Flexible fuel cell sensors and methods of making and using the same are provided. A fuel cell sensor can be used for the detection of, for example, isopropyl alcohol (IPA), and the working mechanism of the fuel cell sensor can rely on redox reactions. The fuel cell sensor can include a proton exchange membrane (PEM), an anode disposed on a first surface of the PEM, a cathode disposed on a second surface of the PEM opposite from the first surface, and a reference electrode disposed on the first surface of the PEM and spaced apart from the anode.

The present invention provides an electrolyte measuring device that makes it possible to detect failure in the device with a high degree of accuracy. The electrolyte measuring device has: an ion-selective electrode to which an ion solution including ions is supplied; a reference electrode; a measurement section to measure a potential difference between the ion-selective electrode and the reference electrode; and a current measurement section to measure an electric current flowing in the reference electrode.

An electrochemical sensor arrangement (10) for a breath alcohol measuring device (100), to a corresponding breath alcohol measuring device (100) as well as to a process for determining a vitality of electrodes of an electrochemical sensor. The electrochemical sensor arrangement comprises an electrochemical sensor with at least two electrodes (12, 14). The electrochemical sensor arrangement further comprises a heat source (16). The heat source is arranged such that it, upon activation, selectively heats one of the electrodes (12) of the electrochemical sensor.

A fluid analyzer for analyzing fluid samples comprising one or more analytes and a method of calibrating such. The fluid analyzer includes a control system to control at least one automated valve to pass at least three calibration reagents through a fluid channel to a secondary ion selective electrode, a primary ion selective electrode, and a reference electrode, and determine calibration information using calibration logic from signals generated by a meter, control the at least one automated valve to selectively pass different subsets of the at least three calibration reagents through the fluid channel to the secondary ion selective electrode, the primary ion selective electrode, and the reference electrode, and determine re-calibration information using the signals generated by the meter and at least one of the calibration information and re-calibration logic.

There is provided a separation analysis method for analyzing a sample component s included in a sample liquid by introducing the sample liquid into a separation flow path filled with a flow path liquid, the method comprising: obtaining a correction factor representing a proportion of a time period from the first point in time when the sample liquid is introduced into the separation flow path, to the second point in time when an interface between the flow path liquid and the sample liquid reaches a predetermined position at the separation flow path, with respect to a time period from the first point in time to the third point in time when an optical characteristic value of the sample component is measured at the predetermined position, and correcting the measured optical characteristic value with the correction factor.

A low-cost, portable potentiostat capable of performing several different electrochemical experiments (e.g. cyclic voltammetry and anodic stripping voltammetry) was designed. The potentiostat runs on one or more batteries and has a battery life of over two weeks. Further, the potentiostat of the present invention is capable of self-calibrating and has a linear dynamic range spanning several orders of magnitude. It is also capable of saving data onto an onboard data storage card and is able to export the data to a computer for additional analysis. The potentiostat requires no peripheral hardware and is suitable for use by those with even minimal training in electrochemistry.

An analysis device measures ion concentration in a sample to detect an abnormality using an ion selective electrode. The analysis device includes an ion selective electrode that obtains a potential based on the ion concentration, a reference electrode that obtains a potential based on a reference liquid, a measurement unit that measures an electromotive force between the ion selective electrode and the reference electrode, an analyzer that analyzes a potential change of the electromotive force in a certain time region, and a storage that stores abnormality analysis data indicating a relation between the potential change and an abnormality of the analysis device. The analyzer acquires a parameter for the potential change of the electromotive force measured by the measurement unit, and analyzes the abnormality of the analysis device based on the parameter and the abnormality analysis data stored in the storage.

A method of calibrating a gas sensor comprises determining a sensitivity of a gas sensor to one or more conditions proximate the gas sensor, determining one or more initial calibration factors comprising a sensitivity of the gas sensor to one or more analytes of interest, determining a current sensitivity of the gas sensor to the one or more conditions proximate the gas sensor by measuring a response of the gas sensor while the one or more conditions proximate the gas sensor varies during operation of the gas sensor, and adjusting the one or more initial calibration factors of the gas sensor based, at least in part on the current sensitivity of the gas sensor to the one or more conditions proximate the gas sensor, and a relationship between the sensitivity of the gas sensor to the one or more analytes of interest to the sensitivity of the gas sensor to the one or more conditions proximate the gas sensor. Related gas detectors, related methods of compensating and calibrating the gas sensors, and methods of determining a functionality of the gas sensors are disclosed.

The present disclosure provides methods for determining impedance of an electrochemical device by electrically connecting a variable impedance in parallel with the electrochemical device; electrically connecting a power supply to the electrochemical device, the power supply generating a power supply current; modulating a current through the variable impedance; measuring a stack current flowing through the electrochemical device; measuring, at the electrochemical device, a voltage across at least a portion of the electrochemical device; and calculating, based on the measured stack current and the measured voltage, the impedance of the electrochemical device. Systems for performing such methods are also provided.

Apparatus (200) for detecting corrosion of a coating (250) of an object (216), the apparatus comprising: an electrically conductive body (202) defining a cavity (204) for containing an electrolyte (206), the body (202) arranged to be, in use, in electrically conductive contact with the object (216) and arranged to isolate, in use, the electrolyte (206) from the object; and a first electrode (208) within the cavity (204), the first electrode (208) for electrical connection to a potentiostat (402) or to a galvanostat and arranged to be, in use, in electrical contact with the electrolyte (206) in the cavity (204); wherein the body (202) comprises a first part (222) and a second part (224), the second part (224) being slidably movable relative to the first part (222) between a retracted position and an extended position.