Applications of PTV Injectors for Problem Solving in the Petrochemical Industry Part 1:- Thermal Desorption with GC and GC-MS
Applications | | GL SciencesInstrumentation
Programmable Temperature Vaporising (PTV) thermal desorption coupled with capillary gas chromatography and mass spectrometry offers a direct, solvent-free approach to analyse solid petrochemical samples. This technique addresses limitations of conventional split, splitless and on-column injections by minimising sample loss, thermal degradation and volatility discrimination, while enabling trace-level sensitivity without extensive sample preparation.
The application note describes four industrial case studies demonstrating PTV thermal desorption as a problem-solving tool: 1) characterisation of hydrocarbon‐contaminated explosive powders, 2) identification of odorous compounds in printed polyethylene film, 3) quantification of residual low-molecular-weight hydrocarbons in reactor and pelletized polyethylene, and 4) direct determination of phthalate ester plasticisers in PVC.
Analyses were performed using Optic Model 2-200 PTV injectors on HP5890 and Chrompack CP9000 GCs, interfaced with VG Trio3 and Trio 1000 single‐quadrupole MS systems (EI at 70 eV; CI with ammonia). Columns included HP-1, DB-5MS, DB-Wax and CP-SIL 8 capillaries. Samples (1–15 mg) were loaded into fritted liners; expert or standard desorption modes programmed ramp rates (e.g. 16 °C/min) and pressure profiles to release volatiles before split or splitless transfer onto cooled columns. Quantification down to 1 ppm was achieved using GC-FID with internal n-heneicosane standards.
PTV thermal desorption enables rapid, high-sensitivity screening of solids without solvent use, streamlining QA/QC workflows, trace contaminant detection and failure analysis across petrochemical, polymer and materials industries.
Advancements may include integration of headspace trapping for ultra-volatile analytes, automation for routine QA/QC, expansion to environmental and catalyst materials, and enhanced injector designs for broader temperature and pressure control.
PTV thermal desorption with GC and GC-MS provides a versatile, robust platform for direct solid sample analysis in the petrochemical sector, offering enhanced sensitivity, reduced sample handling and reliable identification and quantification of complex analytes.
1. Vogt W, Jacob K, Obwexer HW. J Chromatogr. 1979;186:197.
2. Vogt W, Jacob K, Obwexer HW. J Chromatogr. 1982;174:437.
3. Poy FS, Visani F, Terrosi F. J Chromatogr. 1981;217:81.
4. Teske J, Efer J, Engelward W. Chromatographia. 1997;46:580–586.
GC, Thermal desorption
IndustriesEnergy & Chemicals , Homeland Security, Materials Testing
ManufacturerAgilent Technologies, GL Sciences
Summary
Importance of the Topic
Programmable Temperature Vaporising (PTV) thermal desorption coupled with capillary gas chromatography and mass spectrometry offers a direct, solvent-free approach to analyse solid petrochemical samples. This technique addresses limitations of conventional split, splitless and on-column injections by minimising sample loss, thermal degradation and volatility discrimination, while enabling trace-level sensitivity without extensive sample preparation.
Study Objectives and Overview
The application note describes four industrial case studies demonstrating PTV thermal desorption as a problem-solving tool: 1) characterisation of hydrocarbon‐contaminated explosive powders, 2) identification of odorous compounds in printed polyethylene film, 3) quantification of residual low-molecular-weight hydrocarbons in reactor and pelletized polyethylene, and 4) direct determination of phthalate ester plasticisers in PVC.
Methodology and Instrumentation
Analyses were performed using Optic Model 2-200 PTV injectors on HP5890 and Chrompack CP9000 GCs, interfaced with VG Trio3 and Trio 1000 single‐quadrupole MS systems (EI at 70 eV; CI with ammonia). Columns included HP-1, DB-5MS, DB-Wax and CP-SIL 8 capillaries. Samples (1–15 mg) were loaded into fritted liners; expert or standard desorption modes programmed ramp rates (e.g. 16 °C/min) and pressure profiles to release volatiles before split or splitless transfer onto cooled columns. Quantification down to 1 ppm was achieved using GC-FID with internal n-heneicosane standards.
Key Results and Discussion
- Explosive powders: GC-MS revealed C₈–C₂₂ saturated and aromatic hydrocarbons; the faulty batch contained ~3× more hydrocarbons than normal, implicating fuel-oil combustion products in the explosion risk.
- Printed polyethylene film: Thermal desorption detected oxygenated low-molecular-weight species (e.g. oxidation products of peroxide initiators) absent in unprinted film, pinpointing odor sources from the printing process.
- Polyethylene volatiles: Reactor resin and pellet samples exhibited C₈–C₂₄ alkanes/alkenes; complete desorption of up to C₂₂ was confirmed. GC-FID quantification showed reactor powder retained higher volatile content, with individual components measured at ppm levels.
- PVC plasticisers: Direct desorption obviated solvent extraction. GC-FID and GC-MS identified blended di-undecyl and di-iso-undecyl phthalate esters in unknown PVC samples, demonstrating rapid plasticiser profiling.
Benefits and Practical Applications
PTV thermal desorption enables rapid, high-sensitivity screening of solids without solvent use, streamlining QA/QC workflows, trace contaminant detection and failure analysis across petrochemical, polymer and materials industries.
Future Trends and Opportunities
Advancements may include integration of headspace trapping for ultra-volatile analytes, automation for routine QA/QC, expansion to environmental and catalyst materials, and enhanced injector designs for broader temperature and pressure control.
Conclusion
PTV thermal desorption with GC and GC-MS provides a versatile, robust platform for direct solid sample analysis in the petrochemical sector, offering enhanced sensitivity, reduced sample handling and reliable identification and quantification of complex analytes.
Reference
1. Vogt W, Jacob K, Obwexer HW. J Chromatogr. 1979;186:197.
2. Vogt W, Jacob K, Obwexer HW. J Chromatogr. 1982;174:437.
3. Poy FS, Visani F, Terrosi F. J Chromatogr. 1981;217:81.
4. Teske J, Efer J, Engelward W. Chromatographia. 1997;46:580–586.
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