福建碧田铜金银矿床的金属矿物研究

碧田矿床是成因上与燕山晚期次火山岩有关的以银为主的大型铜金银矿床。金属矿物种类复杂，除常见的黄铁矿、黄铜矿、斑铜矿外，还有多种铜铋硫盐矿物（锌砷黝铜矿、铋砷黝铜矿、铋锑黝铜矿、针硫铋铅矿、硫铋铜矿）、钨锡硫化物（硫铁锡铜矿、硫钨锡铜矿）及多金属硫化物。金银矿物除辉银矿外，主要是Ａｕ－Ａｇ系列的自然金、银金矿、金银矿及自然银。这些矿物形成于不同的物理化学条件下，大多数铜矿物、铜铋硫盐矿物和钨锡硫化物是在中高温（２６０—３８０℃）条件下、硫逸度较高（ｌｇｆＳ２＝－８．７４—－１２．０６）、流体盐度高并处于沸腾的状况下形成的；而多金属硫化物和金银矿物则主要是在中低温（１２０—２６０℃）条件下，硫逸度较低（ｌｇｆＳ２＝－１１．６—－１９．５），流体盐度也较低的状况下形成的。     

我国首次发现钒砷锗石

1988年12月我们在四川廿孜某多金属矿床中发现了钒砷锗石。这种矿物首先由Н·М·Мнтряева等(1968)发现于苏联。在我国则属首次发现。与钒砷锗石共生的矿物,除方铅矿、闪锌矿外,还有锌锑黝铜矿、黄铁矿、黄铜矿、斑铜矿、铜蓝、自然金、银金矿、硫铜银矿、硫汞银铜矿、钡长石、钡冰长石、重晶石、曼纳     

夏塞银多金属矿床中硫化物和硫盐系列矿物特征及其意义

夏塞矿主档是大型的热液脉型银多金属矿床,通过对大量矿石光（薄）片观察和电子探针分析表明,除主要（方铅矿、富铁闪锌矿）和次要（黄铁矿、毒砂、磁黄铁矿、黄铜矿等）硫化物外,硫盐毓硫物十分发育,主要有Ｃｕ－Ｓｂ－Ａｇ硫盐（黝铜矿、含银黝铜矿和银黝铜矿）、Ｓｂ－Ａｇ硫盐（深红银矿、辉锑银矿）、Ｐｂ－Ｓｂ硫盐（脆硫锑铅矿、硫锑铅矿）和Ｂｉ－Ｐｂ硫盐（斜方辉饿铅矿）。此外,尚有少（微）量黄锡矿、锡石、自然饿和银金矿等。银的硫盐硫物和硫化物（辉银矿）乃是获得银的主要工业矿物,这些硫盐毓矿物常与硫化物伴生,多沿方铅矿、富铁闪锌矿、黄铁矿等的解理、裂隙或粒间产出,这些研究结果不仅有助于了解矿化作用过程,而且为矿床评价,组分综合利用和选冶提供重要依据。     

西南北海道地区早川、释迦坑矿床的铜铅锌矿化作用

早川与释迦坑矿床的铜铅锌矿化作用特征,集中表现在单位矿脉的构造、矿物组合、矿化阶段以及矿脉中石英和母岩氧同位素组成等方面.早川与释迦坑的矿床中,存在着黄铜矿—黄铁矿—黝铜了—方铅矿—伴有闪锌矿的石英脉(铜铅锌石英脉)以及方铅矿—伴有闪锌矿的石英脉(铅锌石英脉.铜铅锌石英脉较铅锌石英脉更早期形成.铜铅锌石英脉的矿物组合为黄铜矿、黄铁矿、黝铜矿—砷黝铜矿、方铅矿、闪锌矿、硫砷铜矿、车轮矿、板硫锑铅矿、碲银矿、黄锡锌矿、砷等轴硫钒铜矿、Cu-Fe-Zn-Sn-S系矿物、硫碲铋铅矿、硫铜铋铅矿、石英以及磷灰石.铅锌石英脉的矿物组合为方铅矿、闪锌矿、黄铁矿、黄铜矿、黝铜矿、银金矿及石英.随着矿化作用早期向晚期过渡,闪锌矿中的FeS含量有所减低.黝铜矿—砷黝铜矿的单一颗粒中,Sb与As之间的化学组成出现明显的非均质性.     

中国主要伴（共）生银矿床银的赋存状态研究

通过２０多个伴（共）生银矿床银的矿物及组合、银矿物的工艺性质、银的载休矿物及银在矿石中的平衡配分等方面的系统研究，表明中国伴（共）生银矿床中银的重要工业矿物为银锑黝铜矿（黝锑银矿）、深红银矿、螺状硫银矿．不同的矿床其银矿物组合有所变化，反映其成矿的物理－化学条件的差异。银矿物粒度细小，多小于０．０７４ｍｍ，主要以包裹银产在载体矿物中。银的主要载体矿物为方铅矿、闪锌矿、黄铜矿、黄铁矿，视其伴生的主金属矿种不同而变化，因而银在不同矿床中的平衡配分结果也有较大差异。中国现行生产矿山银的选矿回收率与其理想回收率有一定的差距，说明提高银的选矿回收率尚有一定的潜力。     

梭梭井银铅矿床银的赋存状态及其与回收率的关系

该矿床中银品位可达数千g/t.工业矿物为方铅矿、黄铜矿、银黝铜矿、螺状硫银矿—辉银矿、硫铜银矿等.本文在研究银的赋存状态、粒度和分布特征的基础上,探讨了银回收的有效途径.     

北京市得田沟金矿床矿物特征和金的赋存状态

得田沟金矿床是受韧性剪切带控制的石英脉－蚀变岩型金矿床。容矿岩石主要为太古宙受混合岩化的角闪岩相变岩系。矿石矿物主要为黄铁矿、方铅矿、闪锌矿、黄铜矿、碲铅矿及金、银（铋）的单质和化合物等；脉石矿物主要为石英、方解石、绿泥石、绿帘石、绢云母、阳起石等。Ａｕ、Ａｇ（Ｂｉ）主要呈细粒自然金、自然银、碲金银矿、针碲金银矿、碲银矿、六方碲银矿、螺状硫银矿、未定名矿物ＡｇＳ１＋ｘＴｅ１－ｘ和Ｂｉ５Ｔｅ６存在。     

内蒙拜仁达坝超大型Ag-Pb-Zn多金属矿床中针硫锑铅矿的发现与成因意义

在内蒙拜仁达坝超大型Ag-Pb-Zn多金属矿床中,产出针硫锑铅矿。与其共生的金属矿物主要为方铅矿、银黝铜矿、磁黄铁矿、黄铜矿、块硫锑铅矿等。针硫锑铅矿呈长柱状、针状、毛发状、束状和不规则状等,粒度变化较大,一般为0.05～4mm,最大可达12mm。反光显微镜下为灰白色,强非均性,显微硬度VHN100g=93.25～127.39kg/mm2(平均111.05kg/mm2),相当于摩氏硬度3.06～3.40(平均3.24)。矿物主要化学成分质量分数为:Pb52.20%～57.80%(平均54.89%),Sb22.26%～28.13%(平均26.08%),S18.65%～19.62%(平均19.01%),并含有少量的Fe、Cu、Zn、Ag和As等元素。相应的平均化学分子式为(Pb4.91,Cu0.04,Fe0.03,Zn0.01)4.99(Sb3.97,As0.04)4.01S11.00,标准化学式为Pb5Sb4S11。晶体为单斜晶系对称,晶胞参数值a=2.156nm,b=2.349nm,c=0.810nm。矿床中针硫锑铅矿的形成,与成矿温度较低、硫逸度升高以及还原作用密切相关。     

东岗山银多金属矿床银的赋存状态的研究

东岗山银多金属矿床有三种类型，其中最重要的是锡石─硫化物型银矿床。银形成于硫化物成矿后期的硫锑铅矿─方铅矿─黄铜矿─银黝铜矿阶段。银的赋存状态有三种：①以独立矿物相即银黝铜矿的形式赋存于主要矿石矿物之中；②以类质同象替代状态产出，并且不排除次显微状银黝铜矿存在的可能性；③在氧化带的下部则为次生的辉银矿。     

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。     

一种未定名的硫盐矿物——Pb_6Bi_7(Cu,Ag)S_(17)

在河北省涞源的铜铁矿床中,发现了一种未定名的Pb-Bi-Cu的硫盐矿物,它以不规则粒状产于黄铜矿之中,与它共生的有方铅矿、闪锌矿、碲银矿、硫银铋矿和自然银等。该矿物是铅灰色,金属光泽,直径0.003—0.72mm,在显微镜下呈白色微蓝,双反射弱,非均质性明显,H_v=119.75kg/mm~2(50g),D_x=7.04g/cm~3。六个颗粒的平均化学成分值是Pb 36.51,Bi 44.80,S 15.35,Cu 1.82,Ag 1.54,Cr0.105,总计100.135。理论化学式为Pb_6Bi_7(Cu,Ag)S_(17),其中Cu>Ag。X射线衍射的强线值:3.428(10,012),3.059(4.140),2.996(9,041),2.765(5,207),2.247(4,250),2.023(3,133);晶胞参数a=8.811,b=13.060,c=7.106,~(?)_(?)V=817.699~3。Z=1,斜方晶系。     

南秦岭大型钡成矿带中硫钒铜矿的特征及成因意义

在南秦岭下寒武统硅岩建造中的毒重石-重晶石矿床中,产出大量硫钒铜矿.硫钒铜矿呈正方形,长方形及不规则状,粒度大小变化较大,一般为0.01 mm～1 mm,最大可达7 mm.反光显微镜下为淡柠檬黄色,显微硬度134.5 kg/mm2～139.8 kg/mm2,相当于摩氏硬度3.46～3.50.主要化学成分为:Cu 47.18～52.02(平均50.44),V 6.50～14.32(平均11.95),Sn 0.00～12.85(平均2.15),S 31.77～34.34(平均33.29),As 0.00～5.12(平均0.86).Fe 0.00～3.27(平均0.77),部分样品含有极少量的Fe,Ni,Co,Sb,Se,Te,In.相应的平均化学分子式为Cu3.04(V0.90,Sn0.07,Fe0.05,As0.04,Sb0.01)1.07(S3.98,Se0.02)4.00,简化式为:Cu3(V,Sn,As,Fe)S4.矿物为等轴晶系.晶胞参数值a=0.539 2nm.成矿带中硫钒铜矿的形成与钒的富集,与有机质演化受热和生物降解作用有密切联系.     

我国首次发现的杂铅矿

杂铅矿（Izoklakeite）^[1]是一个Ag-Cu—Pb—Sb—Bi硫盐矿物。1984年发现于我国广西芒场锡—多金属矿床块状锡石—石英—硫化物矿石中。与毒砂、黄铜矿、黝铝矿、方铅矿（少）、浓红银矿和自然铋,有时也与自然锑等密切共生。文中给出了杂铅矿的若干特征参数。     

新变种矿物—含锗锡硫钒铜矿

含锗锡硫钒铜矿是硫钒铜矿的含锗锡变种。它产于四川省白玉县呷村银多金属矿床中,反光显微镜下为淡柠檬黄色,形态呈正方形、长方形及不规则状。粒度一般为0.01—0.1mm,最大为0.3mm。显微硬度Hv=137.8kg/mm2,相当于HM=3.49。反射率:589nm 31.54%。主要化学成分为:Cu 52.29—54.71%,S 30.59—32.49%,V 5.70—6.50%,Ge 4.3—6%,Sn2.43—3.56%,还含微量Zn、Fe、As、Sb、Bi等。简化式为:Cu3(V,Ge,Sn)S4。矿物为等轴晶系,ao=10.66,V=1211.36,空间群为P43m,Z=8。     

The Relationship Between Mineralogical Characteristics and Isotopic Composition of Sphalerite,as Exemplified by the Huxu Deposit,China

The relationship between mineralogical characteristics and isotopic composition of sulfides has not received its proper share of attention from geologists, although many references are available concerning the application of sulfur isotopes to geological problems. Located in the vicinity of the contact region between the Yangtze Platform and the South China Caledonian Folding Zone, the Huxu deposit is hosted in a structural zone in quartz-diorite-porphyrite emplaced in Jurassic volcanic rocks. Sphalerite and galena are the principal ore minerals in the deposit. (1) Sphalerite is highly variable in color and this variation can be related to its chemical composition and sulfur isotopic characters. Dark colored sphalerites are poor in Zn and Ni, rich in Pb, Cu, Fe, Ag and Au and have high δ³⁴S values, while the opposite is true for light-colored ones. (2) δ³⁴S of sphalerite is negatively correlated with the contents of Zn and Ni and positively correlated with the contents of Pb, Cu, Ag and Au, with the absolute values of the correlation coefficients being greater than 0.7. The above two characters suggest that the sulfur isotopic composition of sphalerite is controlled not only by the physicochemical conditions under which the mineral was formed, but also by mineralogical characteristics of the host mineral. (3) Apparent correlations exist among the constituent elements in the sphalerite. For example, Zn is negatively correlated with Cu, Pb, Fe, Ag and Au and positively correlated with Ni. (4) Sphalerites of the same color in the same hand specimen always show similar characters with respect to trace element and sulfur isotopes. (5) Two distinct trends of evolution can be recognized between Zn and Cu, Zn and Pb, Zn and Ag and between these elements on one hand and δ³⁴S on the other, reflecting that the ore-forming solutions may have resulted from mixing of fluids of different origins. (6) Pb is uniformly distributed in sphalerite and shows positive correlations with Cu, Fe, Ag and δ³⁴S, suggesting isomorphic substitution in the sphalerite lattice. This project was financially supported by the Open Laboratory of Ore Deposit Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences.     

黝铜矿-砷黝铜矿矿物学研究进展

黝铜矿-砷黝铜矿系列矿物(Tetrahedrite -Tennantite Series Mineral,TTSM)作为含Cu、Ag、S、Sb、As、Hg及少量Au、Fe、Zn、Cd、Bi、Te、Se的硫盐矿物广泛存在于世界各地的Cu、Ag、Au、Pb、Zn多金属矿床中.为了能够更好的认识该系列矿物,提高矿物中有用元素的回收率,扩大黝铜矿型铜矿床的经济效益,本文对TTSM的化学组成和类质同象置换规律,晶胞参数和晶体结构的形变,矿物人工合成和有用元素的浸出试验等研究进展进行了综述.天然TTSM矿物一般化学式为:(Cu,Ag)6 Cu4 (Fe,Zn,Cu,Hg,Ag,Cd)2 (Sb,As,Bi,Te)4 (S,Se)13,其中S-Se、Sb-As-Bi-Te、Ag-Cu、Cu-Hg-Fe-Pb-Zn-Cd的类质同象置换相当普遍;TTSM晶体结构中不同结构位置离子置换规律更多的受限于离子价键,而同一结构位置不同离子的置换除受限于离子价键还受限于该位置空间大小,晶胞参数与离子置换类型和数量密切相关;人工合成实验证实形成TTSM矿物的温度范围为350～540℃,浸出试验证明随反应温度增高、浸出浓度增大、矿物颗粒减小时,TTSM中有用元素的浸出速率增大.     

Sensitive High-Resolution Ion Microprobe U-Pb Zircon and 40Ar-39Ar Muscovite Ages of the Yinshan Deposit in the Northeast Jiangxi Province, South China

The Yinshan deposit in the Jiangnan tectonic belt in South China consists of Pb‐Zn‐Ag and Cu‐Au ore bodies. This deposit contains approximately 83 Mt of the Cu‐Au ores at 0.52% Cu and 0.8 g/t Au, and 84 Mt of the Pb‐Zn‐Ag ores at 1.25% Pb, 1.02% Zn and 33.3 g/t Ag. It is hosted by low‐grade metamorphosed sedimentary rocks and mafic volcanic rocks of the lower Mesoproterozoic Shuangqiaoshan Group, and continental volcanic rocks of the Jurassic Erhuling Group and dacitic subvolcanic rocks. The ore bodies mainly consist of veinlets of sulfide minerals and sulfide‐disseminated rocks, which are divided into Cu‐Au and Pb‐Zn‐Ag ore bodies. The Cu‐Au ore bodies occur in the area close to a dacite porphyry stock (No. 3 stock), whereas Pb‐Zn‐Ag bodies occur in areas distal from the No. 3 stock. Muscovite is the main alteration mineral associated with the Cu‐Au ore bodies, and muscovite and chlorite are associated with the Pb‐Zn‐Ag ores. A zircon sensitive high‐resolution ion microprobe U‐Pb age from the No. 3 dacite stock suggests it was emplaced in Early Jurassic. Three ⁴⁰Ar‐³⁹Ar incremental‐heating mineral ages from muscovite, which are related to Cu‐Au and Pb‐Zn‐Ag mineralization, yielded 179–175 Ma. These muscovite ages indicate that Cu‐Au mineralization occurred at 178.2±1.4 Ma (2σ), and Pb‐Zn‐Ag mineralization at 175.4±1.2 Ma (2σ) and 175.3±1.1 Ma (2σ), which supports a restricted period for the mineralization. The Early Jurassic ages for the mineralization at Yinshan are similar to that of the porphyry Cu mineralization at Dexing in Jiangnan tectonic belt, and suggest that the polymetallic mineralization occurred in a regional transcompressional tectonic regime.     

Mineral systems,their types,and distribution in nature. I. Khibiny,Lovozero, and the Mont Saint-Hilaire

In accordance with the set of species-defining chemical elements in minerals, n-component systems (where n = 1, 2, 3, 4, 5, 6, 7, 8, 9, 10) for all mineral species (4952) known to 2014 inclusive were distinguished. Seventy chemical elements have been established to be species-defining, which are distributed by mineral systems as follows: 1 (29), 2 (62), 3 (68), 4 (61), 5 (61), 6 (55), 7 (49), 8 (38), 9 (28), and 10 (19). The number of mineral species in which certain chemical elements are species-defining has been specified. Oxygen (4041), hydrogen (2755), silicon (1448), calcium (1139), sulfur (1025), aluminum (960), iron (917), sodium (914), copper (616), phosphorous (580), arsenic (575), and magnesium (550) are the leading elements in minerals in the Earth’s crust. It has been found that the most species-defining elements are normally distributed by mineral systems. The distributions of mineral species in various systems from the Khibiny and Lovozero, Kola Peninsula, Russia; and Mont Saint-Hilaire, Quebec, Canada peralkaline plutons were compared and the characters of species-defining element distribution in these localities were compared. Si, Na, K, C, F, Ti, Ce, Zr, Nb, Sr, and Th are “excess” species-defining elements in minerals from the plutons compared to the total number of mineral species, whereas S, Cu, Pb, Cl, B, Te, Ag, Ni, and Be are “scarce” elements.     

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.     

Silver sulfoselenide from ore of the Valunisty Au-Ag deposit,Chukchi Peninsula

Silver sulfoselenide (Ag,Cu)₉Se₂S₄ from ore of the Valunisty Au-Ag deposit on the Chukchi Peninsula is described for the first time. The mineral occurs in mineralized quartz-adularia veins, where it associates with chalcopyrite, sphalerite, galena, and electrum and replaces arsenpolybasite. It forms anhedral grains up to 0.2 mm in size. The reflectivity of sulfoselenide is moderate, no anisotropy is observed, and the microhardness is very low. The chemical composition of the mineral differs from other known members of the Ag-Se-Se-S system: the S/Se ratio of the mineral is 2/1 and the (Ag + Cu)/(Se + S) ratio is about 1.5.