Comprehensive two-dimensional gas chromatography

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Comprehensive Two-dimensional gas chromatography, or GCxGC is a multidimensional gas chromatography technique that was originally described in 1991 by Professor Phillips and his student Liu [1].

GCxGC utilizes two different columns with two different stationary phases. In GCxGC, all of the effluent from the first dimension column is diverted to the second dimension column via a modulator. The modulator quickly traps, then "injects" the effluent from the first dimension column onto the second dimension. This process creates a retention plane of the 1st dimension separation x 2nd dimension separation.

The Oil and Gas Industry were early adopters of the technology for the complex oil samples to determine the many different types of Hydrocarbons and its isomers. Nowadays in these types of samples it has been reported that over 30000 different compounds could be identified in a crude oil with this Comprehensive Chromatography Technology (CCT).

The CCT evolved from a technology only used in academic R&D laboratories, into a more robust technology used in many different industrial labs. Comprehensive Chromatography is used in forensics, food and flavor, environmental, metabolomics, biomarkers and clinical applications. Some of the most well-established research groups in the world that are found in Australia,[2][3] Italy,[4], the Netherlands, Canada,[5] United States,[6][7] and Brazil use this analytical technique.

Modulation: The process[edit]

In GC × GC two columns are connected sequentially, typically the first dimension is a conventional column and the second dimension is a short fast GC type, with a modulator positioned between them. The function of the modulator can be divided into basically three processes:

  1. continuously collect small fractions of the effluent from 1D, ensuring that the separation is maintained in this dimension;
  2. focus or refocus the effluent of a narrow band;
  3. to quickly transfer the 2D fraction collected and focused as a narrow pulse. Taken together, these three steps is called modulation cycle, which is repeated throughout the chromatographic run.

Thermal modulation[edit]

The most frequently used type of modulation is the thermal modulation (patent holder is ZOEX Corporation), where liquid nitrogen is used to (cryogenic) trap (immobilize) all the components eluting from the first dimension. After a fixed time interval a hot stream pulse is mobilizing a part of the compounds again. This hot pulse can be considered as the injection starting point into the second dimension column. The latest version is called a loop-type Thermal modulator where the released compounds are trapped and refocused for a second time (and released again) to have perfect peak shapes and maximum resolution in the second dimension. With the thermal modulator also very volatile compounds can be modulated.

The thermal modulation in practice is a liquid nitrogen cooled loop system that provides the lowest temperature for thermal modulation, and modulates the widest range (C2 to C55) of organic compounds. The temperature at the jet is -189 °C. The maximum temperature of the hot jet is 475 °C. Even methane has been modulated with liquid nitrogen cooled gas jets like those in this type of modulator.

Closed Cycle Refrigerated Loop Modulation[edit]

This loop modulation system eliminates the need for liquid nitrogen for thermal modulation. The system employs a closed cycle refrigerator/heat exchanger to produce -90 °C at the jet. The cooling is done by indirect cooling of gaseous nitrogen and therefore this type modulates volatile and semi volatile compounds over the C6+ range.

Flow modulation[edit]

This is a valve-based approach, where differential flows are used to ‘fill’ and ‘flush’ a sample loop. Flow modulation does not suffer from the same volatility restrictions as thermal modulation, as it does not rely on trapping analytes using a cool jet - meaning volatiles <C5 can be efficiently modulated.[8]

Modulation period[edit]

The time required to complete a cycle is called the period of modulation (modulation time) and is actually the time in between two hot pulses, which typically lasts between 2 and 10 seconds is related to the time needed for the compounds to eluted in 2D.

Sensitivity[edit]

Another key aspect of GC x GC that can be highlighted is that the result from the refocusing in the 1D, which occurs during the modulation, causes a significant increase in sensitivity. The modulation process causes the chromatographic bands in GC × GC systems are 10-50 times closer than in 1D-GC, resulting in values for much better peak widths (FWHM Full Width Half Mass) between 50 ms to 500 ms, which requires detectors with fast response and small internal volumes.

Column set[edit]

The set of columns can be configured with various types. In the original work, column sets were mainly poly(dimethylsiloxane) in the first dimension and poly(ethyleneglycol) in the second dimension. These so-called straight phase column sets are suitable for hydrocarbon analysis. Therefore, these are still used most frequently in the oil and gas industry. For applications that require the analysis of polar compounds in a non-polar matrix, a reverse-phase column set gives more resolution. The first dimension column in this situation is a polar column, followed by a mid-polar second dimension column. Other applications can be configured differently according to their specific needs. For example, they may include chiral columns for optical isomer separation or PLOT columns for volatiles and gas samples.

Optimizing the application is more complex compared to 1D separations, as there are more parameters involved. Flow and oven temperature program are still important, but hot jet pulse duration, length of the second dimension column and modulation time also affect the final results. The output is also different: the GCxGC technique produces a three-dimensional plot rather than a traditional chromatogram, facilitated by specially designed software[9] packages. The new and different way of presenting and evaluating data offers additional information. For example, modern software,[9] can perform group-type separation as well as automated peak identification (with Mass Spectrometry).

Detectors[edit]

Due to the small width of the peak in the second dimension, suitable detectors are needed. Examples include flame ionization detector (FID), (micro) electron capture detector (µECD) and mass spectrometry analyzers such as fast time of flight (TOF). Several authors have published work using quadrupole Mass Spectrometry (qMS), though some trade-offs have to be accepted as these are much slower.

References[edit]

  1. ^ Liu, Zaiyou; Phillips, John B. (1991-06-01). "Comprehensive Two-Dimensional Gas Chromatography using an On-Column Thermal Modulator Interface". Journal of Chromatographic Science. 29 (6): 227–231. doi:10.1093/chromsci/29.6.227. ISSN 0021-9665.
  2. ^ https://web.archive.org/web/20100627210058/http://www.rmit.edu.au/staff/philip-marriott. Archived from the original on June 27, 2010. Retrieved July 9, 2010. Missing or empty |title= (help)
  3. ^ "Home - School of Chemistry - University of Tasmania, Australia". Fcms.its.utas.edu.au. Retrieved 2012-10-13.
  4. ^ "Analytical Food Industry". Sepsci.farmacia.unime.it. Archived from the original on 2012-03-09. Retrieved 2012-10-13.
  5. ^ "Prof. Dr. T. Gorecki - Waterloo Science - University of Waterloo". Science.uwaterloo.ca. Retrieved 2012-10-13.
  6. ^ "Dimandja". Gcxgcroundrobin.org. Retrieved 2012-10-13.
  7. ^ "Robert E. Synovec - UW Dept. of Chemistry". Depts.washington.edu. Retrieved 2012-10-13.
  8. ^ "INSIGHT flow modulator". SepSolve Analytical. Retrieved 2012-10-13.
  9. ^ a b "GC Image Software for Multidimensional Chromatography". Zoex Corp, GC Image LLC. Retrieved 2016-12-21.