Fe۳O۴@SiO۲@Mel-Rh-Cu: A High-Performance, Green Catalyst for Efficient Xanthene Synthesis and Its Application for Magnetic Solid Phase Extraction of Diazinon Followed by Its Determination through HPLC-UV
محل انتشار: نشریه متدهای شیمیایی، دوره: 8، شماره: 4
سال انتشار: 1403
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 35
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شناسه ملی سند علمی:
JR_CHM-8-4_003
تاریخ نمایه سازی: 18 فروردین 1403
چکیده مقاله:
A novel, high-performance, recyclable heterogeneous catalyst functionalized with melamine was advantageously prepared and rhodanine on magnetic silica was successfully carried out. After that, the Cu ions were coordinated with the existing ligands decorated on the magnetic silica surface. This catalyst was identified by different analyses and acted as a recoverable catalyst for xanthene synthesis. Its advantages include the solvent-free conditions of the reaction, the high efficiency of the products in a short period of time, as well as its simple collection from the reaction environment. Moreover, the prepared sorbent has been developed for the extraction of diazinon from different real samples through magnetic solid phase extraction (MSPE). Under optimal conditions, the linear range for measuring diazinon was ۰.۵-۲۰۰ µg L-۱. The coefficient of determination (R۲) was ۰.۹۹۸۵. The limit of detection (LOD) of the method was ۰.۰۸ μg L-۱. Relative standard deviation values (RSD%) for the concentration of ۱۰.۰ μg L-۱ and ۱۰۰ μg L-۱ were between ۵.۳% and ۵.۹%. Finally, the proposed method was used to determine diazinon in orange and agricultural water. The results showed that the percentage of relative recovery of the selected toxin in the studied real samples was between ۹۲ and ۱۰۵.Moreover, the prepared sorbent has been developed for the extraction of diazinon from different real samples through magnetic solid phase extraction (MSPE). The parameters affecting the extraction were optimized by response surface methodology (RSM). The optimal extraction conditions were ۱۵ min for contact time, ۷ mg for sorbent amount, and ۰% (w/v) for NaCl concentration.Moreover, ۲۰ µL of methanol was used to elute the extracted analyte. Under optimal conditions, the linear range for measuring diazinon was ۰.۵-۲۰۰ µg L-۱. The coefficient of determination (R۲) was ۰.۹۹۸۵. The limit of detection (LOD) of the method was ۰.۰۸ μg L-۱. Relative standard deviation values (RSD%) for the concentration of ۱۰.۰ μg L-۱ and ۱۰۰ μg L-۱ were between ۵.۳% and ۵.۹%. Finally, the proposed method was used to determine diazinon in orange and agricultural water. The results showed that the percentage of relative recovery of the selected toxin in the studied real samples was between ۹۲ and ۱۰۵.
کلیدواژه ها:
نویسندگان
Sahar Peiman
Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran
Behrooz Maleki
Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran
Milad Ghani
Department of Analytical Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran
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