An apparatus for measuring the absorbance of a substance in a solution includes at least one sample cell arranged to contain the solution that is at least partially transparent to light of a predefined wavelength spectrum, at least two light passages through the at least one sample cell, each of the light passages having a known path length, an LED light source arrangement including at least two LEDs, each arranged to emit a light output with a wavelength within the predefined wavelength spectrum. A plurality of optical fibers, one for each light passage, is arranged at each LED for receiving the light output and guiding it to the light passages. A method for measuring the absorbance of a substance in a solution includes providing the LED light source arrangement with an associate fiber bundle for each LED.

Spectrophotometric measurements on highly absorbing turbid samples face technical challenges that can be solved by reducing a path length of an optical chamber used during measurement. Reducing the path length requires exceptional control of variables that may be difficult to achieve in unit-use and inexpensive cuvettes. The invention provides a precise inexpensive method for producing an optical cavity useful in making spectrophotometric measurements on high attenuation liquid samples. Two components are shaped such that, when in contact, a central optical chamber and peripheral groove are formed. Liquid adhesive dispensed into the groove wicks around the interface perimeter, sealing the components together when cured. This results in a short precisely controlled path length that reduces chances of mechanical induced distortions (that arise with other bonding methods). The invention provides for manufacturing of a consistent optical chamber with very short path length within a diagnostic cartridge or cuvette.

A flow cell, for detecting a fluidic sample separated by a sample separation apparatus, includes a cuvette, a flow channel formed at least partially in the cuvette and configured to enable a flow of the separated fluidic sample through the flow channel, an electromagnetic radiation inlet at which an excitation electromagnetic radiation beam is couplable into the cuvette, and an electromagnetic radiation outlet at which an emission electromagnetic radiation beam, generated by an interaction between the excitation electromagnetic radiation beam and the separated fluidic sample, is couplable out of the cuvette. A geometry of the cuvette is configured so that at least one point at the excitation backside surface of the cuvette is outside of a direct field of view of the electromagnetic radiation outlet.

In an embodiment, an apparatus (100) is described. The apparatus comprises an infrared, IR, generating system (102). The IR generating system comprises a first IR source (104) configured to produce IR radiation for forming a first IR beam (106) in a first spectral band. The IR generating system further comprises a second IR source (108) configured to produce IR radiation for forming a second IR beam (110) in a second spectral band. The apparatus further comprises a beam manipulation system (112) configured to combine a beam path of the first and second IR beams and direct the first and second IR beams along the beam path through a gas sample region (114). The apparatus further comprises an IR detection system (116) configured to detect an intensity of the first and second IR beams after passage through the gas sample region. The IR detection system is configured to produce a signal (118) from which an indication of a concentration of a target gas in the gas sample region can be derived.

Sensor systems, and flow cells for use with them, which can provide for a universal sensor housing. The senor housing includes a first section which is designed to remain statically in position and a selectable sensor head that may be swapped out as necessary. The specific head is selected based on the types of measurement to be performed at the sensor location and the sensor head can integrate with the housing so only a single wire connection needs to be made to obtain all data from the housing.

A fire detection apparatus 1A includes a detector cover 70A for inhibiting ambient light from entering a detection space 60A, an inner cover 30A that accommodates the detection space 60A and the detector cover 70A, an outer cover 20A that accommodates the inner cover 30A, a first opening 30aA provided in a side portion on an opposite side from a side portion on an installation surface side among side portions of the inner cover 30A, a second opening provided in a side portion on an opposite side from a side portion on an installation surface among side portions of the detector cover 70A, and a flat plate-shaped insect screen 50A provided on the detector cover 70A and configured to substantially cover the entire second opening.

A detection assembly and a method for producing a detection assemblies are disclosed. In an embodiment a detection arrangement includes an emitter configured to generate radiation having a peak wavelength in an infrared spectral range, a detector configured to receive the radiation, a mounting surface comprising at least a first contact surface and a second contact surface for external electrical connection of the detection arrangement, a form body adjoining the emitter and the detector at least in places and deflection optics, on which the radiation impinges during operation of the detection arrangement so that an optical path is formed between the emitter and the detector by the deflection optics, wherein the deflection optics include a scattering body into which the radiation enters during the operation through a surface of the scattering body facing the emitter.

Disposable, pre-sterilized, and pre-calibrated, pre-validated sensor components are provided. The sensor components interact with a sensor system having disposable fluid conduit or bioreactor bag and a reusable sensor assembly. The components can include an optical bench or inset optical component or module designed to be integrated within the disposable fluid conduit or bioreactor bag, which provides an optical light path through the conduit or bag. The sensors systems are designed to store sensor-specific information, such as calibration and production information, in a non-volatile memory chip on the disposable fluid conduit or bag and on the reusable sensor assembly. Methods for calibrating the sensor and for determining a target property of an unknown fluid are also disclosed. The devices, systems and methods relating to the sensor are suitable for and can be outfitted for turbidity sensing.

A gas cell (1) for the spectroscopic, in particular absorption spectroscopic, analysis of a gas, in which the gas is exposed to an incident beam of rays (S) of electromagnetic radiation and a beam of rays (S.sub.A) of electromagnetic radiation exiting the gas is detected to form a measurement signal, wherein the gas cell (1) comprises a body (10) formed by a porous, electromagnetic radiation-scattering material, an in-coupling device (20) for coupling the incident beam of rays (S) into the gas cell (1) and an out-coupling device (30) for coupling the exiting beam of rays (S.sub.A) out of the gas cell (1), wherein, according to the invention, the gas cell is further developed according to the invention by forming a material-free cavity (12) in the body (10), which is surrounded by an inner surface (14) running within the material and is both diffusely reflecting and transmitting the electromagnetic radiation.

An apparatus for analysing a liquid sample comprising particles, comprises: a first chamber (12) and a second chamber (14), and an optical path between the first chamber (12) and the second chamber (14), wherein: the first chamber (12) is a sample chamber comprising: a sample space for receiving the sample; a light input (24) for input of light into the first chamber (12) for interaction with the sample; and an exit aperture (26) arranged for scattered and/or reflected light to pass from the first chamber via the optical path to the second chamber (14); the second chamber (14) is a detection chamber comprising: an input aperture (28) for receiving light from the optical path; and a detector (25) for detecting, or a detector aperture for receiving, light to be detected; wherein the first chamber (12) and the second chamber (14) provide at least one light integrating volume, and wherein the first chamber (12) is configured such that in operation the liquid sample is present in the first chamber (12) and isolated from the second chamber (14).