Abstract:
An ion trap for a mass spectrometer is disclosed. The ion trap includes a ring electrode and first and second electrodes which are arranged on opposite sides of the ring electrode. The ring electrode and the first and second electrodes are configured to generate an electric field based on the received RF signal. The first electrode defines a first aperture and the second electrode defines a second aperture, the first aperture and the second aperture being asymmetric relative to each other and configured to generate a hexapoie field.
Abstract:
A mass spectrometer system is disclosed. The mass spectrometer includes a vacuum chamber defining an enclosed evacuated space and an ion trap disposed in the enclosed space. The ion trap is configured to trap an ionized sample. The mass spectrometer further includes an son detector coupled to the chamber at a location external to the chamber such that sample ions may exit the evacuated space and into the externally-coupled detector without loss of vacuum pressure.
Abstract:
An ion trap for a mass spectrometer is disclosed. The ion trap includes a ring electrode and first and second electrodes which are arranged on opposite sides of the ring electrode. The ring electrode and the first and second electrodes are configured to generate an electric field based on the received RF signal. The first electrode defines a first aperture and the second electrode defines a second aperture, the first aperture and the second aperture being asymmetric relative to each other and configured to generate a hexapole field.
Abstract:
Apparatuses and methods for performing mass analysis are disclosed. One such apparatus may include an ion trap device. The ion trap device may comprise a first end cap having a first aperture and a second end cap having a second aperture, wherein the first aperture and the second aperture may define an ejection axis. The ion trap device may also comprise a ring electrode substantially coaxially aligned between the first and second end caps. The ring electrode may include an opening extending along a radial direction of the ring electrode, wherein the radial direction is substantially perpendicular to the ejection axis. One such method may include ionizing a sample in an ion trap through an opening separating at least part of first and second ring sections of the ion trap and detecting ions ejected though an aperture on an end cap of the ion trap.
Abstract:
In mass spectrometry, the number of ionized sample molecules affects various performance specifications of the resulting spectrum, including resolution, sensitivity, dynamic range, and scan speed. A voltage-controlled lens is used to control the number of electrons emitted from an electron source that enter the ion trap and ionize the target sample molecules. By monitoring a feature of the resulting spectrum, such as the resolution, total ion current, or a combination of these features, the lens voltage may be adjusted to create the optimal number of ions in the trap for a particular sample spectrum scan. Generally, for low concentration samples, the number of electrons introduced to the trap is increased, hence creating more ions in the trap, which in turn increases the intensity of the output signal improving the probability of detecting a sufficient number of ions by raising the intensity well above the noise floor. For higher concentration samples, the number of electrons is reduced, thus reducing interactions in the trap which in turn reduces peak broadening and improves resolution, as well as avoids saturating the detector. Several methods for adjusting the lens voltage may be used. First, the lens voltage may be repeatedly adjusted until the resulting spectrum reaches a desired trade-off between resolution and sensitivity. The lens voltage may also be incrementally increased until the resulting spectrum begins to exhibit space charge effects. Finally, all lens voltages in a list of usable voltage settings may be applied, and all the resulting spectra are compared. The optimal voltage setting is selected and used for subsequent scans.
Abstract:
In one general aspect, a sample is transferred into a mass spectrometer (150) by capturing a sample on a collector (125), inserting the collector (125) into a sample chamber (110) coupled to the mass spectrometer (150) and a vacuum pump (342, 344), evacuating the sample chamber (110) using the vacuum pump (342, 344) to reduce an internal pressure of the sample chamber (110) to a level less than atmospheric pressure, heating the collector (125) to release the sample from the collector, and introducing the sample into the mass spectrometer (150) from the evacuated sample chamber (110).
Abstract:
A chemical analysis system is disclosed wherein, in evacuating a preconcentrator housing (2) prior to desorption, a pump system (13) reduces an internal pressure of the preconcentrator housing to a level substantially equal to an internal pressure of a chemical analyzer such that flow restrictors and/or membranes (15) between the chemical analyzer (7) and the preconcentrator housing (2) may be omitted. The chemical analysis system includes a chemical analyzer (7), a preconcentrator housing (2) coupled to the chemical analyzer, the preconcentrator housing enclosing a temperature control element (5, 18) and a sorbent material (1), the temperature control element configured to heat the sorbent material to adsorb or desorb a chemical of interest; and a pump system (13) coupled to the preconcentrator housing and the chemical analyzer, the pump system configured to evacuate the preconcentrator housing prior to desorption of the chemical of interest.
Abstract:
A chemical analysis system is disclosed wherein, in evacuating a preconcentrator housing (2) prior to desorption, a pump system (13) reduces an internal pressure of the preconcentrator housing to a level substantially equal to an internal pressure of a chemical analyzer such that flow restrictors and/or membranes (15) between the chemical analyzer (7) and the preconcentrator housing (2) may be omitted. The chemical analysis system includes a chemical analyzer (7), a preconcentrator housing (2) coupled to the chemical analyzer, the preconcentrator housing enclosing a temperature control element (5, 18) and a sorbent material (1), the temperature control element configured to heat the sorbent material to adsorb or desorb a chemical of interest; and a pump system (13) coupled to the preconcentrator housing and the chemical analyzer, the pump system configured to evacuate the preconcentrator housing prior to desorption of the chemical of interest.
Abstract:
A chemical preconcentrator (100) includes a conduit (200) defining a flow path (106) between two ends (108A, 108B) and having a heating element (102) disposed within the conduit, such that the heating element has at least one sorbent material (115) deposited directly on at least a portion of a conductive surface of the heating element. Some such heating elements (102) are in the form of electrically conductive strips defining both a plurality of apertures (112, 710) through the strip and a series of undulations (114) spaced along the flow path (106).
Abstract:
In one general aspect, a sample is transferred into a mass spectrometer (150) by capturing a sample on a collector (125), inserting the collector (125) into a sample chamber (110) coupled to the mass spectrometer (150) and a vacuum pump (342, 344), evacuating the sample chamber (110) using the vacuum pump (342, 344) to reduce an internal pressure of the sample chamber (110) to a level less than atmospheric pressure, heating the collector (125) to release the sample from the collector, and introducing the sample into the mass spectrometer (150) from the evacuated sample chamber (110).