Analysis of Trace (mg/kg) Thiophene in Benzene Using Two-Dimensional Gas Chromatography and Flame Ionization Detection
Applications | 2003 | Agilent TechnologiesInstrumentation
Trace levels of thiophene in benzene pose a serious challenge for petrochemical production because sulfur impurities can poison catalysts, reduce product quality, and fail regulatory specifications. Traditional sulfur-selective detectors are costly and complex. A reliable, cost-effective technique that couples high chromatographic resolution with inexpensive detectors is therefore highly valuable in industrial quality control and research laboratories.
This study aims to develop and validate a two-dimensional gas chromatography (2-D GC) method using a simplified Deans switch and standard flame ionization detection (FID) for quantifying thiophene at milligram-per-kilogram levels in benzene. Key goals include achieving complete separation of thiophene from benzene and common hydrocarbon interferences, establishing calibration performance, and comparing results against a GC-atomic emission detector (AED) reference system. Simultaneously, the method is configured to perform ASTM D4492 benzene purity analysis in the same run.
Calibration standards of thiophene in purified benzene were prepared at 0.02, 0.05, 0.1, 0.2, 0.5, 1, and 2 mg/kg. Benzene blanks were purified by three-step recrystallization to ensure <0.003 mg/kg thiophene background. A 4 µL splitless injection was used throughout.
The Deans switch software calculated EPC pressures to maintain 7 mL/min flow on INNOWax and 9 mL/min on PLOT Q. Heart-cut windows were defined based on retention time precision studies of a 2 mg/kg standard (RT = 8.055 min, %RSD = 0.1), yielding a cut between 7.95 and 8.18 min. After transferring the thiophene fraction, complete separation from benzene occurred on the PLOT Q column, allowing FID quantitation.
A seven-point calibration exhibited linear response (R² = 0.9996) over 0.02–2 mg/kg. Retention times and peak areas were stable (RT %RSD ≤ 0.1; area %RSD ≤ 4.8) over multi-day tests. Analysis of a “thiophene-free” benzene sample yielded 0.20 mg/kg (RSD 2.2%), and a styrene-feedstock benzene contained 0.06 mg/kg (RSD 4.8%). Cross-validation with GC-AED produced comparable values (0.2 mg/kg and 0.05 mg/kg). Spiked hydrocarbon blanks confirmed no co-elution of C8/C9 species in the thiophene window.
Using standard FID detectors instead of specialized sulfur monitors reduces cost and complexity without sacrificing sensitivity. The heart-cut 2-D GC approach enhances selectivity and eliminates matrix interferences, enabling simultaneous benzene purity testing (ASTM D4492) and trace sulfur analysis on a single system and in one injection sequence. This versatility is ideal for petrochemical quality control, QA/QC labs, and research environments.
The described 2-D GC method using a simplified Deans switch and FID provides precise, accurate, and cost-effective quantitation of thiophene in benzene at mg/kg levels. It matches the performance of sulfur-selective detectors while enabling simultaneous benzene purity analysis. The approach delivers robust separation from hydrocarbon interferences and demonstrates excellent stability for routine petrochemical quality control.
GC, GCxGC
IndustriesEnergy & Chemicals
ManufacturerAgilent Technologies
Summary
Significance of the Topic
Trace levels of thiophene in benzene pose a serious challenge for petrochemical production because sulfur impurities can poison catalysts, reduce product quality, and fail regulatory specifications. Traditional sulfur-selective detectors are costly and complex. A reliable, cost-effective technique that couples high chromatographic resolution with inexpensive detectors is therefore highly valuable in industrial quality control and research laboratories.
Objectives and Study Overview
This study aims to develop and validate a two-dimensional gas chromatography (2-D GC) method using a simplified Deans switch and standard flame ionization detection (FID) for quantifying thiophene at milligram-per-kilogram levels in benzene. Key goals include achieving complete separation of thiophene from benzene and common hydrocarbon interferences, establishing calibration performance, and comparing results against a GC-atomic emission detector (AED) reference system. Simultaneously, the method is configured to perform ASTM D4492 benzene purity analysis in the same run.
Instrumentation Used
- Agilent 6890N GC with split/splitless injector, electronic pressure control (EPC), and pneumatics control module (PCM)
- Two FIDs (FID A on primary column, FID B on secondary column)
- Simplified Deans switch kit for heart-cutting
- Primary column: HP-INNOWax, 60 m × 0.53 mm × 1 µm film
- Secondary column: HP-PLOT Q, 15 m × 0.53 mm × 40 µm film
- Fixed restrictor: deactivated fused silica tubing, 0.58 m × 0.20 mm ID
- Agilent 7683 autosampler and ChemStation data system
- GC-AED system with sulfur-selective detector for cross-checking
Methodology
Calibration standards of thiophene in purified benzene were prepared at 0.02, 0.05, 0.1, 0.2, 0.5, 1, and 2 mg/kg. Benzene blanks were purified by three-step recrystallization to ensure <0.003 mg/kg thiophene background. A 4 µL splitless injection was used throughout.
The Deans switch software calculated EPC pressures to maintain 7 mL/min flow on INNOWax and 9 mL/min on PLOT Q. Heart-cut windows were defined based on retention time precision studies of a 2 mg/kg standard (RT = 8.055 min, %RSD = 0.1), yielding a cut between 7.95 and 8.18 min. After transferring the thiophene fraction, complete separation from benzene occurred on the PLOT Q column, allowing FID quantitation.
Main Results and Discussion
A seven-point calibration exhibited linear response (R² = 0.9996) over 0.02–2 mg/kg. Retention times and peak areas were stable (RT %RSD ≤ 0.1; area %RSD ≤ 4.8) over multi-day tests. Analysis of a “thiophene-free” benzene sample yielded 0.20 mg/kg (RSD 2.2%), and a styrene-feedstock benzene contained 0.06 mg/kg (RSD 4.8%). Cross-validation with GC-AED produced comparable values (0.2 mg/kg and 0.05 mg/kg). Spiked hydrocarbon blanks confirmed no co-elution of C8/C9 species in the thiophene window.
Benefits and Practical Applications
Using standard FID detectors instead of specialized sulfur monitors reduces cost and complexity without sacrificing sensitivity. The heart-cut 2-D GC approach enhances selectivity and eliminates matrix interferences, enabling simultaneous benzene purity testing (ASTM D4492) and trace sulfur analysis on a single system and in one injection sequence. This versatility is ideal for petrochemical quality control, QA/QC labs, and research environments.
Future Trends and Applications
- Integration with mass spectrometry in the secondary dimension to extend compound identification
- Automation of heart-cut timing and real-time process monitoring for continuous operations
- Miniaturization of 2-D GC hardware for field or on-line installations
- Extension of the method to other trace sulfur and heteroatom impurities in a variety of petrochemical matrices
Conclusion
The described 2-D GC method using a simplified Deans switch and FID provides precise, accurate, and cost-effective quantitation of thiophene in benzene at mg/kg levels. It matches the performance of sulfur-selective detectors while enabling simultaneous benzene purity analysis. The approach delivers robust separation from hydrocarbon interferences and demonstrates excellent stability for routine petrochemical quality control.
References
- ASTM D4492 “Standard Test Method for Purity of Benzene by Gas Chromatography,” Annual Book of ASTM Standards, Vol. 06.04.
- McCurry, J.D. and Quimby, B.D., “Two-dimensional Gas Chromatographic Analysis of Oxygenates and Aromatics in Gasoline Using a Heart-Cutting Technique,” Agilent Technologies Publication 5988-6696EN.
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