Solid Phase Microextraction of Semivolatile Compounds
Aplikace | 1998 | MerckInstrumentace
Solid phase microextraction (SPME) offers a solvent-free approach to isolate semivolatile organic compounds from water, addressing regulatory and environmental demands to reduce hazardous solvent use. By simplifying sample preparation and minimizing waste, SPME enhances routine monitoring and quality control in environmental laboratories.
This application note evaluates a 7 µm polydimethylsiloxane (PDMS) SPME fiber for extracting US EPA-listed polycyclic aromatic hydrocarbons (PAHs) and phthalate esters from spiked water samples. Key goals include assessing method linearity, reproducibility, extraction efficiency, and compatibility with GC/MS analysis.
Samples of 4 mL deionized water spiked at 10–200 ppb levels were equilibrated with the PDMS fiber for 15 minutes. Adsorbed analytes were thermally desorbed in a split/splitless GC injector at 280 °C and transferred onto a narrow-bore PTE-5 capillary column under helium flow. Detection was performed by mass spectrometry over m/z 45–465 in full scan mode.
Response factors for target PAHs and nonpolar phthalates remained close to unity across five concentration levels, with relative standard deviations mostly under 10 %, demonstrating excellent linearity and precision. Parts-per-trillion detection limits are achievable with ion-trap MS. More polar phthalates (dimethyl- and diethyl-phthalate) exhibited low recovery on the nonpolar PDMS fiber, indicating the need for polar phase coatings for these analytes. Chromatograms showed sharp peaks with high signal-to-baseline ratios, confirming efficient analyte transfer and minimal carryover.
Ongoing developments include new fiber coatings tailored for polar and high-molecular-weight analytes, integration with HPLC interfaces, miniaturized field‐deployable systems for on-site monitoring, and further automation for high-throughput environmental screening. Expanded regulatory adoption of SPME methods is anticipated.
The 7 µm PDMS SPME fiber provides a robust, sensitive, and environmentally friendly alternative to traditional solvent-based extractions for semivolatile organics in water. Its ease of use, reproducibility, and compatibility with GC/MS make it an attractive choice for routine environmental analysis.
1. Zhang Z. and Pawliszyn J., Anal. Chem. 65:1843–1852 (1993)
GC/MSD, SPME, Spotřební materiál
ZaměřeníŽivotní prostředí
VýrobceMerck
Souhrn
Significance of the Topic
Solid phase microextraction (SPME) offers a solvent-free approach to isolate semivolatile organic compounds from water, addressing regulatory and environmental demands to reduce hazardous solvent use. By simplifying sample preparation and minimizing waste, SPME enhances routine monitoring and quality control in environmental laboratories.
Objectives and Study Overview
This application note evaluates a 7 µm polydimethylsiloxane (PDMS) SPME fiber for extracting US EPA-listed polycyclic aromatic hydrocarbons (PAHs) and phthalate esters from spiked water samples. Key goals include assessing method linearity, reproducibility, extraction efficiency, and compatibility with GC/MS analysis.
Methodology
Samples of 4 mL deionized water spiked at 10–200 ppb levels were equilibrated with the PDMS fiber for 15 minutes. Adsorbed analytes were thermally desorbed in a split/splitless GC injector at 280 °C and transferred onto a narrow-bore PTE-5 capillary column under helium flow. Detection was performed by mass spectrometry over m/z 45–465 in full scan mode.
Used Instrumentation
- SPME fiber assembly: 7 µm PDMS coating, Supelco catalog no. 57302
- Fiber holder: manual or automated sampling interface
- Gas chromatograph: Finnigan Incos GC/MS system
- Capillary column: 30 m × 0.25 mm ID × 0.25 µm PTE-5 fused silica
- Carrier gas: helium at 40 cm/sec (60 °C)
Main Results and Discussion
Response factors for target PAHs and nonpolar phthalates remained close to unity across five concentration levels, with relative standard deviations mostly under 10 %, demonstrating excellent linearity and precision. Parts-per-trillion detection limits are achievable with ion-trap MS. More polar phthalates (dimethyl- and diethyl-phthalate) exhibited low recovery on the nonpolar PDMS fiber, indicating the need for polar phase coatings for these analytes. Chromatograms showed sharp peaks with high signal-to-baseline ratios, confirming efficient analyte transfer and minimal carryover.
Benefits and Practical Applications
- Eliminates chlorinated solvent use and associated disposal costs
- Reduces sample preparation time (equilibrium in 2–30 min)
- Reusable fibers lower consumable expenses
- Compatible with standard GC or GC/MS systems and autosamplers
- Sensitive detection of volatile, semivolatile, and nonvolatile compounds in water or headspace
Future Trends and Potential Applications
Ongoing developments include new fiber coatings tailored for polar and high-molecular-weight analytes, integration with HPLC interfaces, miniaturized field‐deployable systems for on-site monitoring, and further automation for high-throughput environmental screening. Expanded regulatory adoption of SPME methods is anticipated.
Conclusion
The 7 µm PDMS SPME fiber provides a robust, sensitive, and environmentally friendly alternative to traditional solvent-based extractions for semivolatile organics in water. Its ease of use, reproducibility, and compatibility with GC/MS make it an attractive choice for routine environmental analysis.
Reference
1. Zhang Z. and Pawliszyn J., Anal. Chem. 65:1843–1852 (1993)
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