A spiral tube countercurrent chromatography rotor for separating virus in a two part aqueous solvent is described.

Respective peaks detected on chromatograms created based on data obtained by conducting GC-MS analysis on a target sample are identified based on information stored in a compound database (S1, S2). A retention time list indicating relationships between compounds and measured peak retention times is created based on results of identification of the peak. Then a plurality of compounds in which the measured retention times are identical to each other or are within an allowable range are extracted and are combined into one group (S3, S4). A determination is made whether overlapping identifications exist by determining whether a single group includes a plurality of compounds (S5, S6). Retention times, mass spectrums, and confirmation ion ratio reference values stored in the compound database are used for the respective groups in which overlapping identifications are likely to exist so that a most likely compound candidate is selected (S7).

A centrifuge apparatus includes a plurality of modules, each including a rotatable body, housing and flying leads, assembly. The modules can be selectively interconnected to allow adaptation of the processing capacity of the apparatus to process a liquid to remove components therefrom and/or to process a number of different liquids and allow the separation of one or more types of components therefrom simultaneously.

The present invention discloses a high-speed counter-current chromatograph unreeled by a gear ring, including an upper disc, a middle disc and a lower disc, wherein an unreeling gear ring coaxial with the middle disc is fixed above the middle disc, the lower disc is driven by a driving shaft to rotate, the unreeling gear ring is fixed, gear teeth of the unreeling gear ring are distributed on the inner ring thereof, multiple groups of gears engaged with the unreeling gear ring are arranged along the circumferential direction of the inner ring of the unreeling gear ring, gears between the adjacent groups are not engaged with each other, each group of gears includes two gears that are engaged with each other, wherein one gear drives a separation column, the other gear drives an unreeling shaft, the separation column is installed on a separation shaft, the upper ends of the unreeling shaft and the separation shaft are connected with the upper disc, and the lower ends are connected with the middle disc; meanwhile, the unreeling shaft and the separation column rotate with the rotating bracket; and after a liquid inlet tube passes through center shafts of the upper disc and the middle disc, infusion tubes of multiple groups of separation columns and unreeling shafts are sequentially connected in series therewith and finally led out from a liquid outlet tube.

The present invention discloses a high-speed counter-current chromatograph unreeled by a gear ring, including an upper disc, a middle disc and a lower disc, wherein an unreeling gear ring coaxial with the middle disc is fixed above the middle disc, the lower disc is driven by a driving shaft to rotate, the unreeling gear ring is fixed, gear teeth of the unreeling gear ring are distributed on the inner ring thereof, multiple groups of gears engaged with the unreeling gear ring are arranged along the circumferential direction of the inner ring of the unreeling gear ring, gears between the adjacent groups are not engaged with each other, each group of gears includes two gears that are engaged with each other, wherein one gear drives a separation column, the other gear drives an unreeling shaft, the separation column is installed on a separation shaft, the upper ends of the unreeling shaft and the separation shaft are connected with the upper disc, and the lower ends are connected with the middle disc; meanwhile, the unreeling shaft and the separation column rotate with the rotating bracket; and after a liquid inlet tube passes through center shafts of the upper disc and the middle disc, infusion tubes of multiple groups of separation columns and unreeling shafts are sequentially connected in series therewith and finally led out from a liquid outlet tube.

The present invention relates to a valve unit (100) for a chromatography apparatus, the valve unit comprising a fluid inlet (110) configured to receive an input fluid, a fluid outlet (120) configured to provide an output fluid, a first pair of fluid ports (131,132) configured to be coupled to a first column, a second pair (141,142) of fluid ports configured to be coupled to a second column, a coupling valve assembly (200) configured to direct fluid between a selection of the fluid inlet (110), the fluid outlet (120), the first pair of fluid ports (131,132) and the second pair of fluid ports (141,142) in response to one or more control signals, wherein the coupling valve assembly is configured to direct fluid using a selection of membrane valves coupled by fluid channels comprised in a body of the coupling valve assembly. The invention further relates to a chromatography apparatus comprising the valve unit and a membrane valve comprised in the valve unit.

A dispersed mobile-phase countercurrent chromatography system is described in which solutes are carried by a stream of dispersed mobile phase solvent through a column, or array of serially-connected columns, of stationary phase solvent with which the mobile phase solvent is immiscible. Solutes carried along by the stream of dispersed mobile-phase solvent will be equilibrated between the mobile-phase solvent and the stationary-phase solvent. Because the mobile-phase is dispersed into mini-droplets much smaller in diameter than the column of stationary phase, the enhanced surface/volume ratio of the droplets expedites countercurrent equilibration of different solutes between the mobile-phase solvent and the stationary-phase solvent in accordance with the distribution-coefficients of the solutes between the two solvents. As a result, a solute with a distribution coefficient that favors its dissolving in the stationary phase will be retarded in its migration through the columns compared to a solute with a distribution coefficient that favors its dissolving in the mobile phase. The different migration rates of different solutes bring about their chromatographic separation on the columns, effectively combining the advantages of countercurrent distribution (e.g., elimination of any solid chromatographic matrix, and therefore losses of solutes due to adsorption to the solid matrix and contamination of separated solutes by impurities leached from the solid matrix) and liquid column chromatography (e.g., continuous mode of operation, and scalable from analytical to large industrial separations without any centrifugal or discontinuous mechanical steps).

A dispersed mobile-phase countercurrent chromatography system is described in which solutes are carried by a stream of dispersed mobile phase solvent through a column, or array of serially-connected columns, of stationary phase solvent with which the mobile phase solvent is immiscible. Solutes carried along by the stream of dispersed mobile-phase solvent will be equilibrated between the mobile-phase solvent and the stationary-phase solvent. Because the mobile-phase is dispersed into mini-droplets much smaller in diameter than the column of stationary phase, the enhanced surface/volume ratio of the droplets expedites countercurrent equilibration of different solutes between the mobile-phase solvent and the stationary-phase solvent in accordance with the distribution-coefficients of the solutes between the two solvents. As a result, a solute with a distribution coefficient that favors its dissolving in the stationary phase will be retarded in its migration through the columns compared to a solute with a distribution coefficient that favors its dissolving in the mobile phase. The different migration rates of different solutes bring about their chromatographic separation on the columns, effectively combining the advantages of countercurrent distribution (e.g., elimination of any solid chromatographic matrix, and therefore losses of solutes due to adsorption to the solid matrix and contamination of separated solutes by impurities leached from the solid matrix) and liquid column chromatography (e.g., continuous mode of operation, and scalable from analytical to large industrial separations without any centrifugal or discontinuous mechanical steps).

A flying leads assembly includes a flying lead having an inner layer which forms a liquid passage and an outer layer which acts as a sacrificial layer in use, thereby allowing integrity of the passage to be maintained for a long period of time. A further layer is provided intermediate the inner and outer layers which can be used to provide support to the assembly. The flying lead assembly, or a number of assemblies, are then located in a guide with lubricant material.

A flying leads assembly includes a flying lead having an inner layer which forms a liquid passage and an outer layer which acts as a sacrificial layer in use, thereby allowing integrity of the passage to be maintained for a long period of time. A further layer is provided intermediate the inner and outer layers which can be used to provide support to the assembly. The flying lead assembly, or a number of assemblies, are then located in a guide with lubricant material.