The sensor includes: a collection part 30L, 30M, 30S in which, a plurality of filter members for collecting particulate matter in exhaust gas are arranged in descending order of porosity from an exhaust upstream side to an exhaust downstream side of the exhaust gas; a pair of electrodes 32, 33 which is arranged to each of the plurality of filter members 30L, 30M, 30S and facing each other with the plurality of filter members interposed therebetween; and estimation means 42 to 44 far estimating a particulate matter amount collected on each of the plurality of filter members having different porosities based on a capacitance change amount between the pair of electrodes 32, 33.

A microfluidic diagnostic chip may comprise a main fluid channel comprising a main pump, a secondary fluid channel branching off from the main fluid channel, and a secondary pump within the secondary fluid channel wherein the secondary pump is to pull a particle of analyte of a first size from a fluid passing through the main channel, the fluid comprising particles of analyte of the first size and of a number of larger sizes. A method of analyzing an analyte on a microfluidic chip may comprise pumping, with a main microfluidic pump, a fluid comprising an analyte particle through a main microfluidic channel fluidly coupled to a fluid slot and sorting the analyte particle within the fluid through a secondary microfluidic channel by pulling the analyte particle into the secondary microfluidic channel with a secondary microfluidic pump.

Microfluidic structures and methods for manipulating fluids, fluid components, and reactions are provided. In one aspect, such structures and methods can allow production of droplets of a precise volume, which can be stored/maintained at precise regions of the device. In another aspect, microfluidic structures and methods described herein are designed for containing and positioning components in an arrangement such that the components can be manipulated and then tracked even after manipulation. For example, cells may be constrained in an arrangement in microfluidic structures described herein to facilitate tracking during their growth and/or after they multiply.

A system for characterizing at least one particle from a fluid sample is disclosed. The system includes a filter disposed upstream of an outlet, and a luminaire configured to illuminate the at least one particle at an oblique angle. An imaging device is configured to capture and process images of the illuminated at least one particle as it rests on the filter for characterizing the at least one particle. A system for characterizing at least one particle using bright field illumination is also disclosed. A method for characterizing particulates in a fluid sample using at least one of oblique angle and bright field illumination is also disclosed.

The present disclosure provides apparatuses, systems, and methods for performing particle analysis through flow cytometry at comparatively high event rates and for gathering high resolution images of particles.

The invention relates to a device for determining particle size distribution in a bulk material, such as milled or grinded grain for animal feed. The device comprises an inlet for receiving at least a portion of the bulk material, a sorting mechanism for sorting the received bulk material. Said sorting mechanism comprises at least a first sorting device for sorting said received bulk material into at least two sorted partitions wherein the sorting device are capable of sorting different particle sizes and said at least two sorted partitions have different particle sizes. The invention further comprises a motor or actuator for vibrating said sorting device, a weighing system with at least one sensor for weighing the at least two sorted partitions sorted by said sorting mechanism and a data output for generating output data indicative of a weight of the at least two sorted partitions, so as to allow calculation of the particle size distribution in the bulk material received in the inlet and thus provide information regarding the particle size composition of the milled or grinded grain.

The present disclosure provides apparatuses, systems, and methods for performing particle analysis through flow cytometry at comparatively high event rates and for gathering high resolution images of particles.

A separation system suitable for separating a dry or dried infill preferably including rubber and/or sand, into a plurality of fractions, the separation system includes a first screening means configured to receive a first set of separation screens said set of separation screens being configured to separate infill into a first plurality of fractions, wherein the separation system further includes a pre-analysis unit, a database and a processing unit configured to calculate correlation coefficients and/or deviation values between the first set of composition values and a plurality of second sets of composition values of the database; and a method for separating a dry or dried infill having a composition of materials, preferably including rubber and sand, into a plurality of fractions.

A method and system of determining a filter life are disclosed. In examples, a method comprises capturing aerosol particles on a filter and measuring absorbance spectra of the aerosol particles captured on the filter. The method further comprises identifying one or more aerosol particle types based on the measured absorbance spectra and determining a mass accumulation of each of the one or more aerosol particle types based on the measured absorbance spectra and the aerosol particle type. The method further comprises determining a median particle size of each of the one or more aerosol particle types based on the measured absorbance spectra and the aerosol particle type and determining a filter life based on the determined mass accumulation and the determined median particle size of each of the one or more aerosol particle types.

An apparatus and a method for isolating and/or preparing particles are provided.