A magnetic sector including magnetic means, a yoke including a first magnetic portion, and a deflection gap in the first magnetic portion. The magnetic sector is configured such that the magnetic means are adapted for generating a magnetic field through the deflection gap in order to deflect charged particles moving in the deflection gap. The yoke further includes a second magnetic portion having a magnetic shunt including a shunt passage for the charged particles. The magnetic shunt directs a magnetic flux leaked from the deflection gap into the first magnetic portion.

An accelerator mass spectrometry system for measuring an isotopic ratio of a chemical element in a sample. The system includes an ion source generating a beam of negative ions of the chemical element containing ions of first and second isotopes of the chemical element, a first analyzer section, comprising a first mass analyzer; a tandem accelerator comprising a first accelerating section, a charge stripping section for converting the negative ions into positive ions, and a second accelerating section behind the charge stripping section. A second analyzer section includes a second mass analyzer and an electrostatic analyzer; a particle detector; and a controller system configured to control the first mass analyzer section and the second analyzer section such that the ions of the first and second isotopes traverse the tandem accelerator and ions of only one of the first and second isotopes enter the particle detector. An additional analyzer is located in between the charge stripping section and the second accelerating section and is configured to receive positive ions that have exited the charge stripping section and to separate positive ions having a charge state corresponding to a predetermined charge-state value from positive ions having a charge state not corresponding to the predetermined charge-state value, so as to transmit ions with different charge states in mutually different directions such that only ions having a charge state corresponding to the predetermined charge-state value are transmitted towards the particle detector.

A control system for controlling a magnet of a magnetic sector mass spectrometer comprises a magnetic field sensor for sensing the magnetic field of the magnet and generating an output representative thereof; a set point generator configured to generate an output representative of, or related to, a desired magnetic field of the magnet; and a digital controller configured to receive a variable digital input signal from the output of the magnetic field sensor and a set point digital input signal from the output of the set point generator, and to generate a digital output from which is derived a control signal for controlling a current to the magnet so as to control the magnetic field thereof. The control system is arranged to apply to the digital controller a selected one of a plurality of different controller settings, in accordance with the desired magnetic field of the magnet.

A control system for controlling a magnet of a magnetic sector mass spectrometer comprises a magnetic field sensor for sensing the magnetic field of the magnet and generating an output representative thereof; a set point generator configured to generate an output representative of, or related to, a desired magnetic field of the magnet; and a digital controller configured to receive a variable digital input signal from the output of the magnetic field sensor and a set point digital input signal from the output of the set point generator, and to generate a digital output from which is derived a control signal for controlling a current to the magnet so as to control the magnetic field thereof. The control system is arranged to apply to the digital controller a selected one of a plurality of different controller settings, in accordance with the desired magnetic field of the magnet.

A miniature, low cost mass spectrometer capable of unit resolution over a mass range of 10 to 50 AMU. The mass spectrometer incorporates several features that enhance the performance of the design over comparable instruments. An efficient ion source enables relatively low power consumption without sacrificing measurement resolution. Variable geometry mechanical filters allow for variable resolution. An onboard ion pump removes the need for an external pumping source. A magnet and magnetic yoke produce magnetic field regions with different flux densities to run the ion pump and a magnetic sector mass analyzer. An onboard digital controller and power conversion circuit inside the vacuum chamber allows a large degree of flexibility over the operation of the mass spectrometer while eliminating the need for high-voltage electrical feedthroughs. The miniature mass spectrometer senses fractions of a percentage of inlet gas and returns mass spectra data to a computer.

A miniature, low cost mass spectrometer capable of unit resolution over a mass range of 10 to 50 AMU. The mass spectrometer incorporates several features that enhance the performance of the design over comparable instruments. An efficient ion source enables relatively low power consumption without sacrificing measurement resolution. Variable geometry mechanical filters allow for variable resolution. An onboard ion pump removes the need for an external pumping source. A magnet and magnetic yoke produce magnetic field regions with different flux densities to run the ion pump and a magnetic sector mass analyzer. An onboard digital controller and power conversion circuit inside the vacuum chamber allows a large degree of flexibility over the operation of the mass spectrometer while eliminating the need for high-voltage electrical feedthroughs. The miniature mass spectrometer senses fractions of a percentage of inlet gas and returns mass spectra data to a computer.

The present application relates to a method for improving analytical efficiency and cost effectiveness of oxygen isotope analysis of an aqueous sample. In particular, the present application relates to a method of determining an oxygen isotope composition of an aqueous sample by (a) equilibrating the aqueous sample with CO.sub.2 gas wherein the aqueous sample comprises an effective amount of carbonic anhydrase (CA) enzyme; and (b) measuring the oxygen isotope composition of the CO.sub.2 at equilibrium, wherein the oxygen isotope composition of the CO.sub.2 corresponds to the oxygen isotope composition of the aqueous sample.

The present application relates to a method for improving analytical efficiency and cost effectiveness of oxygen isotope analysis of an aqueous sample. In particular, the present application relates to a method of determining an oxygen isotope composition of an aqueous sample by (a) equilibrating the aqueous sample with CO.sub.2 gas wherein the aqueous sample comprises an effective amount of carbonic anhydrase (CA) enzyme; and (b) measuring the oxygen isotope composition of the CO.sub.2 at equilibrium, wherein the oxygen isotope composition of the CO.sub.2 corresponds to the oxygen isotope composition of the aqueous sample.

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.