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Experimental study of mass-independence of Hg isotope fractionation during photodecomposition of dissolved methylmercury

Dmitry Malinovskiy UGent, Kris Latruwe UGent, Luc Moens UGent and Frank Vanhaecke UGent (2010) JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY. 25(7). p.950-956
abstract
Experiments modelling photolytic decomposition of methylmercury chloride in aqueous solutions of different chemical composition have been performed. Ion-exchange chromatographic separation using Chelex (R) 100 resin was used in order to separate methylmercury from inorganic mercury prior to the isotope ratio measurements by solution nebulization multicollector inductively coupled plasma mass spectrometry (MC-ICPMS). The performance of the chromatographic separation has been evaluated in terms of recovery of both methylmercury and inorganic Hg using synthetic solutions. Both mass-dependent and mass-independent fractionation of Hg isotopes concomitant with the decomposition process have been observed. Mass-independent Hg isotope fractionation (MIF) resulted in selective enrichment of Hg-199 and Hg-201 relative to the other isotopes in the methylmercury molecules and has been attributed to the magnetic isotope effect. The highest extent of MIF of Hg isotopes, expressed as Delta Hg-199 and Delta Hg-201 values, has been observed in acidified solution with low concentration of total dissolved solids (TDS). Progressive decrease in Delta Hg-199 and Delta Hg-201 values in acidified solution with higher concentration of TDS, alkaline solutions of both low and high concentration of TDS, and in a solution of ascorbic acid has been attributed to suppression of the radical pair reaction mechanism, responsible for the occurrence of the magnetic isotope effect, by substances acting as radical scavengers, such as OH- or ascorbic acid. The data obtained in this study demonstrate the significance of spin chemistry effects in the isotope fractionation of mercury.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
CHROMATOGRAPHIC-SEPARATION, RATIO MEASUREMENTS, COORDINATION CHEMISTRY, MERCURY ISOTOPES, AQUEOUS-SOLUTION, HEAVY-ELEMENTS, SPECTROMETRY, PHASE, SEDIMENTS, DEGRADATION
journal title
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY
J. Anal. At. Spectrom.
volume
25
issue
7
pages
950 - 956
Web of Science type
Article
Web of Science id
000279099000005
JCR category
CHEMISTRY, ANALYTICAL
JCR impact factor
4.372 (2010)
JCR rank
5/71 (2010)
JCR quartile
1 (2010)
ISSN
0267-9477
DOI
10.1039/b926650j
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
1113593
handle
http://hdl.handle.net/1854/LU-1113593
date created
2011-02-01 13:30:42
date last changed
2011-02-09 12:08:31
@article{1113593,
  abstract     = {Experiments modelling photolytic decomposition of methylmercury chloride in aqueous solutions of different chemical composition have been performed. Ion-exchange chromatographic separation using Chelex (R) 100 resin was used in order to separate methylmercury from inorganic mercury prior to the isotope ratio measurements by solution nebulization multicollector inductively coupled plasma mass spectrometry (MC-ICPMS). The performance of the chromatographic separation has been evaluated in terms of recovery of both methylmercury and inorganic Hg using synthetic solutions. Both mass-dependent and mass-independent fractionation of Hg isotopes concomitant with the decomposition process have been observed. Mass-independent Hg isotope fractionation (MIF) resulted in selective enrichment of Hg-199 and Hg-201 relative to the other isotopes in the methylmercury molecules and has been attributed to the magnetic isotope effect. The highest extent of MIF of Hg isotopes, expressed as Delta Hg-199 and Delta Hg-201 values, has been observed in acidified solution with low concentration of total dissolved solids (TDS). Progressive decrease in Delta Hg-199 and Delta Hg-201 values in acidified solution with higher concentration of TDS, alkaline solutions of both low and high concentration of TDS, and in a solution of ascorbic acid has been attributed to suppression of the radical pair reaction mechanism, responsible for the occurrence of the magnetic isotope effect, by substances acting as radical scavengers, such as OH- or ascorbic acid. The data obtained in this study demonstrate the significance of spin chemistry effects in the isotope fractionation of mercury.},
  author       = {Malinovskiy, Dmitry and Latruwe, Kris and Moens, Luc and Vanhaecke, Frank},
  issn         = {0267-9477},
  journal      = {JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY},
  keyword      = {CHROMATOGRAPHIC-SEPARATION,RATIO MEASUREMENTS,COORDINATION CHEMISTRY,MERCURY ISOTOPES,AQUEOUS-SOLUTION,HEAVY-ELEMENTS,SPECTROMETRY,PHASE,SEDIMENTS,DEGRADATION},
  language     = {eng},
  number       = {7},
  pages        = {950--956},
  title        = {Experimental study of mass-independence of Hg isotope fractionation during photodecomposition of dissolved methylmercury},
  url          = {http://dx.doi.org/10.1039/b926650j},
  volume       = {25},
  year         = {2010},
}

Chicago
Malinovskiy, Dmitry, Kris Latruwe, Luc Moens, and Frank Vanhaecke. 2010. “Experimental Study of Mass-independence of Hg Isotope Fractionation During Photodecomposition of Dissolved Methylmercury.” Journal of Analytical Atomic Spectrometry 25 (7): 950–956.
APA
Malinovskiy, D., Latruwe, K., Moens, L., & Vanhaecke, F. (2010). Experimental study of mass-independence of Hg isotope fractionation during photodecomposition of dissolved methylmercury. JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 25(7), 950–956.
Vancouver
1.
Malinovskiy D, Latruwe K, Moens L, Vanhaecke F. Experimental study of mass-independence of Hg isotope fractionation during photodecomposition of dissolved methylmercury. JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY. 2010;25(7):950–6.
MLA
Malinovskiy, Dmitry, Kris Latruwe, Luc Moens, et al. “Experimental Study of Mass-independence of Hg Isotope Fractionation During Photodecomposition of Dissolved Methylmercury.” JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY 25.7 (2010): 950–956. Print.