Abstract: The invention relates to a method of determining a charged particle concentration in an analyte (100), the method comprising steps of: i) determining at least two measurement points of a surface-potential versus interface-temperature curve (c1, c2, c3, c4), wherein the interface temperature is defined as a temperature of the interface between a measurement electrode and the analyte (100), wherein the surface-potential is defined at the interface, and ii) calculating the charged particle concentration from locations of the at least two measurement points of said curve (c1, c2, c3, c4).This method, which still is a potentiometric electrochemical measurement, exploits the temperature dependency of a surface-potential of a measurement electrode. The invention further provides an electrochemical sensor and electrochemical sensor system for determining a charged particle concentration in an analyte. The invention also provides various sensors which can be used to determine the charged particle concentration, i.e.

Abstract: A method for determining an analyte in a water sample with a mobile water analyzing system having a basic unit and a test element insertable in the basic unit, the method comprising providing the test element and the basic unit. The test element is inserted into a test element receptacle of the basic unit. The water sample is transported forward from an inlet opening to a measuring section of the test element. A first analyzing of the water sample is performed in the measuring section with an analyzer of the basic unit. The water sample is transported forward from the measuring section to the first reagent section of the test element. The water sample is transported backward from the first reagent section to the measuring section of the test element. A second analyzing of the water sample is performed in the measuring section with the analyzer of the basic unit.

Abstract: Luminescence test measurements are conducted using an assay module having integrated electrodes with a reader apparatus adapted to receive assay modules, induce luminescence, preferably electrode induced luminescence, in the wells or assay regions of the assay modules and measure the induced luminescence.

Abstract: An electrochemical sensor includes a dielectric substrate and a conductive layer formed on a surface of the substrate. The conductive layer includes a working electrode, an electrode lead and a connecting arm connecting the working electrode to the electrode lead. A dielectric layer is positioned over the conductive layer. The dielectric layer has an aperture exposing the working electrode and a portion of the connecting arm. The working electrode, electrode lead and connecting arm may be formed by laser ablation technique to provide precise working electrode sensor parameters.

Abstract: A sensor includes a sheath that is elongated along a longitudinal axis; a spacer positioned within the sheath and defining first and second channels having lengths that extend along the longitudinal axis; a first elongated member positioned within the first channel; and a second elongated member positioned within the second channel. The first elongated member includes an active surface forming a working electrode and the second elongated member including an active surface defining a counter electrode.

Abstract: An electrically passive device and method for in-situ acoustic emission, and/or releasing, sampling and/or measuring of a fluid or various material(s) is provided. The device may provide a robust timing mechanism to release, sample and/or perform measurements on a predefined schedule, and, in various embodiments, emits an acoustic signal sequence(s) that may be used for triangulation of the device position within, for example, a hydrocarbon reservoir or a living body.

Abstract: A method for detecting an organic carbonyl species involves exposing a metal oxide-free film of a polyaniline to an environment suspected of containing an organic carbonyl species, detecting a change in electrical conductivity and/or an optical or luminescent property of the polyaniline, and, correlating the change in electrical conductivity and/or optical or luminescent property to a presence of the organic carbonyl species in the environment. Further, sensors for organic carbonyl species are disclosed having a metal oxide-free film of a polyaniline supported on an electrically insulating substrate. The method and sensors provide a good balance between response time and sensitivity, being considerably faster than metal oxide and metal oxide/polymer based sensors, while having greater sensitivity than other polymer-based sensors.

Abstract: An electrolyte sensor that uses conductive elastomer electrodes. Examples of the intended analytes for sensor use include those found in urine, saliva, blood, feces and spinal fluid, although other analytes exist for electrolyte detection. Conductive elastomer trace electrodes are separated by a gap or channel which can be bridged by an electrolyte and thereby complete an electrical circuit to an alarm or other circuitry. Gap or channel distances vary the level of electrical resistance associated with detecting certain electrolytes.

Abstract: The present invention concerns embodiments of a system for determining the concentration of an analyte in a body fluid which comprises an analytical test element and an instrument separate therefrom, wherein at least a part of the electrical components of the system are comprised of polymer electronics. Embodiments of the analytical test element comprise an area with reagent chemistry for the detection of an analyte and a transponder configured for wireless transmission of lot-specific data and/or measured values. The instrument has a reading module configured for wireless transmission of data, or data and energy, to the test element and an evaluation unit for evaluating the data or measured values received by the transponder.

Abstract: A method for measuring an iodine adsorption number of carbon black includes: (a) electrochemically reducing an unknown amount of iodine adsorbed by a predetermined amount of a carbon black sample; (b) measuring the electrical charge used for reducing the unknown amount of the iodine adsorbed by the carbon black sample; and (c) obtaining the iodine adsorption number from the measured electrical charge. An electrolytic cell and a kit for measuring an iodine adsorption number of carbon black are also disclosed.

Abstract: The invention concerns a reagent system for the so-called on-board control of analytical elements, in particular test strips, containing an organic N-oxide or a nitroso compound. The invention also concerns analytical elements containing a reagent system for a detection reaction and a reagent system for an on-board control. Furthermore, the invention concerns a method for checking analytical elements in which a reagent system for an on-board control is examined optically or electrochemically with the aid of a measuring instrument for changes which could indicate a stress of the analytical element.

Abstract: An electrochemical gas sensor (9) has improved electrochemical measurement properties and housing tightness for an electrolyte at the sites at which the connection lines (11, 21, 31) pass through. The sensor (9) includes a housing (4), containing at least one measuring electrode (1) and a counterelectrode (2) and with electric connection lines (11, 21, 31) from the electrodes (1, 2, 3) to a measuring unit (8) arranged outside the housing (4). The electric connection lines (11, 21, 31) include carbon nanotubes (CNT, Carbon Nanotubes) at least in some sections in the housing (4) in the area of the electrolyte wetting.

Abstract: A catalyst member comprising a blended mixture of nano-scale metal particles compressed with larger metal particles and sintered to form a structurally stable member of any desired shape. The catalyst member can be used in one of many different applications; for example, as an electrode in a fuel cell or in an electrolysis device to generate hydrogen and oxygen.

Abstract: Devices and methods are presented for electronic sensing of chemical and biochemical analytes. An electronic sensor having a at least two electrodes separated by a nanoscale gap wherein the separation between the first electrode and the second electrode forms a cavity capable of containing a fluid wherein two or more posts comprised of an insulating material extend into the cavity from the face of the first electrode to the face of the second electrode. Optionally, the cavity is closed with a bead. Devices according to embodiments of the invention are capable of detecting chemicals and biochemicals through redox cycling events. Additionally, devices and methods according to embodiments of the invention are adapted to identify and sequence nucleic acid molecules.

Abstract: A system for analyzing a liquid is provided. The system comprises: an electrochemical unit having an electrochemical microchamber for receiving a sample of the liquid and electrochemically analyzing the sample; and a microfluidic unit being attached to the electrochemical unit and having microchannels constituted for sampling the sample in situ and feeding the sample to the electrochemical microchamber. Also provided are nucleic acid constructs and cells comprising same for analyte detection.

Abstract: Methods for determining a concentration of an analyte in a sample, and the devices and systems used in conjunction with the same, are provided herein. In one exemplary embodiment of a method for determining a concentration of an analyte in a sample, a sample including an analyte is provided in a sample analyzing device having a working and a counter electrode. An electric potential is applied between the electrodes and a fill time of the sample into the device is calculated. A concentration of the analyte in view of fill time can then be determined. Systems and devices that take advantage of the fill time to make analyte concentration determinations are also provided.

Abstract: The present invention provides a unique solution to the problems of both steady-state and transient signals produced by a variety of interfering stimuli, including humidity, which relies upon the inclusion in a gas sensing electrode in an electrochemical gas sensor of a catalyst material in addition to a first catalyst material reactive to the target gas, the additional, or second, catalyst material producing a response to an interfering stimulus which is of the opposite polarity to that generated by the first catalyst material.

Abstract: The present invention provides a test strip for measuring a concentration of an analyte of interest in a biological fluid, wherein the test strip may be encoded with information that can be read by a test meter into which the test strip is inserted. In one embodiment, a first test strip comprises: a first measurement electrode connectable to a test meter; a first trace loop with a first associated resistance, where the first trace loop is connectable to the test meter; and a second trace loop with a second associated resistance, where the second trace loop is connectable to the test meter. The test meter is adapted to: receive the first test strip; connect to the first measurement electrode, the first trace loop, and the second trace loop; and obtain a first resistance ratio by comparing the first and second associated resistances.

Abstract: A water-proof electrochemical sensor for in situ analysis and real-time monitoring of chemical and biological compounds in a liquid analyte, such as a water column, or a water column/sediment interface, or sediment. The water-proof electrochemical sensor assembly comprises an electrode body that is resistant to high temperatures and pressure and includes a semi-hard o-ring or collar. A resilient elastomeric boot, that has an internal groove which is adapted to form a tight pressure-fit with the collar is installable on the electrode body. One end of the boot has an opening adapted to form an interference fit with a pin contact for electrical connections with external equipment and the other end of the boot has an opening adapted to form an interference fit with the electrode body whereby a water-proof seal is formed.

Abstract: The invention relates to embodiments of an analysis system and to a method for analyzing a sample on an analytical test element, with the analysis system comprising a test element receptacle for receiving and positioning a test element in an analysis position. In an exemplary embodiment, the test element receptacle contains a guide part and a lock part, the guide part having means for guiding a test element into and out of the analysis position, the lock part comprising a frame and a bolt element, which frame and bolt element are connected to one another by a hinge. The bolt element can be pivoted about the hinge between a first position and a second position with respect to the frame. The bolt element comprises a latching lug for engaging in a recess in test element when the bolt element is in the first position and when the test element is positioned in the analysis position.

Abstract: A bilirubin sensor has a working electrode with a first chemical matrix disposed thereon that contains a binder, a substrate electrode with a second chemical matrix dispose thereon that contains a binder and a chemical agent that consumes bilirubin, a reference electrode, a sample chamber containing the working electrode, the substrate electrode and the reference electrode, and a method of measuring bilirubin in a body fluid.

Abstract: Generally, embodiments of the present disclosure relate to analyte determining methods and devices (e.g., electrochemical analyte monitoring systems) that have improved signal response and stability by inclusion of a coating including a hydrogel, a crosslinker, and a swelling modulator, where the coating is disposed proximate to a working electrode of in vivo and/or in vitro analyte sensors, e.g., continuous and/or automatic in vivo monitoring using analyte sensors and/or test strips. Also provided are systems and methods of using the, for example electrochemical, analyte sensors in analyte monitoring.

Abstract: Sensor device for ion channel recordings; liquid-liquid measurements and resistive pulse particle counting comprising; at least one sensor element; the element comprising a diamond thin film substrate and a pore which is a nanopore or a micropore included in the substrate. This device may be used in analysis, for instance the device may be used for single molecule detection of an apialyte (e.g. DNA), for the analysis of interactions between a sensor element and an analyte, for the detection of pore forming entities, or for the determination of ion transfer.

Abstract: Generally, embodiments of the present disclosure relate to analyte determining methods and devices (e.g., electrochemical analyte monitoring systems) that have improved uniformity of distribution of the sensing layer by inclusion of a self-polymerizing hydrogel, where the sensing layer is disposed proximate to a working electrode of in vivo and/or in vitro analyte sensors, e.g., continuous and/or automatic in vivo monitoring using analyte sensors and/or test strips. Also provided are systems and methods of using the, for example electrochemical, analyte sensors in analyte monitoring.

Abstract: An exhaust sensor includes a first sheet of ceramic that is perforated with a vent orifice and, a second sheet of ceramic that is laminated to the first sheet. A palladium circuit trace is positioned between the first sheet and the second sheet of ceramic and a fugitive ink is printed on one of the sheets that is in communication with the vent orifice and the palladium. The fugitive ink volatilizes during a firing process and created a void space that is occupied by a palladium oxide that forms at temperatures around 625-900C.

Abstract: Methods, compositions and kits for analyzing a chemical analyte using an electrochemical cell connected to a measuring apparatus are provided. The electrochemical cell contains a solution having one or more conductive or redox active NPs (nanoparticles), one or more chemical analytes, and an indicator. In addition, the electrochemical cell contains one or more electrodes in communication with the solution. One or more catalytic ECL properties are generated by the interaction of the one or more conductive or redox active NPs and the liquid sample and measured at the one or more electrodes or with an optical detection system.

Abstract: The present invention is directed to devices and methods for carrying out and/or monitoring biological reactions in response to electrical stimuli. A programmable multiplexed active biologic array includes an array of electrodes coupled to sample-and-hold circuits. The programmable multiplexed active biologic array includes a digital interface that allows external control of the array using an external processor. The circuit may monitor, digitally control, and deliver electrical stimuli to the electrodes individually or in selected groups.

Abstract: Method and system for detecting presence of biomolecules in a selected subset, or in each of several selected subsets, in a fluid. Each of an array of two or more carbon nanotubes (“CNTs”) is connected at a first CNT end to one or more electronics devices, each of which senses a selected electrochemical signal that is generated when a target biomolecule in the selected subset becomes attached to a functionalized second end of the CNT, which is covalently bonded with a probe molecule. This approach indicates when target biomolecules in the selected subset are present and indicates presence or absence of target biomolecules in two or more selected subsets. Alternatively, presence of absence of an analyte can be detected.

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 planar electrochemical gas sensor is provided with at least one working electrode (4), at least one counterelectrode (4?), at least one electrolyte-filled planar electrolyte carrier (10), at least one planar housing upper part (3) and at least one planar housing lower part (2). The electrodes (4, 4?) are arranged such that they are in two-dimensional contact with the electrolyte carrier (10). The housing upper part (3) and the housing lower part (2) are connected with one another such that the electrodes (4, 4?) and the electrolyte carrier (10) are pressed against one another in such a way that they are secured against displacement. The housing upper part (3) and the housing lower part (2) are partially in direct two-dimensional contact with one another, and the connection of the housing upper part (3) and the housing lower part (2) in the area of the direct two-dimensional contact is present at least along a closed figure, which surrounds the electrodes (4, 4?) and the electrolyte carrier (10).

Abstract: An explosion-proof sensor for detecting combustible gases is provided with a glass seal (9) for establishing an electrically conductive connection with the interior of the housing. The sensor is improved in terms of the pressure resistance of the housing. The glass seal (9) has a bending-resistant casting compound (16, 17, 18) mechanically stabilizing the glass seal (9) on at least one side.

Abstract: The application generally describes devices, systems, and methods for determination of one or more analytes. Embodiments described herein may be useful as sensors for analytes such as explosives, chemical warfare agents, and/or toxins. In some cases, chemiresistor or chemFET sensor devices for monitoring volatile organics, especially chemical warfare agents such as sarin, are described. Some embodiments comprise functionalised carbon nanotube/conjugated polymer composites (6) as sensing material. In some embodiments, the polymer is poly(3-hexylthiophene), 3PHT, optionally substituted with calixarenes, or hexafluoroisopropanol susbstituted polythiophene, HFIP-PT. Biosensing embodiments are also described, as well as methods of manufacturing the devices.

Abstract: An apparatus and method for electrochemical fluid analysis comprises a chamber (1202) having a depth dimension for accommodating a volume of a fluid under test, first and second electrodes (A1) disposed within the chamber and extending along the depth dimension in spaced relation with each other, and a soluble solid, such as an annealed polymer, e.g. EUDRAGIT occupying a lateral gap between the first and second electrodes. The rate of dissolution as monitored by electrochemical impedance spectroscopy (EIS) of the soluble solid within the fluid depends on the chemical concentration of a corresponding analyte present in solution in the fluid. In one embodiment a silicon-based integrated circuit device defining an upper margin includes an array of electrodes disposed along said upper margin to permit direct exposure of the electrode array to the fluid under test. The device is constructed using CMOS technology.

Abstract: The measuring device has at least one measuring probe, e.g., a physical or electrochemical measuring probe, which is equipped with one or more memory units and which is connected through a cable, e.g., a coaxial cable, to a transmitter which includes a processor. The measuring probe has a ground wire and is connected to the memory unit through a first signal wire, wherein under the control of the processor in accordance with a transmission protocol, the first signal wire and a connecting cable serve for the unidirectional transmission of the analog or digital measuring signal of the measuring probe as well as the preferably bidirectional transmission between the measuring probe and the transmitter of digital operating data which are read from or to be written into the memory unit.

Abstract: The present invention relates to devices, systems, and methods for determination of ionizing radiation. In some embodiments, the devices comprise nanocomposite materials containing nanostructures (e.g., carbon nanotubes) dispersed in radiation sensitive polymers. In some cases, the device may include a conductive pathway that may be affected upon exposure to ionizing radiation. Embodiments described herein may provide inexpensive, large area, low power, and highly sensitive radiation detection materials/devices.

Abstract: A gas sensor and method thereof are provided. The example gas sensor may include first and second electrodes formed on a substrate, a carbon nanotube connecting the first and second electrodes on the substrate, a light source disposed above the carbon nanotube and an ampere meter measuring current flowing between the first and second electrodes.

Abstract: A three-dimensionally ordered macroporous sensor apparatus and method of forming the same. A direct opal film associated with a number of pores can be formed by vertical deposition of one or more nanospheres on a glass substrate. The thickness of the direct opal film can be controlled by concentration of the nanospheres. A mixture of a precursor/monomer of a sensing material and a complexing agent can be filled into the pores associated with the direct opal film, such that the mixture permeates the interstitial spaces between the pores. The nanospheres may then be removed in order to form a three dimensionally-ordered macroporous electrode with an inverse opal structure. Optionally, the sensing material can be coated on an inverse opal backbone structure formed from an external inactive material and utilizing a coating operation.

Abstract: A method of determining chemical oxygen demand (COD) of a water sample which is useful in a probe configuration includes the steps of a) applying a constant potential bias to a photoelectmchemical cell, having a photoactive working electrode optionally a reference electrode and a counter electrode, and containing a supporting electrolyte solution; b) illuminating the working electrode with a light source and recording the background photocurrent produced at the working electrode from the supporting electrolyte solution; c) adding a water sample, to be analysed, to the photoelectrochemical cell; d) illuminating the working electrode with a light source and recording the steady state photocurrent produced with the sample; e) determining the chemical oxygen demand of the water sample using the formula (I): where ? is the Nernst diffusion layer thickness, D is the diffusion coefficient, A is the electrode area, F the Faraday constant and iss the steady state photocurrent.

Abstract: The present invention includes sensors and systems that include a sensor. A sensor includes a sensor polymer, where the polymer includes a repeating unit having an anilineboronic acid-phosphate complex or an anilineboronic acid complexed with an alcohol or diol. The sensor polymer may be a copolymer, such as a random copolymer, a block copolymer, or an alternate copolymer. The present invention also provides methods for using the sensors described herein, including methods for detecting the presence of an analyte, such as CO2, in a fluid.

Abstract: A system for sensing a gas stream constituent comprises: (a) a thermally conductive, electrically insulative substrate, (b) a gas-sensing element mounted on the substrate and capable of sensing the constituent, (c) a reference element mounted on the substrate having electrical properties congruent with the gas-sensing element and being insensitive to the constituent, (d) an electronic circuit interconnecting the gas-sensing element and the reference element. The circuit is capable of actuating both of the elements and measuring the voltage difference between the elements. The voltage difference is proportional to the concentration of the constituent in the gas stream.

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: The present disclosure provides small volume analyte sensors having large sample fill ports, supported analyte sensors, analyte sensors having supported tip protrusions and methods of making and using same.

Abstract: A precious metal testing apparatus and methods adapted to analyze impurities in a precious metal test sample is described. The testing apparatus contains a test probe that has a replaceable portion and that is connected to a meter to measure resistance. The replaceable portion contains or forms a reservoir that includes at least one electrolyte component, a conductive member, and a fibrous tip. The electrolyte component is fluidly associated with a fiber tip and the conductive member contacts an electrical contact located outside the reservoir. Methods of testing and instructions regarding such methods are also included.

Abstract: The present invention relates to an analyzing tool including: a plurality of electrodes 10, 11 and 12 formed in an annular shape with stacked on one another in an axial direction; and a specimen layer formed in an interior of at least one of the plurality of electrodes 10, 11 and 12. The analyzing tool according to the present invention may be configured to include: a first electrode formed in an annular shape; a second electrode formed in an annular shape and inserted through an interior of the first electrode with a space from an inner peripheral surface of the first electrode; and a specimen layer formed between the inner peripheral surface of the first electrode and an outer peripheral surface of the second electrode.

Abstract: A fluid assay system comprises a swab having an absorbent portion for receiving and retaining a fluid sample. The system also comprises an electrode module having at least one electrode, arranged so that it can be selectively placed over the absorbent portion of the swab in order to contact the electrode with the fluid sample. The system further comprises a reader module configured to process signals from the electrode module, with the electrode and reading modules arranged such that they can be coupled together for communication of the signals from the electrode module to the reader module.

Abstract: Provided is an electrochemical sensor device capable of micromachining a channel while maintaining its measurement sensitivity and of reliably quantitating an analyte in a trace amount of a sample. An electrochemical sensor device includes: a channel portion formed in a substrate; and working electrodes for subjecting an analyte in a solution flowing in the channel portion to electrochemical measurement, the electrochemical sensor device includes a plurality of measuring portions individually provided with the working electrodes, and each of the working electrodes has a plurality of conductive protrusion portions formed to protrude from a bottom surface of each of the measuring portions.

Abstract: The present invention relates to a method for distinguishing between a sample and a control liquid in a system for analyzing a specific component in the sample by using an analyzing tool having a working electrode and an counter electrode. This discriminating method includes a first step of applying a voltage between the working electrode and the counter electrode, a second step of measuring a response current at certain intervals by use of the working electrode and the counter electrode, a third step of calculating a relative value for a peak value or an end value of the response current, a fourth step of calculating a change rate of the relative value, and a fifth step of distinguishing between the sample and the control liquid based on the change rate.

Abstract: A method for measuring an iodine adsorption number of carbon black includes: (a) electrochemically reducing an unknown amount of iodine adsorbed by a predetermined amount of a carbon black sample; (b) measuring the electrical charge used for reducing the unknown amount of the iodine adsorbed by the carbon black sample; and (c) obtaining the iodine adsorption number from the measured electrical charge. An electrolytic cell and a kit for measuring an iodine adsorption number of carbon black are also disclosed.

Abstract: An electrochemical sensor, especially for gases, is provided having a mediator compound based on transition metal salts of polybasic acids and/or transition metal salts of polyhydroxycarboxylic acids. The electrochemical sensor also contains a DLC, BDD or a precious metal thin-layer measuring electrode (3). The electrochemical sensor may be used for determining SO2 and H2S.

Abstract: Provided are nanoscale devices suitable for multiplexed, parallel detection of multiple analytes and methods for fabricating such devices.