Influence of modulator injection width on comprehensive two-dimensional gas chromatography peak dimensions.

This study examines how the height and width of peaks exiting the secondary column of a comprehensive two-dimensional gas chromatography (GC × GC) separation are affected by the width of the pulse introduced to the secondary column. A flow-modulated GC × GC apparatus was assembled that allowed input pulse widths to be controlled precisely over a range of 10 to 70 ms. GC × GC chromatograms were obtained using secondary columns containing a polyethylene glycol stationary phase with internal diameters of 0.25 and 0.32 mm. The area, height, and width of peaks emerging from the secondary column were found to be accurately modeled by the convolution of a rectangular function with a Gaussian distribution. The rectangular function represents the input pulse, and the Gaussian distribution represents the broadening that occurs in the secondary column. The minimum peak width that could be produced by the secondary column was determined for a wide range of compounds. Injection pulse widths that matched a compound's minimum peak width produced peaks that were 25% wider than the minimum width and had heights that were 76% of the maximum possible peak height. Increasing the injection width significantly above the minimum width yielded substantially broader peaks with only a modest increase (< 25%) in peak height.

The multi-mode modulator: A versatile fluidic device for two-dimensional gas chromatography.

A fluidic device called the multi-mode modulator (MMM) has been developed for use as a comprehensive two-dimensional gas chromatography (GC x GC) modulator. The MMM can be employed in a wide range of capacities including as a traditional heart-cutting device, a low duty cycle GC x GC modulator, and a full transfer GC x GC modulator. The MMM is capable of producing narrow component pulses (widths <50ms) while operating at flows compatible with high resolution chromatography. The sample path of modulated components is confined to the interior of a joining capillary. The joining capillary dimensions and the position of the columns within the joining capillary can be optimized for the selected modulation mode. Furthermore, the joining capillary can be replaced easily and inexpensively if it becomes fouled due to sample matrix components or column bleed. The principles of operation of the MMM are described and its efficacy is demonstrated as a heart-cutting device and as a GC x GC modulator.

Comprehensive two-dimensional gas chromatography with pattern modulation.

Comprehensive two-dimensional gas chromatography (GC×GC) modulators normally transfer primary column effluent to the head of the secondary column as a series of sharp pulses. Such pulses are produced with time-varying temperature gradients in thermal modulation or with time-varying flow patterns in flow modulation. Thermal modulators produce narrow peaks at optimal flow rates, but require large amounts of consumables or a highly engineered heating/cooling system. Flow modulators involve simpler hardware and no additional consumables. However, flow modulators require a large increase in secondary column flow or transfer only a small portion of the primary effluent to the secondary column. This study examines a new method of producing GC×GC separations with a flow modulator. Instead of injecting narrow pulses, the modulator transfers primary effluent to the secondary column in the form of an intricate injection pattern. The detector signal is deconvoluted and converted to a two-dimensional chromatogram. The high duty cycle of the technique (>50%) leads to deconvoluted peaks with twenty times greater intensity than those produced by conventional modulation with a Deans switch modulator. Pattern modulation can be produced without requiring elevated carrier flows. This study evaluates the efficacy of pattern modulation GC×GC by analyzing a standard mixture of 43 oxygenated organic compounds and an E85 fuel sample.

Analysis of siloxanes in hydrocarbon mixtures using comprehensive two-dimensional gas chromatography.

A comprehensive two-dimensional gas chromatography (GC×GC) method for separating siloxanes from hydrocarbons has been developed using a systematic process. First, the retention indices of a set of siloxanes and a set of hydrocarbons were determined on 6 different stationary phases. The retention indices were then used to model GC×GC separation on 15 different stationary phase pairs. The SPB-Octyl×DB-1 pair was predicted to provide the best separation of the siloxanes from the hydrocarbons. The efficacy of this stationary phase pair was experimentally tested by performing a GC×GC analysis of gasoline spiked with siloxanes and by analyzing biogas obtained from a local wastewater treatment facility. The model predictions agreed well with the experimental results. The SPB-Octyl×DB-1 stationary phase pair constrained the hydrocarbons to a narrow range of secondary retention times and fully isolated the siloxanes from the hydrocarbon band. The resulting GC×GC method allows siloxanes to be resolved from complex mixtures of hydrocarbons without requiring the use of a selective detector.

Iterative trapping of gaseous volatile organic compounds in a capillary column.

The iterative trapping method has been developed for concentrating gaseous volatile organic compounds (VOCs) prior to gas chromatographic analysis. VOCs are trapped in a 50 cm × 0.53 mm metal capillary column coated with a 7 µm thick film of polydimethylsiloxane (PDMS). Iterative trapping does not employ the two-step thermal desorption approach used by most VOC concentrating techniques. Instead, a four-step cycle involving synchronized changes in flow direction and temperature is repeated throughout the sampling process. This iterative process causes VOCs to accumulate within the capillary well past the level where a standard two-step method reaches its saturation limit. Iterative trapping is capable of sampling and desorbing C5 through C11 n-alkanes with uniform efficiency. This new technique, in its current form, is most appropriate for focusing VOCs from gas volumes on the order of 10 mL. Iterative trapping increases the focusing power of a weak sorbent like PDMS and allows narrow chromatographic peaks to be generated without the use of high desorption temperatures or a secondary focusing stage.

High speed Deans switch for low duty cycle comprehensive two-dimensional gas chromatography.

A new high-speed valve-based modulator has been designed and tested for use in comprehensive two-dimensional gas chromatography (GC×GC). The modulator is a Deans switch constructed from two micro-volume fittings and a solenoid valve. Modulator performance was characterized over a wide range of device settings including the magnitude of the switching flow, the gap between the tips of the primary and secondary column, the primary column flow rate, and the carrier gas identity. Under optimized conditions, the modulator was found to be capable of generating narrow pulses (<50ms) of primary effluent with a 2mL/min secondary column flow. This capability will ultimately allow the modulator to be used with GC×GC separations employing a wide range of detectors and secondary column geometries. The main disadvantage of this modulator is that it employs a low sampling duty cycle, and thus it produces separations with sensitivities that are lower than those produced with thermal modulators or differential flow modulators. The efficacy of the new high-speed Deans switch modulator was demonstrated through the GC×GC separation of a hydrocarbon standard and gasoline. Precise quantitation of individual components was possible provided the modulation ratio was kept greater than 2.0.

Recent advances in flow-controlled multidimensional gas chromatography.

The continued development of flow-controlled two-dimensional gas chromatography (2-D GC) is reviewed, with a special emphasis on results published from 2001 through 2011. Heart-cutting 2-D GC continues to be used for isolating selected components in complex mixtures. The programmable and highly precise flows and temperatures produced by modern gas chromatographs have made it easier to selectively transfer analytes to the secondary column and to backflush unwanted components from the primary column. Several new Deans switch interfaces for performing heart-cutting 2-D GC have been introduced, with most attention given to devices that integrate the flow connections into a single unit. Heart-cutting 2-D GC has been used to isolate analytes in a wide variety of complex mixtures including fuels, industrial feedstocks, fragrances, and environmental extracts. Valve-based comprehensive 2-D GC (GC×GC) was also actively developed in the past decade. Valve-based modulation is a simple way to generate GC×GC separations without using cryogenic fluids. More than ten new valve-based modulators were introduced. Diaphragm valves fitted with sample loops are the most common low duty cycle modulators, whereas fluidic modulators that employ differential flow conditions are the most common high duty cycle modulators. Applications of valve-based GC×GC include analysis of hydrocarbon mixtures, essential oils, and environmental samples.

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.

Solvation parameter model of comprehensive two-dimensional gas chromatography separations.

A solvation parameter model was used to generate comprehensive two-dimensional gas chromatography (GC x GC) retention diagrams for 54 solutes on four different stationary phase combinations. Retention diagrams are plots used to predict the relative position of solutes in GC x GC chromatograms. In this study, retention diagrams were based entirely on solute and stationary phase descriptors taken from the literature. The temperature-averaged values of the stationary phase descriptors were used to further simplify the model. The relative positions of the solutes in the retention diagrams were compared with experimentally obtained GC x GC chromatograms. Excellent agreement was observed for each column combination. The model was found to generate primary retention time predictions with standard errors that were approximately 1% of the range of the experimental values and secondary retention time predictions with standard errors that were approximately 5% of the range of the experimental values. It is concluded that the GC x GC solvation parameter model is sufficiently accurate to aid in the identification of optimal column combinations.

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.

Comprehensive two-dimensional gas chromatography using a high-temperature phosphonium ionic liquid column.

A high-temperature ionic liquid, trihexyl(tetradecyl)phosphonium bis(trifluoromethane)sulfonamide, was used as the primary column stationary phase for comprehensive two-dimensional gas chromatography (GC x GC). The ionic liquid (IL) column was coupled to a 5% diphenyl/95% dimethyl polysiloxane (HP-5) secondary column. The retention characteristics of the IL column were compared to polyethylene glycol (DB-Wax) and 50% phenyl/50% methyl polysiloxane (HP-50+). A series of homologous compounds that included hydrocarbons, oxygenated organics, and halogenated alkanes were analyzed with each column combination. This comparison showed that the ionic liquid is less polar than DB-Wax but more polar than HP-50+. The most unique feature of the IL x HP-5 column combination is that alkanes, cyclic alkanes, and alkenes eluted in a narrow band in the GC x GC chromatogram; whereas, these compounds occupied a much larger portion of the DB-Wax x HP-5 and the HP-50+ x HP-5 chromatograms. Each column combination was used to analyze diesel fuel. The IL x HP-5 chromatogram displayed narrow bands for three major compound classes in diesel fuel: saturates, monoaromatics, and diaromatics. The IL column was used at temperatures as high as 290 degrees C for several months without any noticeable changes in column performance.

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.

Model for predicting comprehensive two-dimensional gas chromatography retention times.

A model for approximating the relative retention of solutes in comprehensive two-dimensional gas chromatography (GCxGC) is presented. The model uses retention data from standard single-column temperature-programmed separations. The one-dimensional retention times are first converted into retention indices and then these indices are combined in a simple manner to generate a retention diagram. A retention diagram is an approximation of the two-dimensional chromatogram that has retention order and spacing in both dimensions similar to that found in the experimental chromatogram. If required, the retention diagram can be scaled to more closely resemble the two-dimensional chromatogram. The model has been tested by using retention time data from single-column gas chromatography-mass spectrometry and valve-based GCxGC. A total of 139 volatile organic compounds (VOCs) were examined. Approximately half of the VOCs had a single functional group and a linear alkyl chain (i.e., compounds with the structure Z-(CH(2))(n)-H). The retention diagrams had primary retention orders that were in excellent agreement with the GCxGC chromatograms. The relative secondary retention order for compounds with similar structures was also accurately predicted by the retention diagram. However, the relative secondary retention for compounds with dissimilar structures, such as acyclic alcohols and multi-substituted alkylbenzenes, were less accurately modeled. This study demonstrates how readily available single-column retention time data can be used to provide an a priori estimate of the relative retention of solutes in a GCxGC chromatogram. Such a capability is useful for screening possible combinations of stationary phases.

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.

Method for reducing the ambiguity of comprehensive two-dimensional chromatography retention times.

Comprehensive two-dimensional chromatography generates a two-dimensional chromatogram from a one-dimensional signal array. This process can only be done unambiguously when the range of secondary retention times is less than the modulation period. However, complex samples often produce wider ranges of secondary retention times. Peaks with retention times that exceed the modulation period are said to be "wrapped-around". A simple algorithm has been developed that determines absolute retention times when wrap-around occurs. A sample is first analyzed under standard modulation conditions and then re-analyzed with a modulation period that is increased by an integer fraction of the original modulation period. Retention shifts along the secondary axis are used to determine absolute retention times. A theoretical analysis has been performed to optimize the implementation conditions and characterize the technique limitations. The efficacy of this algorithm has been tested through a series of isothermal GC x GC separations. This method has been found to be particularly useful during the initial stages of method development.

A systematic analysis of a flow-switching modulator for comprehensive two-dimensional gas chromatography.

A simple flow-switching device has been designed for use as a comprehensive two-dimensional gas chromatography modulator. The device is constructed from fused silica tubing, t-unions, and a solenoid valve. A series of experiments were conducted to determine the influence of primary flow, secondary flow, modulation time, and device dimensions on the performance of the modulator. The flow-switching device was found to produce pulses with widths near the theoretical minimum. High-performance was maintained over a wide range of modulation times. The flow-switching device did not introduce extra broadening along the primary retention axis. However, the modulator performance was optimal only over a narrow range of primary to secondary flow ratios. The ideal flow ratio is determined by the dimensions of the tubes that connect the t-unions. A simple flow resistance model has been developed that can predict the dimensions that will produce optimal results for a specified primary to secondary flow ratio. Thus, it is possible to construct a device that operates near the theoretical limit without numerous alterations. Under optimal conditions, the flow switching modulator generates peaks that are narrower than those produced by a diaphragm valve.

Volume and surface area study of tobramycin-polymethylmethacrylate beads.

Polymethylmethacrylate bone cement beads impregnated with antibiotic are a common treatment for patients with persistent articular joint infections or osteomyelitis. They also are used as a prophylaxis for infection in patients with large soft tissue wounds. The current study was designed to evaluate the relationship between bead geometry and elution of the antibiotic tobramycin by methodically varying the shape of the beads for a given set of volumes. Beads of five shapes (spherical to ovoid) and two volumes were prepared and studied. Only 0.9% to 3.3% of the total amount of tobramycin present actually eluted from the beads in a 96-hour period and of this amount, approximately 1/3 eluted within the first 4 hours. The elution mass data indicate the benefit of numerous, small and elliptically shaped beads for maximal antibiotic availability. Additionally, a mathematical model is presented that describes these findings and can be used to predict tobramycin delivery rates from bone cement beads. This model assumes that the antibiotic is delivered through two mechanisms: fast dissolution of tobramycin initially adhering to the bead surface and slow release by diffusion through the polymer. The results generate diffusion coefficients for tobramycin in polymethylmethacrylate bone cement on the order of 2 x 10 cm/s.