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.

Disclosed herein is an apparatus including a structure containing a multiphase fluid and having a transparent window. A collimated light source emits light through the transparent window structure at 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 structure and out through the transparent window structure to impinge upon the photodetector. The photodetector has an actual dynamic range for light detection. Processing circuitry adjusts a power of the collimated light source in a series of steps dependent upon a relationship between an output level of the photodetector and a threshold to cause measurement of the emitted light over an effective dynamic range greater than the actual dynamic range. Properties of the multiphase fluid are determined as a function of the measured emitted light.

Technology is provided for an aqueous solution constituent analyzer. The analyzer includes an ultraviolet light emitting diode (LED) with a current source providing variable current thereto. A spectrometer is positioned for receiving light from the LED transmitted through an aqueous solution. A controller receives radiant flux data for a plurality of wavelengths and determines, based on the radiant flux data, a usable number of the plurality of wavelengths that satisfies a relative uncertainty threshold. The controller can increase the current to the LED if the usable number of wavelengths is less than a minimum threshold and calculate a concentration of a constituent of interest in the solution. The controller can also determine a peak wavelength of the plurality of wavelengths having the greatest intensity value, and decrease the current level to the LED if the peak wavelength has an intensity value greater than a saturation value for the spectrometer.

An optical analysis system and an optical analyzer thereof. The optical analyzer comprises a solid state light source emitter, a uniform mixing or light splitting assembly, a first optical receiver, and a second optical receiver. The solid state light source emitter comprises a light source comprising multiple light-emitting assemblies respectively radiating light having at least one light-emitting peak wavelength and at least one wavelength range; the light emitted by the multiple light-emitting assemblies passes through the uniformly mixing or light splitting assembly to form first light and second light which passes through a fluidic object to be detected to form detection light (i.e., after the second light passes through the fluidic object to be detected, the part of the second light not absorbed by the fluidic object to be detected forms detection light. The first optical receiver receives the first light. The second optical receiver receives the detection light.

A light emitting apparatus has light emitting units. The light emitting units can be respectively provided with current densities, so that the light emitted by each of the light emitting unit has a light intensity, wherein the current densities are different from each other, or partial of the current densities are different from each other. A number of the light emitting units can be larger than or equal to four, all of the four lighting frequencies of the four light emitting units are different from each other, or partial of the four lighting frequencies of the four light emitting units are identical to each other, and the light emitting apparatus and the object under test rotate relative to each other. A light emitting method, a spectrum detection method and a lighting correction method are also illustrated for increasing SNR, correcting the light intensity or the spectrum signal.

Method in which, in order to actuate a wavelength-tunable laser diode in a spectrometer, a power-time function is predetermined instead of a current-time function, wherein the laser diode is tuned periodically over a wavelength range in accordance with the power-time function. For this purpose, a current profile (i) with which the laser diode is actuated is determined from the power-time function and measured values of the voltage (u) present at the laser diode.

Apparatuses and methods for monitoring curing of photocurable material are disclosed. The methods generally include directing an ultraviolet cure light into a photocurable material, wherein the ultraviolet cure light causes the photocurable material to cure; directing a probe light into the photocurable material through an optical fiber during the cure; collecting a back reflection signal from the photocurable material with the optical fiber; and determining a refractive index change of the photocurable material during the cure.

A spectrum detection apparatus has a light emitting apparatus with multiple light emitting units. The light emitting units can be respectively provided with current densities, so that the light emitted by each of the light emitting unit has a light intensity, wherein the current densities are different from each other or identical to each other, or at least two of the current densities provided to the light emitting units are different from each other or identical to each other, and the light emitting apparatus and the object under test rotate relative to each other. A number of the light emitting units can be larger than or equal to four, all of the four lighting frequencies of the four light emitting units are different from each other, or partial of the four lighting frequencies of the four light emitting units are identical to each other.

A method for optical inspection of a feature of interest on a workpiece using an optical measuring system comprising at least one camera and a plurality of light sources, the method comprising: simulating illumination of a workpiece model; training, based on synthetic images obtained from the simulated illumination, an AI agent or an ML model to automatically control the plurality of light sources; inferring, in at least one image captured by the at least one camera, properties of the feature of interest on the workpiece; the trained AI agent controlling the plurality of light sources to select a light setting for illuminating the feature of interest; and optically inspecting the illuminated feature of interest while it is illuminated with the selected light setting.

An optical sensor assembly of a centrifuge of a biological fluid separation system includes a light source configured to emit light having an intensity toward a separation chamber received within the centrifuge, with at least a portion of the light exiting the separation chamber as transmitted light. A light detector receives at least a portion of the transmitted light as received light and transmits a signal based on the received light. A controller receives the signal from the light detector, then determines the location of an interface between two of the separated components within the separation chamber based at least in part of the signal. The controller is programmed to determine whether to control the light source to dynamically adjust the intensity of the light during a biological fluid separation procedure and/or to control the light detector to dynamically adjust an amplification of the signal during the procedure.