Determination of hexachlorocyclopentadiene in water by HS-SPME-GC-MS

A headspace solid-phase microextraction gas chromatography-mass spectrometry(HS-SPME-GC-MS) method was established for the determination of hexachlorocyclopentadiene in water, with using headspace solid-phase microextraction injection, DB-1 chromatographic column separation, and gas chromatography/mass spectrometry detector detection. The effects of coating solid-phase extraction needles, inlet temperatures, solid-phase extraction conditions, salt effects on the determination were systematically investigated, and the method was validated under the optimal experimental conditions. The results showed that hexachlorocyclopentadiene exhibited good linearity with chromatographic peak area within the mass concentration range of 0.1-10 µg/L, with a correlation coefficient of 0.997 and a detection limit of 0.03 µg/L. The actual surface water and wastewater samples were measured, and the monitoring result of wastewater sample was 0.5 µg/L, while the monitoring result of surface water sample was not detected. The actual samples were spiked with 0.5 µg/L and 1.0 µg/L, respectively. The recovery rate was 70%-87%, and the relative standard deviation was 4.14%-13.9%(n=6). This method was simple to operate, did not use organic solvents for extraction, had good precision and high accuracy, which could be used for rapid determination of hexachlorocyclopentadiene in industrial wastewater and surface water.

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Publication Details

Journal
SHILAP Revista de lepidopterología
Published
2025-01-01
DOI
https://doi.org/10.19965/j.cnki.iwt.2023-1226
Primary Topic
Analytical chemistry methods development
Type
article
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article

Determination of hexachlorocyclopentadiene in water by HS-SPME-GC-MS

SHILAP Revista de lepidopterología
Analytical chemistry methods development
article

Determination of hexachlorocyclopentadiene in water by HS-SPME-GC-MS

article en

Abstract

A headspace solid-phase microextraction gas chromatography-mass spectrometry(HS-SPME-GC-MS) method was established for the determination of hexachlorocyclopentadiene in water, with using headspace solid-phase microextraction injection, DB-1 chromatographic column separation, and gas chromatography/mass spectrometry detector detection. The effects of coating solid-phase extraction needles, inlet temperatures, solid-phase extraction conditions, salt effects on the determination were systematically investigated, and the method was validated under the optimal experimental conditions. The results showed that hexachlorocyclopentadiene exhibited good linearity with chromatographic peak area within the mass concentration range of 0.1-10 µg/L, with a correlation coefficient of 0.997 and a detection limit of 0.03 µg/L. The actual surface water and wastewater samples were measured, and the monitoring result of wastewater sample was 0.5 µg/L, while the monitoring result of surface water sample was not detected. The actual samples were spiked with 0.5 µg/L and 1.0 µg/L, respectively. The recovery rate was 70%-87%, and the relative standard deviation was 4.14%-13.9%(n=6). This method was simple to operate, did not use organic solvents for extraction, had good precision and high accuracy, which could be used for rapid determination of hexachlorocyclopentadiene in industrial wastewater and surface water.

SHILAP Revista de lepidopterología
Beijing Zhongke Science and Technology (China) (CN), China National Environmental Monitoring Center (CN), Beijing Municipal Ecological and Environmental Monitoring Center (CN)
Clean water and sanitation
Openalex Percentile: Top 56%
Analytical chemistry methods development
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