A flow cell assembly (16) for a fluid analyzer (14) that analyzes a sample (12) includes (i) a base (350) that includes a base window (350B); (ii) a cap (352) having a cap window (352B) that is spaced apart from the base window (350B); and (iii) a gasket (360) that is secured to and positioned between the base (350) and the cap (352), the gasket (360) having a gasket body (360A) that includes a gasket opening (360B). The gasket body (360A), the base (350) and the cap (352) cooperate to define a flow cell chamber (362). Moreover, an inlet passageway (366) extends into the flow cell chamber (362) to direct the sample (12) into the flow cell chamber (362); and an outlet passageway (368) extends into the flow cell chamber (362) to allow the sample (12) to exit the flow cell chamber (362).

A flow cell assembly (16) for a fluid analyzer (14) that analyzes a sample (12) includes (i) a base (350) that includes a base window (350B); (ii) a cap (352) having a cap window (352B) that is spaced apart from the base window (350B); and (iii) a gasket (360) that is secured to and positioned between the base (350) and the cap (352), the gasket (360) having a gasket body (360A) that includes a gasket opening (360B). The gasket body (360A), the base (350) and the cap (352) cooperate to define a flow cell chamber (362). Moreover, an inlet passageway (366) extends into the flow cell chamber (362) to direct the sample (12) into the flow cell chamber (362); and an outlet passageway (368) extends into the flow cell chamber (362) to allow the sample (12) to exit the flow cell chamber (362).

Apparatus and method for detecting a dissolved gaseous impurity in an aqueous environment, comprises a tube for isolating liquid surface, or a sampler for obtaining a liquid sample from the aqueous environment, a vacuum pump located to exert a vacuum, leaving the surface to evaporate into the vacuum; and a holding compartment for holding evaporated gas which may then be analyzed using electrochemical or spectroscopic methods. The apparatus is useful for detecting levels of ammonia in fish ponds or indeed any impurity that may be dissolved in the water.

A device for monitoring a bioreactor is configured for in-situ analysis, e.g., by NIR, without the need for withdrawing a sample into a sample cell or into an ex-situ arrangement. The device can be inserted into a port of the bioreactor and provides a sample detection region defined by an optical element such as a lens and a photodetector. The electrical signal obtained from a photodetector that is part of the device can be directed to an analyzer via a detachable electrical connection.

Systems and methods are described, and one method includes providing an optical fiber extending into a chamber with a volume of the gas; passing an optical beam, from an optical source, through the optical fiber; applying a spectral analysis to the optical beam as received after passing through the optical fiber, and outputting a corresponding spectral analysis signal; and determining, based on the output spectral analysis signal, whether a liquid is carried by the volume of the gas.

Various approaches preparing Cannabis flower samples for analysis of cannabinoid content, the method comprising the steps of weighing the sample in a portable or benchtop balance; adding, to a container, the weighed sample and a solvent; agitating the vial and thereafter extracting a liquid component therefrom; and analytically analyzing the sample using the solvent based on the weight and a volume of the extracted liquid.

Various approaches preparing Cannabis flower samples for analysis of cannabinoid content, the method comprising the steps of weighing the sample in a portable or benchtop balance; adding, to a container, the weighed sample and a solvent; agitating the vial and thereafter extracting a liquid component therefrom; and analytically analyzing the sample using the solvent based on the weight and a volume of the extracted liquid.

Various embodiments may relate a chemical sensor. The chemical sensor may include a substrate including a first sealed (or isolated) cavity and a second sealed (or isolated) cavity separate from the first sealed (or isolated) cavity. The chemical sensor may also include an emitter in the first sealed (or isolated) cavity, the emitter configured to emit infrared light. The chemical sensor may further include a detector in the second sealed (or isolated) cavity. The chemical sensor may also include a waveguide configured to carry the infrared light from the emitter to the detector. The waveguide may include a sensing portion configured such that a property of the infrared light carried through the sensing portion changes in response to a chemical entity in contact with the sensing portion. The detector may be configured to detect the change in the property (of the infrared light).

A fast, batch and non-invasive identification and screening method of cows with A2 β-casein genotype of producing A2 milk belongs to the cow genotyping field and includes steps of: 1) collecting milk samples of cows; 2) detecting and acquiring mid-infrared spectral data; 3) data preprocessing to remove outliers; 4) dividing the dataset after the preprocessing into a training set and a testing set according to random sampling principle; 5) screening modeling spectral wavebands; and 6) combining different spectrum preprocessing methods with a modeling algorithm to establish classification models, using accuracy, sensitivity, specificity and AUC to evaluate the models, and determining the best classification model. The method can realize rapid and batch identification of cows of producing A2 milk and non A2 milk, and may have advantages of fast, high precision, low cost, simple operation, batch determination, no trauma (no blood collection, hair plucking, and tissue extraction), and strong practicability.

Asphaltene onset pressure of a formation fluid is determined by subjecting the fluid to a plurality of tests where depressurization is conducted at a different depressurization rate for each test while optically monitoring the fluid for asphaltene flocculation. The pressures at which asphaltene flocculation are detected in each test are fit to a curve as a function of depressurization rate, and the curve is extrapolated to a pressure (e.g., 0 psi) to provide the asphaltene onset pressure.