A compact, portable, low-cost electrostatic bioaerosol sampler device is provided for collection of aerosolized biological and non-biological particles. The device may be used for long-term, large-scale deployment. With a low-pressure design, the device can sample a high flowrate of 10 lit/min with a low-power fan. The device collects dust particles with a nominal size range of 1-10 μm, with an efficiency of >60%. The device may include aerosol sensing components, a particle ionizer, and an electrostatic precipitator. A removable cassette includes a ground plate for collection of ionized particles and a high voltage plate opposite the ground plate. A divider may be included beneath the ionizer to facilitate separation of collected particles by size on the ground plate.

A device for scattered light measurement of particles in a gas, comprising a light source, a beam splitter which splits a light beam emitted by the light source into a measuring beam and a reference beam, a light receiving device arranged at a distance from the beam splitter, which comprises at least one lens arranged in the reference beam with an optical axis aligned at an acute angle to the measuring beam, a first light receiver on the side of the lens facing away from the beam splitter, for receiving the scattered light imaged by the latter from a measurement volume in a gas-bearing region between the beam splitter and the lens, and a second light receiver on the side of the lens facing away from the beam splitter for receiving the reference beam imaged by the latter.

A device for scattered light measurement of particles in a gas, comprising a light source, a beam splitter which splits a light beam emitted by the light source into a measuring beam and a reference beam, a light receiving device arranged at a distance from the beam splitter, which comprises at least one lens arranged in the reference beam with an optical axis aligned at an acute angle to the measuring beam, a first light receiver on the side of the lens facing away from the beam splitter, for receiving the scattered light imaged by the latter from a measurement volume in a gas-bearing region between the beam splitter and the lens, and a second light receiver on the side of the lens facing away from the beam splitter for receiving the reference beam imaged by the latter.

The present disclosure provides methods and compositions for preparing linearity control slides to verify linearity of image-based hematology analyzers without the need to make such control slides over and over again for each analyzer each time the analyzer is verified.

The present disclosure provides methods and compositions for preparing linearity control slides to verify linearity of image-based hematology analyzers without the need to make such control slides over and over again for each analyzer each time the analyzer is verified.

The present disclosure discloses a degassing-free underwater dissolved carbon dioxide detection device and a detection method. The degassing-free underwater dissolved carbon dioxide detection device includes a computer, which is used to provide the driving signal and controlling parameters for the power tuning unit; the computer is connected with a laser driving control module and the power tuning unit, respectively; the laser driving control module is connected with a laser; the laser is connected with a photo-isolator; the photo-isolator is connected with a thulium-doped fiber vertical-cavity laser system; the thulium-doped fiber vertical-cavity laser system is connected with a photoacoustic cell system through a fiber collimator; the photoacoustic cell system is connected with a pre-amplifier circuit and a lock-in amplifier in sequence, and the lock-in amplifier is connected with the computer.

The present disclosure discloses a degassing-free underwater dissolved carbon dioxide detection device and a detection method. The degassing-free underwater dissolved carbon dioxide detection device includes a computer, which is used to provide the driving signal and controlling parameters for the power tuning unit; the computer is connected with a laser driving control module and the power tuning unit, respectively; the laser driving control module is connected with a laser; the laser is connected with a photo-isolator; the photo-isolator is connected with a thulium-doped fiber vertical-cavity laser system; the thulium-doped fiber vertical-cavity laser system is connected with a photoacoustic cell system through a fiber collimator; the photoacoustic cell system is connected with a pre-amplifier circuit and a lock-in amplifier in sequence, and the lock-in amplifier is connected with the computer.

An emissions measurement system capable of providing an accurate, real-time measurement of an emissions sample is disclosed. The exhaust may be generated by an internal combustion engine, in which case the system may be sequentially connected to the exhaust from the internal combustion engine. The emissions measurement system can include a laser light opacity sensor, a light scattering sensor, and a particle ionization sensor.

Apparatus and method for separating whole cells from a mixture, e.g., including liquid, other cell types, nucleic acid material, or other components. Focused acoustic energy may be used to move whole cells in a chamber so that the cells exit the chamber via a first outlet rather than a second outlet. A filter may, or need not, be used to assist in separation.

A method for measuring concentrations of blood cell components is provided. The method comprises: obtaining a blood sample from a subject, the blood sample comprising at least one of red blood cells (RBCs), white blood cells (WBCs), and platelets (PLTs); mixing the blood sample with a non-lysing aqueous solution to form a sample mixture comprising a predetermined tonicity; passing the sample mixture through a flow cell; emitting light towards the flow cell; measuring at least one of an amount of light absorbed by the RBCs to obtain an RBC absorption value, an amount of light scattered by WBCs to obtain a WBC scatter value, and an amount of light scattered by PLTs to obtain a PLT scatter value; and determining a concentration of at least one of the RBCs, WBCs, and PLTs present in the sample mixture.