On-line multi-bed sorption trap for VOC analysis of large-volume vapor samples: injection plug width, effects of water vapor and sample decomposition.

A multibed on-line sorption trap is used to preconcentrate organic vapors from air samples and inject the analytes into a GC separation column. Injection plug widths depend on the boiling point for the lipophilic compounds and on the polarity and boiling point for the polar compounds. Injection plug widths are sufficiently small (0.

Design, fabrication, and evaluation of microfabricated columns for gas chromatography.

The design, fabrication, and performance of gas chromatography columns etched in silicon substrates are described. Deep reactive-ion etching formed the 3-m-long, 150-microm-wide, 240-microm-deep rectangular cross section channels. A glass cover plate was anodically bonded to the remaining surface of the substrate forming the gastight channel.

High-speed analysis of residual solvents by flow-modulation gas chromatography.

High-speed gas chromatographic (GC) separation of residual solvents in pharmaceutical preparations, using a flow-modulation technique, is described. These volatile compounds are separated on a series-coupled (tandem) column ensemble consisting of a polyethylene glycol column and a trifluoropropylmethyl/dimethylpolysiloxane column. This column ensemble is operated in stop-flow mode to enhance, or "tune", the separation.

Characterization and quantitative analysis with GC/TOFMS comparing enhanced separation with tandem-column stop-flow GC and spectral deconvolution of overlapping peaks.

Time-of-flight mass spectrometry is unique in that ion abundance ratios are constant over the chromatographic peak profile provided that the peak contains only one component. This provides the means for the automated finding and spectral deconvolution of overlapping chromatographic peaks from completely unknown mixtures if the mass spectra for the overlapping components are sufficiently unique. This can greatly reduce the chromatographic resolution requirements, which allows for very rapid quantitative analysis as well as for high-speed mixture characterization.

GC analysis of human breath with a series-coupled column ensemble and a multibed sorption trap.

The combination of a tandem column ensemble and an on-line microsorption trap is used for the analysis of organic compounds in human breath samples. The four-bed sorption trap uses a series of discreet sorption beds containing three grades of graphitized carbon and a carbon molecular sieve to quantitatively remove most organic compounds from 0.8-L breath samples.

Programmable selectivity for GC with series-coupled columns using pulsed heating of the second column.

A series-coupled ensemble of a nonpolar dimethyl polysiloxane column and a polar trifluoropropylmethyl polysiloxane column with independent at-column heating is used to obtain pulsed heating of the second column. For mixture component bands that are separated by the first column but coelute from the column ensemble, a temperature pulse is initiated after the first of the two components has crossed the column junction point and is in the second column, while the other component is still in the first column. This accelerates the band for the first component.

Portable gas chromatograph with tunable retention and sensor array detection for determination of complex vapor mixtures.

A prototype portable gas chromatograph that combines a multiadsorbent preconcentrator/focuser, a tandem-column separation stage with individual column temperature control and junction point pressure modulation, and a detector consisting of an integrated array of polymer-coated surface acoustic wave microsensors is described. Using scheduled first-column stop-flow intervals and independent temperature programming of the two columns, it is possible to adjust the retention of eluting analyte vapors to maximize vapor recognition with the microsensor array and minimize the time of analysis. A retention window approach is combined with Monte Carlo simulations to guide retention tuning requirements and facilitate pattern recognition analyses.

On-line multibed sorption trap and injector for the GC analysis of organic vapors in large-volume air samples.

A capillary-dimension on-line sorption trap is used to preconcentrate organic vapors from large-volume air samples and inject the organic compounds into the separation column as a relatively narrow vapor plug. The multibed trap is made from a Co-Ni alloy for resistive heating during sample desorption and uses four different carbon-based adsorption materials that are graded from weakest to strongest in the direction of the sample gas flow during sample preconcentration. The flow direction then is reversed for sample injection.

Risk of prevalent HIV infection associated with incarceration among injecting drug users in Bangkok, Thailand: case-control study.

Objectives: To identify risks for HIV infection related to incarceration among injecting drug users in Bangkok, Thailand.

Design: Case-control study of sexual and parenteral exposures occurring before, during, and after the most recent incarceration.

Setting: Metropolitan Bangkok.

High-speed characterization and analysis of orange oils with tandem-column stop-flow GC and time-of-flight MS.

High-speed GC with time-of-flight (TOF) MS detection is used for the characterization and analysis of oils rendered from the peel of five diverse species of orange including bergemot orange, bitter orange, tangerine, mandarin orange, and sweet orange. With a user-defined signal-to-noise threshold of 100, 44 peaks were found and 36 compounds identified in the various oils. Some major constituent components show large concentration ranges over the five species.

Selectivity enhancement for high-speed GC analysis of volatile organic compounds with portable instruments designed for vacuum-outlet and atmospheric-pressure inlet operation using air as the carrier gas.

A tandem ensemble of two 4.5-m-long x 0.25-mm-i.

A portable, high-speed, vacuum-outlet GC vapor analyzer employing air as carrier gas and surface acoustic wave detection.

Vacuum-outlet GC with atmospheric-pressure air as the carrier gas is implemented at outlet pressures up to 0.8 atm using a low-dead-volume polymer-coated surface acoustic wave (SAW) detector. Increases in the system outlet pressure from 0.

High-speed GC and GC/time-of-flight MS of lemon and lime oil samples.

The high-speed GC separation and MS characterization of lime oil and lemon oil samples using programmable column selectivity and time-of-flight mass spectrometry is described. The volatile essential oils are separated on a series-coupled (tandem) column ensemble consisting of a polar trifluoropropylmethyl polysiloxane column and a nonpolar 5% phenyl dimethyl polysiloxane column. Both columns are 7 m long.

Band-trajectory model for temperature-programmed series-coupled column ensembles with pressure-tunable selectivity.

A model and a spreadsheet algorithm is described for the prediction of solute-band migration trajectories in a series-coupled combination of two capillary GC columns with pressure-tunable and -programmable selectivity and operated under temperature-programmed conditions. The model takes into account the acceleration of carrier gas in the two columns as a result of decompression effects, the deceleration of carrier gas as a result of the increase in viscosity during temperature programming, the decrease in solute retention factors with increasing temperature during the temperature program, the differences in retention factors for the two columns, and programmed changes in the carrier-gas flow rates in the two columns during selectivity programming. In the model, the 20-meter-long column ensemble is divided into 1-cm-long intervals, and the carrier-gas velocity and column temperature are assummed to be constant in any interval.

High-speed GC and GC/MS with a series-coupled column ensemble using stop-flow operation.

A pneumatically actuated valve is used to connect the junction point of a series-coupled column ensemble to a ballast chamber containing carrier gas at the ensemble inlet pressure in order to periodically stop the carrier gas flow in the first column. When the valve is opened, mixture components, which have migrated across the column junction, are accelerated toward a time-of-flight mass spectrometer that is used as an ensemble detector. Mixture components, which are still in the first column, are frozen in position.

High-speed analysis of complex indoor VOC mixtures by vacuum-outlet GC with air carrier gas and programmable retention.

A pressure-tunable, series-coupled column ensemble was used with atmospheric pressure air as carrier gas for the vacuum-outlet GC analysis of 42 volatile and semivolatile organic compounds commonly encountered as indoor air pollutants. Separation strategies applicable to a field-portable instrument that will employ a dual-stage preconcentrator and a microsensor array as the detector were developed, where coelution of certain analytes can be tolerated. The capillary column ensemble consists of a 4.

A tandem column ensemble with an atmospheric pressure junction-point vent for high-speed GC with selective control of peak-pair separation.

A series-coupled (tandem) ensemble of two capillary GC columns using different stationary phases and a pneumatically actuated low-volume valve connecting the column junction point to an atmospheric-pressure vent line is used to adjust the ensemble separation of selected pairs of target compounds. The valve is normally closed, and the pressure at the column junction point assumes the value that would occur in the absence of any other connections. The valve can be opened for brief periods of time, thus producing pulses of atmospheric pressure at the column junction point.

Pulsed flow modulation for high-speed GC using a pressure-tunable column ensemble.

A computer-driven pressure controller is used to deliver pressure pulses to the junction point of two series-coupled columns using different stationary-phase chemistries. The column ensemble consists of a trifluoropropylmethyl polysiloxane column followed by a dimethyl polysiloxane column. Each pressure pulse causes a differential change in the carrier gas velocities in the two columns, which lasts for the duration of the pulse.

Programmable control of column selectivity for temperature-programmed GC.

A computer-driven pressure controller connected to the junction point of a series-coupled ensemble of two capillary GC columns having different stationary-phase selectivity is used to obtain on-the-fly (programmable) changes in ensemble selectivity. Changes in the junction-point pressure result in differential changes in the local carrier gas velocity in the two columns, and this results in changes in the pattern of peaks eluting from the ensemble. When used with relatively fast temperature programming (30 degrees C/min), the pattern of eluting peaks can be very sensitive to the time at which a selectivity (junction-point pressure) change is implemented.

Hihg-speed GC/MS of gasoline-range hydrocarbon compounds using a pressure-tunable column ensemble and time-of-flight detection.

A pressure-tunable series-coupled ensemble of two capillary GC columns is combined with a time-of-flight MS detector for the high-speed characterization of mixtures containing hydrocarbon compounds. The column ensemble consists of a nonpolar 5% phenyl poly(dimethylsiloxane) column and a very polar poly(ethylene glycol) column. The TOFMS instrument uses time-array detection to obtain up to 500 complete electron mass spectra per second.

Pressure-tunable column selectivity for high-speed vacuum-outlet GC.

A pressure-tunable ensemble of two series-coupled capillary columns operated at subambient outlet pressure is described. The ensemble consists of a 4.5-m length of nonpolar dimethyl polysiloxane column followed by a 7.