共查询到20条相似文献，搜索用时 171 毫秒
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一、前言在水质监测中,保证采集的样品具有代表性是水质监测重要环节之一,而样品的代表性则取决于采样技术和样品的保存。根据有关部门提出的课题,我们自1984年着手研制RY-86型溶解氧采样器,1986年9月通过由水电部水 相似文献
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近几年来,为配合寻找富铁矿及其他科研任务,对冀东、辽东、豫西、川西等地的前寒武系,及庐枞、宁芜、繁昌和浙西等地的中生代火山岩地层进行了同位素年龄测定和研究。在所内外的大力支持协助下,进行了野外观察和采样,同时接受了所内外兄弟单位送来的样品及有关地层资料。我们对这些样品进行了同位素年龄测定。冀东、辽东、豫西和川西前寒武纪地层的样品,主要用Rb-Sr全岩等时线法,其中对川西的样品并用了少数K-Ar法。对庐枞、宁芜、繁昌和浙西的中生代地层样品,主要用K-Ar法。对浙西的个别样品并用了Rb-Sr全岩等时线法。对测定得到的部分年龄数据,以前曾以不同方式报道。 相似文献
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近红外反射光谱学在岩石矿物研究中的应用Ⅲ．快速测定地质样品中二氧化碳 总被引：1，自引：1，他引：1
使用一组不同岩石矿物性质的25个地质样品,研究了地质样品中二氧化碳含量和近红外漫反射光谱的关系。利用多重散射光校正、标准正常变量转换及导数光谱等化学计量统计学方法,预处理了漫反射光谱数据,获得了偏最小二乘法(PLS)回归的多变量校正方法,建立了应用近红外(NIR)反射光谱学方法无损快速测定各种地质样品中二氧化碳模型。从光谱特性方面解释了大多数进入多变量校正模型的波长与碳酸盐矿物的CO2-3基团光谱吸收有关。NIR估算结果表明,应用二氧化碳校正模型来定量分析地质样品中二氧化碳的方法是可行的。 相似文献
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姚远俊 《华东地质学院学报》1982,(1)
一、前言钋(~(210)Po)法找矿是通过测量岩石或土壤中的钋含量达到找铀矿的目的。存在于岩石或土壤中的钋是通过电化学方法提取,然后测定其α强度来实现的。因此,从样品中提取钋是钋法找矿的关键一环,而外的提取受许多因素的控制和影响,它不仅与采用的分析流程、还原剂的种类有关,而且与样品的颗粒度和样品的化学成分及化学性质有关。所以在制备钋样 相似文献
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近几年在国内外珠宝市场上出现了一种红色透明长石,其天然性引起了广泛的争议。采用常规的宝石学方法、LA—ICP—MS以及紫外-可见分光光度计等测试仪器研究了该红色长石样品的宝石学特征、化学成分及紫外-可见吸收光谱,旨在探讨其致色原因。结果表明,该红色长石样品属于中长石;与黄色长石样品相比,其化学成分中Cu的质量分数为739×10^-6～801×10^-6,远远高于黄色长石的（1．07×10^-6）,而其它微量元素的质量分数则无明显的差别,故认为Cu可能与其呈红色有关;紫外-可见吸收光谱结果显示,该红色长石样品在可见光区的吸收带主要位于566nm处,推测其可能与Cu对可见光的吸收有关。 相似文献
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研究了天然土壤样品热释光测量最佳条件。天然样品热释光测量强度与升温区间、升温速率及仪器灵敏度有关。在不同的地质条件下分别采集样品(北方砂岩,南方花岗岩及重庆滑坡),通过测量,对发光曲线进行对比分析,确定了几种不同地质条件下天然土壤样品热释光测量最佳条件。 相似文献
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样品分解是所有化学及化学—仪器分析方法中必须首先考虑的一个问题。地质样品中的岩石、矿石分解方法,不仅在已出版的许多岩石矿物化学分析著作中作了介绍,而且还有岩矿分解方法的专著。微迹元素测定中的样品分解方法也有了详细论述。 相似文献
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研究了物质粉末衍射强度与样品堆积密度的关系,将粉末样品紧密度导入衍射强度公式。在此基础上推导出直接法测定多组分混合物质量吸收系数及各相浓度的数学公式,并通过实验证明了方法的实用性。还研究了缺乏纯样品以及样品中存在非晶质相、结晶度变化大的柑、择优取向严重的相等特殊情况的实验方法。 该方法不需要向待测样品中加入任何参考物质,不称样,不混样,不损耗纯样品,制样简便,特别适合大批量样品的定量相分析。 相似文献
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Origin of the difference in the distribution behavior of tellurium and selenium in a soil-water system 总被引：4，自引：0，他引：4
Teppei Harada 《Geochimica et cosmochimica acta》2008,72(5):1281-1294
The distribution behavior of tellurium (Te) between soil and water in a synthetic soil-water system was studied coupled with the speciation of Te both in soil and water phases by using X-ray absorption fine structure (XAFS) spectroscopy and a high-performance liquid chromatography connected to an ICP-MS (HPLC-ICP-MS), respectively. The results were compared with a similar data set for Se, which was simultaneously obtained in this study. The oxidation states and host phases of Te and Se in the soil samples were given by XAFS, while the oxidation states in water were given by HPLC-ICP-MS. It was found that both Te and Se in soil are mainly associated with Fe(III) hydroxides under oxic conditions. From the EXAFS analyses, the outer-sphere complex is important for the Se(VI) sorbed on Fe(III) hydroxides in soils, while Se(IV), Te(IV), and Te(VI) form inner-sphere complexes. Under reducing condition, it was found that Te(0) and Se(0) species were formed and that Se was more readily reduced to Se(0) than Te, as is predicted from their Eh-pH diagrams. The reduction process from hexavalent to zerovalent species was different between Se and Te, that is, the direct reduction from Se(VI) to Se(0) was observed for Se, while Te was reduced stepwise from Te(VI) to Te(0) via Te(IV). In terms of the distribution between soil and water, Se distribution to water was much higher than that of Te under wide redox conditions. For Se, selenate is the predominant species in water even under reducing condition due to the much higher solubility of Se(VI) than Se(IV). Furthermore, a much smaller distribution of Te in water was primarily due to the larger affinities of Te(IV) and Te(VI) to Fe(III) hydroxides than Se(VI), which originates from the formation of the inner-sphere complexes of Te(IV) and Te(VI) to Fe(III) hydroxides. 相似文献
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M_(17)树脂在>6mol/L的HCl介质中能同时吸附Se和Te,Se和Te可用水和丙酮分别洗脱,也可用丙酮同时洗脱。从而建立了两个新的Se、Te分离富集体系,使原子荧光测定达到纳克量级。 相似文献
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Allison Forrest Richard Kingsley Jean-Guy Schilling 《Geostandards and Geoanalytical Research》2009,33(2):261-269
Promising methods have been developed recently for the determination of selenium (Se) and tellurium (Te) in geological materials at ng g−1 and lower levels, using hydride generation-inductively coupled plasma-mass spectrometry. Here we report on a new isotope dilution-hydride generation-inductively coupled plasma-mass spectrometry (ID-HG-ICP-MS) method for the simultaneous determination of Se and Te, which is applied to basalts, and modified compared to previous work. The basalts were attacked and dissolved with hydrofluoric and nitric acid, spiked with enriched isotopes, and passed through a cation exchange column (AG 50-X8 100–200 mesh) to separate the major cations that interfere with Se and Te detection (e.g., Fe). The detection limits of this method were 0.010 ng g−1 for Se and 0.0030 ng g−1 for Te, well below the concentrations of Se and Te expected in basalts. The precision of the method for Se was 12.2 to 15.1% and for Te was 4.6 to 7.2% RSD from replicate analyses of basalt reference samples. The accuracy for Se determinations was 61 to 94% and for Te 28 to 100% of values previously reported in the literature for selected USGS reference materials. 相似文献
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The chemistry and mode of occurrences of native tellurium in the epithermal gold ores from Teine, Kobetsuzawa, Mutsu, Kawazu, Suzaki and Iriki in Japan are examined. Mineral assemblages in contact with native tellurium are: quartz‐sylvanite at Teine, quartz‐hessite‐sylvanite‐tellurantimony at Kobetsuzawa, quartz at Mutsu, quartz‐stutzite‐hessite‐sylvanite‐tetradymite at Kawazu, quartz at Suzaki, and quartz‐goldfieldite at Iriki. The peak patterns of XRD for native tellurium from these six ores are nearly identical to that of JCPDS 4–554. Their chemical compositions of Te range from 98.16 to 100.73 wt.%, showing nearly pure tellurium. Other elements detected are: Se of 0–0.85 and Cu of 0–0.74 at Teine, Sb of 0.45–0.47 and Se of 0.19–0.27 at Kawazu, Se of 0.22–1.11 and Sb of 0–0.49 at Suzaki, and Cu of 0.69–0.98, As of 0.22–0.28 and Bi of 0–0.22 wt.% at Iriki. No other elements are detected in the ores of Kobetsuzawa and Mutsu. The ranges of associated minor compositions are consistent with those of the experimental phase. The differences would be related to associate minerals. The mineral assemblages in these ores agree well with the previously proposed experimental phase relations in Au‐Ag‐Te ternary system for 120–280°C. The Suzaki ore has high Te‐Au assemblage: from calaverite‐sylvanite‐krennerite via native tellurium to petzite, with changing mineralization stage, whereas the Kobetsuzawa and the Kawazu ores have high Te‐Ag assemblage of tellurium‐hessite, and native tellurium‐stutzite‐hessite‐sylvanite, respectively. The Teine ore has intermediate assemblage of native tellurium‐sylvanite. The mineral assemblages in the Au‐Ag‐Te system are related to the hydrothermal environment especially to the pH condition, i.e. Au rich assemblages under acidic and Ag rich assemblages under intermediate pH conditions, being supported by alteration mineral species. The other telluriferous epithermal gold deposits not in association with native tellurium such as Agawa, Date, Takeno, Chugu, Chitose, Sado and Kushikino are estimated to have been formed under higher pH conditions as adularia and calcite occur in these deposits. The pH‐Eh diagram for aqueous tellurium species and tellurium minerals at 250°C indicates that the region of native tellurium occurs between those of aqueous telluride and tellurous species at lower pH, being consistent with their mineral assemblages in ores and alteration envelopes. 相似文献
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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 总被引：2，自引：1，他引：1
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。 相似文献
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M17树脂分离富集原子荧光测定岩矿中痕量碲 总被引：4，自引：1，他引：4
本文研究了不同种类树脂对Te的吸附能力,提出了在3mol/L HCl介质中,用M_(17)二甲胺树脂吸附,然后用水洗脱的新途径,使Te有效且无污染地得到分离和富集,实现了原子荧光测定地质试样中ppb级痕量Te。经地矿部标准参考样GSR7-12考察,分析结果与推荐值相符。 相似文献
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氧化性富金斑岩-矽卡岩矿床中碲、硒、铊富集机制的研究进展 总被引：5，自引：1，他引：4
富金斑岩-矽卡岩矿床目前提供了全球几乎所有的硒、碲及部分铊产量,其中氧化性富金斑岩-矽卡岩矿床可共伴生碲、硒、铊等稀散金属。文章从元素地球化学行为、矿床类型、岩浆作用、赋存状态、稀散金属与铜金关系等方面,总结了氧化性富金斑岩-矽卡岩矿床中有关碲、硒、铊富集机制的研究进展。碲、硒具有亲铁和亲硫的特征,而铊具有亲硫和亲石的双重特征,三者具有不同程度的挥发性。岩浆热液型矿床伴生有碲、硒、铊矿化。基性岩浆的注入和岩浆硫化物熔离可能是氧化性富金斑岩-矽卡岩矿床碲、硒、铊富集的主要岩浆作用。氧化性富金斑岩-矽卡岩矿床中铜和金含量通常呈正相关性,发育有丰富的含碲/硒/铊矿物,但碲、硒、铊与铜、金的关系还不清楚。长江中下游成矿带发育多个氧化性矽卡岩金矿、矽卡岩铜金矿,伴生大规模的碲、硒、铊矿化,且已被综合回收利用,该带是探讨氧化性富金矽卡岩矿床中碲、硒、铊富集机制的理想对象。 相似文献
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电感耦合等离子体质谱法同时测定地质样品中锗硒碲 总被引：7，自引：7，他引：0
锗、硒、碲三个元素的分析需要分别采用硝酸-氢氟酸-高氯酸-磷酸、硝酸-氢氟酸-高氯酸两种溶样体系,原子荧光光谱（AFS）、电感耦合等离子体质谱（ICP-MS）两种仪器进行测定,对于大批量地质样品的分析成本高、测试效率低。本文建立了在同一份溶液中用ICP-MS同一种仪器测定锗、硒、碲三元素的方法。样品用硝酸-氢氟酸-硫酸一种体系分解,试液以50%硝酸提取,3%乙醇定容,避免乙醇在复溶时的挥发损失,保证了试样溶液中的乙醇浓度均为最佳增敏作用所需值。试样分解过程中没有使用盐酸,避免了氯离子存在给锗、碲造成的损失。在3%硝酸-3%乙醇介质中硒、碲的灵敏度提高了2.2倍、3.7倍。同时克服了ICP-MS测定硒、碲难电离、灵敏度低的问题,保证了方法稳定性;CCT碰撞池技术消除了氩的多原子离子对硒测定干扰,提高了方法准确度。本方法通过分析国家一级标准物质进行验证,测定值与标准值基本一致,相对标准偏差（RSD,n=4）小于5%,样品前处理过程简单,分析效率高。 相似文献
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武山铜矿床是长江中下游成矿带九瑞矿集区内典型的层控-接触带矽卡岩型铜多金属矿床,铜资源量达到大型,此外还共生硒、碲、钴、镓、铊等关键金属矿产,具备良好的矿产资源综合利用前景,但矿床中关键金属的分布规律、赋存状态和富集机制等研究尚未开展。本文以武山铜矿床为研究对象,系统采集了矿床南矿带接触带矽卡岩型矿体3条勘探线(W3-2、S4-2、N6-1)、北矿带层控硫化物型矿体3条勘探线(E9-2、E2-1、W4-1)和层控矽卡岩型矿体1条勘探线(E7-3)代表性岩矿石样品。通过光学显微镜和扫描电镜的观察,结合全岩地球化学和矿物原位LA-ICP-MS分析,查明了矿床中硒、碲、钴等关键金属的空间分布规律与赋存状态,初步探讨了硒、碲、钴的迁移沉淀机制。研究结果表明矿床中伴生硒、碲、钴的估算资源量分别为5513t、611t和9597t,均达到大-中型规模;武山矿床是成矿带内硒含量最高、潜在资源量最大的矿床。北矿带矿体中Se、Te、Co含量明显高于南矿带,北矿带中部成矿中心向东西远端,矿体中Se、Te、Co含量规律性增高。矿石中Se、Te、Co含量与S含量具有较强的正相关性,矿石中硫化物的含量是关键金属含量主要控制指标;Se和Co富集于含铜黄铁矿矿石、含铜白云岩矿石、含铜矽卡岩矿石(高硫)中;Te富集于含铜黄铁矿矿石和含铜白云岩矿石中。矿床中硒、碲主要以独立矿物和硫化物中类质同象替换两种赋存形式,钴则主要以Co^(2+)类质同象形式进入黄铁矿矿物晶格。矿床中硒、碲随着成矿流体温度降低、硫逸度升高、氧逸度降低、pH值升高逐渐沉淀富集;钴主要随着硫化物的沉淀富集在黄铁矿中。 相似文献
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Geological reference materials (RMs) with variable compositions and NIST SRM 612 were analysed by isotope dilution mass spectrometry for bulk rock concentrations of chalcogen elements (sulfur, selenium and tellurium), rhenium and platinum‐group elements (PGEs: Ru, Pd, Os, Ir and Pt), including the isotope amount ratios of 187Os/188Os. All concentrations were obtained from the same aliquot after HCl‐HNO3 digestion in a high pressure asher at 320 °C. Concentrations were determined after chemical separation by negative TIMS, ICP‐MS and hydride generation ICP‐MS (Se, Te). As in previous studies, concentrations of the PGEs in most RMs were found to be highly variable, which may be ascribed to sample heterogeneity at the < 1 g level. In contrast, S, Se and Te displayed good precision (RSD < 5%) in most RMs, suggesting that part of the PGE budget is controlled by different phases, compared with the chalcogen budget. The method may minimise losses of volatile chalcogens during the closed‐system digestion and indicates the different extent of heterogeneity of chalcogens, Re and PGEs in the same sample aliquot. OKUM, SCo‐1, MRG‐1, DR‐N and MAG‐1 are useful RMs for the chalcogens. NIST SRM 612 displays homogenous distribution of S, Se, Te, Pt and Pd in 30 mg aliquots, in contrast with micro‐scale heterogeneity of Se, Pd and Pt. 相似文献