U-Pb SHRIMP-II ages of titanite and timing constraints on apatite-nepheline mineralization in the Khibiny and Lovozero alkaline massifs (Kola Peninsula)     

N.V. Rodionov  E.N. Lepekhina  A.V. Antonov  I.N. Kapitonov  Yu.S. Balashova  B.V. Belyatsky  A.A. Arzamastsev  S.A. Sergeev 《Russian Geology and Geophysics》2018,59(8):962-974

Results of this study of titanite samples collected from silicate rocks and apatite-nepheline-(sphene) ores from Paleozoic polyphase alkaline nepheline syenite complexes of the Khibiny and Lovozero massifs revealed the possibility of their in-situ U-Pb dating using sensitive high-resolution ion microprobe SHRIMP-II with an accuracy of 1.0-1.5%, which is comparable with that of U-Pb zircon analysis. Employing different approaches to age determination of the formation of the U-Pb system of titanites, the combined isochrons and mixing lines were plotted from the data obtained from the differentiated complex samples (121 analyses of five Khibiny samples and 52 analyses of one Lovozero sample) and apatite-nepheline ores (120 analyses of five Khibiny samples and 88 analyses of three Lovozero samples). They indicate synchronous crystallization of titanite in silicate rocks throughout the complexes: 374.1 ± 3.7 Ma for the Khibiny massif and 380.9 ± 4.5 Ma for the Lovozero massif, and attest to the later formation of phosphate-rare-metal ores: 371.0 ± 4.2 and 361.4 ± 3.2 Ma, respectively. The relatively delayed ore mineralization specific to the Lovozero massif can be accounted for the significantly lower volumes of magmatic melt and ore fluid involved, different thermal conditions, and the pattern of the investigated mineralization. As such, the obtained U-Pb data from titanite make it possible to limit significantly the time interval (most likely, not exceeding 15-20 Ma) comprising the evolution and activity of the ore-magmatic system of major agpaitic complexes, which is probably associated with plume magmatism.  相似文献   

Petrological and Geochemical Constraints on the Protoliths of Serpentine‐Magnetite Ores in the Zhaoanzhuang Iron Deposit,Southern North China Craton     

MENG Jie  LI Houmin  LI Lixing  SANTOSH M.  SONG Zhe  YANG Xiuqing 《《地质学报》英文版》2018,92(2):627-665

The uncommon Mg-rich and Ti-poor Zhaoanzhuang serpentine-magnetite ores within Taihua Group of the North China Craton(NCC) remain unclear whether the protolith was sourced from ultramafic rocks or chemical sedimentary sequences. Here we present integrated petrographic and geochemical studies to characterize the protoliths and to gain insights on the ore-forming processes. Iron ores mainly contain low-Ti magnetite(TiO_2 ~0.1 wt%) and serpentine(Mg#=92.42–96.55), as well as residual olivine(Fo=89–90), orthopyroxene(En=89–90) and hornblende. Magnetite in the iron ores shows lower Al, Sc, Ti, Cr, Zn relative to that from ultramafic Fe-Ti-V iron ores, but similar to that from metamorphic chemical sedimentary iron deposit. In addition, interstitial minerals of dolomite, calcite, apatite and anhydrite are intergrown with magnetite and serpentine, revealing they were metamorphic, but not magmatic or late hydrothermal minerals. Wall rocks principally contain magnesian silicates of olivine(Fo=83–87), orthopyroxene(En=82–86), humite(Mg#=82–84) and hornblende [XMg=0.87–0.96]. Dolomite, apatite and anhydrite together with minor magnetite, thorianite(Th-rich oxide) and monazite(LREE-rich phosphate) are often seen as relicts or inclusions within magnesian silicates in the wall rocks, revealing that they were primary or earlier metamorphic minerals than magnesian silicates. And olivine exists as subhedral interstitial texture between hornblende, which shows later formation of olivine than hornblende and does not conform with sequence of magmatic crystallization. All these mineralogical features thus bias towards their metamorphic, rather than magmatic origin. The dominant chemical components of the iron ores are SiO_2(4.77–25.23 wt%), Fe_2O_3 T(32.9–80.39 wt%) and MgO(5.72–27.17 wt%) and uniformly, those of the wall rocks are also SiO_2(16.34–48.72 wt%), Mg O(16.71–33.97 wt%) and Fe_2O_3 T(6.98–30.92 wt%). The striking high Fe-Mg-Si contents reveal that protolith of the Zhaoanzhuang iron deposit was more likely to be chemical sedimentary rocks. The distinct high-Mg feature and presence of abundant anhydrite possibly indicate it primarily precipitated in a confined seawater basin under an evaporitic environment. Besides, higher contents of Al, Ti, P, Th, U, Pb, REE relative to other Precambrian iron-rich chemical precipitates(BIF) suggest some clastic terrestrial materials were probably input. As a result, we think the Zhaoanzhuang iron deposit had experienced the initial Fe-Mg-Si marine precipitation, followed by further Mg enrichment through marine evaporated process, subsequent high-grade metamorphism and late-stage hydrothermal fluid modification.  相似文献   

火焰原子吸收光谱法和电感耦合等离子体发射光谱法测定硫化矿中的银铜铅锌   总被引：1，自引：1，他引：0  

胡健平  王日中  杜宝华  盛迪波  罗志翔 《岩矿测试》2018,37(4):388-395

过渡金属Cu、Co、Ni、Zn、Pb等及贵金属元素(铂族元素和Au、Ag)高度富集在硫化物中,尤其是富集在岩浆硫化物中,常形成具有工业开采价值的矿产,因而硫化物矿物具有重大的经济价值。而硫化物矿种类多,不同类型硫化物矿中Ag、Cu、Pb、Zn含量高低不同,有些被强酸分解不完全,产生沉淀,导致检测结果波动性较大、精密度偏低。本文针对含黄铁矿、铅和铜分别以方铅矿和黄铜矿形式存在的较难溶的硫化物矿,在矿样中先加盐酸加热除硫后,再用硝酸-氢氟酸-高氯酸三种强酸分解,以新配制的王水提取,使该类样品获得了理想的分解效果,特别是对银、铅含量较高的样品分解效果改善较显著。试液用火焰原子吸收光谱和电感耦合等离子体发射光谱都能准确测定Ag、Cu、Pb、Zn,两种方法的相对误差在±2.32%以内,测定值基本一致,相对标准偏差(RSD,n=12)均小于3.5%,四个元素的检出限均低于0.0090!g/m L,低于文献检出限。  相似文献   

陕北油田二开井段提下钻遇阻原因分析与对策     

王天宝  刘锋  陈亮  厉磊 《地质与勘探》1999,35(4):62-63

陕北油石二开井段遇阻的原因为泥岩的水化膨胀和孔隙性砂岩的泥饼沉积。对策主要有物理方法（如短程起下钻、加大排量等） 、化学方法（加入强抑制剂ＦＡ３６７、加入ＧＰＳ,提高泥饼质量） 等。  相似文献   

福建省金矿成矿地质条件与成矿远景   总被引：1，自引：1，他引：0  

翁朝峰 《福建地质》1998,17(1):24-34

福建省金矿与地层、构造、岩浆岩等成矿地质条件关系密切,金矿赋矿层位有８个,其中以前寒武纪麻源群、龙北溪组和中生代火山岩、火山碎屑岩层位为最主要。金矿主要分布在区域性断裂、火山构造、北东向与北西向两组断裂复合部位及火山基底起部位,韧性剪切带、推覆（剥离）构造发育地段,是金矿重要成矿部位。金矿成矿时代主要有前寒武纪和燕山期两个成矿期,两者在成矿时间上显示继承性,在空间上具有相关性。金矿化在前寒武纪与中  相似文献   

河北省页岩气地质条件评价     

张路锁  常明华 《中国煤炭地质》2014,(3):23-26,31

应用泥页岩厚度、TOC含量、干酪根类型和成熟度等评价参数,对河北省主要的含暗色页岩系地层——中元古界长城系串岭沟组和蓟县系洪水庄组、新元古界青白口系下马岭组、古生界石炭二叠系太原和山西组、新生界古近系沙河街组的页岩气成藏地质条件进行评价,预测固安、霸县沙河街组和沧州、廊坊太原-山西组为页岩气有利勘探目标区。  相似文献   

辽宁鞍本地区沉积变质型富铁矿的成因：Fe、Si、O、S同位素证据   总被引：2，自引：0，他引：2  

李延河  张增杰  侯可军  段超  万德芳  胡古月 《地质学报》2014,88(12):2351-2372

辽宁鞍本地区是我国最重要的鞍山式沉积变质型(BIF)铁矿矿集区,弓长岭铁矿是我国唯一的由鞍山式贫铁矿经后期热液改造形成的大型磁铁富矿.本文在前人工作基础上,对比研究了鞍本地区贫铁矿、富铁矿和蚀变围岩的铁、硅、氧、硫同位素组成特征和空间变化规律,结合磁铁富矿的地质特征,对成矿流体的性质、来源、成矿作用和富矿成矿机制提出了新的认识.指出鞍本地区富铁矿的成矿作用与辽东地区古元古代造山运动结束后(1.85 Ga)地壳抬升引发的非造山岩浆侵入和热液活动有关,成矿溶液由大气降水演化形成,而非变质热液或混合岩化热液;成矿溶液淋滤了辽河群蒸发盐地层中富13C碳酸盐、富34S石膏、CH4等成矿物质,成矿溶液具偏酸性弱还原特征;铁质活化再富集是鞍本地区富铁矿形成的重要机制,成矿溶液与贫铁矿及围岩反应使铁质以Fe2+形式活化迁移.温度降低、氧逸度升高或与大气降水混合是溶液中Fe2+氧化形成磁铁矿沉淀的主要原因;在Fe2+被氧化形成磁铁矿的同时,成矿溶液中的CH4被氧化形成石墨,与磁铁矿一起沉淀下来,形成含石墨磁铁富矿;溶液中SO42-被还原形成富34S黄铁矿.  相似文献   

熔融制样X射线荧光光谱法测定铜矿石中16种主次量元素   总被引：1，自引：1，他引：0       下载免费PDF全文

罗学辉  苏建芝  鹿青  杨理勤  王岚 《岩矿测试》2014,33(2):230-235

铜矿石类型繁多,矿石赋存状态各异,成分复杂。在现有的铜矿石熔融制样X射线荧光光谱（XRF）分析方法中,选取标准物质个数和矿石类型少、分析范围宽,与实际样品类型相差太大,且制备的熔融片质量不高。本文选用铜含量既有良好浓度变化范围,又符合铜矿石常见含量的包括铜金银铅锌钼铜镍等各类矿石的24个标准物质,以四硼酸锂-偏硼酸锂-氟化锂为混合熔剂,熔剂与样品质量比为30：1,以溴化锂为脱模剂,改进样品预处理方式,将通常采用样品预氧化后或熔融中加入脱模剂的方式,改进为加入脱模剂后再用混合熔剂完全覆盖的方法制备了高质量的熔融片,建立了XRF测定铜矿石中铜锌铅硅铝铁钛锰钙钾镁钼铋锑钴镍16种元素的分析方法。分析铜矿石国家标准物质GBW 07164、GBW 07169,各元素的精密度（RSD）为0.1%~5.4%。分析国家标准物质GBW 07163（多金属矿石）、GBW 07170（铜矿石）的测定值与标准值相符;分析实际铜矿石样品,铜锌铅钼铋锑钴镍的测试结果与电感耦合等离子体发射光谱法和其他方法的测定值相符。本文方法扩大了基体的适应性,提高了实际应用价值。  相似文献   

混合酸分解-电感耦合等离子体质谱法测定磷矿石中15种稀土元素   总被引：2，自引：2，他引：0       下载免费PDF全文

郭振华  何汉江  田凤英 《岩矿测试》2014,33(1):25-28

磷矿石中伴生的大量稀土,是继离子型稀土矿后重要的稀土后备资源。对磷矿石稀土元素分析测定方法的研究具有重要意义。本实验采用盐酸-硝酸-氢氟酸-硫酸体系消解、王水提取,建立了应用电感耦合等离子质谱法(ICP-MS)测定磷矿石中15种稀土元素的分析方法。经优化实验选取了合适的称样量以保证分析结果的准确可靠。选择合适的分析同位素及采用干扰校正方程以消除质谱干扰,利用103Rh为内标元素,有效抑制了分析信号的动态漂移,用于测定磷矿石国家标准物质中的15种稀土元素,方法的检出限为0.001~0.021μg/g,精密度均小于6.0%(n=12),加标回收率在95.7%~108.0%。适合推广运用于大批量磷矿石中稀土分量的快速分析  相似文献   

电感耦合等离子体发射光谱法测定磷矿石中磷镁铝铁   总被引：5，自引：1，他引：4       下载免费PDF全文

吴迎春  岳宇超  聂峰 《岩矿测试》2014,33(4):497-500

运用电感耦合等离子体发射光谱法(ICP-AES)分析磷矿石样品中的多元素,通常采用氢氟酸+盐酸+硝酸混合酸分解石样品,其中的氢氟酸是为了彻底分解地质样品中以硅酸盐形式存在的待测元素,但赶除氢氟酸的程序繁琐。本文在实际工作中发现,仅需测定磷矿石中的磷、镁、铝、铁元素时,可不加氢氟酸,四种元素的分析结果已能满足要求,这可能是与样品处理过程中生成的少量氢氟酸有关。为了验证不加氢氟酸的样品分解能力,采用浓硝酸-浓盐酸混合酸(体积比1∶1)加热分解试样,稀酸浸取,溶液冷却定容后直接用ICP-AES测定。分析结果显示溶样酸中是否含有氢氟酸,对磷、镁、铝、铁的测定结果不存在显著影响。方法检出限为磷100μg/g、镁0.3μg/g、铝20μg/g和铁6μg/g。经国家一级标准物质分析验证,方法精密度(RSD)小于5.0%,相对误差小于1.5%。本方法针对性强,分析快速准确,适用于实际工作中不包括钙和硅元素在内的磷矿石简项测定。  相似文献