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1.
西昆仑库地蛇绿岩发育小规模的铬铁矿床,矿体呈豆荚状和层状、似层状,均与纯橄岩紧密伴生。这些纯橄岩主要由橄榄石和副矿物尖晶石组成,与方辉橄榄岩相比,橄榄岩中的橄榄石粒径粗(平均2.5mm),Mg#(88~90)低,这与它们全岩低Mg#(90)值,富Al_2O_3、TiO_2、Cr_2O_3、Fe_2O_3相吻合,与熔融残余成因的纯橄岩明显不同,反映了其很可能是由熔体与方辉橄榄岩反应而成。矿体主要由块状、浸染状及脉状铬铁矿石组成;铬铁矿石中的尖晶石具有低而相对稳定的Cr#(43~56),低于富铬型铬铁矿矿床中的铬铁矿(Cr#60)。块状矿石与纯橄岩呈突变接触,矿石中的尖晶石呈浑圆状,包裹有较多橄榄石、辉石等硅酸盐矿物及角闪石等含水硅酸盐矿物;浸染状铬铁矿石中的尖晶石与橄榄石颗粒构成交织结构,或呈云朵状,沿橄榄石颗粒边界相互连接,矿石的结构构造显示了熔/岩反应成因特征。通过计算分析,我们认为该区富铝型铬铁矿石是由拉斑玄武质熔体与地幔橄榄岩反应而成,由于熔体中含有较高的H_2O,参与反应的熔体可能源于弧后扩张脊环境。 相似文献
2.
西藏罗布莎蛇绿岩中不同产出的纯橄岩及成因探讨 总被引：2，自引：2，他引：0
罗布莎蛇绿岩中的纯橄岩有三种产出情况,除了与豆荚状铬铁矿伴生的薄壳状纯橄岩外,还有产在方辉橄榄岩底部被认为是堆晶岩的厚层状纯橄岩和方辉橄榄岩中的透镜状纯橄岩。厚层状纯橄岩约700～1000m厚,以橄榄石富镁(Fo93～95),单斜辉石低铝富镁(Al2O30.47%～0.85%,Mg#95～97),铬尖晶石高铬低镁(Cr#值平均77,Mg#平均51)为特征。该纯橄岩中的浸染状铬铁矿也是高铬低镁型,但Mg#值(平均59)高于厚层状纯橄岩的副矿物铬尖晶石。薄壳状纯橄岩与厚层状纯橄岩成分相近,其橄榄石Fo92～94,单斜辉石Al2O3<1%和Mg#95～97;铬尖晶石的Cr#值平均71,Mg#值平均52。与薄壳状纯橄岩伴生的块状铬铁矿为高镁高铬型,但Mg#值(平均68)相对更高些,Cr#值平均79。透镜状纯橄岩的特征是橄榄石Fo(91～92)和铬尖晶石Cr#(60左右)均低于前两类纯橄岩,但单斜辉石的Al2O3(1.41%～1.71%)则高于前两者。透镜状纯橄岩的矿物成分与方辉橄榄岩重叠,两者为渐变过渡关系。研究对比表明,罗布莎厚层状纯橄岩不同于经典的蛇绿岩的超镁铁质堆晶岩,认为将其成因解释为拉斑玄武质熔体与地幔橄榄岩的反应较为合理。透镜状纯橄岩与方辉橄榄岩存在成生联系,可能是地幔橄榄岩高度部分熔融的产物,或熔体和方辉橄榄岩在原位发生反应的产物;薄壳状纯橄岩成因与厚层状纯橄岩相同,但与其相伴的块状铬铁矿是否由拉斑玄武质熔体与方辉橄榄岩反应形成,值得商榷。 相似文献
3.
对豆荚状铬铁矿床成因的认识 总被引：15，自引：1，他引：15
文章提出豆荚状铬铁矿床不是上地幔局部溶融后的残余物，而是亏损地幔又经部分溶融形成的溶体发生液相不混溶，导致硅酸盐岩浆和富铬矿浆的形成。当比重不同高度分馏的溶体在上升过程发生了分离，轻熔体上升侵入于岩浆房、重熔体和铬铁矿浆，就地堆积或贯入围岩形成豆荚状铬铁矿床。豆荚状铬铁矿的伴生围岩纯橄岩，不是高度亏损的上地幔残余，可能是与铬铁矿浆伴随的一种硅酸盐熔体 。与大量纯橄岩脉伴随的基性岩、超基性岩脉，也属 相似文献
4.
豆荚状铬铁矿床是工业上冶金级铬铁矿石的最主要来源,对于其成因研究依然是各国地质学家最为关注的热点之一。文章着重概述了近年来国内外地质学者对豆荚状铬铁矿床成因研究的现状和最新进展。最新研究表明,显生宙以来的豆荚状铬铁矿床具有一定的成矿专属性,主要赋存于蛇绿岩套底部(壳-幔边界,即岩石莫霍面)地幔橄榄岩中的一定层位中。世界上含矿的地幔橄榄岩普遍具有垂直熔融分带特征,即上部偏基性,下部偏酸性。豆荚状铬铁矿床与纯橄岩-方辉橄榄岩相密接相关,却很少见有豆荚状铬铁矿床产于二辉橄榄岩中。豆荚状铬铁矿的成矿作用经历了由洋中脊(MOR)扩张环境向岛弧体系俯冲环境的转变过程,而岛弧环境(岛弧、弧后盆地、弧前盆地等)是形成冶金级豆荚状铬铁矿的最为有利的构造环境。富铬铬铁矿与纯橄岩、玻安岩(Boninite)均为亏损地幔橄榄岩再次高度熔融的最终产物,而玻安岩普遍产于岛弧环境。虽然玻安岩不是铬的有效载体,但玻安岩的熔离促使铬铁矿达到进一步的富集。铬铁矿中的铬来自原始地幔,主要来自于地幔橄榄岩中两种辉石的不一致熔融及其对副矿物铬尖晶石的改造。随着部分熔融程度的增高,地幔橄榄岩逐渐向富镁方向演变,而对应的造矿铬尖晶石也逐渐向富镁、富铬方向演变。 相似文献
5.
本文以西藏自治区罗布莎铬铁矿床为例并结合世界其它地区同类矿床实例,讨论了豆荚型铬铁矿床的成因机制。研究表明,铬铁矿与纯橄岩-斜辉辉橄岩都是由同一原始地幔岩(尖晶石二辉橄榄岩)经不同程度熔融的产物。铬铁矿及纯橄岩是这一过程中高度熔融的最终产物。其熔融的机制是两种辉石(斜方辉石和单斜辉石)不一致熔融转变为橄榄石和铬尖晶石,并伴随着副矿物铬尖晶石及造岩矿物成分的调整和再造,从而导致铬铁矿床与纯橄岩的紧密伴生。该研究成果对认识世界上同类矿床的成因有普遍意义。 相似文献
6.
西藏罗布莎不同类型铬铁矿的特征及成因模式讨论 总被引：6，自引：2，他引：4
蛇绿岩地幔橄榄岩中产出的豆荚状铬铁矿是铬的主要来源。已有的研究表明,豆荚状铬铁矿形成于洋中脊或俯冲带的浅部地幔环境。但随着近些年在豆荚状铬铁矿及围岩地幔橄榄岩中不断发现金刚石等深部矿物,人们也开始质疑豆荚状铬铁矿的浅部成因理论。本文系统研究了西藏雅鲁藏布江蛇绿岩带东段的罗布莎豆荚状铬铁矿床,识别出两类铬铁矿,一类以方辉橄榄岩为围岩的致密块状铬铁矿(Cr1#),另一类是以纯橄岩壳为围岩的浸染状铬铁矿(Cr2#)。两类铬铁矿在铬尖晶石的矿物化学成分、PGE和Re-Os同位素特征上存在较大差别,属不同演化过程的结果。地幔橄榄岩的地球化学特征指示罗布莎橄榄岩中存在由低铬且轻稀土亏损和高铬且轻稀土富集的两类方辉橄榄岩。在此基础上,提出豆荚状铬铁矿为多阶段形成的新认识,经历了早期俯冲至地幔过渡带(410~660km)的陆壳和洋壳物质被脱水和肢解,过渡带产生的热和流体促成了地幔的熔融和Cr的释放和汇聚;铬铁矿浆在地幔柱/地幔对流驱动下,运移至过渡带顶部冷凝固结,并有强还原性的流体进入,后者携带了深部形成的金刚石、斯石英等高压矿物,并进入"塑性-半塑性地幔橄榄岩"中;随着物质向上移动,深度降低,早期超高压相矿物发生相变,如斯石英转变成柯石英,高压相的铬铁矿中出溶成柯石英和单斜辉石;在侵位过程和俯冲带环境,含水熔体与方辉橄榄岩反应形成了不含超高压矿物的规模相对较小的浸染状铬铁矿(Cr2#)及纯橄岩壳。 相似文献
7.
豆荚状铬铁矿床的成因——以西藏自治区罗布莎铬铁矿床为例 总被引：7，自引：2，他引：7
本文以西藏自治区罗布莎铬铁矿床为例并结合世界其它地区同类矿床实例,讨论了豆荚型铬铁矿床的成因机制。研究表明,铬铁矿与纯橄岩-斜辉辉橄岩都是由同一原始地幔岩(尖晶石二辉橄榄岩)经不同程度熔融的产物。铬铁矿及纯橄岩是这一过程中高度熔融的最终产物。其熔融的机制是两种辉石(斜方辉石和单斜辉石)不一致熔融转变为橄榄石和铬尖晶石,并伴随着副矿物铬尖晶石及造岩矿物成分的调整和再造,从而导致铬铁矿床与纯橄岩的紧密伴生。该研究成果对认识世界上同类矿床的成因有普遍意义。 相似文献
8.
再论蛇绿岩中豆荚状铬铁矿的成因——质疑岩石/熔体反应成矿说 总被引：9，自引：0，他引：9
着重论述了蛇绿岩地幔橄榄岩中豆荚状铬铁矿的成因,并对现今盛行的岩石/熔体反应成矿说提出了质疑。世界含铬铁矿的地幔橄榄岩均显示上部偏基性、下部偏酸性的垂直熔融分带,与蛇绿岩堆晶岩中上部偏酸性、下部偏基性的岩浆分异垂直层序恰恰相反。豆荚状铬铁矿与熔融剖面上部的纯橄岩或纯橄岩-方辉辉橄岩杂岩带紧密伴生。豆荚状铬铁矿是原始地幔岩高度熔融再造的产物,高铬型铬铁矿与PPG型蛇绿岩伴生,形成于岛弧或弧前盆地环境;高铝型铬铁矿与PTG型蛇绿岩伴生,形成于扩张脊（MOR）或弧后盆地环境。玻安岩（boninite）与高铬型豆荚状铬铁矿无成因关系,铬铁矿（或富铬矿浆）的形成反而为boninite提供了其形成所需的残余地幔;高铝型铬铁矿不是地幔橄榄岩/拉斑玄武质熔体反应形成的,而是富铬矿浆与基性熔体发生再平衡的产物。豆荚状铬铁矿中超高压矿物包体的出现为其地幔深部成因提供了佐证,而boninite形成于浅部较低压的条件;豆荚状铬铁矿中富集强相容元素IPGE（Os、Ir、Ru）合金,boninite富集不相容元素PPGE (Pt、Pd)硫（砷）化物, 而亏损IPGE,显示其形成较晚。因此,boninite与铬铁矿无生因关系,两者均受岛弧（或弧前盆地）环境的制约而在空间上相伴产出。 相似文献
9.
熊庆 《矿物岩石地球化学通报》2021,40(5):前插1-前插3,999-1011
大洋岩石圈形成演化的关键过程是熔体如何从软流圈地幔中抽取、迁移汇集并最终形成洋壳.蛇绿岩可能为揭示上述过程提供关键对象.前人研究发现,熔体在地幔中主要通过网脉状纯橄岩通道发生迁移汇聚,这种地幔通道与壳幔过渡带和洋壳内的岩浆体系共同构成大洋扩张中心的巨型熔体抽取系统.地幔深部来源的熔体在通过纯橄岩通道时,会发生复杂的熔岩相互作用,使得熔体和地幔的组成均发生变化,形成大洋岩石圈壳-幔组成解耦现象.在不同的大洋扩张中心,地幔内熔体迁移方式和过程是多样的,导致大洋岩石圈的结构和组成复杂多变.我国西藏雅江带蛇绿岩形成于多种构造体制(洋中脊、俯冲带等),其地幔内发育较为新鲜的纯橄岩通道样品,如纯橄岩、铬铁矿岩、辉石岩等.这些样品能够为深入研究地幔纯橄岩通道的成因、熔体在通道内的反应迁移过程,以及不同构造体制下大洋岩石圈壳-幔组成解耦与否的原因,提供新的窗口,同时有助于进一步认知大洋扩张中心巨型岩浆-动力系统、壳幔圈层分异和地球物质循环过程. 相似文献
10.
对富铝型豆荚状铬铁矿矿床成因的新认识一一以新疆萨尔托海铬铁矿矿床为例 总被引：2，自引：0，他引：2
萨尔托海铬铁矿矿床产于萨尔托海蛇绿岩块的地幔橄榄岩中,属于富铝型豆荚状铬铁矿床。该矿床与一套橄长岩和辉长岩类岩石紧密伴生,矿体周围常被一薄的绿泥石壳所包裹。本区铬铁矿的形成包括两个阶段:第一阶段是原始地幔岩经高度熔融形成富铬铬铁矿;第二阶段形成富铝铬铁矿。交代作用伴随着新生单斜辉石和斜长石的形成。原始地幔岩的高度熔融以及基性熔体在地幔橄榄岩中的形成和存在是萨尔托海铬铁矿形成的先决条件。 相似文献
11.
E. M. Prasolov S. A. Sergeev B. V. Belyatsky E. S. Bogomolov K. A. Gruzdov I. N. Kapitonov R. Sh. Krymsky V. O. Khalenev 《Geochemistry International》2018,56(1):46-64
This paper reports the first results of a study of 11 isotope systems (3He/4He, 40Ar/36Ar, 34S/32S, 65Cu/63Cu, 62Ni/60Ni, 87Sr/86Sr, 143Nd/144Nd, 206–208Pb/204Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others. 相似文献
12.
奥地利安东帕有限公司 《岩矿测试》2009,28(3):306-306
最新的流行病学研究表明,空气中较高浓度的悬浮细颗粒可能对人类的健康有不利的影响。根据该项研究显示,由于心脏病、慢性呼吸问题和肺功能指标恶化而导致死亡率的升高与细尘粒子有关。这些研究结果已经促使欧盟于1999年4月出台了限制空气中二氧化硫、二氧化氮、氧化氮、铅和颗粒物含量的法案(1999/30/EC),对各项指标包括对可吸入PM10颗粒的浓度提出了新的限制性指标。PM10颗粒是指可以通过预分级器分离采集的气体动力学直径小于10μm的细颗粒。目前研究的兴趣重点逐步偏向PM2.5这些更细微颗粒物,PM2.5这种颗粒物对健康有明显的不利影响。在欧盟指令2008/50/EC中,对PM10和PM2.5都提 相似文献
13.
S. Viswanathan K. Surya Prakash Rao B. Mahabaleswar 《Journal of the Geological Society of India》2013,82(6):621-627
Komatiites are mantle-derived ultramafic volcanic rocks. Komatiites have been discovered in several States of India, notably in Karnataka. Studies on the distribution of trace-elements in the komatiites of India are very few. This paper proposes a simple, accurate, precise, rapid, and non-destructive wavelength-dispersive x-ray fluorescence (WDXRF) spectrometric technique for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in komatiites, and discusses the accuracy, precision, limits of detection, x-ray spectral-line interferences, inter-element effects, speed, advantages, and limitations of the technique. The accuracy of the technique is excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Zr, Nb, Ba, Pb, and Th and very good (within 4%) for Y. The precision is also excellent (within 3%) for Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th. The limits of detection are: 1 ppm for Sc and V; 2 ppm for Cr, Co, and Ni; 3 ppm for Cu, Zn, Rb, and Sr; 4 ppm for Y and Zr; 6 ppm for Nb; 10 ppm for Ba; 13 ppm for Pb; and 14 ppm for Th. The time taken for determining Sc, V, Cr, Co, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, Pb, and Th in a batch of 24 samples of komatiites, for a replication of four analyses per sample, by one operator, using a manual WDXRF spectrometer, is only 60 hours. 相似文献
14.
Most sulfide-rich magmatic Ni-Cu-(PGE) deposits form in dynamic magmatic systems by partial melting S-bearing wall rocks with variable degrees of assimilation of miscible silicate and volatile components, and generation of barren to weakly-mineralized immiscible Fe sulfide xenomelts into which Ni-Cu-Co-PGE partition from the magma. Some exceptionally-thick magmatic Cr deposits may form by partial melting oxide-bearing wall rocks with variable degrees of assimilation of the miscible silicate and volatile components, and generation of barren Fe ± Ti oxide xenocrysts into which Cr-Mg-V ± Ti partition from the magma. The products of these processes are variably preserved as skarns, residues, xenoliths, xenocrysts, xenomelts, and xenovolatiles, which play important to critical roles in ore genesis, transport, localization, and/or modification. Incorporation of barren xenoliths/autoliths may induce small amounts of sulfide/chromite to segregate, but incorporation of sulfide xenomelts or oxide xenocrysts with dynamic upgrading of metal tenors (PGE > Cu > Ni > Co and Cr > V > Ti, respectively) is required to make significant ore deposits. Silicate xenomelts are only rarely preserved, but will be variably depleted in chalcophile and ferrous metals. Less dense felsic xenoliths may aid upward sulfide transport by increasing the effective viscosity and decreasing the bulk density of the magma. Denser mafic or metamorphosed xenoliths may also increase the effective viscosity of the magma, but may aid downward sulfide transport by increasing the bulk density of the magma. Sulfide wets olivine, so olivine xenocrysts may act as filter beds to collect advected finely dispersed sulfide droplets, but other silicates and xenoliths may not be wetted by sulfides. Xenovolatiles may retard settling of – or in some cases float – dense sulfide droplets. Reactions of sulfide melts with felsic country rocks may generate Fe-rich skarns that may allow sulfide melts to fractionate to more extreme Cu-Ni-rich compositions. Xenoliths, xenocrysts, xenomelts, and xenovolatiles are more likely to be preserved in cooler basaltic magmas than in hotter komatiitic magmas, and are more likely to be preserved in less dynamic (less turbulent) systems/domain/phases than in more dynamic (more turbulent) systems/domains/phases. Massive to semi-massive Ni-Cu-PGE and Cr mineralization and xenoliths are often localized within footwall embayments, dilations/jogs in dikes, throats of magma conduits, and the horizontal segments of dike-chonolith and dike-sill complexes, which represent fluid dynamic traps for both ascending and descending sulfides/oxides. If skarns, residues, xenoliths, xenocrysts, xenomelts, and/or xenovolatiles are present, they provide important constraints on ore genesis and they are valuable exploration indicators, but they must be included in elemental and isotopic mass balance calculations. 相似文献
15.
《Applied Geochemistry》2001,16(2):137-159
Five hundred and ninety-eight samples of terrestrial moss (Hylocomium splendens and Pleurozium schreberi) collected from a 188,000 km2 area of the central Barents region (NE Norway, N Finland, NW Russia) were analysed by ICP-AES and ICP-MS. Analytical results for Al, B, Ba, Ca, K, La, Mg, Mn, Na, P, Rb, Si, Sr, Th, U and Y concentrations are reported here. Graphical methods of data analysis, such as geochemical maps, cumulative frequency diagrams, boxplots and scatterplots, are used to interpret the origin of the patterns for these elements. None of the elements reported here are emitted in significant amounts from the smelting industry on the Kola Peninsula. Despite the conventional view that moss chemistry reflects atmospheric element input, the nature of the underlying mineral substrate (regolith or bedrock) is found to have a considerable influence on moss composition for several elements. This influence of the chemistry of the mineral substrate can take place in a variety of ways. (1) It can be completely natural, reflecting the ability of higher plants to take up elements from deep soil horizons and shed them with litterfall onto the surface. (2) It can result from naturally increased soil dust input where vegetation is scarce due to harsh climatic conditions for instance. Alternatively, substrate influence can be enhanced by human activity, such as open-cast mining, creation of ‘technogenic deserts’, or handling, transport and storage of ore and ore products, all of which magnify the natural elemental flux from bedrock to ground vegetation. Seaspray is another natural process affecting moss composition in the area (Mg, Na), and this is most visible in the Norwegian part of the study area. Presence or absence of some plant species, e.g., lichens, seems to influence moss chemistry. This is shown by the low concentrations of B or K in moss on the Finnish and Norwegian side of the (fenced) border with Russia, contrasting with high concentrations on the other side (intensive reindeer husbandry west of the border has selectively depleted the lichen population). 相似文献
16.
Mercury,arsenic, antimony,and selenium contents of sediment from the Kuskokwim River,Bethel, Alaska,USA 总被引：1，自引：0，他引：1
The Kuskokwim River at Bethel, Alaska, drains a major mercury-antimony metallogenic province in its upper reaches and tributaries. Bethel (population 4000) is situated on the Kuskokwim floodplain and also draws its water supply from wells located in river-deposited sediment. A boring through overbank and floodplain sediment has provided material to establish a baseline datum for sediment-hosted heavy metals. Mercury (total), arsenic, antimony, and selenium contents were determined; aluminum was also determined and used as normalizing factor. The contents of the heavy metals were relatively constant with depth and do not reflect any potential enrichment from upstream contaminant sources. 相似文献
17.
18.
《Chemical Geology》2007,236(1-2):13-26
We examined the coprecipitation behavior of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides under two different fluoride forming conditions: at < 70 °C in an ultrasonic bath (denoted as the ultrasonic method) and at 245 °C using a Teflon bomb (denoted as the bomb method). In the ultrasonic method, small amounts of Ti, Mo and Sn coprecipitation were observed with 100% Ca and 100% Mg fluorides. No coprecipitation of Ti, Mo, Sn and Sb in Ca–Al–Mg fluorides occurred when the sample was decomposed by the bomb method except for 100% Ca fluoride. Based on our coprecipitation observations, we have developed a simultaneous determination method for B, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by Q-pole type ICP-MS (ICP-QMS) and sector field type ICP-MS (ICP-SFMS). 9–50 mg of samples with Zr–Mo–Sn–Sb–Hf spikes were decomposed by HF using the bomb method and the ultrasonic method with B spike. The sample was then evaporated and re-dissolved into 0.5 mol l− 1 HF, followed by the removal of fluorides by centrifuging. B, Zr, Mo, Sn, Sb and Hf were measured by ID method. Nb and Ta were measured by the ID-internal standardization method, based on Nb/Mo and Ta/Mo ratios using ICP-QMS, for which pseudo-FI was developed and applied. When 100% recovery yields of Zr and Hf are expected, Nb/Zr and Ta/Hf ratios may also be used. Ti was determined by the ID-internal standardization method, based on the Ti/Nb ratio from ICP-SFMS. Only 0.053 ml sample solution was required for measurement of all 9 elements. Dilution factors of ≤ 340 were aspirated without matrix effects. To demonstrate the applicability of our method, 4 carbonaceous chondrites (Ivuna, Orgueil, Cold Bokkeveld and Allende) as well as GSJ and USGS silicate reference materials of basalts, andesites and peridotites were analyzed. Our analytical results are consistent with previous studies, and the mean reproducibility of each element is 1.0–4.6% for basalts and andesites, and 6.7–11% for peridotites except for TiO2. 相似文献
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20.
S. M. Moosavirad J. Rasouli M. R. Janardhana M. R. Moghadam M. Shankara 《Arabian Journal of Geosciences》2013,6(10):3623-3634
This paper discusses the result of the detailed investigations carried out on the coal characteristics, including coal petrography and its geochemistry of the Pabedana region. A total of 16 samples were collected from four coal seams d2, d4, d5, and d6 of the Pabedana underground mine which is located in the central part of the Central-East Iranian Microcontinent. These samples were reduced to four samples through composite sampling of each seam and were analyzed for their petrographic, mineralogical, and geochemical compositions. Proximate analysis data of the Pabedana coals indicate no major variations in the moisture, ash, volatile matter, and fixed carbon contents in the coals of different seams. Based on sulfur content, the Pabedana coals may be classified as low-sulfur coals. The low-sulfur contents in the Pabedana coal and relatively low proportion of pyritic sulfur suggest a possible fresh water environment during the deposition of the peat of the Pabedana coal. X-ray diffraction and petrographic analyses indicate the presence of pyrite in coal samples. The Pabedana coals have been classified as a high volatile, bituminous coal in accordance with the vitrinite reflectance values (58.75–74.32 %) and other rank parameters (carbon, calorific value, and volatile matter content). The maceral analysis and reflectance study suggest that the coals in all the four seams are of good quality with low maceral matter association. Mineralogical investigations indicate that the inorganic fraction in the Pabedana coal samples is dominated by carbonates; thus, constituting the major inorganic fraction of the coal samples. Illite, kaolinite, muscovite, quartz, feldspar, apatite, and hematite occur as minor or trace phases. The variation in major elements content is relatively narrow between different coal seams. Elements Sc,, Zr, Ga, Ge, La, As, W, Ce, Sb, Nb, Th, Pb, Se, Tl, Bi, Hg, Re, Li, Zn, Mo, and Ba show varying negative correlation with ash yield. These elements possibly have an organic affinity and may be present as primary biological concentrations either with tissues in living condition and/or through sorption and formation of organometallic compounds. 相似文献