Abstract
Series of sorbents, N-sulfonyl-4-hydroxymethyl-1,2,3-triazole functionalized SBA-15 (x-S-SO2-triazole-OH; x = 5–20 wt%), have been developed via a two-step synthesis strategy: first, co-condensation of 6-azidosulfonylhexyltriethoxysilane and tetraethoxysilane to form 6-azidosulfonylhexyl functionalized SBA-15; and second, the Click reaction of 6-azidosulfonylhexyl functionalized SBA-15 with propyn-1-ol to form (x-S-SO2- triazole-OH). The sorbents with abundant hydrogen bonding sites were used in a stir bar-supported micro-solid-phase extraction (SB-μ-SPE) for six selected phenolic compounds in 10 mL water samples, and the 20-S-SO2-triazole-OH sorbent presented the best extraction efficiency. The linearity range for all tested phenols is within 1–1000 ng mL−1 with R value up to 0.9931 and a detection limit (LOD) of 0.03–0.30 ng mL−1. The RSD values were determined in the range of 2–16% and the relative recoveries in the domestic wastewater sample successfully presented a range of 84.5–108.6%.
| Original language | English |
|---|---|
| Article number | 105410 |
| Journal | Microchemical Journal |
| Volume | 159 |
| DOIs | |
| State | Published - Dec 2020 |
Bibliographical note
Publisher Copyright:© 2020 Elsevier B.V.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 6 Clean Water and Sanitation
Keywords
- Azides
- Click reaction
- Functionalization
- Phenolic compounds
- SBA-15
- Triazole
ASJC Scopus subject areas
- Analytical Chemistry
- Spectroscopy
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