Document Type
Article
Publication Date
9-4-2012
Abstract
Previous studies have indicated environmentally persistent free radicals (EPFRs) are formed when hydroxyl- and chlorine-substituted aromatics chemisorbed on Cu(II)O and Fe(III)2O3 surfaces and were stabilized through their interactions with the surface metal cation. The current study reports our laboratory investigation on the formation and stabilization of EPFRs on a Ni(II)O surface. The EPFRs were produced by the chemisorption of adsorbates on the supported metal oxide surface and transfer of an electron from the adsorbate to the metal center, resulting in reduction of the metal cation. Depending on the temperature and the nature of the adsorbate, more than one type of organic radical was formed. A phenoxyl-type radical, with g-value between 2.0029 and 2.0044, and a semiquinone-type radical, with g-value from 2.0050 to as high as 2.0081, were observed. The half-lives on Ni(II)O were long and ranged from 1.5 to 5.2 days, which were similar to what were observed on Fe(III) 2O3. The yields of the EPFRs formed on Ni(II)O were ∼8× higher than on Cu(II)O and ∼50× higher than on Fe(III)2O3. © 2012 American Chemical Society.
Publication Source (Journal or Book title)
Environmental Science and Technology
First Page
9406
Last Page
9411
Recommended Citation
Vejerano, E., Lomnicki, S., & Dellinger, B. (2012). Formation and stabilization of combustion-generated, environmentally persistent radicals on Ni(II)O supported on a silica surface. Environmental Science and Technology, 46 (17), 9406-9411. https://doi.org/10.1021/es301136d