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1.
Robert L. Linnen   《Lithos》2005,80(1-4):267-280
The solubilities of columbite, tantalite, wolframite, rutile, zircon and hafnon were determined as a function of the water contents in peralkaline and subaluminous granite melts. All experiments were conducted at 1035 °C and 2 kbar and the water contents of the melts ranged from nominally dry to approximately 6 wt.% H2O. Accessory phase solubilities are not affected by the water content of the peralkaline melt. By contrast, solubilities are affected by the water content of the subaluminous melt, where the solubilities of all the accessory phases examined increase with the water content of the melt, up to 2 wt.% H2O. At higher water contents, solubilities are nearly constant. It can be concluded that water is not an important control of accessory phase solubility, although the water content will affect diffusivities of components in the melt, thus whether or not accessory phases will be present as restite material. The solubility behaviour in the subaluminous and peralkaline melts supports previous spectroscopic studies, which have observed differences in the coordination of high field strength elements in dry vs. wet subaluminous granitic glasses, but not for peralkaline granitic glasses. Lastly, the fact that wolframite solubility increases with increasing water content in the subaluminous melt suggests that tungsten dissolved as a hexavalent species.  相似文献   
2.
A suite of (Mn1-x Fe x )Nb2O6 (x=0, 0.05, 0.25, 0.50, 0.75, 1) columbite samples has been prepared by solid-state reaction from oxides. X-ray diffraction and spectroscopic investigations have been carried out in order to gain different perspectives on how the solid solution adapts at different length scales to cation mixing. X-ray powder diffraction and powder absorption IR spectroscopy data are presented. The powder diffraction data show that there is no significant excess volume of mixing on the Fe–Mn columbite join. All the unit-cell parameters decrease linearly as a function of increasing Fe content. Substitution of Fe2+ for the larger Mn2+ cation causes a decrease in the volume of the A polyhedron, which also becomes more regular with respect to both bond-length and edge-length distortion parameters. No significant variation of the B site has been observed. Wavenumber shifts of the IR peaks nearly all vary linearly with composition, consistent with linear variations of the lattice parameters. Line broadening has been quantified by autocorrelation analysis of the IR spectra. This is interpreted as suggesting that there is some element of local strain or positional disorder at the length scale of second or third nearest neighbours around sites occupied by Fe.  相似文献   
3.
Structural investigations at high temperature were carried out on natural columbite samples across the join Fe(Nb0.95Ta0.05)2O6–Mn(Nb0.95Ta0.05)2O6. The samples were preliminarily annealed to attain the complete cation-ordered state and avoid the superimposition of the effects of cation ordering during high-temperature studies. Unit-cell parameters of three columbites with different XFe content were measured at regular intervals in the temperature range 25–900 °C using single-crystal X-ray diffraction techniques. The crystal structures of completely ordered ferrocolumbite and manganocolumbite were also refined from intensity data collected at room temperature, 300 and 600 °C. Structural thermal expansion coefficients show positive, linear expansion of a, b, c lattice constants and cell volume. In general, slightly higher expansion occurs along a and c directions. However, anisotropy decreases sharply with decreasing Fe content. Reversibility of thermal expansion in the investigated temperature range was checked by high-temperature diffraction studies under heating-up and cooling-down conditions. Impurities do not play an important role in thermal expansion of columbites; expansion coefficients measured on two crystals of the same sample characterized by different Ti content are in fact almost identical. Structural changes with temperature essentially affect bond lengths: volumes of both A and B octahedral sites increase linearly with temperature, whereas interpolyhedral geometrical parameters do not vary significantly.  相似文献   
4.
The Central Eastern Desert (CED) of Egypt, a part of Neoproterozoic Arabian Nubian Shield (ANS), embraces a multiplicity of rare metal bearing granitoids. Gabal El-Ineigi represents one of these granitic plutons and is a good example of the fluorite-bearing rare metal granites in the ANS. It is a composite pluton consisting of a porphyritic syenogranite (SG; normal granite) and coarse- to medium-grained highly evolved alkali-feldspar granite (AFG; fluorite and rare metal bearing granite) intruded into older granodiorite and metagabbro-diorite rocks. The rock-forming minerals are quartz, K-feldspar (Or94-99), plagioclase (An0-6) and biotite (protolithonite-siderophyllite) in both granitic types, with subordinate muscovite (Li-phengite) and fluorite in the AFG. Columbite-(Fe), fergusonite-(Y), rutile, zircon and thorite are the main accessory phases in the AFG while allanite-(Ce) and epidote are exclusively encountered in the SG. Texture and chemistry of minerals, especially fluorite, columbite and fergusonite, support their magmatic origin. Both granitic types are metaluminous to weakly peraluminous (A/CNK = 0.95–1.01) and belong to the post-collisional A2-type granites, indicating melting of underplated mafic lower crust. The late phase AFG has distinctive geochemical features typical of rare metal bearing granites; it is highly fractionated calc-alkaline characterized by high Rb, Nb, Y, U and many other HFSE and HREE contents, and by extremely low Sr and Ba. Moreover, the REE patterns show pronounced negative Eu anomalies (Eu/Eu1 = 0.03 and 0.06) and tetrad effect (TE1,3 = 1.13 and 1.27), implying extensive open system fractionation via fluid–rock interactions that characterize the late magmatic stage differentiation. The SG is remarkably enriched in Sr, Ba and invariably shows a relative enrichment in light rare-earth elements (LREEs). The SG rocks (569 ± 15 Ma) are characterized by relatively low initial 87Sr/86Sr ratios (0.7034–0.7035) that suggest their derivation from the mantle, with little contamination from the older continental crust. By contrast, the AFG has very high 87Rb/86Sr and 87Sr/86Sr ratios that reflect the disturbance of the Rb-Sr isotopic system and may give an indication for the high temperature magma-fluid interaction. The positive εNd(t) values of AFG (+7.40) and SG (+5.17), corresponding to young Nd-TDM2 ages ranging from 707 to 893 Ma, clearly reflect the juvenile crustal nature of Gabal El-Ineigi granitoids and preclude the occurrence of pre-Neoproterozoic continental crust in the ANS. The field relationships, chemical, petrological and isotopic characteristics of El-Ineigi SG and AFG prove that they are genetically not associated to each other and indicate a complex origin involving two compositionally distinct parental magmas that were both modified during magmatic fractionation processes. We argue that the SG was formed by partial melting of a mid-crustal source with subsequent fractional crystallization. In contrast, the AFG was generated by partial melting and fractionation of Nb- and Ta-rich amphibole (or biotite) of the lower crust. The appreciable amounts of fluorine in the magma appears to be responsible for the formation of rare metal element complexes (e.g., Nb, Ta, Sn and REEs), and could account for the rare metal mineralization in the El-Ineigi AFG.  相似文献   
5.
Summary Titanian ferrocolumbite is a rare accessory mineral in the spodumene-bearing pegmatites at Weinebene, Carinthia, Austria. It contains abundant exsolved niobian rutile and scarce inclusions of cassiterite that may be primary. The titanian ferrocolumbite is relatively homogeneous with Mn/(Mn + Fe) 0.24–0.33, Ta/(Ta + Nb) 0.09–0.13 (atomic ratios) and 0.47–0.88 Ti per 12 cations (2.7–5.0 wt.% TiO2). Natural specimens are considerably disordered but become more ordered on heating. Niobian rutile has Mn/(Mn + Fe) 0.00–0.04 and Ta/(Ta + Nb) 0.26–0.38; it concentrates Fe, Ta, Ti and Sn relative to the Mn- and Nb-enriched ferrocolumbite. The overall scarcity of Nb, Ta-oxide minerals in the spodumene-bearing pegmatites of southern Ostalpen conforms to their general features ranking them with the albite-spodumene type of rare-element pegmatites.With 4 Figures  相似文献   
6.
黄沙坪多金属矿床是湖南最大的铅锌生产基地,并且在与矿床内花岗斑岩接触的矽卡岩带产有隐伏的大型矽卡岩型白钨矿和中型规模的辉钼矿。钨-钼矿化的时代为晚侏罗世,与矿床内花岗斑岩侵入时代一致。然而,已有研究认为,由于该花岗斑岩规模很小,矽卡岩型白钨矿的成矿热液应来自深部岩浆房而非此花岗斑岩。为此,我们对花岗斑岩进行了仔细的镜下观测,并且对其中的副矿物和黑云母以及矽卡岩中的白钨矿进行了电子探针成分分析,应用原位LA-ICP-MS方法测定了矽卡岩中白钨矿的稀土元素含量,试图对白钨矿矿化的物质和流体来源提供确切的证据。通过研究,首次在矿床内花岗斑岩中发现了与未蚀变黑云母伴生的黑钨矿和铌铁矿,表明花岗斑岩至少在岩浆结晶作用晚期或岩浆-热液过渡阶段早期就已发生钨的矿物富集,为确定花岗斑岩是控制钨矿化的成矿岩体提供了依据。此外,发现花岗斑岩中的黑云母(属铁叶云母)含有极高的氟含量(3%),指示其应形成于富含氟的高分异岩浆。研究进一步揭示,矽卡岩中白钨矿的轻稀土元素配分模式与花岗斑岩十分一致,而重稀土元素则显著亏损,而且Eu的含量较花岗斑岩更为富集。这暗示形成白钨矿的成矿流体应直接来自花岗斑岩,即:在早期无水矽卡岩阶段,石榴子石的沉淀导致流体中的重稀土亏损而Eu相对富集;白钨矿随后再从这种流体中沉淀。此外,白钨矿的Eu含量与Sm、Gd含量具有负相关关系,表明Eu的分配是相对独立的行为,主要以Eu2+存在,从而指示沉淀白钨矿的流体具有还原的性质。结合前人的研究成果及本文所提供的新证据,我们认为,形成矽卡岩型白钨矿的钨和成矿热液应来自高分异且富F的花岗斑岩,而所需的钙则可能来自于碳酸盐围岩,即矿床内花岗斑岩应是形成钨钼矿床的物质来源,驱动热液活动的能量来源,和寻找隐伏钨矿床的重要找矿标志。  相似文献   
7.
A.M.R. Neiva   《Ore Geology Reviews》2008,33(3-4):221-238
Cassiterite and wolframite compositions from Sn > W- and W > Sn-bearing quartz veins in Northern and Central Portugal are compared to provide evidence on fluid compositions. In Sn > W-bearing quartz veins, euhedral cassiterite shows sequences of alternating parallel darker and lighter zones. The darker zones are pleochroic, oscillatory zoned, exhibit exsolutions of columbite and ixiolite and are richer in Nb, Ta and Fe than the lighter zones which consist of nearly pure SnO2. Cassiterite from W > Sn-bearing quartz veins is usually zoned, with homogeneous and slightly pleochroic darker zones, which are chemically similar to lighter zones. Both zones have inclusions of rutile and rare ilmenite. The darker zones of cassiterite from the former veins are richer in Nb, Ta and Fe contents and poorer in Ti than the darker and lighter zones of cassiterite from the latter veins. This is attributed to differences in the composition of magmatic hydrothermal fluids.Wolframite compositions from Sn > W- and W > Sn-bearing quartz veins do not show any significant distinction, because they precipitate from relatively similar magmatic hydrothermal fluids. In some deposits, most wolframite crystals are homogeneous, but others are heterogeneous. Inner patches, rich in a hübnerite component, rarely occur in crystals from the Filharoso and Panasqueira deposits. Zoned crystals, showing an increase in Fe and a decrease in Mn from core to rim, were found in the Vale das Gatas deposit. Complex oscillatory zoned crystals occur. In the Carris deposit, later wolframite contains inclusions of scheelite, partially replaces it and is richer in Fe and poorer in Mn than earlier wolframite. Wolframite from Sn > W-bearing quartz veins in the Argozelo deposit and W > Sn-bearing quartz veins from Vale das Gatas and Panasqueira deposits has significant Nb content. This does not depend on the Fe and Mn content of the wolframite, but W content is negatively correlated with Nb content. Only very rare single crystals of wolframite show an increase in W and a decrease in Nb from core to rim. Sn > W-bearing quartz veins contain wolframite poorer in Nb than the darker zones of cassiterite, which exsolved columbite and ixiolite. In W > Sn-bearing quartz veins from Panasqueira and Vale das Gatas, the wolframite has a higher Nb content than the cassiterite, which contains rutile inclusions enriched in Nb, because cassiterite and wolframite are derived from two distinct magmatic hydrothermal fluids of different age. The fluid responsible for wolframite precipitation will have a similar composition to that resulting from the evolution of the fluid responsible for cassiterite precipitation in the Sn > W-bearing quartz veins.  相似文献   
8.
袁晓军  王传礼 《江苏地质》2000,24(4):232-235
从矿床地质特征、矿石的物质组分及其赋存状态、矿石的可选性、开采条件、开采方案、矿山建设与环境保护、开发前景与经济效益等方面,对苏州超大型钽铌矿的开发可能性问题,进行了系统和概要的论述。认为,该矿的潜在价值极大,对基开发必须带来良好的社会效益和经济效益。  相似文献   
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