首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Multivariate curve resolution strategy for non-quadrilinear type 4 third-order/four way liquid chromatography excitation-emission fluorescence matrix data
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Multivariate curve resolution strategy for non-quadrilinear type 4 third-order/four way liquid chromatography excitation-emission fluorescence matrix data

机译:非四轴型4型三阶/四路液相色谱激发 - 发射荧光矩阵数据的多变量曲线分辨率策略

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摘要

For the first time, a third-order/four-way system having instrumental modes depending on each other was experimentally generated and it was successfully resolved. Non-quadrilinear type 4 data, constituted by liquid chromatographic elution times (LC) and excitation-emission fluorescence matrices (EEFMs), were on-line measured using conventional equipment. Thus, third-order/four-way data, valuable for giving rise to highly sensitive and selective methods, were obtained minimizing significantly the experimental work and time, in comparison with the reported strategies for the acquisition of LC-EEFM data. The usefulness of MCR-ALS (multivariate curve resolution-alternating least square) for attaining reliable results from data with two mutually dependent instrumental modes, namely elution time and excitation wavelength modes, was established through the simultaneous quantitation of benz[a]anthracene, chrysene, benzo[b]fluoranthene, and benzo[a]pyrene. Limits of detection in the range 1.0-1.4 ng mL(-1) were achieved for the target polycyclic aromatic hydrocarbons, allowing their determination in about 9 min per sample in leaves of different types of tea.
机译:首次,通过实验生成具有根据彼此的仪器模式的三阶/四路系统,并成功解决。由液相色谱洗脱季节(LC)和激发 - 发射荧光矩阵(EEFMS)构成的非全高二射型数据在线使用常规设备测量。因此,与报告的获取LC-EEFM数据的策略相比,获得了最大限度地减少了对高敏感和选择性方法的三阶/四通数据,可以获得显着的实验工作和时间。通过同时定量苯子[a]蒽,克莱森的同时确定MCR-ALS(多变量曲线分辨率 - 交替总方)用于获得具有两种相互依赖的仪器模式的可靠结果,即洗脱时间和激发波长模式的可靠结果。 ,苯并[b]氟苯,和苯并[a]芘。对于靶多环芳烃,实现了1.0-1.4 Ng ml(-1)范围内的检测限,允许其在不同类型茶叶的叶片中约9分钟的测定。

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