TY - JOUR
T1 - 4-phenyl-1,2,3-triazole functionalized mesoporous silica SBA-15 as sorbent in an efficient stir bar-supported micro-solid-phase extraction strategy for highly to moderately polar phenols
AU - Tanimu, Abdulkadir
AU - Jillani, Shehzada Muhammad Sajid
AU - Alluhaidan, Ayman A.
AU - Ganiyu, Saheed A.
AU - Alhooshani, Khalid
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - A simple and effective strategy for the extraction of highly to moderately polar phenols in water samples was developed by synthesizing a series of 4-phenyl-1,2,3-triazole functionalized SBA-15 sorbents (xN3-Ph-SBA-15; x = 2 – 10 wt%) via two steps: azide functionalization of SBA-15 and its click reaction with phenylacetylene. The formed sorbents, which have a blend of both polar (1,2,3-triazole) and non-polar (long chain alkyl groups) sites were characterized using magic angle spinning NMR, surface area, pore size/pore volume N2 adsorption-desorption isotherms, scanning electron microscopy, and Fourier transform infrared spectroscopy. The surface area and pore size/pore volume were seen to decrease with increasing loading of 4-phenyl-1,2,3-triazole. The sorbents were used in a stir bar-supported micro-solid-phase extraction (SB-µ-SPE) for seven selected phenols in 10 mL water samples, and in combination with gas chromatography – mass spectrometry (GC-MS). A wide number of parameters were studied in the method optimization: 10N3-Ph-SBA-15 was the best sorbent which performed better using 20 mg dosage; 15 min extraction time; 300 µL of ethyl acetate as desorption solvent, 20 min desorption time; and ionic strength set at 0.5 g NaCl. The approach provided the desired linearity range for all tested phenols with R2 value up to 0.9989 and detection limit (LOD) of 0.23–0.37 ng mL−1. Relative standard deviation (RSD) and relative recovery experiments were tested using phenols spiked at 1, 100 and 400 ng mL−1. RSD values were calculated in the range of 2.3–7.5% and the relative recoveries in the wastewater matrix successfully presented a range of 88.5–99.2%.
AB - A simple and effective strategy for the extraction of highly to moderately polar phenols in water samples was developed by synthesizing a series of 4-phenyl-1,2,3-triazole functionalized SBA-15 sorbents (xN3-Ph-SBA-15; x = 2 – 10 wt%) via two steps: azide functionalization of SBA-15 and its click reaction with phenylacetylene. The formed sorbents, which have a blend of both polar (1,2,3-triazole) and non-polar (long chain alkyl groups) sites were characterized using magic angle spinning NMR, surface area, pore size/pore volume N2 adsorption-desorption isotherms, scanning electron microscopy, and Fourier transform infrared spectroscopy. The surface area and pore size/pore volume were seen to decrease with increasing loading of 4-phenyl-1,2,3-triazole. The sorbents were used in a stir bar-supported micro-solid-phase extraction (SB-µ-SPE) for seven selected phenols in 10 mL water samples, and in combination with gas chromatography – mass spectrometry (GC-MS). A wide number of parameters were studied in the method optimization: 10N3-Ph-SBA-15 was the best sorbent which performed better using 20 mg dosage; 15 min extraction time; 300 µL of ethyl acetate as desorption solvent, 20 min desorption time; and ionic strength set at 0.5 g NaCl. The approach provided the desired linearity range for all tested phenols with R2 value up to 0.9989 and detection limit (LOD) of 0.23–0.37 ng mL−1. Relative standard deviation (RSD) and relative recovery experiments were tested using phenols spiked at 1, 100 and 400 ng mL−1. RSD values were calculated in the range of 2.3–7.5% and the relative recoveries in the wastewater matrix successfully presented a range of 88.5–99.2%.
KW - Azides
KW - Click reaction
KW - Phenols
KW - SBA-15
KW - Stir bar-supported micro-solid-phase-extraction
UR - https://www.scopus.com/pages/publications/85055260288
U2 - 10.1016/j.talanta.2018.10.012
DO - 10.1016/j.talanta.2018.10.012
M3 - Article
C2 - 30609546
AN - SCOPUS:85055260288
SN - 0039-9140
VL - 194
SP - 377
EP - 384
JO - Talanta
JF - Talanta
ER -