A multi-channel headspace extraction needle is provided. The extraction needle includes an inner needle tube, a sealed connector, and a needle rod and an outer needle tube respectively installed on a top portion and a bottom portion of the sealed connector. The sealed connector includes a first conduit and a second conduit connected with a tube lumen of the outer needle tube. A sealing layer is disposed between a bottom tube wall of the inner needle tube, which extends into the tube lumen of the outer needle tube, and a sidewall of the outer needle tube. The sidewall of the outer needle tube includes a first through-hole and a second through-hole respectively disposed above and under the sealing layer. The first through-hole is connected with the tube lumen of the outer needle tube and the second through-hole is connected with a tube lumen of the inner needle.

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.

Disclosed herein are a group of gastric cancer VOC markers in saliva and an application thereof in the preparation of a diagnostic reagent of gastric cancer. The markers are a combination of compounds selected from the group consisting of acetaldehyde, 2-methylbutyraldehyde, isopropanol, hexanal, n-butanol, cineole, nonanal, menthone, 2-ethylhexanol, menthol, anethole and dodecanol. The diagnostic reagent is used for detecting the contents of the marker in a saliva sample of a subject to perform the diagnosis of gastric cancer.

The present invention provides a method for measuring moisture content in a separator of secondary battery by using a gas chromatograph equipped with a headspace sampler. The separator of secondary battery may be a safety reinforced separator (SRS) in which inorganic substance particles and a binder polymer are coated on a polyolefin substrate.

Absorbent materials configured to sequester trimethylamine (TMA), absorbent articles made therefrom, related methods of use, methods of measuring a reduction of free TMA, and related methods of making absorbent articles are described.

Methods and systems for sensing headspace vial presence are described herein. In one embodiment, a system can include a sample probe, a fluid source in fluid communication with the sample probe, one or more of a pressure sensor and a flow sensor in fluid communication with the sample probe, and a processor configured to: (a) receive a first set of signals from the one or more of the pressure and flow sensors, execute an ejection procedure to remove a sample vial from the sample probe, receive a second set of signals from the one or more of the pressure sensor and the flow sensor during step (b), (d) detect whether the ejection procedure is successful from the first set of signals and the second set of signals, and (e) in response to the detecting, initiate one or more actions selected from the group consisting of: a remediation and an alert.

The invention relates to a method for monitoring a container treatment installation which has a filling apparatus for filling containers and a closure apparatus for closing containers. The method involves filling a container with a filling material using the filling apparatus and measuring a concentration of a gas in the filling material of the filled container using a measuring device, wherein the filled container is removed in order to measure the concentration upstream of the closure apparatus or the concentration is measured upstream of the closure apparatus. Advantageously, the method allows the low-oxygen filling by the filling apparatus to be able to be monitored in a selective manner.

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.

Beverage processing system for filling a beverage into containers with a filler with several filling valves for filling the beverage into the containers, where the filling valves are each configured having a filling device for filling at least two components of the beverage into one of the containers, a capper for closing the container filled with the beverage, and with a conveyor for transporting the containers at least from the filler to the capper, characterised in that the beverage processing system comprises at least one gas analysis device for quality control of the mixed beverage filled into the containers, and in that the at least one gas analysis device each comprises a gas suctioning device for suctioning gas from a head region of the containers filled with the beverage and an analyzer for analyzing the suctioned gas.

A CMV sampling device includes a thermoelectric cooler, a vacuum pump, and one or more holders for one or more capillary microextractor of volatiles (CMV) tubes. The holder thermally contacts the thermoelectric cooler and the vacuum pump is fluidly connected to the CMV tube. The CMV device is useful for sampling of volatile organic compounds from air. The sampling can be carried out rapidly to achieve a sample within the CMV tube that may be placed into a thermal desorption unit (TDU) coupled to an inlet port for introduction of the volatiles into an analytical instrument, such as, a gas chromatograph (GC), an ion mobility spectrometer (IMS), a liquid chromatograph (LC), and/or a mass spectrometer (MS) for analysis of one or more volatiles.