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中国精品科技期刊2020
杨敏, 方树桔, 谭伟, 李彬, 王红斌. 多壁碳纳米管基质固相分散萃取-HPLC法测定蔬菜中的啶虫脒残留[J]. 食品工业科技, 2013, (19): 299-302. DOI: 10.13386/j.issn1002-0306.2013.19.033
引用本文: 杨敏, 方树桔, 谭伟, 李彬, 王红斌. 多壁碳纳米管基质固相分散萃取-HPLC法测定蔬菜中的啶虫脒残留[J]. 食品工业科技, 2013, (19): 299-302. DOI: 10.13386/j.issn1002-0306.2013.19.033
YANG Min, FANG Shu-ju, TAN Wei, LI Bin, WANG Hong-bin. Multi-walled carbon nanotubes and matrix solid phase dispersion extraction-HPLC for the determination of acetamiprid residue in vegetables[J]. Science and Technology of Food Industry, 2013, (19): 299-302. DOI: 10.13386/j.issn1002-0306.2013.19.033
Citation: YANG Min, FANG Shu-ju, TAN Wei, LI Bin, WANG Hong-bin. Multi-walled carbon nanotubes and matrix solid phase dispersion extraction-HPLC for the determination of acetamiprid residue in vegetables[J]. Science and Technology of Food Industry, 2013, (19): 299-302. DOI: 10.13386/j.issn1002-0306.2013.19.033

多壁碳纳米管基质固相分散萃取-HPLC法测定蔬菜中的啶虫脒残留

Multi-walled carbon nanotubes and matrix solid phase dispersion extraction-HPLC for the determination of acetamiprid residue in vegetables

  • 摘要: 建立了以多壁碳纳米管(MWCNTs)为萃取剂的基质固相萃取(MSPD)、HPLC测定蔬菜中啶虫脒残留的方法。将样品与工业级碳纳米管、无水硫酸镁混合研磨后装柱,并用乙酸乙酯洗脱,高效液相色谱法测定。采用C8柱(3.0mm×100mm,1.8μm)分离,甲醇-水(3∶2,v/v)为流动相,流速0.10mL/min,紫外检测波长250nm,进样量2.5μL,柱温为30℃。结果表明,该方法对蔬菜样品中啶虫脒的回收率为84.0%106.0%,精密度为0.1%12.5%,方法最低检出限为0.0085mg/L。该法简便、快速、准确。 

     

    Abstract: With multi-walled carbon nanotubes (MWCNTs) as extractant, a method based on MSPD, HPLC had been developed for the determination of acetamiprid residue in vegetables.Samples were homogenized with industrial-grade carbon nanotubes and anhydrous magnesium sulfate in a mortar, packed into a cartridge, eluted by ethylacetate, and analyzed by HPLC.The acetamiprid residue was separated on a C 8 (3.0mm ×100mm, 1.8μm) column, with methanol-water (3∶2, v /v) as the mobile phase at the flow rate of 0.10 mL /min, then detected by UV detector at wavelength 210nm.The injection volume was 2.5μL, and the column temperature was 30℃.The results showed that vegetable samples recoveries were between 84.0% ~ 106.0%, with the relative standard deviations (RSDs) of 0.1%12.5%.And the detection lmit was 0.0085 mg /L.The method was simple, rapid, and accurate.

     

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