首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 125 毫秒
1.
纳雍枝铅锌矿床是贵州省内发现的第一个大型铅锌矿床,前人对该矿床进行过大量地质和地球化学研究,对该矿床成因有了一定认识,但其成矿金属来源,特别是其中稀散金属(如Cd)的来源却少有涉及。本文分析了该矿床硫化物和精矿样品的微量元素及镉同位素组成,结合该区域不同地质端元的地球化学数据,来探讨以Cd为代表的稀散金属来源。结果表明,样品的Zn/Cd值变化较大(377～953),均高于川滇黔地区沉积岩的Zn/Cd比值(13～367),而更接近火成岩的Zn/Cd值(515～1319)。精矿和闪锌矿样品的镉同位素组成(δ114/110Cd NIST-3108)变化范围极小(-0.09‰～-0.05‰),与已获得的岩浆岩数据一致(-0.22‰～0.15‰),但明显区别于该地区的碳酸盐岩地层(-0.25‰～0.82‰)。结合精矿的Zn/Cd-δ114/110Cd NIST-3108关系图解和前人研究成果,本文认为该矿床金属成矿物质(如镉、铅等)主要来自基底。  相似文献   

2.
钛同位素标准溶液研制   总被引：1，自引：1，他引：0       下载免费PDF全文
钛同位素组成可用于地球化学和宇宙化学研究中,但目前国内外缺乏钛同位素标准物质.为了满足地质样品钛同位素分析的需要,本文研制了钛同位素标准溶液,报道了钛同位素标准溶液的研制过程和定值结果,包括标准溶液的选择、均匀性和稳定性检验、定值分析及测定数据的统计性检验等.通过初步测定,确定美国Alfa公司生产的Ti单元素溶液作为备选Ti同位素标准溶液.将备选标准溶液分装成150瓶,随机抽取15瓶进行均匀性检验,测试结果的F值均小于临界值,表明备选标准溶液的Ti同位素组成均匀.通过30个月的稳定性检验,标准溶液的特征量值变化在不确定度范围内.采用独家和多家实验室相结合的方法进行定值,标准溶液的特征量值及不确定度推荐为:δ50Ti=-2.23‰±0.14‰,δ49Ti=-1.67‰±0.09‰,δ48Ti=-1.13‰±0.06‰,δ47Ti=-0.57‰±0.05‰.研制的标准溶液可用于钛同位素分析时校正仪器和验证质谱分析过程,有利于不同实验室的测试数据之间的对比和应用.  相似文献   

3.
本研究采集了广东某矿区流域受矿酸性矿山废水(AMD)影响下的地表水、底泥和土壤样品,分析了样品主要的地球化学参数,并对水样进行了Cd稳定同位素的测试。结果表明,从上游到下游,受AMD污染的主要河流水样和底泥样品中重金属元素Cd的含量随着距离增加而降低,与其他重金属元素和大量元素的含量变化趋势一致,p H随着距离的增加而逐渐升高。其中上游拦泥坝水样表现出最高的Cd含量(304.2μg/L)和最低的p H(p H=3.33);底泥中Cd含量普遍较低,介于0.25与39.85μg/g之间,仅在距离拦泥坝下游较近的2个采样点的中达到最高39.85μg/g和38.62μg/g,表明Cd从上游源头向下游迁移的过程中主要以溶解态的形式向下游迁移,且随着距离的增加而逐渐衰减,受污染水体中Cd含量均超过地表水环境质量标准V类水体,远高于底泥中Cd的含量。流域受污染水体Cd的同位素特征值采用?114/110Cdnancy spex表示,其变化范围为:-0.03‰到0.37‰,平均值为(0.19±0.06)‰,与文献(Lambelet et al.2013)报道淡水河流中Cd的同位素分馏值相接近(0.2±0.1)‰。除去其中1个采样点出现最小((-0.03±0.04)‰)镉同位素值,流域受污染河流水体整体富集重的Cd同位素。因此,Cd稳定同位素有可能作为一种新的方法,示踪受地形和水文条件等因素影响的矿山(山地)流域中Cd的污染源及其在环境中的迁移转化过程。  相似文献   

4.
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   

5.
磷(P)是海洋初级生物不可或缺的营养元素,现代海水中溶解态镉与磷的含量线性关系极好,表明镉可能作为海洋初级生物的营养元素而被利用。浮游生物优先摄取轻的镉同位素,使得海水中的镉同位素变化与海洋初级生产力的变化紧密相关。目前镉同位素已成功应用于二叠纪-三叠纪之交古海洋初级生产力的重建。广西桂林晚泥盆世弗拉期-法门期(Frasnian-Famennian, F-F)之交杨堤剖面的镉同位素数据显示,在F-F灭绝事件前,δ~(114)Cd总体偏重(0.03‰～0.49‰),指示当时海洋具有较强的初级生产力;F-F之交,δ~(114)Cd呈现负偏(-0.44‰～-0.01‰),表明这一时期海洋初级生产力显著下降;F-F灭绝事件后,δ~(114)Cd又逐渐增大(-0.04‰～0.13‰),反映灭绝事件后海洋初级生产力的恢复。海洋初级生产力的下降,导致了海洋生态系统中的食物链受到破坏,从而引发了F-F之交的生物灭绝事件。  相似文献   

6.
锂同位素研究是非传统稳定同位素地球化学研究的前沿,已广泛应用于从地表到地幔的岩石圈及流体等固体地球科学的研究领域。准确测定锂同位素比值是应用该同位素体系的前提。本文报道了国际上7种常用地质标准物质(BHVO-2、JB-2、BCR-2、AGV-2、NKT-1、L-SVEC、IRMM-016)的锂同位素组成数据。分析中采用硝酸-氢氟酸混合酸消解岩石标准样品,通过3根阳离子交换树脂(AG50W-X8,200~400目)填充的聚丙烯交换柱和石英交换柱对锂进行分离富集,利用Neptune型多接收器电感耦合等离子体质谱(MC-ICPMS)测定锂同位素比值,使用标准-样品交叉法(SSB)校正仪器的质量分馏。实验得到这7种常用地质标准物质的锂同位素组成与测试精度(2SD)分别为:δ7LiBHVO-2—L-SVEC=4.7‰±1.0‰(n=53),δ7LiJB-2—L-SVEC=4.9‰±1.0‰(n=20),δ7LiBCR-2—L-SVEC=4.4‰±0.8‰(n=8),δ7LiAGV-2—L-SVEC=6.1‰±0.4‰(n=14),δ7LiNKT-1—L-SVEC=9.8‰±0.2‰(n=3),δ7LiL-SVEC—L-SVEC=-0.3‰±0.3‰(n=10),δ7LiIRMM-016—L-SVEC=0.0‰±0.5‰(n=10),这些数据在误差范围内与国际上已发表的数据一致。Li同位素分析精度可以达到大约0.5‰,长期的分析精度即外部重现性≤±1.0‰,达到了国际同类实验室水平。7种常用地质标准物质的锂同位素组成数据的发表为锂同位素研究提供了统一的标准,使地质样品的锂同位素数据的质量监控成为可能。在基质效应的研究中,使用不同量的IRMM-016配制的标准溶液过柱,深入探讨了样品量对锂同位素测定值的影响,结果表明,在现有测试精度下,只要分析样品的锂含量达到100μg/L,且不超过树脂的承载量,样品的锂同位素组成在误差范围内与真值吻合,样品量的大小不影响锂同位素测定结果的准确性。  相似文献   

7.
华北平原典型区水体蒸发氢氧同位素分馏特征   总被引：3，自引：0，他引：3       下载免费PDF全文
马斌  梁杏  靳孟贵  李静  牛宏 《水科学进展》2015,26(5):639-648
为研究华北平原衡水地区水体蒸发氢氧同位素分馏特征,采集不同盐度的深层地下淡水(TDS 为0.61g/L)和浅层地下咸水(TDS为7.97g/L),现场开展室外器皿蒸发实验,获得了当地气象条件下氢氧同位素分馏参数.实验结果显示,淡水及咸水剩余表层水δ18O与剩余水比率f呈指数关系,与瑞利分馏模拟结果一致,δD和δ18O蒸发线斜率分别为4.78和4.69.整个蒸发过程中,淡水及咸水氢氧同位素值增量ΔδD分别为Δδ18O的4.82倍和4.76倍;剩余表层水相对于初始水δD和δ18O的变化量与累积蒸发量之比,淡水分别为2.68‰/cm和0.56‰/cm,咸水分别为2.78‰/cm和0.61‰/cm;而在不同的蒸发时段,剩余表层水δD和δ18O的变化量与蒸发量无明显相关性.受水分子扩散的影响,蒸发皿中氢氧同位素分馏在垂线上分层微弱.由于水体盐度较低,在当地气候条件下进行自由蒸发时,氢氧同位素分馏的盐效应可以忽略.  相似文献   

8.
使用Nu Plasma 1700型MC-ICP-MS的高分辨模式并采用标准-样品交叉法(SSB)测定Si同位素比值,以减少质谱干扰和仪器质量歧视对测定结果的影响。结果表明样品与标准样之间的Si浓度差异程度与Si同位素测量值呈正相关关系,样品与标准样的Si浓度差异低于20%时,Si同位素测量值差异小于0.04‰。测试部分国际常用标准样品的Si同位素组成,结果与文献报道值在误差范围内一致,δ~(30)Si测量精度优于0.07‰/amu。  相似文献   

9.
蓝高勇  吴夏  杨会  唐伟  应启和  王华 《岩矿测试》2017,36(5):460-467
激光同位素光谱分析方法是近些年使用较广泛的一种便捷、快速的测试稳定同位素组成的技术,能同时分析出水中δD、δ~(18)O同位素组成,因其操作简单,检测效率高,体积小,野外现场测试携带方便,迅速在环境、地质、生态和能源等领域得到广泛应用,但是该测试分析方法尚没有相应的国家标准,测试结果得不到有效的溯源,在使用过程中缺乏规范和统一。为此,本文通过在全国范围内12家实验室选取8个比对水样(δD值在-189.1‰~-0.4‰内,δ~(18)O值在-24.52‰~0.32‰内),利用激光同位素光谱法测试比对D/H和18O/16O值,探讨激光同位素光谱仪分析水中δD、δ~(18)O值的准确度和精密度。测试结果表明:各个协作实验室数据准确、稳定,方法的重复性和再现性良好;激光光谱法测定的δD精密度为0.4‰(1σ),δ~(18)O精密度为0.05‰(1σ),与传统稳定同位素质谱的精度几乎一致,因此适用于常规水样中δD、δ~(18)O测定,可以开展野外在线实时检测水中氢氧同位素组成。本研究为开展制定激光同位素光谱法测定环境液态水中δD、δ~(18)O同位素组成标准方法的工作推广和应用提供了参考。  相似文献   

10.
硝酸盐的氮和三氧同位素(δ15N, δ17O和δ18O)及氧同位素非质量分馏(△17O)综合研究, 可以更有效地示踪硝酸盐的来源和形成过程、制约硝酸盐的形成条件。本文详细描述了细菌反硝化法测定10–6级硝酸盐氮和三氧同位素的分析测试方法和实验要点。综合优化改良的细菌反硝化前处理方法、全自动气体预浓缩富集纯化系统和测试流程, 实现了实验室长期测定数据的稳定性, 以及多批次标准样品测定的良好重现性。10 nmol NO– 3标准样品的δ18O和δ15N测试精度分别是0.25‰(1σ)和0.40‰(1σ)。80 nmol NO– 3标准样品的δ18O、δ17O和δ15N的测试精度分别是0.5‰(1σ)、0.4‰(1σ)和0.1‰(1σ), 据此计算出的Δ17O精度为0.46‰(1σ)。  相似文献   

11.
Notations for Cd stable isotope compositions and the use of reference materials are discussed. It is proposed that Cd stable isotope data should be reported as variations of the 114Cd/110Cd ratio/ using either the δ114/110Cd or ε114/110Cd notations. Future publications should report results for BAM-1012 Cd, the only currently available international Cd isotope reference material. It is also recommended that "Münster Cd" and a range of specified geological reference materials are used as additional reference materials. The final choice of a primary "zero-delta" reference standard remains the most important outstanding question.  相似文献   

12.
In this study, the Cd isotopic composition of various geological reference materials and anthropogenic samples was investigated. The measurements were made by multicollector ICP-MS and instrumental mass fractionation was controlled using a "sample-standard bracketing" technique. Cadmium isotopic data are reported relative to an internal Cd solution (Cd Spex) and expressed as the 114 Cd/110Cd delta value. Two other Cd solutions (Prolabo and JMC) were analysed and yielded the same 0% delta value. A fractionated Cd metal sample (Münster Cd) was used as a secondary reference material for Cd isotopic measurements and we obtained a 114 Cd/110 Cd delta value of 4.48% relative to Cd Spex solution. As opposed to multi-stage Cd purification previously published in the literature, a new one step anionic exchange purification using dilute HCl for the analysis of Cd isotopes in geological samples was developed. This method enabled a high recovery (> 95%) and effective separation of the sample matrix to be achieved. The long-term external reproducibility was evaluated at 0.12% (2 standard deviations) for the 114 Cd/110Cd ratio, based on reference solutions and replicated measurements of samples over one year. The variation of Cd isotopic composition of natural terrestrial samples is restricted to a small range of 0.4%, which is similar to previously reported results. In contrast, large variations of Cd isotopic composition were found for anthropogenic samples with values as low as −0.64% for a dust sample issued from a lead smelter and values as high as +0.50% for NIST SRM 2711 (metal-rich soil). These variations are 10 times larger than the reproducibility and suggest that Cd isotopes can be useful as tracers of anthropogenic sources of Cd in the environment.  相似文献   

13.
This study presents a high‐precision Cd isotope measurement method for soil and rock reference materials using MC‐ICP‐MS with double spike correction. The effects of molecular interferences (e.g., 109Ag1H+, 94Zr16O+, 94Mo16O+ and 70Zn40Ar+) and isobaric interferences (e.g., Pd, In and Sn) to Cd isotope measurements were quantitatively evaluated. When the measured solution has Ag/Cd ≤ 5, Zn/Cd ≤ 0.02, Mo/Cd ≤ 0.4, Zr/Cd ≤ 0.001, Pd/Cd ≤ 5 × 10?5 and In/Cd ≤ 10?3, the measured Cd isotope data were not significantly affected. The intermediate measurement precision of pure Cd solutions (BAM I012 Cd, Münster Cd and AAS Cd) was better than ± 0.05‰ (2s) for δ114/110Cd. The δ114/110Cd values of soil reference materials (NIST SRM 2709, 2709a, 2710, 2710a, 2711, 2711a and GSS‐1) relative to NIST SRM 3108 were in the range of ?0.251 to 0.632‰, the δ114/110Cd values of rock reference materials (BCR‐2, BIR‐1, BHVO‐2, W‐2, AGV‐2, GSP‐2 and COQ‐1) varied from ?0.196‰ to 0.098‰, and that of the manganese nodule (NOD‐P‐1) was 0.163 ± 0.040‰ (2s, n = 8). The large variation in Cd isotopes in soils and igneous rocks indicates that they can be more widely used to study magmatic and supergene processes.  相似文献   

14.
Although Zn–Pb deposits are one of the most important Cd reservoirs in the earth, few studies have focused on the Cd isotopic fractionation in Zn–Pb hydrothermal systems. This study investigates the causes and consequences of cadmium and sulfur isotope fractionation in a large hydrothermal system at the Tianbaoshan Zn–Pb–Cd deposit from the Sichuan–Yunnan–Guizhou (SYG) metallogenic province, SW China. Moderate variations in Cd and S isotope compositions have been measured in sphalerite cover a distance of about 78 m. Sphalerite has δ114/110Cd values ranging from 0.01 to 0.57‰, and sulfides (sphalerite, galena and chalcopyrite) have δ34SCDT values ranging from 0.2 to 5.0‰. Although δ34SCDT and δ114/110Cd values in sphalerites have no regular spatial variations, the δ34SCDT values in galena and calculated ore-forming fluid temperatures decreased from 2.1 to 0.2‰ and from about 290 to 130 °C, respectively, from the bottom to the top of the deposit. Heavy Cd isotopes are enriched in early precipitated sphalerite in contrast to previous studies. We suggest that Cd isotopic compositions in ore-forming fluids are heterogeneous, which result in heavy Cd isotope enrichment in early precipitated sphalerite. In comparison with other Zn–Pb deposits in the SYG area, the Tianbaoshan deposit has moderate Cd contents and small isotope fractionation, suggesting differences in origin to other Zn–Pb deposits in the SYG province.In the Tianbaoshan deposit, the calculated δ34S∑S-fluids value is 4.2‰, which is not only higher than the mantle-derived magmatic sulfur (0 ± 3‰), but also quite lower than those of Ediacaran marine sulfates (about 30 to 35‰). Thus, we suggest that reduced sulfur of ore-forming fluids in the deposit was mainly derived from the leaching of the basement, which contains large amount of volcanic or intrusive rocks. Based upon a combination of Cd and S isotopic systems, the Tianbaoshan deposit has different geochemical characteristics from typical Zn–Pb deposits (e.g., the Huize deposit) in SYG area, indicating the unique origin of this deposit.  相似文献   

15.
The Sichuan-Yunnan-Guizhou(SYG)Zn-Pb metallogenic zone in SW China contains＞400 carbonate-hosted hydrothermal Zn-Pb deposits.Some of these,such as the Huize,Tianbaoshan,and Daliangzi deposits,are super-large deposits with significant reserves of Cd,Ge,and Ag.However,the sources of these metals remain controversial.This study investigated the Cd isotopic geochemistry of the Huize deposit,the largest Zn-Pb deposit in the SYG area.Sphalerites formed at three stages in the deposit have different colors:black or dark brown(Stage Ⅰ),red(Stage Ⅱ),and light-yellow(Stage Ⅲ).The δ114/110Cd values of the sphalerites are in the order Stage Ⅲ＜Stage Ⅰ＜Stage Ⅱ.Kinetic isotopic fractionation is likely the key factor causing the lower δ114/110Cd values in the early formed Stage Ⅰ sphalerites than in later-formed Stage Ⅱ sphalerites,with cooling of ore-forming fluids being responsible for the still lower values of the Stage Ⅲ sphalerites.In galena,the δ114/110Cd values are inversely correlated with Cd contents and tend to be higher in high-Zn galena.We speculate that Cd isotopic fractionation was significant during the precipitation of sphalerite and galena,with light Cd isotopes being enriched in galena rather than sphalerite.Comparison of the Cd isotopic signatures and Zn/Cd ratios of different endmembers suggests that the δ114/110Cd values and Zn/Cd ratios of sphalerite from the Huize deposit,as well as other large-scale deposits from the SYG area,are lie in those range of Emeishan basalts and sedimentary rocks and the mean δ114/110Cd values of these deposits show good negative correlation with 1/Cd,suggesting that the ore-forming materials of these deposits were derived from the mixing of Emeishan basalts and sed-imentary rocks.This study demonstrates that Cd isotopes can be useful proxies in elucidating ore genesis in large Zn-Pb deposits.  相似文献   

16.
以柴达木盆地北缘不同构造带代表性原油作为研究对象,采用GC-TC-IRMS技术对原油中正构烷烃单体碳、氢同位素进行测定。利用样品正构烷烃单体碳、氢同位素组成特征及分布模式,进行原油成因类型划分和对比分析。研究结果表明,正构烷烃可溶有机质的δ13C分布在-36‰～-25‰,δD分布在-180‰～-110‰。对比发现,不同构造带原油中正构烷烃单体碳、氢同位素组成特征上存在着比较明显的差别。以-30‰（δ13C）和 -140‰（δD）作为分界,结合同位素曲线的分布型式,可以划分为不同的分布模式判识生烃母质和沉积环境。  相似文献   

17.
Systematic variations in the Cd and Pb isotope ratios in polluted topsoils surrounding the Jinding Pb–Zn mine in China were measured so that the sources of the metals could be traced. The average δ114/110Cd value and 206Pb/207Pb isotope ratio in background soils from the region were +0.41‰ and 1.1902, respectively, whereas the contaminated soil samples had different values, with the δ114/110Cd values varying between −0.59‰ and +0.33‰ and the 206Pb/207Pb isotope ratios varying between 1.1764 and 1.1896. We also measured the Cd and Pb isotopic compositions in oxide ores, sulfide ores, and slags, and found that binary mixing between ores and background soils could explain almost all of the variations in the Cd and Pb isotope ratios in the contaminated soils. This suggests that Cd and Pb pollution in the soils was mainly caused by the deposition of dust emitted during anthropogenic activities (mining and refining). The Pb and Cd isotope ratios clearly showed that contamination in soils in the northeastern part of the area was caused by surface mines and zinc smelters and their slagheaps, while contamination in soils in the southwestern part of the area also came from tailing ponds and underground mines. The main area of soil polluted by dust from Pb–Zn mining processes roughly extended for up to 5 km from the mine itself.  相似文献   

18.
依据实测的燕山地区(1.6～1.0Ga)高于庄组—景儿峪组114个碳、氧同位素数据,研究、讨论了中、新元古界碳酸盐岩碳、氧同位素组成、演化及其地质意义。研究表明,燕山中、新元古界由下至上的地层序列上,碳、氧同位素表现明显的旋回性演化特征,二者多显正相关关系;δ13C在-3‰～3‰区间低幅、高频振荡;δ18O则表现为-2‰～-8‰的高幅、高频波动;δ13C值的增大与沉积环境由潮间向潮下演变、海平面上升、海水变淡、生物量增多相关;降低的δ13C多代表潮间—潮上环境。高于庄组瘤状灰岩及洪水庄组页岩δ13C为低负值,代表最大海泛期沉积。氧同位素组成和变化指示研究区总体为咸化环境,杨庄组上部和雾迷山组下部古海水盐度最高,之后盐度逐渐降低,至雾迷山组上部又有所升高。研究区与天津蓟县和北京十三陵地区的中、新元古代碳酸盐岩碳、氧同位素组成与演化表现出明显的相似性,反映了它们共同受燕山裂陷槽发育的控制;同时,与北美Belt超群和俄罗斯乌拉尔里菲期碳酸盐岩碳、氧同位素组成、演变的高度协同性,又说明了中、新元古代碳酸盐岩中碳、氧同位素组成、演化响应于全球古海洋背景和地球化学条件。  相似文献   

19.
玄武岩标准样品铁铜锌同位素组成   总被引：7，自引：7，他引：0  
报道了三种玄武岩标准样品(BCR-2、BIR-1a和GBW 07105)的铁铜锌同位素数据。实验使用HNO3-HF混合酸消解玄武岩标准样品;AGMP-1阴离子交换树脂分离提纯样品中的铜铁锌,利用多接收等离子体质谱仪(MC-ICPMS)测定铁铜锌同位素比值,分析过程中使用样品-标准-样品交叉法校正仪器的质量分馏。实验得到BCR-2、BIR-1a和GBW 07105标准样品的高精度铁铜锌同位素组成(95%置信水平的不确定度)分别为:δ56FeBCR-2-IRMM014=0.070‰±0.018‰(2SD),δ65 CuBCR-2-SRM976=0.16‰±0.04‰(2SD),δ66 ZnBCR-2-IRMM3702=-0.072‰±0.020‰(2SD);δ56 FeBIR-1a-IRMM014=0.044‰±0.026‰(2SD),δ65CuBIR-1a-SRM976=0.027‰±0.019‰(2SD),δ66 ZnBIR-1a-IRMM3702=0.085‰±0.032‰(2SD);δ56FeGBW 07105-IRMM014=0.126‰±0.039‰(2SD),δ65 CuGBW 07105-SRM976=0.12‰±0.01‰(2SD),δ66ZnGBW 07105-IRMM3702=0.22‰±0.03‰(2SD)。这些数据在误差(不确定度)范围内与国际上已发表的数据是一致的。三个玄武岩标准样品的铁铜锌同位素组成数据的发表为铁铜锌同位素研究提供了统一的标准,使地质样品的铁铜锌同位素数据的质量监控成为可能。  相似文献   

20.
The present study evaluates several critical issues related to precision and accuracy of Cu and Zn isotopic measurements with application to estuarine particulate materials. Calibration of reference materials (such as the IRMM 3702 Zn) against the JMC Zn and NIST Cu reference materials were performed in wet and/or dry plasma modes (Aridus I and DSN‐100) on a Nu Plasma MC‐ICP‐MS. Different mass bias correction methods were compared. More than 100 analyses of certified reference materials suggested that the sample‐calibrator bracketing correction and the empirical external normalisation methods provide the most reliable corrections, with long term external precisions of 0.06 and 0.07‰ (2SD), respectively. Investigation of the effect of variable analyte to spike concentration ratios on Zn and Cu isotopic determinations indicated that the accuracy of Cu measurements in dry plasma is very sensitive to the relative Cu and Zn concentrations, with deviations of δ65Cu from ?0.4‰ (Cu/Zn = 4) to +0.4‰ (Cu/Zn = 0.2). A quantitative assessment (with instrumental mass bias corrections) of spectral and non‐spectral interferences (Ti, Cr, Co, Fe, Ca, Mg, Na) was performed. Titanium and Cr were the most severe interfering constituents, contributing to inaccuracies of ?5.1‰ and +0.60‰ on δ68/64Zn, respectively (for 500 μg l?1 Cu and Zn standard solutions spiked with 1000 μg l?1 of Ti or Cr). Preliminary isotopic results were obtained on contrasting sediment matrices from the Scheldt estuary. Significant isotopic fractionation of zinc (from 0.21‰ to 1.13‰ for δ66Zn) and copper (from ?0.38‰ to 0.23‰ for δ65Cu), suggest a control by physical mixing of continental and marine water masses, characterized by distinct Cu and Zn isotopic signatures. These results provide a stepping‐stone to further evaluate the use of Cu and Zn isotopes as biogeochemical tracers in estuarine environments.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号