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Mass plasma

The situation is similar for class-2 states, involving asymptotically free fragments that conserve the total charge and mass. Plasma states can be represented by linear combinations of class-2 basis functions, whereas the individual fragments themselves can be described by class-1 states for a subset of electrons and PCBs. [Pg.278]

Ferrando, A.A., Green, N.R. The effect of boron supplementation on lean body mass, plasma testosterone levels, and strength in male bodybuilders. Int. J. Sport Nutr. 1993 3 140-149. [Pg.85]

Mass spectrometric investigations of the ionosphere show an abundance of molecular ions such as NO and watercluster ions [4T ]. This is an indication of the result of ion-molecule reactions which change the chemical state of the ions in this plasma ... [Pg.2809]

Much of the energy deposited in a sample by a laser pulse or beam ablates as neutral material and not ions. Ordinarily, the neutral substances are simply pumped away, and the ions are analyzed by the mass spectrometer. To increase the number of ions formed, there is often a second ion source to produce ions from the neutral materials, thereby enhancing the total ion yield. This secondary or additional mode of ionization can be effected by electrons (electron ionization, El), reagent gases (chemical ionization. Cl), a plasma torch, or even a second laser pulse. The additional ionization is often organized as a pulse (electrons, reagent gas, or laser) that follows very shortly after the... [Pg.10]

The positive column is a region in which atoms, electrons, and ions are all present together in similar numbers, and it is referred to as a plasma. Again, as with the corona discharge, in mass spectrometry, plasmas are usually operated in gases at or near atmospheric pressure. [Pg.34]

Particularly in mass spectrometry, where discharges are used to enhance or produce ions from sample materials, mostly coronas, plasmas, and arcs are used. The gas pressure is normally atmospheric, and the electrodes are arranged to give nonuniform electric fields. Usually, coronas and plasmas are struck between electrodes that are not of similar shapes, complicating any description of the discharge because the resulting electric-field gradients are not uniform between the electrodes. [Pg.38]

The various stages of this process depend critically on the type of gas, its pressure, and the configuration of the electrodes. (Their distance apart and their shapes control the size and shape of the applied electric field.) By controlling the various parameters, the discharge can be made to operate as a corona, a plasma, or an arc at atmospheric pressure. All three discharges can be used as ion sources in mass spectrometry. [Pg.43]

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). [Pg.87]

The end or front of the plasma flame impinges onto a metal plate (the cone or sampler or sampling cone), which has a small hole in its center (Figure 14.2). The region on the other side of the cone from the flame is under vacuum, so the ions and neutrals passing from the atmospheric-pressure hot flame into a vacuum space are accelerated to supersonic speeds and cooled as rapid expansion occurs. A supersonic jet of gas passes toward a second metal plate (the skimmer) containing a hole smaller than the one in the sampler, where ions pass into the mass analyzer. The sampler and skimmer form an interface between the plasma flame and the mass analyzer. A light... [Pg.88]

The cold plasmas tend to be unstable, are sometimes difficult to maintain, and provide ion yields that are less than those of the hot plasmas. To obviate the difficulties of the interfering isobaric molecular ions from hot plasmas, it has been found highly beneficial to include a collision cell (hexapole see Chapter 22) before the mass analyzer itself. This collision cell contains a low pressure of hydrogen gas. lon/molecule collisions between the hydrogen and, for example, ArO+... [Pg.94]

Ions produced in the plasma must be transferred to a mass analyzer. The flame is very hot and at atmospheric pressure, but the mass analyzer is at room temperature and under vacuum. To effect transfer of ions from the plasma to the analyzer, the interface must be as efficient as possible if ion yields from the plasma are to be maintained in the analyzer. [Pg.95]

After the skimmer, the ions must be prepared for mass analysis, and electronic lenses in front of the analyzer are used to adjust ion velocities and flight paths. The skimmer can be considered to be the end of the interface region stretching from the end of the plasma flame. Some sort of light stop must be used to prevent emitted light from the plasma reaching the ion collector in the mass analyzer (Figure 14.2). [Pg.95]

The two major difficulties facing the analyst/mass spectrometrist concern firstly how to get the whole of the sample into the plasma flame efficiently and secondly how to do so without destabilizing or extinguishing the flame. Although plasma flames operate at temperatures of 6000 to 8000 K, the mass of gas in the flame is very small, and its thermal capacity is correspondingly small (Figure 15.1). [Pg.97]

Fundamentally, introduction of a gaseous sample is the easiest option for ICP/MS because all of the sample can be passed efficiently along the inlet tube and into the center of the flame. Unfortunately, gases are mainly confined to low-molecular-mass compounds, and many of the samples that need to be examined cannot be vaporized easily. Nevertheless, there are some key analyses that are carried out in this fashion the major one i.s the generation of volatile hydrides. Other methods for volatiles are discussed below. An important method of analysis uses lasers to vaporize nonvolatile samples such as bone or ceramics. With a laser, ablated (vaporized) sample material is swept into the plasma flame before it can condense out again. Similarly, electrically heated filaments or ovens are also used to volatilize solids, the vapor of which is then swept by argon makeup gas into the plasma torch. However, for convenience, the methods of introducing solid samples are discussed fully in Part C (Chapter 17). [Pg.98]

To examine a sample by inductively coupled plasma mass spectrometry (ICP/MS) or inductively coupled plasma atomic-emission spectroscopy (ICP/AES) the sample must be transported into the flame of a plasma torch. Once in the flame, sample molecules are literally ripped apart to form ions of their constituent elements. These fragmentation and ionization processes are described in Chapters 6 and 14. To introduce samples into the center of the (plasma) flame, they must be transported there as gases, as finely dispersed droplets of a solution, or as fine particulate matter. The various methods of sample introduction are described here in three parts — A, B, and C Chapters 15, 16, and 17 — to cover gases, solutions (liquids), and solids. Some types of sample inlets are multipurpose and can be used with gases and liquids or with liquids and solids, but others have been designed specifically for only one kind of analysis. However, the principles governing the operation of inlet systems fall into a small number of categories. This chapter discusses specifically substances that are normally liquids at ambient temperatures. This sort of inlet is the commonest in analytical work. [Pg.103]

The nebulization concept has been known for many years and is commonly used in hair and paint spays and similar devices. Greater control is needed to introduce a sample to an ICP instrument. For example, if the highest sensitivities of detection are to be maintained, most of the sample solution should enter the flame and not be lost beforehand. The range of droplet sizes should be as small as possible, preferably on the order of a few micrometers in diameter. Large droplets contain a lot of solvent that, if evaporated inside the plasma itself, leads to instability in the flame, with concomitant variations in instrument sensitivity. Sometimes the flame can even be snuffed out by the amount of solvent present because of interference with the basic mechanism of flame propagation. For these reasons, nebulizers for use in ICP mass spectrometry usually combine a means of desolvating the initial spray of droplets so that they shrink to a smaller, more uniform size or sometimes even into small particles of solid matter (particulates). [Pg.106]

In practice, direct insertion of samples requires a somewhat more elaborate arrangement than might be supposed. The sample must be placed on an electrode before insertion into the plasma flame. However, this sample support material is not an electrode in the usual meaning of the term since no electrical current flows through it. Heating of the electrode is done by the plasma flame. The electrode or probe should have small thermal mass so it heats rapidly, and it must be stable at the high temperatures reached in the plasma flame. For these reasons, the sort of materials used... [Pg.114]

Samples to be examined by inductively coupled plasma and mass spectrometry (ICP/MS) are commonly in the form of a solution that is transported into the plasma flame. The thermal mass of the flame is small, and ingress of excessive quantities of extraneous matter, such as solvent, would cool the flame and might even extinguish it. Even cooling the flame reduces its ionization efficiency, with concomitant effects on the accuracy and detection limits of the ICP/MS method. Consequently, it is necessary to remove as much solvent as possible which can be done by evaporation off-line or done on-line by spraying the solution as an aerosol into the plasma flame. [Pg.137]

The term nebulizer is used generally as a description for any spraying device, such as the hair spray mentioned above. It is normally applied to any means of forming an aerosol spray in which a volume of liquid is broken into a mist of vapor and small droplets and possibly even solid matter. There is a variety of nebulizer designs for transporting a solution of analyte in droplet form to a plasma torch in ICP/MS and to the inlet/ionization sources used in electrospray and mass spectrometry (ES/MS) and atmospheric-pressure chemical ionization and mass spectrometry (APCI/MS). [Pg.138]


See other pages where Mass plasma is mentioned: [Pg.198]    [Pg.343]    [Pg.561]    [Pg.313]    [Pg.646]    [Pg.268]    [Pg.646]    [Pg.198]    [Pg.343]    [Pg.561]    [Pg.313]    [Pg.646]    [Pg.268]    [Pg.646]    [Pg.2796]    [Pg.2796]    [Pg.2930]    [Pg.4]    [Pg.29]    [Pg.44]    [Pg.56]    [Pg.72]    [Pg.73]    [Pg.87]    [Pg.88]    [Pg.89]    [Pg.92]    [Pg.94]    [Pg.96]    [Pg.97]    [Pg.101]    [Pg.105]    [Pg.135]    [Pg.135]    [Pg.136]   
See also in sourсe #XX -- [ Pg.3 ]




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Basic plasma mass spectrometry

Coupled Plasma Mass Spectrometry

Coupled Plasma Mass Spectrometry (ICP-MS)

Detection plasma mass spectrometry

Determination of Trace Elements and Elemental Species Using Isotope Dilution Inductively Coupled Plasma Mass Spectrometry

Direct current plasma mass spectrometr

Discriminator inductively coupled plasma-mass

Electrothermal vaporization inductively coupled plasma mass spectrometry

Elemental analysis by atomic emission and mass spectrometry with inductively coupled plasmas

Elemental mass spectrometry inductively coupled plasma

Femtosecond-laser ablation-inductively coupled-plasma mass spectrometry

Helium microwave-induced plasma mass

Helium microwave-induced plasma mass spectrometry

High performance liquid inductively coupled plasma-mass

High-performance liquid chromatography-inductively coupled plasma mass

High-performance liquid chromatography-inductively coupled plasma mass spectrometry

High-resolution inductively coupled plasma mass spectrometry

Houk Elemental Analysis by Atomic Emission and Mass Spectrometry with Inductively Coupled Plasmas

ICP-MS (inductively coupled plasma mass spectroscopy

ICP-MS (inductively coupled plasma-mass

Induction coupled plasma mass spectrometry

Inductive Coupled Plasma Mass Spectrometer

Inductive Coupled Plasma Mass Spectrometer ICP-MS)

Inductive coupled plasma mass spectrometry

Inductive coupled plasma mass spectrometry ICP-MS)

Inductive coupled plasma with mass

Inductive coupled plasma with mass spectrometry

Inductively Coupled Plasma Mass Spectrometers (ICP-MS)

Inductively Coupled Plasma Mass Spectrometry Handbook Edited by Simon M. Nelms

Inductively Coupled Plasma Mass Spectrometry Handbook Edited by Simon M. Nelms 2005 Blackwell Publishing Ltd. ISBN

Inductively Coupled Plasma Mass Spectrometry ICPMS)

Inductively couple plasma mass spectrometry

Inductively couple plasma mass spectrometry ICP-MS)

Inductively coupled plasma atomic emission mass

Inductively coupled plasma atomic emission mass spectrometry

Inductively coupled plasma detectors mass spectrometry

Inductively coupled plasma isotope mass analysers

Inductively coupled plasma isotope mass discrimination

Inductively coupled plasma isotope quadrupole mass

Inductively coupled plasma mass

Inductively coupled plasma mass Imaging

Inductively coupled plasma mass applications

Inductively coupled plasma mass characteristics

Inductively coupled plasma mass detection limits

Inductively coupled plasma mass detectors

Inductively coupled plasma mass external calibration

Inductively coupled plasma mass hydride generation

Inductively coupled plasma mass instrumentation

Inductively coupled plasma mass interface system

Inductively coupled plasma mass interferences

Inductively coupled plasma mass internal standard calibration

Inductively coupled plasma mass isobaric interferences

Inductively coupled plasma mass isotopic tracer techniques

Inductively coupled plasma mass multiple-collector

Inductively coupled plasma mass particle distribution

Inductively coupled plasma mass precision limitations

Inductively coupled plasma mass quantification procedures

Inductively coupled plasma mass reference materials

Inductively coupled plasma mass resolution

Inductively coupled plasma mass resonance

Inductively coupled plasma mass sample introduction system

Inductively coupled plasma mass schematic

Inductively coupled plasma mass sector

Inductively coupled plasma mass sector-field

Inductively coupled plasma mass semi-quantitative analysis

Inductively coupled plasma mass semiquantitative analysis

Inductively coupled plasma mass spectrometiy

Inductively coupled plasma mass spectrometric

Inductively coupled plasma mass spectrometric ICP-MS) detection

Inductively coupled plasma mass spectrometry

Inductively coupled plasma mass spectrometry ICP/MS)

Inductively coupled plasma mass spectrometry analytical performance

Inductively coupled plasma mass spectrometry detection limit

Inductively coupled plasma mass spectrometry instrument

Inductively coupled plasma mass spectrometry laser ablation-ICPMS

Inductively coupled plasma mass spectrometry nebulizers used

Inductively coupled plasma mass spectrometry sample preparation

Inductively coupled plasma mass spectrometry solutions introduced into

Inductively coupled plasma mass spectrometry spectral interferences

Inductively coupled plasma mass spectrometry, ICP

Inductively coupled plasma mass spectrometry, determination

Inductively coupled plasma mass spectroscopic interferences

Inductively coupled plasma mass spectroscopy

Inductively coupled plasma mass standard addition calibration

Inductively coupled plasma mass techniques

Inductively coupled plasma mass uncertainty

Inductively coupled plasma mass vacuum system

Inductively coupled plasma optical emission spectrometry-mass

Inductively coupled plasma sector field mass spectrometry

Inductively coupled plasma spectroscopy/mass spectrometric detection

Inductively coupled plasma time-of-flight mass

Inductively coupled plasma time-of-flight mass spectrometry

Inductively coupled plasma-mass spectrometer

Inductively coupled plasma-mass spectrometry analysis

Inductively coupled plasma-mass spectrometry characteristics

Inductively coupled plasma-mass spectrometry instrumentation

Inductively coupled plasma-mass spectrometry interferences

Inductively coupled plasma-mass spectrometry, lead analysis

Inductively coupled plasma-mass spectrophotometry

Inductively coupled-plasma mass spectrometry spectroscopy

Instrumentation plasma mass spectrometry

Interface inductively coupled plasma-mass

Interferences plasma mass spectrometry

Iron plasma-mass spectrometry

Isotope dilution inductively coupled plasma-mass

Isotope dilution inductively coupled plasma-mass spectrometry

Isotope plasma mass spectrometry

Isotopic Analysis via Multi-Collector Inductively Coupled Plasma Mass Spectrometry in Elemental Speciation

Laser Ablation Inductively Coupled Plasma Mass Spectrometers (LA-ICP-MS)

Laser ablation inductively coupled plasma isotope dilution mass spectrometry

Laser ablation inductively coupled plasma mass analytical performance

Laser ablation inductively coupled plasma mass sample preparation

Laser ablation inductively coupled plasma-mass

Laser ablation inductively coupled plasma-mass spectrometry

Laser ablation multicollector inductively coupled plasma mass spectrometry

Laser inductively coupled plasma-mass

Laser inductively coupled plasma-mass spectrometry

Limit plasma mass spectrometry

Liquid chromatography-inductively coupled plasma mass

Liquid chromatography-inductively coupled plasma mass detection

Liquids inductively coupled plasma-mass

Magnetic sector inductively coupled plasma mass

Magnetic sector inductively coupled plasma mass spectrometry , determination

Mass Spectrometry Combined with Inductively Coupled Plasma

Mass spectrometry 252Cf plasma

Mass spectrometry samples plasma

Mass spectroscopy plasma/glow discharge

Memory effects, plasma mass spectrometry

Microwave plasma mass spectrometry

Microwave-induced plasma mass spectrometry

Multi-collector inductively coupled plasma mass spectrometry

Multicollector-inductively coupled plasma-mass

Multicollector-inductively coupled plasma-mass spectrometry

Multiple collector inductively coupled plasma mass spectrometry

Peptides plasma desorption mass spectrometry

Plasma Analysis of Benazepril Using Gas Chromatography with Mass-Selective Detection (GC-MSD)

Plasma Ionization Mass Spectrometry

Plasma desorption mass spectra

Plasma desorption mass spectrometer

Plasma desorption mass spectrometry

Plasma desorption mass spectrometry PDMS)

Plasma desorption mass spectrometry analysis

Plasma desorption mass spectrometry proteins

Plasma desorption mass spectroscopy

Plasma ionization multicollector mass spectrometry

Plasma mass spectrometry

Plasma mass spectrum

Plasma neutral species, mass spectra

Plasma source ion trap mass

Plasma source ion trap mass spectrometer

Plasma-mass spectrometry, inductively

Plasma-source mass spectrometry

Pneumatic nebulization inductively coupled plasma mass

Pneumatic nebulization inductively coupled plasma mass spectrometry

Quadrupole inductively coupled plasma mass

Quadrupole inductively coupled plasma mass spectrometry

Quadrupole plasma mass spectrometry

Quadrupole-based inductively coupled plasma mass spectrometry

Qualitative analysis inductively coupled plasma-mass

Sample inductively coupled plasma-mass

Single-collector inductively coupled plasma mass spectrometry

Solids inductively coupled plasma-mass

Source inductively coupled plasma-mass

The Plasma Desorption Mass Spectrometer

Trace elements inductively coupled plasma-mass

Ultrasonic plasma mass spectrometry

Vapor phase decomposition inductively coupled plasma mass spectrometry

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