首页> 外文期刊>Journal of Agricultural and Food Chemistry >Analytical method for the determination of cyromazine and melamine residues in soil using LC-UV and GC-MSD.
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Analytical method for the determination of cyromazine and melamine residues in soil using LC-UV and GC-MSD.

机译:LC-UV和GC-MSD测定土壤中环丙嗪和三聚氰胺的分析方法。

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A method is reported for the determination of cyromazine and melamine residues in soil. Soil samples are extracted twice via mechanical shaking, each time with 70% acetonitrile/30% 0.050 M ammomium carbonate for 30 min. An aliquot portion of the pooled extracts is subjected to strong cation exchange (SCX) purification on AG 50W-X4 resin. Final analysis is accomplished using liquid chromatography-ultraviolet (LC-UV) detection at a wavelength of 214 nm. Confirmatory analyses can be performed using gas chromatography-mass selective detection (GC-MSD) in the selected ion monitoring (SIM) mode. The limit of detection (LOD) is 2.5 ng injected and the limit of quantification (LOQ) is 10 ppb when using LC-UV for the analysis of N-cyclopropyl-1,3,5-triazine-2,4, 6-triamine (cyromazine) and 1,3,5-triazine-2,4,6-triamine (melamine). The LOD is 0.050 ng injected and the LOQ is 10 ppb when using GC-MSD for confirmatory analyses. The mean procedural recoveries were 97 and 95% and the standard deviations were 16 and 11% for cyromazine and melamine, respectively (n = 24), when using LC-UV. The mean procedural recoveries were 107 and 92% and the standard deviations were 9.9 and 16% for cyromazine and melamine, respectively (n = 29), when using GC-MSD. The method validation study was conducted under U.S. EPA FIFRA Good Laboratory Practice Guidelines 40 CFR 160. The method also passed an Independent Laboratory Validation (ILV) as per U.S. EPA FIFRA Subdivision N.
机译:报道了一种测定土壤中环丙嗪和三聚氰胺残留的方法。通过机械摇动将土壤样品提取两次,每次用70%乙腈/ 30%0.050 M碳酸铵处理30分钟。将合并的提取物的等分部分在AG 50W-X4树脂上进行强阳离子交换(SCX)纯化。使用液相色谱-紫外线(LC-UV)检测在214 nm的波长下完成最终分析。可以在选定的离子监测(SIM)模式下使用气相色谱-质谱选择性检测(GC-MSD)进行确证分析。当使用LC-UV分析N-环丙基-1,3,5-三嗪-2,4,6-三胺时,进样限(LOD)为2.5 ng,定量限(LOQ)为10 ppb (环丙嗪)和1,3,5-三嗪-2,4,6-三胺(三聚氰胺)。使用GC-MSD进行确证分析时,注入的LOD为0.050 ng,LOQ为10 ppb。当使用LC-UV时,氯嘧嗪和三聚氰胺的平均程序回收率分别为97%和95%,标准偏差分别为16%和11%(n = 24)。使用GC-MSD时,环丙嗪和三聚氰胺的平均程序回收率分别为107%和92%,标准偏差分别为9.9%和16%(n = 29)。方法验证研究是根据美国EPA FIFRA良好实验室操作规范40 CFR 160进行的。该方法还通过了美国EPA FIFRA分区N的独立实验室验证(ILV)。

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