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作 者:赵建宏[1] 张梅梅[1] 程相林[1] 王建设[1] 王留成[1] 宋成盈[1] 张家丽[1]
机构地区:[1]郑州大学化工与能源学院,河南郑州450001
出 处:《郑州大学学报(工学版)》2015年第1期37-40,共4页Journal of Zhengzhou University(Engineering Science)
基 金:河南省产学研计划资助项目(142107000007)
摘 要:建立了一种同时定量测定反应液中苯并噻唑和2-巯基苯并噻唑的高效液相色谱分析方法.该方法采用Hypersil C18(150 mm×4.6 mm i.d)型色谱柱,以V(甲醇):V(水)=50∶50作为流动相(用氨水调节流动相的p H为7.0~8.0);检测波长254 nm;柱温30℃;流速0.9 m L/min.结果表明,待测物苯并噻唑和2-巯基苯并噻唑在上述色谱条件下分离良好,两种物质的质量浓度线性范围分别为0.047~0.426 g·L^-1和0.059~0.273 g·L^-1,检出限分别在1.23×10^-3g·L^-1和0.78×10^-3g·L^-1,加标回收率分别在98.20%~101.03%和98.78%~99.76%,测定结果的最大相对标准偏差分别为0.45%和0.63%.A method was presented for the simultaneous determination of benzothiazole and 2-mercaptobenzothiazole in the reaction liquid by high performance liquid chromatography( HPLC). The analysis was performed on a Hypersil C18 column( 150 mm × 4. 6 mm i. d) with 50: 50 methanol-water as the mobile phase( mobile phase with ammonia,p H = 7. 0 ~ 8. 0) at a flow rate of 0. 9 m L / min. The samples were detected at 254 nm with an UV detector and the column temperature was 30 ℃. It was found that benzothiazole and 2-mercaptobenzothiazole could be well separated under the chromatographic conditions. The linear ranges of the mass concentration were 0. 047 ~ 0. 426 g / L and 0. 059 g / L ~ 0. 273 g / L respectively. The recoveries for them were98. 20% ~ 101. 0 3% and 98. 78 % ~ 99. 76%. The maximum relative standard deviations were 0. 45 % and0. 63 % for benzothiazole and 2-mercaptobenzothiazole.
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