A water quality measurement apparatus is provided. The apparatus comprises an electrochemical cell, a pH sensor, a temperature sensor, a control circuit, a power source, a database, and a warning device. The electrochemical cell comprises a working electrode, a reference electrode, and a counter electrode. The control circuit provides predetermined adjustable potentials between the reference electrode and the working electrode and measures electrochemical currents between the working electrode and the counter electrode, to form a current diagram based on the predetermined adjustable potentials and the electrochemical currents. The database stores predetermined reference diagrams based on various pH values and temperatures, and is in communication with the control circuit. The warning device is configured to output warnings, wherein the control circuit triggers the warning device in the condition that the current diagram exceeds the predetermined reference diagram based on the same range of the pH values and the temperatures.

Provided is a method for detecting a test substance. In this method, metal is deposited or a complex containing a test substance and a metal particle is immobilized on a working electrode on an electrode substrate including the working electrode and a counter electrode. An oxidation potential is applied to the working electrode to generate metal ions, then a reduction potential is applied to a portion having an area smaller than an area of the portion to which an oxidation potential is applied in the working electrode to deposit metal on the surface of the portion to which the reduction potential is applied, and current, voltage or charge caused by the metal deposited is measured to detect metal ions or a test substance.

Provided is a method for detecting a test substance. In this method, metal is deposited or a complex containing a test substance and a metal particle is immobilized on a working electrode on an electrode substrate including the working electrode and a counter electrode. An oxidation potential is applied to the working electrode to generate metal ions, then a reduction potential is applied to a portion having an area smaller than an area of the portion to which an oxidation potential is applied in the working electrode to deposit metal on the surface of the portion to which the reduction potential is applied, and current, voltage or charge caused by the metal deposited is measured to detect metal ions or a test substance.

A method of measuring hematocrit is provided. The method for measuring hematocrit includes the following steps. A test strip is provided. The test strip includes a reaction region and a pair of electrodes disposed in the reaction region. A whole blood sample is entered to the reaction region. After the whole blood sample enters the reaction region, a plurality of sets of square wave voltages are intermittently applied to the pair of electrodes based on a square wave voltammetry method to obtain a plurality of feedbacks related to hematocrit. An interval between two adjacent sets of square wave voltages ranges from 0.1 seconds to 4 seconds. A feedback of an n-th set of square wave voltages is obtained to calculate a hematocrit value of the whole blood sample and n is a positive integer greater than 1. A hematocrit value is calculated according to the feedback.

A method of measuring hematocrit is provided. The method for measuring hematocrit includes the following steps. A test strip is provided. The test strip includes a reaction region and a pair of electrodes disposed in the reaction region. A whole blood sample is entered to the reaction region. After the whole blood sample enters the reaction region, a plurality of sets of square wave voltages are intermittently applied to the pair of electrodes based on a square wave voltammetry method to obtain a plurality of feedbacks related to hematocrit. An interval between two adjacent sets of square wave voltages ranges from 0.1 seconds to 4 seconds. A feedback of an n-th set of square wave voltages is obtained to calculate a hematocrit value of the whole blood sample and n is a positive integer greater than 1. A hematocrit value is calculated according to the feedback.

A device, liquid handling cartridge and related method for detecting the presence or absence of a chemical or biological target within a sample. The method includes the steps of: providing an electrochemical cell with a first electrode module and a second electrode; providing an electronic component between the first electrode module and the second electrode; introducing the sample into the electrochemical cell; measuring the potential difference between the first electrode module and second electrode; and confirming the presence of the chemical or biological target if the measured potential difference exceeds a predetermined threshold value.

A sensing platform for continuous water resource monitoring by electrochemical detection and solution parameter correction is provided. The sensing platform employs a solid-state electrolyte three-electrode cell, creating a high ionic strength environment within the solid-state electrolyte membrane, which is in ion exchange equilibria with the sampled solution. This device may be used as a standalone sensor in environments where the water parameters (pH temperature, and ionic strength) are controlled, or in concert with compensation sensors where water parameters are not controlled.

A sensor apparatus for detecting a heavy metal in a sample.

A sensor apparatus for detecting a heavy metal in a sample.

A method and a system for detecting heavy metal ions are provided. The method includes: fixing a pre-manufactured micro-electrode chip on a connecting device, connecting the connecting device to an electrochemical workstation, carrying out setting before detection on the electrochemical workstation, the micro-electrode chip including a counter electrode and a working electrode, carrying out graphene modification treatment on the counter electrode in advance, and carrying out bismuth film modification treatment on the working electrode in advance; and carrying out acid pretreatment on an aqueous solution to be detected, dropwise adding 5 .Math.L to 100 .Math.L of a treated aqueous solution to a working area of the pre-manufactured micro-electrode chip, measuring an I-V curve by the electrochemical workstation subjected to the setting before detection, and determining species and concentrations of heavy metal ions in the aqueous solution according to peak values of voltage and current of the I-V curve.