A gas-phase chemical analyzer has at least one gas chromatography column in gas-flow communication with at least one gas carrying tube of an optical absorption cell, a laser for illuminating molecules in a gas mixture flowing though the at least one gas carrying tube of the optical absorption cell, and a photodetector or photodetecting apparatus for measuring absorption spectra of the gas mixture illuminated by the laser. A first module is provided for statically identifying particular molecules in the gas mixture from other molecules in said gas mixture and a second module is provided for comparing at least selected ones of the particular molecules in the gas mixture with a reference library of absorption spectra of previously identified molecules and for determining the likelihood of a correct identification of the particular molecules in the gas mixture and the previously identified molecules in the reference library.

A flow cell analyzes a fluid sample. A flow cell body contains a reference material and includes at least one hollow chamber to contain the fluid sample. Opposing surfaces of the flow cell body each have at least one transparent portion thereof. An optical path for light traversing through the flow cell body is defined in part by the transparent portions. A switching mechanism adjusts the amount of the reference material in the optical path to effect switching of the flow cell between a reference measurement state and a fluid sample measurement state. The reference measurement state corresponds to a first light intensity measurement and the fluid sample measurement state corresponds to a second light intensity measurement.

An arrangement for measuring gas concentrations in a gas absorption method, wherein the arrangement includes a plurality of light sources, a measuring cell, at least one measuring receiver and an evaluation apparatus. The measuring cell has a narrow, longitudinally-extended beam path with an entrance-side opening diameter B and an absorption length L with L>B, wherein the measuring cell has a gas inlet and a gas outlet wherein a plurality of light sources of different wavelength spectra is grouped into a first light source group wherein an optical homogeniser is interposed between the first light source group and the measuring cell, wherein, in particular, the homogeniser is coupled to the light source group directly or via a common optical assembly.

The invention relates to sealable short-pathlength liquid transmission cells for Fourier-transform infrared spectroscopy applications. In exemplary embodiments, a liquid transmission cell with transmissions sections uses horizontal tubing for inserting and removing fluids from the cell. Angling the tubing relative to a top face of the cell allows small amounts of entrapped air to rise out of the optical path without blocking spectroscopy measurements. The tubing is silver-soldered to the body of the transmission cell to make a leak-free connection.

The invention discloses a crystal purity detecting apparatus, including a machine body, wherein the detecting body is provided with a detecting chamber, and a detecting device is arranged in the detecting chamber, and a symmetric power chamber is arranged in the inner wall of the left and right sides of the detecting chamber. The detecting chamber is provided with a lifting device, the power chamber is provided with a transmission device, and the power chamber is provided with a power device; the invention has the advantages of simple structure, convenient operation and convenient maintenance, and the device can perform various positions on the crystal the detection, the accuracy of the device judgment is high, and the labor intensity of the professional is lowered, so the device has high use and promotion value.

A flow cell analyzes a fluid sample. A flow cell body contains a reference material and includes at least one hollow chamber to contain the fluid sample. Opposing surfaces of the flow cell body each have at least one transparent portion thereof. An optical path for light traversing through the flow cell body is defined in part by the transparent portions. A switching mechanism adjusts the amount of the reference material in the optical path to effect switching of the flow cell between a reference measurement state and a fluid sample measurement state. The reference measurement state corresponds to a first light intensity measurement and the fluid sample measurement state corresponds to a second light intensity measurement.

A laminated fluorescent sensor includes a sealable sensor housing and an optical sensing system embedded inside the sensor housing. The optical sensing system includes a light source (7), a short wave pass filter (8), an air chamber (10), a sensing unit, a long wave pass filter set (12) and an optical signal collecting unit from top to bottom all of which are coaxially set. The optical signal collecting unit is connected with a signal processing system (14); the sensor housing has air inlets (2, 201) and an air pumping port (3), the air inlets (2, 201) are communicated with the air chamber (10) through an air intake passage, the air chamber (10) is communicated with the air pumping port (3) through an air pumping passage. The laminated fluorescent sensor is compact and easy to be arrayed for simultaneously detecting two or more detected objects, has a high signal-to-noise ratio, is applicable in quick detection of micro-trace chemicals including but not limited to explosives and narcotics, provides great detection effects, has distinctly distinguishable signal responses to objects not being detected and to objects being detected, and provides stable and accurate detection.

The present disclosure is directed to a method and apparatus for performing an assay on a dry slide or other solid media using a reduced reading window. In an embodiment, method of performing at least one assay comprises obtaining an image of a fluid sample located on a dry slide, positioning a reading window to correspond to an area of the fluid sample in the image, determining an interference area within the reading window based on light intensity, reducing the reading window to eliminate the interference area from the reading window, and performing at least one assay using the reduced reading window.

An optical analysis device for determining at least one characteristic of a medium in a process environment or a laboratory environment is provided. The optical analysis device includes an optical measuring arrangement with a plurality of components arranged in an interior space of a housing. The housing has at least one entry/exit area for the entry and/or exit of optical radiation, and a mechanical interface for a positionally accurate detachable attachment of the optical analysis device to a location of operation, in particular in a process environment. Advantageously, the mechanical interface spatially overlaps with the optical radiation entry/exit area. This enables fast assembly and disassembly of the optical analysis device in different locations of use.

An object inspection apparatus according to an embodiment disclosed herein includes: a first flipper apparatus configured to rotate a first object; a second flipper apparatus configured to rotate a second object; and a single camera device configured to move from a position corresponding to one of the first flipper apparatus and the second flipper apparatus to a position corresponding to the other, the camera device being configured to inspect object surfaces of the first object and the second object. Each of the first flipper apparatus and the second flipper apparatus includes at least one flipper unit.