摘要:
Close coupled momentum separator with integral removable source volume for particle beam liquid chromatography/mass spectrometry is provided. The inventive PB LC/MS system comprises a momentum separator wherein the skimmers are designed to accommodate the particle beam conical dispersion so as to minimize the number of particles lost in the separator. In addition, the exit of the momentum separator is closely coupled to the entrance of the MS source volume. The PB LC/MS system demonstrates improved linearity in signal and enhanced sensitivity.
摘要:
The components present in the sample with a mobile phase A in 1st section is separated. In 2nd section there is provided with an inserting line of a dilute solution for diluting the mobile phase A and a trapping column which forces the dilute solution to pass but catches the components by connecting said line to said column. In 3rd section, the components caught by the trapping column are introduced into mass spectrometer by using a mobile phase B. It is preferable to use respectively different mobile phases for the mobile phase A and the mobile phase B. It is good to install separating columns in 1st and 3rd sections. It is also desired to add the retaining apparatus of the components separated in 1st section.
摘要:
A reconfigurable multi-mode post-column analysis system improves resolution of liquid chromatography detection data by providing a parking or MS/MS detection mode in which flow of column eluent is substantially reduced to provide greater analysis time within a single eluting detection peak. A micro switching valve unit is reconfigurable between normal (MS) mode that passes column eluent directly to an MS unit, and a peak parking (or MS/MS) mode, in which normal mode column flow is interrupted, and the gradient halted, while more slowly flowing the detection peak of interest through the MS unit. A micro syringe pump contributes to the substantially lower MS/MS flow rate. A MS control unit controls micro switching valve valves to reconfigure between MS and MS/MS modes. After a detection peak, MS mode is reestablished, and the system primary pump returns to normal mode flow rate and gradient conditions. Mode changes can be carried out for each chromatogram detection peak.
摘要:
A mass spectrometer comprising an ionization region for ionizing a sample under atmospheric pressure, an ion sampling aperture for introducing ions generated by the ionization region into a vacuum, and a mass analysis region for mass analyzing the ions on the basis of a high-frequency electric field, wherein: an electrostatic lens for deflecting the direction of the movement of the ion from the center axis of the ion sampling aperture is disposed between the ionization region and the mass analysis region; the center axis of an aperture for introducing ions into the mass analysis region and the center axis of the ion sampling aperture are disposed so as to be shifted in parallel from each other; and the center axis of the ion sampling aperture and the center axis of a cylindrical inner electrode constituting the electrostatic lens are disposed so as to be shifted in parallel from each other to thereby prevent charged droplets or droplets without charge from flowing into the mass analysis region.
摘要:
A reconfigurable multi-mode post-column analysis system improves resolution of liquid chromatography detection data by providing a parking or MS/MS detection mode in which flow of column eluent is substantially reduced to provide greater analysis time within a single eluting detection peak. A micro switching valve unit is reconfigurable between normal (MS) mode that passes column eluent directly to an MS unit, and a peak parking (or MS/MS) mode, in which normal mode column flow is interrupted, and the gradient halted, while more slowly flowing the detection peak of interest through the MS unit. A micro syringe pump contributes to the substantially lower MS/MS flow rate. A MS control unit controls micro switching valve valves to reconfigure between MS and MS/MS modes. After a detection peak, MS mode is reestablished, and the system primary pump returns to normal mode flow rate and gradient conditions. Mode changes can be carried out for each chromatogram detection peak.
摘要:
An apparatus for directly connecting an analytical column and a mass spectrometer comprising a fixed member having at least four holes which respectively introduce washing solution, eluate containing a component eluted from the analytical column, desalting solution and eluent for eluting the component, and a movable member rotated with respect to an axis having at least four tubes around the axis and mounting the four trapping columns, whereby the trapping columns are respectively washed, trapped, desalted and eluted in parallel. Furthermore, a common trapping column may be used instead of the four trapping columns by controlling the apparatus with four analytical modes.
摘要:
A method and device for analyzing samples containing mixtures of organic compounds using vacuum chromatography is disclosed. The method and device are particularly useful for obtaining mass spectra for identification purposes. The method involves passing a sample dissolved in a solvent through a column with a carrier gas and depositing a thin layer of the sample in the interior of a short column. The short column is then attached to an MS interface. The device comprises a combination of a variable molecular separator and a column alignment component. The alignment component may also be used as a direct probe injector. This device and method allow the separation and MS analysis of mixtures of intermediate molecular weight compounds.
摘要:
This application relates to a method and apparatus for coupling an analyte supply, such as a biomolecule separator, to an electrodynamic droplet processor. In one embodiment the biomolecule separator is a capillary liquid chromatography column and the droplet processor includes an droplet generator and an electrodynamic balance. The biomolecule separator and the droplet processor may be fluidly coupled to provide a continuous supply of analyte for analysis. The droplets may be controllably ejected from the electrodynamic balance and deposited on a target substrate for use in detecting the analyte by mass spectrometry, such as MALDI time of flight mass spectrometry. Prior to deposition, each of the droplets is levitated in the electrodynamic balance for a period sufficient to enable evaporation of volatile solvents present in the droplet solution, thereby increasing the analyte concentration in the droplet. The solution may include a MALDI liquid matrix and the target substrate may be a MALDI plate. In one embodiment, the method involves depositing a succession of discrete droplets on the target substrate to form one or more microspots having a high density of analytes. The microspots are then irradiated and the ions produced are analyzed by mass spectrometry. The invention improves the sensitivity of analyte detection while consuming a comparatively small volume of test solution.
摘要:
Disclosed is a method and apparatus for matrix-assisted laser desorption ionization (MALDI), whereby the components of a sample separated by the column of a chromatographic separation device such as a liquid chromatograph or capillary electrophoresis are eluted and deposited on a sample support plate in a continuous track which both concentrates the sample components and preserves the fidelity of the separation. Analysis by MALDI is thus decoupled from the requirements of the separation and deposition and is performed by moving the continuous track relative to a focused laser beam in order to ionize the sample. The deposition capillary is in relative motion to the sample support plate with a speed of motion compatible with the liquid flow rate. In order to prevent the liquid sample from spreading across the sample support plate and to focus it to a pre-defined narrow region, the deposition of the sample is made along a hydrophilic anchor track of a well-defined width of less than 1 mm on the surface of the sample plate.