Issue 20, 2014

Elucidating the role of stable carbon radicals in the low temperature oxidation of coals by coupled EPR–NMR spectroscopy – a method to characterize surfaces of porous carbon materials

Abstract

Recently, the nature of the carbon radicals stabilized in various coals was characterized using Electron Paramagnetic Resonance (EPR) spectroscopy. It was demonstrated that introducing diamagnetic gases, such as He, CO2, or N2, under STP conditions to the coal surface induces the appearance of a new type of carbon surface radical. This interesting phenomenon was not observed for all coal types, which suggests that the use of EPR measurements can provide information on functional groups that exist on the carbon surface. In the current study coupling Nuclear Magnetic Resonance (NMR) with gas flow in situ EPR measurements significantly enhances the ability to characterize the nature of these radicals and the surface functional groups of coal samples. It was observed that the oxidative reaction with aliphatic groups leads to the increase in stable carbon centered radicals. In addition, there are some species of carbon centered radicals that show reversible binding to O2. This phenomena, however, is dependent on the coal rank, sample porosity and the degree of the coal sample to undergo structural changes under the LTO process. These findings shed new light onto the complex heterogeneous low temperature oxidation reactions occurring at the coal surface.

Graphical abstract: Elucidating the role of stable carbon radicals in the low temperature oxidation of coals by coupled EPR–NMR spectroscopy – a method to characterize surfaces of porous carbon materials

Article information

Article type
Paper
Submitted
23 Feb 2014
Accepted
19 Mar 2014
First published
20 Mar 2014

Phys. Chem. Chem. Phys., 2014,16, 9364-9370

Elucidating the role of stable carbon radicals in the low temperature oxidation of coals by coupled EPR–NMR spectroscopy – a method to characterize surfaces of porous carbon materials

U. Green, K. Keinan-Adamsky, S. Attia, Z. Aizenshtat, G. Goobes, S. Ruthstein and H. Cohen, Phys. Chem. Chem. Phys., 2014, 16, 9364 DOI: 10.1039/C4CP00791C

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