Disclosed is a passive wireless device for microfluidic detection of multi-level droplets. A primary inductor channel and a secondary inductor channel each comprise two layers of inductance coils, and the inductance coils of the primary inductor channel and the secondary inductor channel are alternately arranged in each layer. A double-resonance circuit is formed after a liquid conductive material is injected. A first part of a detection channel is disposed between a primary capacitor channel, and a second part of a detection channel is disposed between a secondary capacitor channel. A reading device is used to read a resonant frequency of the double-resonance circuit, and perform detection according to the resonant frequency to obtain information of a corresponding first droplet group and/or second droplet group.

A particulate matter sensor device comprising an enclosure (21) that comprises a flow inlet (11), a flow outlet (12) and a flow channel (2) extending therebetween, a radiation source for emitting radiation into the flow channel (2) for interaction of the radiation with the particulate matter in the flow (20) of an aerosol sample when guided through the flow channel (2), a radiation detector (4) for detecting at least part of said radiation after interaction with the particulate matter. The sensor device comprises a flow modifying device (511) arranged upstream of the radiation detector (4) and/or of the radiation source (3) for modifying the flow (20) for reducing particulate matter precipitation onto the radiation detector (4) and/or onto the radiation source (3) and/or the channel wall sections in close proximity to the detector (4) and/or source (3). The invention also relates to a method of determining parameters of particulate matter in an aerosol sample by using such a particulate matter sensor device.

An exemplary embodiment of an apparatus for detecting microbiological activity in an industrial process may include a plurality of satellite units, a processing unit, and a main analysis unit. Each satellite unit may be configured to sample a liquid from the industrial process at a plurality of respective locations, periodically analyse a sample, carry out an impedance analysis to count and measure the size of particles passing through an orifice, and generate sample results data corresponding to the number and size of particles in each sample. The processing unit may be configured to compare the sample results data to a predetermined criterion and to generate an alert signal if the particle data is outside of the predetermined criterion. The main analysis unit may be configured to carry out a combined impedance and electromagnetic emission analysis of a sample of liquid from the industrial process following generation of the alert signal.

Systems for detecting, capturing, and/or measuring nanoparticles. The system may include a first vacuum chamber, where nanoparticles are formed inside a first cavity of the first vacuum. The system may also include a second vacuum chamber in fluid communication with the first vacuum chamber, a particle collection component positioned within a second cavity of the second vacuum chamber, and a particle collection medium disposed over the particle collection component. Additionally, the system may include a particle counter in fluid communication with the second vacuum chamber, and a control system operably coupled to the component. The control system may be configured to aerosolize the nanoparticles by adjusting a temperature of the component to a first temperature that establishes the medium in the solid phase, and adjusting the temperature of the component to a second temperature to transition the medium from the solid phase to a gaseous phase.

The present disclosure relates to a method for microscopic examination of phytoplankton. The present disclosure solves the problem of decreased counting accuracy of perioptometry in a dry environment. The method is as follows: step 1, making an analyte into a glass slide, performing qualitative identification of the phytoplankton in the field of view; and step 2, drying the glass slide; after drying, counting the phytoplankton and full-slide rare algae on the glass slide microscopically. When the humidity of microscopy room is only 20%, the method of the present disclosure may count a sample accurately, which has a significant increase in counting accuracy compared with the existing perioptometry. The method of the present disclosure effectively solves the problem of failure to perform the perioptometry accurately due to dry ambient humidity.

A particle measuring device includes: a detection unit that detects scattered light generated due to interaction between a particle contained in a liquid sample and light incident thereon, and converts the detected scattered light into a signal; an addition unit that performs a predetermined number of parallel processing on the signal to add the predetermined number of uncorrelated noises thereto and outputs the resulting signals; a binarization unit that binarizes the resulting signals using a binarization threshold set in accordance with the liquid sample, and outputs the binarized signals; a calculation unit that calculates and outputs a value based on the binarized signals; a filter unit that passes a predetermined frequency component of the output of the calculation unit; and a determination unit that determines that the particle is present when an output of the filter unit exceeds a predetermined particle threshold.

A device including a microfluidic channel structure formed on a substrate and including a first channel and a fluid actuator within the microfluidic channel structure. A sense region within the first channel is to receive a fluid flow of target biologic particles for counting in a single file pattern, with the sense region having a volume on a same order of magnitude as a volume of a single one of the target biologic particles.

Described herein are cartridges and devices for operating said cartridges for analyzing a biological sample, such as a blood or saliva sample. Also described herein is an impedance sensor for analyzing a biological sample. Further described herein are methods of determining a cell count or detecting an analyte in a biological sample, which can include transporting the biological sample through a sensor comprising a channel or pore; applying an electrical current or voltage to the channel or pore; detecting an impedance within the channel or pore; and determining a cell count or detecting the analyte based on the detected impedance. Also described herein is an electrowetting electrode array that is configured to transport aqueous solutions using low voltage, such as about 50 volts or less. Further described herein are methods of transporting an aqueous liquid using electrowetting electrodes.

A device for analyzing biological cells is disclosed. The device includes a first platter for positioning a first group of biological cells; a first head positioned adjacently to the first platter for providing first electromagnetic radiation to at least a first subset of the first group of biological cells; and a first electrode positioned adjacently to the first platter for detecting the first electromagnetic having interacted with the first subset of the first group of biological cells for determining impedance values for the first subset of the first group of biological cells.

A solvent compound for a particle counter/imager system, the solvent compound includes a liquid solvent miscible with oil to remove oil from the particle counter/imager system and a liquid dispersive surfactant configured to break large water droplets into smaller droplets less than a predetermined size. The liquid dispersive surfactant is miscible with the solvent and is nontoxic and nonflammable.