Abstract: Provided is a gas sensor capable of accurately obtaining the concentrations of water vapor and carbon dioxide in a measurement gas. A main pumping cell adjusts an oxygen partial pressure of a first internal space such that water vapor and carbon dioxide in the measurement gas are all decomposed in the first internal space. A first measuring pumping cell adjusts an oxygen partial pressure of a second internal space such that hydrogen generated through the decomposition of water vapor is selectively burned. A second measuring pumping cell adjusts an oxygen partial pressure on the surface of a second measuring internal electrode such that carbon monoxide generated through the decomposition of carbon dioxide is all burned on the surface of the second measuring internal electrode.

Abstract: Matrix materials such polymers derivatives to contain a redox active material can be used to form electrodes and probes suitable for use in pH meters and other analyte sensing devices.

Abstract: Analyte sensing devices suitable for measuring pH or other analytes are provided in a variety of form factors, including a hand-held device.

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: The present invention provides a remote monitoring system for monitoring the operation of a fluid treatment system and/or the qualities, characteristics, properties, etc., of the fluid being processed or treated by the fluid treatment system. The present invention also relates to carbon nanotube sensors.

Abstract: The present invention provides a method for the detection of particulates in a sample, wherein the particulates are introduced into a plasma and the potential difference between a common electrode and each of a plurality of indicator electrodes is measured. The invention further provides an electrode array and an apparatus which can be used for the potentiometric detection of particulates in a sample.

Abstract: Provided are an analytical device comprising a pair of hematocrit electrodes (first pair of electrodes) and a pair of glucose electrodes (second pair of electrodes) that allows a sample to sufficiently reach as far as the second pair of electrodes that are provided on a downstream side in a flow path, a method for manufacturing the analytical device, and a measuring apparatus using the analytical device.

Abstract: An electrochemical test cell, containing an anode comprising a metal as an active component; a cathode comprising a porous chemically inert tube containing an active material compatible with the metal of the anode; and an electrolyte; wherein the only metal in contact with the electrolyte is the metal of the anode, is provided. This test cell is useful in a method to evaluate various combinations of materials for suitability as a combination for preparation of a battery.

Abstract: [Objective] An object is to provide a sensor control apparatus and a sensor-control-apparatus control method which can reduce variation in startup time among a plurality of times of execution of detection processing, in consideration of variation in output characteristic among a plurality of gas sensors. [Means for Solution] In a sensor control apparatus, before drive control (S55 to S80) is started, preliminary control is executed so as to supply a constant current to a second oxygen pump cell over a constant time, to thereby control to a constant level the amount of oxygen pumped from a second measurement chamber to the outside of the second measurement chamber (S40 to 50). The preliminary control is executed under control conditions of the sensor control apparatus which are determined for each gas sensor and are associated with the amount of oxygen pumped from the second measurement chamber to the outside thereof.

Abstract: An electrochemical gas sensor, particularly for the detection of ammonia and/or amines, with an ionic fluid as an electrolyte, wherein the ionic fluid contains at least one protic ammonium cation with at least one dissociable hydrogen atom, whereby the at least one protic ammonium cation reacts with the ammonia and/or amines to be measured via deprotonation. The present invention also relates to the use of such a gas sensor.

Abstract: Apparatus and methods are provided for improving sensitivity, throughput, and efficiency of multi-analyte analytical testing. Specifically, an improved Electrochemiluminescence (ECL) analytical apparatus is provided for analytical chemistry, diagnostics, and environmental applications. The ECL apparatus comprises a 96 or more-well plate, where a microarray of working electrodes is placed in each well for high throughput and multi-analyte testing. The microarray of working electrodes connects with a counter electrode forming a two-electrode electrochemical system. Each well is electrically addressable, thereby controlling ECL reactions in flexible modes. The ECL apparatus further comprises a detector of ECL signals, and the detector employs a CCD-chip assembling matrix. Also provided are methods for high-throughput multi-analyte testing.

Abstract: A sensor including: a detection element; terminal members; and a separator, wherein at least one specific first electrode terminal portion and an other first electrode terminal portion are formed on a first main surface of the detection element, wherein a second electrode terminal portion formed on a second main surface of the detection element is disposed so as to be offset from the specific first electrode terminal portion and to overlap with the other first electrode terminal portion in the axial direction, and in a thickness direction, a distance between the detection element and a specific first frame body portion brought into electrical connection with the specific first electrode terminal portion is larger than a distance between the detection element and the other first frame body portion brought into electrical connection with the other first electrode portion.

Abstract: A chronoamperometric method and device to determine concentration of an electrochemically active species in a fluid and pH of the fluid. A plurality of sets of calibration relationships may be determined for a sensor in an aqueous solution, the sensor having one or more working electrodes and one or more reference electrodes. A first plurality of potentials may be applied across the working and reference electrodes of the sensor in solution, and a first plurality of currents and current differences obtained as a function of the applied first plurality of potentials. Concentration of an electrochemically active species may then be determined as a function of the obtained first plurality of currents and current differences using the plural sets of calibration relationships, and pH of the solution may be determined as a function of the obtained first plurality of currents and current differences using the plural sets of calibration relationships.

Abstract: A small, portable, and inexpensive potentiostat circuit that is suitable for wide-spread electrochemical analysis is disclosed. The potentiostat may be fabricated as a stand-alone electrical component or it may be fabricated in conjunction with a Programmable System-on-Chip (SoC) to facilitate on-the-fly calibration and configuration.

Abstract: Described herein is an apparatus comprising an electrochemical cell that employs a capacitive counter electrode and a faradaic working electrode. The capacitive counter electrode reduces the amount of redox products generated at the counter electrode while enabling the working electrode to generate redox products. The electrochemical cell is useful for controlling the redox products generated and/or the timing of the redox product generation. The electrochemical cell is useful in assay methods, including those using electrochemiluminescence. The electrochemical cell can be combined with additional hardware to form instrumentation for assay methods.

Abstract: A sensor having a bifurcated flow path and method for using the same is disclosed. In some embodiments, the sensor has two flow channels into which sample flow is induced by capillary action, wherein the flow channels are in contact with electrodes configured to generate an electrochemical reaction in the flow channels which can be measured and correlated to the level of an analyte in the sample. In some embodiments, the levels of more than one analyte can be measured using a single sensor.

Abstract: A microelectrochemical sensor having a diaphragm, a web, a first and a second electrode. The diaphragm is permeable to ions of a chemical species, is arranged transversely with respect to a cutout in a base body, and closes off the cutout in a fluid-tight fashion. The web is arranged on a first side of the diaphragm between a first partial surface and a second partial surface, and is designed to adjust a temperature of the diaphragm to an operating temperature using electrical energy. The first electrode has a first partial electrode and a second partial electrode, is permeable to fluid, and is arranged on the first side of the diaphragm. The web prevents electrical contact between the first electrode and the diaphragm. The second electrode has a third partial electrode and a fourth partial electrode, is also permeable to fluid, and is arranged on a second side of the diaphragm.

Abstract: Electrochemical test cells are made with precision and accuracy by adhering an electrically resistive sheet having a bound opening to a first electrically conductive sheet. A notching opening is then punched through the electrically resistive sheet and the first electrically conductive sheet. The notching opening intersects the first bound opening in the electrically resistive sheet, and transforms the first bound opening into a notch in the electrically resistive sheet. A second electrically conductive sheet is punched to have a notching opening corresponding to that of first electrically conductive sheet, and this is adhered to the other side of the electrically resistive sheet such that the notching openings are aligned. This structure is cleaved from surrounding material to form an electrochemical cell that has a sample space for receiving a sample defined by the first and second conductive sheets and the notch in the electrically resistive sheet.

Abstract: One or more charge pumps may be used to amplify the output voltage from a chemically-sensitive pixel that comprises one or more transistors. A charge pump may include a number of track stage switches, a number of boost phase switches and a number of capacitors. The capacitors are in parallel during the track phase and in series during the boost phase, and the total capacitance is divided during the boost phase while the total charge remains fixed. Consequently, the output voltage is pushed up.

Abstract: The present disclosure relates to an electrode strip, a sensor strip and a system thereof. The electrode strip includes a substrate, an electrode layer, an insulation layer and a cover. The electrode layer is disposed on the substrate. The electrode layer includes a first electrode set and a second electrode set. The insulation layer includes a groove, a first protrusion and a second protrusion. The first protrusion and the second protrusion divide the groove into two reactive areas such as a first reactive area and a second reactive area. The cover includes a vent-hole connecting to the groove, and the cover is disposed on the insulation layer.

Abstract: Microelectrode comprising a body formed from electrically non-conducting material and including at least one region of electrically conducting material and at least one passage extending through the body of non-conducting material and the region of conducting material, the electrically conducting region presenting an area of electrically conducting material to a fluid flowing through the passage in use. An electrochemical cell which includes such a microelectrode is also disclosed.

Abstract: A sensor includes a housing, at least two electrodes within the housing, an electrolyte providing ionic conductivity between the electrodes and a vent member including a first section including a portion extending through a passage in the housing. The vent member also includes at least one extending member connected to the first section that extends through at least a portion of an interior of the housing. The first section of the vent member is porous so that gas can diffuse from the interior of the housing to an exterior of the housing via the vent member.

Abstract: A miniaturised electrochemical sensor for detection of a component in a gas is provided. The sensor comprises a reference electrode, a counter electrode and a structure comprising a plurality of passages delineated by walls extending along the passages. A working electrode covers the walls of the structure and a layer of an ionomer covers at least part of the working electrode along the walls of the structure. The layer of ionomer is in ion conducting contact with the electrodes. The disclosure further relates to a method of fabricating a miniaturised electrochemical sensor and to a device for measuring content of NO in exhaled breath comprising such a miniaturised electrochemical sensor.

Abstract: An electrochemical sensor having at least two electrodes, and a reservoir chamber containing electrolyte. The reservoir chamber is internally coated with a wicking material to spread the electrolyte evenly over the walls of the reservoir.

Abstract: A five-part internal reference electrode, including a membrane formed in situ, which is useful in automated clinical chemistry analyzers, the method of forming a direct solid state connection to the membrane eliminating the need for the use of an internal reference electrode internal filling solution, and a ganged assembly of said internal reference electrodes with a grounding unit and an external reference electrode.

Abstract: The invention relates to electrodes for electrochemical analysis comprising: —an insulating surface; —carbon nanotubes situated on the insulating surface at a density of at least 0.1 ?mCNT Um?2; and —an electrically conducting material in electrical contact with the carbon nanotubes; wherein the carbon nanotubes cover an area of no more than about 5.0% of the insulating surface. Methods of making such electrodes and assay devices or kits with such electrodes, are also provided.

Abstract: An electrochemical sensor and a method for using an electrochemical sensor are described where the electrochemical sensor comprises a working electrode having thereon one or more redox species that are sensitive to an analyte to be measured and a polymer coating that provides for interaction between the redox species and the analyte.

Abstract: Assay modules, preferably assay cartridges, are described as are reader apparatuses which may be used to control aspects of module operation. The modules preferably comprise a detection chamber with integrated electrodes that may be used for carrying out electrode induced luminescence measurements. Methods are described for immobilizing assay reagents in a controlled fashion on these electrodes and other surfaces. Assay modules and cartridges are also described that have a detection chamber, preferably having integrated electrodes, and other fluidic components which may include sample chambers, waste chambers, conduits, vents, bubble traps, reagent chambers, dry reagent pill zones and the like. In certain preferred embodiments, these modules are adapted to receive and analyze a sample collected on an applicator stick.

Abstract: An electrochemical detector is an electrochemical detector for detecting a substance in a liquid by generating a redox cycle, the electrochemical detector comprising: a first working electrode having a first electrode surface, a second working electrode having a second electrode surface, and a plurality of insulating spacer particles, wherein the first and second electrode surfaces are placed so as to face each other so that an electric field is formed between the first and second electrode surfaces, and the plurality of spacer particles are placed along the first and second electrode surfaces so as to separate the first and second electrode surfaces from each other.

Abstract: A gas sensor including a gas sensor element that extends in an axial direction and has a detection section at a front-end side thereof, and an electrode pad at a rear-end side thereof; a connection terminal that is electrically connected to the electrode pad; and an insulated separator that extends along the axial direction and has an inserting hole into which the connection terminal is inserted. An element side section is arranged within the inserting hole and is connected the electrode pad, and an external circuit side section extends further to the outside in a diametrical direction than an outer surface of the separator through one or more first bending sections from the element side section.

Abstract: A method is provided for determining the presence or amount of an analyte in a sample and includes the steps of contacting a faradaic working electrode to a solution comprising the optionally pre-processed sample and an electrolyte, contacting a capacitive counter electrode to the solution, supplying electrical energy between the faradaic working electrode and the capacitive counter electrode sufficient to provide for faradaic charge transfer at the faradaic working electrode, and measuring at least one of (i) light, (ii) current, (iii) voltage, and (iv) charge to determine the presence or amount of the analyte in the sample.

Abstract: Disclosed herein are embodiments of an apparatus for analysis of electrochemical dissolution. One embodiment comprises a working electrode submerged in a first reaction chamber containing liquid electrolyte, a counter electrode submerged in a second reaction chamber containing liquid electrolyte, a reference electrode submerged in a third reaction chamber and electrolytically connected to the working electrode and an ion conductor electrolytically connecting the first reaction chamber and the second reaction chamber while physically separating the first reaction chamber and the second reaction chamber.

Abstract: Described herein is a device comprising a plurality of first reaction electrodes arranged in an array, the plurality of first reaction electrodes configured to be exposed to a solution and having a capacitance; first circuitry configured to controllably connect the plurality of first reaction electrodes to a bias source and controllably disconnect the plurality of first reaction electrodes from the bias source; and second circuitry configured to measure a rate of charging or discharging of the capacitance. Also described herein is a method of using this device to sequence DNA.

Abstract: An electrochemical sensor for the detection and analysis of an analyte in a solution is disclosed. The electrochemical sensor has an electrically non-conductive support; a plurality of electrodes on the support, each electrode having a first surface and an opposite second surface, said first surface facing towards the support and the second surface facing away from the support. The plurality of electrodes includes a reference electrode, a counter electrode, and a working electrode. The working electrode has a reagent composition containing a reagent for detecting an analyte applied directly to the second surface of the working electrode.

Abstract: An electrochemical sensor for the detection and analysis of an analyte in a solution is disclosed. The electrochemical sensor has an electrically non-conductive support; a plurality of electrodes on the support, each electrode formed from an electrode material and having a first surface and an opposite second surface, said first surface facing towards the support and the second surface facing away from the support. The plurality of electrodes includes a reference electrode, a counter electrode, and a working electrode. The working electrode has a reagent composition containing a reagent for detecting an analyte applied directly to the second surface of the working electrode or dispersed throughout the electrode material of the working electrode.

Abstract: In an electrochemical gas sensor (1), a carrier substrate (2) has an underside (3) and a top side (4), wherein an electrode structure (20) with an electrolyte layer (6) is arranged at the top side (4), while a gas inlet for a measurement gas is formed at the underside (3). A porous region (7) formed of a porous material is provided in the carrier substrate (2), such that diffusion openings in the porous material connect the underside (3) to the top side (4) in a gas-permeable manner, and a connection (5, 27) of a measurement electrode (25, 26) is formed in a gas-tight surface region (33, 34, 35) at the top side (4) adjacent to the porous region (7) and the connection (5, 27) is at least partly covered by the electrolyte layer (6).

Abstract: The present invention relates to a liquid analyzer provided with: a reference electrode S3 that is provided with internal liquid S33 containing a halide ion; and an ion electrode S1 of which a measurable concentration range for a measuring target ion is lower than the concentration of the halide ion in the internal liquid of the reference electrode S3, wherein: the internal liquid S13 of the ion electrode S1 contains the measuring target ion and a halide ion; and the internal liquid S13 of the ion electrode S1 is liquid in which the concentration of the measuring target ion and the concentration of the halide ion in the internal liquid S13 of the ion electrode S1 are regulated such that an osmotic pressure and an isothermal point of the internal liquid S13 of the ion electrode S1 respectively have desired values, and the isothermal point is included in the measurable concentration range, and the concentration of the halide ion is different from the concentration of the halide ion in the internal liquid S33 of

Abstract: A sensor apparatus includes a first electrode and a second electrode at a predefined distance from one another. The sensor apparatus includes a substrate arranged in a predefined first region of the sensor carrier such that the first electrode and the second electrode are substantially electrically decoupled from one another if the outer side of the sensor carrier is substantially free of particles. A third electrode is coupled to a solid electrolyte that is additionally coupled to the second electrode. A diffusion barrier is coupled to the third electrode in a predefined third region and the exhaust gas is applied to the third electrode only in the third region via the diffusion barrier.

Abstract: Corrosion sensor apparatus for detection of contamination affecting metal based components and devices. For example, an apparatus includes: a set of corrosion sensor elements, wherein a width of a first corrosion sensor element is different than a width of a second corrosion sensor element, wherein each corrosion sensor element is susceptible to corrosion caused by an operating environment of the corrosion sensor elements; and a set of reference elements wherein a width of a first reference sensor element is substantially equal to the width of the first corrosion sensor element and a width of a second reference sensor element is substantially equal to the width of the second corrosion sensor element, wherein each reference sensor element is not substantially susceptible to corrosion caused by the operating environment of the corrosion sensor elements.

Abstract: An electrochemical sensor for sensing a gaseous analyte includes a substrate having at least two electrodes disposed thereon, and a carbon nanotube-polyaniline (CNT/PANI) film disposed on the substrate and in contact with at least two electrodes. The CNT/PANI film includes carbon nanotubes coated with a thin layer of polyaniline. The thickness of the polyaniline coating is such that electron transport can occur along and/or between the carbon nanotubes.

Abstract: A method for determining a salt concentration of a hydrocarbon fluid using a conductivity sensor and a hydrocarbon testing solution includes forming the hydrocarbon testing solution. The electropolymerizable monomer is operable to form a resultant associated polymer at a peak potential of the electropolymerizable polymer. The method includes introducing the hydrocarbon testing solution into the conductivity sensor. The method includes inducing a range of potential across the hydrocarbon testing solution such that at least a portion of the electropolymerizable monomer polymerizes. The range of induced potential includes the peak potential of the electropolymerizable polymer. The method includes detecting a range of electrical current associated with the range of potential induced. The method also includes the step of determining the salt concentration of the hydrocarbon fluid using the range of potential induced and the range of electrical current detected.

Abstract: Methods, arrays, and systems for electrochemical sensing are provided. An example of a method includes forming a number of first electrodes, forming a fluidic level having a number of walls that extend substantially vertically from each of the number of first electrodes, and forming a number of second electrodes in contact with the number of walls. In some examples, forming the fluidic level having the number of walls includes embossing an embossing resin.

Abstract: Provided are an amperometric sensor and device for electrochemically quantifying nitrosothiol (RSNO), which is associated with storage and delivery of nitric oxide (NO) in the human body. The amperometric sensor for measuring a concentration of RSNO includes an electrode configured to measure an electric current generated by an oxidation reaction of NO, and a means configured to start and stop photo-induced decomposition of RSNO. Here, the electric current is measured by the oxidation reaction of NO before and after the photo-induced decomposition of RSNO. The amperometric sensor may measure separate signals of RSNO and NO, which are present in the sample at the same time, using one electrode, thereby preventing an inhibition action caused by NO during the measurement of RSNO. Also, the amperometric sensor is simple in structure and easy to manufacture and may be applied to manufacture of a small electrode, and thus may be developed as a sensor for in vivo measurements.

Abstract: The presently disclosed subject matter relates to a microfluidic device for measuring an amount of a molecular species in a sample. The device comprises a body and an electrode assembly, the electrode assembly comprising at least one electrode coupled to the body. The device also includes a gas permeable membrane disposed on at least one electrode and a detector for measuring a current at each of the electrodes. Further, the device comprises a channel defined between a substantially planar substrate and planar cover glass. The presently disclosed subject matter also relates to methods of making the microfluidic device.

Abstract: The presently disclosed subject matter relates to sensors for measuring an amount of a gaseous species in a sample. The sensors comprise a gas permeable polysiloxane network membrane, comprising both alkyl and fluorinated alkyl groups. In some embodiments, the polysiloxane network can be formed from the co-condensation of a mixture of an alkylalkoxysilane and a fluorosilane. The presently disclosed subject matter also relates to methods of making the sensors, methods of selectively measuring an amount of a gaseous species, such as nitric oxide, in a sample, and to compositions comprising the polysiloxane networks.

Abstract: A test strip and a detecting device are disclosed. The test strip can be used with an electrochemical instrument to accurately detect the viscosity and concentration of an analyte of a specimen. The test strip includes a first specimen path, a first electrode set, a redox reagent, a second specimen path, a second electrode set, and a reaction reagent. The redox reagent includes at least a redox pair. When the specimen enters the first specimen path, the redox pair dissolves and generates an electrochemical redox reaction for obtaining a flow time of the specimen. When the specimen enters the second specimen path, the reaction reagent is used to obtain the analyte concentration of the specimen, and the concentration of the analyte can be corrected by the flow time.

Abstract: An electro-chemical sensor for methane is described having a catalyst to react methane or other low molecular weight hydrocarbons and a detector to detect the turnover or reaction rate and using such information to determine the concentration of the methane or other low molecular weight species. The sensor is preferably used for measurements in a wellbore.

Abstract: This disclosure relates to a method of detecting an analyte. The method includes (1) contacting an aqueous solution containing the analyte with an electrochemical detector having a working electrode, a counter electrode, and a solid electrolyte, where the analyte includes a halogen or an oxy-halogen species and the solid electrolyte provides an electrical pathway between the working and counter electrodes; (2) applying a voltage to the detector; and (3) measuring the resultant current change in the detector.

Abstract: A low cost room temperature electrochemical gas sensor for sensing CO and other toxic analyte gases has a solid protonic conductive membrane with a low bulk ionic resistance. A sensing electrode and a count counter electrode, which are separated by the membrane, can be made of mixed protonic-electronic conductors. Embodiments of the inventive sensor also include an electrochemical analyte gas pump to transport the analyte gas away from the counter electrode side of the sensor. Analyte gas pumps for the inventive sensor include dual pumping electrodes situated on opposite sides of the membrane, and include a means for applying a DC power across the membrane to the sensing and counter electrodes. Another embodiment of the inventive sensor has first and second solid protonic conductive membranes, one of which has a sensing electrode and a counter electrode separated by the first membrane, and the other of which has dual pumping electrodes situated on opposite sides of the second membrane.

Abstract: A low cost room temperature electrochemical gas sensor with humidity compensation for sensing CO, alcohol vapors and other toxic analyte gases has a solid protonic conductive membrane with a low bulk ionic resistance. A sensing electrode and a counter electrode, optionally a counter electrode and a reference electrode, which are separated by the membrane, can be made of mixed protonic-electronic conductors, or can be made of a thin electrically conducting film such as platinum. A reservoir of water maintain the solid protonic conductive membrane at constant 100 percent relative humidity to compensate for ambient humidity changes. Embodiments of the inventive sensor also include an electrochemical analyte gas pump to transport the analyte gas away from the counter electrode side of the sensor.