4.7 Article

Quantification of trace transformation products of rocket fuel unsymmetrical dimethylhydrazine in sand using vacuum-assisted headspace solid-phase microextraction

期刊

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
卷 29, 期 22, 页码 33645-33656

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-17844-1

关键词

Vacuum-assisted headspace solid-phase microextraction; Gas chromatography-mass spectrometry; Soil analysis; Transformation products; Dimethylhydrazine; Rocket fuel

资金

  1. Science Committee of the Ministry of Education and Science of the Republic of Kazakhstan [AP05133158, AP09057951]
  2. Ministry of Education and Science of the Republic of Kazakhstan
  3. Division of Analytical Chemistry of the European Chemical Society
  4. Al-Farabi Kazakh National University

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A new method for quantification of unsymmetrical dimethylhydrazine transformation products in sand samples using vacuum-assisted headspace solid-phase microextraction without addition of water followed by gas chromatography-mass spectrometry is proposed. The method offers lower detection limits, better accuracy and precision, and similar or lower cost of sample preparation compared to existing methods.
Quantification of unsymmetrical dimethylhydrazine transformation products in solid samples is an important stage in monitoring of environmental pollution caused by heavy rockets launches. The new method for simultaneous quantification of unsymmetrical dimethylhydrazine transformation products in sand samples using vacuum-assisted headspace solid-phase microextraction without addition of water followed by gas chromatography-mass spectrometry is proposed. Decreasing air evacuation time from 120 to 20 s at 23 degrees C resulted in increased responses of analytes by 25-46% and allowed obtaining similar responses as after evacuation at -30 degrees C. The best combination of responses of analytes and their relative standard deviations (RSDs) was achieved after air evacuation of a sample (m = 1.00 g) for 20 s at 23 degrees C, incubation for 30 min at 40 degrees C, and 30-min extraction at 40 degrees C by Carboxen/polydimethylsiloxane (Car/PDMS) fiber. The method was validated in terms of linearity (R-2=0.9912-0.9938), limits of detection (0.035 to 3.6 ng g(-1)), limits of quantification (0.12-12 ng g(-1)), recovery (84-97% with RSDs 1-11%), repeatability (RSDs 3-9%), and reproducibility (RSDs 7-11%). It has a number of major advantages over existing methods based on headspace solid-phase microextraction-lower detection limits, better accuracy and precision at similar or lower cost of sample preparation. The developed method was successfully applied for studying losses of analytes from open vials with model sand spiked with unsymmetrical dimethylhydrazine transformation products. It can be recommended for analysis of trace concentrations of unsymmetrical dimethylhydrazine transformation products when studying their transformation, migration and distribution in contaminated sand.

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