Abstract: The present invention provides an alkaline water electrolysis anode such that even when electric power having a large output fluctuation, such as renewable energy, is used as a power source, the electrolysis performance is unlikely to be deteriorated and excellent catalytic activity is retained stably over a long period of time. The alkaline water electrolysis anode is an alkaline water electrolysis anode 10 provided with an electrically conductive substrate 2 at least a surface of which contains nickel or a nickel base alloy and a catalyst layer 6 disposed on the surface of the electrically conductive substrate 2, the catalyst layer 6 containing a nickel-containing metal oxide having a spinel structure, wherein the nickel-containing metal oxide contains nickel (Ni) and manganese (Mn), and has an atom ratio of Li/Ni/Mn/O of (0.0 to 0.8)/(0.4 to 0.6)/(1.0 to 1.8)/4.0.

Abstract: The invention relates to a substrate holding and locking system for chemical and/or electrolytic surface treatment of a substrate in a process fluid and a corresponding method. The system comprises a first element, a second element, a reduced pressure holding unit and a magnetic locking unit. The first element and the second element are configured to hold the substrate between each other. The reduced pressure holding unit comprises a pump to reduce an interior pressure inside the substrate holding and locking system below atmospheric pressure. The magnetic locking unit is configured to lock the first element and the second element with each other. The magnetic locking unit comprises a magnet control and at least a magnet. The magnet is arranged at one of the first element and the second element. The magnet control is configured to control a magnetic force between the first element and the second element.

Abstract: A device for providing treatment is disclosed. The device provides proper skin electrical conductivity while still being minimally invasive by adhering to the patient's skin that also implements safety measures that off-the-shelf electrode options do not have. This device includes a graphite powder-based skin counter electrode that has a graphite powder suspended in an electrolyte gel that allows for electrochemical conduction between the graphite particles in the graphite powder. The gel is spread over a first side of a hydrogel layer. A device housing is mounted on the hydrogel layer over the first side. The device housing contains the electrolyte gel and graphite powder, defines an opening or lead opening as well as an empty expansion chamber for gaseous anodic byproduct. A metallic wire or rod extends from the electrolyte gel and through the housing opening and connects to a potentiostat. The second side of the hydrogel layer is adhered to the skin of the patient.

Abstract: The present invention relates to a removable and reusable anode mounting head for use with heater treaters, tanks, pressure vessels and production vessels. More particularly, the present invention provides a reusable anode mounting head with metallic and non-metallic components that enable electrical connection to the vessel and insulation at a connection to the vessel (e.g., via coupling).

Abstract: A liftable electrolytic vessel including at least one anchor assembly being at least partially embedded in each of two opposed core walls to provide anchorage to a lifting accessory of a lifting device; and related method for lifting the electrolytic vessel. Each anchor assembly comprises an anchor having a strap slot, and a strap connected to the anchor and extending from the anchor along and inside at least a portion of the corresponding core wall. The anchor further includes a connector which is sized and configured to receive a fastener or engage a lifting accessory such as a chain or a hook. The anchor assembly may include one anchor provided at each end of the strap. A plurality of anchor assemblies may extend vertically and horizontally within a core of the vessel to offer various anchorage points from an outer surface of the core. Design of the anchor of a first anchor assembly may differ from the design of a second anchor assembly.

Abstract: The present disclosure is directed to cobalt and nickel cobalt phosphide/phosphate electrocatalyst nanoparticles for catalyzing electrochemical reactions, such as water splitting. The nanoparticles are formed into electrodes that have bi-functional oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) capabilities.

Abstract: A method for preventing corrosion of a spent nuclear fuel canister by using electrolytic corrosion protection, according to the present invention, has an effect of enabling a semi-permanent operation and, particularly, has effects of preventing oxidation and corrosion problems of a canister made of a metal material, in consideration of various environmental variables that may cause corrosion, and ensuring the structural stability of the canister so as to enable a semi-permanent operation.

Abstract: The present invention relates to an electrochemical device and a method for operating the electrochemical device for inducing specific behaviours in its chemical kinetics by supplying externally selected random (stochastic) voltage perturbations while the electrochemical system is operating in a non-oscillatory regime.

Abstract: A method for changing an activation state of an interruption module for selectively interrupting at least one passive cathodic protection unit from a metallic structure. The method includes enabling a global positioning system (GPS) receiver in data communication with a controller of the interruption module, receiving GPS time via the GPS receiver from at least one global positioning system satellite in data communication therewith, synchronizing a real-time clock time of a real-time clock in data communication with the controller to GPS time, disabling the GPS receiver and changing the activation state of the interruption module if a predetermined activation state change time of the interruption module is between the local real-time clock time and the GPS time.

Abstract: The present invention provides an electrode for electrolysis in which electrolysis performance is hard to deteriorate and excellent catalytic activity is kept stable over a long period of time even when electric power in which there is a large fluctuation in output, such as renewable energy, is used as a power source. The electrode for electrolysis is an electrode 10 for electrolysis provided with an electrically conductive substrate 2 at least the surface of which contains nickel or a nickel-based alloy, an intermediate layer 4 formed on the surface of the electrically conductive substrate 2 and containing a lithium-containing nickel oxide represented by composition formula LixNi2-xO2 (0.02?x?0.5), and a catalyst layer 6 of a nickel cobalt spinel oxide, an iridium oxide, or the like, the catalyst layer 6 formed on the surface of the intermediate layer 4.

Abstract: An electrolyzer system comprises a stack of one or more electrolyzer cells, each electrolyzer cell comprising first and second half cells respectively comprising first and second electrodes and a separator between the first half cell and the second half cell, wherein a current is applied between the first and second electrodes. The system further comprises first and second electrolyte feed streams for respectively feeding a first electrolyte solution at a first inlet temperature to the first half cells and a second electrolyte solution at a second inlet temperature to the second half cells, first and second electrolyte outlet streams for respectively withdrawing the first and second electrolyte solutions from the first half cells and second half cells, and a temperature control apparatus to control the first inlet temperature at a first specified temperature and to control the second inlet temperature at a second specified temperature.

Abstract: A copper integrated electrode with a convertible oxidation state, a preparation method and an application method are provided. The preparation process is based on an electrochemically induced self-growth method. Copper foam is used as a precursor, soaked in a graphene oxide solution, dried, calcined at high temperature and annealed, and then treated with an alkali solution to obtain the copper integrated electrode with the convertible oxidation state. The working electrode prepared by the nano-catalytic material of the present invention has good denitrification performance in the environmental field, which can achieve nearly 100% nitrate removal rate, nearly 100% nitrogen selectivity and long-term stability. These properties are due to the prepared working electrode having an oxidizable copper (I, II/0, I), oxygen vacancy (O) and a one-dimensional nanowire structure.

Abstract: An electrode, which includes at least one tetragonally crystallized compound containing at least one element selected from the group of Cu and Ag, the crystal lattice of the compound being of the space group I41/amd type. An electrolysis cell includes the electrode.

Abstract: The present invention generally provides a system for metal corrosion protection, including a metallic object to be protected, connectable to an electron source as cathode, an electrically isolating coating disposed on at least a portion of the metallic object, an electrically conductive blanket anode applied on at least a portion of the electrically isolating coating; an electrode electrically connected to the blanket anode and connectable to the electron source. The present invention further proposes a kit for providing corrosion protection to a substrate and method thereof.

Abstract: A desalination device includes a container, first and second electrodes, an anion exchange membrane (AEM), and a power source. The container contains saline water that has an elevated concentration of dissolved salts. The AEM separates the container into first and second compartments into which the first and second electrodes, respectively, are arranged. The AEM has a continuous porous structure and a plurality of negatively-charged oxygen functional groups coupled to the porous structure. The power source is configured to selectively apply a voltage to one of the first and second electrodes. The AEM has a selective permeability when the voltage is applied such that cations in the saline water solution have a first diffusion rate d1 therethrough and anions in the saline water solution have a second diffusion rate d2 therethrough. The first diffusion rate d1 is less than the second diffusion rate d2 and greater than or equal to zero.

Abstract: Disclosed is an integrally combined electrical current carrier, circulation chamber and frame (CCF) formed as a single or double part (CCF) for use in unipolar electrochemical devices, such as a filter press electrolyser apparatus. The CCF is structured to define an internal circulation chamber for circulation of electrolyte, products, and reactants as well as apertures which form flow passageways when the filter press device is assembled. Affixed on opposed surfaces of the CCFs are electrically conductive planar electroactive structures which are in electrical contact with the CCF. The circulation chamber is formed by the depth of the CCF itself between opposing electroactive structures. Multiple CCFs are assembled and compressed together to form the filter press electrolyser apparatus. The flow passageway apertures within the assembled filter press electrolyser are aligned to form flow pathways, located above and below the circulation chambers.

Abstract: The present invention relates to a method of processing a component, wherein the component comprises at least one opening in a surface thereof, the method comprising: placing the component in an electrophoretic fluid comprising particles of a masking material as an electrode, applying a voltage to the component and a counter electrode of the component, depositing particles of the masking material in the electrophoretic fluid into the at least one aperture through electrophoresis to mask the at least one aperture; processing a surface of the component; and removing the masking material in the at least one opening.

Abstract: A metal-free porphyrin based crystalline 2D organic polymer obtained from the condensation of terephthaloyl chloride and 5,10,15,20-tetrakis(4-aminophenyl porphyrin, namely H2TAPP), which is an effective bifunctional electrocatalyst for the oxygen evolution reaction (OER) in basic conditions and the hydrogen evolution reaction (HER) in neutral solutions. The electrochemical response of this material is explored under oxidation and reduction conditions in order to study its catalytic activity, charge transfer and stability.

Abstract: In a method for cathodically protecting and/or passivating a metal section in an ionically conductive material such as steel reinforcement in concrete or mortar, an impressed current or sacrificial anode communicates ionic current to the metal section and a storage component of electrical energy which can be a cell, battery or capacitor is provided as a component of the anode. A current limiter is provided which prevents excess current draining the supply. This can be a semi-conductive device such as a transistor or diode is connected in the path from the anode to the metal section to limit the cathodic protection current to a value of the order of 1 milliamp. When a diode or similar device is used the current can be limited to the reverse leakage current of the diode.

Abstract: An electrode for use in instruments capable of measuring the electrophoretic mobility of particles in solution is disclosed. The electrode is comprised of an inexpensive support member, generally made of titanium, onto a flat surface of which has been connected, generally by microwelding, a flat electrically conductive but chemically inert foil member, preferably platinum. A uniform texture can be generated on the exposed surfaces of the electrode by various means including tumbling the electrode with an abrasive. An oxide layer can be generated on the support member by soaking the composite electrode in an appropriate medium, protecting the exposed surface of the support member from fluid contact with the sample solution, while the foil member, unaffected by the oxidation process, is able to contact the sample solution.