Hf isotope analysis of small zircon and baddeleyite grains by conventional Multi Collector-Inductively Coupled Plasma-Mass Spectrometry

被引:22
|
作者
D'Abzac, Francois-Xavier [1 ]
Davies, Joshua H. F. L. [1 ]
Wotzlaw, Joern-Frederik [1 ,2 ]
Schaltegger, Urs [1 ]
机构
[1] Univ Geneva, Dept Earth Sci, 13 Rue Maraichers, CH-1205 Geneva, Switzerland
[2] ETH, Inst Geochem & Petrol, Clausiusstr 25, CH-8092 Zurich, Switzerland
关键词
Hafnium isotopes; Zircon; Baddeleyite; MC-ICP-MS; Matrix effect; Reference material; U-PB; LU-HF; TRACE-ELEMENT; RATIO ANALYSIS; MC-ICPMS; HAFNIUM; PRECISION; EVOLUTION; TIMS; ABLATION;
D O I
10.1016/j.chemgeo.2016.03.025
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Protocols for solution nebulization (SN) multi collector (MC) ICP-MS analysis of the Hf isotopic composition of accessory minerals (zircon and baddeleyite) selected for high-precision ID-TIMS U-Pb geochronology have improved significantly during the last two decades. Precise crystallization age and Hf isotopic composition from the exact same volume of mineral can be retrieved, provided that time-consuming sample preparation and purification is possible. The present work focuses on the analytical capabilities of SN-MC-ICP-MS for Hf isotope analysis on non-purified reference materials. Analytical issues arise for (i) igneous and metamorphic zircons, often enriched in trace elements and REEs, which increase the amount of isobaric interferences. (ii) Small minerals that challenge the limits of quantification of the apparatus. JMC475 Hf standard, Plesovice and Temora-2 zircons and Phalaborwa baddeleyite were used to characterize the sources of analytical bias and to set up an optimized protocol for Hf isotope analysis of small accessory minerals with accurate correction of the isobaric interferences and accounting for the matrix effects. Doping of JMC475 with major (Zr, Si), trace (U, Th, Y, Ti) and rare earth elements (Ce, Nd, Gd, Dy, Ho, Er) shows that oxide species produced in the ICP induce an offset of the measured Hf-176/Hf-177 ratios that is corrected by normalization to the reference value. The Yb-176 isobaric interference is efficiently removed for samples with Yb/Hf ratios <0.6 using in-run determined Yb-176/Yb-173 reference ratios from Yb doped reference material. This isotopic ratio varies (i) with time and (ii) sample matrix. Plasma loading by Zr is not the source of these variations. We propose that Yb oxidation in the plasma torch is responsible for variations in the Yb-176/Yb-173 ratio. Our dataset shows that matrix matched standards should be preferred for data reduction, and that Plesovice is a good zircon standard because of its availability, quantifiable REEs composition and potential for wide range of Yb doping. Consequently, low Hf concentration solutions from Temora-2 zircons were accurately measured in a small sample volume (<120 mu l), using a short acquisition protocol (50 x 1 s cycles), and sample-standard bracketing for mass bias coefficient determination in a [Hf]similar to 10 ng/g Plesovice solution measured through 80 x 4 s cycles. The repeatability of the measurement (2SD) is improved by factors of up to similar to 4.4 and the limit of quantification is brought down to <2 ng/g Hf, corresponding to zircon minerals of <24 ng. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:12 / 23
页数:12
相关论文
共 50 条
  • [21] Hafnium isotope analysis of mixed standard solutions by multi-collector inductively coupled plasma mass spectrometry: an evaluation of isobaric interference corrections
    Choi M.S.
    Cheong C.-S.
    Kim J.
    Shin H.S.
    Journal of Analytical Science and Technology, 4 (1)
  • [22] Influence of room temperature on magnesium isotope measurements by multi-collector inductively coupled plasma mass spectrometry
    Zhang, Xing-Chao
    Zhang, An-Yu
    Zhang, Zhao-Feng
    Huang, Fang
    Yu, Hui-Min
    RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2018, 32 (13) : 1026 - 1030
  • [23] Determination of Lu and Hf Mass Fractions and 176Hf/177Hf Ratios in Mafic-Ultramafic Rock Reference Materials by Multi-Collector Inductively Coupled Plasma-Mass Spectrometry
    Ma, Qian
    Yang, Yue-Heng
    Yang, Zhi-Ming
    GEOSTANDARDS AND GEOANALYTICAL RESEARCH, 2023, 47 (04) : 869 - 891
  • [24] A novel approach to measure isotope ratios via multi-collector-inductively coupled plasma-mass spectrometry based on sample mixing with a non-enriched standard
    Costas-Rodriguez, Marta
    Lobo, Lara
    Vanhaecke, Frank
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2014, 406 (18) : 4393 - 4399
  • [25] Correction of Errors Caused by Matrix-induced Mass Bias in Quadrupole Inductively Coupled Plasma-Mass Spectrometry Isotope Dilution Method
    Pak, Yong Nam
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2015, 36 (11) : 2788 - 2790
  • [26] Precise and accurate Ga isotope ratio measurements of geological samples by multi-collector inductively coupled plasma mass spectrometry
    Zhang, Yuxu
    Qiao, Pan
    Zhu, Chuanwei
    Fan, Haifeng
    Wen, Hanjie
    ACTA GEOCHIMICA, 2024, 43 (06) : 1054 - 1064
  • [27] Application of a "Continuous-Acquisition-Method" to potassium isotope measurements by multi-collector inductively coupled plasma mass spectrometry
    Gu, Hai-Ou
    Sun, He
    Huang, Chao
    Wang, Fangyue
    Ge, Can
    RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2021, 35 (13)
  • [28] Optimization of a Laser Ablation-Single Collector-Inductively Coupled Plasma-Mass Spectrometer (Thermo Element 2) for Accurate, Precise, and Efficient Zircon U-Th-Pb Geochronology
    Pullen, Alex
    Ibanez-Mejia, Mauricio
    Gehrels, George E.
    Giesler, Dominique
    Pecha, Mark
    GEOCHEMISTRY GEOPHYSICS GEOSYSTEMS, 2018, 19 (10): : 3689 - 3705
  • [29] Lead isotope measurement using a multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS)
    Choi, Hye-Bin
    Ryu, Jong-Sik
    Park, Sanghee
    Lee, Jeonghoon
    JOURNAL OF THE GEOLOGICAL SOCIETY OF KOREA, 2018, 54 (03) : 311 - 318
  • [30] ANALYSIS OF ZIRCON BY LASER ABLATION AND SOLUTION INDUCTIVELY COUPLED PLASMA MASS-SPECTROMETRY
    PERKINS, WT
    PEARCE, NJG
    FUGE, R
    JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1992, 7 (04) : 611 - 616