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1.
A dunite reference material has been prepared as part of the reference materials programme at the National Geophysical Research Institute, Hyderabad, India. The scarcity of reference materials for undertaking the chemical analysis of ultramafic rocks for major and trace elements justified the preparation of such a rock reference material. A 300 kg sample of starting material was collected from an active quarry near the town of Salem in Tamil Nadu, southern India. The sample was homogenized and an invitation for round robin participation was published in Geostandards Newsletter (October 1995). A total of twenty seven international laboratories participated in the study, providing information on the total element concentration of major, minor, trace and rare earth elements. Following data compilation, outlier rejection, and statistical analysis, proposed and indicative total element concentrations are reported for twenty four elements.  相似文献   

2.
地球化学与环境样品分析标准物质和GeoReM数据库   总被引:7,自引:5,他引:2  
在地球化学和环境样品分析中,标准物质发挥着越来越重要的作用。尽管通常要求分析者必须提供量值溯源的测量过程的信息;但大多数论著都未给出标准物质的数据。文章强调标准物质在地球化学分析工作中的重要性,同时将地球化学与环境样品分析标准物质数据库GeoReM介绍给中国的地质分析工作者。GeoReM数据库收录了1880个地球化学和环境样品分析标准物质的定值数据、汇编数据、分析数据及其他相关信息,其中包括156个由中国制备的标准物质的数据。GeoReM数据库还给出了所收录标准物质推荐使用的首选值及其不确定度。尽管这些首选值大多都不是按照国际标准化组织的有关规定而确定的,但是它们的置信度高,因而被广泛应用于仪器校准和分析数据的质量监控。文章还指出要将中国研制的、发表在中文期刊上的标准物质也收录到GeoReM数据库中,这对于促进中国的相关研究,增加国际认可度具有重要意义。  相似文献   

3.
A total of twenty-five bibliographic reviews were published between 1979 and 2004 in Geostandards Newsletter, subsequently renamed Geostandards and Geoanalytical Research, which list more than 5500 papers. These cited references contain information about geochemical reference materials, analytical methods or address general issues concerning the use of reference materials (protocols for sampling, certification, or new analytical techniques). In support of emerging fields of interest in geoanalysis, frequently associated with environmental research, and reflecting the increased breadth in the topics addressed by the Journal, new reference headings were added over time, while retaining the original style and format of the review. Reference management software was used to extract information from these publications related to methods, reference materials and analytes. Major developments during these 25 years, reflecting both advances in laboratory hardware as well as shifts in research interests, can readily be seen in both the types of reference materials being studied and in nature of the new analytical protocols that were developed. These two topics were the core foci of the twenty-five reviews, though much more information might also be extracted from this extensive resource.  相似文献   

4.
We report a new approach to conduct fast and accurate lithium isotope ratio measurements by MC-ICP mass spectrometry after wet chemical sample preparation. In contrast to most previously published methods our MC-ICP-MS set-up did not use a desolvating system to achieve appropriate ion beam intensities and, therefore, was less affected by matrix-induced shifts of the instrumental mass bias. As the total lithium background and build-up in the sample introduction system was low, previous sample residues could be washed out by an extended uptake of the new sample. Elimination of a nitric acid rinse step increased the sample throughput by a factor of two and allowed the instrumental mass bias drift to be tracked more precisely. δ7Li values of powdered silicate rock reference materials and seawater obtained in this study revealed good accuracy and an overall analytical uncertainty of typically 0.5‰ (2s). On the basis of a comparison between our lithium isotope data and compiled literature data, we recommend preliminary average δ7Li values for seawater (+30.8‰) and several silicate rock reference materials (BHVO-1: +5.0‰; JA-1: +5.6‰; JB-2: +4.8‰). The compilation of published δ7Li values for seawater suggests that the observed large lithium isotope differences are due to inter-method and/or interlaboratory bias. Most recently published δ7Li values for seawater show little variation and confirm a constant lithium isotope composition (at the sub ‰ level) of seawater in well mixed ocean basins.  相似文献   

5.
New concentrations for Au, Ir and Ag obtained by instrumental neutron activation analysis are presented for seventy geochemical reference materials. Results in agreement with literature values for Au and Ir down to concentrations of a few ng g−1 were obtained. For Au and Ir concentrations above 10 ng g−1, the repeatability of replicate analyses of reference materials was mostly better than 10%. For concentrations between 1 and 10 ng g−1 the RSD for Ir was 10–30%, whereas for Au it was higher and more variable (20–50%). In addition, concentrations for Cd and Hg are presented for some of the same reference materials. The high RSD at relatively high concentrations seen in gold for some RMs (e.g., WMG-1, WMS-1) did not exist for Ir and suggests homogeneity for this platinum-group element at the sub-sample size used in this study. For the following eight RMs, mostly ultramafic rocks (CHR-Pt+, OREAS-13P, OREAS-14P, PCC-1, UMT-1, WMG-1, WMS-1, WPR-1), Ir measurements agreed within ± 10% of mostly certified or recommended concentrations, which ranged from 2 ng g−1 to 6 μg g−1. For the reference material UB-N, iridium concentration compared favourably to published results obtained by isotope dilution ICP-MS methods and a previously unrecognised heterogeneity is inferred for Au, Hg and Sb, but not for the other measured elements.  相似文献   

6.
A properly developed consensus from a proficiency test is, for all practical purposes, interchangeable with a certified value derived from an interlaboratory comparison. But some scientists have doubts about the metrological status of such values. In particular, the materials are not regarded as equivalent to certified reference materials (CRM) because of a lack of traceability of the consensus value. However, the detailed considerations in this study show that such a distinction is without foundation. The following issues are addressed. (a) Misgivings about the traceability of an interlaboratory consensus are found to be insubstantial because chemical measurements are hardly ever fully traceable. (b) Reproducibility (i.e., interlaboratory) conditions account for all sources of variation in results other than long‐term stability, so lead to a valid estimate of uncertainty. (c) Certification of a reference material according to ISO procedures is homologous with a proficiency test and no more secure against bias in the characterised value and its standard error. In particular, residual (common) bias cannot be fully addressed in either approach. (d) A consensus in itself attests to a valid outcome. (e) Proficiency test providers have access to a powerful method of monitoring long‐term stability that is denied to CRM producers.  相似文献   

7.
海泡石化学成分分析标准物质研制   总被引:2,自引:0,他引:2  
海泡石是一种十分重要的非金属矿,被广泛应用于航空、畜牧、化工环保等领域中,贸易活动十分活跃。鉴于中国一直没有海泡石标准物质,国际上的海泡石标准物质定值组分少,为了满足相关研究需求,本文研制了湖南湘潭的海泡石标准物质(GBW07138)。对Ba、Be、Bi、Cd、Ce、Co、Cr、Cs、La、Li、Lu、U、Nb、Nd、Ni、Pb、SiO2、Al2O3、Fe2O3、MgO、CaO、Na2O、K2O、TiO2共24种组分进行均匀性和稳定性检验。针对不同含量、不同性质的组分,采用合理的国家标准方法检验了20种组分的RSD小于3%,其余4种组分Bi、La、Lu、Mo的RSD略大于3%,方差检验的F值均小于列表临界值[F0.05(29,60)=1.65],表明该标准物质均匀性良好。在稳定性考察期内,24种组分的含量无统计学上的明显变化,表明该标准物质稳定性良好。由9家实验室采用重量法、容量法、X射线荧光光谱法、电感耦合等离子体质谱法等传统化学分析方法和现代仪器分析方法协作定值,最终定值组分63种,涵盖了主量、微量及全部稀土元素,其中海泡石特征组分MgO和烧失量(LOI)的含量分别为18%±0.2%和8.55%±0.19%,这两种组分与现有的标准物质形成一定阶梯性,能够更好地满足海泡石成分分析测试需求。该海泡石标准物质可用于地质找矿、地球化学调查、地质矿产产品测试以及其他行业相关领域样品测试的质量监控标准。而且在研制该标准物质过程中,改良或开发的一些新方法可为后续开发海泡石标准物质提供技术支持。  相似文献   

8.
研制的黄铁矿、黄铜矿、方铅矿和闪锌矿4个标准物质是国内首次成功研制的硫化物矿物成分分析标准物质。样品采用重选、磁选和电磁选等选矿技术提纯矿物,获得纯度大于95%的单矿物样品。黄铁矿和闪锌矿用棒磨机少量多级粉碎至0.147mm,方铅矿和黄铜矿用小型玛瑙球磨机粉碎至0.097mm。经单因素方差分析检验,均匀性符合要求。采用小包装在干燥、充氩气气氛中保存样品,使样品稳定性有足够保证。连续4年定期监测了样品中全硫含量,证明稳定性良好。样品由国内经计量认证的5家实验室采用多种分离富集手段、不同原理方法协同分析。标准值的确定依据数据分布特征而定,对于服从正态分布的元素,用算术平均值作为定值,对不服从正态分布的元素用多参数模式定值。共确定了56个标准值,16个参考值,6个信息值。该批标准物质于1994年12月通过了国家标准物质研究中心组织的专家复审,并于1995年4月被国家技术监督局批准为国家一级标准物质,标准号分别为GBW07267(GSM-1)、GBW07268(GSM-2)、GBW07269(GSM-3)、GBW07270(GSM-4)。  相似文献   

9.
In this study, the Cd isotopic composition of various geological reference materials and anthropogenic samples was investigated. The measurements were made by multicollector ICP-MS and instrumental mass fractionation was controlled using a "sample-standard bracketing" technique. Cadmium isotopic data are reported relative to an internal Cd solution (Cd Spex) and expressed as the 114 Cd/110Cd delta value. Two other Cd solutions (Prolabo and JMC) were analysed and yielded the same 0% delta value. A fractionated Cd metal sample (Münster Cd) was used as a secondary reference material for Cd isotopic measurements and we obtained a 114 Cd/110 Cd delta value of 4.48% relative to Cd Spex solution. As opposed to multi-stage Cd purification previously published in the literature, a new one step anionic exchange purification using dilute HCl for the analysis of Cd isotopes in geological samples was developed. This method enabled a high recovery (> 95%) and effective separation of the sample matrix to be achieved. The long-term external reproducibility was evaluated at 0.12% (2 standard deviations) for the 114 Cd/110Cd ratio, based on reference solutions and replicated measurements of samples over one year. The variation of Cd isotopic composition of natural terrestrial samples is restricted to a small range of 0.4%, which is similar to previously reported results. In contrast, large variations of Cd isotopic composition were found for anthropogenic samples with values as low as −0.64% for a dust sample issued from a lead smelter and values as high as +0.50% for NIST SRM 2711 (metal-rich soil). These variations are 10 times larger than the reproducibility and suggest that Cd isotopes can be useful as tracers of anthropogenic sources of Cd in the environment.  相似文献   

10.
郑存江 《岩矿测试》2005,24(4):284-286
在分析地质标准物质标准值不确定度来源的基础上,提出了在多个实验室协作研制地质标准物质时,协作单位除提供重现性检测数据外,还应分别提供各项目检测数据的合成不确定度。分析方法或实验室之间的平均值的合成不确定度按不等精度方法处理。标准物质标准值的不确定度由分析方法、检测实验室、样品均匀性和样品稳定性的不确定度合成后乘以扩展不确定度置信水平下的包含因子而得。  相似文献   

11.
中国地质标准物质文献索引(1980—2010)   总被引:2,自引:1,他引:1  
汇集了自中国开展地质标准物质研制与应用工作以来发表的中外文献和专著221条,制成按年代编排的文献索引(1980—2010)、按专题(综合性评述、研制成果发表、制备技术与方法、专题评述和专著)编排的文献索引和作者索引。最后对文献的年度分布、各专题和各类(岩石、沉积物和土壤;矿石矿物;贵金属;能源矿产;化学物相;生物、食品材料;形态、有效态;同位素和年代学;电子探针微区)标准物质的文献分布及文献的期刊分布和作者单位分布等作了简单统计。  相似文献   

12.
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   

13.
重晶石矿石成分分析标准物质研制   总被引:3,自引:2,他引:1  
冯静  王瑞敏  张激光 《岩矿测试》2010,29(2):175-178
研制了7个重晶石矿石成分分析标准物质。其中,GSO-1为铁矿型重晶石,GSO-2、GSO-3为萤石型重晶石,GSO-4、GSO-5为石英型重晶石,GSO-6为硫化物型重晶石,GSO-7为黏土型重晶石。样品采用陶瓷衬里的球磨机加工,加工后样品粒度达到-0.074 mm。采用X射线荧光光谱法检验了钡、铜、铅、锌、锆、铝、硅、铁和钙共9种元素的均匀性,并进行振动试验。8个实验室参加定值工作,提供了硫酸钡、氧化钡、三氧化硫和锶的7个标准值,全三氧化二铁的2个标准值,氟化钙的1个标准值及铜、铅、锌和水溶盐等标准值或参考值。2009年4月,7个样品已被国家质量监督检验检疫总局批准为国家一级标准物质,编号为GBW 07811~GBW 07817。  相似文献   

14.
Abundances of twenty four trace elements, including Y and fourteen rare earth elements (REE), are reported for eighty six geological reference materials and four proficiency testing samples. Analytical data were obtained by ICP-MS using solution nebulisation after mixed acid digestion (HF-HClO4) under pressure. Analysed samples cover a wide range of element concentrations and mineralogical compositions, including samples for which there are few previously published data. Precision for elemental determinations in nearly 90% of the samples analysed is better than 5%. Accuracy, estimated by comparison with data from compilations is better than 6% for well characterized reference materials. Results obtained for samples that are low in trace elements are often significantly lower than compiled reference values. A critical discussion of the compiled data sets, especially for Y and the REEs, indicates that some reference values seem to be erroneous.  相似文献   

15.
The International Association of Geoanalysts (IAG) published a protocol for the certification of reference materials in close accord with the International Organisation for Standardisation (ISO) guidelines (Kane et al. 2003). This article supplements that protocol, providing additional discussion of best approaches for pre-selecting laboratories for participation in certification projects. This discussion also makes a distinction between inter-laboratory certifications, where n = 15 is the general standard, and expert laboratory certifications, where a much smaller number of laboratories will be deemed qualified to provide data of the quality needed for certification.  相似文献   

16.
泛滥平原沉积物标准物质研制   总被引:6,自引:6,他引:0  
泛滥平原沉积物能代表流域内元素的平均分布规律并具有普遍的适用性,是地球化学填图工作的重要介质。目前国际上尚无泛滥平原沉积物标准物质,国外相似标准物质的研制注重于环境方面,定值成分较少;我国同类的土壤和水系沉积物标准物质受限于不同工作需要,研制目的各不相同,且多数标准物质不足。为满足需求,本文研制了长江流域、赣江流域、汉水流域、淮河流域、黄河流域、海河流域、黑龙江流域共7个泛滥平原沉积物国家一级标准物质(编号为GBW07385~GBW07391)。此系列标准物质采用X射线荧光光谱压片法测试了26种成分,主量成分的RSD小于1%,微量元素的RSD约为2%,所有成分的RSD均小于7%,方差检验的F值均小于临界值F0. 05(24,25)=1. 96,表明样品的均匀性良好。在23个月的考察期内,检验的24种成分未发现统计学意义的明显变化,证明样品的稳定性良好。由全国13家实验室采用不同原理的、可靠的多种分析方法共同完成了73种元素和化合物共511个特性成分的定值测试,除GBW07386和GBW07388的CO2未能赋值外,其余494个特性成分给出了认定值与不确定度,15个特性成分给出了参考值,是我国同类标准物质定值最为齐全的一个系列。该系列标准物质代表了各自流域元素的背景含量,适用于多目标地球化学调查、土地质量地球化学调查等样品的分析质量监控,亦可用作环境、农业等领域相关样品测试的量值和质量监控标准。  相似文献   

17.
简介了世界大洋锰结核及深海沉积物标准物质概况,评述了它们的特点,同时也汇集了这些样品已确定的特性值。  相似文献   

18.
中国地质标准物质研制和标准方法制定的成果与思考   总被引:10,自引:2,他引:10  
简介了我国地质标准物质研制与标准方法制定的主要成果,重点讨论了其中在管理和技术方面值得思考的问题,并就提高我国地质标准物质水平,加速走向国际,提高国际影响力提出建议。  相似文献   

19.
Reference materials (RM) are essential to achieve traceability of measurements. Specific uses of RM in analytical laboratories are the validation of methods, the calibration of instruments, the quality control and the demonstration of proficiency. This paper describes the certification of a new geochemical reference material, named BRP-1 (Basalt Ribeirão Preto), and acts as the certificate of analysis for this RM. The rock sample was crushed and pulverised at the USGS (Denver, USA), homogenised and split into 1920 bottles, with 55 g each. BRP-1 was transported back to Brazil and the homogeneity between and within bottles was assessed to demonstrate sufficient homogeneity for certification. The chemical characterisation was performed by twenty-five laboratories. Each laboratory received two bottles of BRP-1 and one of BCR-2 (Basalt Columbia River) used for quality control (QC). Reference values and uncertainties were calculated for forty-four constituents of BRP-1, following ISO Guide 35 recommendations and the IAG Protocol. The calculation of each reference value included data of proven traceability from at least ten laboratories using two or more analytical techniques and the uncertainties combines the characterisation and between bottle homogeneity contributions.  相似文献   

20.
X射线荧光光谱用人工标准物质的研制   总被引:4,自引:3,他引:1  
使用高纯物质人工合成的方法,成功研制了4个人工标准物质。该系列标准物质涵盖了钛、钒、锰、铬、钴、镍、铜、锌、砷、铅、铋、铷、锶、钇、锆、铌、钼、钨、钕、钽、铪、镱、锡、钡、铯、镓、锗、镧、铈等29个元素,不同分析元素的含量范围可扩大到0.00x%~8%。该系列标准物质不仅可以补充自然标准的不足,扩展校准曲线含量范围,而且能够修正干扰系数,解决了准确计算分析元素之间的干扰和仪器校正带来的实际困难。用4个人工标准物质取代单元素人工标准的配制方法,减少标准数量,节约了资源以及标准配制的时间,避免了X射线荧光光谱分析工作者的重复劳动,提高了工作效率。研制的4个标准物质经检验均匀性和稳定性良好,量值准确可靠,已被国家质量监督检验检疫总局批准为国家一级标准物质。  相似文献   

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