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1.
At the Matauri Bay halloysite deposit, economically valuable halloysite-rich clays are hosted by a sanidine rhyolite dome (Ar–Ar dated at 10.1?±?0.03?Ma). The rhyolite dome intrudes an older basalt and is overlain by alluvial sediments and a younger basalt (4.0?±?0.7?Ma). A blanket-like, halloysite-rich zone is restricted to depths of 10–30?m from the present day erosion surface. Primary sanidine and plagioclase phenocrysts in rhyolite are completely leached out in the halloysite-rich zone but are only partially leached out at greater depth. Halloysite was formed by hydrolysis and cation leaching of sanidine and plagioclase phenocrysts and groundmass glass in the rhyolite, resulting in loss of K, Ca, Na and Si and enrichment in OH (LOI 6–10%) and Al2O3 (20–30%) relative to least-altered rhyolite with 1.8% LOI and 14.5% Al2O3. Oxygen and hydrogen isotope data indicate the halloysite is supergene rather than hydrothermal in origin, which is consistent with the absence of pyrite, alunite and other acid-sulphate type hydrothermal minerals, and with the blanket-like alteration profile. The dominance of halloysite over kaolinite was favoured by water-saturated weathering conditions during the late Miocene-Pliocene subtropical weathering regime in Northland.  相似文献   

2.
This work discusses the composition, radioactivity, and possible utilization of the kaolin resources in Sinai which are hosted in thick sandstone sequences belonging to the Carboniferous (Wadi Khaboba) and Early Cretaceous (Wadi Iseila and Abansakar) ages. The characterization of kaolin was done by microscopic and SEM examination, supported by XRD and ICP-MS analyses. The studied kaolin resources consist of kaolinite, as the main constituent, associated with subsidiary dickite and halloysite, and minor contribution of smectite and illite. The most dominant non-clay mineral is quartz, besides minor gypsum, dolomite, and hematite. Ferrugination dominates, in most cases, at the upper boundaries of the kaolin lenses, suggesting possible supergene activity. The high Al2O3/SiO2 ratio for the Cretaceous kaolin (0.54, in average) specifies its better grade relative to the Carboniferous kaolin (0.43, in average). The kaolin of the middle part of lens C in Wadi Iseila contains Si/Al molecular ratio of about unity, suggesting high-grade kaolin. The Carboniferous kaolin has enriched the radionuclides: U, Th, and Ra (at disequilibrium state due to leaching of eU relative to Ra) and the REE, relative to that of the Cretaceous age. The Carboniferous kaolin is characterized by a higher contribution of HREE (zircon signature), whereas LREE seems to be more influential for the Early Cretaceous kaolin (monazite signature). In spite of the very high CIA index (93 to 99), none of the analyzed kaolin deposits displays Ce abnormality. The high radioactivity of some Carboniferous kaolin can be a serious impediment for its utilization or its exportation. The kaolin of Sinai does not satisfy the international standards for paperwork industries and refractory manufacturing, but beneficiation may overcome this challenge. However, some lenses have high-grade kaolin with a low percentage of oxides of iron, magnesium, calcium, sodium, and potassium and a low radioactivity, hence nominated for the local refractory industry. The high-grade kaolin of Sinai fulfills the standards required for ceramics manufacturing in the global market. Grade 3 kaolin (< 30%, Al2O3) can be used in the manufacturing of white Portland cement and red glaze manufacturing on both local and global markets.  相似文献   

3.
Abstract: The Milyang pyrophyllite deposit, which is embedded in the Late Cretaceous Yuchon Group of the Kyongsang Supergroup, is one of the largest hydrothermal clay deposits in the Kyongsang basin, southeast Korea. Host rocks of the deposit are porphyritic andesite lava and minor andesitic lapilli tuff. In the Milyang district, a hydrothermally altered zone is about 2 × 3 km in extent; we can recognize the concentric arrangement of advanced argillic, propylitic, and sericitic alteration zones from the central to peripheral parts of the zone. The Milyang pyrophyllite deposit forms a part of the advanced argillic alteration zone. The Milyang pyrophyllite deposit is subdivided into the following four zones based on mineral assemblages: the pyrophyllite zones 1, 2, 3, and the silicified zone. The pyrophyllite zone 1, which occupies the central part of the deposit, comprises mainly pyrophyllite, kaolinite, and diaspore without quartz. Diaspore nodules often concentrate in beds 40–50 cm thick. Andalusite, dumortierite, and tourmaline locally occur as network veins, crack‐filler, or small spherulitic spots. The Al2O3 content of the ore ranges from 27 to 36 wt%. The pyrophyllite zone 2, which constitutes a major part of the deposit, comprises mainly pyrophyllite, kaolinite, and quartz. The Al2O3 content of the ore ranges from 15 to 24 wt%. The pyro‐phyllite zone 3 is the hematite‐rich marginal facies of the deposit. The silicified zone, which occurs as beds and septa, is mostly composed of quartz with minor pyrophyllite and kaolinite; the SiO2 contents range from 79 to 90 wt%. Comparing chemical compositions of the high‐Al ores with those of unaltered host andesite, the Fe, Ca, alkalis, HFSE, and HREE contents are significantly depleted, whereas S, B, As, Sr, and LREE are enriched. The hydrothermal alteration of the Milyang pyrophyllite deposit can be classified into the following four stages: 1) extensive sericitic and propylitic alteration, 2) medium‐temperature (200–250°C) advanced argillic alteration, 3) high‐temperature (250–350°C or more) advanced argillic alteration, and 4) retrograde low‐temperature alteration. The heat and some volatile components such as B and S would be derived from the Pulguksa Granite intruded underneath the deposit.  相似文献   

4.
The Gold Bar district contains five Carlin-type gold deposits and four resources for a combined gold endowment of 1.6 M oz [50 t]. The gold deposits are hosted in Devonian carbonate rocks below parautochthonous and allochthonous Paleozoic siliciclastic rocks emplaced during the Early Mississippian Antler orogeny. The district is in the Battle Mountain-Eureka trend, a long-lived structural feature that localized intrusions and ore deposits of different types and ages.The whole-rock geochemistry of four different mineralized and unmineralized Devonian carbonate rock units (two favorable and two unfavorable) were determined and interpreted in the context of the regional geology. A combination of basic statistics, R-mode factor analysis, isocon plots, and alteration diagrams were utilized to (1) identify favorable geochemical attributes of the host rocks, (2) characterize alteration and associated element enrichments and depletions, and (3) identify the mechanism of gold precipitation. This approach also led to the recognition of other types of alteration and mineralization in host rocks previously thought to be solely affected by Carlin-type mineralization.Unit 2 of the Upper Member of the Denay Formation, with the highest Al2O3, Fe2O3 and SiO2 contents and the lowest CaO content, is the most favorable host rock. Based on the high regression coefficients of data arrays on XY plots that project toward the origin, Al2O3 and TiO2 were immobile and K2O and Fe2O3 were relatively immobile during alteration and mineralization. Specific element associations identified by factor analysis are also prominent on isocon diagrams that compare the composition of fresh and altered equivalents of the same rock units. The most prominent associations are: Au, As, Sb, SiO2, Tl, –CaO and –LOI, the main gold mineralizing event and related silicification and decalcification; Cd, Zn, Ag, P, Ni and Tl, an early base metal event; and MgO, early dolomitization. Alteration diagrams, consisting of XY plots of SiO2/Al2O3, K2O/Al2O3, CO2/Al2O3, [S/Al2O3]/[Fe2O3/Al2O3], provide evidence for progressive silicification, decarbonation (decalcification and dedolomitization), argillization (illite), and sulfidation as a function of gold mineralization. The latter process is identified as the principal mechanism of gold precipitation.The lithogeochemistry of the ores in the Gold Bar district is typical of that documented in classic Carlin-type gold deposits in the region, but the size of the deposits and the intensity of alteration and mineralization are less. The presence of other types of mineralization in the Gold Bar district is also common to most of the other Carlin-type districts located in major mineral belts. The approach used in this study is well suited to the interpretation of multi-element geochemical data from other study areas with superimposed alteration and mineralization.  相似文献   

5.
金洋、蒙西和雪纳高岭土化学成分以SiO2和Al2O3为主,K、Na、Ca、Mg含量低,而Fe、Ti含量较高;矿物成分以高岭石为主,还含有少量一水软铝石、石英、蒙脱石等。XRD和IR分析结果表明,金洋和蒙西高岭石的有序度较高,HI结晶指数分别为1.19和1.23,而雪纳高岭石的衍射峰峰形弥散,对称程度差,HI结晶指数仅有0.56。二甲基亚砜和甲酰胺与煤系高岭土相互作用后均能进入高岭石层间并撑大其晶面间距,其中金洋高岭土的插层率最高,雪纳次之,蒙西高岭土的插层效果最差。  相似文献   

6.
安徽庐枞盆地酸性蚀变岩帽地质地球化学特征研究   总被引:5,自引:4,他引:1  
酸性蚀变岩帽是浅成低温热液系统演化的产物,形成于酸性高氧化性流体的化学条件下;在高硫化型浅成低温热液金矿床中广泛发育,是该类矿床的显著识别特征。通过对酸性蚀变岩帽的野外地质特征、矿物共生组合和地球化学特征研究,能较好阐明浅成低温成矿热液系统的特征、性质、发生和发展演化及成矿作用过程。庐枞矿集区是长江中下游成矿带重要的矿集区之一,盆地内广泛发育以明矾石为特征蚀变矿物的酸性蚀变岩帽,面积超过30km~2,指示盆地内高硫化浅成低温热液系统的存在。目前为止,前期工作主要针对明矾石矿床地质特征和明矾石资源储量进行,该酸性蚀变岩帽的地质地球化学特征研究尚未开展。本次工作通过对酸性蚀变岩帽系统的野外采样、全岩地球化学分析和短波红外光谱测试分析技术(PNIRS测试)分析,确定其主要赋存在砖桥组火山岩中,组成矿物为石英、明矾石、高岭石、地开石,此外有少量绢云母、伊利石、珍珠陶土、叶蜡石、褐铁矿,极少数的叶腊石和黄钾铁矾等,在钻孔深部存在浸染状和半自形粒状黄铁矿。由于受到地表风化剥蚀和不同热热中心的影响,水平方向从矾山明矾石矿床向外围发育石英+明矾石带、石英+高岭石/地开石+明矾石带、石英+高岭石/地开石带、硅化带以及最外围的泥质带即高岭石±绢云母±伊利石带。根据酸性蚀变岩帽的矿物组合和主量元素特征,可将其分为三类:硅质蚀变岩、明矾石蚀变岩和粘土蚀变岩。硅质蚀变岩中SiO_2含量发生明显的富集作用,其余主量元素(K_2O、Na_2O、Al_2O_3、Fe_2O_3、P_2O5)含量显著降低;明矾石蚀变岩和粘土蚀变岩具有相似的地球化学特征,SiO_2、Al_2O_3、Fe_2O_3、P_2O_5元素含量范围变大,K_2O和Na_2O含量降低,且Na_2O降低更加明显;而钛为不活泼元素,在岩石发生蚀变过程中TiO_2含量变化很小。矾山地区的酸性蚀变岩帽的产状、蚀变类型、地球化学特征受构造和地层的双重控制。  相似文献   

7.
《Applied Geochemistry》2002,17(7):885-902
An ancient saprolite has developed on the Palaeoproterozoic granulite, granite gneiss and amphibolite bedrock of the Vuotso–Tankavaara area of central Finnish Lapland. The present day climatic regime in Finnish Lapland lies within the northern boreal zone and so the saprolite there can be regarded as fossil. Cores of saprolite were collected from 4 sections (42 samples) and analyzed chemically and mineralogically. In the study area, progressive weathering of the rocks has been marked by gradual enrichment in Al, Fe and Ti; and depletion of Na, K and Ca. The higher concentration of Fe(III) and water and reduced Na and Ca in weathered bedrock in the 4 sections are indicative of oxidation, hydration and leaching processes involved during weathering. The primary minerals in the saprolite are plagioclase feldspar, K-feldspar, quartz, garnet (almandine) and hornblende; the common secondary minerals are kaolinite, halloysite, and vermiculite in addition to minor amounts of sericite. Intense weathering is indicated by: (1) the presence of kaolinite and halloysite in 4 sections of different bedrock types, and (2) the comparatively lower SiO2/Al2O3 (wt.%) ratio (2.30) of weathered granulites (3 sections) as compared to fresh granulite (4.33) and that of weathered amphibolite (2.68) as compared to fresh amphibolite (3.56). In general, kaolinite and halloysite have formed through the weathering of feldspars, garnet, and biotite. Vermiculite is the most probable alteration product of biotite. The formation of kaolinite and halloysite in Finnish Lapland indicates wetter and warmer climatic conditions during the time of their formation than at present. The possible time for formation of the saprolite is early Cretaceous–early Tertiary into Middle Miocene.  相似文献   

8.
Kaolin deposits of the Swat District in Pakistan are indicated to have derived by hydrothermal alteration of more feldspathic parts of felsic intrusives, which occur enclosed in orthoamphibolites and orthogneisses of the Cretaceous Kohistan Island Arc terrane. These latter “country rocks” formed under epidote–amphibolite conditions that prograde northwards to amphibolite facies, and locally manifest slight metamorphic differentiation. The felsic intrusives exhibit a general decrease in siliceous character from west to east, but are less siliceous than most hosts of world kaolins. They are composed of chemically allied quartz diorite, tonalite, trondhjemite and pegmatoids, which evolved mainly by an orthomagmatic crystal fractionation. These parental rocks are calc-alkaline in nature, and kaolinization has proceeded in Ca-richer environment. This is in variance with the occurrence of most known kaolin deposits over potassic granites or rhyolites. Ca-metasomatism of the “host rocks” is in evidence. Kaolin formation by a supergene process is not displayed.The raw kaolin with contained unaltered plagioclase is characterized by a rather low silica (46.54–50.93%) and potash (<1%), and high alumina (23.54–26.77%), Fe2O3 (1.73–5.45%) and lime (8.13–16.93%) content. Kaolinization proceeded with a decrease in SiO2 and concomitant increase in Al2O3. The same trend is followed with fineness of grain size of washed fractions, in resemblance to other known kaolin deposits of primary as well as secondary origin.  相似文献   

9.
Bauxite deposits are widespread in NW Sardinia. They formed during the middle Cretaceous, in consequence of a period of emergence of the Mesozoic carbonate shelf. In the Nurra area the geometries derived by the Middle Cretaceous tectonic phases controlled the ore typologies. Two bauxite profiles, laying on different bedrocks, were sampled. The bauxitization proceeded from the surface downward, with the accumulation of Al2O3 and residual ‘immobile’ elements (Al, Ti, HFSE), and corresponding mobility and loss of SiO2 and Fe2O3. Epigenetic kaolinite formed close to faults and joints, probably as a result of silicification, introduced by low temperature hydrothermal solutions. Rare earth elements, especially LREE, are concentrated in Fe-rich bauxite horizons, probably due to scavenging by goethite. REE-enrichment is not observed in the boehmite-rich horizons. Very high REE contents are observed in a Fe-depleted horizon due to the occurrence of REE accessory minerals, probably of the bastnäsite group. Conservative indices, including TiO2/Al2O3 and Ti/Cr ratios, and Eu anomalies (Eu/Eu*), suggest that the deposits formed by weathering of sediments derived from mafic rocks of the Hercynian basement. This, in turn, implies that the basement was exposed during middle Cretaceous.  相似文献   

10.
Bauxite deposits of Mainpat Plateau Surguja District, India, are composed of kaolinite, gibbsite, goethite, anatase, and bohemite. Quartz and micas are absent in the samples. The presence of boehmite and goethite are evidences of intense weathering during the formation of the bauxite deposits. The Mainpat Plateau is a mesa landform, at an elevation of around 1,060 m from msl in comparison to the general elevation of 580, consisting of Archaeans (granite?gneisses, phyllite, etc.) at the base, Gondwanas and Deccan basalt, and at the top having a cover of laterite and bauxite. The extremely high values of the chemical index of alteration, and the low values of the alkali metals and alkali earth metals, support an intense weathering origin for the bauxite deposit. There is evidence of deposition in the deposits based on the presence of pisoids in the bauxite samples and the composition of the parent rock. Kaolin minerals were first produced by the hydrolytic weathering of aluminous sediments and then gibbsite was formed as early kaolin was desilicated. The bauxite is having high TiO2 up to 17 %. The Mainpat laterite/bauxite deposits are characterized by having 50?58 % average Al2O3 and 10?30 % Fe2O3.  相似文献   

11.
A red soil profile in Xuancheng, Anhui province, southern China, in the middle to lower reaches of the Yangtze River, was investigated using X‐ray diffraction, X‐ray fluorescence spectrometer, and scanning electron microscopy. The mobile components K2O and Na2O and trace elements Ba and Sr of the Xuancheng section exhibit a general trend of decrease downward along the red soil profile, together with an increase downward of chemical index of alteration (CIA) values, suggesting more intense depletion in the lower portion than in the upper portion. The major components SiO2, Al2O3 and Fe2O3, as well as SiO2/Al2O3, SiO2/Fe2O3 and Al2O3/Fe2O3 ratios, show notable fluctuations along the soil profile, indicating intense climatic oscillations in the area during the Pleistocene age. The clay mineral assemblage of the Xuancheng section can be generally subdivided into three groups, suggesting a general trend of three stages of climate changes. The lower portion of ~10.4–6.3 m depth has a lower illite content and higher abundance of kaolinite and illite–smectite (I/S) clays, indicating that a warm and wet climate prevailed over the episode of ca. 600–350 ka BP. A decrease in abundance of kaolinite and I/S clays and increase in illite content at a depth of ~6.3–2.2 m probably indicate a transition stage of climate change from warm/humid to cool/dry in the period ca. 350–80 ka BP. The higher illite content and lower abundance of kaolinite and I/S clays in the upper portion of ~2.2–0 m depth suggest that a relatively cool and dry climate dominated since ca. 80 ka BP. Based on changes in clay mineralogy and chemical indices of the sediments, seven warm/cold fluctuations were determined in the area since the Middle Pleistocene. Climate changes documented in the Xuancheng section are in agreement with the δ18O records of sediments from the equatorial Pacific Core V28‐238 and the loess–palaeosol sequences in the Loess Plateau of northwestern China. Correlated to the episode of S4 and S5 soil units in the Loess Plateau, the period of ca. 600–350 ka BP in the Xuancheng area was dominated by the particularly strong East Asia summer monsoon, as indicated by its most abundant kaolinite and I/S clays. Fluctuations in clay mineralogy along the Xuancheng soil profile were mainly controlled by both the East Asia summer and winter monsoons in response to the global changes in the Middle–Late Pleistocene. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

12.
Aluminum-containing hexagonally ordered mesoporous silica (Al-MCM-41) with specific surface area of 509.4 m2/g was first synthesized using natural halloysite as source material by hydrothermal treatment, without addition of silica or aluminum regents. The samples were characterized by X-ray diffraction, transmission electron microscopy, N2 adsorption–desorption measurements, and Fourier transform infrared spectra techniques. The results indicate that process parameters, including calcination temperature, pH value, n(SiO2)/n(CTAB)/n(H2O) ratio, and hydrothermal reaction time, show moderate effects on the preparation of Al-MCM-41. SiO2/Al2O3 molar ratio could be effectively modulated by the calcination temperature for halloysite. Furthermore, we first clarified the structural evolution from natural halloysite to mesoporous material Al-MCM-41 at the atomic level.  相似文献   

13.
Hydrothermal ore deposits are typically characterised by footprints of zoned mineral assemblages that extend far beyond the size of the orebody. Understanding the mineral assemblages and spatial extent of these hydrothermal footprints is crucial for successful exploration, but is commonly hindered by the impact of regolith processes on the Earth's surface. Hyperspectral drill core (HyLogger?-3) data were used to characterise alteration mineralogy at the Mt Olympus gold deposit located 35 km southeast of Paraburdoo along the Nanjilgardy Fault within the northern margin of the Ashburton Basin in Western Australia. Mineralogy interpreted from hyperspectral data over the visible to shortwave (400–2500 nm) and thermal (6000–14500 nm) infrared wavelength ranges was validated with X-ray diffraction and geochemical analyses. Spaceborne multispectral (ASTER) and airborne geophysical (airborne electromagnetic, AEM) data were evaluated for mapping mineral footprints at the surface and sub-surface. At the deposit scale, mineral alteration patterns were identified by comparing the most abundant mineral groups detected in the HyLogger data against lithology logging and gold assays. Potential hydrothermal alteration phases included Na/K-alunite, kaolin phases (kaolinite, dickite), pyrophyllite, white mica, chlorite and quartz, representing low-T alteration of earlier greenschist metamorphosed sediments. The respective zoned mineral footprints varied depending on the type of sedimentary host rock. Siltstones were mainly characterised by widespread white-mica alteration with proximal kaolinite alteration or quartz veining. Sandstones showed (1) distal white mica, intermediate dickite, and proximal alunite + kaolinite or (2) widespread white-mica alteration with associated intervals of kaolinite. In both, sandstones and siltstones, chlorite was distal to gold mineralisation. Conglomerates showed distal kaolinite/dickite and proximal white-mica/dickite alteration. Three-dimensional visualisation of the gold distribution and spatially associated alteration patterns around Mt Olympus revealed three distinct categories: (1) several irregular, poddy, SE-plunging zones of >0.5 ppm gold intersected by the Zoe Fault; (2) sulfate alteration proximal to mineralisation, particularly on the northern side of the Mt Olympus open pit; and (3) varying AlIVAlVISiIV–1(Mg,Fe)VI–1 composition of white micas with proximity to gold mineralisation. Chlorite that developed during regional metamorphic or later hydrothermal alteration occurs distal to gold mineralisation. ASTER mineral mapping products, such as the MgOH Group Content used to map chlorite (±white mica) assemblages, showed evidence of correlation to mapped, local structural features and unknown structural or lithological contacts as indicated by inversion modelling of AEM data.  相似文献   

14.
Rare metals in coal deposits have attracted much attention in recent years because of their potential economic significance. This paper reports the abundance and enrichment origin of rare metals in the Late Permian coals (K1 and K2 Coals) of the Moxinpo Coalfield, Chongqing, southwestern China. The K1 Coal is characterized by highly-elevated concentrations of U-Re-V-Cr-Se and Nb(Ta)-Zr(Hf)-REE assemblages; the latter assemblage is also enriched in the K2 Coal. The high temperature ash (815 °C) of the K1 Coal is enriched in V, Cr, Se, Re, U and REE; the ash of the K2 Coal, and also the floor strata of each seam, are enriched in REE, potentially making all of the units economically viable sources for these elements.The minerals in the K1 Coal are mainly represented by kaolinite, illite and mixed-layer illite/smectite, and pyrite, while the minerals in the K2 Coal consist mainly of kaolinite and tobelite [(NH4,K)Al2(AlSi3O10)(OH)2]. Authigenic roscoelite [K(V3 +,Al)2(AlSi3O10)(OH)2] is commonly observed in the K1 Coal under the SEM, and was probably formed by interaction of kaolinite with V derived from permeating U-Re-V-Cr-Se-rich solutions during early diagenesis. The tobelite enriched in the K2 Coal was formed by reaction between kaolinite already present in the coal and NH4 + derived from decomposition of the organic matter during hydrothermal alteration at a relatively high temperature.The mafic tuffs directly underlying the K1 Coal and containing limestone residual breccias not only served as the substrate for coal accumulation but also as the source of sediment from the uplifted areas around the coal basin. The latter is indicated by low Al2O3/TiO2 ratios (from 10.09 to 14.24), positive Eu anomalies enrichment of medium rare earths (relative to upper continental crust), and detrital calcite of terrigenous origin. The highly-elevated concentrations of U-Re-V-Cr-Se assemblages in the coal were derived from exfiltrational hydrothermal solutions and were then deposited in a euxinic environment. The terrigenous materials in the K2 Coal, however, were derived from felsic-intermediate rocks at the top of the Kangdian Upland, although the elevated concentrations of Nb(Ta)-Zr(Hf)-REE assemblages are attributed to the input of hydrothermal solutions.  相似文献   

15.
浙江高岭土矿床中氢氧同位素的研究   总被引:2,自引:0,他引:2       下载免费PDF全文
浙江省是我国高岭土矿的产地之一,矿床主要集中于浙南火山岩地区。浙南地区广泛分布中生代的中酸性火山碎屑岩、熔岩及浅成侵入岩,构造断裂发育,气候温暖湿润,具有风化或热液作用形成高岭土矿床的有利地质条件。  相似文献   

16.
苏州高岭土矿主要由高岭石、7埃洛石、10埃洛石及少量绢云母、蒙脱石、明矾石、三水铝石组成。高岭土矿物形成后因外界地化条件改变发生了以下转变:(1)埃洛石脱水向高岭石转化;(2)次生淋滤埃洛石形成;(3)埃洛石和三水铝石之间的互相转化;(4)Ca型蒙脱石形成;(5)高岭土的磷酸盐化作用;(6)次生淋滤明矾石的形成。矿物生成的先后顺序和共生关系可将矿物形成分为主要成矿期和成矿期后演化两个阶段。矿物的后期演化使优质高岭土进一步富集,改造,形成量大质优的高岭土矿。同时,非高岭土矿物的生成又使部分矿石质量变差,降低了矿石的工业价值。  相似文献   

17.
核桃箐铁铜矿位于滇中武定断陷盆地内,与迤纳厂铁铜矿同属于滇中地区的IOCG型矿产。野外地质调查发现其成矿地质背景和矿床特征虽与迤纳厂铁铜矿有一定相似性,但富集的成矿元素类型和蚀变特征等方面却与迤纳厂不同。核桃箐矿区主要的赋矿地层为落雪组(Pt_2l),成矿元素只大量富集Fe元素,局部富集Cu元素,没有富集Au元素。矿石类型以致密块状磁铁矿石为主,围岩蚀变类型较少但具有一定的分带性,与矿化关系最为密切的蚀变是硅化。岩相学和地球化学研究发现,从围岩到蚀变岩,核桃箐矿区内主要的迁入元素是SiO_2、Al_2O_3、MnO和Na_2O,主要的迁出元素是CaO、MgO、H_2O和CO_2,表明核桃箐矿区内的硅化与去碳酸盐化是同时进行的,而钠化则与其同步或者稍晚于硅化。岩矿地球化学研究表明,核桃箐含矿围岩的n(SiO_2)/n(Al_2O_3) 3. 6,n(Al)/n(Al+Fe+Mn) 0. 5,n(Al_2O_3)/n(Al_2O_3+Fe_2O_3)=0. 12~0. 36,反映其形成于拉张环境、成岩时海水深度较浅的成岩特征。  相似文献   

18.
赣南脉状钨矿的地球化学特征   总被引:2,自引:0,他引:2  
王成发 《矿床地质》1984,3(2):76-84
赣南是世界著名的脉状钨矿产地,许多地学工作者对其作过详细研究。本文在前人工作的基础上,拟对脉状钨矿的某些地球化学特征及分布规律作进一步探讨。一、地质简况赣南位于南岭山系东段(图1)。泥盆纪以前,这里地壳大幅度下陷,沉积了巨厚的复理石建造、碎屑岩建造、碳酸盐建造及火山岩建造。区内震旦系、寒武系、奥陶系广泛分布。下古生代末期的强烈地壳运动,使泥盆纪以前的地层普遍上升褶皱,并伴有大规模酸性  相似文献   

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20.
Anhydrite–pyrite–magnetite–pyroxene–type deposits occur in the Mesozoic volcanic areas of the Middle–Lower Yangtze Valley in China. These deposits are hosted in alkaline basaltic rocks, and are generally accompanied by melanocratic and leucocratic alteration zones, both of which are characterized by a distinct vertical zonation pattern. Investigation of these zones indicates that the chemical compositions of solid solutions and polymorphs of various minerals vary spatially in the alteration profile, upwards from the lowest level, and outwards from the center.Here we report a case study on the Luohe deposit. In the melanocratic-alteration zone, the composition of magnetite (including trace elements Ti, V, Mg, Mn), pyroxene (Mg, Fe2+, Fe3+, Al2O3), plagioclase (AnxAb1 − x), pyrite (Co, Ni) and apatite (F, CeO2 + Y2O3 + La2O3) changes with depth. The isotherms of hydrothermal fluids determined from fluid inclusion data, including homogenization temperature and salinity, also vary with depth.Activity diagrams were constructed from mineral and isotherm analysis to estimate the chemical constraints on the alteration-mineral assemblages and the coexisting hydrothermal solutions for the Na2O–K2O–CaO–MgO–FeO–Fe2O3–A12O3–SiO2–H2SO4–H2S–HCI–H2O system at 350 to 600 °C and 500 bars (50 MPa), assuming that the major alteration mineral assemblages along the profile reflect the nature of the coexisting hydrothermal solutions. The activity diagrams adopted the major minerals as buffers to fix the activities of the aqueous species in the system, simulating the physicochemical conditions of the magnetite–anhydrite–pyroxene equilibrium and of solid solutions of diopside–hedenbergite, grossular–andradite and anorthite–albite found in the profile.This study provides an approach to modeling the chemical constraints of coexisting fluids in ore-alteration zones based on field observations.  相似文献   

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