A contaminant measurement system is provided. The system is operable to detect and measure a concentration level of a preselected contaminant, e.g., lead, in water disposed within a chamber of the system. The system includes a detection agent that is operable to interact with the preselected contaminant in the water. The detection agent can be a plurality of polymeric beads or a membrane, for example. The system has a sensing circuit that includes a pair of electrodes spaced from one another and both at least partially disposed in the water. A controller is communicatively coupled with the sensing circuit and is configured to receive one or more electric signals from the sensing circuit. The controller determines a parameter indicative of the concentration level of the preselected contaminant based on the one or more electrical signals. The controller then determines and outputs the concentration level of the preselected contaminant.

Provided is a heavy metal detecting sensor. The heavy metal detecting sensor includes an electrode and a plurality of amyloid fibers disposed on the electrode, wherein an amount of a redox current of the electrode decreases when the plurality of amyloid fibers react with heavy metal ions.

The biosensor includes a substrate, an electrode pattern positioned on the substrate, a passivation layer which is formed with a plurality of holes spaced apart from each other, and a bead positioned at one or more holes among the plurality of holes, and to which an antibody is attached, the electrode pattern includes a first electrode pattern part and a second electrode pattern part spaced apart from the first electrode pattern part, which has a same height as a height of the first electrode pattern part, and forms an electric field with the first electrode pattern part.

Peroxycarboxylic acid compositions comprising compatible ionic compounds to deliver conductivity signals to enable monitoring of the peroxycarboxylic acid concentration by conductivity when diluted for use are disclosed. Methods of measuring peroxycarboxylic acid concentration by conductivity are also disclosed. Beneficially, conductivity measurement allows a user to determine concentration of the peroxycarboxylic acid at a point of use without cumbersome titration steps to determine the concentration providing various benefits at an application of use.

Embodiments relate generally to systems and methods for identifying the concentration of an electrolyte. A method may comprise scanning a diagnostic micro-electrode of an electrochemical sensor using scanning voltammetry at a plurality of electrolyte concentrations; generating a variable set of readings from the first scanning voltammetry scan using a potential difference between a strong hydrogen adsorption peak and an oxide reduction peak and/or oxide formation peak at each of the plurality of electrolyte concentrations; and determining a correlation by plotting the variable set of readings and the plurality of electrolyte concentrations. In some embodiments, the method may comprise scanning a diagnostic micro-electrode of a second electrochemical sensor using scanning voltammetry, wherein the second electrochemical sensor has been employed; generating a second set of readings; and determining the electrolyte concentration of the electrolyte of the second electrochemical sensor by applying the determined correlation to the second set of readings.

A sensor is configured to sense a parameter of an aqueous liquid. The sensor has an analog output port configured to provide an analog signal indicative of a sensed parameter, and a calibration memory device storing individual digital information indicative of a calibration of the sensor. A digital output port provides a digital signal indicative of the digital information. A treatment system and method is matched to the sensor.

The present invention is in relation to a method and its apparatus, by means of which HCl generation formed from hydrolysis reactions or thermal decomposition of chloride salts is continuously monitored. Its application is in oil refining or in any other area where chloride salts are heated to temperatures high enough to cause hydrolysis reactions or thermal decomposition. The invention allows for a much more sophisticated and precise record of the thermal events that occur as a function of temperature. It also allows the behavior of chloride salts subjected to these conditions to be evaluated, both in model systems and in industrial saline solutions, with respect to the respective content, composition, or presence of components in the oil phase, such as carboxylic (naphthenic acids) or nitrogenous (ammonia or amines) acids.

The present invention relates to sample analysis cartridges comprising micro-environment sensors and methods for assaying coagulation in a fluid sample applied to the micro-environment sensors, and in particular, to performing coagulation assays using micro-environment sensors in a point of care sample analysis cartridge. For example, the present invention may be directed to a sample analysis cartridge including an inlet chamber configured to receive a biological sample, and a conduit fluidically connected to the inlet chamber and configured to receive the biological sample from the inlet chamber. The conduit may include a micro-environment prothrombin time (PT) sensor, and a micro-environment activated partial thromboplastin time (aPTT) sensor.

A liquid sensor for a diaper, and method of manufacturing the same are provided. The liquid sensor includes a plurality of electrochemical cells in series connection. Each of the plurality of electrochemical cells includes an anode, a cathode and a liquid-porous layer including an electrolyte solution. The liquid-porous layer electrically connects the anode to the cathode such that each cell has a respective predetermined potential difference across the cell. Two or more of the plurality of electrochemical cells are operable to be electrically connected by a liquid to form a single electrochemical cell having a potential difference lower than the sum of the predetermined potential differences of the two or more electrochemical cells.

An organic light emitting display device includes a plurality of pixels. Each of the pixels includes an organic light emitting diode, first to third transistors, a storage capacitor, and a first capacitor. The second transistor includes a gate electrode receiving a first scan signal, a first electrode receiving a data signal, and a second electrode connected to a first electrode of the first transistor. The third transistor includes a gate electrode receiving a second scan signal, a first electrode connected to a second electrode of the first transistor, and a second electrode connected to a gate electrode of the first transistor. The storage capacitor includes a first electrode receiving a power voltage and a second electrode connected to the gate electrode of the first transistor. The first capacitor includes a first electrode connected to the gate electrode of the third transistor and a second electrode receiving the power voltage.