Nuclear Field Shift Effect in the Isotope Exchange Reaction of Chromium(III) Using a Crown Ether

2002 ◽  
Vol 106 (30) ◽  
pp. 6911-6914 ◽  
Author(s):  
Toshiyuki Fujii ◽  
Daisuke Suzuki ◽  
Katsubumi Gunji ◽  
Kazuo Watanabe ◽  
Hirotake Moriyama ◽  
...  
2009 ◽  
Vol 267 (3-4) ◽  
pp. 157-163 ◽  
Author(s):  
Toshiyuki Fujii ◽  
Frédéric Moynier ◽  
Philippe Telouk ◽  
Francis Albarède

2011 ◽  
Vol 1 (1) ◽  
pp. 387-392 ◽  
Author(s):  
T. Fujii ◽  
F. Moynier ◽  
A. Agranier ◽  
E. Ponzevera ◽  
M. Abe

AbstractLead isotopes were fractionated by the liquid-liquid extraction technique between an aqueous phase and a crown ether. After purification by ion-exchange chemistry, the 207Pb/206Pb and 208Pb/206Pb isotopic ratios were measured by multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). Isotope fractionations > 0.05‰ have been found. The conventional equilibrium mass-dependent isotope effect estimated by an ab initio calculation was smaller than the Pb isotope fractionation experimentally obtained. Conventional mass-dependent isotope fractionation is not a valuable explanation for our results. The nuclear field shift effect, which results from the isotopic change in the nuclear size and shape, was also estimated by an ab initio method combined with a finite nucleus model. The nuclear field shift effect calculated was in agreement with our experimental results. Therefore, this study reports the first nuclear field shift effect of Pb in an equilibrium ligand exchange reaction.


2008 ◽  
Vol 26 (2) ◽  
pp. 100-112 ◽  
Author(s):  
Toshiyuki Fujii ◽  
Daisuke Suzuki ◽  
Hajimu Yamana

1997 ◽  
Vol 250 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Atsushi Baba ◽  
Masabumi Nishikawa ◽  
Takanori Eguchi

1989 ◽  
Vol 67 (5) ◽  
pp. 857-861 ◽  
Author(s):  
Shin-Ichi Miyamoto ◽  
Tetsuo Sakka ◽  
Matae Iwasaki

The reaction rate of hydrogen isotope exchange between D2 and H2O catalyzed by platinum plate is studied. The exchange reaction is described with the kinetic model which is the modification of that for the exchange reaction catalyzed by alumina-supported platinum catalyst. For the comparison of experimental results with this model relative amount of the number of sites for hydrogen adsorption was estimated from the initial rate of hydrogen isotope exchange between H2 and D2 on the same surface. The results show that the kinetic model is applicable for the plate catalyst if the number of the sites for hydrogen absorption, which is very sensitive to the surface state of the catalyst, was estimated not from the macroscopic surface area but from our scheme. Keywords: hydrogen isotope exchange reaction, platinum plate as catalyst.


2014 ◽  
Vol 141 (6) ◽  
pp. 064311 ◽  
Author(s):  
Annalise L. Van Wyngarden ◽  
Kathleen A. Mar ◽  
Jim Quach ◽  
Anh P. Q. Nguyen ◽  
Aaron A. Wiegel ◽  
...  

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