化学
拉曼散射
吸附
检出限
农药残留
涂层
分子
基质(水族馆)
杀虫剂
分析化学(期刊)
拉曼光谱
色谱法
化学工程
核化学
有机化学
农学
物理
海洋学
工程类
光学
生物
地质学
作者
Mingyu Zhang,Yongtao Tian,Sijia Liu,Yu Wang,Haiyan Li,Yafei Chen,Qing Gao,Xiaodong Wang,Mingli Chen
摘要
ABSTRACT A multifunctional surface‐enhanced Raman scattering substrate Fe 3 O 4 @AgNPs@MIL‐101 was prepared. Rapid SERS detection of pesticide residues was realized by direct pre‐enrichment and separation on the peel surface. MIL‐101 has an ortho‐octahedral framework and large pore size, which endowed Fe 3 O 4 @AgNPs@MIL‐101 with the ability to rapidly adsorb and separate positively charged targets. The introduction of tannic acid realized the in situ growth of AgNPs on the backbone, to modulate the electromagnetic enhancement. Pesticide molecules were adsorbed onto the surface of AgNPs mediated by central S atoms, accompanied by the interaction between pesticide molecules and AgNPs, the corresponding SERS signals of different pesticides were observed. Together with the introduction of magnetic coating Fe 3 O 4 , the molecules were enriched in the hotspot and separated to further enhance the SERS performance. Magnet instead of centrifugation was used to simultaneously perform surface extraction and sample separation for a noninvasive, rapid, immediate, and portable assay. The method was accomplished in measurement of thiram and thiabendazole on apple and tangerine epidermis, and the limits of detection (LODs) were 20 ng/cm 2 and 4 μg/cm 2 , respectively. The recovery was reasonable, and it showed that the procedure is valuable for the rapid and nondestructive surface analysis of residual chemicals.
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