电感耦合等离子体质谱法同时测定地下水中硼溴碘   总被引：6，自引：4，他引：2       下载免费PDF全文

黄光明  窦银萍  张静梅  张培新  高孝礼 《岩矿测试》2008,27(1):25-28

建立了电感耦合等离子体质谱法同时测定地下水中B、Br、I的方法。选定φ=2%(体积分数)的稀NH3.H2O介质消除碘的记忆效应。采用干扰较少的10B和79Br同位素。B、Br、I在0~10 000 ng/mL呈良好的线性关系。方法的检出限为10B 0.176 ng/mL,79Br 0.876ng/mL,127I 0.132 ng/mL;精密度(RSD,n=12)为10B 2.86%,79Br 3.36%,127I 2.69%;10B的阶梯加标回收率为94.6%~101.5%,79Br为98.3%~104.9%,127I为96.5%~102.0%。  相似文献   

便携式Li-K分析仪的研制及其在锂辉石中锂的分析应用   总被引：1，自引：1，他引：0       下载免费PDF全文

焦距  杨啸涛  袁继海  樊兴涛  刘晓  詹秀春 《岩矿测试》2016,35(4):366-372

我国锂钾主要矿产资源大多分布在西部偏远地区,其勘查找矿或综合利用迫切需要现场快速分析技术的支持。本文介绍了自行开发的便携式Li-K分析仪的主要性能及其在锂辉石中锂的分析应用。Li-K分析仪是一种基于大气压的液体阴极辉光放电光谱仪,以待测液体为放电阴极,实现了样品中Li、K等元素的原子化和激发。该仪器以光纤传导CCD光谱仪作为检测器,其波长范围为345~1015 nm,分辨率3 nm;以Li 670.78 nm和K 769.90 nm分析谱线,在仪器最佳工作条件下测定Li、K的精密度(RSD,n=14)均低于2%,检出限为0.03μg/m L,检测范围0.1~10μg/m L。研究表明,不同酸度和酸的类型对谱线强度影响较大,且存在显著的样品基体效应,标准曲线法分析锂辉石中Li的结果偏差高达267%;而标准加入法可克服基体效应的影响,获得与ICP-OES一致性较好的分析结果,为现场开展固体样品中Li的测定奠定了基础。  相似文献   

热解—动力学光度法测定岩石和化探样品中痕量溴     

杨秀清 《国土资源》1989,(1)

以五氧化二钒为熔剂,用热解分离富集痕量溴,吸收于0.036mol/l 氢氧化钾中,在1.34mol/l 硫酸和硝酸混合溶液中,溴离子催化高锰酸钾对碘的氧化,用苯萃取未反应碘,然后用硫氢酸汞—硫酸高铁铵比色法测定溴。本方法灵敏度高,远择性好,操作简便、快速,方法检出限为0.35ppm 溴,标准偏差为11.63％。  相似文献   

Determination of Bromine and Iodine in Twenty-three Geochemical Reference Materials by ICP-MS   总被引：1，自引：0，他引：1  

Jian Y. Chai  Yasuyuki Muramatsu 《Geostandards and Geoanalytical Research》2007,31(2):143-150

Trace amounts (from nanogram to microgram levels) of bromine and iodine were determined by inductively coupled plasma-mass spectrometry (ICP-MS) in twenty-three geochemical reference materials issued by the GSJ, USGS, IAEA etc. The pyrohydrolysis technique was used to separate bromine and iodine from samples analysed in the form of powder. The accuracy and precision of the experimental values were assessed by the comparative analysis of well established reference materials such as USGS AGV-1, BCR-1 and IGGE GBW07312. The measured values agreed well with reported values within a 10% error range. We also report reliable new data for these elements in these geochemical reference materials.  相似文献   

能量色散X射线荧光光谱法测定卤水中痕量溴铷砷   总被引：3，自引：4，他引：3  

樊兴涛  詹秀春  巩爱华 《岩矿测试》2004,23(1):15-18

用模拟卤水建立了能量色散X射线荧光光谱法测定卤水中溴、铷、砷痕量元素含量的方法.实验表明,方法可以直接取样测定,适用于大批量样品的测试分析.方法的精密度RSD(n＝15)小于1%,加标回收率为86.8%～101.6%.卤水中溴、铷、砷的测定结果与比色法、原子吸收和原子荧光法结果相符.  相似文献   

Gold and Platinum-Group Element Analysis of Geochemical and Platinum Reference Materials Using Fluoroxidation Decomposition     

Valentin N. Mitkin 《Geostandards and Geoanalytical Research》2000,24(2):157-170

A novel method is described for the rapid dissolution of various geological, geochemical and related reference samples for the determination of Au and the platinum-group elements. The decomposition procedure is based on reaction with the fluoroxidants, liquid bromine trifluoride or molten potassium tetrafluorobromate. Results by this novel procedure are compared with data obtained by traditional methods of sample decomposition, including fire assay, autoclave techniques and an aqua regia leach. The oxidative fluorination procedure with the subsequent conversion of fluorocomplexes into the chloride form was found to be an effective and rapid method for the quantification of all the precious metals in a range of sample types.  相似文献   

电感耦合等离子体质谱法同时测定地质样品中痕量碘溴硒砷的研究：Ⅱ.土壤及沉积物标准物质分析   总被引：11，自引：8，他引：11  

李冰  史世云等 《岩矿测试》2001,20(4):241-246

样品用碳酸钠和氧化锌混合熔剂半熔，热水提取，然后用强酸性阳离子交换树脂将阴离子形式存在的分析元素与溶液中大量钠、锌等阳离子分离，采用电感耦合等离子体质谱法直接同时测定溶液中的碘、溴、硒、砷。用0.07mol/L的氨水溶液清洗进样系统，有效减少了碘等元素的记忆效应和清洗时间。方法检出限（10σ，DF=100）溴、碘分别为0.15和0.028μg/g，砷、硒分别为0.04和0.004μg/g。用土壤和沉积物等地质标准物质分析验证了方法的准确度和精密度，绝大多数分析结果在标准值的允许误差范围之内。样品10次测定的RSD为0.8%～2.8%。  相似文献   

铼—锇同位素分析中试样化学预处理方法进展   总被引：4，自引：0，他引：4  

张巽  金立新等 《岩矿测试》2002,21(1):49-54

评述了用于Re-Os同位素体系分析的化学前处理技术的发展。简要介绍了卡洛斯管熔样法、Os的CCl4提取、溴提取和微蒸馏方法。卡洛斯管封闭熔样方法，有效地防止了Os的挥发损失和保证了Os同位素平衡，是一种很有发展前景的熔样方法。蒸馏法仍是分离和纯化Os的有效方法，溶剂（CCl4)提取和溴提取法在许多实验室里应用，而微蒸馏则是Os的二次纯化的主要方法。Re的化学分离和纯化仍是离子交换和萃取法。引用主要文献29篇。  相似文献   

沥青铀矿中氧同位素测定方法   总被引：2，自引：0，他引：2  

刘培伦  张文华 《铀矿地质》1997,13(3):176-182,166

本文介绍了一种直接测定沥青铀矿中氧同位素的分析方法－－五氟化溴法，实验分析和数据首次表明，铀氧化物中的氧同位素主要是富轻氧的。  相似文献   

Electron Probe Microanalysis of Bromine in Minerals and Glasses with Correction for Spectral Interference from Aluminium,and Comparison with Microbeam Synchrotron X‐Ray Fluorescence Spectrometry          下载免费PDF全文

Chao Zhang  Jinru Lin  Yuanming Pan  Renfei Feng  Renat R. Almeev  Francois Holtz 《Geostandards and Geoanalytical Research》2017,41(3):449-457

The strong spectral interference between Br‐ and Al‐induced X‐ray lines hampers the utilisation of electron probe microanalysis (EPMA) for measuring Br mass fractions in Al‐bearing minerals and glasses. Through measuring Br‐free Al‐bearing materials, we established an EPMA method to quantify the overlap from AlKα on BrLβ, which can be expressed as a linear function of the Al₂O₃ content. The count rate of the BrLβ peak signal was enhanced by high beam currents and long measurement times. Application of this EPMA method to Al‐ and Br‐bearing materials, such as sodalite and scapolite, and to five experimental glasses yielded Br mass fractions (in the range of 250–4000 μg g^?1) that are consistent with those measured by microbeam synchrotron X‐ray fluorescence (μ‐SXRF) spectrometry. The EPMA method has an estimated detection limit of ~ 100–300 μg g^?1. We propose that this method is useful for measuring Br mass fractions (hundreds to thousands of μg g^?1) in Al‐bearing minerals and glasses, including those produced in Br‐doped experiments. In addition, the natural marialitic scapolite (ON70) from Mpwapwa (Tanzania) containing homogeneously distributed high mass fractions of Br (2058 ± 56 μg g^?1) and Cl (1.98 ± 0.03% m/m) is an ideal reference material for future in situ analyses.  相似文献