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1.
Lisiguangite, CuPtBiS3, is a new mineral species discovered in a PEG-bearing, Co-Cu sulfide vein in garnet pyroxenite of the Yanshan Mountains, Chengde Prefecture, Hebei Province, China. It is associated with chalcopyrite and bornite, galena, minor pyrite, carrolite, molybdenite and the platinum-group minerals daomanite (CuPtAsS2), Co-bearing malanite (Cu(Pt, Co)2S4) sperrylite, moncheite, cooperite and malyshevite (CuPdBiS3), rare damiaoite (Pt2In3) and yixunite (Pt3In). Lisiguangite occurs as idiomorphic crystals, tabular or lamellae (010) and elongated [100] or as aggregates, up to 2 mm long and 0.5 mm wide. The mineral is opaque, has lead-gray color, black streak and metallic luster. The mineral is non-fluorescent. The observed morphology displays the following forms: pinacoids {100}, {010}, {001}, and prism {110}. No twining is observed. The a:b:c ratio, calculated from unit-cell parameters, is 0.6010:1:0.3836. Cleavage: {010} perfect, {001} distinct, {100} may be visible. H Mohs: 21/2; VHN25=46.7-49.8 (mean 48.3) kg/mm2. Tenacity: brittle. Lisiguangite is bright white with a yellowish tint. In reflected light it shows neither internal reflections nor bireflectance or pleochroism. It has weak to moderate anisotropy (blue-greenish to brownish) and parallel-axial extinction. The reflectance values in air (and in oil) for R3, R4 and (imR3, imR4), at the standard Commission on Ore Mineralogy wavelengths are: 37.5, 35.7 (23.4, 22.3) at 470 nm; 38.6, 36.5 (23.6, 22.6) at 546 nm; 39.4, 37.5 (23.6, 22.7) at 589 nm and 40.3, 38.2 (23.7, 22.9) at 650 nm. The average of eight electron-microprobe analyses: Cu 12.98, Pt 30.04, Pd 2.69, Bi 37.65 and S 17.55, totaling 100.91%, corresponding to Cu1.10(Pt 0.83, Pd0.14)Σ0.97Bi0.97S2.96 based on six atoms apfu. The ideal formula is CuPtBiS3. The mineral is orthorhombic. Space group: P212121, a=7.7152(15)?,b=12.838(3)?, c=4.9248(10)?, V=487.80(17)?3, Z=4. The six strongest lines in the X-ray powder-diffraction pattern [d in ? (I) (h k l) are 6.40(30)(020), 3.24(80)(031), 3.03(100)(201), 2.27(40)(051), 2.14(50)(250), 1.865(60)(232). 相似文献
2.
铂双峰矿产在纯橄榄岩铝矿体中。在铝矿石及矿体邻近的砂矿中均可找到。呈块状聚集体或板片状自形晶,与疏钻矿、含锇自然铱紧密共生。脉状的宽20～301μm,长400～500μm,一般10μm×20μm。金属光泽。条痕黑色。HM=3．05。VHN20=92kg／mm2（平均）。{0001}解理完全。性脆。计算密度为10．21g／cm2。反射色;亮黄白带淡蓝色。内反射无。非均质性中等,偏光色为淡蓝或淡黄。双反射或反射多色性在空气中或油中均未见。5个电子探针分析数据平均（wt％）：Cu0．2,Te57.2,Ir24.5,Pt17．2,Bi0．4,总量99．5。实验式为：（IR0．57Pt0.39Cu0.01）0．98（Te1.99Bi0.01）2.00。简化理论式为（11,Pt）Te2。4条最强X射线粉晶衍射线hkl,d,I为：101,2．87（100）;102,2．10（70）;110,1．98（60）;103,1．58O（50）。根据X射线粉晶数据进行指标化,获得铂双峰矿晶胞数据：三方晶系,P3ml,a=0．3973（5）,c＝0．5315（5）um,V＝0．0727nm3,Z=1。铂双峰矿是笔者对双峰矿研究的继续与补充。 相似文献
3.
Heyrovskýite has a composition range from 6(Pb0.83Bi0.10(Ag, Cu)0.07) S . Bi2S3 to 6(Pb0.92Bi0.05(Ag, Cu)0.03) S . Bi2S3. It is orthorhombic. Crystal forms {100}, {010}, {120}, {140}, {250}, and {321} (?) were observed; {010} and {140} are dominant. Elongated c, flattened (010). a:b:c morph=0.432:1:0.128. Cell parameters a=13.705±0.013 Å, b=31.194±0.033, c=4.121±0.003, a:b:c X-ray=0.439:1:0.132. The diffraction symbol is Bb, compatible with Bbmm, Bb21 m, Bbm2. Morphology corresponds to point groups mmm or mm2, reducing the possible space groups to Bbmm and Bbm2. Density at 20 °C is 7.17 g/cm3, calculated, 7.18; Z=4. Micro-indentation hardness (VHN) (50 g load) is 166 to 234 kp/mm2. Strongly anisotropic; reflectance strongly variable, roughly the same as of galena. Etch tests: HNO3 (1:1) and HCl (1:1) positive, FeCl3 20%, HgCl2 5%, KCN 20%, and KOH 40% all negative. Powder data are identical with those for phase II of Otto and Strunz (1968). Heyrovskýite is associated with galena and cosalite at H?rky, Czechoslovakia. 相似文献
4.
富碲马营矿产在纯橄榄岩铬矿体中。在铝矿石及矿体附近的砂矿中均可找到。呈粒状自形结构,直径0．01～0．15mm。与硫铱矿（IrS2）、双峰矿、高台矿、马营矿及（Fe,Ni）9Cu3Ir6S20等紧密共生。有的呈脉状,宽0．1～0．2mm,长1．2mm。金属光泽。不透明,钢灰色,粉末黑色。HM＝3．7。VHN50＝161kg／mm2（范围132～215kg／mm2）。无解理。无断口。性脆。计算密度为12．2g／cm3。反射色亮白带淡黄色调,内反射无,均质性,双反射与反射多色性无。5个电子探针分析数据平均为（％）：Cu0．3,Te32．9,Ir34．7,Pt2．7,Bi28．2,总量98．9。实验式根据原子数3计算为：（Ir(0．92)Pt(0．92)Cu(0．01)）;(1．00)Bi(0．68)Te(1．31)。简化后的理论式为Ir（Te,Bi）2,而（Ir：Bi：Te＝3：2：4）。6条富碲马营矿是强X射线衍射hki、d、I为：210,2．89（60）;311,1．95（100）;511,1．246（70）;520,1．204（60）;440,1．145（60）;533,0．9891（60）。根据X射线粉晶指标化求得马营矿为等轴晶系,空间群：Pa3,a＝0．6486（4）um,V＝0．2729nm3,Z＝4。富碲马营矿是本文作者对马营矿研究的继续与补充。 相似文献
5.
淡红沸石(Stellerite)是辉沸石族矿物之一种,曾在白令海峡中的苏联铜岛、美国阿拉斯加的朱诺、芬兰和苏联东外贝加尔的一些多金属矿床发现过。前人对淡红沸石着重进行了结晶学和热分析的研究,而对其地质产状和成因以及与有关矿化的关系相对少一些。到目前为止,我国还沒有对淡红沸石进行过报导。 相似文献
6.
新矿物双峰矿—铱的二碲化物 总被引：2，自引：1，他引：2
双峰矿产在纯橄榄岩体铬矿体中。在铬矿石及矿体邻近的砂矿中均可找到，呈块状聚集体或板片状与硫铱矿、锇自然铱矿紧密共生。直径０．５￣０．２ｍｍ，脉状的宽０．０５￣０．１０ｍｍ，长０．５￣１．０ｍｍ。金属光泽。条痕黑色。Ｈ（Ｍ）３。ＶＨＮ２０１０８ｋｇ／ｍｍ＾２（平均）。解理：（０００１）完全。性脆。计算密度为１０．１４ｇ／ｃｍ＾３。反射色：亮黄白带蓝色调。内反射无。非均质性中等，偏光色为淡蓝或淡黄。双 相似文献
7.
Yu ZuxiangInstitute of Geology Chinese Academy of Geological Sciences Baiwanzhuang Beijing 《《地质学报》英文版》1997,71(4):486-490
Changchengite occurs in chromite orebodies in dunite and in platinum placer deposits in chromite orebodies nearby. The mineral occurs as massive aggregates or veinlets on margins of iridisite (IrS2) and replaces it. Opaque. Lustre metallic. Colour steel-black. Streak black. Hm = 3.7. VHN20= 165 kg/ mm2. Isotropic. Cleavage none. Density 11.96 g/ cm3. Seven electron microprobe analyses give the following mean chemical results (wt. %): S 7.2, Cu 0.3, Te 0.4, Ir 41.2, Pt 2.8 and Bi 47.3 with total 99.1. The simplified formula is IrBiS. The strongest X-ray powder diffraction lines (hkl, d, I) are 210, 2.75 (70); 211, 2.51 (60); 311, 1.860 (100); 440. 1.090 (50) and 600, 1.027 (50). The X-ray powder diffraction pattern is similar to that of mayingite. After the diffraction data are indexed the mineral is determined to be cubic. The space group is P213 with a = 0.6164(4) nm, V = 0.2342 nm3 and Z = 4. 相似文献
8.
Summary Childrenite and crandallite are described as two new phosphate members in the paragenesis of the Stari Trg mine which comprises vivianite, ludlamite and struvite. Crandallite crystals with very simple rhombohedral habit grow on rhombohedral carbonate and childrenite crystals. The crystal morphology of childrenite is very similar to that at described from other localities. Following forms were measured: {100}, {100}, {110}, {120}, {121}, {221} and {342}. The average chemical composition is Ch91 Eo9 (Ch-childrenite, Eo-eosphorite). Pseudo-orthorhombic unit cell dimensions were calculated: a = 10.390(4) A, b = 13.390(4) A and c = 6.920(2) A. Growth sectors and sector twins of childrenite are described.
With 4 Figures 相似文献
Childrenit und Crandallit aus der Stari Trg Grube (Trepa), Kosovo: Neue Daten
Zusammenfassung Childrenit und Crandallit werden als zwei neue Minerale der Phosphatgruppe beschrieben. Sie stammen aus der Stari Trg Grube in Paragenese mit Vivianit, Ludlamit und Struvit. Die Crandallit-Kristalle mit einfachem rhomboedrischen Habitus, wachsen rhomboedrischen Karbonat- und Childrenit-Kristallen auf. Die Kristallmorphologie von Childrenit ist, verglichen mit der aus anderen Lokalitäten, sehr einfach. Folgende Formen wurden gemessen: {100}, {010}, {110}, {120}, {121}, {221} und {342}. Die durchschnittliche chemische Zusammensetzung ist Ch(91Eo9(Ch-Childrenit, Eo Eosphorit). Eine Kalkulation der pseudo-orthorhombischen Elementarzelle ergab folgende Abmessungen: a = 10.390(4) A, b = 13.390(4) A and c = 6.920(2) A. Schließlich wird das Wachstum and die Zwillingsbildung von Childrenit beschrieben.
With 4 Figures 相似文献
9.
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。 相似文献
10.
M. A. Yudovskaya N. V. Trubkin E. V. Koporulina D. I. Belakovsky A. V. Mokhov M. V. Kuznetsova T. I. Golovanova 《Geology of Ore Deposits》2008,50(7):551-555
Abramovite, a new mineral species, has been found as fumarole crust on the Kudryavy volcano, Iturup Island, Kuriles, Russia. The mineral is associated with pyrrhotite, pyrite, würtzite, galena, halite, sylvite, and anhydrite. Abramovite occurs as tiny elongated lamellar crystals up to 1 mm long and 0.2 mm wide (average 300 × 50 μ m), which make up chaotic intergrowths in the narrow zone of fumarole crust formed at ～600°C. Most crystals are slightly striated along the elongation. The new mineral is silver gray, with a metallic luster and black streak. Under reflected light, abramovite is white with a yellowish gray hue. It has weak bireflectance; anisotropy is distinct without color effects. The chemical composition (electron microprobe) is as follows, wt %: 20.66 S, 0.98 Se, 0.01 Cu, 0.03 Cd, 11.40 In, 12.11 Sn, 37.11 Pb, 17.30 Bi; the total is 99.60. The empirical formula calculated on the basis of 12 atoms is Pb1.92Sn1.09In1.06Bi0.89(S6.90Se0.13)7.03. The simplified formula is Pb2SnInBiS7. The strongest eight lines in the X-ray powder pattern [d, Å (I)(hkl)] are 5.90(36)(100), 3.90(100)(111), 3.84(71)(112), 3.166(26)(114), 2.921(33)(115), 2.902(16)(200), 2.329(15)(214), 2.186(18)(125). The selected area electron diffraction (SAED) patterns of abramovite are quite similar to those of the homologous cylindrite series minerals. The new mineral is characterized by noncommensurate structure composed of regularly alternated pseudotetragonal and pseudohexagonal sheets. The structure parameters determined from the SAED patterns and X-ray powder diffraction data for pseudotetragonal subcell are: a = 23.4(3), b = 5.77(2), c = 5.83(1) Å, α = 89.1(5) °, β = 89.9(7)°, γ = 91.5(7)°, V = 790(8) Å3; for pseudohexagonal subcell: a = 23.6(3), b = 3.6(1), c = 6.2(1) Å, α = 91(2)°, β = 92(1)°, γ = 90(2)°, V = 532(10) Å3. Abramovite is triclinic, space group P(1). The new mineral is named in honor of Russian mineralogist Dmitry Abramov. The type material of abramovite has been deposited in the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow. 相似文献
11.
L. Z. Reznitsky E. V. Sklyarov Z. F. Ushchapovskaya L. F. Suvorova Yu. S. Polekhovsky P. Dzerzanovsky I. G. Barash 《Geology of Ore Deposits》2011,53(8):758-766
Cuprokalininite as an accessory mineral has been found in Cr-V-bearing quartz-diopside metamorphic rock of the Sludyanka Complex,
South Baikal region, Russia. This mineral is named as Cu analogue of kalininite (ZnCr2S4), is associated with quartz, Cr-V-bearing tremolite and mica, calcite, diopside-kosmochlor, goldmanite-uvarovite, dravite-chromdravite,
Cr-V spinellide, karelianite-eskolaite, V-bearing titanite, pyrite, and plagioclase. Cuprokalininite forms euhedral microcrystals
up to 0.05–0.20 mm in size, of octahedral and cuboctahedral habit with faces o {111} and a {100}, and polysynthetic and simple twinning along the {111}. Cleavage and parting were not observed. The mineral is black
with a dark bronze tint, black streak, and metallic luster. The microhardness (VHN) is 356–458 (loadings are 20 and 30 g), 396 kgf/mm2, on average. The Mohs hardness is 4.5–5.0, d
calc = 4.16(2). In reflected light, the mineral is pale-cream-colored, without anisotropy; reflectance values (λ, nm-R, %): 400-34.3, 420-34.1, 440-33.9, 460-33.7, 480-33.5, 500-33.2, 520-33.0, 540-32.8, 560-32.3, 580-32.2, 600-31.9, 620-31.6,
640-31.2, 660-30.9, 680-30.6, 700-30.4. Cubic, space group Fd
[`3]\bar 3
m, Z = 8; unit cell parameter a = 9.814(2) ?, V = 945.2(4) ?3. The strongest lines of the X-ray powder diffraction pattern [d, ? (I) (hkl)]: 3.44 (6)(220), 2.94 (10)(311), 2.44 (6)(400), 1.884 (9)(511, 333), 1.731 (10)(440), 1.133 (6)(751, 555), 1.098 (6)(840),
1.030 (6)(931), 1.002 (10)(844). Chemical composition (mean of 202 microprobe analyses of 11 grains, wt %): Cu 21.03, Fe 0.47,
Zn 0.17, Cr 29.01, V 5.85, As 0.21, Sb 0.08, S 43.25; the total is 100.07. The empirical formula calculated on the basis of
seven ions is (Cu0.98Fe0.02Zn0.01)1.01(Cr1.65V0.34As0.01)2.00S3.99. The type material has been deposited at the Fersman Mineralogical Museum of the Russian Academy of Sciences, Moscow, Russia. 相似文献
12.
云南大硐厂铅锌矿床中的硫碲铋矿A 总被引：1，自引：0，他引：1
硫碲铋矿Ａ产于云南省大硐厂铅锌矿床，与自然铋、辉铋铅矿共生。晶体呈柱状，粒度０．０２￣０．３ｍｍ。反光显微镜下呈淡黄色，弱非均质性，反射率Ｒｃ′＝５２．４％，Ｒ０＝４８．８％（波长为５４０ｎｍ），显微压入硬度Ｈｖ＝４６￣７２ｋｇ／ｍｍ＾２。主要粉晶谱线：３．０６５（１０），２．１２０（７），１．３４６（５），２．２２０（４）。三方晶系，空间群为Ｄ３ｄ＾５－Ｒ３↑－ｍ，晶胞参数ａ＝０．４２４１ｎｍ， 相似文献
13.
Gerhard Vavra 《Contributions to Mineralogy and Petrology》1994,117(4):331-344
The internal morphologies of zircon crystals from different types of granitoids (alkaline, calcalkaline and anatectic) are revealed by cathodoluminescence imaging and are described in terms of growth rates of the crystal faces relative to each other. Zircons in the alkaline granitoids are characterized by high and constant growth rates of {010} relative to the pyramidal forms and by symmetric grwoth of {011}. Zircons in the calcalkaline and anatectic granitoids are characterized by fluctuating or gradually decreasing relative growth rates of {010}, by asymmetric and highly variable growth of {011}, and by a tendency of {110} to become grwoth-inhibited. Corrosion events are interspersed during zircon growth in the calcalkaline magmas. In the calcalkaline and anatectic magmas, a discontinuity breaks the morphological evolution at late stages of crystallization. The discontinuity coincides with a sharp drop in cathodoluminescence. The growth behaviour of each crystal form is analysed and compared with predictions made by the periodic bond chain (PBC) theory. It is argued that the relative growth rate of {010} depends on supersaturation, that the growth rates of {011} faces are changed in response to different ratios of adsorbing cations (Na, K, Al), and that {110} faces become growth-inhibited by the adsorption of H2O or trace elements enriched in the residual liquid. Morphological and chemical discontinuities at late stages of crystallization are reasonably explained by the formation of larger growth units (from smaller ionic entities) in the residual liquid. Important factors controlling the zircon morphology in different types of granitoids are: high cooling rates (alkaline magmas), magma mixing (calcalkaline magmas), enrichment of H2O and trace elements in residual liquids (calcalkaline and anatectic magmas), and the major element chemistry of the magma, possibly the ratio of Na and K to Al (agpaicity). 相似文献
14.
Transmission electron microscopy (TEM) has been used to investigate deformation microstructures of synthetic stishovite specimens deformed at 14 GPa, 1,300°C. Geometrical characteristics of numerous dislocations have been characterized by dislocation contrast and stereographic analyses in order to identify the easy slip systems of stishovite. TEM data allowed us to characterize the following slip systems: 〈100〉{001}, 〈100〉{010}, 〈100〉{021}, [001]{100}, [001]{110}, [001]{210} and
Observation of sub-grain boundaries and scalloped edge dislocations suggest that climb has been activated in the specimens. 相似文献
15.
We present here a numerical modelling study of dislocations in perovskite CaTiO3. The dislocation core structures and properties are calculated through the Peierls–Nabarro model using the generalized stacking
fault (GSF) results as a starting model. The GSF are determined from first-principles calculations using the VASP code. The
dislocation properties such as collinear, planar core spreading and Peierls stresses are determined for the following slip
systems: [100](010), [100](001), [010](100), [010](001), [001](100), [001](010),
and All dislocations exhibit lattice friction, but glide appears to be easier for [100](010) and [010](100).
[001](010) and [001](100) exhibit collinear dissociation. Comparing Peierls stresses among tausonite (SrTiO3), perovskite (CaTiO3) and MgSiO3 perovskite demonstrates the strong influence of orthorhombic distortions on lattice friction. However, and despite some quantitative
differences, CaTiO3 appears to be a satisfactory analogue material for MgSiO3 perovskite as far as dislocation glide is concerned. 相似文献
16.
1974年在一水晶矿石英脉晶洞中,发现了一种含Ba、Li的硅酸盐新矿物--纤钡锂石。我们对纤钡锂石进行了光性研究、比重测定、差热及热失重分析、红外光谱分析、X射线单晶结构分析等工作,现分述如下。 相似文献
17.
18.
新矿物汉江石的理想分子式为Ba2CaV23＋[（Si3AlO10）（OH）2]F（CO3）2。矿物呈黄绿色、深绿色,显微镜下呈浅绿色、淡绿色;单斜晶系,空间群为C2,a=0.52050（12）nm,b=0.9033（2）nm,c=3.2077（8）nm,β=93.49（8）°,V=1.5054（8）nm3,Z=4;二轴晶,正延性,负光性,一组完全解理,干涉色为三级绿,多色性明显,浅绿色-黄绿-深绿色;折射率α=1.615,β=1.655,γ=1.700（589 nm）,2Vobs=114°～115°,2Vcalc=88.8°;显微硬度平均值203 kg/mm2,相当于莫氏硬度4;实测密度平均3.69 g/cm3,计算密度3.78 g/cm3。X射线粉晶衍射的强谱线有1.5866 nm（7）（002）、0.5340 nm（91）（006）、0.4010 nm（10）（ī14）、0.3209 nm（23）（027）、0.2676 nm（100）（ī110）、0.2294 nm（29）（ī37）和0.2008 nm（11）（228）。汉江石的晶体结构由硅酸盐结构单元TOT（二八面体型）和碳酸盐结构单元Ba2Ca（CO3）2F交替组成,可能有3个多型,即1M型,2M型和3T型。 相似文献
19.
黄铁矿成因形态学 总被引：25，自引：5，他引：20
在1981—1986年野外工作的基础上,作者对胶东三县四个金矿床黄铁矿晶体形态进行了系统研究,对其中2495粒晶体进行了统计,对300粒晶体进行了测角,对60粒晶体进行了微形貌观察。根据以上实际工作及国内外有关资料提出了黄铁矿晶休常见单形出现频率的定量资料与晶体微形貌的特点,特别是{210}面上负条纹的特征与成因探讨。并讨论了黄铁矿晶体形态与分带性,与形成温度,与主、微量成分,与共生组合及与矿化等的关系。查明黄铁矿形态及其晶面微形貌的发育与硫逸度、温度、冷却速度等密切相关。在以上基础上提出了胶东四个金矿床中蚀变岩型金矿及石英脉型金矿两种成因类型黄铁矿形态特征上的五点差异。最后对黄铁矿研究方法要点进行了总结。 相似文献
20.
The morphological theory of Hartman and Perdok (1955, 1956) allows to deduce the character of a growth form {hkl} on the basis of structural data alone. Its application to the structure of whewellite leads to the identification of forms {100}, {010}, {021}, {011}, {12 \(\bar 1\) } and {121} which show during the growth a flat surface profile (flat forms F). These forms occur very frequently in the crystals we grew from pure aqueous solutions at supersaturation β≦1,90. Other forms, {001} and {10 \(\bar 1\) }, possibly show a double character (F or S, where S stays for related faces showing a stepped profile during the growth) according to the bonds assumed within some periodic bond chains (PBCs). Alternative ways of bonding water molecules lead to different structures of the same PBC. The different energy corresponding to these structures may explain the complex morphology of both natural and synthetic crystals grown at high β values. 相似文献