Oxygen

About: Oxygen is a research topic. Over the lifetime, 48149 publications have been published within this topic receiving 1113788 citations. The topic is also known as: O & Oxygen.

Free oxygen radicals regulate plasma membrane Ca2+- and K+-permeable channels in plant root cells.

Abstract: Free oxygen radicals are an irrefutable component of life, underlying important biochemical and physiological phenomena in animals. Here it is shown that free oxygen radicals activate plasma membrane Ca2+- and K+-permeable conductances in Arabidopsis root cell protoplasts, mediating Ca2+ influx and K+ efflux, respectively. Free oxygen radicals generate increases in cytosolic Ca2+ mediated by a novel population of nonselective cation channels that differ in selectivity and pharmacology from those involved in toxic Na+ influx. Analysis of the free oxygen radical-activated K+ conductance showed its similarity to the Arabidopsis root K+ outward rectifier. Significantly larger channel activation was found in cells responsible for perceiving environmental signals and undergoing elongation. Quenching root free oxygen radicals inhibited root elongation, confirming the role of radical-activated Ca2+ influx in cell growth. Net free oxygen radical-stimulated Ca2+ influx and K+ efflux were observed in root cells of monocots, dicots, C3 and C4 plants, suggesting conserved mechanisms and functions. In conclusion, two functions for free oxygen radical cation channel activation are proposed: initialization/amplification of stress signals and control of cell elongation in root growth.

Concentration of Ce3+ and Oxygen Vacancies in Cerium Oxide Nanoparticles

Abstract: Temperature variations of the electron magnetic resonance (EMR) spectra and magnetization measurements are used to show that Ce3+ ions in concentration ≃18% are present in 3 nm CeO2 nanoparticles supported on silica aerogel. It is argued that the presence of Ce3+ implies the defect structure CeO2-x for ceria nanoparticles due to oxygen vacancies. This transformation of Ce4+ to Ce3+ driven by oxygen vacancies may be the key to understanding the catalytic properties of ceria.

Singlet oxygen in natural waters

Abstract: MANY studies have shown that singlet molecular oxygen can oxidise a variety of organic substances1–7. These studies have included biologically important compounds present in the aquatic environment such as amino acids4,7 and pollutants like polycyclic aromatic hydrocarbons5 and pesticides6. No data, however, have been obtained to demonstrate that reactions involving singlet oxygen (often called oxygenations) are sufficiently rapid to be significant in natural waters. The most likely mechanism for oxygenation in the environment was originally proposed by Kautsky8 by which light energy absorbed by a sensitiser is transferred to ground-state oxygen to form singlet oxygen, which in turn reacts with the organic substance, or ‘acceptor’ (A), to form a peroxide. Here we present evidence that rapid photochemical generation of singlet oxygen occurs in inland and coastal water bodies of the south-eastern United States.

The use of ilmenite as an oxygen carrier in chemical-looping combustion

Abstract: The feasibility of using ilmenite as oxygen carrier in chemical-looping combustion has been investigated. Itwas found that ilmenite is an attractive and inexpensive oxygen carrier for chemical-looping combustion.Alaboratory fluidizedbed reactor system, simulating chemical-looping combustion by exposing the sample to alternating reducing and oxidizing conditions,was used to investigate the reactivity. During the reducing phase, 15 g of ilmenite with a particle size of 125–180μm was exposed to a flow of 450mLn/min of either methane or syngas (50% CO, 50% H2) and during the oxidizing phase to a flow of 1000mLn/min of 5% O2 in nitrogen. The ilmenite particles showed no decrease in reactivity in the laboratory experiments after 37 cycles of oxidation and reduction. Equilibrium calculations indicate that the reduced ilmenite is in the form FeTiO3 and the oxidized carrier is in the form Fe2TiO5 +TiO2. The theoretical oxygen transfer capacity between these oxidation states is 5%. The same oxygen transfer capacity was obtained in the laboratory experiments with syngas. Equilibrium calculations indicate that ilmenite should be able to give high conversion of the gases with the equilibrium ratios CO/(CO2 + CO) and H2/(H2O+H2) of 0.0006 and 0.0004, respectively. Laboratory experiments suggest a similar ratio for CO. The equilibrium calculations give a reaction enthalpy of the overall oxidation that is 11% higher than for the oxidation of methane per kmol of oxygen. Thus, the reduction from Fe2TiO5 +TiO2 to FeTiO3 with methane is endothermic, but less endothermic compared to NiO/Ni and Fe2O3/Fe3O4, and almost similar to Mn3O4/MnO.