Abstract:
A measuring device (10) and a measuring method measure a concentration of gaseous and/or aerosol components of a gas mixture. A reaction carrier (14) has a flow channel (42) defining a reaction chamber (46) with an optically detectable reaction material (48) to react with at least one component or with a reaction product of the component. The measuring device (12) includes a gas delivery unit (2) and detection unit (3) having a lighting device (37) for lighting the reaction chamber (46). An optical sensor (38) detects the reaction. An evaluation unit (4) evaluates data of the optical sensor (38) to determines a concentration. The gas delivery unit (2) includes a gas delivering device (28) delivering the gas mixture through the gas outlet channel (18) and a control/regulation unit (31) which controls/regulates a flow of the gas mixture through the flow channel (42) depending on at least one reaction speed parameter.
Abstract:
An apparatus includes a pipe through which a multiphase fluid flows, with a transparent window structure formed in the pipe. A collimated light source emits light through the transparent window structure into the pipe having a wavelength at which a component of a desired phase of the multiphase fluid is absorptive. A photodetector is positioned such that the emitted light passes through the multiphase fluid in the pipe to impinge upon the photodetector. The photodetector has an actual dynamic range for collimated light detection. Processing circuitry is configured to continuously adjust a power of the collimated light source dependent upon an output level of the photodetector so as to cause measurement of the emitted light over an effective dynamic range greater than the actual dynamic range, and determine a property of the multiphase fluid as a function of the power of the collimated light source.
Abstract:
In one embodiment, a surface analyzer system comprises a radiation targeting assembly to target a radiation beam onto a surface; and a scattered radiation collecting assembly that collects radiation scattered from the surface. The radiation targeting assembly generates primary and secondary beams. Data collected from the reflections of the primary and secondary beams may be used in a dynamic range extension routine, alone or in combination with a power attenuation routine.
Abstract:
An inspection device for inspecting defects of an inspection object including a light source for irradiating a luminous flux to the inspection object; an optical system for guiding reflected light from the inspection object; a photoelectric image sensor having a plurality of photoelectric cells arranged, for converting the light guided to detection signals; a detection signal transfer unit having channels each constituted by a signal correction unit, a converter and an image formation unit, and corresponding to each of a plurality of regions formed by dividing the photoelectric image sensor, respectively; and an image synthesis unit for forming an image of the surface of the object by synthesizing partial images outputted; the inspection device inspecting defects of the object by processing the synthesized image; whereby it becomes possible to correct a detection signal from said photoelectric cell close to a predetermined reference target value.
Abstract:
Biopolymeric array scanners that are capable of automatically selecting a dye specific scale factor to employ for a plurality of different dyes, as wells as methods for making and using the same, are provided. In many embodiments, the actual dye specific scale factor automatically selected by the scanner is one that is equal to a preset “master” scale factor, so that the scanner reads any supported dye using the same constant scale factor. The dye specific scale factor selection is typically made by reference to a collection of nominal scale factors for each member of the plurality of dyes. In using the subject scanners, a user simply inputs the one or more dyes being used in a given array assay, and the scanner automatically reads the array using an automatically chosen dye specific scale factor for the selected dyes. Also provided are methods of obtaining collections of nominal scale factors and computer readable mediums comprising the same. The subject invention finds use in a variety of different applications, including both genomics and proteomics applications.
Abstract:
The present invention provides instruments for analyzing a multiplicity of fluorescent dyes using a multiplicity of amplifying photodetectors, methods for using the instruments, methods for setting the instrument parameters, and methods for resetting the instrument parameters following a changed in photodetector amplification. The present invention is particularly applicable in the field of flow cytometry.
Abstract:
Errors in applying liquid sample are judged during biochemical analysis wherein a droplet of liquid sample is applied to an analysis medium containing a reagent, which chemically reacts with a specific constitutent in the liquid sample, the analysis medium is then incubated, the optical densities of the analysis medium are determined, and concentration of the specific constituent in the liquid sample is determined from the optical densities of the analysis medium thus determined. The method for judging errors in applying a liquid sample comprises the steps of determining the optical density of the analysis medium plural times with the passage of time while the analysis medium is being incubated, and calculating the difference between the maximum value and the minimum value of the optical densities thus determined for the analysis medium. The difference is compared with a predetermined threshold value. In cases the difference is smaller than the threshold value, it is judged that errors occurred in applying a liquid sample to the analysis medium.
Abstract:
A fluorescence and phosphorescence detection device includes a fluorescence and phosphorescence sensor, a data acquiring unit, and an emission detection unit. The fluorescence and phosphorescence sensor includes a light source that emits an excitation light of a predetermined wavelength, and a photodetection unit that detects fluorescence emission and phosphorescence emission excited from the paper sheet by the excitation light. The data acquiring unit acquires a time-series waveform of a signal outputted from the fluorescence and phosphorescence sensor in response to the detection of the emission in the photodetection unit. The emission detection unit detects the fluorescence emission from the time-series waveform of a period in which the excitation light is emitted from the light source and detects the phosphorescence emission from an attenuation curve appearing on the time-series waveform of a period in which emission of the excitation light from the light source is stopped.
Abstract:
Disclosed herein are specimen analysis apparatus and method of analyzing specimen using the same. The specimen analysis apparatus includes a cartridge configured to accommodate at least three pH indicators having different properties and an analyzer configured to determine whether a specimen is acidic or basic using one of the pH indicators. The analyzer determines a pH measurement value using another pH indicator selected based on whether the specimen is acidic or basic.
Abstract:
A fluorescence and phosphorescence detection device includes a fluorescence and phosphorescence sensor, a data acquiring unit, and an emission detection unit. The fluorescence and phosphorescence sensor includes a light source that emits an excitation light of a predetermined wavelength, and a photodetection unit that detects fluorescence emission and phosphorescence emission excited from the paper sheet by the excitation light. The data acquiring unit acquires a time-series waveform of a signal outputted from the fluorescence and phosphorescence sensor in response to the detection of the emission in the photodetection unit. The emission detection unit detects the fluorescence emission from the time-series waveform of a period in which the excitation light is emitted from the light source and detects the phosphorescence emission from an attenuation curve appearing on the time-series waveform of a period in which emission of the excitation light from the light source is stopped.