Real time direct analysis

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... 

Even a technique as complicated as direct liquid-introduction mass spectrometry has been coupled with reactor systems to provide real-time compositional analysis, as described in a series of articles by Dell Orco and colleagues.32-34 In their work, these authors used a dynamic dilution interface to provide samples in real time to un-modified commercial ionization sources (electrospray (ESI) and atmospheric pressure chemical ionization (APCI)). Complete speciation was demonstrated due to the unambiguous assignment of molecular weights to reactants, intermediates, and products. 

Real-Time Direct Fourier Transform IR Hollow Waveguide Gas Analysis... 

Thin-Layer Chromatography-Direct Analysis in Real Time in Analysis... 

THIN-LAYER CHROMATOGRAPHY-DIRECT ANALYSIS IN REAL TIME IN ANALYSIS OF SMALL ORGANIC... 

Badjagbo K, Picard P, Moore S, et al. Direct atmospheric pressure chemical ionization-tandem mass spectrometry for the continuous real-time trace analysis of benzene, toluene, ethylbenzene and xylenes in ambient air. J Am Soc Mass Spectrom. 2009 20 829-36. 

Prior to the widespread implementation of supervisory control and data acquisition (SCADA) and human-machine interface (HMI) systems, most SPC and SQC was performed by quality-control departments as an off-line process. Data was collected from test stations, laboratories, etc. and statistical analysis was performed later. SCADA/HMI systems, however, have made it feasible to provide plant-floor SPC charts using data collected in real time directly from the process. Fabricators that want to standardize SPC and SQC to increase their use find they need the two following functions (1) provide the plant floor with SPC charts and (2) make data collected by SCADA systems available for off-line analysis. Available is SPC and SQC software to support these efforts. Recognize that the bulk of SPC s value is derived from process improvements developed from offline SQC analysis. 

The block diagram in Fig. 8.5 shows the architecture of the Real-Time Process Analysis System at the system level. The direct chip-to-chip connection of the... 

The data are very comprehensive with direct applications to reliability, risk, and event analysis of nuclear power plants. Information has been assembled on failure frequency, modes, repairs, and maintenance. Rate Information is based on demands calculated. The time period covered varies from the early 1970 s to the present. Using real time access, the output format if the event can be varied by selection of 20 generic and detailed categories. 

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. 

The scanning transmission electron microscope (STEM) was used to directly observe nm size crystallites of supported platinum, palladium and first row transition metals. The objective of these studies was to determine the uniformity of size and mass of these crystallites and when feasible structural features. STEM analysis and temperature programmed desorption (TPD) of hydrogen Indicate that the 2 nm platinum crystallites supported on alumina are uniform In size and mass while platinum crystallites 3 to 4 nm in size vary by a factor of three-fold In mass. Analysis by STEM of platinum-palladium dn alumina established the segregation of platinum and palladium for the majority of crystallites analyzed even after exposure to elevated temperatures. Direct observation of nickel, cobalt, or iron crystallites on alumina was very difficult, however, the use of direct elemental analysis of 4-6 nm areas and real time Imaging capabilities of up to 20 Mx enabled direct analyses of these transition metals to be made. Additional analyses by TPD of hydrogen and photoacoustic spectroscopy (PAS) were made to support the STEM observations. 

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. 

Another method to detect energy transfer directly is to measure the concentration or amount of acceptor that has undergone an excited state reaction by means other than detecting its fluorescence. For instance, by chemical analysis or chromatographic analysis of the product of a reaction involving excited A [117, 118]. An early application of this determined the photolyzed A molecules by absorption spectroscopic analysis. [119-121], This can be a powerful method, because it does not depend on expensive instrumentation however, it lacks real-time observation, and requires subsequent manipulation. For this reason, fluorescence is the usual method of detection of the sensitized excitation of the acceptor. If it is possible to excite the donor without exciting the acceptor, then the rate of photolysis of the acceptor (which is an excited state reaction) can be used to calculate the FRET efficiency [122],... 

A new family of ionization techniques allows ions to be created under ambient conditions and then collected and analyzed by MS. They can be divided into two major classes desorption electrospray ionization (DESI) and direct analysis in real time (DART). 

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