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1.
Herein, Ag nanoparticles (NPs) modified MoS2 (Ag−MoS2) was applied to the surface of glassy carbon (GC) to produce a robust electrochemical sensor for the detection of thiabendazole, a common antifungal in the post-harvesting of fruits. Cyclic voltammetry studies confirmed thiabendazole exhibited an irreversible, diffusion-controlled process on Ag−MoS2 with a two-fold increase in peak current than the pristine MoS2. A square wave voltammetry was used for the detection of TBZ. The developed sensor exhibited a linear range between 1–10 μM with LOD down to 0.1 μM (S/N>3). Analysis of TBZ in mango and banana matrices gave a recovery of 91.6–100.4 % indicating the suitability of the sensor for food safety monitoring.  相似文献   
2.
An efficient analytical method is presented involving effective sample clean-up with solid-phase extraction and HPLC-UV analysis for the simultaneous determination of carbendazim, thiabendazole, and o-phenylphenol residues in lemons. Sample preparation involves extraction with acetonitrile acidified with trifluoroacetic acid and an ethyl acetate/petroleum ether mixture. Purification of the crude extract was carried out with liquid–liquid partitioning after addition of an aqueous ammonia solution. Final clean-up was performed on polymeric reversed-phase cartridges pretreated with sodium dodecyl sulfate. Chromatographic analysis was performed on a reversed-phase HPLC column isocratically eluted with an acetonitrile/water/ammonia mixture and UV detection at 254 nm. The chromatographic method is repeatable, reproducible, and sensitive. Fungicide recoveries from lemon samples fortified at levels of 5 and 1 mg kg–1 were 81–85% for carbendazim, 96–98% for thiabendazole, and 81–106% for o-phenylphenol with coefficients of variation of 2.5–7.4%. Detection limits for carbendazim, thiabendazole, and o-phenylphenol in lemons were 0.21, 0.27, and 0.51 mg kg–1, respectively.  相似文献   
3.
A series of new chlorinated thiabendazoles (6am) have been synthesized from readily available anilines and 4-cyanothiazole in moderate to good yields. All synthesized compounds were fully characterized using 1H NMR, 13C NMR, IR, and mass spectrometry. Additionally, the structure of the compound (6f) was confirmed by single-crystal X-ray diffraction. In addition, synthesis of 2-substituted benzimidazoles and 2-phenyl benzothiazole was investigated using our optimized conditions and the outcome is presented herein.  相似文献   
4.
In this paper, a novel format for selective solid-phase extraction based on a molecularly imprinted polymer (MIP) is described. A small amount of MIP has been synthesized within the pores of commercial polyethylene (PE) frits and attached to its surface using benzophenone (BP), a photo-initiator capable to start the polymerisation from the surface of the support material. Key properties affecting the obtainment of a proper polymeric layer, such as polymerisation time and kind of cross-linker were optimised. The developed imprinted material has been applied as a selective sorbent for cleaning extracts of thiabendazole (TBZ), as model compound, from citrus samples. The use of different solvents for loading the analyte in the imprinted frits was investigated, as well as the binding capacity of the imprinted polymer. Imprinted frits showed good selectivity when loads were performed using toluene and a linear relationship was obtained for the target analyte up to 1000 ng of loaded analyte. Prepared composite material was applied to the SPE of TBZ in real samples extracts, showing an impressive clean-up ability. Calibrations showed good linearity in the concentration range of 0.05-5.00 μg g(-1), referred to the original solid sample, and the regression coefficients obtained were greater than 0.996. The calculated detection limit was 0.016 μg g(-1), low enough to satisfactory analysis of TBZ in real samples. RSDs at different spiking levels ranged below 15% in all the cases and imprinted frits were reusable without loss in their performance.  相似文献   
5.
A new sample preparation method based on SBA‐15 assisted electromembrane extraction coupled with corona discharge ion mobility spectrometer was developed for the determination of Thiabendazole as a model basic pesticide in fruit juice samples. The addition of SBA‐15 in the supported liquid membrane in electromembrane extraction system not only can lead to enhancement of the effective surface area, but also introducing the negatively charged silanol groups into supported liquid membrane might improve migration of positively charged analytes toward the supported liquid membrane and finally into the acceptor solution. To investigate the effect of the presence of SBA‐15 in the supported liquid membrane on the extraction efficiency, a comparative study was carried out between the conventional electromembrane extraction and SBA‐15/electromembrane extraction methods. Under the optimized conditions, SBA‐15/electromembrane extraction method showed higher extraction efficiencies in comparison with conventional electromembrane extraction method. SBA‐15/electromembrane extraction method exhibited a low limit of detection (0.9 ng/mL), high preconcentration factor (167) and high recovery (83%). Finally, the applicability of SBA‐15/electromembrane extraction method was studied by the extraction and determination of Thiabendazole as a model basic pesticide in fruit juice samples.  相似文献   
6.
随着经济的高速发展,环境问题正在日益引起人们的广泛关注.在实际生产中,农药和塑化剂长期存在滥用的问题,使其成为最为广泛的环境污染源并对生态环境、食品、人畜等造成严重的危害.针对环境中农药和塑化剂的残留问题,开发一种灵敏、快速的高效检测分析方法,采用三维荧光结合化学计量学方法用于环境水样中噻菌灵(TBZ)与双酚A(BPA...  相似文献   
7.
The net analyte signal (NAS)-based method HLA/GO, modification of the original hybrid linear analysis (HLA) method, has been used to determine carbendazim, fuberidazole and thiabendazole in water samples. This approach was used after a solid-phase extraction (SPE) step, using the native fluorescence emission spectra of real samples, previously standardized by piecewise direct standardization (PDS). The results obtained show that the modification of HLA performs in a similar way that partial least-squares method (PLS-1). The NAS concept was also used to calculate multivariate analytical figures of merit such as limit of detection, selectivity, sensitivity and analytical sensitivity (γ−1). With this purpose, blanks of methanol and ternary mixtures, with the target analyte at low concentration and the other two ranging according to the calibration matrix, were used, with different results. Detection limits calculated in the last way are more realistic and show the influence of the other components in the sample. Selectivity for carbendazim is higher than the corresponding values for fuberidazole and thiabendazole, whereas sensitivity, as well as the values obtained for their detection limits, are lower for carbendazim, followed by thiabendazole and fuberidazole. Results obtained by modification of HLA vary in the same way that the ones obtained by PLS-1.  相似文献   
8.
建立了一种可同时测定浓缩菠萝汁中噻菌灵和多菌灵残留量的反相高效液相色谱分析法。浓缩菠萝汁样品与水按一定比例稀释后,经过调节溶液的pH值、离心、过滤,用混合相固相萃取小柱(Mixed-mode SPE)进行提取、净化,并用配有二极管阵列检测器(DAD)的液相色谱仪检测,外标法定量。使用噻菌灵和多菌灵对照品进行添加回收率测定,结果显示,本方法对噻菌灵的检出限为0.020 mg/kg,回收率为75.7%~93.3%;对多菌灵的检出限为0.020 mg/kg,回收率为80.8%~99.2%;测定的相对标准偏差均不大于5.7%。本方法简单、快速、准确,能满足常规噻菌灵和多菌灵残留量检测的需要。  相似文献   
9.
A simple, rapid and reproducible analytical method for thiabendazole (TBZ) and imazalil (IMA) in citrus fruit and banana has been developed. The method involves the use of an ion-exchange cartridge for sample clean-up followed by ion-pair high-performance liquid chromatography with ultraviolet detection. The recoveries of TBZ and IMA from citrus fruits spiked at levels of 10 μg/g and 5 μg/g were in the range of 94–98% and 93–98% with coefficients of variation of 0.5–2.2% and 1.6–2.7%, respectively. The recoveries of TBZ and IMA from banana spiked at levels of 3 μg/g and 2 μg/g were 94% and 94% with coefficients of variation 1.1% and 4.9%, respectively. The detection limits for TBZ and IMA were 0.1 μg/g in citrus fruit and 0.05 μg/g in banana.  相似文献   
10.
建立了反相高效液相色谱-双波长检测法同时测定苹果及浓缩苹果汁中多菌灵、噻菌灵、吡虫啉、吡虫清4种农药残留量的方法。苹果样品经乙腈提取,加水稀释,而浓缩苹果汁样品直接用体积分数20%乙腈稀释后,利用CH2Cl2液-液萃取净化。分析时用C18色谱柱分离,以乙腈-0.05%冰乙酸系统梯度洗脱,选择246 nm和280 nm双波长检测。该方法4种农药的线性关系良好(r≥0.9999),检出限均为0.002 mg/kg,加标回收率在84.3%~109.1%范围内,相对标准偏差为2.0%~5.4%。本方法能够满足农药残留检测要求。  相似文献   
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