Patent classifications
G01N15/06
Dynamic Modification of Bioaerosol Detection with Genetic Identification
A bioaerosol detector is operated in accordance with one or more first inputs. Operating the bioaerosol detector includes filtering pathogens from the air, extracting genetic material from the filtered pathogens, and analyzing the extracted genetic material to identify the filtered pathogens. While operating the bioaerosol detector in accordance with the one or more first inputs, a change is identified in an operating condition for the bioaerosol detector. In response, the bioaerosol detector is operated in accordance with one or more second inputs. At least one input of the one or more second inputs is distinct from a respective input of the one or more first inputs.
METHOD FOR MEASURING CONCENTRATION OF MICRO/NANO PARTICLE
A method for measuring the concentration of a micro/nano particle, including: allowing the to-be-measured micro/nano particle to bind with one or more kinds of marker to form a new particle, the new particle having a change in at least one of particle size, charge state, and particle morphology compared with the to-be-measured micro/nano particle or the marker; measuring the particle size, charge state, or particle morphology of the new particle and the to-be-measured micro/nano particle or the marker, and counting the new particle and the to-be-measured micro/nano particle or the marker respectively to obtain their respective count results, and, on the basis of the count results, calculating the concentration of the to-be-measured micro/nano particle bound with the marker. The method of the present application has the advantages of high measurement accuracy, low measurement limit, and stability of chemical reagents.
METHOD FOR MEASURING CONCENTRATION OF MICRO/NANO PARTICLE
A method for measuring the concentration of a micro/nano particle, including: allowing the to-be-measured micro/nano particle to bind with one or more kinds of marker to form a new particle, the new particle having a change in at least one of particle size, charge state, and particle morphology compared with the to-be-measured micro/nano particle or the marker; measuring the particle size, charge state, or particle morphology of the new particle and the to-be-measured micro/nano particle or the marker, and counting the new particle and the to-be-measured micro/nano particle or the marker respectively to obtain their respective count results, and, on the basis of the count results, calculating the concentration of the to-be-measured micro/nano particle bound with the marker. The method of the present application has the advantages of high measurement accuracy, low measurement limit, and stability of chemical reagents.
Concentration measuring device
A concentration measuring device includes a circulation passage, an aspirator, a differential pressure sensor, and a control unit. The aspirator is disposed in a fuel tank and is connected to the circulation passage. While a gas flows from a gaseous layer within a fuel tank through the circulation passage due to a negative pressure generated in the aspirator, the differential pressure sensor measures a pressure difference of the gas within the circulation passage between an upstream side of a narrowed part, having a narrower passage area than an adjacent portion of the circulation passage, and a downstream side of the narrowed part. The control unit is configured to calculate a density of the fuel vapor from the pressure difference of the gas and to calculate a concentration of the fuel vapor from the density of the fuel vapor.
SOOT SENSOR SYSTEM
A soot sensing system includes a soot sensor having a first element, and circuitry to an amount of soot accumulated on the element and to control heating of the element in response to the soot accumulation. An electrostatic repelling voltage (ERV) may be applied to a sensor/heater element(s) during a contamination prevention mode (CPM) to repel ash and reduce contamination of the sensor. A pulsed heating voltage (PHV) may be applied to the elements during the CPM and a pulsed ERV may be applied to the elements during the “off” period of the PHV. All voltage to the elements may be turned off during the CPM and the elements may be floating/ground. A PHV may be applied to the elements during the CPM and no voltage may be applied to the elements during the “off” period of the PHV. A heating voltage may be applied to the elements during a CPM corresponding to a cold start.
INDOOR AIR QUALITY MONITOR
Apparatus and associated methods relate to monitoring air quality. At least one of temperature, humidity, and particulate concentrations is measured by an indoor air quality monitor, which may be disposed in a spot location. Air from that spot location is drawn into the housing of the indoor air quality monitor via a fan assembly. The air drawn into the housing is directed passed at least one of a temperature sensor, a humidity sensors, and a particulate detector. The air is then expelled back outside the housing through an outlet in a non-planar upper surface of the housing. A processor generates the indoor air quality summary based on the measured temperature, humidity, and particulate concentration.
Inflammatory marker measurement method, inflammatory marker measurement apparatus, inflammatory marker measurement program, and recording medium storing the program
An inflammatory marker is calculated using a nonlinear function including, as variables, a parameter associated with an erythrocyte aggregation and another parameter associated with an erythrocyte density. The parameter associated with the erythrocyte aggregation is calculated based on a syllectogram measured from a blood specimen. The parameter associated with the erythrocyte density is measured from the blood specimen.
Inflammatory marker measurement method, inflammatory marker measurement apparatus, inflammatory marker measurement program, and recording medium storing the program
An inflammatory marker is calculated using a nonlinear function including, as variables, a parameter associated with an erythrocyte aggregation and another parameter associated with an erythrocyte density. The parameter associated with the erythrocyte aggregation is calculated based on a syllectogram measured from a blood specimen. The parameter associated with the erythrocyte density is measured from the blood specimen.
APPARATUSES, SYSTEMS, AND METHODS FOR DETERMINING GAS EMSSION RATE DETECTION SENSITIVITY AND GAS FLOW SPEED USING REMOTE GAS CONCENTRATION MEASUREMENTS
Apparatuses systems and methods for gas emission rate detection sensitivity and probability of detection (PoD) based on emission rate. A measurement system may be characterized by its ability to detect gas plumes as a function of the emission rate of those plumes. The measurement system may be characterized based on a generalized PoD function which expresses PoD relative to emission rate as a function of gas concentration noise and gas flow speed. In an example application, the PoD may be used to estimate a cumulative distribution of gas plumes which were not detected based on a cumulative distribution of measured gas plumes. In another example application, the PoD may be used to refine an estimate for a measured emission rate.
Dynamic modification of bioaerosol detection with genetic identification
A bioaerosol detector is operated in accordance with one or more first inputs. Operating the bioaerosol detector includes filtering pathogens from the air, extracting genetic material from the filtered pathogens, and analyzing the extracted genetic material to identify the filtered pathogens. While operating the bioaerosol detector in accordance with the one or more first inputs, a change is identified in an operating condition for the bioaerosol detector. In response, the bioaerosol detector is operated in accordance with one or more second inputs. At least one input of the one or more second inputs is distinct from a respective input of the one or more first inputs.