Smith, Matthew

Analysis and reactions of aqueous selenide and other reduced inorganic selenium compounds under anoxic conditions

Type:
Names:
Creator (cre): Smith, Matthew, Thesis advisor (ths): Wallschlaeger, Dirk, Degree committee member (dgc): Dillon, Peter, Degree committee member (dgc): Belzile, Nelson, Degree committee member (dgc): Gueguen, Celine, Degree granting institution (dgg): Trent University
Abstract:

Selenide is cited as a geochemically important selenium (Se) species, but it is unknown whether selenide is a stable aqueous ion in natural waters. The feasibility of using anoxic anion exchange chromatography (AEC) coupled to dynamic reaction cell-inductively coupled plasma-mass spectrometry to separate aqueous selenide was investigated with the goal of quantifying this anion to determine its importance in reducing waters.

It was possible to qualitatively identify selenide using AEC, but much of the aqueous selenide oxidises to Se0 faster than the separation procedure could be completed. AEC analyses of solutions containing polyselenides produced peaks for unidentified Se compounds, which have been assigned tentative structures Se2O22-, Se2O32-, and Se2O62- based on close matches in retention time to stable S compounds.

The results of this work show that aqueous selenide can be qualitatively observed in synthetic solutions using AEC, but it is unknown whether these conditions are relevant to natural waters.

Author Keywords: anoxic speciation, polyselenides, selenide, selenium geochemistry, selenium speciation, selenoselenate

2014