首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
Five Belgian sedimentary rock reference materials have been prepared and distributed by the Geology, Petrology and Geochemistry Laboratory (Liège University, Belgium). Thirty-six laboratories participated in the international co-operative study. The individual data received from the participating laboratories are listed. Tables of compiled results are presented for major, minor and trace elements. These updated values are summarized into means, associated standard deviations, medians, and concentration ranges. "Recommended" (or proposed) values are presented.  相似文献   

2.
研制了霓霞正长岩,粗面岩,花岗闪长岩,辉长石,流纹岩及白云岩6种不同类型的岩石标准物质,对用X射线荧光光谱均匀性检验实际取样量进行了探讨,选择分析测试方法时,除采用了标准方法和长期应用的分析方法外,还采用了近年发展起来的新技术新方法,在定值中应用了多参数统计定值模式,给出了69个元素的标准值和参考值,该批标准物质于1991年1月经国家技术监督局审核批准为国家一级标准物质,编号分别为GBW07109  相似文献   

3.
4.
Nine rock reference samples "Sedimentary rock series" issued by the Geological Survey of Japan (GSJ) were analysed for up to 31 elements by neutron activation analysis (NAA); 14MeV-NAA for Si and Al, fission track method for U, radiochemical and instrumental NAA for rare-earth elements, and instrumental NAA for the remaining elements, with reactor neutrons for the latter three. The present results are compared with reported values.  相似文献   

5.
Six sedimentary rook types are proposed as geochemical standards: an arkosic sandstone, a quartzitic sandstone, a shale, a marl, a dolomitic limestone and an evaporite. Localities where these might be obtained are given, and alternative suggestions invited.  相似文献   

6.
We present new reference values for nineteen USGS, GSJ and GIT‐IWG rock reference materials that belong to the most accessed samples of the GeoReM database. The determination of the reference values and their uncertainties at the 95% confidence level follows as closely as possible ISO guidelines and the Certification Protocol of the International Association of Geoanalysts. We used analytical data obtained by the state‐of‐the‐art techniques published mainly in the last 20 years and available in GeoReM. The data are grouped into four categories of different levels of metrological confidence, starting with isotope dilution mass spectrometry as a primary method. Data quality was checked by careful investigation of analytical procedures and by the application of the Horwitz function. As a result, we assign a new and more reliable set of reference values and respective uncertainties for major, minor and a large group of trace elements of the nineteen investigated rock reference materials.  相似文献   

7.
Nine new rock reference samples of the "Sedimentary rock series", Chert JCh-1, Dolomite JDo-1, Lake sediment JLk-1, Limestone JLs-1, Stream sediments JSd-1 to JSd-3, and Slates JS1-1 and JSl-2 have been prepared by the Geological Survey of Japan(GSJ). Thirty major, minor and trace elements were determined using atomic absorption spectrometry, flame emission spectrometry, infrared absorption spectrometry and wet chemical techniques. The results of homogeneity tests showed that almost all elements, with a few exceptions, are considered to be distributed homogeneously in each reference sample.  相似文献   

8.
New Series of Rock and Sediment Geochemical Reference Materials   总被引:1,自引:0,他引:1  
Certified or reference values for sixty six to sixty seven elements and element oxides are given for geochemical reference materials recently prepared by the Institute of Geophysical and Geochemical Exploration (IGGE), including limestone (GSR-13), granitic gneiss (GSR-14), amphibolite (GSR-15), lake sediment (GSS-9) and stream sediments (GSD-1a, GSD-13, GSD-14). These samples supplement the GSR 1-6, GSD1-8 and GSD 9-12 certified reference materials already prepared and characterized by the IGGE.  相似文献   

9.
Two rock samples from the San Marcos Gabbro and the Lakeview Mountain Tonalite of the Southern California Batholith were prepared as U.S. Geological Survey reference samples. These samples were chosen to supply reference data for rocks having intermediate silica contents in the range of 45-60 percent. Unpublished data by members of the U.S. Geological Survey and some published data are summarized, and provisional estimates of the major and minor oxide and traceelement contents are given.  相似文献   

10.
A double‐spike method in combination with MC‐ICP‐MS was applied to obtain molybdenum (Mo) mass fractions and stable isotope compositions in a suite of sedimentary silicate (marine, lake, stream, estuarine, organic‐rich sediment, shales, slate, chert) and carbonate reference materials (coral, dolomite, limestones, carbonatites), and a manganese nodule reference material, poorly characterised for stable Mo isotope compositions. The Mo contents vary between 0.076 and 364 μg g?1, with low‐Mo mass fractions (< 0.29 μg g?1) found almost exclusively in carbonates. Intermediate Mo contents (0.73–2.70 μg g?1) are reported for silicate sediments, with the exception of chert JCh‐1 (0.24 μg g?1), organic‐rich shale SGR‐1b (36.6 μg g?1) and manganese nodule NOD‐A‐1 (364 μg g?1). The Mo isotope compositions (reported as δ98Mo relative to NIST SRM 3134) range from ?1.77 to 1.03‰, with the intermediate precision varying between ± 0.01 and ± 0.12‰ (2s) for most materials. Low‐temperature carbonates show δ98Mo values ranging from 0.21 to 1.03‰ whereas δ98Mo values of ?1.77 and ?0.17‰ were obtained for carbonatites CMP‐1 and COQ‐1, respectively. Silicate materials have δ98Mo values varying from ?1.56 to 0.73‰. The range of δ98Mo values in reference materials may thus reflect the increasingly important relevance of Mo isotope investigations in the fields of palaeoceanography, weathering, sedimentation and provenance, as well as the magmatic realm.  相似文献   

11.
The concentration of boron was determined in twenty one geochemical reference materials (silicate rocks) by isotope dilution inductively coupled plasma-mass spectrometry. Boron was extracted from the rocks using HF digestion, suppressing boron volatilisation through boron-mannitol complexation. Sample solutions, in a diluted HCl matrix, were analysed by ICP-MS without any separation of boron from the matrix elements. The results obtained were in agreement with the literature data and indicate that using the described procedure, trace amounts of boron can be very easily determined in complex matrices with rapidity and precision. With the instrumentation and reagents used in this study, this procedure can be used for the determination of 0.5 μg g−1 boron in a 15 0 mg silicate rock sample. Replicate analyses of the twenty one geochemical reference materials (GRM), ranging in boron concentration from 1.35 to 15 7 μg g−1, yielded precisions (relative standard deviation) varying between 0.9 and 9.8%.  相似文献   

12.
The zirconium content of six carbonate rock reference samples has been determined by a spectrophotometric method using xylenol orange after sample decomposition by acid digestion or alkali fusion. The interference of calcium was eliminated by adding the same concentration of calcium to the blank solution.  相似文献   

13.
A procedure for the determination of chlorine by the isotope dilution technique (ID) using negative thermal ionisation mass spectrometry (N-TIMS) is described. Silicate samples of about 10 mg were spiked and decomposed with hydrofluoric acid, and chlorine was isolated by precipitation of silver chloride after neutralisation with Ca(OH)2. The ammonical solution of AgCl was then subjected to N-TIMS. Replicate analyses of rock reference materials, typically of JB-1 and JR-1, demonstrated the high quality of the analyses (precision for Cl was ± 1-2%). We present here the most precise data sets of chlorine concentrations in nine igneous rock reference materials, three basalts (JB-1, JB-2, JB-3), two andesites (JA-3, AGV-1), two rhyolites (JR-1, JR-2) and two granodiorites (JG-3, GSP-1). The chlorine concentrations found ranged from 152 μg g-1 in AGV-1 to 1008 μg g-1 in JR-1. Our results presented here are partly (but not completely) in agreement with recommended values, where they are available. The N-TIMS ID technique can thus be used as a means of determining low chlorine contents in silicate materials to high precision.  相似文献   

14.
In this study the homogeneity of the zinc isotopic composition in the NIST SRM 683 reference material was examined by measuring the Zn isotopic signature in microdrilled sample powders from two metal nuggets. Zinc was purified using AG MP‐1M resin and then measured by MC‐ICP‐MS. Instrumental mass bias was corrected using the “sample‐standard bracketing” method and empirical external normalisation with Cu doping. After evaluating the potential effects of varying acid mass fractions and different matrices, high‐precision Zn isotope data were obtained with an intermediate measurement precision better than ± 0.05‰ (δ66Zn, 2s) over a period of 5 months. The δ66ZnJMC‐Lyon mean values of eighty‐four and fourteen drilled powders from two nuggets were 0.11 ± 0.02‰ and 0.12 ± 0.02‰, respectively, indicating that NIST SRM 683 is a good isotopic reference material with homogeneous Zn isotopes. The Zn isotopic compositions of seventeen rock reference materials were also determined, and their δ66Zn values were in agreement with most previously published data within 2s. The δ66Zn values of most of the rock reference materials analysed were in the range 0.22–0.36‰, except for GSP‐2 (1.07 ± 0.06‰, n = 12), NOD‐A‐1 (0.96 ± 0.03‰, = 6) and NOD‐P‐1 (0.78 ± 0.03‰, = 6). These comprehensive data should serve as reference values for quality assurance and interlaboratory calibration exercises.  相似文献   

15.
We present a concerted international effort to cross-calibrate five synthetic Th isotope reference materials (UCSC Th "A", OU Th "U", WUN, IRMM-35 and IRMM-36), and six rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2, USGS BHVO-2, LV18) using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). We then compare our new values with a compilation of literature mass spectrometric data for these reference materials and derive recommended "consensus"230Th/232Th values for each. We also present isotope dilution U and Th concentration data for four rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2).  相似文献   

16.
本文通过沉积岩系及其构造控制因素讨论,认为柯坪块隆在古生代属于塔里木克拉通拗陷的西北缘,其沉积演化和构造演化主要与塔里木地块近似。沉积岩系有两大类型:一是稳定台地相沉积;二是滨岸咸化泻湖相、河流相和山麓相沉积,柯坪块隆及其推覆体的出现主要是在二叠纪海西运动未期,起因于南天山冒地槽褶皱隆升导致的重力扩展作用而发生的构造变形。  相似文献   

17.
During the five-year period (April 1981 - March 1986), a series of fifteen rock reference samples, "Igneous rock series", has been prepared by the Geological Survey of Japan (GSJ). Based on the data available (published and communicated), consensus values for major, minor and trace elements have been derived; these values are presented for this second series of samples as well as for the first series of two samples, Granodiorite JG-1 and Basalt JB-1.  相似文献   

18.
四川冕宁前寒武纪重晶石岩的热水沉积特征及其矿床成因意义倪志耀,莫怀毅(成都理工学院,成都610059)(四川地矿局一○九队,四川冕宁615602)关键词重晶石岩,热水沉积,前寒武纪,四川冕宁热水沉积成岩成矿是近二十年来逐渐认识的一种新的成岩成矿作用,...  相似文献   

19.
A micropaleontological analysis was made using materi-als from exploration wells Geobuk-1 (Td:2 72 2 .5m) andOkdom-1 (Td:2 90 3 .7m) for the purpose of biostratigraphicand paleoenvironmental interpretation of the Cheju sedimenta-ry basin.Two wells yield relatively abundant microfossilssuch as dinoflagellates,calcareous nannofossils,pollen andspores.The biostratigraphic and paleoenvironmental settingsanalyzed by microfossil assemblages seem to be closely relatedto the framework of the local t…  相似文献   

20.
We have measured 87Sr/86Sr and 143 Nd/144 Nd isotope ratios in different batches and aliquots of the new US Geological Survey (USGS) reference materials (RMs) BCR-2, BHVO-2, AGV-2 and GSP-2 and the original USGS RMs BCR-1, BHVO-1, AGV-1 and GSP-1 by thermal ionisation mass spectrometry. In addition, we also analysed the eight Max-Planck-Institut-Dingwell (MPI-DING) reference glasses. Nearly all isotope ratios obtained in the different aliquots and batches agree within uncertainty limits indicating excellent homogeneity of the USGS powders and the MPI-DING glasses. With the exception of GSP-2, the new USGS RMs are also indistinguishable from the ratios found in the original USGS RMs (87Sr/86Sr: 0.704960, 0.704958 (BCR-1, -2), 0.703436, 0.703435 (BHVO-1, -2), 0.703931, 0.703931 (AGV-1, -2); 143 Nd/144 Nd: 0.512629, 0.512633 (BCR-1, -2), 0.512957, 0.512957 (BHVO-1, -2); 0.512758, 0.512755 (AGV-1, -2)). This means that for normalisation purposes in Sr and Nd isotope geochemistry BCR-2, BHVO-2 and AGV-2 can well replace BCR-1, BHVO-1 and AGV-1 respectively.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号