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Atmospheric-pressure chemical

One of the first successful techniques for selectively removing solvent from a solution without losing the dissolved solute was to add the solution dropwise to a moving continuous belt. The drops of solution on the belt were heated sufficiently to evaporate the solvent, and the residual solute on the belt was carried into a normal El (electron ionization) or Cl (chemical ionization) ion source, where it was heated more strongly so that it in turn volatilized and could be ionized. However, the moving-belt system had some mechanical problems and could be temperamental. The more recent, less-mechanical inlets such as electrospray have displaced it. The electrospray inlet should be compared with the atmospheric-pressure chemical ionization (APCI) inlet, which is described in Chapter 9. [Pg.55]

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]

The LC/TOF instmment was designed specifically for use with the effluent flowing from LC columns, but it can be used also with static solutions. The initial problem with either of these inlets revolves around how to remove the solvent without affecting the substrate (solute) dissolved in it. Without this step, upon ionization, the large excess of ionized solvent molecules would make it difficult if not impossible to observe ions due only to the substrate. Combined inlet/ionization systems are ideal for this purpose. For example, dynamic fast-atom bombardment (FAB), plas-maspray, thermospray, atmospheric-pressure chemical ionization (APCI), and electrospray (ES)... [Pg.163]

El = electron ionization Cl = chemical ionization ES = electrospray APCI = atmospheric-pressure chemical ionization MALDI = matrix-assisted laser desorption ionization PT = plasma torch (isotope ratios) TI = thermal (surface) ionization (isotope ratios). [Pg.280]

Electrospray Ionization (ES) and Atmospheric Pressure Chemical Ionization (APCI)... [Pg.283]

Thus, either the emitted light or the ions formed can be used to examine samples. For example, the mass spectrometric ionization technique of atmospheric-pressure chemical ionization (APCI) utilizes a corona discharge to enhance the number of ions formed. Carbon arc discharges have been used to generate ions of otherwise analytically intractable inorganic substances, with the ions being examined by mass spectrometry. [Pg.388]

Samples containing mixtures of peptides can be analyzed directly by electrospray. Alternatively, the peptides can be separated and analyzed by LC/MS coupling techniques such as electrospray or atmospheric pressure chemical ionization (APCI). [Pg.417]

The ion guides are frequently used to transmit ions from an atmospheric-pressure inlet/source system (electrospray ionization, atmospheric-pressure chemical ionization) into the vacuum region of an m/z analyzer. [Pg.426]

AIR. (atmospheric) air, a standard for nitrogen and chlorine isotopes APCL atmospheric-pressure chemical ionization, also called plasmaspray API. atmospheric-pressure ionization... [Pg.445]

Pure Elements. AH of the hehum-group elements are colorless, odorless, and tasteless gases at ambient temperature and atmospheric pressure. Chemically, they are nearly inert. A few stable chemical compounds are formed by radon, xenon, and krypton, but none has been reported for neon and belium (see Helium GROUP, compounds). The hehum-group elements are monoatomic and are considered to have perfect spherical symmetry. Because of the theoretical interest generated by this atomic simplicity, the physical properties of ah. the hehum-group elements except radon have been weU studied. [Pg.5]

A liquid chromatography-mass spectrometry (LC-MS) method that can quantitatively analyze urinar y normal and modified nucleosides in less than 30 min with a good resolution and sufficient sensitivity has been developed. Nineteen kinds of normal and modified nucleosides were determined in urine samples from 10 healthy persons and 18 breast cancer patients. Compounds were separ ated on a reverse phase Kromasil C18 column (2.1 mm I.D.) by isocratic elution mode using 20 mg/1 ammonium acetate - acetonitrile (97 3 % v/v) at 200 p.l/min. A higher sensitivity was obtained in positive atmospheric pressure chemical ionization mode APCI(-i-). [Pg.351]

An on-line chromatography/atmospheric pressure chemical ionization tandem mass spectrometry (LC-APCI/MS/MS) methods was developed for rapid screen of pharmacokinetics of different drugs, including 5 (98RCM1216). The electron impact mass spectrum of 5 and ethyl 9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7Ff-pyrido[l,2,3- fe]-l,4-benzoxazine-6-carboxylate was reported (97MI28). Electron impact/Fourier transform... [Pg.268]

I. Fener, V. Pichon, M-C. Hennion and D. Barcelo, Automated sample preparation with exti action columns by means of anti-isoproturon immunosorbents foi the determination of phenylurea herbicides in water followed by liquid chi omatography-diode aixay detection and liquid cliromatogi aphy-atmospheric pressure chemical ionization mass spectrometiy , 7. Chromatogr. 777 91-98 (1997). [Pg.132]

P Dugo, L. Mondello, E. Sebastian , R. Ottana, G. Eirante and G. Dugo, Identification of minor oxygen heterocyclic compounds of citi us essential oils by liquid chromatography-atmospheric pressure chemical ionisation mass specti ometiy , J. Liq. Chromatogr. 22 2991-3005 (1999). [Pg.133]

B. Herbreteau, A. Salvador, M. Lafosse and M. Dreux, SFC with evaporative lightscattering detection and atmospheric-pressure chemical-ionisation mass specti ometiy for methylated glucoses and cyclodextiins analysis, Analusis 27 706-712 (1999). [Pg.169]

C. Aguilar, I. Feirer, R Bonnll, R. M. Marce and D. Barcelo, Monitoring of pesticides in river water based on samples previously stored in polymeric cartridges followed by on-line solid-phase extraction-liquid cliromatography-diode array detection and confirmation by atmospheric pressure chemical ionization mass spectrometry . Anal. Chim. Acta 386 237-248 (1999). [Pg.374]

S. Lacorte and D. Barcelo, Determination of parts per trillion levels of organophospho-rus pesticides in groundwater by automated on-line liquid- solid extraction followed by liquid chr omatography/atmospheric pressure chemical ionization mass spectrometry using positive and negative ion modes of operation . Anal. Chem. 68 2464- 2470 (1996). [Pg.374]

D. Puig, L. Silgoner, M. Grasserbauer and D. Barcelo, Part-per-trillion level determination of priority methyl-, nirto-, and clilor ophenols in river water samples by automated online liquid/solid exrtaction followed by liquid chr omatography/mass spectr ometry using atmospheric pressure chemical ionization and ion spray interfaces . Anal. Chem. 69 2756-2761 (1997). [Pg.374]

I. Eeirer, M. C. Hennion and D. Barcelo, Immunosorbents coupled on-line with liquid chi omatography/atmospheric pressure chemical ionization/mass specti ometiy for the part per trillion level determination of pesticides in sediments and natural waters using low preconcenti ation volumes . Anal. Chem. 69 4508-4514 (1997). [Pg.375]

Atmospheric pressure chemical ionization (APCI) Chemical ionization at atmospheric pressure. [Pg.372]

A number of analytical techniques such as FTIR spectroscopy,65-66 13C NMR,67,68 solid-state 13 C NMR,69 GPC or size exclusion chromatography (SEC),67-72 HPLC,73 mass spectrometric analysis,74 differential scanning calorimetry (DSC),67 75 76 and dynamic mechanical analysis (DMA)77 78 have been utilized to characterize resole syntheses and crosslinking reactions. Packed-column supercritical fluid chromatography with a negative-ion atmospheric pressure chemical ionization mass spectrometric detector has also been used to separate and characterize resoles resins.79 This section provides some examples of how these techniques are used in practical applications. [Pg.407]

Textured Tin Oxide Films Produced by Atmospheric Pressure Chemical Vapor Deposition from Tetramethyltin and Their Usefulness in Producing Light Trapping in Thin-Film Amorphous Silicon Solar Energy Mater., 18 263-281 (1989)... [Pg.106]

Atmospheric Pressure Chemical Vapor Deposition of Tungsten suicide, " J. Electrochem. Soc., 137(5) 1623-1626 (May 1990)... [Pg.342]

In the following chapters, the basic principles of HPLC and MS, in as far as they relate to the LC-MS combination, will be discussed and seven of the most important types of interface which have been made available commercially will be considered. Particular attention will be paid to the electrospray and atmospheric-pressure chemical ionization interfaces as these are the ones most widely used today. The use of LC-MS for identification and quantitation will be described and appropriate applications will be discussed. [Pg.23]

The pump must provide stable flow rates from between 10 ttlmin and 2 mlmin with the LC-MS requirement dependent upon the interface being used and the diameter of the HPLC column. For example, the electrospray interface, when used with a microbore HPLC column, operates at the bottom end of this range, while with a conventional 4.6 mm column such an interface usually operates towards the top end of the range, as does the atmospheric-pressure chemical ionization (APCI) interface. The flow rate requirements of the different interfaces are discussed in the appropriate section of Chapter 4. [Pg.27]

Ionization methods that may be utihzed in LC-MS include electron ionization (El), chemical ionization (Cl), fast-atom bombardment (FAB), thermospray (TSP), electrospray (ESI) and atmospheric-pressure chemical ionization (APCI). [Pg.52]

Cl is not the only ionization technique where this aspect of interpretation must be considered carefully fast-atom bombardment, thermospray, electrospray and atmospheric-pressure chemical ionization, described below in Sections 3.2.3, 4.6, 4.7 and 4.8, respectively, all produce adducts in the molecular ion region of their spectra. [Pg.54]


See other pages where Atmospheric-pressure chemical is mentioned: [Pg.38]    [Pg.60]    [Pg.71]    [Pg.73]    [Pg.163]    [Pg.277]    [Pg.377]    [Pg.248]    [Pg.218]    [Pg.359]    [Pg.37]    [Pg.52]    [Pg.7]    [Pg.7]    [Pg.14]   
See also in sourсe #XX -- [ Pg.12 , Pg.17 , Pg.42 , Pg.57 , Pg.81 , Pg.89 , Pg.226 , Pg.413 , Pg.419 ]




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APCI (atmospheric-pressure chemical

Atmosphere pressure chemical ionization

Atmosphere pressure chemical ionization APCI)

Atmospheric pressure chemical APPI)

Atmospheric pressure chemical Electrospray ionization

Atmospheric pressure chemical acid derivatives

Atmospheric pressure chemical applications

Atmospheric pressure chemical calibration

Atmospheric pressure chemical comparative studies

Atmospheric pressure chemical desorption methods

Atmospheric pressure chemical environmental pollutants

Atmospheric pressure chemical impurities

Atmospheric pressure chemical ionisation

Atmospheric pressure chemical ionisation APCI)

Atmospheric pressure chemical ionisation-mass spectrometry

Atmospheric pressure chemical ionization , ESI

Atmospheric pressure chemical ionization applications

Atmospheric pressure chemical ionization carotenoid analysis

Atmospheric pressure chemical ionization characterized

Atmospheric pressure chemical ionization chromatography

Atmospheric pressure chemical ionization corona discharge

Atmospheric pressure chemical ionization desorption

Atmospheric pressure chemical ionization flow rate through

Atmospheric pressure chemical ionization heated nebulizer interface

Atmospheric pressure chemical ionization matrix effects

Atmospheric pressure chemical ionization photoionization

Atmospheric pressure chemical ionization process

Atmospheric pressure chemical ionization tandem mass

Atmospheric pressure chemical ionization used with

Atmospheric pressure chemical ionization voltage

Atmospheric pressure chemical ionization-mass

Atmospheric pressure chemical ionization-mass spectrometry

Atmospheric pressure chemical mass analyzers

Atmospheric pressure chemical matrix

Atmospheric pressure chemical matrix effects

Atmospheric pressure chemical method development

Atmospheric pressure chemical mobile phases

Atmospheric pressure chemical photoionization

Atmospheric pressure chemical principles

Atmospheric pressure chemical probe temperature

Atmospheric pressure chemical separation techniques

Atmospheric pressure chemical source-analyzer interfaces

Atmospheric pressure chemical spectrometry

Atmospheric pressure chemical technique)

Atmospheric pressure chemical vapor

Atmospheric pressure chemical vapor deposition

Atmospheric pressure chemical vapour

Atmospheric pressure chemical vapour deposition

Atmospheric pressure metal organic chemical

Atmospheric pressure metal organic chemical vapor deposition

Atmospheric-pressure chemical analysis

Atmospheric-pressure chemical ionization

Atmospheric-pressure chemical ionization APCI)

Atmospheric-pressure chemical ionization advantages

Atmospheric-pressure chemical ionization and mass

Atmospheric-pressure chemical ionization and mass spectrometry

Atmospheric-pressure chemical ionization disadvantages

Atmospheric-pressure chemical ionization inlet

Atmospheric-pressure chemical ionization lipid analysis

Atmospheric-pressure chemical ionization mass spectroscopy

Atmospheric-pressure chemical ionization mechanism

Atmospheric-pressure chemical ionization negative ions produced

Atmospheric-pressure chemical ionization suitability

Atmospheric-pressure chemical ionization techniques

Atmospheric-pressure-chemical-ionization adducts

Atmospheric-pressure-chemical-ionization combined with electrospray interface

Atmospheric-pressure-chemical-ionization flow rates

Atmospheric-pressure-chemical-ionization interface

Atmospheric-pressure-chemical-ionization molecular-weight limit

Atmospheric-pressure-chemical-ionization operation

Chemical pressure

Compounds atmospheric-pressure chemical

Desorption (continued atmospheric pressure chemical

Desorption atmospheric pressure chemical

Desorption atmospheric pressure chemical ionization DAPCI)

Detection systems atmospheric pressure chemical

Electron-capture atmospheric pressure chemical ionization

Experimental atmospheric-pressure chemical

HPLC-atmospheric pressure chemical ionization

HPLC-atmospheric pressure chemical ionization mass spectrometry

Heated nebulizer-atmospheric pressure chemical

Heated nebulizer-atmospheric pressure chemical ionization

High atmospheric pressure chemical

Interface atmospheric-pressure chemical ionisation

Interfaces atmospheric-pressure chemical

Ionization methods atmospheric-pressure chemical

Liquid chromatography-atmospheric pressure chemical ionization

Liquid chromatography/atmospheric pressure chemical

Liquid chromatography—mass atmospheric-pressure chemical

Mass atmospheric pressure chemical

Mass spectrometry detectors atmospheric pressure chemical ionization

Supercritical atmospheric pressure chemical

The Atmospheric-Pressure Chemical Ionization Interface

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