The present disclosure relates to an electrochemical sensor for determining a measurand correlating with a concentration of an analyte in a measuring fluid, comprising: a sensor membrane designed to be in contact with the measuring fluid for detecting measured values of the measurand; a probe housing which has at least one immersion region designed for immersion into the measuring fluid, wherein the sensor membrane is arranged in the immersion region of the probe housing; and a measurement circuit which is at least partially contained in the probe housing and is designed to generate and output a measurement signal dependent on the measurand, wherein the sensor membrane contains an optically detectable substance for marking the sensor membrane.

The present disclosure includes a mobile system for calibrating, verifying and/or adjusting a sensor, the mobile system having a valve unit, wherein by setting, in particular controlling, the valve unit, the process variable present at a calibration site can be set, in particular controlled, to at least one specifiable reference value for the process variable. The present disclosure further includes a method for calibrating, verifying and/or adjusting a sensor by means of the mobile system.

The present invention relates to the technical field of glucose detection, and in particular to an enzyme-free glucose sensor and a fabrication method and use thereof. In the present invention, Magnolia grandiflora L. leaves are used as a carbon-based catalyst, which serve as a base material to well disperse nickel atoms and improve the catalytic activity of a material. A prepared Ni@NSiC nano-molecular layer is used to modify a pretreated white glassy carbon electrode (GCE) to obtain a highly-active material-modified working electrode Ni@NSiC/GCE, and then glucose is detected through cyclic voltammetry (CV) and chronoamperometry (CA).

A method for determining contamination of a biosensor in which the biosensor is loaded into a test meter and a sample is then applied. First and second predetermined test voltages are applied between spaced electrodes of the biosensor for respective first and second predetermined time intervals. First and second current values are measured during the respective first and second predetermined time intervals. Reference values are determined based on the measured first and second current values. Based on one or more of the reference values, a determination of contamination is made. Reporting of the analyte concentration of the sample can be suppressed based on the determination.

A system configured to detect defects in a first oxygen sensor is disclosed. The system is configured to detect defects in a first oxygen sensor. The system includes an X-ray imaging device configured to capture a production X-ray image of the first oxygen sensor and an electronic processor configured to use a trained oxygen sensor defect detection model to identify a defect of the first oxygen sensor by producing a pseudo X-ray image by simulating a projection of a fan beam through CT data of a second oxygen sensor. The electronic processor is also configured to measure, via the trained oxygen sensor defect detection model, a fan-beam distortion in the production X-ray image; select, via the trained oxygen sensor defect detection model, the pseudo X-ray image based on the fan-beam distortion; perform a comparison, via the trained oxygen sensor defect detection model, of the production X-ray image to the pseudo X-ray image; and, classify, based on the comparison, the production X-ray image as representing an improperly assembled oxygen sensor.

A microbial sensor, system, and method that can be used to determine a chemical environment and/or substrate concentrations in anaerobic or aerobic environments, such as soils, sediments and ground waters, are disclosed. An exemplary system uses one or more (e.g., inert) measurement electrodes and a reference electrode. The reference electrode can include an electrode exposed to atmospheric oxygen (e.g., a cathode) or an electrode exposed to stable anaerobic or aerobic conditions. The exemplary microbial sensor system measures open-circuit voltage to characterize the chemical (oxidizing or reducing) environment and/or recovery voltage to measure substrate concentrations in the subsurface.

An evaluation and control unit (100) for a broadband lambda probe (200) and a method for operating the same are disclosed. The evaluation and control unit (100) comprises pins (RE, IPE, APE, MES) connectable to electrical wires (201, 202, 203, 204) of electrochemical cells (210, 211) of the broadband lambda probe (200), a controller (103), a ASIC reference potential source (102), wherein the ASIC reference potential source (102) is operable by means of the controller (103), a switch assembly (104) connected to each of the pins (RE, I PE, APE, MES), wherein the switch assembly (104) comprises a first transistor (T.sub.Wire) and a second transistor (T.sub.ECU), wherein the switch reference potential source (105) is connected to a gate side of the first and second transistors (T.sub.Wire, T.sub.ECU), wherein the controller (103) is configured to vary the switch reference potential (V.sub.SW) applied to the gate side of the first and second transistors (T.sub.Wire, T.sub.ECU), wherein the switch assembly (104) is configured to allow a limiting current flowing to the drain side of the first transistor (T.sub.Wire) from the ASIC reference potential if the potential at the gate side of the first and second transistors (T.sub.Wire, T.sub.ECU) is at a predetermined voltage between values of an open and closed switch.

The present invention relates to a method and a device for the chemical-free determination of the chemical oxygen demand (CODs) in aqueous samples. The object of the invention, to develop a method that compensates for the disadvantages of the standard method and at the same time is at least as good as this, in that it can determine the COD quickly and with a high measurement frequency without chemicals and is cheap and has a low personnel requirement and should be simple to automate, is achieved in that the chemical oxygen demand of aqueous samples is determined by non-specific oxidation of water components at an electrode (11), assisted by (ultra)sound from a sound source (15) in a frequency range in which no significant quantities of oxidative species are formed, i.e. below the cavitation threshold.

An electrochemical fuel cell measures ethanol in human breath and a process maintains such an electrochemical fuel cell. The electrochemical fuel cell includes a first electrode (1), a second electrode (2) and a third electrode (3). The first electrode (1) is used as a measuring electrode in a regular operating mode of the electrochemical fuel cell and as a measuring electrode or as a reference electrode in a maintenance mode of the electrochemical fuel cell. The second electrode (2) is used as a counter electrode in the regular operating mode of the electrochemical fuel cell and as a measuring electrode or as a reference electrode in the maintenance mode of the electrochemical fuel cell. The third electrode (3) is used as a counter electrode in the maintenance mode of the electrochemical fuel cell.

A method of using mass and force indicators in electrochemical gas sensor management is provided. The method includes measuring a change in mass of an electrochemical gas sensor and determining a status of the electrochemical gas sensor based on results of the measuring of the change in mass.