scispace - formally typeset
P

Peter Johnston

Researcher at Johnson Matthey

Publications -  63
Citations -  4091

Peter Johnston is an academic researcher from Johnson Matthey. The author has contributed to research in topics: Catalysis & Acetylene. The author has an hindex of 23, co-authored 61 publications receiving 3695 citations. Previous affiliations of Peter Johnston include Cardiff University.

Papers
More filters
Journal ArticleDOI

Tunable gold catalysts for selective hydrocarbon oxidation under mild conditions

TL;DR: It is shown that nanocrystalline gold catalysts can provide tunable active catalysts for the oxidation of alkenes using air, with exceptionally high selectivity to partial oxidation products and significant conversions.
Journal ArticleDOI

Selective oxidation of glycerol to glyceric acid using a gold catalyst in aqueous sodium hydroxide

TL;DR: Glycerol is oxidised to glyceric acid with 100% selectivity using either 1% au/charcoal or 1% Au/graphite catalyst under mild reaction conditions.
Journal ArticleDOI

Oxidation of glycerol using supported Pt, Pd and Au catalysts

TL;DR: In this paper, the role of the base is discussed and it is proposed that the base aids the initial dehydrogenation via H-abstraction of one of the primary OH groups of glycerol and, in the way, the rate limiting step in the oxidation process is overcome.
Journal ArticleDOI

Identification of single-site gold catalysis in acetylene hydrochlorination

TL;DR: An in situ x-ray absorption fine structure study of gold/carbon (Au/C) catalysts under acetylene hydrochlorination reaction conditions is performed and it is demonstrated that highly active catalysts comprise single-site cationic Au entities whose activity correlates with the ratio of Au(I):Au(III) present.
Journal ArticleDOI

Discovery, Development, and Commercialization of Gold Catalysts for Acetylene Hydrochlorination

TL;DR: The use and disadvantages of the mercury catalyst and the advent of the gold catalysts for vinyl chloride monomer is discussed, and the nature of the active site and the possible reaction mechanism are discussed.