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1.
Hydrothermal alteration of a quartz‐K‐feldspar rock is simulated numerically by coupling fluid flow and chemical reactions. Introduction of CO2 gas generates an acidic fluid and produces secondary quartz, muscovite and/or pyrophyllite at constant temperature and pressure of 300°C and 200 MPa. The precipitation and/or dissolution of the secondary minerals is controlled by either mass‐action relations or rate laws. In our simulations the mass of the primary elements are conserved and the mass‐balance equations are solved sequentially using an implicit scheme in a finite‐element code. The pore‐fluid velocity is assumed to be constant. The change of rock volume due to the dissolution or precipitation of the minerals, which is directly related to their molar volume, is taken into account. Feedback into the rock porosity and the reaction rates is included in the model. The model produces zones of pyrophyllite quartz and muscovite due to the dissolution of K‐feldspar. Our model simulates, in a simplified way, the acid‐induced alteration assemblages observed in various guises in many significant mineral deposits. The particular aluminosilicate minerals produced in these experiments are associated with the gold deposits of the Witwatersrand Basin.  相似文献   

2.
In order to evaluate the extent of CO2–water–rock interactions in geological formations for C sequestration, three batch experiments were conducted on alkali feldspars–CO2–brine interactions at 150–200 °C and 300 bars. The elevated temperatures were necessary to accelerate the reactions to facilitate attainable laboratory measurements. Temporal evolution of fluid chemistry was monitored by major element analysis of in situ fluid samples. SEM, TEM and XRD analysis of reaction products showed extensive dissolution features (etch pits, channels, kinks and steps) on feldspars and precipitation of secondary minerals (boehmite, kaolinite, muscovite and paragonite) on feldspar surfaces. Therefore, these experiments have generated both solution chemistry and secondary mineral identity. The experimental results show that partial equilibrium was not attained between secondary minerals and aqueous solutions for the feldspar hydrolysis batch systems. Evidence came from both solution chemistry (supersaturation of the secondary minerals during the entire experimental duration) and metastable co-existence of secondary minerals. The slow precipitation of secondary minerals results in a negative feedback in the dissolution–precipitation loop, reducing the overall feldspar dissolution rates by orders of magnitude. Furthermore, the experimental data indicate the form of rate laws greatly influence the steady state rates under which feldspar dissolution took place. Negligence of both the mitigating effects of secondary mineral precipitation and the sigmoidal shape of rate–ΔGr relationship can overestimate the extent of feldspar dissolution during CO2 storage. Finally, the literature on feldspar dissolution in CO2-charged systems has been reviewed. The data available are insufficient and new experiments are urgently needed to establish a database on feldspar dissolution mechanism, rates and rate laws, as well as secondary mineral information at CO2 storage conditions.  相似文献   

3.
The distribution of trace amounts of Na, Rb and Cs, between muscovite, phlogopite, sanidine and hydrothermal solution have been studied by ion exchange in a temperature range from 400 to 800°C.These distributions have been expressed with a partition ratio Paq?mx = (XK)aq(XK)m (where X is Na, Rb or Cs).In the case of Na and Cs in muscovite, even for the dilute solutions, the ratio Paq?mx is not the equilibrium constant kx of exchange reactions. In other cases, Paq?mx does not depend on the trace alkali ion concentration in silicates (X) and is equal to kx. Variations of Px or kx with T are greater for Na and Cs than for Rb. Generally, kx decreases with increase in T. The function log Px = f(1T) is not linear for Na or Cs, but in the case of Rb, f(1T) is linear and the standard enthalpy and entropy of exchange reactions have been estimated by applying the Arrhenius relation.The distribution relations obtained between silicate and vapour phase permit the determination of distributions of Na, Rb and Cs between two minerals mI and mII, relative to K. These have been expressed with the partition ratio Qx =(XK)mI(XK)mII. Variations of Qx with T are not remarkable, and even for Rb between phlogopite and feldspar are negligible. Nevertheless, one may use the distributions of Rb and Cs between muscovite and feldspar for geothermometry. Experimental results have been applied to some rocks by effecting corrections from the major element composition of the natural minerals. Estimated temperatures are near to 400°C in the granites and pegmatite studied here.  相似文献   

4.
Lattice Preferred Orientation (LPO) of quartz and muscovite are measured in a micaceous quartzite using SEM based Electron Backscatter Diffraction (EBSD) analysis. The measurements were done in a thin section prepared parallel to the K1K3 plane of the anisotropy of magnetic susceptibility (AMS) ellipsoid, which is equivalent to the XZ plane of the strain ellipsoid. Bulk data from the sample reveal that quartz c-axis develop an oblique single girdle LPO pattern indicating a dextral sense of shear. A similar pattern is produced by poles to the basal planes (001) of muscovite, which implies that muscovite controls the LPO of quartz in the rock. Petrofabric analysis of quartz is performed in domains viz. (I) not containing muscovite, (II) between two muscovite grains, and (III) rim of quartz grains around a muscovite grain. Quartz LPO pattern in Domain-III is noted to be similar to the bulk LPO recorded from the whole sample, thus confirming that muscovite was critical in textural evolution of the rock. The study thus establishes that a minor mineral phase in a rock can control the LPO of the major mineral phase, thus playing a significant role in development of bulk texture of the rock. The advantages of domainal petrofabric analysis in evaluation of slip systems in minerals in different parts of a rock, and vorticity quantification are discussed.  相似文献   

5.
Geochemistry of biotites from granitic rocks,Northern Portugal   总被引：2，自引：0，他引：2  
The biotites from a series of rocks ranging in composition from tonalite to granite have been analysed for both major and trace elements.The relations between chemical composition and paragenesis of the biotites are studied. Most biotites co-exist with potassium feldspar and ilmenite. Variations in composition can be correlated with the occurrence of amphibole, primary muscovite and aluminosilicates in the rocks.Variation diagrams of the trace element contents and element ratios of biotite are compared to those of the host rocks. Fractionation of elements can be defined more accurately as the influence of other mineral phases is eliminated.Variations in the proportions of the octahedrally co-ordinated Al, Ti and Fe3+ are correlated with the conditions of crystallization and comparisons made with biotites from other suites of calc-alkali rocks.In the light of the experimental data available, the petrographic observations and the chemical data it is apparent that biotites crystallized from systems in which fO2 was buffered, its values remaining close to that of the buffer FMQ. From the same data, a temperature of 800°C for fO2 = 10?14to 10?15 bars is deduced as prevalent during the crystallization of the tonalites while for the granites, at a temperature of crystallization of 680°C, fO2 = 10?16to 10?18 bars.A calc-alkali trend of fractionation is therefore apparent with decreasing fO2 while fH2O2 remains relatively high.  相似文献   

6.
禹州方山铝土矿是河南省已知铝土矿勘查区中含钾量最高的一个矿区。方山高钾铝土矿赋存于石炭系上统本溪组中,硬质黏土是构成高钾铝土矿的主体,高钾铝土矿层最厚79.47m,最薄1.98m,平均18.78m;主要含铝矿物为一水硬铝石,高钾铝土矿的化学成分与铝土矿基本相同,全矿区w(K2O)的平均值为3.75%,最高10.16%,最低0.04%。矿区很少有云母等含钾矿物的存在,高钾铝土矿中的K2O不完全来源于含钾矿物,也非矿区内仅存交换吸附阳离子能力最低的高岭石所致,况且方山铝土矿周边的寒武系张夏组水泥灰岩中w(K2O)<2%,在方山地段含铝岩系中能形成w(K2O)超过10%的地层实属罕见,方山铝土矿中K2O的来源尚需进一步研究。  相似文献   

7.
几种镁铁矿物平衡共生的成分标志   总被引：3，自引：0，他引：3  
阎月华 《地质科学》1997,32(3):267-274
本文以晋冀内蒙边界地区变质岩中主要镁铁质造岩矿物辉石,闪石为例,阐明镁铁矿物平衡共生的一条普遍规律,即平衡共生的正辉石,钙闪石之间有相同的镁铁比,其分配系数等于或接近于1.引用冀东,吉南,泰山和南极凯西站等地的实例,论证了此规律同时存在于黑云母与钙闪石,黑云母与正辉石之间,也存在于辉长岩和花岗岩等岩浆岩的橄榄石和正辉石,角闪石与黑云母等矿物对之间。这是判断镁铁矿物是否平衡的成分标志。  相似文献   

8.
作为战略性矿产资源之一,高纯石英已广泛应用于集成电路、半导体芯片、太阳能等高新技术产业中,但是能够生产高纯石英的原料矿床极为稀缺,我国尤为紧缺高纯石英原料矿。鄂东南地区是湖北省脉石英矿床的主要分布区。本文针对鄂东南付家山脉石英矿床,通过光学显微镜、扫描电子显微镜观察了脉石英的脉石矿物类型和包裹体特征,采用电感耦合等离子发射光谱法(ICP-OES)对原矿进行了微量元素分析,旨在获得付家山脉石英矿床的杂质元素特征,进而评价矿床用作高纯石英原料的潜力。结果表明,付家山脉石英矿石SiO2含量大于99.95%,杂质元素主要为Al、K、Fe、Ti、Ca等,脉石矿物主要有白云母、钾长石、铁氧化物等,流体包裹体较为发育。杂质元素分析结果表明,付家山脉石英原矿质量达到低端高纯石英标准,经传统工艺提纯后,可能具有生产中高端高纯石英的潜力。  相似文献   

9.
The Parnell Quartz Monzonite in the Pilbara Block of Western Australia is a Proterozoic (1731 ± 14 Ma) pluton characterized by high modal K‐feldspar and a greater abundance of hornblende relative to biotite, as is typical of Phanerozoic monzonitic rocks in eastern Australia. The only geochemical features reflecting its setting in an Archaean terrain are high Na2O, Ni and Cr. The pluton is zoned, with an increase in K‐feldspar, quartz and biotite and a decrease in plagioclase and hornblende from margin to core. Chemically, this zoning is reflected by systematic variation of CaO, K2O, Na2O, Sr and Rb, but ferromagnesian elements have irregular trends, implying preferential extraction of feldspars relative to mafic minerals during differentiation of the magma. The unusual geochemical trends are explained by a model involving ‘in situ’ feldspar fractionation of a K‐rich residual liquid from a mafic crystalline mush.

A parent magma similar to the average rock composition of the pluton is deduced because high ferromagnesian trace element abundances preclude extensive fractionation of mafic minerals. Geochemical and isotopic constraints suggest that the ultimate source was chemically similar to a shoshonitic basaltic andesite, that must have been emplaced beneath the eastern margin of the Pilbara Block in the Early Proterozoic. Subsequent partial melting of this postulated underplated source at ～ 1700 Ma to produce the Parnell Quartz Monzonite was probably associated with tectonism in the Gregory Range Complex.  相似文献   

10.
Marly rock is a sensitive rock group of landslides in the Three Gorges reservoir area, China. It is composed predominantly of carbonate and clay minerals, water–rock interaction (WRI) of which could activate landslides in the reservoir area. To study the mechanism by which WRI affects the mechanical properties of marly rock, samples were collected from two boreholes (depth 301.78 and 307.14 m) and slope surface. Then, laboratory tests were designed to study the quantitative relationship between mineral contents and mechanical properties of intact rock, to analyze both change process of mineral composition and microstructure under short-term and long-term WRI. Finally, the change in mechanical properties and its effect on slope stability are suggested. This study indicates that the uniaxial compressive strength and Poisson ratio can be estimated by linear regression equations: (1) σ c = 8.959 × (C/Q) ? 0.744 × CM + 58.516; (2) μ = 0.014 × (C/Q) ? 0.001 × CM + 0.234. The chemical reactions of WRI mainly included dissolution and ion exchange. On the slope surface, dissolution mainly acts on calcite, illite, dolomite, feldspar and other minerals dissolved in water. Underground, both chemical reactions of dissolution and ion exchange easily approach equilibrium with long-term seepage. Small-size minerals and micropores damage the stable microstructure of marly rock. These changes of minerals and microstructure can trigger shallow slope failure and develop deep creep deformation along some crash zones in the reservoir shoreline.  相似文献   

11.
The high field strength elements (HFSE: Zr, Hf, Nb, Ta, and W) are an important group of chemical tracers that are increasingly used to investigate magmatic differentiation processes. Successful modeling of these processes requires the availability of accurate mineral-melt partition coefficients (D). To date, these have largely been determined by ion microprobe or laser ablation-ICP-MS analyses of the run products of high-pressure, high-temperature experiments. Since HFSE are (highly) incompatible, relatively immobile, high-charge, and difficult to ionize, these experiments and their analysis are challenging. Here we explore whether high-precision analyses of natural mineral-melt systems can provide additional constraints on HFSE partitioning.The HFSE concentrations in natural garnet and amphibole and their alkaline host melt from Kakanui, New Zealand are determined with high precision isotope dilution on a multi-collector-ICP-MS. Major and trace element compositions combined with Lu-Hf isotopic systematics and detailed petrographic sample analysis are used to assess mineral-melt equilibrium and to provide context for the HFSE D measurements. The whole-rock nephelinite, ∼1 mm sized amphiboles in the nephelinite, and garnet megacrysts have similar initial Hf isotope ratios with a mean initial 176Hf/177Hf(34 Ma) = 0.282900 ± 0.000026 (2σ). In contrast, the amphibole megacrysts are isotopically distinct (176Hf/177Hf(34 Ma) = 0.282830 ± 0.000011). Rare earth element D values for garnet megacryst-nephelinite melt and ∼1 mm amphibole-nephelinite melt plotted as a function of ionic radii show classic near-parabolic trends that are in excellent agreement with crystal lattice-strain models. These observations are consistent with equilibrium between the whole-rock nephelinite, the ∼1 mm amphibole grains within the nephelinite and the garnet megacrysts.High-precision isotope dilution results for Zr and Hf in garnet (DZr = 0.220 ± 0.007 and DHf = 0.216 ± 0.005 [2σ]), and for all HFSE in amphibole are consistent with previous experimental findings. However, our measurements for Nb and Ta in garnet (DNb = 0.0007 ± 0.0001 and DTa = 0.0011 ± 0.0006 [2σ]) show that conventional methods may overestimate Nb and Ta concentrations, thereby overestimating both Nb and Ta absolute D values for garnet by up to 3 orders of magnitude and underestimating DNb/DTa by greater than a factor of 100. As a consequence, the role of residual garnet in imposing Nb/Ta fractionation may be less important than previously thought. Moreover, garnet DHf/DW = 17 and DNb/DZr = 0.003 imply fractionation of Hf from W and Nb from Zr upon garnet crystallization, which may have influenced short-lived 182Hf-182W and 92Nb-92Zr isotopic systems in Hadean time.  相似文献   

12.
The trace element compositions of melts and minerals from high-pressure experiments on hydrous pyroxenites containing K-richterite are presented. The experiments used mixtures of a third each of the natural minerals clinopyroxene, phlogopite and K-richterite, some with the addition of 5% of an accessory phase ilmenite, rutile or apatite. Although the major element compositions of melts resemble natural lamproites, the trace element contents of most trace elements from the three-mineral mixture are much lower than in lamproites. Apatite is required in the source to provide high abundances of the rare earth elements, and either rutile and/or ilmenite is required to provide the high field strength elements Ti, Nb, Ta, Zr and Hf. Phlogopite controls the high levels of Rb, Cs and Ba.Since abundances of trace elements in the various starting mixtures vary strongly because of the use of natural minerals, we calculated mineral/melt partition coefficients (DMin/melt) using mineral modes and melting reactions and present trace element patterns for different degrees of partial melting of hydrous pyroxenites. Rb, Cs and Ba are compatible in phlogopite and the partition coefficient ratio phlogopite/K-richterite is high for Ba (1 3 6) and Rb (12). All melts have low contents of most of the first row transition elements, particularly Ni and Cu ((0.1–0.01) × primitive mantle). Nickel has high DMin/melt for all the major minerals (12 for K-richterite, 9.2 for phlogopite and 5.6 for Cpx) and so behaves at least as compatibly as in melting of peridotites. Fluorine/chlorine ratios in melts are high and DMin/melt for fluorine decreases in the order apatite (2.2) > phlogopite (1.5) > K-richterite (0.87). The requirement for apatite and at least one Ti-oxide in the source of natural lamproites holds for mica pyroxenites that lack K-richterite. The results are used to model isotopic ageing in hydrous pyroxenite source rocks: phlogopite controls Sr isotopes, so that lamproites with relatively low 87Sr/86Sr must come from phlogopite-poor source rocks, probably dominated by Cpx and K-richterite. At high pressures (>4 GPa), peritectic Cpx holds back Na, explaining the high K2O/Na2O of lamproites.  相似文献   

13.
Biotite‐muscovite‐garnet gneisses at Einasleigh contain quartz‐feldspar veins composed of the same minerals as found in the enclosing rock. The vein‐gneiss boundaries are commonly irregular and on a microscopic scale, gradational.

Certain amphibolite layers contain quartz‐feldspar veins composed of the same minerals as found in the amphibolite. Hornblende‐rich extraction zones surround these veins, and material balance calculations show that all or nearly all of the vein‐forming matter was locally derived. Variation in the abundance of hornblende and plagioclase in the amphibolite as a function of distance from a quartz‐feldspar vein can be expressed by error‐function curves, thus suggesting that the mineral‐segregation process was diffusion‐controlled. During the mineral rearrangement, the Na and Ca contents of plagioclase have evidently remained unchanged, but the vein hornblende has become slightly richer in Fe+3, Mg, and Ca, and poorer in Si and Al relative to hornblende in the adjacent amphibolite.

A certain biotite‐plagioclase rock forms layers and boudins in the gneisses and contains pegmatite veins composed of the same minerals as found in the host rock. The plagioclase in these veins is more sodic than that in the host rock while the biotite contains slightly more Ti and Fe+2 and less Si and Mg than the biotite of the enclosing rock.

The data indicate that significant portions of the vein‐forming matter at Einasleigh were locally derived. The chemistry of some minerals has changed slightly during the segregation process, resulting possibly from different diffusion rates for the different mineral‐forming constituents.  相似文献   

14.
河北东坪金矿区水泉沟岩体的地球化学特征   总被引：17，自引：0，他引：17       下载免费PDF全文
魏菊英  苏琪 《地质科学》1994,29(3):256-266
水泉沟岩体主要由二长岩构成。主要矿物是碱性长石和斜长石,它们的含量高达80%以上。石英不多见,暗色矿物含量少。副矿物主要是磁铁矿、石榴石、榍石和锆石。交代结构发育,蚀变现象普遍。主要化学组分和微量元素含量及δ18O值变化范围大。该二长岩体是由老片麻岩经热液碱交代作用而成。  相似文献   

15.
Compositions, proportions, and equilibrium temperature of coexisting two-feldspar in crystalline rocks are of great importance to classification in petrography and interpretation of petrogenesis. Crystalline rocks are usually composed of 4-6 minerals (phases), depending on their independent chemical components and the equilibrium temperature of crystallizations. In general, number of mineral phases can be determined by the “Phase Rule”. According to the mass balance principle, bulk composition of coexisting two-feldspar could be evaluated from the bulk chemistry of a rock, provided that the compositions of the coexisting mafic mineral phases containing calcium, sodium, and potassium oxides are determined, e.g., by microprobe analysis. The compositions, proportions, and temperature of two-feldspar in equilibrium can thus be simultaneously resolved numerically from bulk composition of the rock, by incorporating the activity/composition relations of the ternary feldspars with the mass balance constraints. Upon the numerical approximation method presented in this paper, better-quality, internally consistent data on feldspar group could usually be obtained, which would be expected more realistic and accurate in consideration of thermodynamic equilibria in the system of crystalline rocks, as well as bulk chemistry of a rock and the composing minerals.  相似文献   

16.
Manganoan ilmenite was identified in Juina, Brazil kimberlitic rocks among other megacrysts. It forms oval, elongated, rimless grains comprising 8–30 wt.% of the heavy fraction. Internally the grains are homogeneous. The chemical composition of Mn-ilmenite is almost stoichiometric for ilmenite except for an unusually high manganese content, with MnO = 0.63–2.49 wt.% (up to 11 wt.% in inclusions in diamond) and an elevated vanadium admixture (V2O3 = 0.21–0.43 wt.%). By the composition, Mn-ilmenite megacrysts and inclusions in diamond are almost identical. The concentrations of trace elements in Mn-ilmenite, compared to picroilmenite, are much greater and their variations are very wide. Chondrite-normalized distribution of trace elements in Mn-ilmenite megacrysts is similar to the distribution in Mn-ilmenites included in diamond. This confirms that Mn-ilmenite in kimberlites is genetically related to diamond. The finds of Mn-ilmenite known before in kimberlitic and related rocks are late- or postmagmatic, metasomatic phases. They either form reaction rims on grains of picroilmenite or other ore minerals, or compose laths in groundmass. In contrast to those finds, Mn-ilmenite megacrysts in Juina kimberlites are a primary mineral phase with a homogeneous internal structure obtained under stable conditions of growth within lower mantle and/or transition zone. In addition to pyrope garnet, chromian spinel, picroilmenite, chrome-diopside, and magnesian olivine, manganoan ilmenite may be considered as another kimberlite/diamond indicator mineral.  相似文献   

17.
Minerals occurring in dry and modally metasomatized spinel lherzolites from western Victoria have been analysed by proton microprobe for Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Ba, Pb, Br, rare-earth elements (REE), Th and U. Mass-balance calculations demonstrate that these trace elements are contained in specific acceptor minerals and do not occur in significant concentrations at clean grain boundaries. The level of particular trace elements in the rock depends on the presence of specific phases: for example high levels of REE, Sr (and U, Th, Br) require apatite, while Ba, Nb and Ta are strongly concentrated in amphibole±mica. Mantle metasomatism in these spinel lherzolites is inferred to result from an open-system process involving infiltration of fluids released by crystallizing silicate melts. This process produces metasomatic zones with different modal mineralogy and hence greatly different trace-element signatures. The data demonstrate that large-ion-lithophile (LIL) and high-field strength (HFS) elements in metasomatized spinel lherzolites are strongly concentrated in non-refractory phases, which will break down easily in heated volumes such as the walls of magma conduits. The heterogeneity observed in trace-element patterns of intraplate alkali basaltic rocks may not reflect source heterogeneity, but may result largely from contamination by metasomatized mantle wall rock. The KDs for most trace elements show little temperature dependence except for KDSr between orthopyroxene and clinopyroxene where KD decreases with increasing temperature. The generally uniform KDs can be used to test for disequilibrium in such assemblages.  相似文献   

18.
ABSTRACT

Mashhad granitoids and associated mafic microgranular enclaves (MMEs), in NE Iran record late early Mesozoic magmatism, was related to the Palaeo-Tethys closure and Iran-Eurasia collision. These represent ideal rocks to explore magmatic processes associated with Late Triassic closure of the Palaeo-Tethyan ocean and post-collisional magmatism. In this study, new geochronological data, whole-rock geochemistry, and Sr–Nd isotope data are presented for Mashhad granitoids and MMEs. LA–ICP–MS U–Pb dating of zircon yields crystallization ages of 205.0 ± 1.3 Ma for the MMEs, indicating their formation during the Late Triassic. This age is similar to the host granitoids. Our results including the major and trace elements discrimination diagrams, in combination with field and petrographic observations (such as ellipsoidal MMEs with feldspar megacrysts, disequilibrium textures of plagioclase), as well as mineral chemistry, suggest that MMEs formed by mixing of mafic and felsic magmas. The host granodiorite is a felsic, high K calc-alkaline I-type granitoid, with SiO2 = 67.5–69.4 wt%, high K2O (2.4–4.2 wt%), and low Mg# (42.5–50.5). Normalized abundances of LREEs and LILEs are enriched relative to HREEs and HFSEs (e.g. Nb, Ti). Negative values of whole-rock εNd(t) (?3 to ?2.3) from granitoids indicate that the precursor magma was generated by partial melting of enriched lithospheric mantle with some contributions from old lower continental crust. In the MMEs, SiO2 (53.4–58.2 wt%) is lower and Ni (3.9–49.7 ppm), Cr (0.8–93.9 ppm), Mg# (42.81–62.84), and εNd(t) (?2.3 to +1.4) are higher than those in the host granodiorite, suggesting a greater contribution of mantle-derived mafic melts in the genesis of MMEs.  相似文献   

19.
The pegmatite province of the Southeastern Desert (SED) is part of a pegmatite district that extends from Egypt (extends to 1200 km2). Rare metal pegmatites are divided into (1) unzoned, Sn-mineralized; (2) zoned Li, Nb, Ta and Be-bearing; and (3) pegmatites and pegmatites containing colored, gem-quality tourmaline. The Rb/Sr data reflect a crustal origin for the rare metal pegmatites and indicate that the original SED magma was generated during the peak of regional metamorphism and predates the intrusion of post-tectonic leucogranites. These bodies developed an early border zone consisting of coarse to very coarse muscovite quartz alkali feldspar, followed by an intermediate zone of dominant quartz feldspar muscovite rock. Garnet, tourmaline, beryl, galena, pyrite, amblygonite, apatite and monazite are rare accessories in both zones. Cassiterite tends to concentrate in replacement zones and along fractures in albite quartz muscovite-rich portions. The highest concentrations of cassiterite occur in irregular greisenized zones which consist dominantly of micaceous aggregates of green Li-rich muscovite, quartz, albite and coarse-grained cassiterite. The different metasomatic post-solidification alterations include sodic and potassic metasomatism, greisenization and tourmalinization. Geochemically, the pegmatite-generating granites have a metaluminous composition, showing a differentiation trend from coarse-grained, unfractionated plagioclase-rich granite towards highly fractionated fine- to medium-grained, local albite-rich rock. Economically important ore minerals introduced by volatile-rich, rare metal-bearing fluids, either primarily or during the breakdown of the primary mineral assemblages, are niobium-tantalum oxides, Sn-oxides (cassiterite), Li-silicates (petalite, spodumene, euctyptite, and pollucite), Li-phosphates (amblygonite, montebrasite and lithopilite) and minor REE-minerals (Hf-zircon, monazite, xenotime, thorian, loparite and yttrio-fluorite). The pollucite is typically associated with spodumene, petalite, amblygonite, quartz and feldspar. The primary pollucite has Si/Al (at) ratios of 2.53-2.65 and CRK of 79.5- 82.2. Thorian loparite is essentially a member of the loparite (NaLREETi2O6)-lueshite (NaNbO3)-ThTi2O6-ThNb4O12 quaternary system with low or negligible contents of other end-member compositions. The mineral compositionally evolved from niobian loparite to niobian thorian and thorian loparite gave rise to ceriobetafite and belyankinite with high ThO2 contents. Thorian loparite is metamict or partly metamict and upon heating regains a structure close to that of synthetic loparite NaLaTi2O6.  相似文献   

20.
In the process of steam stimulation exploitation of viscous crude oil, the injected water, at high temperature and under high pressure, reacts intensively with the host rock. This kind of water–rock interaction in Liaohe Shuguang Oil Field was studied on the basis of analysis of water composition changes, laboratory experiments, mineral saturation indices analysis, and mass balance calculation. Compared with the injected water, the changes of the composition of discharged water are mainly the distinct decrease of pH, Na+, SiO2 and Cl−, as well as the increase of K+, Ca2+, Mg2+, SO 4 2− and HCO 3 − . Laboratory experiments under field conditions showed: the dissolution sequence of minerals quantitatively is quartz>potassium feldspar>albite, and the main change of clay minerals is the conversion of kaolinite to analcime. Mass balance calculation indicated during the process of steam stimulation, large quantities of analcime are precipitated with the dissolution of large amounts of quartz, kaolinite, potassium feldspar, and CO2. These results correlated very well with the experimental results. The calculated results of Liaohe Shuguang Oil Field showed that during the steam stimulation for viscous crude oil, the amounts of minerals dissolved (precipitated) are huge. To control the clogging of pore spaces of oil reservoirs, increased study of water–rock interaction is needed.  相似文献   

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