4.7 Article

Assessment of commercial porous polyethylene frit for extraction of polycyclic aromatic hydrocarbons from water

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 413, 期 11, 页码 3005-3015

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03236-4

关键词

Porous polyethylene frit; Commercial sorbent; Polycyclic aromatic hydrocarbons; Water

资金

  1. National Natural Science Foundation of China [21507116]
  2. Fundamental Research Funds for the Central Universities, China University of Geosciences (Wuhan) [CUGL160409]

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UMPESP is an effective sorbent for extracting PAHs from water samples, with better desorption and sorption efficiencies compared to LDPEP, and comparable to SR. It has a shorter equilibrium time and larger surface area, making it suitable for the extraction of PAHs.
Exploring commercial and inexpensive sorbents for extraction of organic pollutants is still an active area of research. Ultrahigh molecular weight polyethylene sieve plate (UMPESP) is a commercially available, low-cost, and porous frit, which has been widely used in solid-phase extraction cartridges to fix the filling materials. In this work, UMPESP was investigated for the extraction of polycyclic aromatic hydrocarbons (PAHs) from water samples. The desorption and sorption efficiencies of UMPESP were first evaluated and compared with two previously reported sorbents, low-density polyethylene plastic pellet (LDPEP) and silicone rod (SR). The comparative results showed that quantitative desorption of analytes from UMPESP, which could be easily achieved with 2 x 1.5 mL n-hexane, was more effective than that of LDPEP (>6 x 1.5 mL n-hexane) and comparable to that of SR. Additionally, shorter equilibrium time was rendered by UMPESP (shaking for 120 min) compared with SR (>480 min), due to the porous structure and larger surface area of the former. Different parameters that affect the extraction efficiency, including organic modifier, ionic strength, and pH value, were then studied. The optimized method coupled with gas chromatography-mass spectrometry afforded good linearity in a concentration range of 10-5000 ng L-1 (except acenaphthene in the range of 25-5000 ng L-1) with coefficients of determination ranging from 0.9957 to 0.9995 and relative standard deviations below 13.8%. The limits of detection and quantification were 0.04-3.35 ng L-1 and 0.13-11.16 ng L-1, respectively. Finally, the method was successfully applied to determine PAHs in real water samples, and the results showed no statistically significant difference with the concentrations derived from liquid-liquid extraction.

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