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1.
新疆萨尔托海铬铁矿中的Fe-Ni-As-S矿物研究 总被引：2，自引：1，他引：1
新疆萨尔托海铬铁矿是一个典型的与蛇绿岩有关的高铝型豆荚状铬铁矿,其中矿石铬尖晶石发生了明显的热液蚀变,发育了富Cr的蚀变环边,形成高铁铬铁矿,Cr#在蚀变后升高,发生了Cr元素的次生富集。在矿石颗粒间隙中的Fe-Ni-As-S矿物组合主要为镍黄铁矿-赫硫镍矿-针镍矿-砷镍矿。围岩纯橄岩普遍发育强烈的蛇纹石化,其中的Fe-Ni-As-S矿物组合为赫硫镍矿-镍黄铁矿-砷镍矿,还有少量的针镍矿和铜矿物。通过对硫化物的成分对比分析,认为矿石中的镍黄铁矿和赫硫镍矿都属于岩浆演化的产物(600℃),与赫硫镍矿和针镍矿一样,均从贫S的母岩浆中通过岩浆熔离过程形成。围岩和矿石中的含砷矿物以及围岩中的镍黄铁矿都是晚期热液活动的结果,其中砷镍矿具有特殊的蠕虫状-乳滴状结构,与围岩中的赫硫镍矿和镍黄铁矿共生。围岩和矿石中Fe-Ni-As-S矿物组合的形态和成分差异,说明金属矿物的整体演化从岩浆期到热液期经历了从贫S到富As的环境变化,最终形成了现在所观察到的复杂Fe-Ni-As-S矿物组合。 相似文献
2.
对张家界杆子坪黑色岩系型镍钼矿进行矿物学分析和扫描电镜研究,发现镍主要赋存于铁-方硫镍矿[(Ni,Fe)S2]、针镍矿(NiS)、方硫镍矿(NiS2)、硫镍矿(NiNi2S4)、辉砷镍矿(NiAsS)、紫硫镍矿(FeNi2S4)、镍黄铁矿[(Fe,Ni)9S8]等;钼主要以"胶硫钼矿"的形式存在。镍钼矿物多与黄铁矿、脉石矿物交代共生,反映出矿物嵌布关系的复杂性。镍钼矿物嵌布粒度不均匀且细小,给选矿带来很大的难度。 相似文献
3.
青海化隆地区拉水峡铜镍矿床地质、
地球化学特征及成因 总被引：3，自引：1，他引：2
拉水峡铜镍矿床位于化隆基性—超基性岩带中,岩体几乎全岩发生铜、镍硫化物矿化,且已遭受强烈蚀变,以角闪岩为主。岩浆期主要金属硫化物矿物组合为磁黄铁矿、黄铜矿、镍黄铁矿;热液蚀变期主要有紫硫镍矿、黄铁矿、黄铜矿、针镍矿等;氧化表生期主要为含镍高岭石、含镍绿泥石、孔雀石等。矿石轻稀土元素富集和负Eu异常明显,说明岩浆演化过程中发生了大量斜长石等的分离结晶作用。∑PGE含量平均为2460.46×10-9,(Pd+Pt)/(Os+Ir+Ru)值为0.40~2.00,表明铂族元素与岩浆深部熔离作用密切相关;但Pt/Pd(0.01~2.62)、Pd/Ir(0.91~8.77)说明热液作用对铂族元素具有一定的富集作用。S同位素组成变化范围很小,δ34S平均值为2.24‰,硫化物中的S以地幔S为主。拉水峡矿床的形成经历了岩浆融离贯入、热液叠加改造及表生氧化作用3个阶段。 相似文献
4.
金川低品位镍矿石工艺矿物学特性研究 总被引：2，自引：1，他引：1
金川低品位镍矿石属发生较强烈氧化的难处理型镍资源,矿石中镍的品位为0.51%,主要以紫硫镍矿形式存在。紫硫镍矿由磁黄铁矿、黄铁矿蚀变而来,呈现铁高、硫低、镍低的特点,选矿中可浮性较差。主要矿物的工艺嵌布粒度统计分析表明,矿石中镍矿物和黄铜矿均属微细粒嵌布的范畴,磁铁矿则具不均匀细粒嵌布的特点。单纯从粒度分布特征来看,选矿中欲使90%以上的镍矿物获得解离,以选择-0.026 mm的磨矿细度较为适宜,此时-600目部分约占95%左右。与磁铁矿嵌连关系密切的紫硫镍矿占其总量的95%以上,选矿过程中要提高镍的回收率,必须尽可能多地回收磁铁矿。矿石中脉石矿物主要为蛇纹石与绿泥石,易泥化,减少和消除脉石矿物对选别的影响至关重要。 相似文献
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6.
东天山主要铜镍矿床中磁黄铁矿的矿物标型特征及其成矿意义 总被引：3，自引：4，他引：3
东天山是中国最重要的岩浆铜镍硫化物矿带之一,产有黄山东、黄山、香山、葫芦等大中型铜镍矿床。图拉尔根、白石泉两处镍铜矿床为近年来在新疆地区铜镍找矿中的重大发现,两者均属于与镁铁质-超镁铁质杂岩有关的岩浆熔离-贯入型矿床。矿物共生组合以磁黄铁矿 镍黄铁矿 黄铜矿为特征,磁黄铁矿系矿石中最主要组成部分。文章以X射线衍射、扫描电镜、电子探针分析并辅以常规显微镜,查明这些矿床中磁黄铁矿均系Co、Ni的最主要载体矿物,Co、Ni元素主要以游离状态的硫化物(或硫砷化物)形式存在,如镍辉砷钴矿、钴辉砷镍矿、镍黄铁矿及紫硫镍矿等矿物。它们多以微细包裹体或出溶体形式随机地分布于磁黄铁矿内部,而少量的Co、Ni元素则以类质同像方式存在于磁黄铁矿晶格之中。图拉尔根、白石泉、葫芦三矿床中磁黄铁矿在多型结构以及微量元素地球化学方面均表现出一定的差异,系由两矿床容矿岩石基性程度及成矿温度之差异引起。 相似文献
7.
辉石巨晶中的硫化物及其成因 总被引：8，自引：1，他引：8
我国一些地区玄武岩辉石巨晶中的硫化物球泡(0.02-0.05mm)呈点阵式、散布式、定向带状或微裂隙羽状分布。硫化矿物组合是磁黄铁矿-镍黄铁矿-黄铜矿,其中以磁黄铁矿为主(～90％)。根据硫化物的规则排布以及高温矿物组合推测点阵式、散布式硫化物形成于地幔。是由溶解了～1％S的硅酸盐熔体在减压上升过程中析出过饱和的硫所致。 相似文献
8.
贵州遵义黄家湾下寒武统牛蹄塘组镍-钼富集层电子探针研究 总被引：8，自引：1，他引：7
对贵州遵义黄家湾下寒武统牛蹄塘组镍-钼富集层进行电子探针研究,发现镍主要赋存于黄铁矿、针镍矿、辉砷镍矿、铁辉砷镍矿、紫硫镍矿、赫硫镍矿;钼主要以"碳硫钼矿"的形式存在。镍钼硫化物多与黄铁矿、白铁矿交代共生,反映矿物经历了不同的成矿阶段。岩石中不仅富集Ni、Mo元素,而且Se元素存在超常富集,可以视为热液作用或生物作用的结果。遵义黄家湾下寒武统Ni-Mo富集层应为海底热液沉积和生物沉积混合成因,其物源较为复杂。 相似文献
9.
宁芜云台山黄铁矿矿床中黄铁矿矿物以自形晶为主 ,次为他形粒状 ;黄铁矿晶胞参数为 5 .415 2 3～ 5 .41843× 10 -10 m ,晶体化学式为 (Fe0 .9968Co0 .0 0 0 6Ni0 .0 0 2 6) 1.0 0 0 0 S2 .0 597;黄铁矿红外吸收光谱主吸收峰值为 34 8cm-1,最小透过率为 30 .0 0 %～ 48.80 % ,透过率极差为 31.13～ 47.5 1;黄铁矿中Fe平均含量为 45 .44 % ,S平均含量 5 3.91% ,具有富S特征 ;Co/Ni平均值为 0 .2 1;稀土元素总量平均为2 1.84× 10 -6,具有明显负铈异常 (δCe :0 .76～ 0 .93)和负铕异常 (δEu :0 .72～ 0 .90 ) ;硫同位素组成δ3 4S为 7.0 0‰～ 2 3.0 0‰ ,黄铁矿是含矿热液以堆积、充填和交代方式形成 ,黄铁矿床为火山热水沉积矿床。 相似文献
10.
通过差热-热重分析、X射线粉末衍射（XRD）及磁化率分析等手段,对天然黄铁矿样品在氮气中受热发生的矿物相 变过程进行了综合研究。不同温度下黄铁矿煅烧产物的XRD物相分析结果显示,低于500℃时,黄铁矿无显著变化;随着 温度的升高（500~600℃）,黄铁矿开始转变为单斜磁黄铁矿,进而生成六方磁黄铁矿,磁化率显著升高;700℃~800℃的 煅烧产物主要为六方磁黄铁矿,磁化率明显下降,直至900℃进一步形成更稳定的陨硫铁（FeS）,磁化率接近于零。在黄 铁矿物相开始转变的温度（500~600℃）区间,黄铁矿生成单斜磁黄铁矿的速率大于单斜磁黄铁矿转化为六方磁黄铁矿的速 率;高温（700~900℃）时,黄铁矿转化为单斜磁黄铁矿的速率低于单斜磁黄铁矿转化为六方磁黄铁矿的速率,表现为黄铁 矿直接生成六方磁黄铁矿。 相似文献
11.
矿物晶体收藏近年来成为一大热点,雄黄晶体艳丽,是地质类博物馆和矿物收藏家收藏的矿物种类之一,然而光照下雄黄不稳定,雄黄与光的反应倍受关注。因硫砷化合物的光化学灵敏度,硫砷化合物是一种重要的光学材料,国外开展了雄黄与光作用的反应产物和机理研究工作,雄黄与光的反应产物有副雄黄、砷华和χ-物相,在光照下雄黄通过As_4S_5分子间接地转变为副雄黄。作为药用矿物,As_2O_3是药用雄黄的组成部分,又是毒性成分,As_2O_3的来源与受到的高热和光照等有关,国内中医药界加强了对雄黄的物质成分的研究,还需加强光照对药用雄黄成分影响的研究。 相似文献
12.
本文简单了极化曲线反应极限电流强度确定矿体表面积的基本原理，阐述了单矿体和多矿物极化曲线反应极限电流强度确定矿体表面积的实验研究方法和结果，并说明极化曲线反应极限电流强度确定矿体表面积是有可能的。 相似文献
13.
非接触极化曲线视反应电位差区分矿体矿物成分及确定其边界的实验研究 总被引：2，自引：0，他引：2
本文用非接触极化曲线视反应电位差区分矿体矿物成分和确定矿体边界的基本原理，着重阐述矿物非接触极化曲线视反应电位差特征的实验研究方法和结果，并指出非接触极化曲线视反应电位差区分矿体矿物成分和确定矿体边界是有可能的。 相似文献
14.
Glaucophane and pyroxene breakdown reactions in the Pennine units of the Eastern Alps 总被引：1，自引：0，他引：1
Abstract New occurrences of crossite and jadeitic pyroxene are described from a thick metabasite unit within the upper levels of the Peripheral Schieferhülle in the Tauern Window, Austria. Unusual textures are preserved which provide evidence for the reactions and mechanisms involved in the breakdown of crossite and jadeitic pyroxene. Zones of albite and chlorite, produced by reaction between crossite and paragonite, have been preserved due to sluggish reaction kinetics during decompression from the blueschist to the greenschist facies. The zonal sequence is interpreted in terms of chemical potential gradients in Na, Mg and Al, which have been established by overstepping the equilibrium boundary. Breakdown textures of jadeite-acmite pyroxene to a symplectite of albite + hematite + actinolite, and of crossite to talc and actinolite are also described.
The occurrence of crossite and jadeitic pyroxene at high levels within the Peripheral Schieferhülle implies that even upper levels of the structural sequence have undergone blueschist facies metamorphism with pressures in excess of 8 kbar during the Alpine collisional event. 相似文献
The occurrence of crossite and jadeitic pyroxene at high levels within the Peripheral Schieferhülle implies that even upper levels of the structural sequence have undergone blueschist facies metamorphism with pressures in excess of 8 kbar during the Alpine collisional event. 相似文献
15.
Seal or cap-rock integrity is a safety issue during geological carbon dioxide capture and storage (CCS). Industrial impurities such as SO2, O2, and NOx, may be present in CO2 streams from coal combustion sources. SO2 and O2 have been shown recently to influence rock reactivity when dissolved in formation water. Buoyant water-saturated supercritical CO2 fluid may also come into contact with the base of cap-rock after CO2 injection. Supercritical fluid-rock reactions have the potential to result in corrosion of reactive minerals in rock, with impurity gases additionally present there is the potential for enhanced reactivity but also favourable mineral precipitation.The first observation of mineral dissolution and precipitation on phyllosilicates and CO2 storage cap-rock (siliciclastic reservoir) core during water-saturated supercritical CO2 reactions with industrial impurities SO2 and O2 at simulated reservoir conditions is presented. Phyllosilicates (biotite, phlogopite and muscovite) were reacted in contact with a water-saturated supercritical CO2 containing SO2, or SO2 and O2, and were also immersed in the gas-saturated bulk water. Secondary precipitated sulfate minerals were formed on mineral surfaces concentrated at sheet edges. SO2 dissolution and oxidation resulted in solution pH decreasing to 0.74 through sulfuric acid formation. Phyllosilicate dissolution released elements to solution with ∼50% Fe mobilized. Geochemical modelling was in good agreement with experimental water chemistry. New minerals nontronite (smectite), hematite, jarosite and goethite were saturated in models. A cap-rock core siltstone sample from the Surat Basin, Australia, was also reacted in water-saturated supercritical CO2 containing SO2 or in pure supercritical CO2. In the presence of SO2, siderite and ankerite were corroded, and Fe-chlorite altered by the leaching of mainly Fe and Al. Corrosion of micas in the cap-rock was however not observed as the pH was buffered by carbonate dissolution. Ca-sulfate, and Fe-bearing precipitates were observed post SO2-CO2 reaction, mainly centered on surface cracks and an illite rich illite-smectite precipitate quantified. Water saturated impure supercritical CO2 was observed to have reactivity to rock-forming biotite, muscovite and phlogopite mineral separates. In the cap-rock core however carbonates and chlorite were the main reacting minerals showing the importance of assessing actual whole core. 相似文献
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The extent to which kinetic barriers to nucleation and growth delay the onset of prograde metamorphic reaction, commonly known as overstepping, is related to the macroscopic driving force for reaction, termed reaction affinity. Reaction affinity is defined in the context of overstepping as the Gibbs free‐energy difference between the thermodynamically stable, but not‐yet‐crystallized, products and the metastable reactants. Mineral reactions which release large quantities of H2O, such as chlorite‐consuming reactions, have a higher entropy/volume change, and therefore a higher reaction affinity per unit of temperature/pressure overstep, than those which release little or no H2O. The former are expected to be overstepped in temperature or pressure less than the latter. Different methods of calculating reaction affinity are discussed. Reaction affinity ‘maps’ are calculated that graphically portray variations in reaction affinity on equilibrium phase diagrams, allowing predictions to be made about expected degrees of overstepping. Petrological consequences of variations in reaction affinity include: (i) metamorphic reaction intervals may be discrete rather than continuous, especially in broad multivariant domains across which reaction affinity builds slowly; (ii) reaction intervals may not correspond in a simple way to reaction boundaries and domains in an equilibrium phase diagram, and may involve metastable reactions; (iii) overstepping can lead to a ‘cascade effect’, in which several stable and metastable reactions involving the same reactant phases proceed simultaneously; (iv) fluid generation, and possibly fluid presence in general, may be episodic rather than continuous, corresponding to discrete intervals of reaction; (v) overstepping related to slowly building reaction affinity in multivariant reaction intervals may account for the commonly abrupt development in the field of certain index mineral isograds; and (vi) P–T estimation based on combined use of phase diagram sections and mineral modes/compositions on the one hand, and classical thermobarometry methods on the other, may not agree even if the same thermodynamic data are used. Natural examples of the above, both contact and regional, are provided. The success of the metamorphic facies principle suggests that these kinetic effects are second‐order features that operate within a broadly equilibrium approach to metamorphism. However, it may be that the close approach to equilibrium occurs primarily at the boundaries between the metamorphic facies, corresponding to discrete intervals of high entropy, dehydration reaction involving consumption of hydrous phases like chlorite (greenschist–amphibolite facies boundary) and mica (amphibolite–granulite facies boundary), and less so within the facies themselves. The results of this study suggest that it is important to consider the possibility of reactions removed from equilibrium when inferring the P–T–t evolution of metamorphic rocks. 相似文献
18.
在75℃和pH=1.04～2.46时采用间歇型实验方法测定了天然白钨矿在HCl溶液中的溶解速率,揭示了溶解反应的动力学机理。结果表明,Ca的释放速率随反应时间保持稳定,并随pH降低而增大。W的释放行为则更为复杂,在反应初期与Ca呈一致溶解,之后由于钨酸表面层(中间产物)的形成,W的释放量和释放速率明显下降。这说明白钨矿的溶解作用由早期的表面化学反应转变为化学反应-扩散控制过程,从而导致W、Ca呈不一致溶解。pH越小,不一致溶解出现的时间越早。酸性溶液中白钨矿的溶解速率方程为v=k[H+]n,以W和Ca计算的速率常数k分别为0.65×10-5mol/m2s和1.04×10-5mol/m2s,反应级数n则分别为1.20和1.26。结合他人研究结果,白钨矿的溶解反应相对于H+可能为一级反应。 相似文献
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Determining whether a reaction can be written between a set of minerals within error is an example of the more general problem of determining whether a set of compositions are coplanar within error. Generally if the compositions are of minerals, ‘within error’ should allow the minerals to maintain stoichiometry. The problem is addressed via the addition of a ‘bogus’ composition to the set, and calculating the reaction coefficients for a reaction between the compositions in this augmented set. A reaction can be written if a confidence interval on the reaction coefficient of ‘bogus’ includes zero. The reaction coefficients can be solved for directly when the problem is posed in terms of least squares with equality constraints. The confidence interval is determined with a bootstrap method, allowing the result to depend on the scatter of the data around the solution of the least squares problem, not on the data uncertainties 相似文献