A gas phase component analysis device and a gas phase component analysis method that can prevent degradation of the device due to an unnecessary component and can obtain excellent detection sensitivity are provided. A gas phase component analysis device (1) includes a heating unit (2) configured to heat a specimen to generate a gas phase component composite, a first column (31) into which the gas phase component composite is introduced, a second column (32) that is a separation column connected with the first column (31) through a connection unit (33), an isothermal oven (3) housing the first column (31), the second column (32), and the connection unit (33), a detection unit (4) configured to detect a gas phase component having passed through the second column (32), and a suction unit (5) connected with the connection unit (33).

We disclose a microfabricated device for both extracting and preconcentrating samples for gas chromatography analysis. The device includes a conduit with at least two sections and multiple ports which may be connected to multiple gas chromatography columns. The inner surface of the conduit may be coated with multiple sorbents which bind volatile analytes with different affinities. The sections of the conduit may be divided by a thermal barrier which inhibits heat transfer between sections. Consequently, each section may be independently heated to encourage desorption of volatile analytes. The disclosed device separates and concentrates volatile analytes into different pools according to their chemical and physical properties before they enter a gas chromatography column that is optimized for that pool. The device reduces the amount of heat and time needed to perform gas chromatography analysis as well as avoids the need for purified gas sources typically used for the moving phase.

A method of monitoring catalytic performance of a catalyst used in a reforming process, comprising a) collecting gaseous component data from the reforming process; b) calculating a gaseous component ratio from the gaseous component data; and c) utilizing the gaseous component ratio to estimate an amount of catalytic activity remaining in the catalyst used in the reforming process, a number of days on stream remaining for the catalyst used in the reforming process, or both.

A hand-held microfluidic testing device is provided that includes a housing having a cartridge receiving port, a cartridge for input to the cartridge receiving port having a sample input and a channel, where the channel includes a mixture of Raman-scattering nanoparticles and a calibration solution, where the calibration solution includes chemical compounds capable of interacting with a sample under test input to the cartridge and the Raman-scattering nanoparticles, and an optical detection system in the housing, where the optical detection system is capable of providing an illuminated electric field, where the illuminating electric field is capable of being used for Raman spectroscopy with the Raman-scattering nanoparticles and the calibration solution to analyze the sample under test input to the cartridge.

A hand-held microfluidic testing device is provided that includes a housing having a cartridge receiving port, a cartridge for input to the cartridge receiving port having a sample input and a channel, where the channel includes a mixture of Raman-scattering nanoparticles and a calibration solution, where the calibration solution includes chemical compounds capable of interacting with a sample under test input to the cartridge and the Raman-scattering nanoparticles, and an optical detection system in the housing, where the optical detection system is capable of providing an illuminated electric field, where the illuminating electric field is capable of being used for Raman spectroscopy with the Raman-scattering nanoparticles and the calibration solution to analyze the sample under test input to the cartridge.

Systems, methods and computer program products for cannabis analysis, such as a system that has a cannabis analysis data server and a plurality of mobile cannabis analysis devices that are communicatively coupled to a network. The mobile devices perform physical analyses of a physical sample and communicate resulting data to the cannabis analysis data server with a unique identifier. The mobile cannabis analysis devices may also monitor device and external environmental conditions that affect the performance and communicate these to the cannabis analysis data server. The cannabis analysis data server performs analyses on the received data from the mobile devices. Based on the sample analyses, the cannabis analysis data server generates sample analysis reports and communicates them to a user. The cannabis analysis data server may also generate data to control the operation of the mobile cannabis analysis devices based on the operation and environmental data received from the devices.

Apparatuses and associated methods are described for the efficient evaluation of C1-containing substrates, and especially for such evaluation conducted locally, or on-site, at a prospective facility for implementation of a biological conversion process for desired end product using a C1 carbon source. The exact composition of a given, industrial C1-containing substrate, as well as the range in composition fluctuations, are generally difficult to reproduce at a remote facility (e.g., a laboratory or a pilot-scale or demonstration-scale process), as required for the accurate prediction/modeling of commercial performance to justify large capital expenditures for commercial scale-up.

A modular gas detection system includes a primary gas chromatograph, a constant volume extractor positionable to provide a continuous fluid sample to the primary gas chromatograph, and a total hydrocarbon analyzer. The modular gas detection system also includes a processing device and a memory device including instructions executable by the processing device for causing the processing device to perform operations. The operations include adjusting a detection scheme of the primary gas chromatograph to update a detection range for the continuous fluid sample to detect different hydrocarbons within a single column. Further, the operations include controlling routing of the continuous fluid sample from the constant volume extractor to the primary gas chromatograph and the total hydrocarbon analyzer.

A hybrid trap including a replaceable open-tubular capillary trap followed by a packed trap is used to collect, preconcentrate, and recover a sample, such as VOCs and SVOCs found in air. The capillary stage prevents losses and carryover of the heavy fraction and can also collect the particles in air that contain the heavier SVOCs, also preventing them from reaching the packed stage. The packed stage traps lighter organic compounds that are not as prone to carryover due to channeling. The ionic species within the collected VOCs and SVOCs at the capillary trap can be converted to volatile compounds that allow gas chromatography-mass spectrometry.

A portable gas analysis apparatus for conducting a gas flow, in particular for highly volatile compounds, includes a seeker measurement path and a separation measurement path. The seeker measurement path extends from a sample gas inlet opening to a first air exit opening, wherein a connecting path branches off from the seeker measurement path to a separation measurement path, and said separation measurement path extends from the connecting path to a second air exit opening and is connected to a carrier gas inlet opening, wherein the gas analysis apparatus has a control element which is designed for reversing the gas flow in the connecting path.