Mass analyzer types

Hybrid Mass Spectrometer A tandem mass spectrometer comprised of multiple mass analyzers of different types. A Q-TOF is a hybrid, but a triple quadmpole is not. Ideally, a hybrid instrument harnesses the best features of each mass analyzer type to produce a system perhaps greater than the sum of the parts. 

ESI and MALDI sources have been coupled to many different mass analyzer types. Of these mass analyzers, five will be discussed next and are shown in Figure 4.5. To achieve the highest performance from these analyzers, an experienced operator will tune the mass spectrometer to improve the resolution, sensitivity, and signal-to-noise SIN) level. Tuning is essential to achieve optimum performance, but it differs for each mass spectrometer and will not be covered in this chapter. 

Applications of the mass analyzer types for discovery and development stage metabolite detection, characterization, and identification along with each analyzer type s limitations and advantages are discussed in the following section. 

Commercial LITs were introduced in 2002 as either a stand-alone mass spectrometer (LTQ) [318] or as part of a triple quadrupole (Q-Trap) [319] or in 2005 as part of hybrid tandem mass spectrometers (LTQ-Orbitrap and LTQ-FTICR) [88,90], Application of LTQ-FTICR for metabolism studies has been reviewed by Shipkova et al. [90], In comparison to other mass analyzer types, FTICR-based mass spectrometers are not very popular for metabolite identification studies due to availability of less expensive and more user-friendly LTQ-Orbitrap and Q-TOF-based systems. Another limitation associated with the FTICR-based hybrid mass spectrometers is the TOF effect, which results in efficient trapping of only the high-mass ions [90],... 

Why do we need mass analyzers Obviously, it is not enough to generate ions by different ionization techniques (see Section 4) but it is also necessary to separate them from each other. Mass analyzers are used for ion separation, and several mass analyzer types are commercially available. Overview of these mass analyzers can be simplified by considering two basic physical phenomena ... 

Positive ions are obtained from a sample by placing it in contact with the filament, which can be done by directing a gas or vapor over the hot filament but usually the sample is placed directly onto a cold filament, which is then inserted into the instrument and heated. The positive ions are accelerated from the filament by a negative electrode and then passed into a mass analyzer, where their m/z values are measured (Figure 7.1). The use of a suppressor grid in the ion source assembly reduces background ion effects to a very low level. Many types of mass analyzer could be used, but since very high resolutions are normally not needed and the masses involved are quite low, the mass analyzer can be a simple quadrupole. 

If a sample solution is introduced into the center of the plasma, the constituent molecules are bombarded by the energetic atoms, ions, electrons, and even photons from the plasma itself. Under these vigorous conditions, sample molecules are both ionized and fragmented repeatedly until only their constituent elemental atoms or ions survive. The ions are drawn off into a mass analyzer for measurement of abundances and mJz values. Plasma torches provide a powerful method for introducing and ionizing a wide range of sample types into a mass spectrometer (inductively coupled plasma mass spectrometry, ICP/MS). 

For solids, there is now a very wide range of inlet and ionization opportunities, so most types of solids can be examined, either neat or in solution. However, the inlet/ionization methods are often not simply interchangeable, even if they use the same mass analyzer. Thus a direct-insertion probe will normally be used with El or Cl (and desorption chemical ionization, DCl) methods of ionization. An LC is used with ES or APCI for solutions, and nebulizers can be used with plasma torches for other solutions. MALDI or laser ablation are used for direct analysis of solids. 

The choice of a mass spectrometer to fulfill any particular task must take into account the nature of the substances to be examined, the degree of separation required for mixtures, the types of ion source and inlet systems, and the types of mass analyzer. Once these individual requirements have been defined, it is much easier to discriminate among the numerous commercial instruments that are available. Once suitable mass spectrometers have been identified, it is then often a case of balancing capital and running costs, reUability, ea.se of routine use, after-sales service, and manufacturer reputation. 

Different types of mass analyzer can be used as quadrupoles. 

The main advantages of the ms/ms systems are related to the sensitivity and selectivity they provide. Two mass analyzers in tandem significantly enhance selectivity. Thus samples in very complex matrices can be characterized quickly with Htde or no sample clean-up. Direct introduction of samples such as coca leaves or urine into an ms or even a gc/lc/ms system requires a clean-up step that is not needed in tandem mass spectrometry (28,29). Adding the sensitivity of the electron multiplier to this type of selectivity makes ms/ms a powerhil analytical tool, indeed. It should be noted that introduction of very complex materials increases the frequency of ion source cleaning compared to single-stage instmments where sample clean-up is done first. 

Apart from the quadrupole and TOP analyzers described in Sect. 3.2.2, the most important types of mass analyzer used in common dynamic SIMS instruments employ a magnetic-sector field. 

Instruments are available that can perform MS/MS type experiments using a single analyzer. These instruments trap and manipulate ions in a trapping cell, which also serves as the mass analyzer. The ion trap and fourier transform ion cyclotron resonance (FT-ICR) mass spectrometers are examples. 

Tandem mass spectrometry (MS-MS) uses more than one mass analyzer for structural and sequencing studies that have been found very useful for anthocyanin characterization. These mass analyzers may be of the same type (triple or quadru-poie)85,86 Qj. such as ion trap quadrupole, - and quadrupole-time-of-flight... 

Different types of mass analyzers have been used for anthocyanin analysis single or triple quadrupole mass analyzers, TOP mass analyzer,ion trap mass analyzers,and the combination of analyzers cited above. " ... 

Specific surface areas of the catalysts used were determined by nitrogen adsorption (77.4 K) employing BET method via Sorptomatic 1900 (Carlo-Erba). X-ray difiraction (XRD) patterns of powdered catalysts were carried out on a Siemens D500 (0 / 20) dififactometer with Cu K monochromatic radiation. For the temperature-programmed desorption (TPD) experiments the catalyst (0.3 g) was pre-treated at diflferent temperatures (100-700 °C) under helium flow (5-20 Nml min ) in a micro-catalytic tubular reactor for 3 hours. The treated sample was exposed to methanol vapor (0.01-0.10 kPa) for 2 hours at 260 °C. The system was cooled at room temperature under helium for 30 minutes and then heated at the rate of 4 °C min . Effluents were continuously analyzed using a quadruple mass spectrometer (type QMG420, Balzers AG). 

Mass analyzers interrogate and resolve ions produced by an ion source based on their m/z ratios. Several types of mass analyzers are utilized for proteomic analysis including time-of-flight (TOF) quadrupoles, ion traps, and Fourier transform ion cyclotron resonance (FTICR). Mass analyzers may be assembled in hybrid configurations. MS instruments such as quadrupole TOF and quadra-pole ion trap-FTICR facilitate diversified applications and achieved great success. 

There are now several different types of machines that are all capable of microanalysis. All have advantages and disadvantages, but the choice of which to use is often governed by expense and availability to a particular institution. Electron probe microanalysis is by far the most popular, but here particle-induced X-ray emission (PIXE), the laser microprobe mass analyzer (LAMMA), electron energy loss spectroscopy (EELS), and secondary ion mass spectrometry (SIMS) are also considered. 

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