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中国精品科技期刊2020
赵鸿宾,冷天翠,刘晓梦,等. 微波法制备猕猴桃生物质碳点及应用于金银花中Fe3+的检测[J]. 食品工业科技,2022,43(3):246−253. doi: 10.13386/j.issn1002-0306.2021040147.
引用本文: 赵鸿宾,冷天翠,刘晓梦,等. 微波法制备猕猴桃生物质碳点及应用于金银花中Fe3+的检测[J]. 食品工业科技,2022,43(3):246−253. doi: 10.13386/j.issn1002-0306.2021040147.
ZHAO Hongbin, LENG Tiancui, LIU Xiaomeng, et al. Preparation of Kiwifruit Biomass Carbon Dots by Microwave Method and Application of Fe3+ Detection in Honeysuckle[J]. Science and Technology of Food Industry, 2022, 43(3): 246−253. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021040147.
Citation: ZHAO Hongbin, LENG Tiancui, LIU Xiaomeng, et al. Preparation of Kiwifruit Biomass Carbon Dots by Microwave Method and Application of Fe3+ Detection in Honeysuckle[J]. Science and Technology of Food Industry, 2022, 43(3): 246−253. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021040147.

微波法制备猕猴桃生物质碳点及应用于金银花中Fe3+的检测

Preparation of Kiwifruit Biomass Carbon Dots by Microwave Method and Application of Fe3+ Detection in Honeysuckle

  • 摘要: 为建立一种快速检测Fe3+的方法,以猕猴桃汁为碳源,乙二胺为表面修饰剂,采用微波法制备猕猴桃生物质碳点(CDs)。制备的生物质碳点富含-OH、-NH和C-O等基团,粒径约为2.5 nm,易溶于水且稳定。该碳点在365 nm紫外光照射下发出蓝色荧光。基于Fe3+对猕猴桃生物质碳点荧光猝灭效应,进而建立一种检测Fe3+的方法。当Fe3+的加入量在0.2~10 μmol/L范围内,碳点的荧光猝灭程度(F/F0)随Fe3+浓度的增加而呈线性下降(R2=0.9934),检出限(S/N=3)为0.12 μmol/L。将该方法用于测定金银花中Fe3+的含量,其回收率在98.82%~103.20%,RSD介于1.67%~2.05%之间。该检测方法操作简便,快速,选择性好。

     

    Abstract: In order to establish a rapid detection method for Fe3+, the kiwifruit biomass carbon dots (CDs) were prepared by microwave method with kiwifruit juice as carbon source and ethylenediamine as surface modifier. The CDs were rich in -OH, -NH and C-O groups, had an average particle size about 2.5 nm, which were soluble in water and stable. The CDs emitted blue fluorescence under 365 nm ultraviolet light. A new and rapid detection method for Fe3+ was established with the CDs based on the fluorescence quenching effect of Fe3+. When the addition amount of Fe3+ from 0.2 to 10 μmol/L, the fluorescent intensity (F/F0) of CDs decreased linearly with the increase of Fe3+(R2=0.9934), and the limit of detection (S/N=3) was 0.12 μmol/L. This detection method was applied to the determination of Fe3+ content and the recovery was 98.82%~103.20% , RSD was between 1.67% and 2.05%. The operation of this detection method was simple, rapid and strong selective.

     

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