Articles

Advanced Capillary Column Technology Improves Analysis of Volatile Amines

26 Oct 2020

Short-chain volatile amines, such as monomethylamine, diethylamine, and triethylamine, are of great importance in the petrochemical industry and play a critical role is inhibiting corrosion. Volatile amines are used as gas-scrubbing agents to remove hydrogen sulfide from refinery and natural gas streams, as well as for removing carbon dioxide during the production of ammonia. While accurate data on volatile amine content is vital for optimizing the manufacture of compounds of many different classes, gas chromatographic analysis can be quite challenging due to their basic nature and high polarity. Because of these characteristics, amines will interact with active sites in the analytical column and along the sample pathway, resulting in broad, tailing peaks that are difficult to integrate accurately.

In order to improve chromatography for volatile amines, capillary columns must be highly inert and offer good retention and efficiency at low temperatures. In addition, they must be able to withstand tough matrices, as amines are often analyzed in the presence of water, alcohol, or ammonia. Base-modified polyethylene glycol columns are one option, but they suffer from relatively poor stability and a loss of efficiency below 60 °C. Siloxane columns are another option, but most commercially available siloxane-based columns for amine applications work well for pure samples, but perform poorly in the presence of tough matrices, such as water (Figure 1). Until recently, commercially available columns for the analysis of volatile amines suffered from short lifetimes and displayed poor reproducibility in amine response. A new column developed by Restek, the Rtx-Volatile Amine column, offers improved chromatographic performance and stability.

Figure 1: Short-chain volatile amines often exhibit broad, tailing peaks when analyzed in water on typical volatile amine capillary columns.
Short-Chain Amine Peaks Broaden, Tail, and Split When Analyzed on Typical Volatile Amine Columns

GC_PC1242

Conditions

ColumnConventional volatile amine column, 60 m, 32 mm ID
Standard/SampleShort-chain amines
Diluent:Water
Injection
Inj. Vol.:1 µL split (split ratio 15:1)
Inj. Temp.:220 °C
Split Vent Flow Rate:30 mL/min
Oven
Oven Temp.:40 °C (hold 10 min) to 250 °C at 20 °C/min (hold 10 min)
Carrier GasH2, constant flow
Flow Rate:2 mL/min
Linear Velocity:35 cm/sec
DetectorFID @ 250 °C
InstrumentAgilent/HP6890 GC
AcknowledgementCourtesy of Gilbert Baele, Taminco (Antwerp, Belgium)

New Rtx-Volatile Amine Column Produces Stable, Symmetrical Peaks

In order to assure symmetrical peaks and good reproducibility, both surface deactivation and polymer stability were considered in the development of the Rtx-Volatile Amine capillary GC column. Proper deactivation reduces surface adsorption of short-chain amines, which improves peak shape significantly. As shown in Figure 2, highly symmetrical peaks are obtained for monomethylamine, diethylamine, and triethylamine, as well as for methanol. In addition, the film thickness was increased in order to maintain efficiency at temperatures as low as 40 °C, and the stationary phase was intensively cross-linked in order to improve mechanical stability in the presence of water. The result is a new column chemistry that reliably produces good peak shape and response for volatile amines. As shown in Figure 3, even after 40 injections of amines in water, peak shapes are almost identical.

Figure 2: When analyzed on new Rtx-Volatile Amine columns, chromatography is greatly improved and symmetrical peaks are obtained for both early eluting amines and methanol.
Short-Chain Amines on Rtx-Volatile Amine

GC_PC1243

Conditions

ColumnRtx-Volatile Amine, 60 m, 0.32 mm ID (cat.# 18078)
Standard/SampleShort-chain amines
Diluent:Water
Injection
Inj. Vol.:1 µL split (split ratio 15:1)
Inj. Temp.:220 °C
Split Vent Flow Rate:30 mL/min
Oven
Oven Temp.:40 °C (hold 10 min) to 250 °C at 20 °C/min (hold 10 min)
Carrier GasH2, constant flow
Flow Rate:2 mL/min
Linear Velocity:35 cm/sec
DetectorFID @ 250 °C
InstrumentAgilent/HP6890 GC
AcknowledgementCourtesy of Gilbert Baele, Taminco (Antwerp, Belgium)
Figure 3: Peak shape for amine compounds is virtually unchanged, even after 40 injections.
Stability Overlay: 1st and 40th Injections of Short-Chain Amines in Water on Rtx-Volatile Amine

GC_PC1244

Conditions

ColumnRtx-Volatile Amine, 60 m, 0.32 mm ID (cat.# 18078)
Standard/SampleShort-chain amines
Diluent:Water
Injection
Inj. Vol.:1 µL split (split ratio 15:1)
Inj. Temp.:220 °C
Split Vent Flow Rate:30 mL/min
Oven
Oven Temp.:40 °C (hold 10 min) to 250 °C at 20 °C/min (hold 10 min)
Carrier GasH2, constant flow
Flow Rate:2 mL/min
Linear Velocity:35 cm/sec
DetectorFID @ 250 °C
InstrumentAgilent/HP6890 GC
AcknowledgementCourtesy of Gilbert Baele, Taminco (Antwerp, Belgium)

Practical Solutions for Analyzing Volatile Amines

The strong dipole in the basic amino group is what causes the interactions with the surface silanols that result in nonlinear adsorption effects. In practice, derivatization can be used to reduce these interactions, but it is time-consuming and can produce secondary matrix effects that alter recoveries. Derivatization can be avoided by using an Rtx-Volatile Amine GC column as the robust column chemistry minimizes reactivity and elutes the amine compounds in sharp peaks, even in the presence of water. Priming is another technique that is often used in amine analysis. In this approach, several initial injections of a high boiling point amine are performed so that the priming amine compound reacts with any active sites and provides a systemic, but short-lived, deactivation. While, using a properly deactivated analytical column provides a better long-term solution, priming can be useful in that the priming compound can, at least temporarily, deactivate non-column parts of the sample pathway, including the injection and detection port liners.

In addition to its inertness and tolerance of aqueous matrices, the Rtx-Volatile Amine column also offers high loadability. As shown in Figures 4-7, this column provides excellent chromatographic separations of impurities in pyridine, diethylamine, triethylamine, and isopropylamine. In addition, when analyzing ammonia and water, both compounds elute as nearly symmetrical peaks (Figure 8).

Summary

A new stationary phase for short-chain amine applications has been developed using nonpolar stabilized polysiloxane. Rtx-Volatile Amine columns are extremely inert, assuring accuracy and sensitivity when analyzing volatile amines, including free ammonia. In addition, the highly robust phase withstands repeated water injections, resulting in improved column lifetime.

Figure 4: Impurities in pyridine.
Impurities in Pyridine on Rtx-Volatile Amine

GC_PC1246

Conditions

ColumnRtx-Volatile Amine, 60 m, 0.32 mm ID (cat.# 18078)
Standard/SamplePyridine
Injection
Inj. Vol.:1 µL split (split ratio 15:1)
Inj. Temp.:250 °C
Oven
Oven Temp.:120 °C
Carrier GasH2, constant flow
Flow Rate:2 mL/min
DetectorFID @ 250 °C
InstrumentAgilent/HP6890 GC
Figure 5: Impurities in diethylamine.
Impurities in Diethylamine on Rtx-Volatile Amine

GC_PC1247

See Figure 4 for conditions.

Figure 6: Impurities in triethylamine.
Impurities in Triethylamine on Rtx-Volatile Amine

GC_PC1248

See Figure 4 for conditions.

Figure 7: Impurities in isopropylamine.
Impurities in Isopropylamine on Rtx-Volatile Amine

GC_PC1249

See Figure 4 for conditions.

Products Mentioned


Colonne capillaire Rtx-Volatile Amine, L 60 m, DI 0.32 mm, 5.0 µm

Authors

  • Jaap de Zeeuw

    Jaap is a world-renowned chromatographer with over 40 years of experience, including 15 years with Restek and 27 years with Varian/Chrompack prior to joining Restek. Throughout his career, Jaap has focused the chromatographic challenges of industrial analysis. For his 1979 graduation from The Institute for Higher Education, where he specialized in chemistry, Jaap authored a paper titled "The Challenge of Coating Flexible Fused Silica Capillary Columns" and has since distinguished himself as an authority on the subject. Jaap has been directly involved with the creation of numerous chemically bonded columns, including the first bonded PEG column and the stabilized PLOT columns widely used in the petrochemical arena. He has also helped develop new techniques, such as fast GC-MS using vacuum GC technology (low-pressure GC or LPGC). Over his innovative career, he has filed several patents for his work. Based out of the Netherlands, Jaap is extensively published and regularly travels internationally to share his knowledge. After retiring from Restek, Jaap founded CreaVisions, where he works as a GC Consultant and teaches master classes on key GC topics as well as on creativity in science.

    View all posts
  • Ron Stricek
  • Gary Stidsen

    Gary has over 30 years of experience in chromatography, including sample preparation techniques, air sampling, and chromatographic analysis. He specializes in gas chromatography with an emphasis on the environmental and petroleum markets. Gary has been at Restek for almost 20 years and has played an instrumental role in developing many key products and numerous applications. During this time, he has served as the innovations lab manager, product manager for both the GC Column and air sampling lines, and director of research and innovation, where he was responsible for all aspects of research and new product development. Gary is currently our business manager overseeing reference standards, air sampling, and sample preparation.

    View all posts
PCTJ1676