Development and validation of a pneumatic model for the reversed-flow differential flow modulator for comprehensive two-dimensional gas chromatography.

The development of the reversed fill/flush modulator represents a significant advancement in flow-modulated, comprehensive two-dimensional gas chromatography (GC × GC). Compared to the forward flush/fill modulator, the reversed-flow modulator is less susceptible to baseline anomalies and peak tailing as a result of modulator channel overfilling or insufficient purging of high concentration analytes. Flow reversal requires the addition of a bleed capillary not present in the forward-flow modulator. Selecting the appropriate restriction of the bleed capillary is critical. If the bleed capillary is too restrictive, eluate from the first-dimension column can split between the modulator channel and second-dimension column, which also results in baseline artifacts. To gain a better understanding of the reversed-flow modulator, a comprehensive pneumatic model was developed. The model was validated by comparing calculated and measured hold-up times. The errors in calculated hold-up times were less than 1% of the measured values. The model can be used to predict first-dimension eluate splitting and determine the optimal bleed capillary dimensions to prevent its occurrence. Calculation of the modulator hold-up time can be used to determine the maximum collection time to ensure comprehensive analysis and optimal flush times for partial fill operation.

Comparison of Temperature Programmable Split/Splitless and Cool On-Column Inlets for the Determination of Glycerol and Glycerides in Biodiesel by Gas Chromatography with Flame Ionization Detection.

The European Standard EN 14105:2011-07 is an analysis method for quantifying free glycerol and residual mono-, di- and triacylglycerides impurities in biodiesel by gas chromatography. The method specifies an "on-column injector or equivalent device" as the means of sample introduction. Cool on-column (COC) would appear to be an ideal choice, particularly for quantifying triacylglycerides, as it provides high quantitative accuracy and precision with minimal mass discrimination. However, there are a few drawbacks in using COC for this application. The relatively high concentration of the biodiesel in the prepared samples impedes solvent focusing of early eluting compounds such as glycerol, causing band broadening and shifts in retention time compared with the external calibration standards. More problematic is method robustness when using a metal retention gap. Repeated injections onto the retention gap cause the method control specification to fail within relatively few injections. As an alternative, a temperature programmable split/splitless (TPSS) inlet was investigated for performance equivalency. The results demonstrate that the TPSS yields concentration measurements indistinguishable from the COC inlet at the 95% confidence level. In addition, the robustness of the TPSS far exceeds that of the COC inlet by eliminating the performance control failure and providing solvent focusing for the early eluting peaks.

Stationary phase selection and comprehensive two-dimensional gas chromatographic analysis of trace biodiesel in petroleum-based fuel.

The GC×GC solvation parameter model has been used to identify effective stationary phases for the separation of fatty acid methyl esters (FAMEs) from petroleum hydrocarbons. This simple mathematical model was used to screen the 1225 different combinations of 50 stationary phases. The most promising pairs combined a poly(methyltrifluoropropylsiloxane) stationary phase with a poly(dimethyldiphenylsiloxane) stationary phase. The theoretical results were experimentally tested by equipping a GC×GC instrument with a DB-210 primary stationary phase and an HP-50+ secondary stationary phase. This instrument was used to analyze trace levels of FAMEs in kerosene. The FAMEs were fully separated from the petroleum hydrocarbons on the secondary dimension of the 2-D chromatogram. The resulting GC×GC method was shown to be capable of accurately quantifying FAME levels as low as 2 ppm (w/w). These results demonstrate the utility of the solvation parameter model for identifying optimal stationary phases for high resolution GC×GC separations. Furthermore, this work presents an effective method for determining the level of biodiesel contamination in aviation fuel and other petroleum-based fuels.

Comprehensive two-dimensional gas chromatography analysis of high-ethanol containing motor fuels.

A comprehensive 2-D GC (GC x GC) instrument equipped with a flow-switching modulator was used to determine the concentration of ethanol and eight other alcohols in a retail pump sample of E85 fuel. E85 is a mixture of ethanol and gasoline where the ethanol concentration can range from 70 to 85 vol%. The increased peak capacity and selectivity generated by GC x GC analysis allowed the alcohols to be fully resolved from the gasoline hydrocarbons. GC x GC analysis was compared to the performance obtained with the standard analytical method for determining ethanol in fuel ethanol (ASTM D5501) and the standard method for determining oxygenate concentrations in gasoline (ASTM D4815). The GC x GC analysis required 14 min while the combined ASTM D5501 and ASTM D4815 analyses required more than 60 min. The ethanol concentration obtained by GC x GC was in excellent agreement with the value obtained by the D5501 method. Poorer agreement was observed between the GC x GC and D4815 concentrations for the other alcohols present in E85. In all cases, the differences could be attributed to deficiencies in the D4815 method that led to coelutions between the alcohols and gasoline hydrocarbons.

Analysis of biodiesel/petroleum diesel blends with comprehensive two-dimensional gas chromatography.

Comprehensive two-dimensional gas chromatography (GCxGC) is used to analyze petroleum diesel, biodiesel, and biodiesel/petroleum diesel blends. The GCxGC instrument is assembled from a conventional gas chromatograph fitted with a simple, in-line fluidic modulator. A 5% phenyl polydimethylsiloxane primary column is coupled to a polyethylene glycol secondary column. This column combination generates chromatograms where the fatty acid methyl esters (FAMEs) found in biodiesel occupy a region that is also populated by numerous cyclic alkanes and monoaromatics found in petroleum. Fortunately, the intensities of the petroleum hydrocarbon peaks are far lower than the intensities of the FAME peaks, even for blends with low biodiesel content. This allows the FAMEs to be accurately quantitated by direct integration. The method is calibrated by analyzing standard mixtures of soybean biodiesel in petroleum diesel with concentrations ranging from 1 to 20% v/v. The resulting calibration curve displays excellent linearity. This curve is used to determine the concentration of a B20 biodiesel/petroleum diesel blend obtained from a local retailer. Excellent precision and accuracy are obtained.

A comprehensive two-dimensional gas chromatography method for analyzing extractable petroleum hydrocarbons in water and soil.

A flow-switching two-dimensional gas chromatography (GCxGC) apparatus has been constructed that can operate at temperatures as high as 340 degrees C. This system is employed to analyze complex hydrocarbon mixtures such as diesel fuel, gas-oil, motor oil, and petroleum contaminated environmental samples. The GCxGC system generates two-dimensional chromatograms with minimal overlap between the aliphatic and aromatic regions This allows these compound classes to be independently quantitated without prior fractionation. The GCxGC system is used to analyze extracts of spiked water samples, wastewater, and soil. The accuracy of the method is compared to that of the Massachusetts Extractable Petroleum Hydrocarbons (MA EPH) method. The GCxGC system generates a quantitative accuracy similar to the MA EPH method for the analysis of spiked water samples. The GCxGC method and the MA EPH method generate comparable levels of total hydrocarbons when wastewater is analyzed, but the GCxGC method detects a significantly higher aromatic content and lower aliphatic content. Both the GCxGC method and MA EPH method measure comparable levels of aromatics in the soil samples.

Microfluidic deans switch for comprehensive two-dimensional gas chromatography.

A microfluidic Deans switch was used as a comprehensive two-dimensional gas chromatography (GCxGC) modulator. The simplicity and wide temperature range of the Deans switch make it a promising alternative to existing modulation techniques. However, the Deans switch is a low duty cycle modulator; that is, it samples only a small portion of the primary column effluent. Like all low duty cycle modulators, the Deans switch produces inconsistent transfer of components from the primary to the secondary column if the primary peaks are undersampled. Theoretical simulations and experimental studies show that the relative standard deviation (RSD) of the fraction of material transferred from the primary column to the secondary column is less than 1% if the modulation ratio is greater than 2.5. But the RSDs increase rapidly as the modulation ratio is decreased below 2.5. Deans switch GCxGC was validated by analyzing the aromatic content of gasoline. A fast analysis (<10 min) produced narrow primary peaks and a modulation ratio of 1.7. The quantitative results were in good agreement with results obtained with differential flow modulation GCxGC and GC/MS, but the RSDs of single-component levels were approximately three times greater. The Deans switch modulator was also used for a slower gasoline analysis (33 min run time) that produced modulation ratios near 5. In this case, the quantitative results and RSDs were in excellent agreement with the differential flow GCxGC and GC/MS results. These studies demonstrate that a Deans switch can be an effective modulator provided that modulation ratios greater than approximately 2.5 are employed.

Analysis of aromatic compounds in gasoline with flow-switching comprehensive two-dimensional gas chromatography.

A comprehensive two-dimensional gas chromatography (GC x GC) instrument has been created by coupling a flow-switching modulator and a standard gas chromatograph. The instrument was used to characterize the aromatic composition of gasoline. The high-resolution separation produced by flow-switching GC x GC allowed gasoline aromatics to be fully resolved from saturated components. The aromatic compounds were further separated into groups having the same carbon number. A standard gasoline sample was analyzed to evaluate the quantitative accuracy and precision of this technique. The data show that flow-switching GC x GC produces results that are comparable to gas chromatography-mass spectrometry (GC-MS) and thermal modulation GC x GC. The simple, low-cost, and robust nature of flow-switching GC x GC makes it an ideal technique for the routine analysis of aromatic compounds in gasoline.

Two-dimensional gas chromatography analysis of components in fuel and fuel additives using a simplified heart-cutting GC system.

Multidimensional gas chromatography (MGC) using heart cutting is an old idea that can benefit from the performance of modern instruments and capillary columns to provide fast, reliable separation of target analytes from complex sample matrices. A simplified heart-cutting switch is described that uses these improvements to provide very narrow precise heart cuts between columns of different selectivity. This system is used to analyze ppm levels of 4,6-dimethydibenzothiophene in diesel fuel using a standard flame ionization detector instead of a complex sulfur-selective detector. MGC systems also offer the possibility of faster analysis speed by using two short columns of different selectivity instead of very long columns to resolve compounds from complex matrices. The analysis of alcohols in denatured fuel ethanol using the MGC system is performed over six times faster than the standard American Society for Testing and Materials methodology.