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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Optimization of photo-polymerized sol-gel monolithic stationary phases prepared in polyacrylate-coated fused-silica capillaries for capillary electrochromatography
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Optimization of photo-polymerized sol-gel monolithic stationary phases prepared in polyacrylate-coated fused-silica capillaries for capillary electrochromatography

机译:聚丙烯酸酯包覆的熔融石英毛细管中制备的光聚合溶胶-凝胶整体固定相的优化,用于毛细管电色谱

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The preparation of photo-polymerized sol-gel monolithic stationary phases (MSP) within 100μm internal diameter polyacrylate-coated fused-silica capillaries for use in capillary electrochromatography (CEC) was optimized. Eight mixtures containing different amounts of methacryloxypropyltrimethoxysilane (MPTMS) as the polymeric precursor, hydrochloric acid solution as the catalyst, toluene as the porogen and bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide (Irgacure 819) as the photo-initiator were irradiated at 370nm inside the capillaries in order to complete the MSP polymerization, according to a fractional factorial experimental design 2_(IV)~(4-1). All the preparation procedure, from capillary pretreatment until the MSP is ready to use in CEC, were made in less than four hours in mild conditions. A high pressurization injection device (HPID) useful for micro-volume syringes was built in order to achieve practical, controlled and precise injections of sols, solvents and electrolytes in the capillaries. The eight MSP were equally washed, conditioned and submitted to CEC procedures via short-end injection, which showed higher efficiency and peak height taking shorter analysis time. Electrochromatographic behaviors of the MSP were corroborated with morphological characterizations by scanning electron microscopy. The optimum condition, which allowed the separation of standard mixture containing thiourea (marker compound), naphthalene, acenaphthene, fluorene, phenanthrene and anthracene in twelve minutes without external pressure assistance, showed efficiencies up to 51,460N/m, relative standard deviation from 0.05 to 3.3% for migration/retention time and from 0.14 to 1.6% for relative area (considering thiourea as an internal standard) and also showed no statistical evidence that three MSP prepared at the same condition are different within 95% confidence interval.
机译:优化了内径为100μm的聚丙烯酸酯涂层熔融石英毛细管中的光聚合溶胶-凝胶整体固定相(MSP)的制备,用于毛细管电色谱(CEC)。八种混合物分别包含不同数量的甲基丙烯酰氧基丙基三甲氧基硅烷(MPTMS)作为聚合物前体,盐酸溶液作为催化剂,甲苯作为致孔剂和双(2,4,6-三甲基苯甲酰基)-苯基膦氧化物(Irgacure 819)作为光引发剂根据分数阶乘实验设计2_(IV)〜(4-1),在毛细血管内部370nm处进行辐照以完成MSP聚合。从毛细管预处理到MSP准备在CEC中使用,所有准备过程均在温和条件下不到四小时完成。为了在毛细血管中实现溶胶,溶剂和电解质的实用,控制和精确注射,建立了适用于微量注射器的高压注射装置(HPID)。对8个MSP进行均等清洗,调理,并通过短时进样进行CEC程序处理,结果表明,更高的效率和峰高可缩短分析时间。 MSP的电色谱行为通过扫描电子显微镜得到形态学特征的证实。最佳条件可以在12分钟内分离出含有硫脲(标记化合物),萘,,芴,菲和蒽的标准混合物,而无需外部压力辅助,其效率高达51,460N / m,相对标准偏差为0.05至迁移/保留时间为3.3%,相对面积为0.14至1.6%(以硫脲为内标),也没有统计证据表明在相同条件下制备的三种MSP在95%置信区间内不同。

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