One variation of a method includes, during a calibration period: triggering collection of an initial bioaerosol sample by an air sampler located in an environment; and triggering dispensation of a tracer test load by a dispenser located in the environment; accessing a detected barcode level of a barcode detected in the initial bioaerosol sample; accessing a true barcode level of the barcode contained in the tracer test load; and deriving a calibration factor for the environment based on a difference between the detected barcode level and the true barcode level. The method further includes, during a live period succeeding the calibration period: triggering collection of a first bioaerosol sample by the air sampler; accessing a detected pathogen level of a pathogen detected in the first bioaerosol sample; and interpreting a predicted pathogen level of the pathogen in the environment based on the detected pathogen level and the calibration factor.

One variation of a method for detecting pathogens in an environment includes, during a first sampling period: triggering collection of a pathogen sample from ambient air in the environment by an air sampler; and tracking a first organic load of the first pathogen sample via a detection subsystem integrated within the air sampler, the first organic load representative of a first amount of organic matter present in the first pathogen sample. In response to the first organic load exceeding a threshold organic load defined for the environment, the method further includes: interpreting presence of a set of pathogens in the environment via genetic analysis of the first pathogen sample; and, in response to detecting presence of a first pathogen, in the set of pathogens, in the first pathogen sample, transmitting a notification indicating presence of the first pathogen in the environment to a user associated with the environment.

An air quality indicator for indicating high fine particle levels in an environment of interest. The indicator includes a frame maintaining first and second air filter media. The first air filter medium differs from the second air filter medium at least in terms of a change in visual appearance (e.g., color) when subjected to air flow containing fine particles.

The present invention provides a wide-area sample-based reader design which serves as a diagnostic detection device for bio-particles.

A method is provided for diagnosing the operation of a photometric particle analyzer. The method may determine when the operation is degraded from normal operating conditions, automatically, and the result displayed locally as well as being transmitted to a remote observer. The present invention may be used by optical photometric particle analyzers, or by analyzers that measure other properties of particles collected on filters.

A particle component analyzing device is provided. The particle component analyzing device comprises: a catching body which catches a particle in an aerosol which is subject to measurement, an energy beam irradiating unit which irradiates an energy beam to the particle which is caught by the catching body, and an analyzer which analyzes at least any of a component and an amount of the particle based on a desorbed component of the particle which is desorbed from the catching body by irradiation of the energy beam, wherein the catching body has a temperature measuring unit, the particle component analyzing device further comprising a controlling unit which controls an output of the energy beam irradiating unit based on a temperature of the catching body which is measured by the temperature measuring unit.

A fuel filter inspection method includes capturing an image of a fuel filter sample using an imaging device and sending the captured image to an image processor. The method further includes the image processor receiving the captured image, thresholding the captured image to generate a binary image, determining sizes for a plurality of particles present in the binary image, comparing the size of each of particle of the plurality of particles to a particle size threshold, and quantifying the number of particles of the plurality of plurality of particles with a size greater than the particle size threshold. The method further includes the image processor comparing the number of particles of the plurality of particles with a size greater than the particle size threshold to a particle count threshold, and modifying a graphical user interface to indicate a state of the fuel filter sample based on the comparison.

Systems and methods for monitoring air particulate matter are provided herein that capture particles from the air for analysis. Particles are captured using electrostatic and/or mechanical means to deflect particles toward a substrate. Electrostatic precipitation causes charged carriers to deflect towards a charged substrate. Filtration-based means employ filters and/or fibers to capture particles from air flowing therethrough. A sensor such as a camera is used to read the captured particles. An illumination source directs light towards the substrate, causing the particles to scatter light, which the sensor can detect and derive information or imaging therefrom, which can also be used for further particle or pollution analyses. The substrate can be replenished using electrostatic techniques such as reverse electrostatic force, or mechanical means such as cleaning using a brush or replacing a tape substrate. Dynamic PM monitoring detects and makes adjustments such as those related to air volume, imaging characteristics and substrate replenishment.

Sample monitoring and flow control systems and methods are disclosed for monitoring of airborne particulates. A system may include a particle collection filter. The system also includes a fluid moving device for moving a sample through the particle collection filter. Further, the system includes a light source configured to direct irradiating light towards the particle collection filter. The system also includes a light detector positioned to receive the irradiating light passing through the particle collection filter and configured to generate a signal representative of an amount of the received light. Further, the system includes a controller configured to receive the signal and to control the fluid moving device based on the amount of the received light.

A filter toxin and antigen detector assembly for detecting the presence or absence of toxins or antigens within air handling systems, ventilators, respirators, continuous positive airway pressure devices (CPAP), and bilevel positive airway pressure (BIPAP) devices is disclosed. The filter toxin and antigen detectors may be attached to an air filter, or placed (such as in the form of a test cartridge or test strip) onto a port or other portion of a respiration device to determine if the device is clean for further medical use. The filter toxin and antigen detectors disclosed herein utilize lateral flow immunochromatographic assay technology having a sample window allowing air flow therethough. The filter toxin and antigen detector will give an immediate presence indication, such as by changing color, thus providing a fast indication of whether or not harmful toxins or antigens are present within an airborne environment.