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Compounds atmospheric-pressure chemical

In general, APCI is better suited for heteroatom-containing molecules, and electrospray for ionic compounds. Atmospheric pressure chemical ionization is... [Pg.138]

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]

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]

If a high -molecular-weight compound is being studied by LC-MS, the analyst has little choice in the ionization method to use, with atmospheric-pressure chemical ionization (APCl) being wholly inappropriate. However, when low -molecular-weight componnds are involved, both electrospray ionization and APCl are potentially of value. [Pg.242]

Kohler M, NV Heeb (2003) Determination of nitrated phenolic compounds in rain by liquid chromatography/ atmospheric pressure chemical ionization mass spectrometry. Anal Chem 75 3115-3121. [Pg.43]

Most reported triazine LC applications are reversed-phase utilizing C-8 and C-18 analytical columns, but there are also a few normal-phase (NH2,CN) and ion-exchange (SCX) applications. The columns used range from 5 to 25-cm length and from 2 to 4.6-mm i.d., depending on the specific application. In general, the mobile phases employed for reversed-phase applications consist of various methanol and/or acetonitrile combinations in water. The ionization efficiency of methanol and acetonitrile for atmospheric pressure chemical ionization (APcI) applications were compared, and based on methanol s lower proton affinity, the authors speculated that more compounds could be ionized in the positive ion mode when using methanol than acetonitrile in the mobile phase. [Pg.441]

S., Simultaneous determination of urinary cystathionine, lanthionine, S-(2-aminoethyl)-L-cysteine and their cyclic compounds using liquid chromatography-mass spectrometry with atmospheric pressure chemical ionization, /. Chromatogr. B, 698, 301, 1997. [Pg.305]

Various analyzers have been used to analyze phenolic compounds. The choice of the MS analyzer is influenced by the main objective of the study. The triple quadrupole (QqQ) has been used to quantify, applying multiple reaction monitoring experiments, whereas the ion trap has been used for both identification and structure elucidation of phenolic compounds. Moreover, time-of-flight (TOF) and Fourier-transform ion cyclotron resonance (FT-ICR) are mainly recommended for studies focused on obtaining accurate mass measurements with errors below 5 ppm and sub-ppm errors, respectively (Werner and others 2008). Nowadays, hybrid equipment also exists, including different ionization sources with different analyzers, for instance electrospray or atmospheric pressure chemical ionization with triple quadrupole and time-of-flight (Waridel and others 2001). [Pg.60]

In addition to the dissolved elements and compounds in the oceanic water column, a wide variety of water column chemicals are found in marine organisms and organic detritus. For example, a milliliter of surface seawater can contain on the order of 10 million viruses, 1 million bacteria, 100,000 phytoplankton, and 10,000 zooplankton [9]. With the advent of soft ionization processes for mass spectrometry systems, scientists have been able to study these marine organisms at molecular level. The use of electrospray ionization (ESI see Section 2.1.15), atmospheric pressure chemical ionization... [Pg.239]

Currently no comprehensive libraries have been developed for methods, such as ESI (see Section 2.1.15) and atmospheric pressure chemical ionization (APCI see Section 2.1.8), used to ionize compounds after LC separation. Generally these types of library are user generated for a specific purpose. [Pg.315]

Several years later, the next step in the application of MS-MS for mixture analysis was developed by Hunt et al. [3-5] who described a master scheme for the direct analysis of organic compounds in environmental samples using soft chemical ionisation (Cl) to perform product, parent and neutral loss MS-MS experiments for identification [6,7]. The breakthrough in LC-MS was the development of soft ionisation techniques, e.g. desorption ionisation (continuous flow-fast atom bombardment (CF-FAB), secondary ion mass spectrometry (SIMS) or laser desorption (LD)), and nebulisation ionisation techniques such as thermospray ionisation (TSI), and atmospheric pressure ionisation (API) techniques such as atmospheric pressure chemical ionisation (APCI), and electrospray ionisation (ESI). [Pg.152]

HPLC - Beckman 125 binary gradient pumps, 168 diode-array detector, 507 autosampler MS - Ion-trap mass spectrometer Finnigan LCQ equipped by APCI (atmospheric pressure chemical ionization), data analyzed in negative mode, spectra confirming found compounds were obtained from tandem mass spectromectry (MS/MS). [Pg.215]

Atmospheric Pressure Chemical Ionization (APCI)/MS APCI/MS is used to analyze compounds of intermediate molecular weight (100-1,500 da) and intermediate polarity and is particularly useful for the analysis of biochemicals such as triacylglycerides, carotenoids, and lipids (Byrdwell, 2001). For volatile, nonpolar compounds of low molecular weight, GC/MS is preferred to APCl/MS whereas APl-electrospray/ MS provides better results for larger, more polar materials. The selection of APCl/MS over GC/MS or APl-electrospray/MS depends on the compounds to be analyzed. Many LC/MS instruments can be easily switched between APCl/MS and APl-electrospray/MS so that it can be rapidly determined which ionization process is more suitable to a given chemical. Additional manipulations such as pre and postcolumn derivatization reactions (Nagy et al., 2004 Peters et al., 2004) or coulometric oxidation (Diehl et al., 2001) can make the chemicals of interest more amenable to detection by APCI. [Pg.162]

J.E. Rodriguez, Atmospheric Pressure Chemical Ionization of Nitro-Organic Compounds in Mass Spectrometry and Ion Mobility Spectrometry, MS Thesis, New Mexico State University, Las Cruces, NM, USA, May 1996. [Pg.199]

MW 272 Da), the control compound in the study (Fig. 2.13), and WY234 (fCa 5 pM, MW 253 Da Fig. 2.14). 17j8-Estradiol is a relatively less polar material and was studied in the negative atmospheric pressure chemical ionization (APCI) mode since it produced a weak APCI spectrum in the positive mode and no spec-... [Pg.89]

Atmospheric pressure chemical ionization (APCI) is the most common alternative to ESI in LC/MS. Whereas the application of ESI is generally recommended in the case of polar compounds, which may have a high molecular weight (up to 1 million Da), the problem-solving domain of APCI is limited to compounds with an MW smaller than 1000 Da. However, less polar compounds are accessible than with ESI. [Pg.342]

For the determination of organotin compounds (tributyltin, triphenyltin, triethyltin, and tetra-ethyltin) a MAE is proposed before the normal phase (NP) HPLC/UV analysis [35], In organotin and arsenic speciation studies, hydride generation is the most popular derivatization method, combined with atomic absorption and fluorescence spectroscopy or ICP techniques [25,36], Both atmospheric pressure chemical ionization (APCI)-MS and electrospray ionization ESI-MS are employed in the determination of butyltin, phenyltin, triphenyltin, and tributyltin in waters and sediments [37], A micro LC/ESI-ion trap MS method has been recently chosen as the official EPA (Environmental Protection Agency) method (8323) [38] it permits the determination of mono-, di-, and tri- butyltin, and mono-, di-, and tri-phenyltin at concentration levels of a subnanogram per liter and has been successfully applied in the analysis of freshwaters and fish [39], Tributyltin in waters has been also quantified through an automated sensitive SPME LC/ESI-MS method [40],... [Pg.539]


See other pages where Compounds atmospheric-pressure chemical is mentioned: [Pg.3615]    [Pg.3615]    [Pg.142]    [Pg.246]    [Pg.525]    [Pg.345]    [Pg.424]    [Pg.426]    [Pg.830]    [Pg.1146]    [Pg.26]    [Pg.54]    [Pg.102]    [Pg.33]    [Pg.94]    [Pg.216]    [Pg.22]    [Pg.63]    [Pg.231]    [Pg.698]    [Pg.241]    [Pg.225]    [Pg.84]    [Pg.189]    [Pg.49]    [Pg.136]    [Pg.191]    [Pg.150]    [Pg.417]    [Pg.481]    [Pg.180]    [Pg.190]   


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Atmospheric pressure chemical

Chemical Compounding

Chemical compounds

Chemical pressure

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