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John B. Moffat

Researcher at University of Waterloo

Publications -  208
Citations -  4945

John B. Moffat is an academic researcher from University of Waterloo. The author has contributed to research in topics: Catalysis & Oxidative coupling of methane. The author has an hindex of 37, co-authored 208 publications receiving 4838 citations. Previous affiliations of John B. Moffat include University of Tokushima & University of Guelph.

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A new radical oxygen site on silica prepared by the sol-gel method from ethyl orthosilicate

TL;DR: In this article, a stable radical species is generated on the surface of silica prepared by the sol-gel method from ethyl orthosilicate by the surface reaction between carbon monoxide and oxygen, while a small number of the radicals are observable on the silica sample evacuated at 950 K.
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Removal of NO2 from Gaseous Streams by Sorption and Conversion on 12-Tungstophosphoric Acid.

TL;DR: Although no formation of N 2 is observed, the process, which is at least partially reversible, offers some interesting possibilities for the removal of NO 2 from the gas phase.
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Comparison of the Oxidative Coupling Reactions of Benzene with Those of Methane of Rare Earth Oxide Catalysts

TL;DR: In this article, the authors compared the oxidative coupling of benzene with that of methane on La2O3, CeO2, Pr6O11, and Sm 2O3 at temperatures greater than 1048 K.
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Synergistic effects in the oxidation of methane on strontium and lead hydroxyapatites

TL;DR: In this article, the oxidation of methane has been investigated on lead hydroxyapatite (PbHAp), strontium hydroxymatic acid (SrHAp) and their binary mixtures at 873 K.
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ESR study of the active oxygen species on hydroxyapatite activated by heat treatment

TL;DR: In this paper, the ESR spectra of the active oxygen radical (O 2 − ) formed on the hydroxyapatite (HAP) were analyzed and a quartet signal was derived from the interaction of an unpaired electron with three equivalent phosphorus atoms, which was attributed to the different active species for O 2 produced by the series of treatments: formation of O 2 − on thermally activated HAP, reaction of the O 2− species with propylene, heating at 673-973 K and treatment with O 2.