scholarly journals Testing miniaturized extraction chromatography protocols for combined 87 Sr / 86 Sr and δ 88/ 86 Sr analyses of pore water by MC‐ICP‐MS

Author(s):  
Claudio Argentino ◽  
Federico Lugli ◽  
Anna Cipriani ◽  
Giuliana Panieri
2020 ◽  
Vol 27 (9) ◽  
pp. 9686-9696 ◽  
Author(s):  
Atta Rasool ◽  
Tangfu Xiao ◽  
Salar Ali ◽  
Waqar Ali ◽  
Wajid Nasim

2017 ◽  
Vol 112 (3) ◽  
pp. 246-251 ◽  
Author(s):  
Athena Marie Gallardo ◽  
Chit Than ◽  
Carolyn Wong ◽  
Ralf Sudowe

2006 ◽  
Vol 60 (2) ◽  
Author(s):  
A. Bartošová ◽  
P. Rajec ◽  
A. Klimeková

AbstractThree methods have been used for the determination of 99Tc in soils and solid radioactive wastes using 99mTc as a yield monitor. In the method one and three the samples were leached in low concentrated nitric and sulphuric acid. Many contaminants were then co-precipitated with Fe(OH)3 in alkali media and Tc in the supernatant was separated using anion-exchange extraction chromatography. There were made also some studies how to improve the chemical recovery of 99mTc in the process of chromatography. In the method two the sample was ashed and then leached in 8 mol dm−3 HNO3 and after iron precipitation, technetium was separated on chromatographic column. The chemical recovery of 99mTc was optimized in the process of chromatography and leaching. Typical recoveries of technetium determined with 99mTc tracer for all these methods were in the range 39 %–87 %.The 99Tc activity was measured using proportional low-background beta detector after one week of staying to allow decay of 99mTc activity. 99Tc was also determined by the non-radiometric method using inductively coupled plasma mass spectrometer.


Talanta ◽  
2013 ◽  
Vol 106 ◽  
pp. 1-7 ◽  
Author(s):  
C. Gautier ◽  
M. Coppo ◽  
C. Caussignac ◽  
I. Laszak ◽  
P. Fichet ◽  
...  

2014 ◽  
Vol 29 (10) ◽  
pp. 1858-1870 ◽  
Author(s):  
Christian Pin ◽  
Abdelmouhcine Gannoun ◽  
Alain Dupont

A straightforward separation scheme is described for the separation of Sr, Pb, and Nd from silicate rocks.


2006 ◽  
Vol 3 (1) ◽  
pp. 53-64 ◽  
Author(s):  
H. Biester ◽  
D. Selimović ◽  
S. Hemmerich ◽  
M. Petri

Abstract. Halogens are strongly enriched in peat and peatlands and such they are one of their largest active terrestrial reservoir. The enrichment of halogens in peat is mainly attributed to the formation of organohalogens and climatically controlled humification processes. However, little is known about release of halogens from the peat substrate and the distribution of halogens in the peat pore water. In this study we have investigated the distribution of chlorine, bromine and iodine in pore water of three pristine peat bogs located in the Magellanic Moorlands, southern Chile. Peat pore waters were collected using a sipping technique, which allows in situ sampling down to a depth greater than 6m. Halogens and halogen species in pore water were determined by ion-chromatography (IC) (chlorine) and IC-ICP-MS (bromine and iodine). Results show that halogen concentrations in pore water are 15–30 times higher than in rainwater. Mean concentrations of chlorine, bromine and iodine in pore water were 7–15 mg l−1, 56–123 μg l−1, and 10–20 μg l−1, which correspond to mean proportions of 10–15%, 1–2.3% and 0.5–2.2% of total concentrations in peat, respectively. Organobromine and organoiodine were the predominant species in pore waters, whereas chlorine in pore water was mostly chloride. Advection and diffusion of halogens were found to be generally low and halogen concentrations appear to reflect release from the peat substrate. Release of bromine and iodine from peat depend on the degree of peat degradation, whereas this relationship is weak for chlorine. Relatively higher release of bromine and iodine was observed in less degraded peat sections, where the release of dissolved organic carbon (DOC) was also the most intensive. It has been concluded that the release of halogenated dissolved organic matter (DOM) is the predominant mechanism of iodine and bromine release from peat.


2001 ◽  
Vol 371 (1) ◽  
pp. 49-53 ◽  
Author(s):  
Yan-Qin Ji ◽  
Jin-Ying Li ◽  
Shang-Geng Luo ◽  
Tao Wu ◽  
Jun-Ling Liu

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