High-precision Ru isotopic measurements by multi-collector ICP-MS

The Analyst ◽  
2002 ◽  
Vol 127 (6) ◽  
pp. 775-780 ◽  
Author(s):  
Harry Becker ◽  
Claude Dalpe ◽  
Richard J. Walker
The Analyst ◽  
2004 ◽  
Vol 129 (1) ◽  
pp. 32-37 ◽  
Author(s):  
Maria Schönbächler ◽  
Mark Rehkämper ◽  
Der-Chuen Lee ◽  
Alex N. Halliday

2019 ◽  
Vol 40 (6) ◽  
pp. 206-214
Author(s):  
Yangtao Zhu ◽  
Ming Li ◽  
Zaicong Wang ◽  
Zongqi Zou ◽  
Zhaochu Hu ◽  
...  

2020 ◽  
Vol 545 ◽  
pp. 119648 ◽  
Author(s):  
Jing-Jing Fan ◽  
Jie Li ◽  
Qiang Wang ◽  
Le Zhang ◽  
Jing Zhang ◽  
...  

2002 ◽  
Vol 188 (1-2) ◽  
pp. 65-83 ◽  
Author(s):  
Kenneth D. Collerson ◽  
Balz S. Kamber ◽  
Ronny Schoenberg

2018 ◽  
Vol 4 (3) ◽  
Author(s):  
Josefina Pérez-Arantegui ◽  
Francisco Laborda

Abstract Inorganic mass spectrometry has been used as a well-known analytical technique to determine elemental/isotopic composition of very diverse materials, based on the different mass-to-charge ratios of the ions produced in a specific source. In this case, two mass spectrometric techniques are explained and their analytical properties discussed: inductively coupled plasma mass spectrometry (ICP-MS) and thermal ionisation mass spectrometry (TIMS), since they are the most used in art and archaeological material studies. Both techniques combine advantageous analytical properties, like low detection limits, low interferences and high precision. The use of laser ablation as sample introduction system in ICP-MS allows to avoid sample preparation and to perform good spatial-resolution analysis. The development of new instruments, improving the mass separation and the detection of the ions, specially multicollection detectors, results in high-precision isotopic analysis. A summary of the important applications of these mass spectrometric techniques to the analysis of art and archaeological materials is also highlighted.


2021 ◽  
Author(s):  
Mitsuru Suzuki ◽  
Tsuyoshi Iizuka ◽  
Kota Yamamoto ◽  
Takafumi Hirata

2018 ◽  
Vol 33 (2) ◽  
pp. 175-186 ◽  
Author(s):  
Leah E. Morgan ◽  
Danielle P. Santiago Ramos ◽  
Brett Davidheiser-Kroll ◽  
John Faithfull ◽  
Nicholas S. Lloyd ◽  
...  

Potassium isotopic compositions measured by MC-ICP-MS in cold-plasma, high-resolution mode indicate terrestrial variability in 41K/39K ratios.


Author(s):  
Kaiyun Chen ◽  
Zhian Bao ◽  
Honglin Yuan ◽  
Nan Lv

This study presents a practical method for high-precision Fe isotope determination without column chromatography purification for iron-dominated mineral samples using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). A series of comparable...


2021 ◽  
Author(s):  
Qingqing Zhao ◽  
Degao Zhai ◽  
Ryan Mathur ◽  
Jiajun Liu ◽  
David Selby ◽  
...  

Abstract Whether giant porphyry ore deposits are the products of single, short-lived magmatic-hydrothermal events or multiple events over a prolonged interval is a topic of considerable debate. Previous studies, however, have all been devoted to porphyry Cu and Cu-Mo deposits. In this paper, we report high-precision isotope dilution-negative-thermal ionization mass spectrometric (ID-N-TIMS) molybdenite Re-Os ages for the newly discovered, world-class Chalukou porphyry Mo deposit (reserves of 2.46 Mt @ 0.087 wt % Mo) in NE China. Samples were selected based on a careful evaluation of the relative timing of the different vein types (i.e., A, B, and D veins), thereby ensuring that the suite of samples analyzed could be used to reliably determine the age and duration of mineralization. The molybdenite Re-Os geochronology reveals that hydrothermal activity at Chalukou involved two magmatic-hydrothermal events spanning an interval of 6.92 ± 0.16 m.y. The first event (153.96 ± 0.08/0.63/0.79 Ma, molybdenite ID-N-TIMS Re-Os age) was associated with the emplacement of a granite porphyry dated at 152.1 ± 2.2 Ma (zircon laser ablation-inductively coupled plasma-microscopic [LA-ICP-MS] U-Pb ages), and led to only minor Mo mineralization, accounting for <10% of the overall Mo budget. The bulk of the Mo (>90%) was deposited in less than 650 kyr, between 147.67 ± 0.10/0.60/0.76 and 147.04 ± 0.12/0.72/0.86 Ma (molybdenite ID-N-TIMS Re-Os ages), coincident with the emplacement of a fine-grained porphyry at 148.1 ± 2.6 Ma (zircon LA-ICP-MS U-Pb ages). The high-precision Re-Os age determinations presented here show, contrary to the finding of a number of studies of porphyry Cu and Cu-Mo systems, that the giant Chalukou porphyry Mo deposit primarily formed in a single, short-lived (<650 kyr) hydrothermal event, suggesting that this may also have been the case for other giant porphyry Mo deposits.


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