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The group set the groundwork for further development. In 1979, Thaller et. al. introduced an iron-hydrogen fuel cell as a rebalancing cell for the chromium-iron redox flow battery [19] which was adapted 1983 for the iron-redox flow batteries by Stalnake et al. [20] Further development went into the fuel cell as a separate system. [11] [12] [21]
A typical flow battery consists of two tanks of liquids which are pumped past a membrane held between two electrodes. [1]A flow battery, or redox flow battery (after reduction–oxidation), is a type of electrochemical cell where chemical energy is provided by two chemical components dissolved in liquids that are pumped through the system on separate sides of a membrane.
A metal–air electrochemical cell is an electrochemical cell that uses an anode made from pure metal and an external cathode of ambient air, typically with an aqueous or aprotic electrolyte. [1] [2] During discharging of a metal–air electrochemical cell, a reduction reaction occurs in the ambient air cathode while the metal anode is oxidized.
The iron compounds produced on the largest scale in industry are iron(II) sulfate (FeSO 4 ·7H 2 O) and iron(III) chloride (FeCl 3). The former is one of the most readily available sources of iron(II), but is less stable to aerial oxidation than Mohr's salt ( (NH 4 ) 2 Fe(SO 4 ) 2 ·6H 2 O ).
When metallic iron (oxidation state 0) is placed in a solution of hydrochloric acid, iron(II) chloride is formed, with release of hydrogen gas, by the reaction Fe 0 + 2 H + → Fe 2+ + H 2. Iron(II) is oxidized by hydrogen peroxide to iron(III), forming a hydroxyl radical and a hydroxide ion in the process. This is the Fenton reaction.
Metals in the middle of the reactivity series, such as iron, will react with acids such as sulfuric acid (but not water at normal temperatures) to give hydrogen and a metal salt, such as iron(II) sulfate: Fe (s) + H 2 SO 4 (l) → FeSO 4 (aq) + H 2 (g) There is some ambiguity at the borderlines between the groups.
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Metallic bonding is a type of chemical bonding that arises from the electrostatic attractive force between conduction electrons (in the form of an electron cloud of delocalized electrons) and positively charged metal ions. It may be described as the sharing of free electrons among a structure of positively charged ions .