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1.
四川石棉大水沟碲矿床是世界首例独立碲多金属矿床。包裹体的相态和成分特征表明,矿石和变质分异脉体富含CO2、CO2-H2O(低盐度流体)和CO2-H2O-NaCl(高盐度流体)三种体系的流体包裹体,成矿作用与前两种体系的流体有关。薄片中普遍存在包裹体的自然爆裂现象,大多数包裹体在均一前发生泄漏或爆裂。矿物温度计表明,磁黄铁矿阶段成矿温度约500℃, 辉碲铋矿阶段约400℃ ,流体密度变化在1.04~0.76 g/cm3之间,成矿压力分别为450~500 MPa和240~300 MPa,矿化是在高温高压条件下发生的。  相似文献   

2.
新疆望峰金矿床流体包裹体地球化学及矿床成因类型   总被引:6,自引:2,他引:4  
张莉  刘春发  武广 《岩石学报》2009,25(6):1465-1473
西天山东缘的望峰金矿床受胜利达坂韧性剪切带的控制,成矿过程包括早、中、晚3个阶段,自然金和矿石矿物主要形成于中阶段。岩相学、显微测温及单个包裹体成分激光拉曼光谱研究表明,望峰金矿床石英中的流体包裹体有CO2-H2O型、纯CO2型、NaCl-H2O溶液型和含子晶多相等4种类型。早阶段石英中原生包裹体主要是CO2-H2O型,其盐度1.62%~8.03% NaCl eqv.,流体密度0.73~0.89g/cm3,均一温度为250~390℃,气相成分为CO2。中阶段石英中的原生包裹体包括了所有4种类型,其CO2-H2O型和NaCl-H2O溶液型包裹体的均一温度分别为210~340℃和230~300℃,显示了流体沸腾现象的存在。CO2-H2O型包裹体的盐度0.83%~9.59% NaCl eqv.,密度0.77~0.95g/cm3,气相成分为CO2±CH4±N2。晚阶段石英只发育水溶液包裹体,具有较低的盐度(0.35%~3.87% NaCl eqv.)和均一温度(120~214℃)。根据CO2-H2O型包裹体估算早、中阶段流体包裹体捕获压力分别为110~300PMa和90~250MPa,成矿深度为9~11km。总体而言,望峰金矿床由低盐度、低密度、富CO2的变质流体系统形成,流体减压沸腾导致矿质沉淀,属于中深带的造山型金矿系统。  相似文献   

3.
小秦岭东桐峪金矿床的流体包裹体研究   总被引:4,自引:2,他引:2  
东桐峪金矿床位于小秦岭金矿田的中西部,其含金石英脉受韧性剪切构造带的控制。该矿床的构造-成矿过程可划分为4个阶段:Ⅰ黄铁矿-乳白色石英脉阶段;Ⅱ灰白色石英-黄铁矿阶段;Ⅲ石英-多金属硫化物阶段;Ⅳ石英-碳酸盐阶段。相对于小秦岭地区的其他金矿床,东桐峪金矿床的流体包裹体研究资料相对缺乏。文章表明,该矿床内的流体包裹体类型主要为CO2-H2O包裹体和水溶液包裹体,见少量纯液相CO2包裹体。显微测温表明,Ⅰ阶段的构造-成矿流体以中温、富CO2等挥发分为特征,包裹体均一温度为221~392℃,盐度w(NaCleq)为5.5%~7.9%,密度为0.84~0.93 g/cm3;Ⅱ阶段和Ⅲ阶段以CO2-H2O±CH4流体为主,包裹体均一温度为205~350℃(Ⅱ阶段)和224~271℃(Ⅲ阶段),盐度w(NaCleq)集中于5.1%~7.1%,密度为0.83~0.96 g/cm3;Ⅳ阶段的流体演化为中-低温、低盐度的盐水溶液体系,包裹体均一温度为175~185℃。文章对该矿床各成矿阶段的压力进行了估算,Ⅰ、Ⅱ、Ⅲ阶段的流体最小捕获压力分别为123~160 MPa、160~170 MPa、170 MPa左右。  相似文献   

4.
藏南折木朗造山型金矿成矿流体地球化学和成矿机制   总被引:5,自引:4,他引:1  
折木朗金矿位于青藏高原雅鲁藏布江缝合带东段的南侧,矿体受大型脆-韧性剪切带的次级断裂控制。系统的显微测温和激光拉曼测定显示折木朗金矿矿石中存在3类流体包裹体: NaCl-H2O溶液包裹体(类型Ⅰ);含CO2盐水溶液包裹体(类型Ⅱ),此类包裹体又分为两相(Ⅱa)和三相(Ⅱb)2个小类;Ⅲ纯气相包裹体。折木朗金矿床中流体包裹体显微测温显示该矿成矿流体的盐度范围为2.31%~7.39% NaCleqv,平均值为5.33%% NaCleqv,峰值为4.0%~7.0% NaCleqv;均一温度的范围为164.5~273.1℃,峰值为220~240℃,平均值为221.0℃。相对应的密度范围为0.82~0.93g·cm-3,峰值为0.84~0.90g·cm-3,平均值为0.88g·cm-3。折木朗金矿床成矿流体具有富含CO2、低盐度、低密度、中低温度的特征,与造山型金矿成矿流体相似。此外,同位素测定显示成矿流体的氢氧碳同位素组成分别为δDH2O=-36.7‰~-107.5‰,δ18OH2O=4.1‰~5.5‰,δ13C=-9.6‰~-11.5‰,说明成矿流体主要为变质水,但有地幔流体的加入。综合成矿地质特征和成矿流体的证据,提出折木朗金矿为陆陆碰撞造山型金矿。  相似文献   

5.
云南哀牢山老王寨大型造山型金矿成矿流体地球化学   总被引:12,自引:4,他引:8  
云南哀牢山金矿带是我国最重要的喜马拉雅期金矿带,而老王寨是其中最大的金矿。流体包裹体研究显示:老王寨金矿含金石英脉中流体包裹体类型主要为NaCl-H2O型和CO2-H2O型,其均一温度为102~302℃, 峰值为160~180℃;流体盐度范围变化较大,介于2.5%~12.9% NaCleqv之间,峰值为6.0%~7.5% NaCleqv,显示老王寨成矿流体具有中低盐度和中低温度的特征。 氢氧同位素测定显示成矿流体δDH2O=-115‰~-90‰,δ18OH2O=5.2‰~6.8‰,显示其组成主要为岩浆水,可能与有机沉积物发生过同位素交换。流体包裹体碳同位素组成(δ13C为-6.5‰~-3.9‰)基本落在幔源碳变化范围之内,说明其中CO2可能来自地壳深部,甚至上地幔。综合成矿地质特征和成矿流体的证据,提出老王寨金矿为喜马拉雅期造山型金矿。  相似文献   

6.
简单体系水溶液包裹体pH和Eh的计算   总被引:2,自引:0,他引:2  
刘斌 《岩石学报》2011,27(5):1533-1542
流体包裹体pH和Eh参数的计算一直处于探索阶段。已经发表的计算公式,由于缺少高压(>1bar)环境下化学组分反应平衡常数,常常利用常压(1大气压)下化学组分反应平衡常数代替而推导出的,对于大多数自然界捕获的包裹体,不可避免地产生较大计算误差。根据水溶液包裹体中离子反应热力学特征,结合前人推导的计算公式,我们分别建立简单体系水溶液包裹体pH和Eh计算公式。由于利用较高压(>1bar)化学反应平衡常数,基本上解决不同条件下、特别在较高温度、压力下捕获的水溶液包裹体pH和Eh的计算难题。4种简单体系水溶液包裹体pH计算公式:① H2O包裹体:pH=pKw② CO2-H2O包裹体: 3-(mCO2Ka,1+KW)· -2mCO2Ka,1Ka,2=0③ NaCl-H2O包裹体: 2= ④ CO2-H2O-NaCl包裹体: 3+ 2-(mCO2·Ka,1+Kw)· -2mCO2·Ka,1·Ka,2- =0计算数值精度分析表明:CO2-H2O和NaCl-H2O包裹体的pH值按照公式计算,相同或接近于实际测定的天然酸雨、海水pH数值范围。CO2-H2O-NaCl包裹体与Crerar(1978)公式计算误差不超过10%。4种简单体系水溶液包裹体Eh的计算,引用Ryzhenko and Bryzgalin (1984)年推导的Eh公式。文中列举了3个实例,详细叙述不同类型包裹体捕获温度、压力下pH和Eh计算过程。自然界中水溶液包裹体成分十分复杂,本文涉及的只是自然界几种简单体系水溶液包裹体,给出的pH和Eh公式只对特定组分组合反应平衡条件有效,它不适合另外一种组分组合平衡条件下的关系,因此使用时务必注意平衡的组分组合条件。  相似文献   

7.
江西黄沙石英脉型钨矿床流体包裹体研究   总被引:13,自引:0,他引:13  
黄沙钨矿床是赣南地区一大型石英脉型钨多金属矿床。本文采用"流体包裹体组合"的研究方法,对黄沙钨矿床主成矿阶段早期的黑钨矿-石英脉和晚期的硫化物-(黑钨矿)-石英脉石英中的流体包裹体进行了显微测温和拉曼探针的分析。研究表明,黑钨矿-石英脉中包裹体主要为水溶液包裹体和含CO2水溶液包裹体,硫化物-(黑钨矿)-石英脉中主要发育水溶液包裹体。黑钨矿-石英脉中包裹体的均一温度明显高于硫化物-(黑钨矿)-石英脉中的包裹体,但两者水溶液包裹体的盐度相差不大。激光拉曼探针测试表明,两期矿脉中水溶液包裹体的组分主要为水,在黑钨矿-石英脉中的含CO2水溶液包裹体,除CO2外,还检测到CH4和N2组分。研究表明,以CO2逸失为特征的流体不混溶作用是早期黑钨矿-石英脉含矿流体中的金属络合物分解并沉淀成矿的主要机制,晚期硫化物-(黑钨矿)-石英脉中矿质的沉淀则主要是流体的混合作用导致。  相似文献   

8.
常海亮  韩友科 《矿床地质》1998,17(Z6):1071-1074
板苍河金矿是典型的岩浆热液型金矿床。石英中发育的裹体有: ① 富CO2包亵体; ②含L CO2多相包裹体; ③ 两相气液包裹体; ④ 有机质包裹体; ⑤ 单相水溶液包裹体。群体包裹体成份分析结果中SO42-高,在冷冻法测定时出现乩S水合物,而激光拉曼探针分析结果证实其中有较多的H2S、HS-和有机质。在对这种包裹体进行详细研究基础上,对有关问题进行了有益的讨论。  相似文献   

9.
河北省青龙满族自治县四拨子-六拨子钼铜矿位于燕辽成矿带东部,是近年来发现的中型钼铜矿床。辉钼矿呈细脉状、网脉状、浸染状、薄膜状赋存于长城系石英砂岩及白云岩中的矽卡岩带,钼矿化与硅化关系密切。矿体呈似层状、脉状和透镜状。矿床的形成经历了矽卡岩期和石英-硫化物期,铜和钼矿化主要形成于石英-硫化物期。研究表明,矽卡岩期矿物以发育液体包裹体为特征,石英-硫化物期石英中主要发育液体包裹体、含CO2两相和三相包裹体。矽卡岩期成矿流体为高-中温(192~497℃)、中-低盐度(5.41%~16.53% NaCleqv)、中-低密度(0.59~0.92g/cm3)的NaCl-H2O体系。石英-硫化物期成矿流体为中-低温(主要变化于160~330℃)、低盐度(2.07%~15.17% NaCleqv)和中低密度(0.69~1.01g/cm3)的NaCl-H2O-CO2 (±CH4/N2)型流体。石英的δDSMOW为-128‰~-80‰,δ18OSMOW值为9.6‰~14‰,δ18OH2O值为-3.61%~5.30‰,表明成矿流体具有岩浆水混合大气降水的特征。硫化物的δ34S变化于-0.9‰~5.7‰,平均值为2.9‰,表明成矿物质中硫来自深部岩浆。成矿时代为早侏罗世早期,成矿作用与花岗斑岩岩浆期后热液活动有关。  相似文献   

10.
杨孝强  厉子龙 《岩石学报》2013,29(10):3446-3456
北疆阿尔泰造山带南缘晚古生代超高温麻粒岩存在高铝斜方辉石+夕线石+石英和尖晶石+石英等超高温特征矿物组合,其退变质作用主要以典型的降压反应矿物堇青石的形成为标志。对其中新发现的石榴子石及石英流体包裹体开展显微测温和激光拉曼探针分析,结果表明:基质中的石英以及被石榴子石包裹的石英中孤立分布的原生流体包裹体成分为近纯CO2(部分含少量的N2),均一温度在10.1~29℃之间,其对应的密度在0.631~0.861g/cm3。石榴子石中的原生和假次生CO2包裹体费米峰差在104.1cm-1左右,低于石英中CO2包裹体的费米峰差(~104.7cm-1),暗示其密度低于石英中的CO2包裹体。由CO2流体包裹体密度所得到的等容线从P-T轨迹退变质阶段的下方穿过结合区域地质背景,我们初步认为阿尔泰超高温麻粒岩的形成与幔源岩浆底侵有关。基性岩浆的底侵不但提供了异常高的地温梯度,同时其所释放的大量CO2降低了水活度,使得变质作用峰期的特征矿物得以保存。低密度的CO2流体指示了阿尔泰超高温麻粒岩沿顺时针P-T轨迹紧随超高温峰期变质之后快速抬升降压,捕获的同变质流体包裹体因腔体体积增大而密度降低的一种退变质过程。  相似文献   

11.
In steady state the stable isotopic composition of nitrogen and oxygen in tropospheric N2O is balanced by isotopically light N2O emitted from soils and oceans and isotopically heavy N2O as a return flux from the stratosphere.However,no such balance was reached in calculations given by Kim and Caig(1993).Modifications have been made on their calculations based on the most recent reports on annual global emission of N2O.It is considered that the nitrogen and oxygen isotope budget in tropospheric N2O are approximately in balance if isotopic fractionation effects during the production of N2O in soils and furthermore this paper puts forward further evidence for validating the above results.  相似文献   

12.
In the Sanandaj-Sirjan zone of metamorphic belt of Iran, the area south of Hamadan city comprises of metamorphic rocks, granitic batholith with pegmatites and quartz veins. Alvand batholith is emplaced into metasediments of early Mesozoic age. Fluid inclusions have been studied using microthermometry to evaluate the source of fluids from which quartz veins and pegmatites formed to investigate the possible relation between host rocks of pegmatites and the fluid inclusion types. Host minerals of fluid inclusions in pegmatites are quartz, andalusite and tourmaline. Fluid inclusions can be classified into four types. Type 1 inclusions are high salinity aqueous fluids (NaCleq >12 wt%). Type 2 inclusions are low to moderate salinity (NaCleq <12 wt%) aqueous fluids. Type 3 and 4 inclusions are carbonic and mixed CO2-H2O fluid inclusions. The distribution of fluid inclusions indicate that type 1 and type 2 inclusions are present in the pegmatites and quartz veins respectively in the Alvand batholith. This would imply that aqueous magmatic fluids with no detectable CO2 were present during the crystallization of these pegmatites and quartz veins. Types 3 and 4 inclusions are common in quartz veins and pegmatites in metamorphic rocks and are more abundant in the hornfelses. The distribution of the different types of fluid inclusions suggests that CO2 fluids generated during metamorphism and metamorphic fluids might also contribute to the formation of quartz veins and pegmatites in metamorphic terrains.  相似文献   

13.
Elastic and thermoelastic constants of large single crystals of Ca2MgSi2O7 and Ca2ZnSi2O7 have been derived from ultrasonic resonance frequencies of plane-parallel plates and their shift upon variation of temperature, respectively. In addition, coefficients of thermal expansion and dielectric constants were determined. Both species possess quite similar properties. As observed in other isotypic magnesium and zinc compounds, the mean elastic stiffness and the deviation from the Cauchy relations are significantly larger in the zinc compound, due to a covalent contribution of the Zn–O bond. Positive thermoelastic constants T44 and T66 in Ca2MgSi2O7 allow temperature-independent ultrasonic generators and oscillators to be manufactured.  相似文献   

14.
含Ti硅酸盐玻璃在基础科学研究和应用技术开发上均有重要价值,亟需对其进行准确的成分分析,为进一步的科研工作提供重要的数据支撑.对玻璃进行电子探针分析时,由于样品的易损性和其中(Na和K)阳离子在电子束轰击下极易发生迁移和扩散,因此往往需要经过条件实验来确定合适的分析条件,确保样品在该条件下能够保持尽量稳定的状态,才能获...  相似文献   

15.
Numerical models on thermal structure, convective flow of solid, generation and transportation of H2O-rich fluid in subduction zones are consolidated to have a comprehensive view of the subduction zone processes: heat balance, circulation of H2O magmatism–metamorphism, growth of arcs and continental margins. A large scale convection model with steady subduction of a cold old slab (130 Myr old) predicts rapid ( 100 Myr) cooling of subduction zones, resulting in cessation of magmatism. The model also predicts that the mantle temperature beneath arcs and continental margins is greatly affected by the effective temperature of the subducting slab, i.e., the age of the subducting slab. If subduction of a young hot slab, including ridge subduction, occurs every 60 to 120 Myr as is suggested for eastern Asia, the average temperature beneath arcs is increased by about 300 °C, which may explain the long-lasting magmatism in eastern Asia. Associated with subduction of young slabs and ridges, thermal structure and circulation of H2O are greatly modified to cause a transition from (1) normal arc magmatism, (2) forearc mantle melting, to (3) slab melting to produce a significant amount (100 km3) of granitic melts, associated with both high-P/T and low-P/T type metamorphism. The last stage of (3) can result in formation of a granitic batholith belt and a paired metamorphic belts. Synthesis of the numerical models and observations suggest that episodic subduction of young slabs and ridges can explain heat source for generating a large amount of granitic magmas of batholiths, synchronous formation of batholith and regional metamorphic belts, and PT conditions of the paired metamorphism. Even the high-P/T metamorphism requires an elevated geothermal structure in the forearc region, associated with ridge subduction. Although the emplacement of the batholiths and the regional metamorphic belts, and the mass balance in subduction zones are not well constrained at present, the episodic event associated with ridge subduction is thought to be essential for net growth of arcs and continental margins, as well as for the long-term heat balance in subduction zones.  相似文献   

16.
Hydrometallurgical processing of spent hydrodesulphurisation (HDS) catalyst for the recovery of molybdenum using sodium carbonate and hydrogen peroxide mixtures was investigated. The results indicated that the recovery of molybdenum was largely dependent on the concentrations of Na2CO3 and H2O2 in the reaction medium, which controls the acidity of the leach liquor and carry over of impurities such as Al, Ni, P, Si and V. Leaching process was exothermic and leaching efficiency of molybdenum decreased with increasing solid to liquid ratio. Large scale leaching of spent catalyst, under optimum conditions: 20% pulp density, 85 g/L Na2CO3, 10 vol.% H2O2 and 1 h reaction, resulted a leaching efficiency of 84% Mo. The obtained leach liquor contained (g/L): Mo — 22.0, Ni — 0.015 and Al — 0.82, P — 1.1, Si — 0.094 and minor quantities of V — 8 mg/L, As and Co — < 1 mg/L. Recovery of Mo from leach solution as MoO3 of 97.30% purity was achieved by ammonium molybdate precipitation method.  相似文献   

17.
18.
Freshwater marshes could be a source of greenhouse gases emission because they contain large amounts of soil carbon and nitrogen. These emissions are strongly influenced by exogenous nitrogen. We investigate the effects of exogenous nitrogen on ecosystem respiration (CO2), CH4 and N2O emissions from freshwater marshes in situ in the Sanjiang Plain Northeast of China during the growing seasons of 2004 and 2005, using a field fertilizer experiment and the static opaque chamber/GC techniques. The results show that there were no significant differences in patterns of seasonal variations of CO2 and CH4 among the fertilizer and non-fertilizer treatments, but the seasonal patterns of N2O emission were significantly influenced by the exogenous nitrogen. Seasonal averages of the CO2 flux from non-fertilizer and fertilizer were 987.74 and 1,344.35 mg m 2 h 1, respectively, in 2004, and 898.59 and 2,154.17 mg m 2 h 1, respectively, in 2005. And the CH4 from the control and fertilizer treatments were 6.05 and 13.56 mg m 2 h 1 and 0.72 and 1.88 mg m 2 h 1, respectively, in 2004 and 2005. The difference of N2O flux between the fertilizer and non-fertilizer treatments is also significant either in 2004 and 2005. On the time scale of 20-, 100-, and 500-year periods, the integrated global warming potential (GWP) of CO2 + CH4 + N2O released during the two growing seasons for the treatment of fertilizer was 97, 94 and 89%, respectively, higher than that for the control, which suggested that the nitrogen fertilizer can enhance the GWP of the CH4 and N2O either in long time or short time scale.  相似文献   

19.
The viscosity of a synthetic andesite-like melt was measured in the low viscosity range (101-106 Pa s) using the falling sphere(s) method and in the high viscosity range (108-1013 Pa s) using parallel-plate viscometry. Falling sphere experiments with melts containing 2.3 and 5.6 wt.% H2O were carried out in an internally heated gas pressure vessel (IHPV) at 500 MPa confining pressure. The sinking velocity of Pt and Pd spheres and in one case of a corundum sphere was used to measure the melt viscosity. In addition, a creep experiment was performed at ambient pressure using a glass containing 2.73 wt.% H2O . A more water-rich glass (5.6 wt.% H2O ) was investigated with a high pressure parallel-plate viscometer at 400 MPa confining pressure in an IPHV. By combining our new data with previous results for a similar melt composition we derived the following expression to describe the viscosity η (in Pa s) as a function of temperature T (in K) and water content w (in wt.%)
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20.
We report here a single-crystal polarized-light study of stoppaniite, ideally (Fe,Al,Mg)4(Be6Si12O36)(H2O)2(Na,□), from Capranica (Viterbo). Polarized-light FTIR spectra were collected on an oriented (hk0) section, doubly polished to 15 μm. The spectrum shows two main bands at 3,660 and 3,595 cm−1; the former is strongly polarized for E c, while the latter is polarized for E //c. A sharp and very intense band at 1,620 cm−1, plus minor features at 4,000 and 3,228 cm−1 are also polarized for E //c. On the basis of literature data and considering the pleochroic behavior of the absorptions, the 3,660 cm−1 band is assigned to the ν3 stretching mode and the 1,620 cm−1 (associated with an overtone 2*ν2 at 3,230 cm−1) band to the ν2 bending mode of “type II” water molecules within the structural channels of the studied beryl. The sharp band at 3,595 cm−1 is not associated with a corresponding ν2 bending mode; thus it is assigned to the stretching vibration of O–H groups in the sample. The minor 4,000 cm−1 feature can be assigned to the combination of the O–H bond parallel to c with a low-frequency metal-oxygen mode such as the Na–O stretching mode. The present results suggest that the interpretation of the FTIR spectrum of Na-rich beryl needs to be carefully reconsidered.  相似文献   

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