Provided is a supercritical fluid device equipped with a back pressure regulator for creating a pressurized state in which a mobile phase in a separation/extraction unit of an analysis flow passage is kept in a supercritical fluid state. One end of a pipe is connected to an outlet side of the back pressure regulator, and the other end of the pipe is open to the atmosphere. A heating unit is provided on the pipe, and the heating unit includes a plurality of electrically independent heaters arranged on mutually different portions of the pile along the pipe. A power supply controller is connected to the heaters, and the power supply controller is configured to supply heating power to one or more heaters selected among the plurality of heaters, but to not supply heating power to the other heaters.

A system for performing gas chromatography analyses in accordance with the present disclosure includes an analytical column and a column oven. The analytical column has an inlet portion coupled to an injector for receiving a material sample and an outlet portion coupled to a detector. The analytical column is adapted to direct the material sample from the injector to the detector. The column oven is adapted to heat the analytical column for separating constituent components of the material sample for detection by the detector.

A column protection gas supply channel (4) is connected to a channel (17) for carrier gas present between a sample vaporization chamber (12) and an MS section (2). During a standby, a column (11) may be protected on the downstream side of a merging section (16) of the column protection gas supply channel (4) and the channel (17) for carrier gas by supplying column protection gas through the column protection gas supply channel (4). At this time, there is remaining carrier gas in the channel (17) for carrier gas on the upstream side of the merging section (16). Accordingly, when carrier gas is then supplied at a time of start of an analysis, a certain amount of carrier gas is already present inside the channel (17). Therefore, the time required to completely replace the column protection gas in the channel (17) by the carrier gas is reduced, and the standby time until the start of the analysis may be reduced.

A method of performing a chromatographic separation includes generating a spatial temperature gradient along a length of a chromatographic column in a liquid chromatography system. A sample is injected into a flow of a mobile phase to the column and a flow of a mobile phase having a composition gradient is provided to the column after the sample is received at the column. The spatial temperature gradient is moved along the length of the column from the column inlet to the column outlet during the time that the composition gradient traverses the column. This coordination of the composition gradient with the movement of the spatial thermal gradient yields a significant increase in peak capacity per unit time compared with conventional separation techniques performed in a conventional isothermal column environment.

A sample analysis method includes directing a sample that contains one or more SVOC components to a GC column to temporally separate components present in the sample. Output gas from the GC column is expanded into a sample cell. The sample cell is held at a temperature and pressure that are lower than the temperature and pressure at an outlet of the GC column. The volume of the sample cell is sufficiently large for maintaining the one or more SVOC components in a gaseous phase. Infrared spectra of the components in the sample cell are obtained using a Fourier transform infrared spectrometry system.

A chromatography system includes a separation column that separates a sample carried by a compressible mobile phase flow into analytes and a splitter in fluidic communication with the separation column to receive and divide the compressible mobile phase flow into first and second mobile phase streams in accordance with a split ratio. A thermally modulated variable restrictor is coupled between the splitter and a detector. The restrictor receives the first mobile phase stream from the splitter and has a temperature element in thermal communication with the first mobile phase stream to exchange heat therewith. A controller, in communication with the restrictor, dynamically adjusts a temperature setting of the temperature element of the restrictor to adjust the heat exchange between the thermally modulated variable restrictor and the first mobile phase stream in order to keep the split ratio constant throughout a chromatographic run.

The present disclosure relates to the regulation of carbon dioxide expansion in a carbon dioxide based chromatographic system. In particular, the present disclosure relates to minimizing or eliminating the deleterious effects of carbon dioxide expansion on one or more of the solvent, the analyte(s) of interest, the separation, the detection of the analyte(s) of interest, and other related aspects in a carbon dioxide based chromatographic system.

A system for performing gas chromatography analyzes in accordance with the present disclosure includes an analytical column and a column oven. The analytical column has an inlet portion coupled to an injector for receiving a material sample and an outlet portion coupled to a detector. The analytical column is adapted to direct the material sample from the injector to the detector. The column oven is adapted to heat the analytical column for separating constituent components of the material sample for detection by the detector.

Provided is a supercritical fluid device equipped with a back pressure regulator for creating a pressurized state in which a mobile phase in a separation/extraction unit of an analysis flow passage is kept in a supercritical fluid state. One end of a pipe is connected to an outlet side of the back pressure regulator, and the other end of the pipe is open to the atmosphere. A heating unit is provided on the pipe, and the heating unit includes a plurality of electrically independent heaters arranged on mutually different portions of the pile along the pipe. A power supply controller is connected to the heaters, and the power supply controller is configured to supply heating power to one or more heaters selected among the plurality of heaters, but to not supply heating power to the other heaters.

The invention relates to a method for analysing hydrocarbons, with the implementation of a gas chromatography separation according to a first controlled temperature profile, to separate a sample into a plurality of analytes and the detection of at least one of said analytes by measurement of a variation of the resonance frequency of at least one resonator of nano-electromechanical system (NEMS) type covered with a functional layer made to vibrate at the resonance frequency thereof, under the effect of an adsorption or desorption of the analyte by the functional layer, the resonator being subjected to a second controlled temperature profile, lower than the first profile.