Abstract:
A both ultraviolet-visible and double monochromatic fluorescence dual detector has a small inner-casing, which combines both ultraviolet-visible and double monochromatic fluorescence dual detector widely used in the high performance liquid chromatography by taking the first to use deuterium lamp as the individual light source of the dual detectors, the individual sample detection cell and the individual electrical circuit, the device comprises a detection optical member, which including a first monochromatic spectroscopic device—raster G1, a second monochromatic spectroscopic device—raster G2, a light source, four groups of lens needed for processing the light paths; and a detection electromechanical member, which includes: a central controller, a proposed amplifying module, an auto gain module, a noise processing module and a logarithm amplifying module. The dual detector realizes the sensitivity and stability, also the elimination of noise and drift.
Abstract:
A processing apparatus includes: a light emission unit configured to emit light to a surface of a particle dispersed liquid applied to a base material, the particle dispersed liquid having particles dispersed in a solvent; a reflected light amount monitoring unit configured to detect an amount of the light reflected, and monitor a temporal variation of the detected value; and a condition adjustment unit configured to adjust a condition for a particle securing process, the particle securing process being performed to remove the solvent and secure the particles onto the base material, wherein, when the temporal variation falls within a predetermined range after the value has reached an extreme value, securing of the particles is determined to have been completed.
Abstract:
Disclosed is a system for controlling focus, angle of incidence and intensity of an electromagnetic beam over a spectrum of wavelengths, and methodology for optimizing investigation of samples which demonstrate low specular reflectance and/or are depolarizing of a polarized beam of electromagnetic radiation, such as solar cells.
Abstract:
A system for measuring optical detector linearity according to the present invention employs a laser source that illuminates an integrating sphere. The sphere randomizes the laser signal phase and produces a uniform intensity over the sphere output. A collimator expands the sphere output for entry into an interferometer, where the incident optical energy is amplitude modulated in a sinusoidal fashion by a linear mechanical mirror movement. Optical band filters eliminate significant harmonic content being present on a pre-detected optical signal. Sampling of the detected signal energy is performed synchronous to the mechanical mirror position to assure sinusoidal response. The sampled signals are processed to separately determine signal harmonic components attributed to detector non-linearity and multiple laser reflections within the system. The system utilizes at least two measurements at two different laser intensities. An optional third measurement of background radiance may be applied to the first two measurements to enhance accuracy.
Abstract:
A device (1; 10; 20; 30; 40) for optically examining the interior of a turbid medium (5) is provided. The device comprises an illumination system (2; 12; 22; 32; 42) adapted for illuminating a turbid medium (5) to be examined and an imaging device (106) adapted for generating images from detected light. The illumination system (2; 12; 22; 32; 42) is adapted to be operable in at least a first mode in which a wide area image is acquired by illuminating the turbid medium (5) and a surrounding area. From this wide area image, the region or regions of interest (110) at which the turbid medium (5) is actually situated can be determined. Then, these regions of interest (110) can be illuminated in a second mode. Thus, no light which has not been coupled to the turbid medium (5) and which might cause overexposure of the detector unit of the imaging device (106) will reach the imaging device (106).
Abstract:
A device (1; 10; 20; 30; 40) for optically examining the interior of a turbid medium is provided. The device comprises an illumination system (2; 12; 22; 32; 42) adapted for illuminating a turbid medium to be examined and an imaging device (106) adapted for generating images from detected light. The illumination system (2; 12; 22; 32; 42) is adapted to be operable in at least a first mode in which a large area is illuminated and a second mode in which at least one selected region (110) of the large area is illuminated.
Abstract:
Die vorliegende Erfindung betrifft ein Verfahren zur Überwachung der Befüllung einer Kapsel mit einem Medikament, ein entsprechendes Befüllungsverfahren die zugehörigen Vorrichtungen, sowie ein Computerprogramm zur Steuerung des Verfahrens und der Vorrichtung. Bei dem Überwachungsverfahren wird, nachdem wenigstens ein Teil der Kapsel mit einer vorgegebenen Füllmasse von vorgegebener geschlossener Kontur aus dem Medikament befüllt wurde, in einem ersten Schritt wenigstens die im Teil der Kapsel nach der Befüllung befindliche Füllmasse digitalbildgebend aufgezeichnet, in einem zweiten Schritt aus der digitalbildgebenden Aufzeichnung die Kontur der im Teil der Kapsel befindlichen Füllmasse ermittelt und in einem dritten Schritt die Kontur analysiert wird, um eine Bewertung der Befüllung im Vergleich zur vorgegebenen Kontur vorzunehmen. Es ist erfindungsgemäß vorgesehen mittels Regelung des optischen Systems äußere Einflüsse auf die Bildeigenschaften auszugleichen.
Abstract:
An apparatus for enhancing the selectivity for spectroscopic measurements of analytes in a turbid medium is described. In one example, spatial filters are used to select only certain radii from the medium to be imaged. This selection is accomplished by placing an optical obstruction on the surface of the medium or at an image plane of the surface later in the optical imaging system. In one implementation, this is achieved by placing a fiber bundle at an image plane of the collecting optical system and then using a spacer of appropriate size at the center of the fiber bundle to act as a central obstruction.
Abstract:
A sample analyzer with an optical detection device and a sample analysis method of the sample analyzer are disclosed. The optical detection device includes a fluid chamber, a light source and a light detector. The fluid chamber includes an illumination zone. An analyte flows through the illumination zone so as to form a sample stream. The light source illuminates the illumination zone to excite cell articles, reacted with a reagent, of the sample stream to emit a light signal. The light detector detects the fluorescent lights and transforms it into an electric signal. The light detector can include a silicon photomultiplier.
Abstract:
A sample analyzer with an optical detection device and a sample analysis method of the sample analyzer are disclosed. The optical detection device includes a fluid chamber, a light source and a light detector. The fluid chamber includes an illumination zone. An analyte flows through the illumination zone so as to form a sample stream. The light source illuminates the illumination zone to excite cell articles, reacted with a reagent, of the sample stream to emit a light signal. The light detector detects the fluorescent lights and transforms it into an electric signal. The light detector can include a silicon photomultiplier.