Abstract: A water testing and measuring system is disclosed including a water generator configured to generate water by extracting water vapor from ambient air. A compound generator is configured to apply a compound to the water generated by the water generator. A processor is in communication with the water generator and the compound generator. A measurement device is in communication with the water generator, the compound generator and the processor.

Abstract: A surface modified electrode is provided. The surface modified electrode includes a glassy carbon electrode (GCE) and a nanomaterial disposed on the glassy carbon electrode. The nanomaterial comprises carbon nanotubes (CNTs), and at least one of thallium oxide nanoparticles (Tl2O3.NPs), thallium oxide (Tl2O3) nanopowder, and thallium oxide carbon nanotube nanocomposites (Tl2O3.CNT NCs). A polymer matrix is configured to bind the glassy carbon electrode with the nanomaterial. A method of preparing the surface modified electrode is also disclosed. The surface modified electrode can be implemented in a biosensor for detecting a biological molecule, like choline.

Abstract: Solid-contact electrodes include a molecular redox buffer that is covalently attached to one of the components of the electrodes. These electrodes can be incorporated into electrochemical sensor systems. The electrode components are an electron conductor, a membrane and optionally, an interlayer. The electrode includes covalent attachment of the molecular redox buffer to the interlayer, to the electron conductor or the membrane. The interlayer includes nanoporous carbon such as CIM-carbon. The molecular redox buffer includes a well-defined redox pair, e.g., a complex of Co(II)/Co(III). The electrodes are ion-selective electrodes (ISEs) or reference electrodes. Methods include constructing solid contact electrodes and using the electrodes in electrochemical sensor systems to determine the quantity of an analyte in a sample. The electrochemical sensor systems include disposable paper-based devices and/or wearable devices for measuring analytes in a sample.

Abstract: A sensor arrangement for determining at least one measurand of a measuring medium includes at least one first sensor with a first sensing element used to record measured values of a first measurand of the measuring medium, a housing having a housing wall which surrounds a housing interior containing the first sensing element, wherein the housing interior contains a medium in particular, a liquid which has a predetermined value of the first measurand.

Abstract: It is described an integrated gas sensor device comprising a silicon substrate and an oxide layer on the silicon substrate, as well as a working electrode, a counter electrode and a reference electrode, on the oxide layer, the working electrode and the counter electrode having respective active area exposed to an environmental air through at least a plurality of first openings and a plurality of second openings in the oxide layer in correspondence of the working electrode and of the counter electrode, further comprising an electrolyte layer portion and a hydrogel layer portion on the electrolyte layer portion, the electrolyte and hydrogel layer portions having a same size, suitable to cover at least the working, counter and reference electrodes, the hydrogel layer portion acting as a “quasi solid state” water reservoir.

Abstract: A detector for detecting radiation is generally described. The detector can comprise at least one ionic semiconductor material. For example, the ionic semiconductor material comprises a thallium halide and/or an indium halide. Electrical contacts are formed on the semiconductor material to provide a voltage to the detector during use. At least one of the electrical contacts may comprise a liquid that contains ions. In some instances, at least one electrical contact comprises a metal, such as Cr, Ti, W, Mo, or Pb. In some embodiments, the detector comprises both an electrical contact comprising liquid comprising ions and an electrical contact comprising a metal selected from a group consisting of Cr, Ti, W, Mo, and Pb. Detectors for detecting radiation, as described herein, may have beneficial properties.

Abstract: An electrode system for measuring the concentration of an analyte under in-vivo conditions comprises a counter-electrode having an electrical conductor, a working electrode having an electrical conductor on which an enzyme layer containing immobilized enzyme molecules for catalytic conversion of the analyte is arranged, and a diffusion barrier that slows the diffusion of the analyte from body fluid surrounding the electrode system to enzyme molecules. The enzyme layer is in the form of multiple fields that are arranged on the conductor of the working electrode at a distance from each other.

Abstract: An electrochemical sensor apparatus and electrochemical sensing method within an aqueous system are described, using one or more working electrodes of boron doped diamond (BDD). A cathodic reduction process provides a cathodic measurement and, substantially simultaneously, an anodic oxidation process provides an anodic measurement. A sum of a content of two equilibrium species within the aqueous system is obtained using both the cathodic measurement and the anodic measurement. One example measures total free chlorine by simultaneously measuring hypochlorous acid (HOCl) and hypochlorite ion (OCl?).

Abstract: The purpose of the invention is to provide a method for accurately quantifying a chemical substance by a substitutional stripping voltammetry technique. A method is provided for quantifying a chemical substance contained in a sample solution, and the method comprises preparing a measurement system. The measurement system comprises a pair of working electrodes (a first and a second electrodes), a counter electrode, and a gel-coated electrode. This gel-coated electrode comprises an electrode surface, a stripping gel, and a protection gel, and the protection gel covers the stripping gel.

Abstract: The chip includes electrodes on a substrate. The electrodes include a working electrode, a reference electrode, and a counter electrode. The reference electrode is constructed so as to not have an intrinsic potential. A self-assembly monolayer is positioned on the reference electrode. The self-assembly monolayer includes spacers and active probes. The active probes are configured to have a higher affinity for a capture probe than the spacers have for the capture probe.

Abstract: Nanostructures comprising carbon and metal catalyst that are formed on a substrate, such as a silicon substrate, are contacted with a composition that, among other useful modifications, protects the nano structures and renders them stable in the presence of oxidizing agents in an aqueous environment. The protected nano structures are rendered stable over an extended period of time and thereby remain useful during such period as components of an electrode, for example, for detecting electrochemical species such as free chlorine, total chlorine, or both in water.

Abstract: Method for electrochemically detecting different oxidant and halide anion species in a sample. According to one embodiment, the method uses a sensor including a boron-doped diamond working electrode, a platinum mesh counter electrode, a silver/silver chloride reference electrode, a potentiostat coupled to the three electrodes, and a computer coupled to the potentiostat. The sensor measures current resulting from differential pulse non-stripping voltammetry, thereby enabling different oxidants and halide anions from a plurality of such species to be detected by distinct responses. Peaks in the current signal result at characteristic voltages when a species is oxidized to a higher oxidation state, and the concentration of a particular species is determined by the magnitude of the current peak. The sensor response time is rapid and shows high sensitivity and selectivity for oxidants and halide anions. The sensor may be a hand-held or in-line device and may be used in a feedback-control system.

Abstract: A method and apparatus measures the presence of total residual oxidant species in aqueous environments. More specifically, the apparatus is operable to measure hypohalites (e.g., hypochlorite and hypobromite) in water containing halide salts using electrochemistry. The apparatus can be a sensor having four electrodes—a reference electrode, a working electrode, and two auxiliary electrodes. The fourth electrode, i.e., the second auxiliary electrode, can be used to generate ionized water near and in contact with the working electrode. The ionized water can clean the working electrode to minimize effects due to scaling or biofilm formation. As such, the working electrode does not need the capability to clean itself. Thus, other elements, originally believed to be unsuitable for use in saline aqueous environments, can be used for the electrodes, for example, gold.

Abstract: A chloramine amperometric sensor includes a sensor body with an electrolyte disposed inside the sensor body. A membrane is coupled to the sensor body and adapted to pass chloramine therethrough. A reference electrode is disposed in the electrolyte and coupled to a first conductor. A second conductor is coupled to a working electrode that is disposed proximate the membrane. The working electrode is constructed from a noble metal in non-compact form. The non-compact form can be a Gas Diffusion Electrode, which can include metal mesh, carbon paper, carbon cloth, metal/carbon powder loaded on a porous membrane or any combination thereof.

Abstract: A method of producing a silver halide photographic emulsion in which a silver ion concentration in precipitation of a silver halide emulsion in a precipitation bath is controlled, wherein a precipitation bath in which stirring is conducted rapidly and uniformly, and crystal formation and crystal growth are uniformly performed is used, the method comprises the steps of: in a start period of precipitation, quantitavely adding a silver nitrate solution and a halogen salt solution at a constant ratio flow rate; when an EAg value reaches a designated EAg value region in the vicinity of a preset target EAg value, starting a control of an adding rate of the halogen salt solution by using a controller which has an operation period equal to or shorter than 1 sec.

Abstract: A thick film electrochemical microsensor device for measuring or regulating chlorine and bromine in water, comprising a substrate to which is applied an optimum arrangement of at least two electrodes. The device is especially useful for measuring or regulating chlorine and bromine levels in swimming pool or spa water. A method of measuring or regulating ions of at least one of chlorine and bromine in water is also described, which comprises contacting the water with the microsensor of the present invention; measuring the current output of the microsensor; determining the level of at least one of chlorine and bromine indicated by the current output; and generating a signal.

Abstract: A thick film electrochemical micro-sensor apparatus for detection and quantification of trace metal ions in water, comprising a substrate to which is applied an arrangement of electrodes comprising at least one of a first type of working electrode, at least one of a second type of working electrode, a counter electrode, a reference electrode, and optionally pH and temperature detectors. The apparatus is especially useful for detection and quantification of trace metal ions in water and effluent. A method of detecting and quantifying trace metal ions using the electrochemical micro-sensor apparatus is also described comprising contacting the water or effluent with the sensor of the present invention, applying a voltage selected for the trace metal ion to be detected, measuring the current output of the micro-sensor, determining if the current output indicates the presence of the trace metal ion, and generating a signal.

Abstract: Processes and devices are disclosed for continuously detecting at least one substance in a gaseous or liquid mixture by means of a sensor electrode to which is applied a variable potential. In an alternative, the substances are concentrated at the surface of the sensor electrode, their concentration is determined by measuring the electrode capacity, the thus obtained measurement value is correlated with the substance and the substance. concentrated at the surface of the sensor electrode is then removed. In another alternative, one or several detection cycles are carried out. In each detection cycle, at least one substance is concentrated at the surface of the sensor electrode, the potential is brought to at least one potential characteristic of the electrochemical reaction of at least one substance, the resulting current is measured and the thus obtained measurement values are correlated with the substances.

Abstract: The present invention provides an electrochemical sensor for the detection of hydrogen chloride. In general, the electrochemical sensor comprises a housing having disposed therein a working electrode, a reference electrode and a counter electrode. The electrochemically active surface of the working electrode preferably comprises a gold film having a thickness of approximately 1000 to 3000 .ANG.. Electrical connection is maintained between the working electrode and the counter electrode via an electrolyte present within the housing. The electrochemical gas sensor preferably further comprises circuitry for maintaining the working electrode at a potential in the range of approximately 1025 to approximately 1400 mV versus the normal hydrogen electrode. The present invention also provides a method of using such a sensor to detect hydrogen chloride.

Abstract: The sensor electrode has a sensing surface intended to contact a liquid medium for continuous measuring, in combination with a counter electrode and a reference electrode, of the hydrogen peroxide concentration over a concentration range from 0.005 mole/liter to 3 mole/liter, said sensor consisting of a carbon electrode having an open circuit potential between -65 and -85 mV, said open circuit potential being measured with respect to a Ag/AgCl/saturated Cl.sup.- reference electrode in an alkaline solution having a pH between 10.5 and 14, said solution containing hydrogen peroxide at a concentration of more than 0.5 mole/liter.

Abstract: The invention relates to an electrochemical sensor to determine the concentration of a gas to be quantified, comprising a housing, a measuring electrode comprising a catalystically active material which causes a reaction of the gas to be quantified, a counterelectrode comprising a carbon material, and a solid electrolyte in contact with the measuring electrode and the counterelectrode, wherein the solid electrolyte is prepared by swelling a solid matrix comprising an acrylate polymer with an electrolytic solution comprising at least one acid, and wherein the carbon material in the counterelectrode has a specific surface of at least 40 m.sup.2 /g and comprises reversibly oxidizable or reducible electrochemically active surface compounds.

Abstract: An in-situ procedure is described for measuring chlorate ion concentration in aqueous media containing the same by employing electrodes, particularly microelectrodes which generate a sigmoidal-type response at high chlorate ion concentration, and which exhibit catalytic properties toward chlorate ion electroreduction or electrooxidation.

Abstract: Accordingly, the present invention provides an electrochemical sensor comprising at least two electrochemically active electrodes, a non-aqueous electrolyte system and a diffusion barrier membrane through which the analyte in its gas phase is mobile but through which the non-aqueous electrolyte system is substantially immobile. The diffusion barrier membrane thus allows an analyte in its gas phase to enter the sensor, while substantially preventing the non-aqueous electrolyte from exiting the sensor.

Abstract: The present invention provides an electrochemical sensor for the detection of hydrogen chloride. In general, the electrochemical sensor comprises a housing having disposed therein a working electrode, a reference electrode and a counter electrode. The electrochemically active surface of the working electrode preferably comprises a gold film having a thickness of approximately 1000 to 3000 .ANG.. Electrical connection is maintained between the working electrode and the counter electrode via an electrolyte present within the housing. The electrochemical gas sensor preferably further comprises circuitry for maintaining the working electrode at a potential in the range of approximately 1025 to approximately 1400 mV versus the normal hydrogen electrode. The present invention also provides a method of using such a sensor to detect hydrogen chloride.

Abstract: An electrochemical detection cell (320), which is usable either for potentiometric or electrolytic conductivity detection, has a capillary (305), which controls electrolyte flow. A gas stream containing detectable substances is input through a non-wettable plastic capillary (306). A reaction zone (310) through which both gas and liquid flow is internally wettable. Reference electrode (309) and either electrode (311) or (312) may be used for potentiometric detection. Sensor electrodes (311) and (312), both in the reaction zone, are used for conductivity detection. The electrolyte is fed through the capillary (305) gravimetrically from a reservoir, and the gas stream is supplied by a pyrolysis furnace. The mechanism of ionization in the gas phase ionization detector (GPELCD) is described.