Presentation on theme: "Atomic Mass Spectrometry Yongsik Lee 2004. Introduction ► Atomic mass spectrometry Versatile and widely used tool All elements can be determined ►"— Presentation transcript:
Atomic Mass Spectrometry Yongsik Lee 2004
Introduction ► Atomic mass spectrometry Versatile and widely used tool All elements can be determined ► Advantage over AOS Detection limits are 1000 times better Simple spectra Measure atomic isotope ratios ► Disadvantage Cost – 100 or 1000 times expensive Instrumental drift – 5% per hour Interference effects
11A General Features ► Atomization = same as AOS ► Conversion to ions = same as AOS ► Separation of ions by mass-to-charge ratio ► Counting the number of ions of each type
Atomic weights in MS ► Atomic mass unit (amu) = dalton (Da) Relative scale where mass of C12 is 12 amu Carbon-12 scale 1 amu = (1/12)(12g / Navo) = x g/atom of C12 ► Exact mass CH4, CH3D, CH2D2, CHD3, CD4 ► Nominal mass A whole-number precision
Chemical atomic weight ► Average atomic weight Fractional abundance x isotope mass ► m/z Atomic or molecular mass / charges of ions If Z=+1, m/z = mass
Atomic mass of Zr ► (51.5 x 90) + (11.2 x 91) + (17.1 x 92) + (17.4 x 94) + (2.8 x 96) = ► The average mass of these 100 atoms would be / 100 = 91.3 (to 3 significant figures). ► 91.3 is the relative atomic mass of zirconium.
MS of chlorine molecule ► Fragmentation When chlorine is passed into the ionisation chamber, an electron is knocked off the molecule to give a molecular ion, Cl2+. These ions won't be particularly stable, and some will fall apart to give a chlorine atom and a Cl+ ion. ► If the Cl atom formed isn't then ionised in the ionisation chamber, it simply gets lost in the machine - neither accelerated nor deflected. ► The Cl+ ions will pass through the machine and will give lines at 35 and 37, depending on the isotope. ► You will also record lines for the unfragmented Cl2+ ions. ► Both atoms could be 35Cl, both atoms could be 37Cl, or you could have one of each sort. That would give you total masses of the Cl2+ ion of: = 70 = 72 = 74 ► That means that you would get a set of lines in the m/z = 70 region
Ion deflection ► Atoms can be deflected by magnetic fields - provided the atom is first turned into an ion. ► Electrically charged particles are affected by a magnetic field although electrically neutral ones aren't. ► Stage 1: Ionisation The atom is ionised by knocking one or more electrons off to give a positive ion. This is true even for things which you would normally expect to form negative ions (chlorine, for example) or never form ions at all (argon, for example). Mass spectrometers always work with positive ions. ► Stage 2: Acceleration The ions are accelerated so that they all have the same kinetic energy. ► Stage 3: Deflection The ions are then deflected by a magnetic field according to their masses. The lighter they are, the more they are deflected.The amount of deflection also depends on the number of positive charges on the ion - in other words, on how many electrons were knocked off in the first stage. The more the ion is charged, the more it gets deflected. ► Stage 4: Detection The beam of ions passing through the machine is detected electrically.
Basic Principle - deflection ► subject something to a sideways force, it will move in a curve deflected out of its original path ► The amount of deflection for a given sideways force depends on the mass of the ball. ► If you knew the speed of the ball the size of the force, ► Then you could calculate the mass of the ball The less the deflection, the heavier the ball.
Mass analyzer ► ► separate ions to measure m/z and intensity ► resolution
Electron multipliers ► General characteristics Rugged and reliable High current gains Nanosecond response time Requires enough Kinetic energy ions ► Acceleration required for quadrupoles ► types Discrete dynode emp Continuous dynode emp
Electron multipliers ► Discrete dynode electron multiplier (figure 11-2 a) Similar to PMT Cu/Be surface ► Burst of electrons ► when struck by energetic ions or electrons 20 dynodes = gain of 10 million ► Continuous dynode electron multiplier (figure 11-2 b) Trumpet shaped Made of glass of highly Pb doped Electrical potential across the length of transducer Gain of 100 thousand – 100 million
Multi Cannel Plate (MCP)
Faraday Cup ► principle Ions strike the collector electrode Charge of the positive ions is neutralized by a flow of electrons Electron flow cause a potential drop over a resistor High impedance amplifier ► advantages Independent of the energy, mass, chemical nature of the ion Inexpensive and simple ► disadvantages Low response speed Less sensitive than EMP
Photographic plate ► Photographic plate Silver bromide emulsion are sensitive to energetic ions Frequently used for spark source instrument Simultaneous observation of wide m/z possible
Magnetic sector analyzer
► ► For fixed radius and charge can use permanent magnet, vary A and B potential (V) or variable electromagnet, fixed A and B potential (V)
Double focusing analyzer ► ► Single-focusing magnetic sector analyzers have Rmax < 2000 translational energy aberrations angular aberrations Addition of electrostatic analyzer simultaneously minimizes both ► ► Electrostatic analyzer focuses ions of unique m/z at entrance slit to magnetic sector
Quadrupole analyzer ► ► ions travel parallel to four rods opposite pairs of rods have rapidly alternating potentials (AC) ions try to follow alternating field in helical trajectories stable path only for one m/z value for each field frequency ► ► Harder to push heavy molecule - m/zmax < 2000 ► ► Rmax ~ 500
Time of flight analyzer ► ► Generate pulse of ions (by laser, electrons) with same initial energy ► ► Ions travel down field-free tube separate according to mass light ions arrive first, heavy ions arrive later Unlimited mass range m/zmax > 100 kDa ► ► Poor resolution Rmax < 1000 ► ► Poor sensitivity
Summary ► ► One of most powerful analytical tools: sensitive (10-6 to <10-13 g) range of ion sources for different situations elemental composition for small and large MW- biomolecules limited structural information qualitative and quantitative analysis of mixtures composition of solid surfaces isotopic information in compounds ► ► But complex instrumentation expensive ► ► high resolution structure obtained indirectly complex spectra/fragmentation for hard ionization sources simple spectra for soft ionization sources