A thermal desorption tube for chromatography and mass spectrometry analysis. The thermal desorption tube includes a sorbent and a plurality of focusing agents loaded at known, relative amounts onto the sorbent. Each focusing agent is a compound that chromatographically elutes within a retention time similar to a retention time of a target analyte and has a mass spectrum similar to a mass spectrum of the target analyte. The thermal desorption tube is configured to be further loaded with a sample having the target analyte.

The invention relates to a system and micro monitor apparatus, a space-, time-, and cost-efficient device to concentrate, identify, and quantify organic compounds in gas environments. The invention further relates to a method centered on gas chromatography for identifying and quantifying organic compounds in gas environments, using air as the carrier gas, without the need for a compressed pre-bottled purified carrier gas.

The present disclosure relates to an article inspection system and method, an electronic device, and a storage medium, and relates to the field of security inspection technology. The system includes: a pre-concentration sampling module configured to concentrate and sample gas molecule of the article under inspection to obtain a sample; a gas chromatography module; an internal circulation gas path module; and an ion migration tube module connected to the internal circulation gas path module and configured to form a fingerprint spectrum of the article under inspection from a spectrum of the pre-separated sample molecules, so as to identify a kind of the article under inspection according to the fingerprint spectrum. The present disclosure improves the efficiency and accuracy of article inspection, and realizes intelligent inspection of articles.

The disclosed embodiments relate to the design of a preconcentrator system for preconcentrating air samples. This preconcentrator system includes a plurality of preconcentrators that preconcentrate the air samples prior to chemical analysis, and a delivery structure comprising a manifold that selectively routes a sample airflow to the plurality of concentrators so that the plurality of preconcentrators receive a sample airflow concurrently or individually.

The disclosed embodiments relate to the design of a preconcentrator system for preconcentrating air samples. This preconcentrator system includes a plurality of preconcentrators that preconcentrate the air samples prior to chemical analysis, and a delivery structure comprising a manifold that selectively routes a sample airflow to the plurality of concentrators so that the plurality of preconcentrators receive a sample airflow concurrently or individually.

Systems for measuring a product quality attribute of an analyte of a biological sample include a first flow control device, a sample purification device, a second flow control device in fluid communication with first and second sample analyzers, where the first sample analyzer includes a first chromatography column, and a control unit configured so that during operation of the system, the control unit adjusts a configuration of the second flow control device to direct a portion of the biological sample to one of the first and second sample analyzers, and determines a product quality attribute of an analyte of the biological sample based on an analysis of the portion of the biological sample by the one of the first and second sample analyzers.

A gas analysis device and a gas analysis method capable of performing measurement in a direct mode and a trap mode without carrying out a complicated control. The gas analysis device includes a branching section that branches a target gas, a mass spectrometer that carries out mass spectrometry of one branched target gases, a trap section that holds the other branched target gases, a gas chromatograph that analyzes the other branched target gas held by the trap section, and a controller that controls the flow path of the one branched target gas and the other branched target gas. The branching section is controlled so that, while the thermal analysis is being carried out by the thermal analysis device, the branching section continuously branches the supplied target gas and discharges one branched target gas and the other branched target gas, and when the thermal analysis has been completed, the other branched target gas held by the trap section is supplied to the gas chromatograph.

The present disclosure is directed to systems and methods for automated column sparging of preconcentration columns for analytic testing. A system embodiment includes, but is not limited to, a selection valve fluidically coupled with a gas source and with an eluent source, the selection valve including a mixing portion to mix gas from the gas source and eluent from the eluent source to provide a bubbled eluent stream; and a preconcentration column in fluid communication with the selection valve, the preconcentration column configured to receive the bubbled eluent stream from the selection valve and direct the bubbled eluent stream into an interior of the preconcentration column.

A gas chromatography guard column assembly is disclosed including a guard column having an inlet and an outlet. The guard column is disposed in a coil having a column coil aspect ratio of less than 15. A gas chromatography system is disclosed including an oven cavity, a heater assembly, an inlet, a guard column, an analytical column, and a detector. The guard column is in fluid communication with the inlet and is disposed in a guard column coil. The analytical column is in fluid communication with the guard column and is disposed in an analytical column coil. The detector is in fluid communication with the analytical column. The analytical column coil has an analytical column coil central axis aligned with a central axis of the heater assembly, and the guard column coil has a guard column coil central axis remote from the central axis of the heater assembly.

The present invention discloses a method of determining the presence of autoimmune disease with the use of glycan biomarkers. A method of improving the detection sensitivity of trace glycans from a mixture of glycans and a microfluidic chip therefor are also disclosed.