ORCID Profile
0000-0002-9273-3679
Current Organisation
Jordan University of Science and Technology
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Publisher: Elsevier BV
Date: 02-2020
DOI: 10.1016/J.CHEMOSPHERE.2019.124921
Abstract: The interplay of phenolic molecules with 3d transition metals, such as Fe and Cu, and their oxide surfaces, provide important fingerprints for environmental burdens associated with thermal recycling of e-waste and subsequent generation of notorious dioxins compounds and phenoxy-type Environmental Persistent Free Radicals (EPFRs). DRIFTS and EPR measurements established a strong interaction of the phenol molecule with transition metal oxides via synthesis of phenolic- and catecholic-type EPFRs intermediates. In this contribution, we comparatively examined the dissociative adsorption of a phenol molecule, as the simplest model for phenolic-type compounds, on Cu and Fe surfaces and their partially oxidized configurations through accurate density functional theory (DFT) studies. The underlying aim is to elucidate the specific underpinning mechanism forming phenoxy- or phenolate-type EFPRs. Simulated results show that, the phenol molecule undergoes fission of its hydroxyl's O-H bond via accessible activation energies. These values are lower by 46.5-74.1% when compared with the analogous gas phase value. Physisorbed molecules of phenol incur very low binding energies in the range of -2.1 to -5.5 over clean Cu/Fe and their oxides surfaces. Molecular attributes based on charge transfer and geometrical features are in accord with the very weak interaction in physisorbed states. Thermo-kinetic parameters established over the temperature region of 300 and 1000 K, exhibit a lower activation energy for scission of phenolic's O-H bonds over the oxide surfaces in reference to their pure surfaces (24.7 and 43.0 kcal mol
Publisher: Elsevier BV
Date: 12-2018
Publisher: Elsevier BV
Date: 11-2014
Publisher: Elsevier BV
Date: 10-2014
Publisher: Elsevier BV
Date: 10-2018
Publisher: Elsevier BV
Date: 05-2018
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for mohammad al-harahsheh.