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  2. Nernst equation - Wikipedia

    en.wikipedia.org/wiki/Nernst_equation

    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 ...

  3. Standard electrode potential (data page) - Wikipedia

    en.wikipedia.org/wiki/Standard_electrode...

    Variations from these ideal conditions affect measured voltage via the Nernst equation. Electrode potentials of successive elementary half-reactions cannot be directly added. However, the corresponding Gibbs free energy changes (∆G°) must satisfy ∆G° = – z FE°,

  4. Permanganate - Wikipedia

    en.wikipedia.org/wiki/Permanganate

    In a strongly basic or alkaline solution, permanganate(VII) is reduced to the green manganate ion, MnO 2− 4 with an oxidation state of +6. MnO − 4 + e − → MnO 2− 4. In a neutral solution, however, it gets reduced to the brown manganese dioxide MnO 2 with an oxidation state of +4. 2 H 2 O + MnO − 4 + 3 e − → MnO 2 + 4 OH −

  5. Standard electrode potential - Wikipedia

    en.wikipedia.org/wiki/Standard_electrode_potential

    Bipolar electrochemistry scheme. In electrochemistry, standard electrode potential, or , is a measure of the reducing power of any element or compound.The IUPAC "Gold Book" defines it as; "the value of the standard emf (electromotive force) of a cell in which molecular hydrogen under standard pressure is oxidized to solvated protons at the left-hand electrode".

  6. Half-reaction - Wikipedia

    en.wikipedia.org/wiki/Half-reaction

    For oxidation-reduction reactions in basic conditions, after balancing the atoms and oxidation numbers, first treat it as an acidic solution and then add OH − ions to balance the H + ions in the half reactions (which would give H 2 O).

  7. Tafel equation - Wikipedia

    en.wikipedia.org/wiki/Tafel_equation

    The Tafel equation is an equation in electrochemical kinetics relating the rate of an electrochemical reaction to the overpotential. [1] 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.

  8. Reducing agent - Wikipedia

    en.wikipedia.org/wiki/Reducing_agent

    In the above equation, the Iron (Fe) has an oxidation number of 0 before and 3+ after the reaction. For oxygen (O) the oxidation number began as 0 and decreased to 2−. These changes can be viewed as two "half-reactions" that occur concurrently: Oxidation half reaction: Fe 0 → Fe 3+ + 3e −; Reduction half reaction: O 2 + 4e − → 2 O 2−

  9. Pourbaix diagram - Wikipedia

    en.wikipedia.org/wiki/Pourbaix_diagram

    Pourbaix diagram of iron. [1] The Y axis corresponds to voltage potential. In electrochemistry, and more generally in solution chemistry, a Pourbaix diagram, also known as a potential/pH diagram, E H –pH diagram or a pE/pH diagram, is a plot of possible thermodynamically stable phases (i.e., at chemical equilibrium) of an aqueous electrochemical system.