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Mass spectrometry real-time

Brum, J. 8t Dell Orco, P., Online mass spectrometry Real-time monitoring and kinetics analysis for the photolysis of idoxifene Rapid Commun. Mass Spectrom. 1998, 12, 741-745. [Pg.357]

Brum, J., Dell Orco, P. (1998) On-line Mass Spectrometry Real-time Monitoring and Kinetics Analysis for the Photolysis of Idoxifene. Rapid Commun. Mass Spectrom. 12 741-745. [Pg.142]

Schramm, E., et al. (2009) Trace detection of organic compounds in complex sample matrixes by single photon ionization ion trap mass spectrometry real-time detection of security-relevant compounds and online analysis of the coffee-roasting process. Analytical Chemistry, 81, 4456-4467. [Pg.475]

The application of a selective pyrolysis process to the recovery of chemicals from waste PU foam is described. The reaction conditions are controlled so that target products can be collected directly from the waste stream in high yields. Molecular beam mass spectrometry is used in small-scale experiments to analyse the reaction products in real time, enabling the effects of process parameters such as temperature, catalysts and co-reagents to be quickly screened. Fixed bed and fluidised bed reactors are used to provide products for conventional chemical analysis to determine material balances and to test the concept under larger scale conditions. Results are presented for the recycling of PU foams from vehicle seats and refrigerators. 12 refs. [Pg.79]

An advantage of the microbore gas chromatrography/time-of-flight mass spectrometry (GC/TOFMS) method over the other two approaches is that separation efficiency need not be compromised for speed of analysis. The rapid deconvolution of spectra ( scan rate ) with TOFMS makes it the only MS approach to achieve several data points across a narrow peak in full-scan operation. However, the injection of complex extracts deteriorates performance of microbore columns quickly, and an increased LOD and decreased ruggedness result. Microbore columns may be used in water analysis if the LOD is sufficiently low, but they can rarely be used in real-life applications to complicated extracts. [Pg.763]

Laser desorption methods (such as LD-ITMS) are indicated as cost-saving real-time techniques for the near future. In a single laser shot, the LDI technique coupled with Fourier-transform mass spectrometry (FTMS) can provide detailed chemical information on the polymeric molecular structure, and is a tool for direct determination of additives and contaminants in polymers. This offers new analytical capabilities to solve problems in research, development, engineering, production, technical support, competitor product analysis, and defect analysis. Laser desorption techniques are limited to surface analysis and do not allow quantitation, but exhibit superior analyte selectivity. [Pg.737]

Of the methods developed for the identification of hydrocarbon mixtures, only coupled gas chromatography-mass spectrometry holds any real promise of certain identification and this only at a prohibitive cost in time spent characterising minor peaks. It would be far more efficient to develop rapid screening procedures which would eliminate all but a few possibilities, and then use gas chromatography-mass spectrometry to isolate and identify a few key peaks to confirm the characterisation. This is precisely the scheme adopted independently by a number of laboratories. [Pg.384]

The ability of the new precursors to decompose thermally to yield singlephase CIS was investigated by powder XRD analysis and EDS on the nonvolatile solids from the TGA experiments of selected compounds. Furthermore, using TGA-evolved gas analysis (EGA), the volatile components from the degradation of the SSPs could be analyzed via real-time fourier transform infrared (FTIR) and mass spectrometry (MS), thus providing information for the decomposition mechanism.3 The real-time FTIR spectrum for 7 and 8 shows absorptions at approximately 3000,1460,1390,1300, and 1250 cm-1 (see Fig. 6.7). [Pg.166]

This presentation will summarize developments in laser ablation with emphasis on LIBS (laser induced breakdown spectroscopy) and inductively coupled plasma mass spectrometry (ICPMS) as analytical tools for real time chemical analysis (Fig. 1) (Russo et al. [Pg.295]

DGE a AC AMS APCI API AP-MALDI APPI ASAP BIRD c CAD CE CF CF-FAB Cl CID cw CZE Da DAPCI DART DC DE DESI DIOS DTIMS EC ECD El ELDI EM ESI ETD eV f FAB FAIMS FD FI FT FTICR two-dimensional gel electrophoresis atto, 10 18 alternating current accelerator mass spectrometry atmospheric pressure chemical ionization atmospheric pressure ionization atmospheric pressure matrix-assisted laser desorption/ionization atmospheric pressure photoionization atmospheric-pressure solids analysis probe blackbody infrared radiative dissociation centi, 10-2 collision-activated dissociation capillary electrophoresis continuous flow continuous flow fast atom bombardment chemical ionization collision-induced dissociation continuous wave capillary zone electrophoresis dalton desorption atmospheric pressure chemical ionization direct analysis in real time direct current delayed extraction desorption electrospray ionization desorption/ionization on silicon drift tube ion mobility spectrometry electrochromatography electron capture dissociation electron ionization electrospray-assisted laser desorption/ionization electron multiplier electrospray ionization electron transfer dissociation electron volt femto, 1CT15 fast atom bombardment field asymmetric waveform ion mobility spectrometry field desorption field ionization Fourier transform Fourier transform ion cyclotron resonance... [Pg.11]

How much detail does a student need to know and how much detail should a textbook then contain This is an almost unsolvable problem because of the diversity of students and their analytical needs. The majority of students will eventually move on into special fields in (bio)chemistry, molecular or systems biology or polymer chemistry. For them mass spectrometry will only be one of the commodities to help them solve their problems, which are defined by their field of activity, not the analytical technique. How much of the basics in mass spectrometry will they need to know Again, this depends on the problem at hand. For many a routine application of commercial instalments and the manufacturers manuals will suffice. However, if the problem is not routine the analytical technique cannot be either. Mass spectrometry is and, most probably, will remain a rather complex technique. To fully exploit its tremendous potential, but, equally important, to avoid its many pitfalls, a deeper understanding of the mechanisms and the technology will be mandatory. This book will, hopefully, help students to lay the basis for this expertise and, once the need arises, allow them to go back to the more specialized literature at a later time. It is in this sense that I hope this book will be a real help to many of them. [Pg.403]

We discussed the fundamentals of mass spectrometry in Chapter 10 and infrared spectrometry in Chapter 8. The quadrupole mass spectrometer and the Fourier transform infrared spectrometer have been adapted to and used with GC equipment as detectors with great success. Gas chromatography-mass spectrometry (GC-MS) and gas chromatography-infrared spectrometry (GC-IR) are very powerful tools for qualitative analysis in GC because not only do they give retention time information, but, due to their inherent speed, they are also able to measure and record the mass spectrum or infrared (IR) spectrum of the individual sample components as they elute from the GC column. It is like taking a photograph of each component as it elutes. See Figure 12.14. Coupled with the computer banks of mass and IR spectra, a component s identity is an easy chore for such a detector. It seems the only real... [Pg.351]

J. Wang, S. Wasmus, and R.F. Savinell, Evaluation of ethanol, 1 -propanol, and 5-propanol in a direct oxidation polymer-electrolyte fuel cell—A real-time mass spectrometry study, J. Electrochem. Soc. 142(12), 4218-4224 (1995). [Pg.323]

Steeghs M, Bais HP, de Gouw J, Goldan P, Kuster W, Northway M, Fall R, Vivanco JM (2004) Proton-transfer-reaction mass spectrometry as a new tool for real time analysis of root-secreted volatile organic compounds in arabidopsis. Plant Physiol 135 47-58... [Pg.176]

Kristensen GH, Klausen MM, Hansen VA, Lauritsen FR (2010) On-line monitoring of the dynamics of trihalomethane concentrations in a warm public swimming pool using an unsupervised membrane inlet mass spectrometry system with off-site real-time surveillance. Rapid Commun Mass Spectrom 24(l) 30-34... [Pg.136]

Greaser, C. S. Lamarca, D. G. Brum, J. Werner, C. New, A. P dos Santos, L. M. E. Reversed-Phase Membrane Inlet Mass Spectrometry Applied to the Real-Time Monitoring of Low Molecular Weight Alcohols in Chloroform. Anal. Chem. 2002, 74, 300-304. [Pg.669]

Nedelkov, D., Rasooly, A., and Nelson, R. W. (2000). Multitoxin biosensor-mass spectrometry analysis A new approach for rapid, real-time, sensitive analysis of staphylococcal toxins in food. Int.. Food Microbiol. 60,1-13. [Pg.40]

ESI-MS has been used for the quantification of a number of substrates and products of enzymatic reactions [56,57]. Hsieh et al. report the use of ion spray mass spectrometry (a technical variation of electrospray ionization) coupled to HPLC for the kinetic analysis of enzymatic reactions in real time [58]. The hydrolysis of dinucleotides with bovine pancreatic ribonuclease A and the hydrolysis of lactose with 3-galactosidase were monitored and the resulting data were used for the estimation of and v x of these reactions. Another field of application of electrospray mass spectrometry is the screening of combinatorial libraries for potent inhibitors [31,59]. [Pg.14]


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See also in sourсe #XX -- [ Pg.386 , Pg.402 , Pg.403 , Pg.404 , Pg.405 , Pg.406 , Pg.407 ]




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