Mass spectrometry quadrupole instruments

In mass spectrometers, ions are analysed according to the ml7. (mass-to-charge) value and not to the mass. While there are many possible combinations of technologies associated with a mass-spectrometry experiment, relatively few forms of mass analysis predominate. They include linear multipoles, such as the quadrupole mass filter, time-of-flight mass spectrometry, ion trapping forms of mass spectrometry, including the quadrupole ion trap and Fourier-transform ion-cyclotron resonance, and sector mass spectrometry. Hybrid instruments intend to combine the strengths of the component analysers. 

Yost, R. A. Boyd, R. K. 1990. Tandem mass spectrometry quadrupole and hybrid instruments. Methods Enzymol., 193,154-200. 

Figure 8 Atomika Dynamic In Depth Analyzer (ADIDA), quadrupole-based-imaging secondary ion mass spectrometry (SIMS) instrument.

Bier, M. E. and Schwartz, J. C., Electrospray ionization quadrupole ion trap mass spectrometry, in Electrospray Ionization Mass Spectrometry Fundamentals, Instrumentation, and Applications, Cole, R. Ed., John Wiley Sons, New York, 1997, chap 7. 

Munson and Field reported in 1966 on a technique of ionizing molecules by gas phase ion-molecule reactions, which they called chemical ionization (Cl). In this way, break-up of the molecules can be greatly reduced or even avoided. Thus, measured ion currents can be correlated with the densities of the respective parent neutral compounds, allowing for on-line monitoring of rather complex gas mixtures. The fundamental principles of gas phase ion chemistry on which Cl is based, as well as the instrumentation for Cl, have been reviewed in great detail by Harrison." The wide variety of Cl methods that has been developed includes Medium Pressure Mass Spectrometry, Fourier Transform Mass Spectrometry, Quadrupole Ion Trap Mass Spectrometry, Pulsed Positive Ion-Negative Ion Chemical Ionization, and Atmospheric Pressure Ionization Mass Spectrometry (API-MS). Of these, API-MS has developed into a very reliable and widely used technique for analysis of VOCs in flavor release studies and human breath. A variety of API-MS applications in these fields of research has been described in a recent volume by Roberts and Taylor. ... 

Volume rv is entitled Theory and Instrumentation and is composed of six parts Fundamentals, New Ion Trapping Techniques, Fourier Transform Mass Spectrometry, Quadrupole Rod Sets, 3D-Quadrupole Ion Trap Mass Spectrometry, and Photochemistry of Trapped Ions. 

Py/GC/MS. pyrolysis, gas chromatography, and mass spectrometry used as a combined technique Py/MS. pyrolysis and mass spectrometry used as a combined technique oa-TOF. orthogonally accelerated time of flight Q. quadrupole field or instrument... 

The most widely regarded approach to accomplish the determination of as many pesticides as possible in as few steps as possible is to use MS detection. MS is considered a universally selective detection method because MS detects all compounds independently of elemental composition and further separates the signal into mass spectral scans to provide a high degree of selectivity. Unlike GC with selective detectors, or even atomic emission detection (AED), GC/MS may provide acceptable confirmation of the identity of analytes without the need for further information. This reduces the need to re-inject a sample into a separate GC system (usually GC/MS) for pesticide confirmation. Through the use of selected ion monitoring (SIM), efficient ion-trap or quadrupole devices, and/or tandem mass spectrometry (MS/MS), modern GC/MS instruments provide LODs similar to or lower than those of selective detectors, depending on the analytes, methods, and detectors. 

Currently PCR and mass spectrometry are performed by two separate instruments. However, there is no reason why PCR followed by simple automated cleanup and mass spectrometry cannot be incorporated into a single integrated instrument. Essentially every configuration of the modern ESI mass spectrometer has been used successfully for the analysis of PCR products, from the highest to the lowest resolution involving. Fourier transform ion cyclotron resonance (FTICR), triple quadrupole, quadrupole-time of flight (Q-TOF), and ion trap.22-24 MS discriminates between two structurally related PCR products by MW difference. Mass accuracy is needed to differentiate the... 

The concept of peak capacity is rather universal in instrumental analytical chemistry. For example, one can resolve components in time as in column chromatography or space, similar to the planar separation systems however, the concept transcends chromatography. Mass spectrometry, for example, a powerful detection method, which is often the detector of choice for complex samples after separation by chromatography, is a separation system itself. Mass spectrometry can separate samples in time when the mass filter is scanned, for example, when the mass-to-charge ratio is scanned in a quadrupole detector. The sample can also be separated in time with a time-of-flight (TOF) mass detector so that the arrival time is related to the mass-to-charge ratio. 

The most important gas phase analytical techniques are mass spectrometry and gas phase chromatography. If the total gas pressure is <10-4-10-8 Torr, a mass spectrometer such an omegatron or a quadrupole instrument may be inserted into the reactant volume. However, in most cases, the pressure is in excess of this, and gas must be delivered to a mass spectrometer via a leak, such as a Metrosil pellet or a capillary constriction, situated as closely as possible to the reaction volume. 

The instrumental analysis for the identification of UV filters degradation products formed during the fungal treatment process was performed by means of HPLC coupled to tandem mass spectrometry using a hybrid quadrupole-time-of-flight mass spectrometer (HPLC-QqTOF-MS/MS). Chromatographic separation was achieved on a Hibar Purospher STAR HR R-18 ec. (50 mm x 2.0 mm, 5 pm, from Merck). In the optimized method, the mobile phase consisted of a mixture of HPLC grade water and acetonitrile, both with 0.15% formic acid. The injection volume was set to 10 pL and the mobile phase flow-rate to 0.3 mL/min. 

Multiple mass analyzers exist that can perform tandem mass spectrometry. Some use a tandem-in-space configuration, such as the triple quadrupole mass analyzers illustrated (Fig.3.9). Others use a tandem-in-time configuration and include instruments such as ion-traps (ITMS) and Fourier transform ion cyclotron resonance mass spectrometry (FTICRMS or FTMS). A triple quadrupole mass spectrometer can only perform the tandem process once for an isolated precursor ion (e.g., MS/MS), but trapping or tandem-in-time instruments can perform repetitive tandem mass spectrometry (MS ), thus adding n 1 degrees of structural characterization and elucidation. When an ion-trap is combined with HPLC and photodiode array detection, the net result is a profiling tool that is a powerful tool for both metabolite profiling and metabolite identification. 

The layout of an ICP-MS is shown schematically in Figure 8.17 and comprises three essential parts the ICP torch, the interface and the mass spectrometer. The ICP torch differs little from that discussed earlier and the mass spectrometer is very similar to those used for organic mass spectrometry and discussed in Chapter 9. Typically a quadrupole instrument would be used. The construction of the interface is shown in Figure 8.18 and is based on the use of a pair of water-cooled cones which divert a portion of the sample stream into the ion optics of the mass spectrometer whence the mass spectrum is produced by standard mass spectrometer operation. Some modern instruments also incorporate a so-... 

TOF analyzers are especially compatible with MALDI ion sources and hence are frequently coupled in aMALDI-TOF configuration. Nevertheless, many commercial mass spectrometers combine ESI with TOF with great success. For proteomics applications, the quadrupole TOF (QqTOF) hybrid instruments with their superior mass accuracy, mass range, and mass resolution are of much greater utility than simple TOF instruments.21,22 Moreover, TOF instruments feature high sensitivity because they can generate full scan data without the necessity for scanning that causes ion loss and decreased sensitivity. Linear mode TOF instruments cannot perform tandem mass spectrometry. This problem is addressed by hybrid instruments that incorporate analyzers with mass selective capability (e.g., QqTOF) in front of a TOF instrument. 

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