标题: 应用微胞电动层分析Benzimidazole类杀菌剂
Analysis of Benzimidazole Fungicides by Micellar Electrokinetic Chromatography
作者: 王瑞雄
Wang, Jui-Hsiung
谢有客
Hsieh, You-Zung
应用化学系硕博士班
关键字: 微胞电动层;顶空固相微萃取法
公开日期: 1997
摘要: 本研究针对常用的 benzimidazole 类杀菌剂:Benomyl, Carbendazim, Fuberidazole,Thiabendazole 和 Thiophanate-methyl,以微胞电动层析建立一个快速、高效率和高准确度的分析方法。在pH值为7.91,16mM的磷酸盐缓冲溶液中,添加50mM的十二烷基磺酸钠盐,可在7分钟内完全分离 benzimidazole 类杀菌剂。接着并以超临界流体萃取法作为样品前处理方法,萃取水果样品中 benzimidazole 类杀菌剂,当苹果样品添加10ppm benzimidazole 类杀菌剂时,最佳化的萃取条件为萃取温度 65°C,超临界二气化碳的密度 0.85g/mL,萃取的超临界二气化碳体积25毫升,其回收率的结果在74.44%和92.37%之间,最后并将此方法应用到其他的水果样品上。
本研究也应用顶空固相微萃取法作为含煤油与柴油的纵火残迹样品之前处理方法,并以直交表实验计划法寻找萃取时的最佳化条件。经由实验的结果发现以直交表实验计划法可以迅速得到最佳化的萃取条件,而干扰物被萃出的量亦相当有限,不致影响图谱的判别,跟传统的静态顶空方法比较起来,顶空固相微萃取法拥有较高的灵敏度,很适合用于煤油与柴油 的 纵火残迹样品之前处理。
The purpose of this study was to develop a rapid, high efficiency and high accuracy method applied to the analysis of benzimimdazole fungicides (Benomyl, Carbendazim, Fuberidazole, Thiabendazole and Th-iophanate-methyl ) by micellar electrokinetic chromatography (MEKC).In the analysis benzimidazole fun-gicides, we used pH=7.91 16mM phosphate buffer containing 50mM SDS as separation media. The benz-imidazole fungicides were completely separated within 7minutes. Sample pretreatment was performed by supercritical fluid extraction (SFE).Recoveries ranging from 74.44% to92.37% to 92.37% were obtained for apple samples spiked with benzimidazole fungicides at 10ppm.The availability of the technique was also evaluated in several fruit samples.
This study also presents a rapid and simple mdthod, i. e.,headspace solid phase microextraction (HS SPME), for kerosene and diesel in arson debris sample preparation. Via an orthogonal array experimental design,the optimal conditions of headspace solid phase microextraction were obtained. Furthermore, only limited interference components were coextracted.Compared to the traditional static headspace technique,the proposed method has a higher sensitivity.
URI: http://140.113.39.130/cdrfb3/record/nctu/#NT863500015
http://hdl.handle.net/11536/63552
显示于类别:Thesis