Galvanic replacement synthesis of Cu@Zeolitic imidazolate framework-8 reinforced hollow fiber for hollow fiber solid-phase microextraction of diazinon and malathion followed by HPLC-UV determination

IF 3.7 Q1 CHEMISTRY, ANALYTICAL Talanta Open Pub Date : 2025-08-01 Epub Date: 2025-03-17 DOI:10.1016/j.talo.2025.100433
Zahra Doraghi , Heshmatollah Alinezhad , Milad Ghani
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Abstract

This paper represents the synthesis of zinc-based metal-organic framework-8 by the solvothermal method followed by doping of copper (Cu) metal by the purely chemical galvanic replacement method in the synthesized ZIF-8 substrate. Subsequently, the Cu doped ZIF-8 was used as an adsorbent in the hollow fiber solid-phase microextraction (HF-SPME) method for the extraction and determination of organophosphorus pesticides (OPPs), especially diazinon and malathion, from real samples contentiously from tomato, cucumber, apple, and well water. Optimization was done through the Plackett-Burman design and Box-Behnken design. Limits of detection (LODs) of 0.29 µgL−1 and 0.54 µgL−1, while limits of quantification (LOQs) of 0.96 µgL−1 and 1.79 µgL−1 were recorded for diazinon and malathion, respectively. The linear dynamic ranges (LDRs) for both analytes were established as 1–200 µg L⁻¹ and 2–500 µg L⁻¹ with determination coefficients (R²) of 0.9953 for diazinon and 0.9968 for malathion, indicating excellent linearity. The enrichment factors (EFs) were determined to be 152 for diazinon and 146 for malathion. RSDs% were obtained in the range of 4.21 % - 5.78 % for intra-day and 3.53 % - 6.24 % for inter-day precision. The results obtained from the experiments indicate that the developed method has a significant ability to extract and analyze selected analytes in a wide range of real-world samples, which proves the effectiveness and reliability of the method.

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电偶取代合成Cu@Zeolitic咪唑酸骨架-8增强中空纤维,对中空纤维固相微萃取重氮肼和马拉硫磷进行HPLC-UV测定
本文采用溶剂热法合成了锌基金属-有机骨架-8,然后在合成的ZIF-8衬底上用纯化学电替换法掺杂金属铜。随后,以Cu掺杂的ZIF-8为吸附剂,采用中空纤维固相微萃取(HF-SPME)法,对番茄、黄瓜、苹果、井水等样品中的有机磷农药(OPPs),特别是二嗪农和马拉硫磷进行了萃取和测定。通过Plackett-Burman设计和Box-Behnken设计进行优化。重氮肼和马拉硫磷的检出限分别为0.29µgL−1和0.54µgL−1,定量限分别为0.96µgL−1和1.79µgL−1。两种分析物的线性动态范围(ldr)分别为1-200µg L -⁻¹和2-500µg L -⁻¹,重氮肼和马拉硫磷的测定系数(R²)分别为0.9953和0.9968,线性良好。重氮磷的富集因子为152,马拉硫磷为146。日内精密度rsd %为4.21% ~ 5.78%,日内精密度rsd %为3.53% ~ 6.24%。实验结果表明,所建立的方法在广泛的实际样品中提取和分析选定的分析物的能力很强,证明了该方法的有效性和可靠性。
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来源期刊
Talanta Open
Talanta Open Chemistry-Analytical Chemistry
CiteScore
5.20
自引率
0.00%
发文量
86
审稿时长
49 days
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