Determination of low-level radiostrontium, with emphasis on in situ pre-concentration of Sr from large volume of freshwater sample using Powdex resin

2015 ◽  
Vol 146 ◽  
pp. 88-93 ◽  
Author(s):  
Jumpei Tomita ◽  
Masayoshi Yamamoto ◽  
Teo Nozaki ◽  
Yoshihiko Tanimura ◽  
Tetsuya Oishi
2019 ◽  
Vol 11 (31) ◽  
pp. 3943-3957
Author(s):  
Imma Tolosa ◽  
Carlos Guitart ◽  
Marianela Mesa-Albernas ◽  
Carolina Funkey ◽  
Roberto Cassi

A large volume sampling technique is used to develop and validate a home-made SPE system connected to a particle collector in situ pump for high sample pre-concentration and determination of petroleum hydrocarbons and their 13C/12C isotope ratio.


1998 ◽  
Vol 102 (50) ◽  
pp. 10289-10299 ◽  
Author(s):  
Björn Klotz ◽  
Søren Sørensen ◽  
Ian Barnes ◽  
Karl H. Becker ◽  
Thomas Etzkorn ◽  
...  

Minerals ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 67
Author(s):  
Britany L. Kulka ◽  
Jonathan D. Dolinschi ◽  
Kurt D. Leinenweber ◽  
Vitali B. Prakapenka ◽  
Sang-Heon Shim

The bridgmanite–akimotoite–majorite (Bm–Ak–Mj or BAM) triple point in MgSiO3 has been measured in large-volume press (LVP; COMPRES 8/3 assembly) and laser-heated diamond anvil cell (LHDAC). For the LVP data, we calculated pressures from the calibration provided for the assembly. For the LHDAC data, we conducted in situ determination of pressure at high temperature using the Pt scale at synchrotron. The measured temperatures of the triple point are in good agreement between LVP and LHDAC at 1990–2000 K. However, the pressure for the triple point determined from the LVP is 3.9 ± 0.6 GPa lower than that from the LHDAC dataset. The BAM triple point determined through these experiments will provide an important reference point in the pressure–temperature space for future high-pressure experiments and will allow mineral physicists to compare the pressure–temperature conditions measured in these two different experimental methods.


2022 ◽  
Author(s):  
Qingze Li ◽  
Xiping Chen ◽  
Lei Xie ◽  
Tiexin Han ◽  
Jiacheng Sun ◽  
...  

Abstract Here, simultaneous in-situ calibration of pressures and temperatures was performed in a hinge-type second-stage cubic large volume press (LVP) up to 15 GPa and 1400 K by an acoustic travel-time approach. Based on the recently reported P-t S and P-T-t P -t S equations for Al2O3 buffer rod, the cell pressures and temperatures in the chamber of LVP were in-situ determined, in comparison with those by conventional off-line (or fixed-points) pressure calibration method and direct thermocouple measurement, respectively. It is found that the cell pressures of the LVP chamber are significantly reduced after annealing at simultaneous high pressures and high temperatures, owing to the stress relaxation as accumulate in the LVP chamber. This acoustic travel-time method is validated to be a good way for precise determination of thermal (cell) pressures at high temperature conditions, and is of great importance and necessity to conduct in-situ physical property measurements under extreme high P-T conditions, especially when the precious synchrotron X-ray/neutron diffraction beams are not available.


Author(s):  
Britany Kulka ◽  
Jonathan Dolinschi ◽  
Kurt Leinenweber ◽  
Vitali Prakapenka ◽  
Sang-Heon Shim

The akimotoite--majorite--bridgmanite (Ak--Mj--Bm) triple point in MgSiO3 has been measured in large-volume press (LVP; COMPRES 8/3 assembly) and laser-heated diamond anvil cell (LHDAC). For the LVP data, we calculated pressures from the calibration by Leinenweber (2012). For the LHDAC data, we conducted \textit{in situ} determination of pressure at high temperature using the Pt scale by Dorogokupets and Dewaele (2007) at synchrotron. The measured temperatures of the triple point are in good agreement between LVP and LHDAC at 1990-2000 K. However, the pressure for the triple point determined from the LVP is 3.9+/-0.6~GPa lower than that from the LHDAC dataset. The triple point determined through these experiments will provide an important reference point in the pressure-temperature space for future high-pressure experiments and allow mineral physicists to compare the pressure--temperature conditions measured in these two different experimental methods.


2020 ◽  
Vol 48 (6) ◽  
pp. 765-773 ◽  
Author(s):  
Rui-Qin GAO ◽  
Xiao-Lin HOU ◽  
Lu-Yuan ZHANG ◽  
Wei-Chao ZHANG ◽  
Meng-Ting ZHANG

2007 ◽  
Vol 275 (2) ◽  
pp. 291-297 ◽  
Author(s):  
A. Okubo ◽  
J. Zheng ◽  
M. Yamada ◽  
T. Aono ◽  
T. Nakanishi ◽  
...  

2010 ◽  
Vol 68 (4-5) ◽  
pp. 812-815 ◽  
Author(s):  
A. Baeza ◽  
J.A. Corbacho
Keyword(s):  

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


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