Topic
Hydrogen peroxide
About: Hydrogen peroxide is a research topic. Over the lifetime, 42583 publications have been published within this topic receiving 1043732 citations. The topic is also known as: H2O2 & dioxidane.
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TL;DR: It is reported that gold nanoparticles grafted on nanoparticulate diamond catalyze the formation of hydroxyl radicals from hydrogen peroxide with at least 79 % efficiency and reach a turnover number of 321 000, many orders of magnitude higher than any currently available catalysts.
Abstract: The Fenton reaction consists of the generation of highly aggressive hydroxyl radicals from hydrogen peroxide and is widely used to degrade organic pollutants. Due to its general applicability, the Fenton reaction is employed in water and soil disinfection/remediation and for removal of non-biodegradable chemicals. The main limitation of the Fenton reaction is the consumption of stoichiometric amounts of transition metals, mostly iron. There is considerable incentive in developing a catalytic Fenton process using exclusively hydrogen peroxide and a catalyst. Herein we report that gold nanoparticles grafted on nanoparticulate diamond catalyze the formation of hydroxyl radicals from hydrogen peroxide with at least 79 % efficiency and reach a turnover number of 321 000, many orders of magnitude higher than any currently available catalysts. This extraordinary activity is derived directly from the nanometric diameters of gold and diamond (“nanojewels”) and from the remarkable inertness of the diamond surface. The Fenton reaction, in which highly aggressive hydroxyl radicals (HOC) are generated from H2O2 by reduction with Fe II ,C u II , or other transition metal salts, is a general process that can be used for the degradation/mineralization of recalcitrant organic pollutants as well as for disinfection. [1–4] In spite of the wide applicability of the Fenton reaction for decomposing almost any organic compound, its widespread use for pollution abatement and disinfection is limited by the need for stoichiometric amounts of Fe II or other transition metals. Most of the efforts to transform the Fenton reaction from a stoichiometric to a catalytic process have met with failure or at best can produce HOC with remarkably low efficiency. [5] For instance, the photo-Fenton process requires transparency of the solution (a prerequisite not frequently fulfilled in polluted waters or soils) and consumes “expensive” photons as stoichiometric reagents. A large number of iron-containing solids such as iron-exchanged zeolites and montmorillonites have also been reported as heterogeneous
183 citations
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TL;DR: The results presented here suggest strongly that the reactive species is singlet oxygen generated via the Haber-Weiss reaction and not, as usually assumed, the hydroxyl radical, .OH, generated by the same reaction.
Abstract: Characteristic chemiluminescence emission of singlet (1 delta g) molecular oxygen at 1268 nm is reported from a Haber-Weiss reaction. The reaction consists of mixing aqueous hydrogen peroxide with a solution of potassium superoxide, solubilized by 18-crown-6 ether in carbon tetrachloride or in dry acetonitrile at room temperature. Since the discovery of the enzyme superoxide dismutase by J.M. McCord and I. Fridovich [(1968) J. Biol. Chem. 243, 5733-5760], the identity of the reactive oxidant in superoxide-generating systems in biology has remained a chemical mystery. The results presented here suggest strongly that the reactive species is singlet oxygen generated via the Haber-Weiss reaction and not, as usually assumed, the hydroxyl radical, .OH, generated by the same reaction.
183 citations
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TL;DR: An aqueous solution of hydrogen carbonate facilitated oxidative hydrogen peroxide production from water on a WO3/BiVO4 photoanode with the simultaneous production of hydrogen (H2) on a Pt cathode even at an applied voltage far lower than the theoretical electrolysis voltage under simulated solar light.
183 citations
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TL;DR: The chemical mechanism and reaction intermediates generated during conversion of amino acids into aldehydes by myeloperoxidase-generated HOCl are detailed.
183 citations
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TL;DR: The observed pseudo-first order rate constant for the reaction between a horseradish peroxidase (HRP) variant (R38L)HRPC and hydrogen peroxide saturates at high peroxide concentrations is consistent with a two-step mechanism involving the formation of an HRP-HO intermediate, and Spectrophotometric titrations show that arginine 38 modulates the reactivity of HRP compound I.
183 citations