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1.
新变种矿物—含锗锡硫钒铜矿   总被引:3,自引:0,他引:3  
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。  相似文献   

2.
铋砷黝铜矿在中国的发现与研究   总被引:1,自引:0,他引:1  
铋砷黝铜矿产于广东陆丰中低温热液黄铁矿矿床中,呈它形粒状嵌布在黄铁矿内,粒径0.05~0.22mm,与黄铜矿、针硫铋铝矿共生。反射免呈灰色微带蓝色,均质性。显微硬度Hv=295.5kg/mm2。电子探针成分分析(平均值)为:S24.4%,Cu38.25%,As13.03%,Bi17.人83%,Sb0.48%,Zn2.39%,Fe2.13%,Te1.47%,化学式为:Cu10(Fe0.65Zn0.63Cu0.49)1.77(As2.97Bi1.46Sb0.07)4、50(S12.8Te0.20)13。X射线粉晶衍射强线:2.95(10),2.55(3),1.866(5),1.727(4),1.041(5)。晶胞参数α=1.0218nm。  相似文献   

3.
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。  相似文献   

4.
南秦岭大型钡成矿带中硫钒铜矿的特征及成因意义   总被引:2,自引:0,他引:2  
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.  相似文献   

5.
烧锅营子金矿床的黄铁矿形成于早、中、晚3期,是主要的矿石矿物和载金矿物,其中以中期黄铁矿为最主要的载金者.黄铁矿的化学成分为:TFe43.34%~45.52%,S46.58%~48.86%,与标准黄铁矿相比显示亏铁、亏硫特点.黄铁矿内含丰富的微量元素,有Au、Ag、As、Sb、Bi、Cu、Zn、Pb、Co、Ni、W、Mo、Se等.其中Au、Ag、Cu、Pb、Zn、Bi含量较高,而As、Sb低,Se极低.其Au/Ag(多大于0.5)、(Cu+Pb+Zn)/(Co+Ni+As)(4.26)、Co/Ni(>> 1)比值表明其属中温岩浆热液矿床.  相似文献   

6.
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.  相似文献   

7.
内蒙古巴彦宝力道金矿区物化探综合找矿方法及其应用   总被引:1,自引:0,他引:1  
尹忠  李峰  刘萍 《物探与化探》2004,28(3):224-227,232
巴彦宝力道金矿区位于内蒙古苏尼特左旗,区内发育与金矿化有关的破碎蚀变带和糜棱岩化带。通过研究地质及物化探工作成果,建立本区地球物理、地球化学成矿模式,采用相关分析和"格氏法"等方法,确定了矿床元素轴向分带序列为:As Sb Hg Bi Li Sr Ba Ag Pb Au Cu Zn Sn V Co Cr Ni Ti Mo W,前缘晕元素为As、Sb、Hg、Bi,主成矿元素为Au、Cu、Zn,尾晕元素为Ti、Mo、W。据轴向分带特征,确定金矿体剥蚀程度的判别指标为w(As)×w(Sb)×w(Bi)/w(Ti)×w(Mo)×w(W)。建立了找矿标志,为下一步地质找矿提供了依据。  相似文献   

8.
陕西洛南发现含碲黝铜矿   总被引:1,自引:0,他引:1  
曹恩魁 《矿物学报》1991,11(3):278-280,T001
陕西洛南发现的含碲黝铜矿产于含碲金石英脉中。呈不规则粒状,粒径0.1—0.4mm。实测维氏硬度为227kg/mm~2,相当摩氏硬度4.1。400—700nm波段反射率色散值为35.10—24.13%。颜色指数:R=24.87;x=0.3283;y=0.3130,λd=489;Pe=0.075。四个颗粒电子探针分析结果(%):Cu 41.70—42.39,平均42.133;Zn 5.09—5.59,平均5.345;Fe 0.02—0.30,平均0.145;Ag 0.00—0.10,平均0.033;Sb 14.93—16.79,平均16.023;As 6.09—7.57,平均6.655;S 23.91—24.55,平均24.228;Te 4.93—6.46平均5.645。根据分析结果的平均值计算矿物化学式:(Cu_(10.0593)Ag_(0.0052)_(10.0645)(Zn_(1.3353)Cu_(0.6232)Fe_(0.0415)_(2.00)(Sb_(2.1319)As_(1.4398)_(3.5717)(S_(12.2841)Te_(0.7159)_(13.00),简化式Cu_(10)Zn_2(Sb,As)_4(S,Te)_(13)  相似文献   

9.
冶炼副产品硫酸镍组成成分复杂,准确分析杂质元素As、Zn、Co含量对设计硫酸镍提纯工艺有重要意义。采用硝酸-盐酸-氢氟酸-高氯酸体系对样品进行前处理,优化仪器工作条件,建立了电感耦合等离子体发射光谱法(ICP-AES)测定冶炼副产品硫酸镍中As、Zn、Co的方法。本实验分别以As 189.042nm,Zn 206.200nm,Co 228.616nm为分析谱线。实验结果表明:待测溶液中20g/L硫酸镍基体及1g/L Cu、20mg/L Cd、Cr、Fe、Sb、Ca、Mg、Al、Mn、Sn、Bi等共存杂质元素对As、Zn、Co的测定结果基本无影响。As、Zn、Co的标准曲线线性相关系数均在0.9999以上,方法检出限为0.0021~0.026mg/L,方法定量限为0.0063~0.078mg/L。采用实验方法测定冶炼副产品硫酸镍实际样品中As、Zn、Co,所得结果的相对标准偏差(RSD,n=11)介于1.51%~2.77%之间,加标回收率在89.6%~108.4%之间。  相似文献   

10.
文中给出了一个包含两大类五亚类八个型式的金矿床成矿模式图。浙江省火山岩区金矿的找矿标志有:矿床产出条件、围岩蚀变、同位素组成、包裹体、矿物共生组合、矿物组构及其标型特征。例如,该火山岩区重要金矿床的黄铁矿中,相对富含Pb、Zn、Mo、Sn、As,Sb和Bi,而贫Co、Ni、Se和Te;并且S/se、Ag/Au、Pb/Ni、Se/Te和(As+Sb+Bi)/(Se+Te)比值较高,Co/Ni、Ag/Pb、Ag/Zn、Cu/Zn和(Co+Ni)/(Pb+Zn)比值较低。Ⅰ、Ⅵ、Ⅶ式金银矿床中闪锌矿的化学成分富Fe、Mn,贫Cd、Hg;尤其贫Ge、Ga、Tl而富Au、Ag、Sn、Bi;晶体结构αo值约为5.4167~5.4191A。闪锌矿比重较低(d<4.05)、反射率(R)较高(高于纯闪锌矿0.24~1.61%),并且只有一个红外吸收峰(310~313cm~(-1))的特点。  相似文献   

11.
四川石棉金矿床中的黝铜矿族矿物   总被引:3,自引:0,他引:3  
王小春  张哲儒 《矿物学报》1999,19(4):470-474
四川石棉西部碳酸盐岩系中的金矿床产于泥盆系中统,受层间蚀变破碎带控制。其中分布有为数较多的黟同矿族矿物,与黄铁矿、黄铜矿、方铅矿、闪锌矿和Au-Ag系列矿物共同组成矿石的矿物组合和Au-Cu-Ag-Pb-As-Sb-Bi的元素组合。电子探针分析表明黝铜矿族矿物有同铜矿、黝铜矿、砷黝铜矿和锌砷黝铜帮等,其中,Fe-Zn、AsSb之间分别呈完全类质同象。在垂向上,黝铜矿的成分自上而下由富锌锑向富铁砷演  相似文献   

12.
R. O. Sack 《Petrology》2017,25(5):498-515
Possible topologies of miscibility gaps in arsenian (Cu,Ag)10(Fe,Zn)2(Sb,As)4S13 fahlores are examined. These topologies are based on a thermodynamic model for fahlores whose calibration has been verified for (Cu,Ag)10(Fe,Zn)2Sb4S13 fahlores, and conform with experimental constraints on the incompatibility between As and Ag in (Cu,Ag)10(Fe,Zn)2(Sb,As)4S13 fahlores, and with experimental and natural constraints on the incompatibility between As and Zn and the nonideality of the As for Sb substitution in Cu10(Fe,Zn)2(Sb,As)4S13 fahlores. It is inferred that miscibility gaps in (Cu,Ag)10(Fe,Zn)2As4S13 fahlores have critical temperatures several °C below those established for their Sb counterparts (170 to 185°C). Depending on the structural role of Ag in arsenian fahlores, critical temperatures for (Cu,Ag)10(Fe,Zn)2(Sb,As)4S13 fahlores may vary from comparable to those inferred for (Cu,Ag)10(Fe,Zn)2As4S13 fahlores, if the As for Sb substitution stabilizes Ag in tetrahedral metal sites, to temperatures approaching 370°C, if the As for Sb substitution results in an increase in the site preference of Ag for trigonal-planar metal sites. The latter topology is more likely based on comparison of calculated miscibility gaps with compositions of fahlores from nature exhibiting the greatest departure from the Cu10(Fe,Zn)2(Sb,As)4S13 and (Cu,Ag)10(Fe,Zn)2Sb4S13 planes of the (Cu,Ag)10(Fe,Zn)2(Sb,As)4S13 fahlore cube.  相似文献   

13.
黝铜矿族矿物的EPMA研究   总被引:3,自引:0,他引:3  
根据产自约20个不同矿床的黝铜矿族矿物的大量电子探针分析结果以及一些文献资料分析,黝铜矿族矿物是一类复杂的类质同象矿物系列。本文还对黝铜矿族矿物的分类命名规则以及相应的矿物种和变种名称提出意见和建议。  相似文献   

14.
Chemical compositions of tetrahedrite—Ag-rich tetrahedrite—freibergite solid solutions (Ag-rich tetrahedritess) and homogenization temperatures of fluid inclusions in quartz and carbonates of seventeen samples from nine veins in the El Zancudo deposit, Antioquia, Colombia, were investigated to reveal the origin of silver in Ag-rich tetrahedritess, to derive their crystallization temperatures and to examine the relationship between chemical compositions of Ag-rich tetrahedritess and their crystallization temperatures. The ores consist of arsenopyrite, pyrite, sphalerite, Ag-rich tetrahedritess, galena, boulangerite, andorite, owyheeite, diaphorite, jamesonite, miargyrite, bournonite, chalcopyrite, and electrum. Ag-rich tetrahedritess forms about 10 volume % of the total ores and is one of the most common and widely distributed sulfosalts in this deposit. Ag-rich tetrahedritess is rich in Ag (1.13 to 31.02 wt%) and Sb (22.93 to 29.82 wt%), and poor in As (0.06 to 2.43 wt%), consistent with the reported incompatibilities of Ag and As in Ag-rich tetrahedritess. The Zn/(Zn + Fe)-, Ag/(Ag + Cu)- and Sb/(Sb + As + Bi)-atomic ratios exhibit some variations among the veins. Ag-rich tetrahedritess with higher Ag/(Ag + Cu) ratios coexist with diaphorite, whereas those with lower ratios are not associated with this sulfosalt. Ag-rich tetrahedritess in the assemblages of Ag-rich tetrahedritess+ sphalerite and of Ag-rich tetrahedritess+ bournonite + galena shows no Zn ↔ Fe and Cu ↔ Ag variations between core and rim, respectively, negating the possibility of solid state reaction during cooling. Ag-rich tetrahedritess is thus regarded as primary phase. Homogenization temperatures of primary fluid inclusions in quartz and carbonates co-existing with Ag-rich tetrahedritess define the mineralization temperatures of 134 to 263°C. Independent crystallization temperatures of Ag-rich tetrahedrite estimated based on Zn/(Zn + Fe) and Ag/(Ag + Cu) ratios of the Ag-rich tetrahedritess associated with silver minerals such as miargyrite, andorite and diaphorite using Sack's thermochemical database lie in a range between 170 and ∼250°C. Both results are thus in good agreement.  相似文献   

15.
Twenty eight electron microprobe analyses of freibergite from the Mount Isa (Queensland) Pb-Zn-Ag stratiform orebody, range in silver content from 18.4 to 42.5 wt. % Ag. These values significantly extend the tetrahedrite-freibergite series. The compositional range based on twenty-one complete analyses is indicated by the formula (Ag,Cu)9.21–11.44(Fe,Zn)1.59–2.31(Sb,As)3.87–4.43S13.0. As far as could be determined, Mount Isa freibergite is homogeneous and no marked compositional changes were detected either across individual grains, or in different grains of the same electron microprobe sample. The linear, atom for atom, replacement of copper by silver reported for lower silver bearing tetrahedrites continues in Mount Isa freibergite. A maximum silver content of about 51 wt. % Ag is predicted. X-ray investigations indicate however that in contrast to the structural expansion with increasing silver content reported for argentian tetrahedrite, Mount Isa freibergite contracts with increase in silver. The extrapolated lattice parameter for the theoretical freibergite (Ag10(Fe,Zn)2Sb4S13) end member is of the same order as tetrahedrite.  相似文献   

16.
广东陆丰发现黝铜矿族系列矿物。根据矿物硬度、反射率、X衍射和电子探针分析数据,鉴定其为黝铜矿、砷黝铜矿、锌锑黝铜矿、锌砷黝铜矿、铋砷黝铜矿和碲砷黝铜矿。研究表明,在陆丰矿床中发现如此多黝铜矿亚种以及Fe、Zn、As、Sb、Bi和Te分别呈全完类质同象系列是极为罕见的。通过黝铜矿系列的研究,为在该区乃至东南沿海找矿开拓了新的思路  相似文献   

17.
雷蕴芬  林月英等 《矿物学报》1991,11(1):78-82,T002
未定名硫化物矿物是一个稀少矿物,它发现于内蒙古铅锌矿的钛卡岩矿床中。共生太物有黄铜矿、闪锌矿、方铅矿。它呈黑色,金属光泽,不透明,硬度为165-214kg/mm^2。反射铯为灰色微带蓝色,弱非均质性,深蓝--黄褐色。化学成分(wt%):S32.32、Cu6.46、Fe6.56、Zn54.29、Pb0.31、Cd0.2c、CO0.03(平均),分子式(Zn0.84Fe0.11Cu0.09)1.04S。X射线分析数据与闪锌矿相同,d值和晶胸参数比闪锌矿(含铁)的小,晶胞参数比人工合成闪锌矿的大。粉晶主要强线为3.108(100)、1.906(50)、1.628(30)、1.240(20)、1.103(20)。  相似文献   

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