铊矿物晶体化学和地球化学

对世界上已经发现报道的56个铊矿物种类、晶体化学和地球化学特征以及铊矿物产出的地质条件进行了系统总结。将铊矿物分为硫化物、氧化物和含氧盐等六大类,其中铊硫化物矿物占绝大多数。在低温还原环境下,铊表现出强烈的亲硫性,可以与As、Sb、Pb、Hg、Cu和Au等元素结合形成两种形式的铊硫化物矿物：①Tl_wB_yS_z（铊作为唯一的金属元素）,②Tl_wA_xB_yS_z（除了铊以外还有其他的金属元素）。低温成矿域中贱金属矿床是铊矿物的主要产出场所。对目前铊矿物学研究的现状、最新进展和存在的问题进行了综述和探讨。     

安康矿不相称超晶格有序及相似矿物的晶体化学

安康矿是一种柱红石类新矿物,共化学组成为Ba0.8（Ti,V,Cr）8O16。通讨X光单晶工作。发现其结构在平行c轴方向上,存在一维的不相称超晶格有序。亚结构同柱红石结构,修正的晶胞参数a=10.118（1）A c=2.956（3）A。不相称超结构属四维的布拉维类,可能的超空间群有。不相称超结构与大孔道中的空位、以及由空位引起大阳离子沿c方向上的位移有关     

Crystal Chemistry Research of Minerals of Nigerite Group and Its Significance

SinceJacobsonandWebb (194 7)firstlyfoundthenigeriteinNigeria ,mineralogistshavefounditinmanycountriessuchasRussia (EastSiberia ,195 8) ,China(Hunan ,196 3) ,Portugal (196 5 ) ,Australia (1976 )andsoon .Greyetal.(1979)determinedaccuratelythecrystalstructureofnigerite (2 4R) .In 1988,Chenfoundakindofendmembermineralofnigerite ,whichisMg riched .ByapprovingofCommissiononNewMineralsandMineralNames (CNMMN) ,thismineralwasnamedpengzhizhongite .Inthepast ,somemineralogistsdidnotfurtherdis t…     

库车坳陷三叠系碎屑重矿物成分及其物源属性

库车坳陷三叠系发育良好,出露齐全,主要由陆相碎屑岩组成。本文运用电子探针微区成分分析方法,对库车坳陷北部三叠系砂岩中石榴石、电气石、铬尖晶石进行了矿物化学成分分析。结果显示,碎屑石榴石主要富含铁铝榴石,其次为镁铝榴石、锰铝榴石,钙铝榴石含量较低,他们主要来自于低级-高级变质岩和花岗岩;电气石主要来自于变质沉积岩和花岗岩;铬尖晶石则主要源自岛弧玄武岩、洋岛玄武岩和与俯冲相关的橄榄岩。综合石榴石与电气石研究结果表明,上三叠统碎屑物质更多的来自于高级变质岩和花岗岩,而下三叠统碎屑物质主要源自低级变质岩和花岗岩。通过对比西天山榴辉岩、片麻岩中石榴石成分,本文所研究的高镁石榴石以低钙铝榴石含量与榴辉岩中石榴石相区别,而与片麻岩中石榴石成分相似。西天山榴辉岩在三叠纪时期可能尚未剥露至地表,但片麻岩已有相当范围的出露。上三叠统的碎屑铬尖晶石可能主要来自于中天山及南天山的岛弧岩浆岩及蛇绿岩,部分源自洋岛玄武岩,为南天山为多岛海造山提供了沉积学证据。     

黑龙江省砂宝斯金矿床矿石矿物与金矿物特征研究

为给砂宝斯金矿床的勘探和利用提供依据,本文总结了多年的野外观察资料,并通过镜下鉴定、人工重砂、电子探针等方法对该矿床的矿石矿物、金矿物特征进行了系统研究。结果表明,该矿床的矿石类型为贫硫化物微细粒浸染型金矿石,矿石矿物主要为黄铁矿,次为毒砂,含有较多的微量元素;脉石矿物主要为石英。矿石结构主要为半自形-自形、他形、交代、固溶体分离结构,浸染状或细脉浸染状构造。金矿物主要为自然金,其赋存状态以硫化物中包裹金和脉石粒间金为主,主要为微粒金及次显微金,呈微细分散状态。除Au元素外,矿床中其他元素均不具有综合利用价值,有害元素含量低。     

Chemistry of Kornerupine and Associated Minerals, a Wet Chemical, Ion Microprobe, and X-Ray Study Emphasizing Li, Be, B and F Contents

Kornerupine and associated minerals in 31 samples of high-graderocks relatively rich in Al and Mg were analysed by wet chemistry,ion microprobe mass analyser, electron microprobe and X-raypowder diffraction. For 11 samples of kornerupine and threesamples of biotite (F only) analysed by both wet chemical andion microprobe methods, the best agreement was obtained forB₂O₃, whereas the ion microprobe Li₂O values were systematicallysomewhat higher than the wet chemical values. The wet chemicalmethods give Li₂O=0–0?19 wt.%; BeO=0–0?032 wt.%;B₂O₃=0–4?01 wt.%; and F=0?07–0?77 wt.% in kornerupine,whereas ion microprobe analyses on other kornerupines give valuesup to 0?35 wt.% Li₂O, O066 wt.% BeO, and 4?72 wt.% B₂O₃. Thesum B+Al+Fe³⁺+Cr is close to 6?9 atoms per 22 (O, OH, F) or21?5 (O) in kornerupine. In general, Li/Fe ratios decrease as follows: kornerupine ?sapphirinebiotite> Crd (Na<0?03 per 18 oxygens)>tourmaline, garnet,orthopyroxene. However, for cordierite with Na>004, Li/Fedecreases as follows: cordierite>kornerupine. Sapphirineand sillimanite are the only associated minerals to incorporatesignificant boron (0?1–0?85 wt.% B₂O₃) and then only whenthe single site for B in kornerupine is approaching capacity.Sillimanite B₂O₃ contents increase regularly with kornerupineF. Fractionation of fluorine increases as follows: kornerupine<biotite<tourmaline,and K^krn-BtD=(F/OH)^Krn/(F/(OH)^Bt (assuming ideal anion composition)increases with biotite Ti. Kornerupine B₂O₃ content is a measureof B₂O₃ activity in associated metamorphic fluid, whereas sillimaniteB₂O₃ content increases with temperature, exceeding 0?4 wt.%whenT=900?C at very low water activities. New data on 11 kornerupines and literature data indicate thatthe unit cell parameters a, c, and V decrease with increasingB content and b, c, and V increase with increasing Fe³⁺ content.In Fe³⁺-poor kornerupines, b increases with Mg and with (Mg+ Fe²⁺) but the effect of Mg on b via the substitution ^VIMg+^IVSi=^VIAl+^IVAloverwhelms the effect of Fe²⁺=Mg substitution.     

金、银矿物及含银的硫化物的电子探针定量分析

金、银矿物在岩石中通常量微,颗粒小,产出形式也比较复杂,用电子探针分析,不仅可以快速准确定出矿物名称,而且配合电子探针的附件背散射电子图象装置、X射线面分布图象装置等可以进一步查清金、银元素的赋存状态。本文主要对该类矿物的定量方法作一介绍。     

苏北东海花岗质岩石中主要造岩矿物和副矿物的地球化学特征

苏北东海地区主侵入花岗岩类岩石属Ⅰ型花岗岩类。其主要造岩矿物为阳起角闪石、富镁黑云母、更长石、钾长石和石英。主要副矿物为榍石、磷灰石、锆石、磁铁矿等。主侵入岩体的形成温度为910—690℃,logfo_2=-12,fH_2O=(1.3—1.8)×10~8Pa,log(fH_2O/f_(HF))=3—4。第一类过渡元素富集于角闪石、黑云母和榍石中,而在更长石、钾长石和石英中明显亏损。由于榍石、角闪石、黑云母和更长石对全岩REE含量的贡献最大,因此它们控制了本区花岗岩类岩石的稀土配分模式。前三者富重稀土,负Eu异常较强,斜长石相对富轻稀土,并表现为正Eu 异常。因此可以认为随着花岗质岩浆中铁镁矿物和斜长石的分离,将会导致残余岩浆中第一类过渡元素、重稀土元素和Eu的亏损。     

Geology and Mineral Chemistry of Uranium- and Thorium-bearing Minerals in Rare-Metal (NYF) Pegmatites of Um Solimate,South Eastern Desert,Egypt

The garnet muscovite granitic pegmatite of Um Solimate, in southern Egypt, represents a promising asset for strategic and economic metals, especially Bi–Ni–Ag–Nb–Ta as well as U and Th. The ore bodies occur as large masses, pockets and/or veins of very coarse-grained pegmatites, which consist mainly of K-feldspar, quartz and albite with subordinate muscovite, garnet, and biotite. Radiometric data revealed that eU- and eTh-contents of the pegmatites reach up to 39 ppm and 82 ppm, respectively. The studied pegmatites are enriched in primary U and Th minerals (uraninite, coffinite, thorianite and uranothorite) as well as Hf-rich zircon and monazite, which give rise to anomalous radioactive zones. Niobium-tantalium-bearing minerals (i.e. ferrocolumbite, microlite and uranopyrochlore), xenotime, barite, galena, fluorite, and apatite are ubiquitous, and, consequently, the studied pegmatites belong tothe Niobium–Yttrium–Fluorine-type (NYF) family. The noble metal mineralization includes argentite (Ag2S), native Ni and Bi as well as bismite and bismoclite. In addition, beryl and tourmaline are observed in pegmatites near the contact with metasediments and ultramafic bodies. The observed compositional variations of Ta/(Ta+Nb) and Mn/(Mn+Fe) ratios in columbite (0.08–0.45 and 0.11–0.57, respectively) and Hf contents in zircon (3.54–6.46 wt%) may reflectan extreme degree of magmatic fractionation leading to formation of the pegmatite orebody.     

我国矿物晶体结构与晶体化学研究进展及新成果(2000-2019)

矿物的晶体结构与晶体化学是矿物学的重要基础研究领域之一,21世纪以来,随着国家对地勘行业的重视,以及平面探测技术单晶衍射仪、微区、微量衍射等实验技术的应用与计算机软硬件能力的提高,我国矿物晶体结构与晶体化学研究得到飞速发展.矿物晶体结构测定与研究是伴随着新矿物的发现而发展的,新矿物的发现是矿物晶体结构研究的基石,又为新...     

Minerals of the viridine hornfels from Darmstadt,Germany

Viridine containing the highest amounts of Mn₂O₃ detected thus far (up to 20.5 mol % “Mn₂SiO₅”) coexists in a metasedimentary hornfels with spessartine, Mn-phlogopite (mangan-ophyllite), Mn-phengite (alurgite), hematite, quartz and probably some primary braunite. In layers poorer in viridine spessartine is absent but piemontite appears as an additional phase. Microprobe analyses of all these phases are presented which indicate very strong fractionation of Mg and Mn in coexisting phlogopite and garnet, and of Fe and Mn in coexisting hematite and braunite. Sericitic aggregates consisting of phengitic muscovite and braunite are interpreted as retrograde alteration products of viridine, but might partly be pinitic alterations of a former Mg-rich cordierite. Due to the occurrence of the assemblage spessartine-viridine-quartz Mn-cordierite cannot have been a stable phase prior to retrograde alterations. In general the stability field of viridine is extended towards higher temperatures as compared to that of pure andalusite, Al₂SiO₅. Due to the coexistence of phlogopite and muscovite (phengite) the temperature of contact metamorphism cannot have exceeded some 550°–650° C depending on the prevailing water pressure.     

2010年玉树Ms7.1地震前后大气物理化学遥感信息

利用高分辨率卫星遥感数据反演了地表温度、水汽、CO总量和CH4体积分数的时空变化,讨论了这种变化与2010年4月14日青海玉树Ms 7.1地震以及地震断裂带的关系.利用MODIS LIB数据反演的玉树地震前后的温度数据表明,在主震前亮温和地表温度出现高值,高值异常高于震前几年的同期平均温度并沿NW向断裂带分布;这与测量...     

细粒沉积物(岩)中重矿物提取方法的改进

随着近百年的重矿物研究,从沉积物中提取重矿物的实验方法已经形成了固定模式,然而这些传统方法都是对砂岩粗颗粒矿物研究经验的积累,并不适用于泥质含量高的细粒沉积物.根据溶胶稳定(DLVO)理论,悬浮于溶液中的微细颗粒会因分子间作用力的相互吸引絮凝成团,从而影响细粒沉积物中重矿物提取的效果.实验研究证明,影响重矿物提取的主要因素是微细矿物颗粒间的絮凝作用,而并非有机重液的黏度.如何克服微粒间的絮凝作用是提取泥岩和粉砂岩中重矿物的关键.实验对比分析表明,添加分散剂的超声波振动和自然沉降法可以在克服絮凝作用的前提下有效去除泥质成分,同时对粉砂级矿物进行精确的粒径分选;离心分离同样也可以克服微粒间的絮凝作用,在重液分离过程中使重矿物顺利从轻矿物中分离.以上3种方法的联合使用可以弥补传统的重矿物提取方法的不足,并显著提高泥岩、粉砂岩中重矿物的提取率.     

论SNS边坡柔性防护工程实践中的几个问题

随着SNS边坡柔性防护新技术在坡面地质灾害防护特别是崩塌落石防护领域的推广及成功应用,与其自身特点相对应的一些疑问在SNS的设计及施工中被广大工程技术人员提出.文章试图对业内人士普遍关心的几个问题作一简要论述.望能为广大工程技术人员在SNS边坡柔性防护技术的实践中提供理论帮助并消除相关疑问.     

富钙长石-橄榄石包体与其他部分典型包体W-L边的成因

球粒陨石中的富Ca、Al包体(简称CAI)形成于星云演化的最初始阶段,保存了大量星云形成和演化的各种信息。研究认为,包体的成因主要包括星云直接凝聚和熔融结晶,少部分甚至经历过高温蒸发过程。部分CAI最外层具有由一种或几种矿物组成的Warking-Lovering边(简称为W-L边),CAI和其W-L边对于认识早期星云环境和界定CAI的形成时间等均具有重要意义。目前,对于W-L边的形成过程研究并不深入,且一直存在争议。本文主要介绍了三个典型包体:C#1(富钙长石-橄榄石包体)、GRV 022459-2RI5(A型包体)和GRV 021579-3RI5(富尖晶石球粒状包体)及其W-L边的矿物岩石学和氧同位素组成特征。C#1包体明显经历过熔融结晶过程,W-L边氧同位素组成具有与包体内部矿物相似的富~(16)O同位素特征,表明W-L边的成因与包体的形成过程密切相关,形成于同一富~(16)O同位素组成区域,且W-L边属于包体熔融结晶过程后期的产物。矿物岩石学特征表明,GRV 022459-2RI5属于星云直接凝聚形成,其W-L边为包体形成过程最晚期星云凝聚产物。GRV021579-3RI5经历过熔融结晶过程,其W-L边为包体结晶最后阶段的产物。     

Platinum-Group Elements in Sulphide Minerals, Platinum-Group Minerals, and Whole-Rocks of the Merensky Reef (Bushveld Complex, South Africa): Implications for the Formation of the Reef

The concentrations of platinum-group elements (PGE), Co, Re,Au and Ag have been determined in the base-metal sulphide (BMS)of a section of the Merensky Reef. In addition we performeddetailed image analysis of the platinum-group minerals (PGM).The aims of the study were to establish: (1) whether the BMSare the principal host of these elements; (2) whether individualelements preferentially partition into a specific BMS; (3) whetherthe concentration of the elements varies with stratigraphy orlithology; (4) what is the proportion of PGE hosted by PGM;(5) whether the PGM and the PGE found in BMS could account forthe complete PGE budget of the whole-rocks. In all lithologies,most of the PGE (65 up to 85%) are hosted by PGM (essentiallyPt–Fe alloy, Pt–Pd sulphide, Pt–Pd bismuthotelluride).Lesser amounts of PGE occur in solid solution within the BMS.In most cases, the PGM occur at the contact between the BMSand silicates or oxides, or are included within the BMS. Pentlanditeis the principal BMS host of all of the PGE, except Pt, andcontains up to 600 ppm combined PGE. It is preferentially enrichedin Pd, Rh and Co. Pyrrhotite contains, Rh, Os, Ir and Ru, butexcludes both Pt and Pd. Chalcopyrite contains very little ofthe PGE, but does concentrate Ag and Cd. Platinum and Au donot partition into any of the BMS. Instead, they occur in theform of PGM and electrum. In the chromitite layers the whole-rockconcentrations of all the PGE except Pd are enriched by a factorof five relative to S, Ni, Cu and Au. This enrichment couldbe attributed to BMS in these layers being richer in PGE thanthe BMS in the silicate layers. However, the PGE content inthe BMS varies only slightly as a function of the stratigraphy.The BMS in the chromitites contain twice as much PGE as theBMS in the silicate rocks, but this is not sufficient to explainthe strong enrichment of PGE in the chromitites. In the lightof our results, we propose that the collection of the PGE occurredin two steps in the chromitites: some PGM formed before sulphidesaturation during chromitite layer formation. The remainingPGE were collected by an immiscible sulphide liquid that percolateddownward until it encountered the chromitite layers. In thesilicate rocks, PGE were collected by only the sulphide liquid. KEY WORDS: Merensky Reef; Rustenburg Platinum Mine; sulphide; platinum-group elements; image analysis; laser ablation ICP-MS     

西藏甲玛铜多金属矿床中铋矿物及其与铜矿化关系

西藏墨竹工卡县甲玛铜多金属矿床中,矽卡岩型铜矿石的铋质量分数最高可达0.23%,且分布较广泛,可作为伴生有用组分综合回收利用.根据化学分析,铋含量的高低与矿石类型有关.铋与矽卡岩型铜矿石的关系最为密切,铜矿化越强,铋含量越高.在垂向上,中浅部矽卡岩型矿体中的铋含量高于深部的矽卡岩,与矿化分带中的Cu元素矿化带较一致.通过电子探针分析,甲玛矿床中含铋矿物主要有硫铋铜矿、辉碲铋矿、针硫铋铅矿、针辉铋铜矿、辉铋锑矿及含铋黝铜矿和斑铜矿等.硫铋铜矿是甲玛矿床中分布最广、最主要的铋矿物,其主要呈它形粒状、叶片状或乳滴状分布于斑铜矿、辉铜矿、黝铜矿等硫化物中.根据矿物的产出形态及电子探针分析,甲玛矿床中存在不同成矿世代的硫铋铜矿:分布于斑铜矿中呈它形粒状、叶片状的硫铋铜矿和在斑铜矿中呈乳滴状的硫铋铜矿.前者是硫铋铜矿的主要产出形态,其成分接近硫铋铜矿的理论值;但后者往往成分发生变化,Bi偏低,Cu、S偏高.甲玛矿石中铋不仅应该被综合利用,且是铜矿化的重要找矿标志.     

The Stability of Andradite, Hedenbergite, and Related Minerals in the System Ca--Fe--Si--O--H

Phase relations for the bulk compositions 3CaO·2FeO_x·3SiO₂+excessH₂O and CaO·FeO_x·2SiO₂+excess H₂O were determinedusing conventional hydrothermal techniques with solid phaseoxygen buffers to control fO₂. Andradite, Ca₃Fe³⁺₂Si₃O₁₂, synthesized above 550 °C hasan average unit cell edge, a_o, of 12.055±0.001 Å,and an index of refraction, n, of 1.887±0.003. Belowthis temperature, a_o increases whereas n decreases, indicatingthe formation of a member of the andradite-hydroandradite solidsolution. At 2000 bars P_fluid andradite is stable above an f_O2of 10¹⁵ bar at 800 °C and 10-³² bar at 400 °C. At lowerf_O2 andradite+fluid gives way at successively lower temperaturesto the condensed assemblages magnetite+wollastonite, kirschsteinite(CaFe²⁺SiO₄)+ wollastonite and kirschsteinite+xonotlite (Ca₆Si₆O₁₇(OH)₂). Synthetic hedenbergite, CaFe²⁺Si₂O₆, has average unit cell dimensionsof a_o = 9.857± 0.004 Å, b_o = 9.033±0.002Å, c_o = 5.254±0.002 Å and ß = 104.82°±0.03°,and refractive indices of n = 1.731±0.003 and n = 1.755±0.005.At 2000 bars P_fiuid, hedenbergite is stable below an f_O2 of10-¹³ bar at 800 °C and 10-²⁸ bar at 400 °C. Above thesef_O2 values, hedenbergite+O₂ breaks down to andradite+magnetite+quartz. The mineral pair andradite +hedenbergite thus limit the f_O2range possible for their joint formation under equilibrium conditions. The hydration of wollastonite to xonotlite occurs at much lowertemperatures than previous experimental work indicated. A tentativehigh temperature limit for this reaction is set at 185°±15°C and 5000±25 bars and 210°±15 °Cand 2000±20 bars. Inasmuch as the growth of xonotlitefrom wollastonite + H₂O was never accomplished, this high temperaturelimit does not represent an equilibrium univariant curve. Nine phases were encountered in the study of andradite and hedenbergite.They are andradite, hedenbergite, magnetite, wollastonite, kirschsteinite,xonotlite, quartz, ilvaite, and vapor (fluid). An invariantpoint analysis using the method of Schreinemakers shows thetopologic relations of the reactions involved. The resultinggrid can be used to interpret natural occurrences.     

缅甸地质矿产特征与矿业投资环境分析

缅甸位于中国西南和印度洋之间,是“一带一路”中缅经济走廊的重要节点,也是中国西南通向印度洋、连接东南亚的便捷通道。缅甸固体矿产资源较为丰富,但地质工作研究程度较低,因而具有良好的矿业投资前景,尤其是近年来缅甸政府陆续更新了矿业政策,对外国赴缅矿业投资的限制进行了优化,以此吸引更多的投资者在缅进行矿业勘查开发,振兴缅甸矿业经济。文中介绍了缅甸地质与矿产资源概况、近十年勘查开发形势及主要矿山开发现状,重点解读了近年来缅甸政府颁发的新的《矿业法》和《矿业法实施细则》等文件,以期更加深入地理解缅甸矿业政策的新变化、新动向和新趋势,为中资企业开展缅甸矿业投资开发提供依据。同时,提出相关的建议,包括需要及时跟进矿业市场动态、了解在缅项目负面清单、科学把握政策要点、提前研判与缅甸政府合作的优劣模式以及履行企业社会责任等。笔者分析缅甸资源禀赋和矿业开发现状、深入解读缅甸新颁布的矿业法和矿业政策,对企业在缅甸矿产勘查和矿业投资合作具有一定指导意义。