2022
DOI: 10.1021/acs.jafc.2c03983
|View full text |Cite
|
Sign up to set email alerts
|

Fluorine-Functionalized Covalent-Organic-Framework-Coated Stir Bar for the Extraction of Benzoylurea Insecticides in Pear Juice and Beverage Followed by High-Performance Liquid Chromatography–Ultraviolet Detection

Abstract: A fluorinated covalent organic framework (COF), named F-COF, was fabricated via simple room-temperature synthesis. With the characteristics of rich fluorine atoms, hydrophobicity, and large conjugated structure, F-COF was evaluated for the extraction of five benzoylurea insecticides (BUs) containing fluorine atoms, benzene ring, and urea bridge. Specifically, F-COF-coated stir bars were prepared by physical adhesion and exhibited higher extraction recovery (73–93 versus 40–85%) toward BUs than commercial stir … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 16 publications
(3 citation statements)
references
References 43 publications
0
3
0
Order By: Relevance
“…With the effect of "fluorine affinity", fCOFs have been used for the detection and adsorption of fluorinated pesticides. [69,70] For instance, a fCOF (COF-(CF 3 ) 2 ) synthesized by post-synthesis modification exhibits strong interaction with the fluorinated pesticides (Figure 4B). [45] Though the BET specific surface area after post-synthesis modification shows some decrease, COF-(CF 3 ) 2 still possesses a BET specific surface area of 1533 m 2 g −1 .…”
Section: Adsorptionmentioning
confidence: 99%
“…With the effect of "fluorine affinity", fCOFs have been used for the detection and adsorption of fluorinated pesticides. [69,70] For instance, a fCOF (COF-(CF 3 ) 2 ) synthesized by post-synthesis modification exhibits strong interaction with the fluorinated pesticides (Figure 4B). [45] Though the BET specific surface area after post-synthesis modification shows some decrease, COF-(CF 3 ) 2 still possesses a BET specific surface area of 1533 m 2 g −1 .…”
Section: Adsorptionmentioning
confidence: 99%
“…Typically, COFs are stable and ordered crystalline structures with great potential in sample pretreatment [25][26][27][28][29]. As a highly effective adsorbent, COFs have been widely used in the enrichment of food hazards [30][31][32] and the removal of environmental pollutants [33][34][35]. However, most of COFs constructed with dynamic imine bonds suffer from instability, so it is essential to synthesize COFs based on irreversible chemical reactions.…”
Section: Introductionmentioning
confidence: 99%
“…The adsorption affinity of adsorbents (FSMP-2 and ASMP) toward adsorbates (TePT and 5CT) can be reflected by the ΔH ads , 45 which were calculated by DFT (Figure 5). The ΔH ads between TePT and FSMP-2 (−188.38 kJ mol −1 ) was significantly lower than that between TePT and ASMP (−18.65 kJ mol −1 ).…”
Section: ■ Introductionmentioning
confidence: 99%