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Updated: Jun 17, 2025

Fabrication of a Dipole-assisted Solid Phase Extraction Microchip for Trace Metal Analysis in Water Samples
Published on: August 7, 2016
Methyltrimethoxysilane modified tin dioxide microspheres with hydrophobic networks and abundant adsorbed oxygen for
Caixia Ji1, Hongwei Wu2, Anying Long3
1Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, 453007, People's Republic of China.
Abstract:
Methyltrimethoxysilane (MTMS) modified tin dioxide microspheres (MTMS/SnO2) were prepared by a facile hydrothermal method and heated reflux reaction strategy. The characterization results indicate that the modification of MTMS induced the formation of a hydrophobic network within the composites, while maintaining abundant adsorbed oxygen species. Subsequently, the MTMS/SnO2 microspheres were used as a solid-phase microextraction (SPME) coating for the efficient extraction and sensitive determination of trace polychlorinated biphenyls (PCBs) in aqueous solutions coupled to gas chromatography-mass spectrometry. MTMS/SnO2 coating exhibited superior extraction performances for PCBs compared with commercial SPME and pure SnO2 microspheres coatings, owing to the hydrophobic crosslinking and adsorbed oxygen-enhanced hydrogen bonding. The proposed analytical method presented respectable linearity in the concentration range 0.25-1000 ng L-1, with low limits of detection varying from 0.036 to 0.14 ng L-1 for seven PCBs and excellent precision, with relative standard deviations of 5.7-9.8% for a single fiber and 8.2-13.1% for five fibers. Finally, the proposed method was successfully used for determination of PCBs in real water with recoveries ranging from 75.8 to 115.6%. This study proposed a new type SPME coating of MTMS/SnO2 microspheres, which extended the potential of SnO2 in capturing and determining organic pollutants.
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