Search results
Results from the WOW.Com Content Network
In outer sphere redox reactions no bonds are formed or broken; only an electron transfer (ET) takes place. A quite simple example is the Fe 2+ /Fe 3+ redox reaction, the self exchange reaction which is known to be always occurring in an aqueous solution containing the aquo complexes [Fe(H 2 O) 6] 2+ and [Fe(H 2 O)6] 3+.
Free radical reactions are redox reactions that occur as part of homeostasis and killing microorganisms. In these reactions, an electron detaches from a molecule and then re-attaches almost instantly. Free radicals are part of redox molecules and can become harmful to the human body if they do not reattach to the redox molecule or an antioxidant.
In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...
The values below are standard apparent reduction potentials (E°') for electro-biochemical half-reactions measured at 25 °C, 1 atmosphere and a pH of 7 in aqueous solution. [1] [2] The actual physiological potential depends on the ratio of the reduced (Red) and oxidized (Ox) forms according to the Nernst equation and the thermal voltage.
In electrochemistry, the Randles–Ševčík equation describes the effect of scan rate on the peak current (i p) for a cyclic voltammetry experiment. For simple redox events where the reaction is electrochemically reversible, and the products and reactants are both soluble, such as the ferrocene/ferrocenium couple, i p depends not only on the concentration and diffusional properties of the ...
The decomposition of a reaction into half reactions is key to understanding a variety of chemical processes. For example, in the above reaction, it can be shown that this is a redox reaction in which Fe is oxidised, and Cl is reduced. Note the transfer of electrons from Fe to Cl.
The Tafel equation was first deduced experimentally and was later shown to have a theoretical justification. The equation is named after Swiss chemist Julius Tafel. It describes how the electrical current through an electrode depends on the voltage difference between the electrode and the bulk electrolyte for a simple, unimolecular redox reaction.
The reaction will proceed towards the lower energy - reducing for the blue curve, oxidizing for the red curve. The green curve illustrates equilibrium. The following derivation of the extended Butler–Volmer equation is adapted from that of Bard and Faulkner [3] and Newman and Thomas-Alyea. [5] For a simple unimolecular, one-step reaction of ...