concentrations in stream sediment samples displayed weak-positive anomalies, while silver (Ag) displayed a weak-negative anomaly. Bi, Te, Ag, and Au anomalies are regarded as indicators of Te deposits; the greater the ratio of Te?+?Bi/Au?+?Ag, the larger the possibility of an independent tellurobismuthite deposit. The ratio calculated from our samples is 7.288. Five locations were identified for prospecting for Te minerals by this model, including the northern part of the Dashuigou Te deposit, Majiagou, Tizigou, southeastern Miaoping, and northern Baishuihe. These five regions are within the Dashuigou dome anticline, the exposed strata of which are controlled by tracing the tensile shear fracture; the metallogenic geological conditions and geochemical characteristics are the same as those of the known Dashuigou Te deposit. Already, Te–Bi veins have been found in some of these areas.     

个旧卡房矿田锡-铜矿床伴生金（银）矿赋存状态及其富集规律

云南个旧锡多金属矿区卡房矿田伴生金矿主要赋存于中三叠统个旧组卡房段地层的中上部,矿化受花岗岩侵入的热液活动、变玄武岩及NE向和EW向褶皱、断裂构造控制。伴生金矿床可分为含金（银）多金属矽卡岩硫化锡铜矿床及含金脉（层）状锡铅矿床。金主要呈银金矿、自然金等独立矿物出现,主要载金矿物有自然铋、毒砂、辉钼矿等,其中以自然铋含金量最高。金矿化在变玄武岩底界之下6～20m处矿化最强,最富集。     

A New Variety of Mineral—Argentian Mercurian Gold

Argentian mercurian gold,golden-yellow in colour,is a variety of native gold containing Ag and Hg,coccurring as hexagonal and tetragonal crystals in hairy,milk-droplet or irregular forms.Its microhardness Hv=91kg/mm^2,equivalent to 3.04on Mons‘scale,and the reflectance is 70.35%(589nm).Chemical analysis gave:Au 56.05-67.33,Ag18.29-31.06 and Hg 10-14.82%,as well as minor Cu.In a few samples Bi or Fe was also detected.The simplified formula is (Au0.52Ag0.36Hg0.09Cu0.02)0.99.X-ray analysis suggests the mineral is of isometric system,with space group=Oh^5-Fm3m,a0=0.40803nm,V=0.06739nm^3,and Z=4.Argentian mercurian gold occurs in a Ag-multimetal deposit at Xiacun,Baiyu County,Sichuan Province,As observed in the mining district,the mineral is distributed along the fissures of the main metallic minerals pyrite,tetrahedrite,chalcopyrite,arsenopyrite,galena,sphalerite,etc.,or in the sulfide veinlets developed in the.fissures of these minerals.Also found in the mineral deposit are native gold,argentite,sulvanite,bournonite,boulangrite,etc.     

小秦岭金矿田中的两种罕见矿物—碲铅铋矿和自然碲

碲铅铋矿和自然碲产于河南省小秦岭含金石英脉矿床中。碲铅铋矿化学成分平均值(%)为:Te44.06,Bi40.24,Pb14.23,并含有微量的Ag、Au、Hg、Fe、Ni、Cu等元素。理论化学式为(Bi,Pb)_3Te_4,其中Bi>Pb。共生矿物有自然金、碲金矿、破银矿、碲铅矿、碲金银矿、碲铋矿;方铅矿、闪锌矿、黄铁矿、黄铜矿等。 自然碲反射色为纯白微带乳色,非均质性清楚,偏光色为蓝灰-棕灰色。显微硬度为H_v=85.1kg/mm~2(25g)。共生矿物有碲金银矿、碲银矿、黄铜矿等。化学成分中碲含量达98.44％,并含Ag、Cu、W、Fe、Pt等微量元素。     

内蒙古宁城地区煌斑岩与金矿

内蒙古宁城地区出露加里东海西期煌斑岩脉群，其中云斜煌斑岩内，沿燕山期韧性剪切片理化带，分布金矿体。煌斑岩是客观找金的标志。金矿体中硅化，绿泥石化，方解石化发育。主要金属矿物是黄铁矿。金主要以显微次显微自然金包裹体，赋存于黄铁矿内。     

四方铜金矿CuAu在我国发现

四方铜金矿产于新疆玛纳斯县清水河上游萨尔达拉含铂基性-超基性岩体中。岩体主要为暗绿色蛇纹石化斜辉辉橄岩,岩石化学成分多数为正常系列,少数为铝过饱和系列。岩体长9公里,宽140米,是一个向南倾斜的单斜岩墙。岩体侵入到泥盆系头苏泉组的黑灰色粉砂质板岩中。外接触带仅几十厘米到1米左右宽,以绿泥石化、绿帘石化、蛇纹石化为主,其次是碳酸岩化。内接触带有1米多宽,以蛇纹石化、透辉石化、透闪石化为主,个别地段有阳起石、透闪石软玉。