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低共熔溶剂液液微萃取法测定皮革中富马酸二甲酯

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建立了一种基于低共熔溶剂液液微萃取结合气相色谱质谱联用法检测皮革中富马酸二甲酯的分析方法。合成了7种不同的低共熔溶剂,研究了低共熔溶剂和分散剂种类、萃取液中乙腈含量、超声萃取温度和时间及萃取剂体积等对萃取效率的影响。采用水/乙腈混合液(体积比10︰1)作为超声萃取溶剂,以氯化胆碱:六氟异丙醇(摩尔比1︰3)组成的低共熔溶剂作为微萃取萃取剂时萃取效率最高。在优化的条件下,富马酸二甲酯在0。005~2。0 mg/L浓度范围内线性关系良好,定量检出限为0。025 mg/kg,在0。1、0。5、2。0 mg/L 3个不同浓度添加水平下加标回收率在81。5%~105。7%,相对标准偏差在3。2%~8。5%。该方法采用水和绿色溶剂进行前处理,减少了有机试剂的用量,操作过程简单快速,适用于测定皮革中富马酸二甲酯的含量。
Determination of Dimethyl Fumarate in Leather Using Liquid-Liquid Microextraction with Deep Eutectic Solvents
An analytical method for the determination of dimethyl fumarate in leather was developed based on liq-uid-liquid microextraction with deep eutectic solvent ( DES) combined with gas chromatography and mass spectrome-try.Seven different eutectic solvents were synthesized.The effects of the types of eutectic solvent and dispersant,the content of acetonitrile in the extraction solution,the temperature and time of ultrasonic extraction and the volume of extractant on the extraction efficiency were studied.The extraction efficiency was the highest when water/acetonitrile mixture ( volume ratio 10︰1) was used as the solvent,and the DES composed of choline chloride and hexafluoroiso-propanol ( molar ratio 1 ︰ 3) was used as the extractant.Under the optimized conditions,the linear relationship is good in the concentration range of 0.005~2.0 mg/L,the quantitative detection limit is 0.025 mg/kg,and the stand-ard recovery is in the range of 81.5% to 105.7% under the three different concentration levels of 0.1 mg/L,0.5 mg/L and 2.0 mg/L.The relative standard deviation is between 3.2% and 8.5%.The pretreatment with water and green solvent reduces the amount of organic reagent,the operation process is simple and rapid,and it is suitable for the determination of dimethyl fumarate in leather.

deep eutectic solventliquid-liquid microextractiondimethyl fumaratehexafluoroisopropanolgas chromatography and mass spectrometry

卢鸯、任冰、陈芃旭、王玲霞、沈金金

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浙江省轻工业品质量检验研究院,浙江 杭州310018

低共熔溶剂 液液微萃取 富马酸二甲酯 六氟异丙醇 气相色谱质谱联用法

2025

中国皮革
中国皮革和制鞋工业研究院

中国皮革

影响因子:0.157
ISSN:1001-6813
年,卷(期):2025.54(1)