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首页> 外文期刊>RSC Advances >Ionic liquid-based carbon nanotube coated magnetic nanoparticles as adsorbent for the magnetic solid phase extraction of triazole fungicides from environmental water
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Ionic liquid-based carbon nanotube coated magnetic nanoparticles as adsorbent for the magnetic solid phase extraction of triazole fungicides from environmental water

机译:离子液体基碳纳米管涂覆磁性纳米粒子作为磁性固相萃取三唑杀菌剂的吸附剂,从环境水中萃取

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摘要

Ionic liquid-based magnetic carbon nanotubes (IL-Fe _(3) O _(4) @MWCNTs) were synthesized as a novel adsorbent for magnetic solid-phase extraction (MSPE) for the determination of six triazole fungicides, i.e. penconazole (Pen), tebuconazole (TEB), epoxiconazole (Epo), bitertanol (Bit), fenbuconazole (Fen) and difenoconazole (Dif), from aqueous solution by gas chromatography coupled to mass spectrometry. Scanning electron microscopy (SEM), Fourier transform infrared spectrometry (FT-IR), X-ray diffraction (XRD) and Energy Dispersive X-ray (EDX) spectrometry were used to characterize the adsorbent. Some important factors governing the extraction efficiency such as adsorbent type, dilution conditions, adsorbent amount, extraction time, desorption time and ionic strength were investigated and optimized. Under the optimal conditions, the enrichment factors of the method for the analytes were in the range of 125 to 1242. A good linearity was observed in the range of 0.5–50 ng mL ~(?1) for Epo, Bit, Fen, and Dif, 1–50 ng mL ~(?1) for Teb and 2–50 ng mL ~(?1) for Pen, respectively, with the correlation coefficients ranging from 0.9968 to 0.9999. The limits of detection (LODs) and the limits of quantification (LOQs) of the method were within the range 0.05–0.22 ng mL ~(?1) and 0.23–0.75 ng mL ~(?1) , respectively. The southern end of the Beijing-Hangzhou Grand Canal water (Hangzhou, China) was used to verify the applicability of the developed method for the determination of the targets.
机译:In离子液体基磁性碳纳米管(IL-Fe _(3)O _(4)o _(4)o _(4)o ~mwnts)作为磁性固相萃取(MSPE)的新型吸附剂,用于测定六个三唑杀真菌剂,即Penconazole(笔),通过气相色谱法通过气相色谱法通过气相色谱法从水溶液中加入水溶液,Tebuconazole(TEB),苯嘧啶(钻头),富核醇(钻头),芬琥珀酰唑(DIF)。扫描电子显微镜(SEM),傅里叶变换红外光谱法(FT-IR),X射线衍射(XRD)和能量分散X射线(EDX)光谱法用于表征吸附剂。针对吸附型,稀释条件,吸附量,提取时间,解吸时间和离子强度等提取效率的一些重要因素进行了研究和优化。在最佳条件下,分析物方法的富集因子在125至1242的范围内。在EPO,BIT,FEN和SEP,BIT,FEN和SEP的范围内,观察到良好的线性度在0.5-50ng mL〜(α1)的范围内用于TEB的1-50ng mL〜(α1)分别用于笔的TEB和2-50ng mL〜(α1),相关系数范围为0.9968至0.9999。该方法的检测限(LOD)和定量限制(LOQs)的限制分别在0.05-0.22ng ml〜(α1)和0.23-0.75ng ml〜(α1)范围内。北京杭州大运河水(杭州)南端用于验证开发方法确定目标的适用性。

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