Two phase electrolytes used as halogen traps in metal halogen secondary cells and batteries
AssigneeEco-Control, Inc.
InventorsAlfred M. Ajami, Fraser M. Walsh, Dennis N. Crouse
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AssigneeEco-Control, Inc.
InventorsAlfred M. Ajami, Fraser M. Walsh, Dennis N. Crouse
Estimating the term…
Organic-aqueous two-phase electrolytes are disclosed in which the organic phase is capable of complexing halogen in cells and batteries of the type which utilize the electrochemical reaction X.sub.2 .revreaction.2X.sup.-, where X is Br, Cl, I or a combination of these halides. The organic phase of the two-phase electrolyte contains an organic halogen salt which provides both conductivity and the ability to complex halogens and prevent them from being dissolved in the aqueous phase of the electrolyte of the cell or battery in which they are used.
A method for improving the performance of current delivering electrochemical systems of the type which utilize a halogen selected from the group consisting of bromine, chlorine, iodine, and mixtures thereof as an electrochemically active agent which reacts electrochemically at a halide electrode and which system includes a metal electrode and an aqueous metal halide electrolyte phase in which halogens are soluble, wherein the improvement comprises using an organic halogen complexing phase which has two components, one of which is an organic solvent which is insoluble in water, the second component being an organic salt which is soluble in the organic solvent, forms complexes with halogens which do not crystallize out of the solvent at any point during halogen addition, and which do not react irreversibly with free halogens, the organic halogen complexing phase remaining insoluble with the aqueous electrolyte phase during charging and discharging of the current delivery system, the organic salt of the halogen complexing phase forming a reversible complex with the halogen to store halogen during charging of the system and to release halogen during discharging of the system, the halogen complexing phase preventing halogens from dissolving in the aqueous phase.
An electrochemical cell comprising a case, a porous, conductive halide electrode, a Me electrode where Me is selected from the group consisting of zinc and cadmium, an aqueous electrolyte in which halogens are soluble containing an inorganic salt of the formula MX, where M is selected from the group consisting of cadmium and zinc, and X is selected from the group consisting of bromide, chloride, iodide and combinations thereof, and an organic halogen complexing phase, said organic phase having two components, one of which is an organic solvent which is insoluble in water, the second component being an organic salt which is soluble in the organic solvent, forms complexes with halogens which do not crystallize out of the solvent at any point during halogen addition, and which do not react irreversibly with free halogens, the organic halogen complexing phase remaining insoluble with the aqueous electrolyte during charging and discharging of the current delivery system, the organic salt of the halogen complexing phase forming a reversible complex with the halogen to store halogen during charging of the system and to release halogen during discharging of the system, the halogen complexing phase preventing halogens from dissolving in the aqueous electrolyte.
Dependencies are inferred from the claim text.
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Composed of a half-cell of a fuel-cell type and a half-cell of the secondary-cell type: zinc-halogen cells or batteries
Accumulators not provided for in groups H01M10/05-H01M10/34: zinc-halogen accumulators
Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation: energy storage using batteries
Climate change mitigation technologies in the production process for final industrial or consumer products: manufacturing or production processes…
Term ended 27 Dec 1994 (estimated)
USPTO file history isn’t available for this patent, so only indexed dates are shown.
This invention relates to water insoluble organic electrolytes useful for complexing halogens and more particularly to two-phase electrolytes useful as an electrolyte for electrochemical cells and batteries of the type which utilize a halogen as its electrochemically active agent.
Voltaic cells which include an aqueous solution of zinc or cadmium halide as an electrolyte are known, but are frequently characterized by a relatively high self-discharge rate, low capacity, and high internal resistance. Since elemental halogen is soluble in the aqueous electrolyte, it is difficult to keep metallic zinc or cadmium and elemental halogen apart while simultaneously achieving a system in which a good percentage of the theoretical energy storage capacity can be realized.
Recently, various attempts have been made to prevent elemental halogen from migrating to the zinc or cadmium electrode. For example, U.S. Pat. No. 3,352,720 to G. R. Wilson et al teaches the use of water insoluble polymeric amine halogen complexes in place of the elemental halogen. While the structures disclosed in the Wilson et al patent function as halogen cells, they nevertheless suffer from less than optimum capacities and self-discharge rates because of the low stability of the polyhalogens employed.
FIG. 1 is a cross-sectional view of a cell of the type in which the complexing electrolytes of the present invention are useful;
FIG. 2 is a graph which illustrates ionic conductivities;
FIG. 3 is a schematic of a regenerative fuel cell in which a recirculating electrolyte of the present invention is useful; and,
At the outset, it is desirable to comment on certain terms that are used throughout this specification and claims. For example, the terms "zinc electrode" and "bromide electrode" are not intended to imply that the electrodes are formed from these material exclusively. As is conventional practice, the terms are used merely to indicate the electrochemically active element reacting. The metal and halogen electrodes of the cells with which the electrolytes of the present invention are employed, are electrically conductive, and preferably porous and noncorrosive. Carbon in its various forms is a preferred material. The carbon of the metal electrode serves as a plating surface for zinc or cadmium.
Furthermore, although reference is made to one counter electrode and one metal electrode, it is obvious that the compounds of the invention are useful in cells which include more than one pair of electrodes and with batteries of two or more cells constructed in accordance with methods known to those skilled in the art. Because cadmium is electrochemically similar to zinc, it is also obvious that the zinc of the electrode and the electrolyte can be replaced by cadmium. Although bromine is used throughout this specification and claims, it will be apparent to those skilled in the art that chlorine, iodine, or any combination of bromine, chlorine, and iodine may be substituted therefore.
During discharge of the well-known zinc bromine cell the following half reactions occur: