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  Types of Mass Spectrometry

Mass Spectrometer at ASU
Mass Spectrometer at Arizona State University (ASU)

   Secondary Ion Mass Spectrometry (SIMS)

SIMS is a technique for the characterization of solid surfaces and thin films. It uses the process of ion formation by bombarding the surface to be tested with a highly collimated beam of primary ions. The surface then emits material through a sputtering process - only a fraction of these emitted particles is ionized. These secondary ions are measured with a mass spectrometer to determine the quantitative elemental, isotopic or molecular composition of the surface. SIMS is the most sensitive surface analysis technique, but it is more difficult to obtain quantitative results compared to other techniques.

megaSIMS-2 picture (small) spacer megaSIMS-2 picture (small) spacer megaSIMS-1 picture (small) spacer megaSIMS-4 picture (small)

Take a 360-degree tour of the MegaSIMS Laboratory: High Res QT, 4.1 MB - click, hold, and drag your mouse slowly left, right, up, or down over the image.

    Gas Source Mass Spectrometry

Gas source mass spectrometers are used for measuring isotopic ratios of light elements, which includes hydrogen, carbon, nitrogen, and oxygen. Samples are prepared in gaseous form, often hydrogen, nitrogen, or carbon dioxide, and inlet into the mass spectrometer for analysis.

    Resonance Ionization Mass Spectrometry (RIMS)

RIMS is designed to determine the relative weights of an atomic nuclei.

    Total Reflection X-Ray Florescence

In-Situ analysis used the Genesis Science team members, which is unique in the fact that it does not require extraction allowing the solar wind regimes to remain intact during analysis and non-destructive to particle.

    Plasma Mass Spectrometry

A non-invasive method of extraction, allows the science team members to study particles by using differential chemical etching.

    Accelerator Mass Spectrometry

Accelerator mass spectrometry (AMS) differs from other forms of mass spectrometry in that it accelerates ions to extraordinarily high kinetic energies before mass analysis. AMS is exceptional in its ability to sensitively and accurately analyze elemental and isotopic compositions

    How it all works

Generally negative ions are created (atoms are ionized) in an ion source. It is preferable, but not necessary that the charges be the same for each atom. These ions are introduced to the gas phase and they enter an electrostatic accelerator that accelerates them to very high kinetic energy by presenting ever more positive electrical potentials. Half-way through the accelerator they impact a sheet of carbon. The impact strips off many of the ion's electrons, converting it into a positively charged ion. In the second half of the accelerator the now positively charged ion is accelerated away from the highly positive center of the electrostatic accelerator, which previously attracted the negative ion. When the ions leave the accelerator they are positively charged and are moving very fast. Next, the exact ion velocities must be filtered such that only a narrow selection of ion velocities is allowed to pass to allow for proper mass analysis. A device called a velocity selector, which utilizes both electric fields and magnetic fields to allow only ions of a specific charge and kinetic energy to pass, most frequently accomplishes this. The ions then pass through at least one mass analyzer, most often a magnetic or electric sector. For example with a magnetic sector, the atom, at its known velocity (relative to mass) and charge is released into a magnetic field perpendicular to it velocity. This field causes the particle's path to curve in a circular arc. The radius of this circular arc is related to the mass-to-charge ratio of the particle. Dedicated detectors for each isotope or element then detect the ions.

 
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Curator: Aimee Meyer
Updated: November 2009