Determination of Bismuth in Eighty-Three Geochemical Reference Samples by Atomic Absorption Spectrometry

The bismuth content of eighty-three geochemical reference samples has been determined by atomic absorption spectrometry using either a hydride generation and heated quartz cell atomizer or a solvent extraction and carbon tube atomizer. The agreement between the present results and published data is generally good.     

Determination of Thallium in Eighty-Seven Geochemical Reference Samples by Atomic Absorption Spectrometry

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.     

Determination of Silver in Seventy-Three Geochemical Reference Samples by Atomic Absorption Spectrometry

The silver content of seventy-three geochemical reference samples has been determined by atomic absorption spectrometry using an air-acetylene flame or a graphite furnace atomizer, after extraction of silver as iodide with methyl isobutyl ketone (MIBK). A comparison with published data shows clearly the need for much more data on most reference samples.     

Determination of Beryllium in Eighty Geological Reference Samples by Atomic Absorption Spectrometry

The beryllium content of eighty geological reference samples has been determined by atomic absorption spectrometry using a nitrous oxide-acetylene flame or a carbon tube atomizer, after extraction of beryllium as acetylacetonate with methylisobutylketone (MIBK). The agreement between the present results and published data is generally good.     

Determination of Cadmium and Lead in Seventy-seven Geological Reference Samples by Atomic Absorption Spectrometry

The cadmium and lead contents of seventy-seven geological reference samples have been determined by atomic absorption spectrometry using an air-acetylene flame or a carbon tube atomizer, after extraction of cadmium and lead as iodides with methylisobutylketone (MIBK). The agreement between the present results and published data is generally good.     

Determination of Arsenic and Antimony in Eighty-Five Geochemical Reference Samples by Automated Hydride Generation and Electrothermal Atomic Absorption Spectrometry

The arsenic and antimony contents of 85 geochemical reference samples have been determined by atomic absorption spectrometry with hydride generation and heated quartz cell atomizer. The sample is decomposed with a mixture of perchloric, nitric and hydrofluoric acids and potassium permanganate solution; interferences are eliminated by addition of potassium iodide, aluminium chloride and ascorbic acid. The agreement between the present results and published data is fairly good.     

Flameless atomic-absorption determination of gold in geological materials

Gold in geologic material is dissolved using a solution of hydrobromic acid and bromine, extracted with methyl isobutyl ketone, and determined using an atomic-absorption spectrophotometer equipped with a graphite furnace atomizer. A comparison of results obtained by this flameless atomic-absorption method on U.S. Geological Survey reference rocks and geochemical samples with reported values and with results obtained by flame atomic-absorption shows that reasonable accuracy is achieved with improved precision. The sensitivity, accuracy, and precision of the method allows acquisition of data on the distribution of gold at or below its crustal abundance.     

Determination of Gold in Sixty Geochemical Reference Samples by Flameless Atomic Absorption Spectrometry

The gold content of sixty geochemical reference samples has been determined by atomic absorption spectrometry using a graphite furnace atomizer after digestion of sample with aqua regia and extraction of gold as chloride by methylisobutylketone. A comparison with published data shows clearly the need for much more data on most samples before consensus values could be assigned.
La teneur en or dans soixante échantillons géochimiques de référence a été déterminée par le spectromètre d'absorption atomique équipé d'un four à graphite. L'échantillon a été mis en solution avec de l'eau régale et l'or extrait avec du methylisobutylketone. Un examen des données publiées sur l'or montre qu'il faut davantage de résultats pour fixer des valeurs de consensus dans la plupart des échantillons.     

AFS-230E型双道原子荧光光度计常见故障及排除方法

简要介绍北京海光仪器公司生产的AFS-230E型双道原子荧光光度计中的气路控制系统、原子化器温度、空心阴极灯电源的电路原理等常见故障及排除方法。     

双道氢化物原子荧光法同时测定地球化学样品中的微量砷和锑

已有大量研究工作表明砷是各种类型金矿床的极有效的探途元素,它也是许多热液多金属矿床的通用指示元素。锑作为指示元素做的工作比砷少,但是根据已有资料,它也是锑矿床、金矿床及多金属矿床的指示元素。我国最近发表的《苗龙金矿的发现》一文中很好地说明了砷及锑对找金矿的指示作用。     

石墨炉原子吸收法测定矿石中痕量金

本试验确立的聚三氟氯乙烯—磷酸三丁酯(1∶0.6)为固定相,反相萃取色层分离富集、石墨炉原子吸收法测定矿石中痕量金的分析方案,在选定的条件下,基本上无背景吸收和共存元素的影响。实测绝对灵敏度为8.9×10~(-12)克/1%吸收;检出限为1.1×10~(-4)克/吨、定量测定下限为2.2×10~(-4)克/吨;     

流动注射HG-AFS法同时测定化探样品中的砷和汞

建立了流动注射HG-AFS测定痕量砷和汞的分析方法。把砷和汞放入20%的王水介质中,它们被硫脲-抗坏血酸预还原,待测量溶液澄清之后,将溶液与硼氢化钾一起导入反应器,产生的氢化物载气导入原子化器中测定,测定结果符合国家标准。本法改进了流动注射HG-AFS法测定砷、汞的分析方法。     

电热石墨管炉原子吸收法测定铝土矿中镓

铝土矿中镓的测定多沿用罗丹明B光度法,无火焰原子吸收法测定镓国内外也有一些资料报导,但都经萃取分离再用石墨管炉测定。 电热石墨管炉法测定镓,其中铝的干扰严重,资料[2]曾为此选用萃取法来消除影响。其它资料对一些干扰影响萃取法事先分离。我们分析的矿物是铝土矿,其中铝对镓测定的干扰是首先要解决的问题。我们反复试验,证明铝对镓用电热石墨管炉     

原子荧光光谱法测定地质样品中As、Sb、Bi、Hg——需要注意的问题及解决方法

通过总结实际工作及查阅文献,分析了样品制备、酸度、硼氢化钾浓度对As、Sb、Bi、Hg测定的准确性及灵敏度的影响,确定了仪器测定过程中负高压、载气流量、原子化器高度及温度、元素干扰对测定结果的影响,并总结了在日常测定过程中仪器故障排除、测量误差的控制及测量过程中潜在的问题及解决方法.     

Study and Application of Geochemical Reference Materials in the Institute of Geophysical and Geochemical Exploration (IGGE), China

In order to meet the needs of geochemical mapping and geochemical exploration, 125 geochemical reference materials have been successively prepared by the Institute of Geophysical and Geochemical Exploration (IGGE) since 1978. They include certified reference materials of stream sediments (GSD1-14), soils (GSS1-16; ASA 1–6, for analysis of available elements), various rocks (GSR1-6, GSR13-15), biological material (GSV1-4 and GSB 1–10), synthetic silicates (GSES I 1–11) and limestones (GSES II 1–9 for spectral analysis). They also include geochemical reference materials for ore analysis: Cu-Pb-Zn ores (GSO1-4), Cu-Pb-Zn concentrates (GSO5-7), platinum-group element (PGE) ores (GPt5-6 and GPt9-10), silver ores (GAg1-6) and geochemical reference materials for Au (GAu8-14) and PGE determination (GPt1-4, and GPt7-8). A multi-laboratory collaborative analysis scheme was adopted in the certification procedure of the IGGE. Dozens of competent laboratories with hundreds of senior analysts in China participated in the certification analysis. These samples have been supplied to more than thirty countries and more than 4000 customers from national industrial, agricultural, environmental, scientific and educational fields. Most of the geochemical reference materials are used for the calibration of measuring apparatus, evaluation of analytical methods, certification studies, quality control and laboratory accreditation programmes.     

Geochemical behavior of Pt and Pd in coastal marine sediments,southeastern margin of the Japan Sea

Eighty-one argillaceous marine sediments collected from the southeastern coastal margin of the Japan Sea were analyzed for Pt and Pd by atomic absorption spectrometry using a graphite furnace atomizer after solvent extraction separation. The average Pt (1.2 ± 0.5 ppb) and Pd(1.6 ± 0.9 ppb) contents are generally similar to those of the published crustal abundances. The Pt or Pd is generally enriched in the fine sediment fraction, and positively correlated with Cu, Pb and water depth. The inverse correlation between the Pt or Pd content and redox potential of the sediment suggests that significant amounts of Pt and Pd are supplied in their dissolved forms, and reduced to their metallic states. It is concluded that the Pt and Pd distributions in the coastal marine sediments are controlled by the geological characteristics of the studied area, grain size and redox potential of sediments, water depths, and dissolved O₂ concentration of sea water.     

Analyses of the United States Geological Survey Geochemical Exploration Reference Samples GXR-I to - 6

Analyses of the United States Geological Survey geochemical exploration reference samples (GXR) 1–6 are reported for 36 elements and compared with published values.     

微波消解电感耦合等离子体质谱法测定黑色页岩中稀有稀土元素

采用硝酸-氢氟酸-过氧化氢于微波消解仪中分解样品,电感耦合等离子体质谱法测定贵州遵义地区某黑色页岩中稀有稀土元素的含量。对页岩标准物质(GBW 07107)和水系沉积物地球化学成分分析标准物质(GBW07305、GBW 07310)的分析,测定值与标准值相一致。对黑色页岩的分析结果较好,方法精密度(RSD,n=6)各元素均小于4%,加标回收率为97.9%~100.1%。方法准确度高、简单、快捷,一次溶样可同时测定多种元素。     

Reference Materials for Geochemical Studies: New Analytical Data by ICP-MS and Critical Discussion of Reference Values

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.     

Determination of partial geoidal parameters over the Indian sub-continent

The paper presents values of partial geoidal parametersN, ξ and η which define the departure of the geoid from the reference spheroid, at 1° intervals over the Indian subcontinent. These values represent contributions arising from the gravity anomaly data over the entire earth's surface, except for that from a 6°×6° element around the immediate neighbourhood of the point. Complete values of these parameters at a point can be obtained simply by adding to these partial values, contributions from the 6°×6° element circumscribing that point. The objective of the study was to provide a ready basis for updating the geoidal parameters at the initial reference point as and when the density and quality of local gravity data around it improve. These computations once made, would also facilitate calculation of geoidal parameters at a fairly large number of astro-geodetic stations apart from that at the initial reference point, which should lead to considerably more precise value of the absolute datum of the Indian geodetic dasystem.