Redox

About: Redox is a research topic. Over the lifetime, 26853 publications have been published within this topic receiving 862368 citations. The topic is also known as: reduction-oxidation & reduction-oxidation reaction.

Relationship between redox activity and chemical speciation of size-fractionated particulate matter

Abstract: Although the mechanisms of airborne particulate matter (PM) related health effects remain incompletely understood, one emerging hypothesis is that these adverse effects derive from oxidative stress, initiated by the formation of reactive oxygen species (ROS) within affected cells. Typically, ROS are formed in cells through the reduction of oxygen by biological reducing agents, with the catalytic assistance of electron transfer enzymes and redox active chemical species such as redox active organic chemicals and metals. The purpose of this study was to relate the electron transfer ability, or redox activity, of the PM samples to their content in polycyclic aromatic hydrocarbons and various inorganic species. The redox activity of the samples has been shown to correlate with the induction of the stress protein, hemeoxygenase-1. Size-fractionated (i.e. < 0.15; < 2.5 and 2.5 – 10 μm in diameter) ambient PM samples were collected from four different locations in the period from June 2003 to July 2005, and were chemically analyzed for elemental and organic carbon, ions, elements and trace metals and polycyclic aromatic hydrocarbons. The redox activity of the samples was evaluated by means of the dithiothreitol activity assay and was related to their chemical speciation by means of correlation analysis. Our analysis indicated a higher redox activity on a per PM mass basis for ultrafine (< 0.15 μm) particles compared to those of larger sizes. The PM redox activity was highly correlated with the organic carbon (OC) content of PM as well as the mass fractions of species such as polycyclic aromatic hydrocarbons (PAH), and selected metals. The results of this work demonstrate the utility of the dithiothreitol assay for quantitatively assessing the redox potential of airborne particulate matter from a wide range of sources. Studies to characterize the redox activity of PM from various sources throughout the Los Angeles basin are currently underway.

Organic Radical Battery Approaching Practical Use

Abstract: The electrochemical redox reactions of organic polymers bearing robust unpaired electrons were investigated to determine the applicability of these polymers to rechargeable batteries. Such an “orga...

Hydrogen evolution from water induced by visible light mediated by redox catalysis

Abstract: Noble metal dispersions are suitable for mediating light-induced hydrogen1–5 and oxygen6–8 evolution from water. We report here a dramatic improvement of the hydrogen production rate when very finely dispersed platinum is used as a mediator in reaction (1). The first observations of the dynamics of intervention of the Pt particles in the redox events are presented. A centrifuged colloidal Pt catalyst stabilised by polyvinyl alcohol showed exceptionally high activity in promoting hydrogen evolution from water via 2MV+ + H2O→PtH2 + 2OH− + 2MV2+ (1) where MV+ stands for reduced methylviologen. The latter is produced photochemically in aqueous solution containing Ru(bipy)32+ as a sensitiser and EDTA as an electron donor. At 10−3 M Pt the reoxidation of MV+ requires only 15 µs and leads to quantitative formation of H2.

Identifying the Active Site in Nitrogen-Doped Graphene for the VO2+/VO2+ Redox Reaction

Abstract: Nitrogen-doped graphene sheets (NGS), synthesized by annealing graphite oxide (GO) with urea at 700–1050 °C, were studied as positive electrodes in a vanadium redox flow battery. The NGS, in particular annealed at 900 °C, exhibited excellent catalytic performance in terms of electron transfer (ET) resistance (4.74 ± 0.51 and 7.27 ± 0.42 Ω for the anodic process and cathodic process, respectively) and reversibility (ΔE = 100 mV, Ipa/Ipc = 1.38 at a scan rate of 50 mV s–1). Detailed research confirms that not the nitrogen doping level but the nitrogen type in the graphene sheets determines the catalytic activity. Among four types of nitrogen species doped into the graphene lattice including pyridinic-N, pyrrolic-N, quaternary nitrogen, and oxidic-N, quaternary nitrogen is verified as a catalytic active center for the [VO]2+/[VO2]+ couple reaction. A mechanism is proposed to explain the electrocatalytic performance of NGS for the [VO]2+/[VO2]+ couple reaction. The possible formation of a N–V transitional bon...