Mass spectrometers configuration

Mass spectrometer configuration. Multianalyzer instruments should be named for the analyzers in the sequence in which they are traversed by the ion beam, where B is a magnetic analyzer, E is an electrostatic analyzer, Q is a quadrupole analyzer, TOP is a time-of-flight analyzer, and ICR is an ion cyclotron resonance analyzer. For example BE mass spectrometer (reversed-geometry double-focusing instrument), BQ mass spectrometer (hybrid sector and quadrupole instrument), EBQ (double-focusing instrument followed by a quadrupole). 

Various mass spectrometer configurations have been used for the detection of explosives, such as ion traps, quadrupoles and time-of flight mass analyzers and combinations as MS/MS systems. The ionization method is usually APCI with corona discharge [24, 25]. An example is given in Figure 20, which shows the schematic diagram of an explosive mass spectrometer detector [25]. It is based on an ion trap mass analyzer, an APCI source with corona discharge and a counter-flow introduction (CFI) system. The direction of the sample gas flow introduced into the ion source is opposite to that of the ion flow produced by the ion source. 

Various mass spectrometer configurations have been used for the detection of explosives, such as ion traps, quadrupoles, and time-of-flight (TOF) analyzers and tandem mass spectrometer (MS/MS) combinations. Also, various modes of ionization have been employed, depending on the specific application in the detection of explosives. 

The ion source used for the generation of biomolecular parent ions is critical, and only recently have the so-called soft ionization methods been developed.2 Electron-impact ionization sources fall into the category of hard sources, whereby the sample must be in the vapor phase initially, and the ionization process produces a very large number of fragments. Soft methods were introduced to overcome the problems associated with the thermal instability and involatility of macromolecular analytes. Soft ionization produces few fragments under relatively mild conditions. In Table 15.1 a comparison is shown between the three main soft ionization methods some of these values are strongly dependent on individual mass spectrometer configurations and the desired resolution. 

Refer to Figures 19-48 to 19-51, p. 209, for the details of the rest of the mass spectrometer configuration. 

A typical mass spectrometer configuration is shown in Figure 10.1 [1]. The main components are briefly discussed in the following [1] ... 

Aside from the smgle mass filter, the most connnon configuration for quadnipole mass spectrometers is the triple-quadnipole instrument. This is the simplest tandem mass spectrometer using quadnipole mass filters. Typically, the... 

Typical MS/MS configuration. Ions produced from a source (e.g., dynamic FAB) are analyzed by MS(1). Molecular ions (M or [M + H]+ or [M - H]", etc.) are selected in MS(1) and passed through a collision cell (CC), where they are activated by collision with a neutral gas. The activation causes some of the molecular ions to break up, and the resulting fragment ions provide evidence of the original molecular structure. The spectrum of fragment ions is mass analyzed in the second mass spectrometer, MS(2). 

In Dynamic Secondary Ion Ma s Spectrometry (SIMS), a focused ion beam is used to sputter material from a specific location on a solid surface in the form of neutral and ionized atoms and molecules. The ions are then accelerated into a mass spectrometer and separated according to their mass-to-charge ratios. Several kinds of mass spectrometers and instrument configurations are used, depending upon the type of materials analyzed and the desired results. 

Each type of mass spectrometer has its associated advantages and disadvantages. Quadrupole-based systems offer a fairly simple ion optics design that provides a certain degree of flexibility with respect to instrument configuration. For example, quadrupole mass filters are often found in hybrid systems, that is, coupled with another surface analytical method, such as electron spectroscopy for chemical analysis or scanning Auger spectroscopy. 

It is possible to measure equilibrium constants and heats of reaction in the gas phase by using mass spectrometers of special configuration. With proton-transfer reactions, for example, the equilibrium constant can be determined by measuring the ratio of two reactant species competing for protons. Table 4.13 compares of phenol ionizations. 

Qualitative or quantitative mass spectrometric analysis can be made by one of two alternative configurations. Either the sample is decomposed in the high vacuum chamber of the mass spectrometer (MS) itself or reaction proceeds in an external system at higher pressure (e.g. a microbalance)... 

Figure 3.6 Schematics of three configurations of mass spectrometer capable of accurate mass measurement (a) forward-geometry (b) reverse-geometry (c) tri-sector. From applications literature published by Micromass UK Ltd, Manchester, UK, and reproduced with permission.

What is the configuration of a Q-ToF mass spectrometer and what are its anaiyticai strengths ... 

Various tandem MS instrument configurations have been developed, e.g. sector instruments, such as CBCE, CBCECB or CECBCE, and hybrid instruments, e.g. BCECQQ (B = magnetic sector analyser, E = electrostatic analyser, C = collision cell, Q = quadrupole mass spectrometer), all with specific performance. Sector mass spectrometers have been reviewed [168],... 

The quadrupole mass filter is the most abundant mass analyser today and RF-only multipoles are used as transmission devices/collision regions in various instrumental configurations. The mass filter is used extensively as a stand-alone mass analyser and as an analyser in multistage mass spectrometers. 

FTIR in multiply hyphenated systems may be either off-line (with on-line collection of peaks) [666,667] or directly on-line [668,669]. Off-line techniques may be essential for minor components in a mixture, where long analysis times are required for FT-based techniques (NMR, IR), or where careful optimisation of the response is needed. In an early study a prototype configuration comprised SEC, a triple quadrupole mass spectrometer, off-line evaporative FTIR with splitting after UV detection see Scheme 7.12c [667]. Off-line IR spectroscopy (LC Transform ) provides good-quality spectra with no interferences from the mobile phase and the potential for very high sensitivity. Advanced approaches consist of an HPLC system incorporating a UV diode array, FTIR (using an ATR flow-cell to obtain on-flow IR spectra), NMR and ToF-MS. 

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... 

It should be pointed out that FAB, MALDI, and ESI can be used to provide ions for peptide mass maps or for microsequencing and that any kind of ion analyzer can support searches based only on molecular masses. Fragment or sequence ions are provided by instruments that can both select precursor ions and record their fragmentation. Such mass spectrometers include ion traps, Fourier transform ion cyclotron resonance, tandem quadrupole, tandem magnetic sector, several configurations of time-of-flight (TOF) analyzers, and hybrid systems such as quadrupole-TOF and ion trap-TOF analyzers. 

Topics which will be presented in this chapter include the hardware, software, automation, valve and column configurations, and integration used in comprehensive 2DLC. Aspects of the 2DLC experiment in conjunction with multichannel detectors such as UV diode array optical detectors and mass spectrometers are discussed along with the handling of the data, which is expected to expand in scope in the future as chemometric methods are more widely used for data analysis. 

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