Abstract:
A system to remove sodium and Sulfur from a feed stream containing alkali metal sulfides and polysulfides in addition to heavy metals. The system includes an electrolytic cell having an anolyte compartment housing an anode in contact with an anolyte. The anolyte includes alkali metal sulfides and polysulfides dissolved in a polar organic solvent. The anolyte includes heavy metal ions. A separator includes an ion conducting membrane and separates the anolyte compartment from a catholyte compartment that includes a cathode in contact with a catholyte. The catholyte includes an alkali ion-conductive liquid. A power source applies a voltage to the electrolytic cell high enough to reduce the alkali metal and oxidize Sulfur ions to allow recovery of the alkali metal and elemental sulfur. The ratio of sodium to Sulfur is such that the open circuit potential of the electrolytic cell is greater than about 2.3V.
Abstract:
A system treats off gas from a waste incinerator to decrease potentially negative aspects of the off gas to the environment. The system includes a waste incinerator and a plasma oxidizer. The waste incinerator includes an incineration chamber to contain a waste material during at least a portion of an incineration process of the waste material. The waste incinerator also includes an exhaust outlet to exhaust an off gas from the incineration process of the waste material. The plasma oxidizer is coupled to the waste incinerator to receive and oxidize the off gas from the exhaust outlet of the waste incinerator. The plasma oxidizer includes a non-thermal gliding electric arc oxidation system to generate the plasma.
Abstract:
Molten salt electrolytes are described for use in electrochemical synthesis of hydrocarbons from carboxylic acids. The molten salt electrolyte can be used to synthesize a wide variety of hydrocarbons with and without functional groups that have a broad range of applications. The molten salt can be used to synthesize saturated hydrocarbons, diols, alkylated aromatic compounds, as well as other types of hydrocarbons. The molten salt electrolyte increases the selectivity, yield, the energy efficiency and Coulombic efficiency of the electrochemical conversion of carboxylic acids to hydrocarbons while reducing the cell potential required to perform the oxidation.
Abstract:
The present invention provides a molten sodium secondary cell. In some cases, the secondary cell includes a sodium metal negative electrode, a positive electrode compartment that includes a positive electrode disposed in a molten positive electrolyte comprising Na-FSA (sodium-bis(fluorosulonyl)amide), and a sodium ion conductive electrolyte membrane that separates the negative electrode from the positive electrolyte. One disclosed example of electrolyte membrane material includes, without limitation, a NaSICON-type membrane. Non-limiting examples of the positive electrode include Ni, Zn, Cu, or Fe. The cell is functional at an operating temperature between about 100 C and about 150 C, and preferably between about 110 C and about 130 C.
Abstract:
The present invention provides a secondary cell having a negative electrode compartment (15) and a positive electrode compartment (25), which are separated by an alkali ion conductive electrolyte membrane (40). An alkali metal negative electrode (20) disposed in the negative electrode compartment (15) oxidizes to release alkali ions as the cell discharges and reduces the alkali ions to alkali metal during recharge. The positive electrode compartment (25) includes a positive electrode (30) contacting a positive electrode solution (35) that includes an alkali metal compound and a metal halide. The alkali metal compound can be selected from an alkali halide and an alkali pseudo-halide. During discharge, the metal ion reduces to form metal plating on the positive electrode. As the cell charges, the metal plating oxidizes to strip the metal plating to form metal halide or pseudo halide or corresponding metal complex.
Abstract:
A process of producing metal that includes adding a quantity of a alkoxide (M(OR)x) or another metal salt to a cathode compartment of an electrolytic cell and electrolyzing the cell. This electrolyzing causes a quantity of alkali metal ions to migrate into the cathode compartment and react with the metal alkoxide, thereby producing metal and an alkali metal alkoxide. In some embodiments, the alkali metal is sodium such that the sodium ions will pass through a sodium ion selective membrane, such as a NaSICON membrane, into the cathode compartment.
Abstract:
The present invention provides a rechargeable battery. The battery includes a honeycomb separator (20) which defines therein a plurality of cells separated from adjacent cells by thin, non-porous cell walls (30) of a substantially non-porous, alkali ion conductive ceramic membrane material. The battery includes a plurality of positive electrodes (55), each positive electrode (55) being disposed in a respective positive electrode cell (65) of the honeycomb separator (20). Each positive electrode cell (65) contains a positive electrode electrochemical material that undergoes electrochemical reduction during battery discharge and electrochemical oxidation during battery charge. Negative electrodes (50) are disposed in respective negative electrode cells (60) of the honeycomb separator (20). Each negative electrode cell (60) contains a negative electrode electrochemical material that undergoes electrochemical oxidation during battery discharge and electrochemical reduction during battery charge. The positive (55) and negative (50) electrodes are disposed in the cells of the honeycomb separator (20) in a checkerboard pattern.
Abstract:
A Fischer Tropsch ("FT") unit (100) includes at least one FT reactor tube (60). The FT reactor tube (60) is configured to convert syngas into one or more hydrocarbon products. Inside the tube is a nano-sized catalyst particles dispersed in a micro-fibrous substrate. The FT reactor tube (60) may be positioned within a cooling block (10) that may be made of aluminum or another metal. The cooling block (10) includes an aperture (15), wherein the FT reactor tube (60) is housed within the aperture (15). At least one cooling channel (20) is located on the cooling block (10). The cooling channel (20) houses at least one cooling tube (70) that is designed to dissipate the heat produced by the FT reaction.
Abstract:
Ammonia is synthesized using electrochemical and non-electrochemical reactions. The electrochemical reactions occur in an electrolytic cell (110) having a lithium ion conductive membrane (112) that divides the electrochemical cell (110) into an anolyte compartment (114) and a catholyte compartment (116). The catholyte compartment (116) includes a porous cathode (120) closely associated with the lithium ion conductive membrane (112). The overall electrochemical reaction is: 6LiOH + N2-> Li3N (s) + 3H2O + 3/2O2. The nitrogen (128) may be produced by a nitrogen generator (130). The non-electrochemical reaction involves reacting lithium nitride with water and/or steam as follows: Li3N (s) + 3H2O-> 3LiOH + NH3 (g). The ammonia is vented and collected. The lithium hydroxide is preferably recycled and introduced into the anolyte compartment. The electrolytic cell (110) is shut down prior to reacting the lithium nitride with water. The cathode (120) is preferably dried prior to start up of the electrolytic cell (1 10) and electrolyzing Li+ and N2 at the cathode (120).
Abstract:
Electrochemical processes to convert alkali sulfates into useful chemical products, such as syngas, alkali hydroxide, and sulfur are disclosed. An alkali sulfate is reacted with carbon to form carbon monoxide and alkali sulfide. In one embodiment, the alkali sulfide is dissolved in water and subjected to electrochemical reaction to form alkali hydroxide, hydrogen, and sulfur. In another embodiment, the alkali sulfide is reacted with iodine to form alkali iodide sulfur in a non-aqueous solvent, such as methyl alcohol. The alkali iodide is electrochemically reacted to form alkali hydroxide, hydrogen, and iodine. The iodine may be recycled to react with additional alkali sulfide. The hydrogen and carbon monoxide from both embodiments may be combined to form syngas. The alkali hydroxide from both embodiments may be recovered as a useful industrial chemical.