Abstract:
Provided is a chemical test apparatus for testing a chemical used to process a substrate, the chemical test apparatus including a first line providing an inlet through which the chemical is introduced, and a passage through which the chemical moves, a second line having an end and another end connected to two separate points of the first line, and providing a passage in which the chemical introduced into the first line is filled, a discharge line connected to a lower end of the first line, and a valve disposed between the first line and the discharge line at least below portions of the first line connected to the second line, to open or close a passage through which the chemical moves from the first line to the discharge line.
Abstract:
An optical sensing system for sensing hydrogen in a fluid comprising a first optical sensor comprising a first optical fiber, wherein an end portion of the first optical fiber is coated with a first hydrogen-sensitive multilayer on an end surface perpendicular to a longitudinal axis of the first optical fiber, the first multilayer being adapted to change its optical properties dependent on a hydrogen partial pressure in the fluid and dependent on a temperature of the fluid, with a known first characteristic; a second optical sensor comprising a second optical fiber, wherein an end portion of the second optical fiber is coated with a second hydrogen-sensitive multilayer on an end surface perpendicular to the longitudinal axis of the second optical fiber, the second multilayer being adapted to change its optical properties dependent on the hydrogen partial pressure in the fluid and dependent on a temperature of the fluid, with a known second characteristic which is different from the first characteristic; at least one light source adapted for coupling light into the first optical fiber and the second optical fiber, at least one light detector adapted for detecting light reflected by the first and second multilayer, a control unit adapted for calculating the hydrogen partial pressure in the fluid by using the first characteristic and the second characteristic and an output signal of the at least one light detector.
Abstract:
A system for measuring the blood loss comprises a measuring device that determines a hemoglobin concentration of fluid within a container utilizing a light source and a light detector. The container receives blood and other fluids from a patient during a medical procedure. Light from the light source is passed through the blood and other fluids in the container and is detected by the light detector. Based upon a magnitude of light detected, a hemoglobin concentration of the fluid in the container can be determined. A volume-measuring device determines the volume of blood and fluid in the container. Knowing the hemoglobin concentration and volume of fluid in the container, the volume of patient blood loss in the container can be determined. The blood loss measuring device in combination with infusion systems maintains a real-blood volume status so that proper infusion of blood, crystalloid and/or colloid solutions occurs.
Abstract:
An optical sensor is arranged in an indentation of a dust line, the indentation being equipped with at least one gas inlet nozzle for removing the dust from the optical sensor. Dust is transported through the dust line. An optical property of the dust is measured using at least one optical sensor arranged in an indentation of the dust line, and the dust is then removed from the optical sensor by blowing in air using the at least one gas inlet nozzle arranged in the indentation.
Abstract:
A holding is presented. The holding device includes a male connector comprising a first male extension and a second male extension that extend out of opposite surfaces of a male central disk, an electromagnetic guiding device continuously passing through a central hole that continuously passes through the first male extension, the male central disk and the second male extension, a reflector that is in a direct physical contact with a first end of the electromagnetic guiding device that ends at a top surface of the first male extension, and a holder that covers the first male extension to hold the reflector, and maintain the physical contact between the first end of the electromagnetic guiding device and the reflector.
Abstract:
Activation of an enzyme in a bodily fluid is detected based on the amount of cleavage of a substrate for the enzyme. The substrate is tagged with two fluorescent dyes—a donor and an acceptor. The tagged substrate is presented to the bodily fluid. A device emits energy at a first wavelength into the bodily fluid, and detects energy at second and third wavelengths emitted by the dyes in response to the energy at the first wavelength. Prior to enzymatic cleavage of the substrate, the acceptor emits energy at the third wavelength in response to energy at the second wavelength received through fluorescent resonant energy transfer (FRET) from the donor. After enzymatic cleavage of the substrate, the donor emits energy at the second wavelength. The device can determine the concentration of activated enzyme within the bodily fluid based on the relative intensities of energy, at the second and third wavelengths.
Abstract:
An apparatus for estimating a property of a fluid downhole, is provided an includes: an optical fiber that receives light emitted from a light source and including an unclad portion adapted for contacting the fluid; a photodetector for receiving optical signals from the portion; and a spectrometer for obtaining an evanescent spectrum of the fluid from the portion. A method and a system are included.
Abstract:
This invention relates to semi-batch type copolymerization processes. More specifically, the processes of the present invention are directed to the production of compositionally uniform copolymers, including the production of such copolymers from dissimilar monomers, e.g., from monomers with significantly different reactivity ratios.
Abstract:
Activation of an enzyme in a bodily fluid is detected based on the amount of cleavage of a substrate for the enzyme. The substrate is tagged with two fluorescent dyes—a donor and an acceptor. The tagged substrate is presented to the bodily fluid. A device emits energy at a first wavelength into the bodily fluid, and detects energy at second and third wavelengths emitted by the dyes in response to the energy at the first wavelength. Prior to enzymatic cleavage of the substrate, the acceptor emits energy at the third wavelength in response to energy at the second wavelength received through fluorescent resonant energy transfer (FRET) from the donor. After enzymatic cleavage of the substrate, the donor emits energy at the second wavelength. The device can determine the concentration of activated enzyme within the bodily fluid based on the relative intensities of energy at the second and third wavelengths.
Abstract:
Real time biofilm monitoring systems are provided. Said systems comprise single or multiple fiber-optic probes detecting wavelength-specific fluorescence from biomarkers of fouling organisms; a compact optoelectronic interface and data acquisition system interfaced with said probes, wherein said probe or probes are bifurcated and contain at least one excitation and at least one emission filter permitting the simultaneous resolution of multiple biomarkers.