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In my previous blog, I discussed the possibility of backflash in splitless GC injection and its effect on quantitative reproducibility and carry-over.While much is written in the literature on optimization of splitless injection conditions, little is available on the implementation and optimization of increased head pressure (pressure pulsed) injection, so we will concentrate on this aspect of injection optimization.
In my previous blog, I discussed the possibility of backflash in splitless GC injection and its effect on quantitative reproducibility and carry-over.
While much is written in the literature on optimization of splitless injection conditions, little is available on the implementation and optimization of increased head pressure (pressure pulsed) injection, so we will concentrate on this aspect of injection optimization.
In most split/splitless GC injection systems there is a finite volume within the liner in which the gaseous sample needs to be maintained. If the gaseous volume of the sample exceeds the liner volume, then backflash occurs and analyte may be deposited onto the non-heated surfaces within the septum purge, split, and even carrier gas inlet lines leading into and out of the inlet. Subsequent backflashed injections risk re-solubilizing some of this deposited material and “pulling” it back into the inlet and ultimately onto the column as the inlet empties under splitless conditions, thus contaminating the injected sample vapor.
The risk of “backflash” can be assessed using simple calculators into which the GC inlet operating parameters are entered, along with some information on sample solvent and injection volume, and an assessment is made of the vapor volume created on injection against the available internal volume of the inlet liner used.
Analysis conditions and backflash assessment for injection of a predominantly aqueous sample is shown in Figure 1.
Note: inlet pressure can be found from the instrument software or instrument front panel and will be determined by the column dimensions and the carrier gas flow (for splitless injection). Alternatively this pressure may be calculated using an offline calculator, again based upon the required column flow and column dimensions.(See here for a pressure/flow calculator https://www.agilent.com/en/support/gas-chromatography/gccalculators)
In the above example, the liner volume is exceeded by the volume of sample vapor created and therefore there is risk of backflash and carry-over, leading to potential contamination and quantitation issues. Sample solvents with high expansion coefficients, such as water, are particularly problematic as small injection volumes lead to large vapor volumes.
Obviously one way to overcome these issues is to inject a lower sample volume, however in splitless injection, which is typically used for the analysis of trace analytes, this may lead to an issue with the detectability of analytes and sensitivity of the method. An alternative way to overcome backflash is to reduce the volume of sample vapor which is created during the injection by increasing the pressure within the inlet which constrains the expansion of the sample. This is known as “pressure pulsed” injection and the increased pressure applied within the inlet is typically reduced prior to the end of the splitless period to re-establish the required pressure and flow through the column for the analysis.
With this approach in mind, a further assessment may be made to identify the inlet pressure required to constrain the vapor volume created with our 1-mL aqueous sample injection to within the available volume of the inlet liner – as shown in Figure 2.
Figure 2 indicates that an increased head pressure of between 30 psi and 50 psi (typically the upper limit of the pulse pressure available in most systems) would lead to the solvent vapor volume being constrained within the liner and therefore a reduced possibility of backflash and carryover.
The implementation of pressure pulsed injection requires the addition of two further variables (1 and 2 below) to the splitless injection method which now typically must define:
It is important to note from Figure 3 that there is a finite time required to move from the higher pulse pressure to the pressure required for the analytical separation and even though the rate of pressure reduction is high (98psi/min.) This will still take 15 s to recover from a 30-psi pulse to the 5.4-psi required for the analysis. Careful consideration is required in setting the pressure pulse time in relation to the splitless time (time at which the split vent is opened) as, in our experience, the relationship between the pressure pulse end time and the splitless time can be critical in determining the reproducibility of the injection. In some cases it is more favorable for the split to be opened whilst the pressure is high, and the pulse time relative to the splitless time often requires some empirical optimization.
Figure 4 shows chromatograms resulting from splitless and pulsed splitless injections of an aqueous sample containing 5% dimethylformamide (DMF) (aq) followed by a water “wash” injection and a subsequent ‘”standard” injection containing ethyl hexanol (5.55 mins) and benzaldehyde (6.15 mins).
The top chromatogram of Figure 4, generated using standard splitless conditions, shows a large amount of carryover of the DMF (retention time 5.05 mins.) in both the subsequent water wash and the “standard” chromatograms. In the bottom chromatogram, a pressure pulsed injection of 50 psi for 1.5 min with a 2-min splitless time is used to reduce carryover. While there is a very small amount of DMF carryover into the water wash injection, this is an extremely challenging application example and the amount of carryover is drastically reduced in comparison to the standard splitless experiment. The subsequent “standard” injection shows no trace of DMF.
It is very important to note that when using pressure pulsed injection, the usual rules of splitless injection apply and it is important that the initial oven temperature is at least 10 °C below the boiling point of the injection solvent to allow for good peak focusing, Further, the initial hold time for the oven temperature may require some empirical optimization in order to derive the best peak shape/ efficiency, however the hold time should not be any less than the splitless time.
Under some circumstances, peak slitting may be observed when undertaking pulsed pressure injection which can be attributed to the rapid change in pressure at the end of the pressure pulse. If this occurs, first extend the time between the end of the pressure pulse and the splitless (purge-on) time and, if unsuccessful, alter the ramp rate of pressure reduction at the end of the pressure pulse from 98 psi per min to 20 psi per min and lengthen the splitless time commensurately. The use of a retention gap (1-3 m) of fused silica prior to the analytical column may also help to reduce the effects of peak splitting.
It is also recommended that the inlet septum is changed regularly in order to avoid analyte losses during sample addition into the inlet under the increased pressure conditions. Whenever pressure pulsed splitless injection is implemented, one needs to not only assess the reduction in carry-over, an assessment of the precision of analytes of interest should also be made to ensure appropriate conditions have been selected. Figure 5 (top) shows the assessment of repeatability using the pressure pulsed injection conditions of Figure 4, clearly highlighting variability of peak area of the ethyl hexanol and benzaldehyde peaks. By shortening both the pressure pulse and splitless times (liner clearance time can be calculated at 0.18 mins), this variability is eliminated to within the required reproducibility requirements.
Tony Taylor is the technical director of Crawford Scientific and ChromAcademy. He comes from a pharmaceutical background and has many years research and development experience in small molecule analysis and bioanalysis using LC, GC, and hyphenated MS techniques. Taylor is actively involved in method development within the analytical services laboratory at Crawford Scientific and continues to research in LC-MS and GC-MS methods for structural characterization. As the technical director of the CHROMacademy, Taylor has spent the past 12 years as a trainer and developing online education materials in analytical chemistry techniques.