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1.
沈崇辉 《矿物学报》2020,40(3):313-322
对安徽大黄山假象绿松石和磷灰石进行了详细的显微镜、背散射图像(BSE)观察,在此基础上,对假象绿松石和磷灰石进行了电子探针原位化学分析和岩石地球化学分析。研究表明,大黄山假象绿松石具磷灰石晶体形态,致密微晶-鳞片状、不规则球粒紧密堆积状和球粒状变胶结构,BSE背散射图像显示大黄山假象绿松石和磷灰石中均含有细小独居石矿物包裹体。全岩化学分析和电子探针原位分析表明大黄山假象绿松石为磷铜铁矿端元-富铝端元固溶体矿物。P_2O_5为大黄山假象绿松石和磷灰石共同的主要化学成分,F、Cl、S为二者共同的次要化学成分,且含量接近,大黄山假象绿松石和磷灰石微量元素原始地幔标准化蛛网图和稀土元素球粒陨石标准化配分型式图分布趋势相同,绿松石主要成矿物质来源于磷灰石。根据磷灰石中稀土元素特征值(δEu=0.25~0.28,δCe=1.20~1.27)和大黄山假象绿松石稀土元素特征值(δEu=0.33~0.47,δCe=0.80~1.88),综合分析判断大黄山假象绿松石为热液蚀变交代磷灰石成因。  相似文献   

2.
安徽马鞍山地区假象绿松石的研究   总被引:8,自引:1,他引:8  
笔者在马鞍山地区发现了假象绿松石。在矿物和矿床的很多特征上,假象绿松石与结核状和细脉状绿松石是相似的,但是,假象绿松石保留了磷灰石的晶体形态,其成矿母岩是磷灰石-磁铁矿-阳起石脉岩,假象绿松石的生成需要特定的岩石,地质构造,围岩(母岩)蚀变和地表氧化等条件,因此,它在世界上是罕见的。  相似文献   

3.
绿松石的热性能分析在对其水的结构特征、呈色机理等的研究中具有重要指示作用.采用热重-差热分析(TG-DSC)、红外光谱(IR)和X-射线粉晶衍射(XRD) 分析方法, 对安徽马鞍山具磷灰石假象绿松石的热性能特征进行了研究.研究结果显示从室温到1100℃, 假象绿松石的热相变可划分为6个变化阶段: 100~200℃时, 为吸附水脱水阶段; 250~330℃, 假象绿松石中羟基和晶格水分子脱失; 330~750℃为非晶态物相阶段; 约750℃时为新物相形成阶段; 750~1100℃为具磷石英结构磷酸铝的形成阶段; 1100℃时磷酸铝的结晶有序度增加.假象绿松石结构及水的存在形式、总量和结合方式制约和影响着颜色的变化.   相似文献   

4.
湖北竹山寒武纪碳硅质板岩层间破碎带内大量块状、结核状磷钙铝矾--纤磷钙铝石系列矿物,与绿松石伴生,是地表水淋滤作用形成的,化学成分分析显示,SO2-4浓度是磷钙铝矾--纤磷钙铝石系列矿物形成的决定因素.该系列矿物是一个复杂的多矿物组成的微晶集合体,主要矿物种属有磷铝矾、磷钙铝矾、纤磷钙铝石、沸水硅磷铝石等.该系列矿物磷和硫的含量高,能够吸附较丰富的多金属元素,并能聚集多种阴离子团,形成一道有效的地球化学障,对环境保护和生态学研究具有独特的意义.  相似文献   

5.
张辉  饶冰  唐勇  刘丛强 《云南地质》2006,25(4):403-404
目前,根据磷灰石溶解度模型、P在碱性长石与熔体相间的分配以及黑云母、锰铝榴石、透锂长石与对应的磷酸盐(包括斜磷锰铁矿、磷铝锂石-羟磷锂铝石)的平衡研究,已对过铝质岩浆中P的归宿进行了有效的平衡。但未见锰铝榴石-磷灰石的平衡研究。由于锰铝榴石-磷灰石矿物共生组合是花岗岩和LET型伟晶岩中最常见的矿物组合,直到岩浆演化晚期才出现锂辉石-磷铝锂石-羟磷锂铝石的组合。为此,本文实验研究锰铝榴石-磷灰石平衡反应,对过铝质岩浆体系中P溶解度起控制作用。  相似文献   

6.
采用x射线粉晶衍射(XRD)、博里叶变换红外光谱(FTI码以及拉曼光谱等方法对安徽马鞍山具磷灰石假象的绿松石进行了研究。结果表明:其主要矿物组成为绿松石,保留了磷灰石六边形的形态特征。XRD~U试的特征谱线d值为36745~36748(111)、29008~29025(123)、34247~34293(2101、32709~32781(113)、61626~61781(011)3020130~20162(301),与绿松石的标准衍射谱线基本致。红外光谱测试分析表明:3510~3465cm。间的谱带归属绿松石0(OH)的伸缩振动,3300~3070cm’间的谱带归属为绿松Nu(M-H。O)伸缩振动,1210-1012cm’间的谱带归属为绿松石U3口O。)ira缩振动,在838cm。附近的吸收谱带归属为绿松石6(OH)弯曲振动,655-480cm。间的谱带归属为绿松石u4(P04)弯曲振动。拉曼光谱测试分析表明:3466cm’附近的尖锐拉曼谱峰归属于绿松石(OH)基团的伸缩振动所致,宽缓的拉曼谱峰3281cm’~03078cm’归属于绿松石中水合络离子的伸缩振动,798cm’谱峰则是由于OH的弯曲振动所致。  相似文献   

7.
安徽马鞍山磷铝石宝石矿物学特征研究   总被引:3,自引:1,他引:2  
周彦  亓利剑  戴慧  张青  蒋小平 《岩矿测试》2014,33(5):690-697
近年来在安徽马鞍山地区所在的绿松石矿体附近,相继发现一种绿色、半透明的磷铝石,部分达到宝石级别。本文采用电子探针、X射线粉晶衍射仪、扫描电镜、傅里叶变换红外光谱仪、紫外可见光谱仪等测试技术,对该地区磷铝石的化学成分、矿物成分、微观结构和光谱特征进行对比验证和综合分析,研究其水的赋存形式,进而对磷铝石的呈色机制作了深入探讨。电子探针分析显示该地区磷铝石的化学成分主要以Al、P元素组成,含微量的Fe、V元素。X射线粉晶衍射与红外吸收光谱分析表明主要矿物为磷铝石,基本不含有其他杂质矿物;磷铝石是一种水合磷酸盐矿物,含有结晶水以及少量结构水的矿物,且结晶水与结构水多与Al3+(Fe3+)相结合的形式存在。偏光显微镜和扫描电镜观察显示磷铝石整体以鳞片状集合体产出,微观上多以短柱状及板片状堆积,单个晶体显示斜方晶系结晶生长习性。紫外可见吸收光谱中639 nm处吸收谱峰由Fe3+与V3+联合所致,300、423、864 nm处吸收峰由Fe3+所致,说明Fe3+与V3+的共同作用是马鞍山地区磷铝石呈现绿色的主要原因。本研究对于认识该类磷铝石的宝石矿物学性质以及颜色成因具有一定意义。  相似文献   

8.
羟磷铝锂石是南平稀有金属花岗伟晶岩中的重要标型矿物,可分为原生和次生两大类,最主要的是前者,一般呈块体状,共生矿物主要有销长石,钾长石,锂辉石,铌钽矿物。本文详细讨论了南平羟磷铝锂石的化学成分、X射线粉晶衍射资料、红外光谱和差热分析结果。南平原生羟磷铝锂石的交代蚀变作用十分发育,按其先后顺序,交代蚀变矿物组合有:石英—叶钠长石、次生羟磷铝锂石、细晶销长石—石英—次生磷灰石、次生复杂磷酸盐矿物和绢云母。  相似文献   

9.
桂林附近洞穴磷酸盐矿物   总被引:2,自引:0,他引:2  
洞穴矿物是洞穴环境下表生沉积作用的产物。据目前所知,次生洞穴矿物已达118种,其中磷酸盐矿物有29种。我们通过研究,在桂林附近的岩溶洞穴中鉴定出氢氧磷灰石、磷铝石、磷铝钾石及磷钙铝石等四种洞穴磷酸盐矿物。  相似文献   

10.
石振荣 《江苏地质》2008,32(2):109-112
湖北竹山县寒武纪碳硅质板岩层间破碎带内有大量蓝色的磷钙铝矾、纤磷钙铝石混合物与绿松石共生,物理性质表现为致密坚硬而性脆,吸水性强。化学成分分析硅和铝的含量高,磷含量少,并含有少量的硫和铜,是溶液为酸性时的产物。  相似文献   

11.
云南磷铝石谱学特征研究   总被引:1,自引:0,他引:1  
使用电子探针、X射线粉晶衍射仪、傅里叶变换红外光谱仪、激光拉曼光谱仪、紫外可见分光光度计等仪器,对最近在云南发现的一种达到宝石级别的磷铝石进行了化学成分、矿物组成、红外吸收光谱、拉曼光谱、紫外可见吸收光谱等方面的研究。化学成分分析结果表明,该磷铝石的主要化学成分为P和Al,并含有少量的Fe和V;X射线粉晶衍射结果显示,该磷铝石的矿物成分主要为磷铝石,杂质较少;红外光谱与拉曼光谱分析均检出磷酸根基团的特征峰,红外光谱分析还显示有结晶水与结构水的存在;紫外可见吸收光谱在300和420 nm附近的吸收归属于Fe3+,630 nm附近较宽缓的吸收带由Fe3+和V3+共同产生。并将磷铝石与绿松石进行了谱学方面的对比分析,以便更好地区分两者。  相似文献   

12.
Over 700 apatite grains from a range of rock types have been analysed by laser-ablation microprobe ICPMS for 28 trace elements, to investigate the potential usefulness of apatite as an indicator mineral in mineral exploration. Apatites derived from different rock types have distinctive absolute and relative abundances of many trace elements (including rare-earth elements (REE), Sr, Y, Mn, Th), and chondrite-normalised trace-element patterns. The slope of chondrite-normalised REE patterns varies systematically from ultramafic through mafic/intermediate to highly fractionated granitoid rock types. (Ce/Yb)cn is very high in apatites from carbonatites and mantle-derived lherzolites (over 100 and over 200, respectively), while (Ce/Yb)cn values in apatites from granitic pegmatites are generally less than 1, reflecting both HREE enrichment and LREE depletion. Within a large suite of apatites from granitoid rocks, chemical composition is closely related to both the degree of fractionation and the oxidation state of the magma, two important parameters in determining the mineral potential of the magmatic system. Apatite can accept high levels of transition and chalcophile elements and As, making it feasible to recognise apatite associated with specific types of mineralisation. Multivariate statistical analysis has provided a user-friendly scheme to distinguish apatites from different rock types, based on contents of Sr, Y, Mn and total REE, the degree of LREE enrichment and the size of the Eu anomaly. The scheme can be used for the recognition of apatites from specific rock types or styles of mineralisation, so that the provenance of apatite grains in heavy mineral concentrates can be determined and used in geochemical exploration.  相似文献   

13.
矾山磷铁矿床稀土元素地球化学特征   总被引:3,自引:0,他引:3  
程春 《化工矿产地质》2001,23(2):104-108
矾山磷铁矿床赋存于矾山杂岩体内 ,呈层状产出 ,是由深源富钾铁镁质岩浆演化而形成的晚期矿床。矾山杂岩体由三期侵入岩和脉岩组成 ,矿床产于第一期侵入岩中。第一期侵入岩较其它期次侵入岩REE含量高 ,按辉石岩—黑云母辉石岩—磷灰石岩的顺序增加。矿床稀土元素地球化学特征及主要元素含量表明 :在岩桨演化晚期 ,在贫硅和缺少足够“Ca2 +”的条件下 ,稀土元素极易代替“Ca2 +”而进入磷灰石晶格形成补尝类质同象。这对于研究矿床形成的物理化学环境和岩桨的演化具有重要意义。  相似文献   

14.
X射线衍射分析和化学成分研究表明,磷灰石为氟磷灰石,榍石成分中存在着的主要类质同象替代是(Fe~(3+)、Al)+(F,OH)~-=Ti~(4+)+O~(2-)。磷灰石和榍石是碱性辉长岩的REE、Ba、Zr等微量元素的主要载体;它们是在较高氧逸度的条件下结晶的。磷灰石的Sr同位素特征说明形成双龙桥碱性辉长杂岩的物质来源于上地幔。  相似文献   

15.
Apatite is a versatile mineral crystallizing at different stages of silicic magma evolution. Its composition may record that of magma, but could also be affected by interaction with fluids. The focus of this study is the well-recognized magma mingling process that was previously detected using plagioclase composition and in this study complementary record is sought in apatite. The apatite was analysed in two dioritic enclaves (primitive and hybrid) and host quartz monzonite, which is an igneous rock emplaced at ca. 340 Ma in mylonitized Góry Sowie gneisses (NE Bohemian Massif). The apatite was analysed in-situ by microprobe that allowed for chemical characterization of different apatite populations in quartz monzonite and analyses of thin acicular apatite in the enclaves. Apatite population in the quartz monzonite was chemically distinct from that in both enclave types and characterized by higher Y and lower Ce contents, such values are usually typical for peraluminous magmas. As such, the apatite transfer from felsic to mafic magma should be well recorded in apatite composition, which was not the case. Monzonite apatite composition was not commonly observed in the hybrid enclave despite massive plagioclase transfer and only rare resorbed cores with low Ce and Y contents were present. However, such low Ce and Y cores crystalized at the latest stage of apatite crystallization in the quartz monzonite, whereas the plagioclase transfer was an early episode. Therefore, we conclude that apatite transfer was limited during mingling and the apatite composition in the quartz monzonite is best explained by an early Cl-Ce-rich fluid removal and then fractional crystallization, while apatite in the primitive enclave is affected only by fractional crystallization. Altogether, Ce and Y composition of apatite is a valuable tool to record diverse magmatic processes such as fluid removal and precipitation from fluid in addition to fractionation of different REE phases and should be further explored.  相似文献   

16.
REE示踪沉积物物源研究进展   总被引:101,自引:0,他引:101  
REE作为一种重要的沉积物物源示踪剂运用很广。在介绍了REE性质的基础上,对海水、河水、沉积岩、河流及边缘海沉积物中的REE元素丰度与配分模式特征进行了深入综述,概述了影响和控制REE丰度、模式及分馏特征的主要因素;论述了REE的物泊示踪意义以及在国内外应用情况与存在问题:源岩风化对REE分馏的影响;颗粒运及沉积时水动力分选对REE分馏可能造成的影响,即不同粒级中的REE不同的丰度与配分模式和碎屑  相似文献   

17.
The concentrations of trace elements in apatite from granitoid rocks of the Mt Isa Inlier have been investigated using the laser‐ablation inductively coupled plasma‐mass spectrometry (ICP‐MS) microprobe. The results indicate that the distribution of trace elements (especially rare‐earth elements (REE), Sr, Y, Mn and Th) in apatite strongly reflects the chemical characteristics of the parental rock. The variations in the trace‐element concentrations of apatite are correlated with parameters such as the SiO2 content, oxidation state of iron, total alkalis and the aluminium saturation index (ASI). The relative enrichment of Y, HREE and Mn and the relative depletion of Sr in the apatites studied reflect the degree of fractionation of the host granite. Apatites from strongly oxidised plutons tend to have higher concentrations of LREE relative to MREE. Manganese concentrations are higher in apatite from reduced granitoids because Mn2+substitutes directly for Ca2+. The La/Ce ratio of apatite is well‐correlated with the whole‐rock K2O and Na2O contents, as well as with the oxidation state and ASI. Because apatite trace‐element composition reflects the chemistry of the whole rock, it can be a useful indicator mineral for the recognition of mineralised granite suites, where particular mineralisation styles are associated with granitoids that have specific geochemical fingerprints.  相似文献   

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