石墨炉原子吸收光谱法测定土壤样品中镉

采用磷酸氢二铵作基体改进剂塞曼扣背景石墨炉原子吸收光谱法测定土壤样品中镉，方法检出限DL=0．012μg／g，精密度RSD在3．55％～7．33％，满足了土壤样品中镉测定的镉质量要求。     

涂钨热解石墨管－石墨炉原子吸收法测定天然水中痕量钡

选择涂钨热解石墨管测钡,克服了钡的碳化物形成而提高了方法的灵敏度,采用钙做基体补偿不仅克服钙对测钡的影响,同时也对测钡起增敏作用,结合其它测定条件的优化实现了石墨炉原子吸收法测定天然水中的痕量钡。其线性范围在０～７０μｇ／Ｌ检出限３．３ｐｇ,特征质量为２．９ｐｇ／１％吸收,对５μｇ／ＬＢａ试液测定１１次,其ＲＳＤ为６．９％,加标回收率８９％～１２０％。方法经标样分析验证,结果与标准值相符。     

黄陵断穹核部鳞片石墨矿地球化学特征与成因研究

黄陵断穹核部石墨矿是我国鳞片(晶质)石墨矿的主要产区,对该区石墨矿的研究具有重要理论和实际意义。该区已有石墨矿研究成果多侧重于矿床地质方面,对矿床成因分析缺乏地球化学支撑。为此,本文从地球化学层面查明石墨矿原岩类型,碳质富集岩相、变质作用和晶质石墨的形成,为矿床成因和成矿作用提供地球化学依据。通过系统采集区内主要石墨矿样品,进行主量元素、微量元素、稀土元素和同位素分析,根据矿床地球化学原理和分析方法,阐明石墨矿的物质来源,成矿元素集散行为和矿床形成机制。根据主量元素含量和组合,推断石墨的原岩为碳质粉砂质泥岩。微量元素的双重性指示石墨矿的物质有两个来源:中太古代野马洞岩组和中太古代东冲河片麻杂岩。独特的稀土元素配分型式说明物源转化为原岩时存在着强烈的地球化学反应。石墨矿的碳同位素组成支持碳质来自有机物的观点。     

氢化物发生-原子荧光光谱法直接测定地球化学样品中痕量碲

采用硝酸-氢氟酸-高氯酸溶解样品,以Fe3 作减缓剂,不需分离富集,用氢化物发生-原子荧光光谱法直接测定地球化学样品中痕量碲.对测定介质、KBH4浓度、铁盐的作用等条件进行试验.方法检出限为0.0031μg/g,精密度(RSD,n=11)＜6.10%.方法用于国家一级地球化学标准物质中痕量碲的测定,结果与标准值一致.     

川西高原地区岩石中硒的地球化学特征和影响因素

川西高原土壤、水体等多种介质研究表明,该地区的硒含量偏低,天然土壤剖面硒为0.06～0.16μg/g,表层土壤中硒含量为0.075～0.204μg/g,沉积物中硒含量为0.069～0.310μg/g,地表水中硒含量为nd～0.096μg/L,地下水中硒含量为nd～0.058μg/L,均低于我国相应环境介质中硒的平均含量,影响到当地人体健康。本文采集川西高原地区80件岩石样品,同时采集6套岩心样品,这些样品主要以板岩、砂岩、灰岩和页岩为主。采用原子荧光光谱法(AFS)测定硒含量,研究川西高原阿坝地区岩石与岩心样品中硒的地球化学特征和低硒的影响因素。结果表明:岩石硒含量范围为0.030～0.282μg/g,平均值0.09μg/g,低于硒土壤背景值。不同类型岩石中的硒含量大小为:页岩灰岩板岩砂岩。岩石中硒含量在不同地区也表现出较大的差异:松潘阿坝壤塘马尔康九寨沟若尔盖红原,可能是受到岩石类型及有机质和地质环境的影响所致。岩心各剖面的硒含量最小值为0.02～0.07μg/g,最大值为0.21～0.34μg/g,平均值为0.06～0.17μg/g,各钻孔的硒含量明显低于硒的地壳丰度。本研究认为,硒的分布受地质环境、有机质、岩石致密性等条件限制,低硒的地质环境是导致岩石中的硒含量较低的最主要因素。     

原子吸收分光光度法与氢醌容量法测定矿石中金的比对

本文对矿石中金的两种分析方法进行了比对。结果表明原子吸收分光光度法要优于氢醌容量法。     

火焰原子吸收法测定化探样品中的银铜铅锌

样品经硝酸、氢氟酸、高氯酸分解，制成硝酸溶液，经巯基棉层析柱过滤富集Ag，并用2mol／LHBr溶液洗脱，用火焰原子吸收法测定洗脱液中的Ag和滤液中的Cu，Pb，Zn。用该法测定化探样品中银和铜铅锌，检出限低，结果准确度和精密度均令人满意。     

原子吸收分光光度法快速测定铬铁矿中钙、镁、锰

通过在标液中加入相应的Sr来消除离子干扰,采用原子吸收分光光度法快速测定CaO、MgO、MnO的含量,方法经国家标准物质验证,其RSD<2%(n=6)。其结果与标准值相符。方法达到了准确、简便、快速、实用性强。     

氢化物发生-原子荧光光谱法测定砷等元素分析探讨

本文分析探讨氢化物发生—原子荧光光谱法测定土壤中低质量浓度的砷、锑、铋的方法实验。     

Organic Geochemistry of the Early Jurassic Oil Shale from the Shuanghu Area in Northern Tibet and the Early Toarcian Oceanic Anoxic Event

This paper presents new geological and geochemical data from the Shuanghu area in northern Tibet, which recorded the Early Toarcian Oceanic Anoxic Event. The stratigraphic succession in the Shuanghu area consists mostly of grey to dark-colored alternating oil shales, marls and mudstones. Ammonite beds are found at the top of the Shuanghu oil shale section, which are principally of early Toarcian age, roughly within the Harplocearasfalciferrum Zone. Therefore,the oil shale strata at Shuanghu can be correlated with early Toarcian black shales distributing extensively in the European epicontinental seas that contain the records of an Oceanic Anoxic Event. Sedimentary organic matter of laminated shale anomalously rich in organic carbon across the Shuanghu area is characterized by high organic carbon contents, ranging from 1.8% to 26.1%. The carbon isotope curve displays the δ^13C values of the kerogen (δ^13Ckerogen) fluctuating from -26.22 to -23.53‰ PDB with a positive excursion close to 2.17‰, which, albeit significantly smaller, may also have been associated with other Early Toarcian Oceanic Anoxic Events (OAEs) in Europe. The organic atomic C/N ratios range between 6 and 43, and the curve of C/N ratios is consistent with that of the δ^13Ckerogen values. The biological assemblage,characterized by scarcity of benthic organisms and bloom of calcareous nannofossils (coccoliths), reveals high biological productivity in the surface water and an unfavorable environment for the benthic fauna in the bottom water during the Oceanic Anoxic Event. On the basis of organic geochemistry and characteristics of the biological assemblage, this study suggests that the carbon-isotope excursion is caused by the changes of sea level and productivity, and that the black shale deposition, especially oil shales, is related to the bloom and high productivity of coccoliths.