兖州矿区山西组 3煤层中微量元素的特征分析   总被引：7，自引：2，他引：7  

刘桂建  杨萍玥  彭子成  王桂梁 《地球化学》2003,32(3):255-262

通过对兖州矿区山西组3煤层21个样品中全硫、硫化物硫、有机硫和具有环境意义的微量元素Cu、Pb、Zn、As、U、Th含量的测试，分析了微量元素在研究区煤层垂直方向上的变化特征及主要形成原因，并发现煤层中所选的微量元素、硫化物琉及全硫在煤层顶、底或煤层夹矸样品中含量相对较高。微量元素与硫化物硫、全硫的相关系数表明，所研究的微量元素与硫化物硫和全硫有明显的正相关关系，而且研究区3煤层中全硫的含量取决于硫化物硫的含量。同时还研究了原煤中微量元素的含量与灰产率的关系，并将研究区微量元素同世界和中国同类煤中的微量元素的含量进行了比较。  相似文献   

The Role of Organic Matter During Metal Enrichment in Permian Kupferschiefer of the Rudna Mine,Southwest Poland     

孙玉壮  WILHELM PüTTMANN 《中国地球化学学报》2003,22(1):1-10

The bulk composition of organic matter and saturated and aromatic hydrocarbons extracted from 16 samples collected from two Kuperschiefer profiles in the Rudna mine,Southwest Poland has been analyzed to study the role of organic matter during base metal enrichment in the Kupferschiefer shale.The results indicated that the extract yields and saturated hydrocarbon yields decreased with increasing base metal contents.GC and GC/MS analyses indicated that n -alkanes and alkylated aromatic compounds were depleted and may have served as hydrogen donators for thermochemical sulfate reduction.The enrichment of base metal is closely connected with the destruction of hydrocarbons.  相似文献   

内蒙古白云鄂博矿区富钾板岩的热水沉积成因特征   总被引：3，自引：1，他引：3  

肖荣阁  史淑玲  安国英  张汉成  费红彩 《现代地质》2003,17(3):281-286,T005,T006

通过对白云鄂博富钾板岩的岩石学、矿物学及岩石化学的研究,提出富钾板岩是一种热水沉积钾长石岩的认识。富钾板岩是白云鄂博矿区的一种重要岩性,与上下岩层呈不规则层状或夹层产出,致密状微晶或隐晶质结构。其中钾长石含量在80%以上,X射线衍射分析表明其2θ(2-01)=21 00,2θ(060)=41 800,2θ(2-04)=50 560,求得三斜度Δ=0 91,有序度δ=0 89,属于典型的低钠、低温、有序最大的微斜长石,微斜长石成分占98%以上。岩石中富含微量元素B、F、Sr、Ba,平均质量分数分别为26×10-6、3386×10-6、119×10-6和1735×10-6,结合X射线衍射分析表明微斜长石中有冰长石成分。稀土元素以轻稀土富集、重稀土亏损、个别出现正铕异常为特征。根据热水流体中钾浓度与温度的相关性及热水沉积、交代和充填物中经常出现钾长石矿物,分析认为白云鄂博矿区出现的富钾板岩是热水沉积钾长石岩,其形成于火山期后的溶液活动阶段。  相似文献   

单道扫描电感耦合等离子体发射光谱法测定珊瑚礁中主量和微量元素   总被引：1，自引：0，他引：1       下载免费PDF全文

林学辉  刘昌岭 《岩矿测试》2003,22(3):225-227

建立了用单道扫描电感耦合等离子体发射光谱法测定珊瑚礁中主量和微量元素的方法。珊瑚礁样品经酸溶解后,直接进行Ca、Mg、K、Na、V、Sr、Ba、Co、Ni、Pb、Li、Rb的测定,方法检出限为0.0004～0.1mg/L,精密度RSD<5%(n=6),样品的加标回收率为97%～105%。测定w(CaO)为50%的样品,结果与传统的EDTA容量法相符。方法经碳酸盐岩石国家一级标准物质验证可行,已用于大批量的珊瑚礁样品的测定。  相似文献   

流体包裹体方法在油气源追踪对比中的应用——以四川盆地碳酸盐岩大型气田为例   总被引：14，自引：4，他引：14  

陶士振张宝民  赵长毅 《岩石学报》2003,19(2):327-336

本文运用流体包裹体方法，基于薄片观察和岩矿学研究，探讨了四川盆地碳酸盐岩大型气田的气源。首先对包裹体的生源属性、多期捕获和后生变化进行了精细的鉴别分析。在此基础上，通过成岩自生矿物微量元素、包裹体相组成、均一温度、初熔温度等参数鉴别多期演化的油气充注。通过烃类包裹体化学成分初步鉴别出煤成气和油型气。根据烃类包裹体的相组成鉴别有机质可能来源于腐泥型源岩还是腐殖型源岩。最后根据同期包裹体生物标志物确定某一期次的油气所对应的烃源层。结果表明研究成果符合地质实际，为传统的油气源追踪对比研究提供了一个重要有效的辅助方法。  相似文献   

底质不连续面类型、成因及遗迹学特征     

齐永安  徐华山 《地质科技情报》2003,22(1):41-46

底质不连续面是沉积作用中断时所形成的一种地层界面。根据底质的粘结程度可将底质不连续面划分为两大类：固底不连续面和硬底不连续面。固底不连续面中的简单停积面依靠沉积序列的变化来识别，界面上、下的生物地层带是连续的；而复成停积面上、下的生物地层带不连续。在硬底不连续面中，硬底的上、下地层属于同一个沉积体系，而继承性岩底的上、下地层则属于不同的沉积体系，其间发生过重大的沉积间断。根据底质控制的Glossifungites遗迹相和Trypanites遗迹相可以有效地识别各类不连续面并解释其成因。三种类型的不连续面具有层序地层学意义：①侵蚀性不连续面，包括低水位侵蚀面（LSE）和海进侵蚀面（TSE）；②无沉积间断面；③沉积性不连续面（凝缩段）。  相似文献   

Laser Ablation ICP-MS Analysis of Geological Materials Prepared as Lithium Borate Glasses   总被引：9，自引：0，他引：9  

Stephen M. Eggins 《Geostandards and Geoanalytical Research》2003,27(2):147-162

A simple, rapid and precise method is described for determining trace elements by laser ablation (LA)-ICP-MS analysis in bulk geological materials that have been prepared as lithium borate glasses following standard procedures for XRF analysis. This approach reliably achieves complete sample digestion and provides for complementary XRF and LA-ICP-MS analysis of a full suite of major and trace elements from a single sample preparation. Highly precise analysis is enabled by rastering an ArF excimer laser (λ= 193nm) across fused samples to deliver a constant sample yield to the mass spectrometer without inter-element fractionation effects during each analysis. Capabilities of the method are demonstrated by determination of twenty five trace elements (Sc, Ti, V, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba, REE, Hf, Ta, Pb, Th and U) in a diverse range of geological reference materials that includes peridotites, basalts, granites, metamorphic rocks and sediments. More than 90% of determinations are indistinguishable from published reference values at the 95% confidence level. Systematic bias greater than 5% is observed for only a handful of elements (Zr, Nb and U) and may be attributed in part to inaccurate calibration values used for the NIST SRM 612 glass in the case of Zr and Nb. Detection limits for several elements, most notably La, are compromised at ultra-trace levels by impurities in the lithium borate flux but can be corrected for by subtracting appropriate procedural blanks. Reliable Pb analysis has proved problematic due to variable degrees of contamination introduced during sample polishing prior to analysis and from Pt-crucibles previously used to fuse Pb-rich samples. Scope exists for extending the method to include internal standard element/isotope spiking, particularly where integrated XRF analysis is not available to characterise major and trace elements in the fused lithium borate glasses prior to LA-ICP-MS analysis.  相似文献   

A Reappraisal of Rb, Y, Zr, Pb and Th Values in Geochemical Reference Material BHVO-1     

William J. Chazey III  Clive R. Neal  Jinesh C. Jain  William S. Kinman 《Geostandards and Geoanalytical Research》2003,27(2):181-192

The geochemical reference material BHVO-1 was analysed by a variety of techniques over a six year period. These techniques included inductively coupled plasma-mass spectrometry and atomic emission spectroscopy (ICP-MS and ICP-AES, respectively), laser ablation ICP-MS and spark source mass spectroscopy. Inconsistencies between the published consensus values reported by Gladney and Roelandts (1988, Geostandards Newsletter) and the results of our study are noted for Rb, Y, Zr, Pb and Th. The values reported here for Rb, Y, Zr and Pb are generally lower, while Th is higher than the consensus value. This is not an analytical artefact unique to the University of Notre Dame ICP-MS facility, as most of the BHVO-1 analyses reported over the last ten to twenty years are in agreement with our results. We propose new consensus values for each of these elements as follows: Rb = 9.3 ± 0.2 μg g-1 (compared to 11 ± 2 μg g-1), Y = 24.4 ± 1.3 μg g-1 (compared to 27.6 ± 1.7 μg g-1), Zr = 172 ± 10 μg g-1 (compared to 179 ± 21 μg g-1), Pb = 2.2 ± 0.2 μg g-1 (compared to 2.6 ± 0.9 μg g-1) and Th = 1.22 ± 0.02 μg g-1 (compared to 1.08 ± 0.15 μg g-1).  相似文献   

富水水库中微生物成因的显微针铁矿及其对微量元素的富集   总被引：3，自引：0，他引：3       下载免费PDF全文

车遥  胡宝林  夏林  孙振亚  王利忠 《地球学报》2003,24(2):161-166

通过对湖北省富水水库坝基渗漏水及其析出物的研究，探讨了现代沉积环境（水库）中显微铁矿物形成的机理及微生物在铁的生物矿化中的作用和意义。对析出物中微量元素的富集特征也进行了初步研究。用化学分析方法测试出坝基渗漏水中阳离子以Ca^2 、Mg^2 、K^ 、Na^ 为主，Fe^2 和Fe^3 含量极少，阴离子以HCO3^-为主。析出物的化学成分以铁的氧化物为主。采用X射线衍射、差热分析、红外光谱和穆斯堡尔谱，以及透射电镜和扫描电镜等测试手段，分析研究了析出物的物相和形貌特征。析出物的主要矿物相为针铁矿、石英、伊利石、蒙脱石和微量方解石，呈弱结晶状态。由析出物中显微针铁矿特殊的形貌特征及其特征的穆斯堡尔谱图推测出富水水库沉积环境中显微针铁矿是由铁细菌形成。ICP－MS测试测试结果表明，析出物中不仅富集了铁，还富集了Yb、Pb、Dy、Zn、Co、Be、Eu、Sm和Tb等微量元素。微量元素的富集是微生物与显微针铁矿共同作用的结果。  相似文献   

河北省黄壁庄水库坝基渗漏单井示踪试验研究     

杜国平  董巧云  冷元宝  崔琳 《地球物理学进展》2003,18(3):395-399

以河北省黄壁庄水库副坝坝基的渗漏塌坑为例，利用“九五”国家重点科技成果推广项目“智能化地下水动态参数测量仪”在天然流场下，测量出水库自然渗漏量地下水的渗透流速流向、垂直向流速流向，每米含水层的渗透系数等工程必须的水文地质参数。确定性地诊断和检测出黄壁水库坝基渗漏隐患出现的具体位置和高程，从而为大坝的渗漏处理和安全处理提供详细的现场测量数据。  相似文献