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Time-of-flight ion-trap

Quadrupole mass spectrometers were used in both the early ICP-MS instrument development research and the first commercial instruments. To date, quadrupole-based ICP-MS instruments continue to be predominant. During the last several years, ICP ion sources have been coupled with mass spectrometers of several different designs, including double-sector, single-sector, time-of-flight, ion trap, and Fourier transform ion cyclotron resonance. [Pg.94]

The ions from the ion beam are separated by their mass to charge ratio (m/z) (where commonlyz= 1), providing the series mi/zi, m2/z2, m3/z3,...mn/Zn that will give the mass spectrum. The ion separation can be done using special ion optics that differentiate the mass spectrometers as follows magnetic sector instruments, quadrupole, time-of-flight, ion trap, Wein filter, ion cyclotron resonance, etc. [Pg.134]

Sheath-flow and nanospray ESI interfaces have successfully coupled CE to almost every mode of MS including the use of quadrupole, time-of-flight, ion-trap, and magnetic sector instruments. CE-MS has been employed in the analysis of a wide range of analytes but has been especially successful in biological assays. The mass selectivity of MS detection is especially useful in complex DNA, protein, and carbohydrate separations. [Pg.354]

Other types of mass spectrometer may use point, array, or both types of collector. The time-of-flight (TOF) instrument uses a special multichannel plate collector an ion trap can record ion arrivals either sequentially in time or all at once a Fourier-transform ion cyclotron resonance (FTICR) instrument can record ion arrivals in either time or frequency domains which are interconvertible (by the Fourier-transform technique). [Pg.201]

Commercial mass analyzers are based almost entirely on quadrupoles, magnetic sectors (with or without an added electric sector for high-resolution work), and time-of-flight (TOE) configurations or a combination of these. There are also ion traps and ion cyclotron resonance instruments. These are discussed as single use and combined (hybrid) use. [Pg.280]

Almost any type of analyzer could be used to separate isotopes, so their ratios of abundances can be measured. In practice, the type of analyzer employed will depend on the resolution needed to differentiate among a range of isotopes. When the isotopes are locked into multielement ions, it becomes difficult to separate all of the possible isotopes. For example, an ion of composition CgHijOj will actually consist of many compositions if all of the isotopes ( C, C, H, H, 0, O, and 0) are considered. To resolve all of these isotopic compositions before measurement of their abundances is difficult. For low-molecular-mass ions (HjO, COj) or for atomic ions (Ca, Cl), the problems are not so severe. Therefore, most accurate isotope ratio measurements are made on low-molecular-mass species, and resolution of these even with simple analyzers is not difficult. The most widely used analyzers are based on magnets, quadrupoles, ion traps, and time-of-flight instruments. [Pg.365]

Electrospray ionization mass spectrometry (ESI-MS) is an analytical method for mass determination of ionized molecules. It is a commonly used method for soft ionization of peptides and proteins in quadmpole, ion-trap, or time-of-flight mass spectrometers. The ionization is performed by application of a high voltage to a stream of liquid emitted from a capillaty. The highly charged droplets are shrunk and the resulting peptide or protein ions are sampled and separated by the mass spectrometer. [Pg.458]

Tandem mass spectrometry (MS/MS) is a method for obtaining sequence and structural information by measurement of the mass-to-charge ratios of ionized molecules before and after dissociation reactions within a mass spectrometer which consists essentially of two mass spectrometers in tandem. In the first step, precursor ions are selected for further fragmentation by energy impact and interaction with a collision gas. The generated product ions can be analyzed by a second scan step. MS/MS measurements of peptides can be performed using electrospray or matrix-assisted laser desorption/ionization in combination with triple quadruple, ion trap, quadrupole-TOF (time-of-flight), TOF-TOF or ion cyclotron resonance MS. Tandem... [Pg.1191]

Martinez Bueno MJM, Agiiera A, Gomez MJ, Hernando MD, Garcia JE, Fernandez-Alba AR (2007) Application of liquid chromatography/quadrupole-linear ion trap mass spectrometry and time-of-flight mass spectrometry to the determination of pharmaceuticals and related contaminants in wastewaters. Anal Chem 79 9372-9384... [Pg.227]

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... [Pg.493]

Rapid scanning mass spectrometers providing unit resolution are routinely used as chroaatographic detectors. Ion separation is accomplished using either a magnetic sector, quadrupole filter or ion trap device. Ions can also be separated by time-of-flight or ion cyclotron resonance mass analyzers but these devices are not widely used with chromatograidiic inlets and will not be discussed here [20]. [Pg.991]

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. [Pg.386]

B magnetic sector E = electric sector Q = quadrupole mass filter ToF = time-of-flight mass spectrometer IT = ion trap FTICR = Fourier-transform ion-cyclotron resonance. [Pg.386]

B, magnetic sector Q, quadrupole mass Hlter ToF, time-of-flight spectrometer IT, ion trap FTICR, Fourier-transform ion-cyclotron resonance. [Pg.387]

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... [Pg.28]

Chien, B. M. Michael, S. M. Fubman, D. M. Enhancement of resolution in matrix-assisted laser desorption using an ion-trap storage/reflectron time-of-flight mass spectrometer. Rapid Comm. Mass Spectrom. 1993, 7,837-843. [Pg.199]

Different mass analysers can be combined with the electrospray ionization source to effect analysis. These include magnetic sector analysers, quadrupole filter (Q), quadrupole ion trap (QIT), time of flight (TOF), and more recently the Fourrier transform ion cyclotron resonance (FTICR) mass analysers. Tandem mass spectrometry can also be effected by combining one or more mass analysers in tandem, as in a triple quadrupole or a QTOF. The first analyzer is usually used as a mass filter to select parent ions that can be fragmented and analyzed by subsequent analysers. [Pg.237]

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. [Pg.262]

Q Quadrupole, IT Ion trap, ToF Time of flight, ICR Ion cyclotron resonance... [Pg.277]

Sectors(EB 8E EBE Quadnipole (Q, QqQ) Ion trap, Orbitrap Time of flight (TOP) Hybrids (BEqQ QTOF.)... [Pg.42]

Magnetic and electrostatic sectors, quadrupole, and time of flight analyzers belong to the first group, while ion trap, Orbitrap and Fourier transform ion cyclotron resonance analyzers separate ions in time. [Pg.54]


See other pages where Time-of-flight ion-trap is mentioned: [Pg.198]    [Pg.921]    [Pg.1085]    [Pg.2869]    [Pg.1434]    [Pg.1457]    [Pg.1433]    [Pg.198]    [Pg.921]    [Pg.1085]    [Pg.2869]    [Pg.1434]    [Pg.1457]    [Pg.1433]    [Pg.1232]    [Pg.69]    [Pg.32]    [Pg.2390]    [Pg.12]    [Pg.189]    [Pg.195]    [Pg.251]    [Pg.1029]    [Pg.468]    [Pg.101]    [Pg.55]    [Pg.440]    [Pg.58]    [Pg.61]    [Pg.68]    [Pg.358]    [Pg.385]    [Pg.455]    [Pg.162]    [Pg.48]    [Pg.277]   
See also in sourсe #XX -- [ Pg.237 , Pg.238 , Pg.262 ]




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Ion trapping

Quadrupole ion trap -time of flight mass spectrometer

Time-of-flight

Trapped ions

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