A method and a device for measuring an oxygen content of a headspace gas in a beverage can. The beverage can is oriented upside down to allow the headspace gas to collect at the bottom. A hollow piercer on a piercing head forms a sampling opening in the bottom of the can through which the sampling tube penetrates. The liquid level in the beverage can is lowered to establish a direct connection of the gas-filled headspace and the sampling opening. Then the headspace gas is transported from the headspace to a sensor unit via the sampling tube and/or the hollow piercer or the piercing head. The oxygen content and/or an oxygen partial pressure and/or a headspace volume of the headspace gas are determined by the sensor unit. The sampling opening is closed off airtight by sealing elements arranged on the piercer or the piercing head.

A device determines an oxygen content of a headspace gas in a liquid-filled container. The device contains a piercer, a sampling tube, a piercing head on which the piercer and the sampling tube are disposed, a pump, a ring line, and a sensor unit disposed within the ring line and used to determine the oxygen content and/or an oxygen partial pressure of the headspace gas of the liquid-filled container. The ring line is configured such that the headspace gas of the liquid-filled container can be sampled via the piercer or the piercing head by use of the pump and can be returned into the headspace of the liquid-filled container via the sampling tube.

A method for extracting and detecting volatile organic compounds includes steps as follows. At least one effervescent tablet is provided, wherein the effervescent tablet is produced by mixing an acidic compound and an alkaline compound homogeneously. An extraction and detection apparatus is provided, wherein the extraction and detection apparatus includes an extraction chamber, an injection tube and a detection instrument. An extraction step is performed, wherein a liquid matrix is put into the extraction chamber, and the effervescent tablet is added into the liquid matrix to generate bubbles, the volatile organic compounds are extracted from the liquid matrix by the bubbles, and the bubbles enter into the headspace of the extraction chamber. A detection step is performed, wherein the volatile organic compounds extracted during the extraction step are transferred to the detection instrument via the injection tube so as to detect the volatile organic compounds.

An ion molecule reactor for generating analyte ions from analytes comprises: a) a reaction volume in which reagent ions can interact with the analytes in order to form analyte ions; b) at least one analyte inlet for introducing the analytes along an inlet path into the reaction volume whereby, preferably, the inlet path runs essentially along at least a first section of the predefined transit path in the reaction volume; c) at least one reagent ion source and/or at least one reagent ion inlet for providing reagent ions into the reaction volume; d) optionally, at least one ion guide comprising an electrode arrangement which is configured for producing an alternating electrical, magnetic and/or electromagnetic field, that allows for guiding the reagent ions and/or the analyte ions at least along a section of the predefined transit path, preferably along the whole transit path, through the reaction volume. There is also provided a sampler comprising one or more chambers, wherein each chamber is configured for receiving an individual sample and comprises an inlet and an outlet, such that a gaseous fluid flow can pass through each of the chambers.

A sample extraction device and a desorption device for use in gas chromatography (GC), gas chromatography-mass spectrometry (GCMS), liquid chromatography (LC), and/or liquid chromatography-mass spectrometry (LCMS) are disclosed. In some examples, the sample extraction device includes a lower chamber holding a sorbent. The sample extraction device can extract sample headspace gas from a sample vial by placing the sorbent inside the vial and creating a vacuum to increase recovery of low volatility compounds, for example. Once the sample has been collected, the sample extraction device can be inserted into a desorption device. The desorption device can control the flow of a carrier fluid (e.g., a liquid or a gas) through the sorbent containing the sample and into a pre-column and/or a primary column of a chemical analysis device for performing GC, GCMS, LC, LCMS, and/or some other chemical analysis process.

The floating-type contamination measurement apparatus according to embodiments of the present invention can provide a body part; a buoyancy providing part, which is received to the body part and provides buoyancy to the body part; and a measurement part, which is received to the body part and measures the level of contamination in a closed space.

A sample container, sampling system and operating methods permit representative sampling from a liquid phase or boiling liquid, a gaseous phase, a containment sump, containment atmosphere, or condensation chamber of a nuclear power plant following a severe accident. A sample container obtaining an environmental sample includes an outer chamber surrounded by an outer container wall, being directly fluidically connected to the environment through a passage opening in the outer container wall and being fillable with a liquid at least in a base region. An inner chamber surrounded by an inner container wall is fluidically connected to the base region through a passage opening in the inner container wall, has connections for sampling and conveyor medium lines and is otherwise pressure and media tightly sealed from the environment. A pneumatically or hydraulically actuatable closure device for the passage opening between the outer and inner chambers has an actuation medium line connection.

Embodiments herein include a method for detecting a health condition of a subject. The method can include obtaining a biological sample from the subject and placing it into a container having a headspace surrounding the biological sample. The method can include contacting a gas from the headspace with a chemical sensor element, the chemical sensor element including one or more discrete graphene varactors. The method can include sensing and storing capacitance of the discrete graphene varactors to obtain a sample data set. Other embodiments are also included herein.

An example of an apparatus and method for sampling food. The apparatus includes a sampling unit for collecting the food. The apparatus further includes a transfer unit connected to the sampling unit. In addition, the apparatus includes an extraction system and a valve disposed between the transfer chamber and the extraction chamber.

A cooling-assisted inside needle capillary adsorption trap device for sampling and delivering volatile and semi-volatile analytes to an analytical device is disclosed. The device includes an inside needle capillary adsorption trap having a first end and a second end and a side aperture located between the first and second ends. The side aperture enables entering the carrier gas into the INCAT and flowing upon the surface of the sorbent (when injected into the GC injector) for complete releasing and eluting of the analytes from the interior surface of the needle. A sorbent is multiwall carbon nanotube/polyaniline and is coated onto the interior surface of the needle between the second end and the side aperture to entrap an analyte within a sample. The cooling-assisted inside needle capillary adsorption trap device also includes a cooling device configured to cool the sorbent.