共查询到20条相似文献，搜索用时 31 毫秒
1.
Silver content of silicate rook samples rarely exceeds 200 ppb. For determining such low levels of silver, a solid sampling flame atomic absorption method has been developed and has been applied to the analysis of several silicate rock reference samples. These results are compared with the sparse published data. Using silver as an example, the usefulness of solid sampling procedures for testing the repartition of volatile trace elements during the processing of new rock reference samples is illustrated. 相似文献
2.
A procedure for the analysis of geochemical samples has been developed based on direct atomic-emission spectrometry for the determination of silver, gold and the platinum-group elements. Instrumentation comprised a DC arc emission two-jet plasmatron coupled to a diffraction spectrograph and multichannel analyser for recording emission spectra. Spectrum analysis used a comprehensive library of spectral lines for practically all elements excited using this emission source. The software programme for the automatic registration of spectra and subsequent data processing are described and results presented for a number of geochemical reference materials. 相似文献
3.
4.
微波消解-石墨炉原子吸收光谱法测定痕量银的研究 总被引：2，自引：0，他引：2
传统的应用石墨炉原子吸收光谱法测定化探样品中的痕量银,一般采用盐酸-硝酸-氢氟酸-高氯酸电热板加热溶样,使用铱、铂为基体改进剂,但存在分析流程繁琐、成本高等缺点。相比于电热板消解法,微波消解技术的高压密闭消解和微波快速加热等特点,具有酸用量少、消解完全、消解过程损失少等优点。本文对传统的微波消解和仪器工作参数进行了改良,确定了最佳测定条件。建立了HNO_3-H_2O_2高压密闭消解样品,石墨炉原子吸收法测定水系沉积物、土壤、岩石中痕量银的方法。采用65%的HNO_3和H_2O_2微波消解溶样,加入12 g/L硫脲为介质,消除了基体干扰。方法检出限为0.018μg/g,将所建立的分析方法用于沉积物标准物质(GBW07309、GBW07311)、土壤标准物质(GBW07402、GBW07404)和岩石标准物质(GBW07103、GBW07104)验证,结果显示测定值与推荐值吻合,准确度△lg C(GBW)≤±0.024、RE(GBW)≤±5.71%,精密度RSD(GBW)≤5.97%。该分析方法适用于大批化探样品中痕量银的测定。 相似文献
5.
V. I. Nefedov N. M. Zhavoronkov G. V. Machavariani Ya. V. Salyn V. A. Makeev V. I. Zelenov 《Physics and Chemistry of Minerals》1982,8(5):193-196
Depth profiling analysis of native gold samples using X-ray photoelectron spectroscopy (XPS) shows the surface layers of lode gold to be significantly enriched with silver to a depth of 0.02–0.04 microns and the surface layers of placer gold to be depleted of silver up to a depth of several microns. The change in the surface composition of gold samples taken from oxidation zones is of more complicated character. Model experiments suggest the surface segregation of silver in lode gold samples to be due to outward diffusion and oxidation of silver at the surface. In placer gold the depletion of silver is caused by leaching of the latter from the surface layers. 相似文献
6.
Xianzhong Cheng Kun Shao Shangyue Shen Shenghong Hu Haiou Qiu 《Geostandards and Geoanalytical Research》2011,35(4):461-469
A rapid and inexpensive method was developed for the determination of trace silver in polymetallic ore samples by use of eggshell membrane (ESM), a natural biomaterial, as the solid‐phase extraction (SPE) adsorbent coupled with flame atomic absorption spectrometry (FAAS). The ESM was used for the separation/pre‐concentration of silver, and the parameters affecting sensitivity, such as pH, sample flow rate, eluent volume and eluent flow rate, were carefully investigated. ESM was found to be an effective solid phase extractant for the adsorption of trace silver over a wide range of acidity from 0.02 to 0.50 mol l?1 HNO3. The sample solution in 0.4 mol l?1 HNO3 was pumped through an ESM microcolumn at the rate of 1.0 ml min?1. Silver was absorbed, and then eluted with a solution of 1.0% m/v thiourea–0.5% v/v HCl. Under these optimal conditions, ESM exhibited a good enrichment efficiency for silver with a dynamic adsorption capacity of 1.7 mg g?1. The proposed method was applied to the FAAS determination of trace silver in polymetallic ores and geological reference materials, GSO‐2, 3 and 5, and GSD‐11, GSD‐12, and the determined values were in good agreement with certified values. 相似文献
7.
Reference Materials for Geochemical Studies: New Analytical Data by ICP-MS and Critical Discussion of Reference Values 总被引：13，自引：0，他引：13
Peter Dulski 《Geostandards and Geoanalytical Research》2001,25(1):87-125
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
8.
原子吸收工作曲线的两种拟合方式的研究,采用国家一级标准物质GBW07209(矿石中金和银成分分析标准物质)、GBW07255(GAg1)(银矿石中银成分分析标准物质)、GBW07256(GAg2)(银矿石中银成分分析标准物质)、GBW07305a(水系沉积物成分分析标准物质)、GBW07307a(水系沉积物成分分析标准物质)、GBW07311(水系沉积物成分分析标准物质)、GBW07405(土壤成分分析标准物质-黄红壤)进行实验,得出两种拟合方式的使用条件以及在实际工作中如何取舍的结论。 相似文献
9.
Shigeru Terashima 《Geostandards and Geoanalytical Research》1989,13(2):277-281
The thallium content of eighty-seven geochemical reference samples has been determined by atomic absorption spectrometry using an air-acetylene flame or a graphite furnace atomizer, after extraction of thallium as chloride with methylisobutylketone (MIBK). A comparison with published data show clearly the need for much more data on most reference samples. 相似文献
10.
Shigeru TERASHIMA 《Geostandards and Geoanalytical Research》1994,18(2):199-202
The mercury content of 118 geochemical reference samples have been determined by combustion followed by cold vapor atomic absorption spectrometry. The negative interference from volatile halogen and sulfur was eliminated by a packing of sodium carbonate in the combustion tube and addition of magnesium oxide to the samples. A comparison with published data show clearly the need for much more data on most reference samples. 相似文献
11.
The Haenam–Jindo area, located on the southwestern margin of the Korean Peninsula, was the site of vigorous volcanic activity during the Late Cretaceous and Early Tertiary periods. Large parts of the area record strong hydrothermal alteration, and there exist many clay–alunite and gold–silver deposits. We undertook potassium–argon (K–Ar) age dating of five mineral samples (including adularia, sericite and alunite) from the Eunsan, Moisan and Gasado epithermal gold–silver deposits in this area. The purities of the samples were confirmed by X‐ray diffraction analysis. The K–Ar ages of adularia from the Eunsan deposit and adularia and sericite from the Moisan deposit (related to gold–silver mineralization) are 75.0 ± 1.6, 74.7 ± 1.6 and 75.1 ± 1.6 Ma, respectively. The similarity of these ages, combined with the close proximity and similar geochemical characteristics of the deposits, indicates that the mineralization occurred as part of a single hydrothermal system. The K–Ar ages of alunite at the surface and adularia at depth within the Gasado deposit are 82.2 ± 1.9 and 70.7 ± 1.9 Ma, respectively, revealing that the clay–alunite and gold–silver mineralization formed at different ages. K–Ar age data indicate that the gold–silver mineralization in this area occurred mainly at 75–70 Ma, resulting from hydrothermal activity in the Haenam–Jindo area (82–70 Ma). This is the first time that the mineralization of precious metals in Korea has been identified during this period. 相似文献
12.
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
13.
以遥感地质方法为主导,结合运用地质矿产、地球化学和地球物理等多元地学数据,对泗洋铅锌矿点成矿条件进行综合分析研究,建立遥感信息找矿标志,并通过顶宅银矿点的验证,最后以该标志圈定了3处找矿有利地段,为泗洋—凤迹晚侏罗世火山喷发盆地的找矿提供参考依据。 相似文献
14.
Gold, Palladium and Tellurium in South African, Chinese and Japanese Geological Reference Samples 总被引：1，自引：0，他引：1
Reliable rock reference materials for Au, Pd and Te are scarce. We report here our analytical data on these three elements in 46 NIM, IGGE and GSJ reference samples in order to accumulate analytical data on these samples. 相似文献
15.
M. SANKAR DAS 《Geostandards and Geoanalytical Research》1979,3(2):199-205
Trace element data compiled on, geoshemical reference samples present invariably skewed distributions. It is proposed to treat such data as lognormally distributed and to compute geometric means (Xgm ) as probable values. As examples, the Xgm values derived for some trace elements in some rock reference samples are compared with the "recommended" values and with the "gamma" values of Christie. 相似文献
16.
用于多接收器等离子体质谱测定的铁铜锌同位素标准溶液研制 总被引：3，自引：3，他引：0
近十来年铁铜锌同位素研究已经成为热门研究领域,铁铜锌同位素分析方法日趋成熟,但是铁铜锌同位素标准物质却十分匮乏。目前欧盟参考物质及测量研究所(IRMM)有1个铁同位素标准物质和1个锌同位素标准物质,前者售罄,后者价格昂贵;美国国家标准局(NIST)有1个铜同位素标准物质。为了适应我国铁铜锌同位素研究的发展,本文使用铁铜锌元素浓度标准溶液作为备选标准溶液研制了铁铜锌三个同位素标准溶液(CAGS-Fe、CAGS-Cu和CAGS-Zn)。三个备选标准溶液经过F检验均匀性良好;在38个月内δ56Fe、δ57Fe、δ65Cu、δ66Zn和δ68Zn值没有显著性变化,具有良好的稳定性;主要特性值的推荐值及95%置信水平的不确定度为:CAGS-Fe,δ56FeIRMM014(‰)=0.80±0.05,δ57FeIRMM014(‰)=1.20±0.10;CAGS-Cu,δ65CuIRMM976(‰)=0.57±0.06;CAGS-Zn,δ66ZnIRMM3702(‰)=-0.77±0.10,δ68ZnIRMM3702(‰)=-1.55±0.13。本文研制的标准溶液可用于多接收器等离子体质谱仪测定铁铜锌同位素时的仪器校正和质谱分析过程监控,对于不同实验室的测试数据对比具有重要意义。 相似文献
17.
18.
提出了一种化探找金、银的新方法,该法采用一种混合浸取剂,以螯合吸附剂对采集到的化探次生晕样品进行偏提取.对偏提取的金、银含量,利用液珠萃取比色法进行金、银含量测定,从而达到化探直接找金、银的目的.该法克服了化探找金工作中的“粒金效应”.该设备简单、易操作. 相似文献
19.
John LYNCH 《Geostandards and Geoanalytical Research》1996,20(2):277-287
The collection and preparation of two soil reference samples and two till reference samples are described. Like their predecessors the LKSD series and the STSD series, the TILL series are characterized for total elements and for elements derived by partial extractions. Provisional data are presented for major, minor and trace elements. In addition, information data from a single source are provided for a number of elements derived by EPA digestions 3050 and 3051; these data allow a comparison with other partial extractions reported herein. 相似文献
20.
在高氯酸-硫脲介质中用原子吸收光谱法同时测定地质及选冶样品中银和铜已有文献报道;但在王水-硫脲介质中存在铜对银的测定干扰.本文采用盐酸-氢氟酸-硝酸-高氯酸四酸溶矿,王水提取、硫脲络合,用火焰原子吸收光谱法对银精矿中铜、银进行连续测定.通过筛选不同的样品消解方法,试验了硫脲介质浓度的影响,对共存元素的干扰进行消除.结果表明:四酸溶矿效果最好;通过加入过量的硫脲并控制其浓度在20 g/L以内,使溶液中银的白色沉淀与硫脲生成可溶的Ag[SC(NH2)2]3+配离子,消除了铜对银测定的干扰.该方法用于样品分析,相对标准偏差RSD(n =6)铜为1.20％～2.11％,银为0.61％ ～1.18％;加标回收率铜为96.5％ ～ 107.0％,银为97.3％ ～ 104.7％.测定值与碘量法、火试金法结果相符.本法具有简单、实用、成本低等优点,可满足银精矿选矿工艺生产的需要. 相似文献