scholarly journals LA-ICP-MS Calibrations for Intact Rock Samples with Internal Standard and Modified Constant-Sum Methods

2012 ◽  
Vol 03 (02) ◽  
pp. 168-174 ◽  
Author(s):  
Sheng Peng ◽  
Qinhong Hu
2020 ◽  
Vol 545 ◽  
pp. 119648 ◽  
Author(s):  
Jing-Jing Fan ◽  
Jie Li ◽  
Qiang Wang ◽  
Le Zhang ◽  
Jing Zhang ◽  
...  

2019 ◽  
Vol 34 (5) ◽  
pp. 940-953 ◽  
Author(s):  
Zhian Bao ◽  
Kangjun Huang ◽  
Tianzheng Huang ◽  
Bing Shen ◽  
Chunlei Zong ◽  
...  

This study presents a chemical protocol for the separation of Mg that is particularly adapted for diverse igneous rock samples, especially for high-K and low-Mg rocks.


2021 ◽  
Author(s):  
Seung-Gu Lee ◽  
Tsuyoshi Tanaka

<p></p><p>Eu has only two isotopes (151Eu and 153 Eu). Eu and Gd are one of the rare earth elements that are very difficult to completely separate from each other. Eu isotope ratio can be determined by MC-ICP-MS using internal Sm or Gd spikes to correct for mass discrimination. NIST3117a ultrapure chemical reagent shows almost no Eu isotope fractionation regardless of the kind of normalization isotope pair. However, Eu isotope ratio in the silicate rocks was effected by Gd matrix during MC-ICP-MS measurement if a trace amount of Gd impurity remains in the purified Eu fraction. In this report, we tried to determine optimizing conditions for precise and accurate Europium isotope ratio measurements in geological samples using MC-ICP-MS. The pure Eu fraction with almost no Gd matrix separated from geological samples and NIST3117a ultrapure chemical reagent show almost same degree of Eu isotope fractionation regardless of the kind of normalization isotope pair. However, Eu isotope ratio in the silicate rocks was effected by Gd matrix during MC-ICP-MS measurement using if 154 Gd interference relative to 154 Sm as internal standard is more than ca. 0.1%. Particularly, highly fractionated granite and high silica volcanic rock with extremely low Eu concentration compared to Gd require high – purity Eu separation with a high recovery rate to obtain the true value of the Eu isotope fractionation in the geological rocks. <br></p><br><p></p>


Author(s):  
John D. Greenough ◽  
Alejandro Velasquez ◽  
Mohamed Shaheen ◽  
Joel Gagnon ◽  
Brian J. Fryer ◽  
...  

Trace elements in native gold provide a “fingerprint” that tends to be unique to individual gold deposits. Fingerprinting can distinguish gold sources and potentially yield insights into geochemical processes operating during gold deposit formation. Native gold grains come from three historical gold ore deposits; Hollinger, McIntyre (quartz-vein ore), and Aunor near Timmins, Ontario, at the western end of the Porcupine gold camp and the south-western part of the Abitibi greenstone belt. Laser-ablation, inductively-coupled plasma mass spectrometry (LA ICP MS) trace element concentrations were determined on 20 to 25 µm wide, 300 µm long rastor trails in ~ 60 native gold grains. Analyses used Ag as an internal standard with Ag and Au determined by a scanning electron microscope with an energy dispersive spectrometer. The London Bullion Market AuRM2 reference material served as the external standard for 21 trace element analytes (Al, As, Bi, Ca, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Pd, Pt, Rh, Sb, Se, Si, Sn, Te, Ti, Zn; Se generally below detection in samples). Trace elements in native gold associate according to Goldschmidt’s classification of elements strongly suggesting that element behavior in native Au is not random. Such element behavior suggests that samples from each Timmins deposit formed under similar but slightly variable geochemical conditions. Chalcophile and siderophile elements provide the most compelling fingerprints of the three ore deposits and appear to be mostly in solid solution in Au. Lithophile elements are not very useful for distinguishing these deposits and element ABSTRACT CUT OFF BY SOFTWARE


2016 ◽  
Vol 31 (4) ◽  
pp. 1012-1022 ◽  
Author(s):  
Bao Zhian ◽  
Yuan Honglin ◽  
Zong Chunlei ◽  
Liu Ye ◽  
Chen Kaiyun ◽  
...  

A new glass-making method was developed to allow the in situ analysis of trace elements and lead isotopes in rock samples.


1995 ◽  
Vol 51 (3) ◽  
pp. 312-318 ◽  
Author(s):  
M. Barbaro ◽  
B. Passariello ◽  
S. Quaresima ◽  
A. Casciello ◽  
A. Marabini

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