An atom probe directs two or more pulsed laser beams onto a specimen, with each laser beam being on a different side of the specimen, and with each laser beam supplying pulses at a time different from the other laser beams. The laser beams are preferably generated by splitting a single beam provided by a laser source. The laser beams are preferably successively aligned incident with the specimen by one or more beam steering mirrors, which may also scan each laser beam over the specimen to achieve a desired degree of specimen ionization.

A gas ionization chamber, includes a first electrode, a fence electrode disposed below the first electrode, a second electrode disposed below the fence electrode, a first dielectric layer disposed between the first electrode and the fence electrode, and a second dielectric layer disposed between the fence electrode and the second electrode. The first and second electrodes, and the first and second dielectric layers include a plurality of aligned holes forming channels configured to permit gas flow between the first electrode to the second electrode through an opening in the fence electrode, the plurality of aligned holes being arranged in a pattern having a central region with a first set of aligned holes and a peripheral region having a second set of aligned holes, and wherein a diameter of at least one hole of the first set of aligned holes is less than or equal to about 0.5 millimeters.

A sample support is a sample support for sample ionization, including: a substrate formed with a plurality of through holes opening to a first surface and a second surface on a side opposite to the first surface; a conductive layer provided not to block the through hole in the first surface; and a frame body provided in a peripheral portion of the substrate to surround an ionization region in which a sample is ionized when viewed in a thickness direction of the substrate, in which a marker for recognizing a position in the ionization region is provided in the frame body.

A method for measuring the chirality of molecules in a sample of chiral molecules, the sample including at least one chemical species, the method including the steps of: introducing the sample of chiral molecules into an ionisation area; ionising the molecules by electromagnetic radiation in the ionisation area; and detecting a distribution of electrons produced by ionisation and emitted at the front and back of the ionisation area relative to the axis, z, of propagation of the electromagnetic radiation; wherein the electromagnetic radiation is elliptically polarised, the ellipticity varying continuously and periodically as a function of time, the method further including a step of: determining the chirality of the molecules from the electron distribution detected continuously as a function of time. A system is also provided for measuring the chirality of molecules using such a method.

A method for detecting and analyzing olefins in petroleum by electrospray ionization mass spectrometry can include obtaining a hydrocarbon sample comprising at least about 90 wt % of saturate compounds; producing a solution comprising the hydrocarbon sample and a metal salt, the metal salt comprising a metal ion; forming olefin-metal ion complexes by electrospray ionization; and detecting the olefin-metal ion complexes using mass spectrometry.

An ion mobility spectrometry method is described comprising: providing a sample; generating molecular ions from the sample; separating the molecular ions according to their mobility characteristics; fragmenting at least some of the separated molecular ions to form sub-molecular fragment ions in a fragmentation zone; separating at least some of the fragment ions according to their mobility characteristics; wherein the separation and fragmentation steps are performed at a pressure of at least 50 mbar; detecting at least some of the separated fragment ions; and identifying at least one molecular ion based on its mobility characteristics and/or the mobility characteristics of at least one detected fragment ion.

The present invention provides a method enabling a quantitative analysis of a polymer by MALDI mass spectrometry, and a method for manufacturing a sample for MALDI mass spectrometry for a quantitative analysis of a polymer. To that end, the methods can increase reproducibility of a MALDI spectrum by making uniform the thickness of a sample affecting the pattern in a polymer MALDI spectrum. The sample according to the present invention is applicable also to a commercial MALDI-TOF instrument, and, thus, can quantitatively analyze a polymer in a more efficient and faster manner.

A first container for housing a reagent and a second container for housing the first container inside are provided. The pressurization mechanism pressurizes a pressurization space formed outside the first container in the second container to pressurize the inside of the first container communicating with the pressurization space. The reagent is drawn out from the pressurized inside of the first container through a pipe.

The present invention relates to a composition analysis technology of ultramicro-volume liquid by laser ablation plasma mass spectrometry. Using a pipette gun to extract the liquid to be detected in a low-temperature environment, dropping the liquid into a dropping pit in a dropping plate, the liquid level is slightly higher than an overflow table in the dropping plate; dropping different liquid samples into different dropping pits by the same method; gradually covering the dropping pit with an analysis film having an area 1.5 times larger than that of the dropping plate from one side of the dropping plate, tightly adhering the thin film onto the dropping plate by using a transparent adhesive tape, the thin film is in close contact with the liquid level; placing the dropping plate covered by the thin film in a LA-ICPMS universal solid sample chamber, and then setting parameters for ablation.

Provided is a sample support body that includes: a substrate having a first surface and a second surface opposite to each other; and a conductive layer provided on at least the first surface. A plurality of through-holes, which open to the second surface and a third surface of the conductive layer which is located on a side opposite to the substrate, are formed in the substrate and the conductive layer. At least one of the second surface and the third surface is subjected to surface treatment for providing a difference in an affinity with water between a surface close to the second surface and a surface close to the third surface.