Abstract: A process for making a cathode active material for a lithium ion battery is described. The process includes (a) a step of synthesizing a mixed oxide of formula Li1+xTM1?xO2 at a temperature ranging from 750 to 1000° C. in an oxidizing atmosphere, where TM is a combination of two or more transition metals of Mn, Co and Ni and, optionally, at least one more metal of Ba, Al, Ti, Zr, W, Fe, Cr, K, Mo, Nb, Mg, Na and V, and x is a number ranging from zero to 0.2, (b) a step of cooling down the material obtained from step (a) to a temperature ranging from 100 to 400° C., (c) a step of adding at least one reactant of BF3, SO2 and SO3 at the temperature of 100 to 400° C., and (d) a step of cooling down to a temperature of 50° C. or below.

Abstract: An electrolyte composition for use in a battery system including a silicon-based negative electrode having active material particles is provided. The electrolyte composition includes a polar solvent selected from the group consisting of ethylene carbonate, propylene carbonate, sulfolane, ?-butyrolactone, and combinations thereof and at least one lithium salt dissolved in the polar solvent at a concentration of at least 2 moles of the at least one lithium salt per 1 liter of the polar solvent. The at least one lithium salt and the polar solvent add dipoles to the electrolyte composition configured for reducing an electric field present at a surface of each of the active material particles in the silicon-based negative electrode of the battery system.

Abstract: A process for preparing surface-modified carbon, comprising adding carbon material to a solution of a reaction product of primary aromatic amine and excess molar amount of nitrite source, and recovering surface-modified carbon bearing redox-active sites. Surface-modified carbon material, electrodes and capacitors based thereon are also provided.

Abstract: Process for making a cathode active material for a lithium ion battery, said process comprising the following steps: (a) treating a mixed oxide according to general formula Li1+xTM1?xO2 with at least one aromatic di-, tri- or tetracarboxylic acid or with a combination of at least two of the foregoing, wherein TM is a combination of Mn and Ni and, optionally, at least one more metal selected from Ba, Al, Co, Ti, Zr, W, Fe, Cr, K, Mo, Nb, Ta, Mg and V, and x is in the range of from zero to 0.2, (b) subjecting said precursor to heat treatment a temperature in the range of from 500 to 800° C.

Abstract: The present application provides a self-powered drug-delivery device. The device includes a chamber having a wall. The chamber contains a fluid and is in connection with an administration means. The device also includes a displacement-generating battery cell. The device further includes an electrically-controlled battery unit, which includes the displacement-generating battery cell coupled to the chamber by a coupling means. The displacement-generating battery cell includes an element that changes shape as a result of charge or discharge of the battery cell so as to cause a displacement within the battery unit. The arrangement of the battery unit, the coupling means, the wall, the chamber, and the administration means is such that the displacement derived from the battery unit is conveyed by the coupling means to cause displacement of the wall of the chamber such that the fluid is expelled from the chamber to force a drug towards the administration means.

Abstract: Asymmetric electrochemical cell apparatus, and methods of operating such apparatus to produce electrolyzed water.

Abstract: The present invention relates to the production of electrolyzed aqueous solutions in an electrochemical cell. More particularly, the invention relates to an asymmetric electrochemical cell device for producing electrolyzed water or aqueous solution, while controlling the pH of the solution. The invention further relates to methods of operating said device and to the use thereof for microbial disinfection and/or pesticide removal.

Abstract: A method of bromide ion and iodide ion selective removal from seawater or the like by electrochemical desalination; and a device therefor. The method includes (a) providing a capacitive deionizing cell with high surface area activated carbon electrodes; (b) flowing the seawater through the cell; and (c) applying a voltage to charge and discharge the electrodes.

Abstract: The present application provides a self-powered drug-delivery device. The device includes a chamber having a wall. The chamber contains a fluid and is in connection with an administration means. The device also includes a displacement-generating battery cell. The device further includes an electrically-controlled battery unit, which includes the displacement-generating battery cell coupled to the chamber by a coupling means. The displacement-generating battery cell includes an element that changes shape as a result of charge or discharge of the battery cell so as to cause a displacement within the battery unit. The arrangement of the battery unit, the coupling means, the wall, the chamber, and the administration means is such that the displacement derived from the battery unit is conveyed by the coupling means to cause displacement of the wall of the chamber such that the fluid is expelled from the chamber to force a drug towards the administration means.

Abstract: Methods of scavenging acid in a lithium-ion electrochemical cell are provided. An electrolyte solution that contains an acid or is capable of forming the acid is contacted with a polymer comprising a nitrogen-containing acid-trapping moiety selected from the group consisting of: an amine group, a pyridine group, and combinations thereof. The nitrogen-containing acid-trapping moiety scavenges acidic species present in the electrolyte solution by participating in a Lewis acid-base neutralization reaction. The electrolyte solution comprises a lithium salt and one or more solvents and is contained in the electrochemical cell that further comprises a first electrode, a second electrode having an opposite polarity from the first electrode, and a porous separator. Lithium ions can be cycled through the separator and electrolyte solution from the first electrode to the second electrode, where acid generated during the cycling is scavenged by the polymer comprising a nitrogen-containing acid-trapping moiety.

Abstract: The present application provides a self-powered drug-delivery device. The device includes a chamber having a wall. The chamber contains a fluid and is in connection with an administration means. The device also includes a displacement-generating battery cell. The device further includes an electrically-controlled battery unit, which includes the displacement-generating battery cell coupled to the chamber by a coupling means. The displacement-generating battery cell includes an element that changes shape as a result of charge or discharge of the battery cell so as to cause a displacement within the battery unit. The arrangement of the battery unit, the coupling means, the wall, the chamber, and the administration means is such that the displacement derived from the battery unit is conveyed by the coupling means to cause displacement of the wall of the chamber such that the fluid is expelled from the chamber to force a drug towards the administration means.

Abstract: Apparatus, and methods of operating such apparatus to produce disposable towels moistened with aqueous solution containing hypohalous acid.

Abstract: A process for making a cathode active material for a lithium ion battery is described. The process includes (a) a step of synthesizing a mixed oxide of formula Li1+xTM1?xO2 at a temperature ranging from 750 to 1000° C. in an oxidizing atmosphere, where TM is a combination of two or more transition metals of Mn, Co and Ni and, optionally, at least one more metal of Ba, Al, Ti, Zr, W, Fe, Cr, K, Mo, Nb, Mg, Na and V, and x is a number ranging from zero to 0.2, (b) a step of cooling down the material obtained from step (a) to a temperature ranging from 100 to 400° C., (c) a step of adding at least one reactant of BF3, SO2 and SO3 at the temperature of 100 to 400° C., and (d) a step of cooling down to a temperature of 50° C. or below.

Abstract: Methods of scavenging acid in a lithium-ion electrochemical cell are provided. An electrolyte solution that contains an acid or is capable of forming the acid is contacted with a polymer comprising a nitrogen-containing acid-trapping moiety selected from the group consisting of: an amine group, a pyridine group, and combinations thereof. The nitrogen-containing acid-trapping moiety scavenges acidic species present in the electrolyte solution by participating in a Lewis acid-base neutralization reaction. The electrolyte solution comprises a lithium salt and one or more solvents and is contained in the electrochemical cell that further comprises a first electrode, a second electrode having an opposite polarity from the first electrode, and a porous separator. Lithium ions can be cycled through the separator and electrolyte solution from the first electrode to the second electrode, where acid generated during the cycling is scavenged by the polymer comprising a nitrogen-containing acid-trapping moiety.

Abstract: The present application provides a self-powered drug-delivery device. The device includes a chamber having a wall. The chamber contains a fluid and is in connection with an administration means. The device also includes a displacement-generating battery cell. The device further includes an electrically-controlled battery unit, which includes the displacement-generating battery cell coupled to the chamber by a coupling means. The displacement-generating battery cell includes an element that changes shape as a result of charge or discharge of the battery cell so as to cause a displacement within the battery unit. The arrangement of the battery unit, the coupling means, the wall, the chamber, and the administration means is such that the displacement derived from the battery unit is conveyed by the coupling means to cause displacement of the wall of the chamber such that the fluid is expelled from the chamber to force a drug towards the administration means.

Abstract: Asymmetric electrochemical cell apparatus, and methods of operating such apparatus to produce electrolyzed water.

Abstract: A lithium ion battery includes a positive and a negative electrode, and a nanoporous or microporous polymer separator soaked in electrolyte solution and disposed between the electrodes. At least two different chelating agents are included and selected to complex with: i) two or more different transition metal ions; ii) a transition metal ion in two or more different oxidation states; or iii) both i) and ii). The at least two different selected chelating agents are to complex with transition metal ions in a manner sufficient to not affect movement of lithium ions across the separator during operation of the battery. The chelating agents are: dissolved or dispersed in the electrolyte solution; grafted onto the polymer of the separator; attached to the binder material of the negative and/or positive electrode; disposed within pores of the separator; coated on a surface of the separator; and/or coated on a surface of an electrode.

Abstract: Embodiments include a displacement-generating battery cell for driving a drug-delivery device. The cell includes at least one volume-changing element. The cell also includes a housing formed according to a concertina-shaped design with folds in the walls thereof and containing an internal chemical reaction system. The arrangement of the chemical reaction system is such that as the cell is discharged, the volume-changing element expands, thereby lengthening the battery and thus reducing the extent of said folds, such that the cell becomes taller to reflect the expansion of the volume-changing component.

Abstract: A lithium ion battery includes positive and negative electrodes, and a nanoporous or microporous polymer separator soaked in an electrolyte solution, between the positive electrode and the negative electrode. Chelating agent(s) are included to complex with transition metal ions while not affecting movement of lithium ions across the separator during operation of the lithium ion battery. The chelating agents are: dissolved in the electrolyte solution; grafted onto the polymer of the separator; attached to the binder material of the negative and/or positive electrode; coated on a surface of the separator; and/or coated on a surface of the negative and/or positive electrode. The chelating agents are selected from: ion traps in molecular form selected from polyamines, thiols and alkali metal salts of organic acids; polymers functionalized with alkali metal salts of organic acids; polymers functionalized with nitrogen-containing functional groups; and polymers functionalized with two or more functional groups.

Abstract: A lithium ion battery includes a positive and a negative electrode, and a nanoporous or microporous polymer separator soaked in electrolyte solution and disposed between the electrodes. At least two different chelating agents are included and selected to complex with: i) two or more different transition metal ions; ii) a transition metal ion in two or more different oxidation states; or iii) both i) and ii). The at least two different selected chelating agents are to complex with transition metal ions in a manner sufficient to not affect movement of lithium ions across the separator during operation of the battery. The chelating agents are: dissolved or dispersed in the electrolyte solution; grafted onto the polymer of the separator; attached to the binder material of the negative and/or positive electrode; disposed within pores of the separator; coated on a surface of the separator; and/or coated on a surface of an electrode.