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.

A method of producing a mass spectrum from a time-varying transient signal detected in a mass spectrometer, the method comprising: performing a Fourier transform of the transient signal to produce a first set of complex amplitudes wherein each of the complex amplitudes corresponds to a respective frequency of a first set of frequencies; generating a second set of complex amplitudes, wherein each of the complex amplitudes corresponds to a respective frequency of a second set of frequencies with a minimum spacing less than the inverse of the duration of the transient signal; optimizing the second set of complex amplitudes to produce an improved second set; generating a mass spectrum from at least some of the improved second set of complex amplitudes; wherein optimizing the second set of complex amplitudes to produce an improved second set of complex amplitudes is based on an objective function subject to some phase constraints.

A method of producing a mass spectrum from a time-varying transient signal detected in a mass spectrometer, the method comprising: performing a Fourier transform of the transient signal to produce a first set of complex amplitudes wherein each of the complex amplitudes corresponds to a respective frequency of a first set of frequencies; generating a second set of complex amplitudes, wherein each of the complex amplitudes corresponds to a respective frequency of a second set of frequencies with a minimum spacing less than the inverse of the duration of the transient signal; optimizing the second set of complex amplitudes to produce an improved second set; generating a mass spectrum from at least some of the improved second set of complex amplitudes; wherein optimizing the second set of complex amplitudes to produce an improved second set of complex amplitudes is based on an objective function subject to some phase constraints.

An isotope mass spectrometer including: an electron cyclotron resonance ion source, a front-end analysis device, a back-end analysis device and an ion detector; where the electron cyclotron resonance ion source is connected with the front-end analysis device, and is used for generating ion beams of multivalent charge states; the front-end analysis device is connected with the back-end analysis device, selects and separates the ion beams, and receives ion beams of constant, microscale and trace levels; the back-end analysis device is connected with the ion detector, and is used for eliminating a background of an isotope to be measured at an ultratrace level; and the ion detector is used for receiving ion beams of the ultratrace level, and carrying out energy measurement and separation on the ion beams of the ultratrace level, so as to obtain the isotope to be measured at the ultratrace level.

An isotope mass spectrometer including: an electron cyclotron resonance ion source, a front-end analysis device, a back-end analysis device and an ion detector; where the electron cyclotron resonance ion source is connected with the front-end analysis device, and is used for generating ion beams of multivalent charge states; the front-end analysis device is connected with the back-end analysis device, selects and separates the ion beams, and receives ion beams of constant, microscale and trace levels; the back-end analysis device is connected with the ion detector, and is used for eliminating a background of an isotope to be measured at an ultratrace level; and the ion detector is used for receiving ion beams of the ultratrace level, and carrying out energy measurement and separation on the ion beams of the ultratrace level, so as to obtain the isotope to be measured at the ultratrace level.

A system, method and computer program product are provided for calculating one or more indicative properties including one or more of the cetane number, octane number, pour point, cloud point and aniline point of oil fractions, from the density and Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) of a sample of an oil sample.

Systems and methods are provided for modifying or selecting processing conditions for bright stock formation based on compositional characterization of the feedstock and/or bright stock products. In some aspects, the compositional information can include Z-class characterization of the components of a feed and/or bright stock product, optionally in combination with carbon number and/or molecular weight for the components. The compositional information can be used to select processing conditions to allow for removal and/or modification of selected components within a bright stock in order to improve throughput and/or provide desirable cold flow properties.

A process and system for the extraction of metals and gases contained on planets and asteroids (mining and refining) and for space debris remediation may include geographically localizing a material to be extracted/remediated; performing a risk analysis on the material to determine whether the material presents a serious risk of instantaneous fracture or disaggregation; using the risk analysis to qualify or refuse the material; capturing and stabilizing the qualified material in an ablation cylinder on a plasma machine (PERT station); deploying multiple magnetic hydraulic cylinders around the qualified material; equalizing and stabilizing the PERT station and the qualified material; performing ablation and destruction of the qualified material; and transforming pure elements from the ablation cylinder.

A process and system for the extraction of metals and gases contained on planets and asteroids (mining and refining) and for space debris remediation may include geographically localizing a material to be extracted/remediated; performing a risk analysis on the material to determine whether the material presents a serious risk of instantaneous fracture or disaggregation; using the risk analysis to qualify or refuse the material; capturing and stabilizing the qualified material in an ablation cylinder on a plasma machine (PERT station); deploying multiple magnetic hydraulic cylinders around the qualified material; equalizing and stabilizing the PERT station and the qualified material; performing ablation and destruction of the qualified material; and transforming pure elements from the ablation cylinder.

A method of isotope ratio mass spectrometry comprising: flowing a liquid mobile phase through a separation device; reducing the flow rate of the mobile phase through the separation device for at least a portion of time that at least one molecular species is emerging from the separation device to achieve a desired isotope ratio precision, wherein the flow rate is reduced from a first rate to a second rate corresponding to a higher theoretical plate height of the separation device; and mass analyzing the molecular species that has emerged from the separation device at least while the flow rate is reduced; and determining at least one isotope ratio from the intensities of mass peaks of at least two isotopologues, wherein the mass analysis is performed with mass resolving power high enough to resolve the two most abundant mass peaks at the nominal mass of at least one of the isotopologues.