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使用大孔强阴离子交换树脂预处理水样对叔丁基二甲基硅烷化后采用气相色谱-质谱法测定神经毒气水解产物的效率。

Efficiency of pretreatment of aqueous samples using a macroporous strong anion-exchange resin on the determination of nerve gas hydrolysis products by gas chromatography-mass spectrometry after tert.-butyldimethylsilylation.

作者信息

Kataoka M, Tsuge K, Seto Y

机构信息

National Research Institute of Police Science, Kashiwa, Chiba, Japan.

出版信息

J Chromatogr A. 2000 Sep 8;891(2):295-304. doi: 10.1016/s0021-9673(00)00640-3.

Abstract

A pretreatment procedure, using a macroporous strong anion-exchange resin (MSA) has been established for the determination of nerve gas hydrolysis products by gas chromatography-mass spectrometry (GC-MS) after tert.-butyldimethylsilyl (TBDMS) derivatization. Aqueous solutions of methylphosphonic acid (MPA) and three alkyl methylphosphonic acids (AMPAs) (ethyl, isopropyl and pinacolyl methylphosphonic acid), were retained on the MSA column, and then quantitatively eluted with 0.1 M hydrochloric acid. The neutralized column eluate was dried, and MPA and AMPAs were derivatized with N-methyl-N-(tert.-butyldimethylsilyl)-trifluoroacetamide and analyzed by GC-MS. The column eluate was also analyzed in order to determine the exact hydrolysis product levels by capillary electrophoresis using borate and benzoate buffer (pH 6). The MSA pretreatment was examined for the clean-up of aqueous extracts of three types of soils and an aqueous solution containing 10% sucrose, which is regarded as model for a typical soft drink, after spiking with MPA and AMPAs. MPA and AMPAs were quantitatively recovered in the MSA eluate fraction from those samples, except for MPA from volcanic acid and alluvial soils. The yields of TBDMS derivatives were remarkably improved, compared with for which no pretreatment was used and also for those in which a strong cation-exchange resin was used. The achieved detection limits of MPA and AMPAs ranged from 0.12 to 0.18 microg/g of soil (S/N=3). The established MSA method was applied to the pretreatment of spiked sea water, two types of beverages, Pepsi Cola and canned coffee. Although the yields of TBDMS derivatives of MPA and AMPAs in sea water (in a range between 44 and 96%) and AMPAs in Pepsi Cola (in a range between 58 and 92%) were rather high, those for MPA in the Pepsi Cola (27%) and those for MPA and AMPAs in the canned coffee (in a range between 5 and 17%) were low.

摘要

已建立一种预处理方法,使用大孔强阴离子交换树脂(MSA),用于在叔丁基二甲基甲硅烷基(TBDMS)衍生化后,通过气相色谱 - 质谱联用(GC-MS)测定神经毒气水解产物。甲基膦酸(MPA)和三种烷基甲基膦酸(AMPA)(乙基、异丙基和频哪基甲基膦酸)的水溶液保留在MSA柱上,然后用0.1 M盐酸定量洗脱。将中和后的柱洗脱液干燥,MPA和AMPA用N - 甲基 - N -(叔丁基二甲基甲硅烷基)- 三氟乙酰胺衍生化,并通过GC-MS分析。还对柱洗脱液进行分析,以便使用硼酸盐和苯甲酸盐缓冲液(pH 6)通过毛细管电泳确定确切的水解产物水平。在用MPA和AMPA加标后,对MSA预处理用于净化三种类型土壤的水提取物以及含有10%蔗糖的水溶液(被视为典型软饮料的模型)进行了研究。除了来自火山土和冲积土的MPA外,MPA和AMPA在MSA洗脱液部分中从这些样品中被定量回收。与未使用预处理以及使用强阳离子交换树脂的情况相比,TBDMS衍生物的产率显著提高。MPA和AMPA的检测限达到0.12至0.18μg/g土壤(S/N = 3)。所建立的MSA方法应用于加标海水、两种饮料(百事可乐和罐装咖啡)的预处理。虽然海水中MPA和AMPA的TBDMS衍生物产率(在44%至96%之间)以及百事可乐中AMPA的产率(在58%至92%之间)相当高,但百事可乐中MPA的产率(27%)以及罐装咖啡中MPA和AMPA的产率(在5%至17%之间)较低。

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