Simplified coupled chemo‐mechanical modeling of cement pastes behavior subjected to combined leaching and external sulfate attack     

B. Bary 《国际地质力学数值与分析法杂志》2008,32(14):1791-1816

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铜锡复合成矿研究进展与展望     

李欢  吴经华  孙文博  刘飚 《地质学报》2023,97(1):262-277

铜与锡具有不同的地球化学性质,然而铜锡共生或复合成矿现象在世界主要铜、锡成矿带中比较常见,如中国的右江、南岭(湘南)、大兴安岭南段(内蒙东部)、葡萄牙伊比利亚、秘鲁安第斯、英格兰德文郡、德国厄尔士山、日本西南、俄罗斯远东、加拿大新不伦瑞克等成矿带均为铜锡复合矿床的集中产区。铜锡复合矿床主要为岩浆热液矿床,以矽卡岩型、脉状矿床为主,兼有火山热液沉积型、斑岩型及云英岩型等。铜矿体的主要矿石矿物为黄铜矿,兼有斑铜矿、黝铜矿、辉铜矿等;锡矿体的主要矿石矿物为锡石,兼有黝锡矿。铜锡复合矿床的成矿物质来源(尤其是铜、锡成矿元素的来源是否具有一致性)尚有不少争议,锡普遍被认为是岩浆来源,而铜的来源具有多样性。成矿流体演化过程中的氧化还原环境的改变及流体的混合是导致铜锡复合成矿的主要原因。目前对于铜锡复合成矿的研究,主要是从矿床的年代学、单矿物(黄铜矿、锡石)微量元素及传统同位素地球化学、流体包裹体等方面入手,但对厘定铜锡复合成矿过程的作用有限。铜锡复合矿床的成因及勘查模型的建立具有重要的理论价值及现实意义。本文提出未来研究可以从多种非传统稳定同位素(例如Cu、Sn、W、Zn同位素)的联合示踪探索、成...  相似文献   

内蒙古拜仁达坝及维拉斯托银多金属矿床的硫和铅同位素研究   总被引：10，自引：3，他引：7  

江思宏  聂凤军  刘翼飞  云飞 《矿床地质》2010,29(1):101-112

拜仁达坝和维拉斯托是近年来在内蒙古东部地区发现的2个大型银多金属矿床,文章对其开展了硫和铅同位素研究。结果表明,拜仁达坝矿床矿石中硫化物的δ34S值为-4.0‰～+1.6‰,维拉斯托矿床矿石中硫化物的δ34S值为-0.8‰～+2.0‰,与岩浆热液型矿床的硫同位素值接近,表明这2个矿床中的硫主要来自岩浆。拜仁达坝矿区43件金属硫化物的206Pb/204Pb值为18.333～18.515,207Pb/204Pb值为15.532～15.656,208Pb/204Pb值为38.057～38.610;维拉斯托矿区20件金属硫化物的206Pb/204Pb值为18.304～18.377,207Pb/204Pb值为15.520～15.610,208Pb/204Pb值为38.112～38.435。拜仁达坝东矿区矿石中的铅同位素组成与维拉斯托矿区相似,变化范围小,相对贫放射性铅同位素,并且均为混合铅。矿石中的铅可能来自围岩地层及深源岩浆。  相似文献   

粤北302铀矿床同位素地球化学研究   总被引：11，自引：1，他引：10  

沈渭洲  凌洪飞  邓平  朱捌  黄国龙  谭正中 《铀矿地质》2010,26(2):80-87

位于粤北诸广山岩体东南部的302铀矿床是我国规模较大、埋藏较深的花岗岩型铀矿床之一。该矿床产于印支期油洞岩体和燕山早期长江岩体的断裂蚀变带内,矿区内NWW向基性岩脉十分发育,矿体呈似脉状、扁豆状或透镜状。同位素研究表明,矿石的沥青铀矿Sm-Nd和U-Pb等时线年龄（70 Ma）与油洞岩体（232 Ma）、长江岩体（160 Ma）的年龄相差巨大;主成矿期成矿流体的δDH2O值为-65‰～-82‰（平均为-75‰）,δ18OH2O值为6.8‰～0.6‰（平均为3.9‰）,反映出成矿流体主要由地幔流体组成;方解石的δ13C值为-8.4‰～-5.3‰,表明矿化剂ΣCO2也来自地幔;矿区内辉绿岩的（87Sr/86Sr）i值为0.70861～0.70882,花岗岩的（87Sr/86Sr）i值为0.73519～0.77152,萤石的（87Sr/86Sr）i值为0.71474～0.71697,表明成矿组分Sr可能来源于基性脉岩（幔源）与赋矿花岗岩体（壳源）,并呈不同程度的混合,而主成矿组分铀主要来源于赋矿花岗岩体。  相似文献   

地质钻探中的井漏及堵漏材料研究     

毛洪江 《西北地质》2010,43(3):141-146

通过对钻探过程中井漏的复杂地质因素分析,提出了水化膨胀复合材料体系,并对该体系进行了膨胀性、封堵性及复合桥接堵漏模拟实验。实验结果表明,堵漏材料PAR具有很强的吸水膨胀性能,可膨胀至原体积的几十倍,且时间快有利于形成快速的封堵。材料PAR与稻谷和锯末形成的复合堵漏材料具有很强的堵塞率,可达70%以上。承压堵漏测量装置中测试表明:复合堵漏体系不仅能形成封堵,而且能够承受一定的压差。在云南临仓市勐简乡铅锌矿钻探过程中,运用复合堵漏体系满足了该地区复杂地矿钻探需要。  相似文献   

Evaluation of a Quality Control Monitor Material for the Routine Electron Probe Microanalysis of Kimberlite Exploration Garnets     

Deon De Bruin 《Geostandards and Geoanalytical Research》2010,34(3):257-264

Election probe microanalysis of indicator minerals is extensively used in the exploration for kimberlite deposits, the evaluation of specific kimberlite occurrences for their diamond bearing potential and to classify grains into different chemical and lithological mantle associations. Kimberlite exploration programmes can involve several tens of thousands of indicator mineral analyses. Procedures for monitoring data quality and consistency of analyses across large data sets are commonly absent. Suitable monitor minerals should be used to verify the data quality of kimberlite exploration and evaluation data sets. This material should have a suitable composition, be homogenous, be available in sufficient quantities and have a similar appearance to the unknown samples. Garnet P1, a megacryst garnet from the Premier kimberlite, was found to have a suitable composition as a monitor for kimberlite garnet analyses. Data were collected on the monitor material at regular intervals during routine analyses, over an extended period, both as a fixed grain mounted on the sample holder and as separate grains set within batches of routine samples. The data were evaluated to assess the quality and consistency in the analyses of large data sets over time. The monitor material was also analysed at independent laboratories using their routine analytical set-up and calibration procedures for comparative purposes. Values are given for the mean ± 2s range, which can serve as guide values for acceptable analyses for all elements.  相似文献   

GGR Biennial Review: Atomic Absorption,Inductively Coupled Plasma-Atomic Emission Spectrometry,Neutron Activation Analysis and X-Ray Fluorescence Spectrometry Review for 2008–2009     

L. Paul Bédard  Kathryn L. Linge 《Geostandards and Geoanalytical Research》2010,34(4):343-352

This review describes developments major and in trace element determination using atomic absorption spectroscopy (AAS), inductively coupled plasma-atomic emission spectrometry (ICP-AES), instrumental neutron activation analysis (INAA), and X-ray fluorescence (XRF) spectrometry that were reported in 2008 and 2009. Publication levels were comparable to those of previous years, except for XRF which showed an increase in the number of articles published in the past 2 years. In terms of number of publications and impact, the most active field was AAS, while INAA was the least active. As expected for well-established and mature methods, novel developments for all four analytical techniques were relatively sparse. For AAS, the most notable publications concerned developments in sample introduction, particularly focussing on solid samples, increasing analyte sensitivity, and higher sample throughput. For ICP-AES, publication of developments in sample introduction, remediation of matrix effects and calibration continues. Compared with past years, there was a clear focus on sample preconcentration methods, but very few publications reporting new hyphenated speciation methods. For INAA, there were several publications exploring the accuracy and robustness of the method, as well as the requirements for INAA to meet criteria for a primary method of measurement. Two other related techniques, delayed neutron activation analysis, and prompt gamma activation analysis, were also described. Hyphenated XRF techniques showed interesting developments in enabling XRF and XRD analysis on the same spot, and further work characterising and calibrating three-dimensional micro-XRF shows promising results for investigating sample heterogeneity.  相似文献   

Accurate and Precise Elemental Abundance of Zinc in Reference Materials by an Isotope Dilution Mass Spectrometry TIMS Technique     

Osama Y. Ghidan  Robert D. Loss 《Geostandards and Geoanalytical Research》2010,34(2):185-191

A thermal ionisation mass spectrometric technique enabled the abundance of Zn in geological and biological reference materials and water samples to be measured by double spiking isotope dilution mass spectrometry enriched in the ⁶⁷Zn and ⁷⁰Zn isotopes. In the past, thermal ionisation mass spectrometry proved to be difficult for low-level zinc isotopic measurements. The size of Zn samples used for isotopic determination, in particular the biological RMs, represents an important breakthrough. These results represent the most accurate and precise concentrations measured for Zn in these samples. The maximum fractional uncertainty was that for TILL-3 (2%), while the minimum fractional uncertainty was 0.7% for both BCR-1 and W-2. The inhomogeneity of Zn in HISS-1 was revealed while other reference materials appeared homogeneous at the 95% confidence uncertainty. The certified concentration of Zn in HISS-1 and IMEP-19 by their producers are 28% and 3.8% higher than the values measured in this work. These are the first Zn concentration measurements in these materials by the isotope dilution-TIMS technique, except for BCR-1, NIES N^o 9 and IMEP-19. Reducing the blank enabled accurate measurement in water at the ng g^-1 level demonstrating the applicability of the technique for low-level Zn samples.  相似文献   

Sulfur Concentration in Geochemical Reference Materials by Solution Inductively Coupled Plasma‐Mass Spectrometry     

Monica E. Erdman  Cin‐Ty A. Lee  Wenbo Yang  Lynn Ingram 《Geostandards and Geoanalytical Research》2014,38(1):51-60

With implications for the origin of ore deposits, redox state of the atmosphere, and effects of volcanic outgassing, understanding the sulfur cycle is vital to our investigation of Earth processes. However, the paucity of sulfur concentration measurements in silicate rocks and the lack of well‐calibrated reference materials with concentrations relevant to the rocks of interest have hindered such investigations. To aid in this endeavour, this study details a new method to determine sulfur concentration via high mass resolution solution inductively coupled plasma‐mass spectrometry (ICP‐MS). The method is based on an aqua regia leach, involving relatively rapid sample preparation and analysis, and uses small test portion masses (< 50 mg). We utilised two independently prepared standard solutions to calibrate the analyses, resulting in 4% accuracy, and applied the method to eight geochemical reference materials. Measurements were reproducible to within ~ 10%. Sulfur concentrations and isotopes of six reference materials were measured additionally by elemental analyser‐combustion‐isotope ratio mass spectrometry to independently evaluate the accuracy of the ICP‐MS method. Reference materials that yielded reproducible measurements identical to published values from other laboratories (JGb‐1, JGb‐2 and MAG‐1) are considered useful materials for the measurement of sulfur. Reference materials that varied between studies but were reproducible for a given test portion perhaps suffer from sample heterogeneity and are not recommended as sulfur reference materials.  相似文献   

Precise and Accurate In Situ Determination of Lead Isotope Ratios in NIST,USGS, MPI‐DING and CGSG Glass Reference Materials using Femtosecond Laser Ablation MC‐ICP‐MS     

Chen Kaiyun  Yuan Honglin  Bao Zhian  Zong Chunlei  Dai Mengning 《Geostandards and Geoanalytical Research》2014,38(1):5-21

Lead isotope ratio data were obtained with good precision and accuracy using a 266 nm femtosecond laser ablation (fLA) system connected to a multi‐collector ICP‐MS (MC‐ICP‐MS) and through careful control of analytical procedures. The mass fractionation coefficient induced by 266 nm femtosecond laser ablation was approximately 28% lower than that by 193 nm excimer laser ablation (eLA) with helium carrier gas. The exponential law correction method for Tl normalisation with optimum adjusted Tl ratio was utilised to obtain Pb isotopic data with good precision and accuracy. The Pb isotopic ratios of the glass reference materials NIST SRM 610, 612, 614; USGS BHVO‐2G, BCR‐2G, GSD‐1G, BIR‐1G; and MPI‐DING GOR132‐G, KL2‐G, T1‐G, StHs60/80‐G, ATHO‐G and ML3B‐G were determined using fLA‐MC‐ICP‐MS. The measured Pb isotopic ratios were in good agreement with the reference or published values within 2s measurement uncertainties. We also present the first high‐precision Pb isotopic data for GSE‐1G, GSC‐1G, GSA‐1G and CGSG‐1, CGSG‐2, CGSG‐4 and CGSG‐5 glass reference materials obtained using the femtosecond laser ablation MC‐ICP‐MS analysis technique.  相似文献