Patent classifications
H01J49/38
METHOD AND PROGRAM FOR APPROXIMATELY IDENTIFYING MOLECULAR STRUCTURE OF MULTICOMPONENT MIXTURE
A method identifies the molecular structure of each component in a multicomponent mixture. The method includes (1) subjecting the multicomponent mixture to mass spectrometry to identify the formula of a molecule attributed to each obtained peak, and to identify abundance of the molecule; (2) subjecting the multicomponent mixture to collision induced dissociation; (3) performing mass spectrometry on each fragment ion generated via the collision induced dissociation in (2) to identify the core structure forming each fragment ion and abundance thereof; (4) dividing the molecules attributed to each peak in (1) into classes based on a type and number of heteroatoms, and a DBE value, and on all the molecules belonging to each class, estimating the existence state and abundance thereof; and (5) determining the core structure forming each molecule, for which the existence state is estimated in (4), and determining and assigning a side chain and a cross-link thereto.
Fourier transform mass spectrometer
A quadrupole is filled with ions and the ions are cooled by applying a pressure and gas flow within the quadrupole. Ions are trapped in the quadrupole by applying a DC voltage and an RF voltage to quadrupole rods of the quadrupole, one or more DC voltages to a plurality of auxiliary electrodes of the quadrupole, and a DC voltage and an RF voltage to an exit lens at the end of the quadrupole. The ions are coherently oscillated after the filling and cooling by applying a coherent excitation between at least two rods of the quadrupole rods. The coherently oscillating ions are axially ejected through the exit lens and to a destructive detector for detection by changing one or more voltages of the one or more DC voltages of the plurality of auxiliary electrodes and changing the DC voltage of the exit lens.
Fourier transform mass spectrometer
A quadrupole is filled with ions and the ions are cooled by applying a pressure and gas flow within the quadrupole. Ions are trapped in the quadrupole by applying a DC voltage and an RF voltage to quadrupole rods of the quadrupole, one or more DC voltages to a plurality of auxiliary electrodes of the quadrupole, and a DC voltage and an RF voltage to an exit lens at the end of the quadrupole. The ions are coherently oscillated after the filling and cooling by applying a coherent excitation between at least two rods of the quadrupole rods. The coherently oscillating ions are axially ejected through the exit lens and to a destructive detector for detection by changing one or more voltages of the one or more DC voltages of the plurality of auxiliary electrodes and changing the DC voltage of the exit lens.
METHOD FOR DETECTING AROMATIC HYDROCARBONS AND/OR DIAMONDOIDS USING FOURIER TRANSFORM ION CYCLOTRONIC RESONANCE MASS SPECTROMETRY COUPLED WITH THE ATMOSPHERIC PRESSURE PHOTOIONIZATION SOURCE
The present invention relates to the field of organic geochemistry wherein a method for accessing high molecular mass aromatic hydrocarbons and diamondoids was developed from comprehensive characterization carried out by high resolution spectrometry coupled with the atmospheric pressure photoionization source (APPI FT-ICR MS). Based on the compositional profile of diamondoids and aromatic hydrocarbons, it is possible to quickly and robustly classify oils in relation to their origin and thermal evolution. It is verified that the compositional detail provided by the APPI(+)-FT-ICR MS analysis allowed the development of new molecular indicators, accessed without the need for any preliminary separation technique, in order to become a powerful tool for prospecting the use of oils exploited for specific purposes.
METHOD FOR DETECTING AROMATIC HYDROCARBONS AND/OR DIAMONDOIDS USING FOURIER TRANSFORM ION CYCLOTRONIC RESONANCE MASS SPECTROMETRY COUPLED WITH THE ATMOSPHERIC PRESSURE PHOTOIONIZATION SOURCE
The present invention relates to the field of organic geochemistry wherein a method for accessing high molecular mass aromatic hydrocarbons and diamondoids was developed from comprehensive characterization carried out by high resolution spectrometry coupled with the atmospheric pressure photoionization source (APPI FT-ICR MS). Based on the compositional profile of diamondoids and aromatic hydrocarbons, it is possible to quickly and robustly classify oils in relation to their origin and thermal evolution. It is verified that the compositional detail provided by the APPI(+)-FT-ICR MS analysis allowed the development of new molecular indicators, accessed without the need for any preliminary separation technique, in order to become a powerful tool for prospecting the use of oils exploited for specific purposes.
Optimized electromagnetic field on side-on FT-ICR mass spectrometers
Improvements to a side-on Penning trap include a feedback system for stabilizing the magnetic field. This system includes a magnetic sensor that measures the magnetic field and a solenoid coil that in response to the magnetic field measurements increases or decreases the overall magnetic field. Improvements also include a number of different configurations of the two sets of PCB electrodes used to produce the quadrupole electric field. Dimensions of the PCB electrodes are optimized, an equipotential surface electrode is added, and additional ring electrodes are added to produce a purer quadrupole field. A central disk electrode is segmented to direct charged particles to the trap center to make the trap useful for applications other than mass spectrometry. Finally, outer ring electrodes are segmented to increase the path of charged particles, thereby increasing sensitivity.
Optimized electromagnetic field on side-on FT-ICR mass spectrometers
Improvements to a side-on Penning trap include a feedback system for stabilizing the magnetic field. This system includes a magnetic sensor that measures the magnetic field and a solenoid coil that in response to the magnetic field measurements increases or decreases the overall magnetic field. Improvements also include a number of different configurations of the two sets of PCB electrodes used to produce the quadrupole electric field. Dimensions of the PCB electrodes are optimized, an equipotential surface electrode is added, and additional ring electrodes are added to produce a purer quadrupole field. A central disk electrode is segmented to direct charged particles to the trap center to make the trap useful for applications other than mass spectrometry. Finally, outer ring electrodes are segmented to increase the path of charged particles, thereby increasing sensitivity.
ULTRA-COMPACT MASS ANALYSIS DEVICE AND ULTRA-COMPACT PARTICLE ACCELERATION DEVICE
A mass analyzer includes a main substrate, an upper substrate adhered to the main substrate, and a lower substrate. A mass analysis room (cavity) is formed in the main substrate and penetrates from an upper surface of the first main substrate to a lower surface of the first main substrate. A vertical direction (Z direction) to the main substrate by the upper substrate, both sides of the lower substrate, a travelling direction (X direction) of charged particles and a right angle to the Z direction by the main substrate, and both sides of a right-angled direction (Y to Z direction) and the X direction by a side surface of the main substrate are surrounded. A central hole is open in the side plate of the main substrate that the charged particles enter. The charged particles enter the mass analysis room through the central hole formed in the first main substrate.
ULTRA-COMPACT MASS ANALYSIS DEVICE AND ULTRA-COMPACT PARTICLE ACCELERATION DEVICE
A mass analyzer includes a main substrate, an upper substrate adhered to the main substrate, and a lower substrate. A mass analysis room (cavity) is formed in the main substrate and penetrates from an upper surface of the first main substrate to a lower surface of the first main substrate. A vertical direction (Z direction) to the main substrate by the upper substrate, both sides of the lower substrate, a travelling direction (X direction) of charged particles and a right angle to the Z direction by the main substrate, and both sides of a right-angled direction (Y to Z direction) and the X direction by a side surface of the main substrate are surrounded. A central hole is open in the side plate of the main substrate that the charged particles enter. The charged particles enter the mass analysis room through the central hole formed in the first main substrate.
Methods for the diagnosis and risk assessment of plasmalogen deficiency mediated diseases of aging
The present invention relates to methods for the diagnosis and risk assessment of plasmalogen deficiency mediated diseases of aging. The present invention describes the relationship between plasmalogen biosynthesis dysfunction and the biochemical and clinical manifestations of age related disorders. Specifically the present invention describes an increased prevalence of colon cancer, prostate cancer, lung cancer, breast cancer, ovary cancer, kidney cancer, cognitive impairment and dementia in subjects suffering from adult onset plasmalogen biosynthesis disorder (AO-PBD).