首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Simultaneous multicomponent spectrophotometric monitoring of methyl and propyl parabens using multivariate statistical methods after their preconcentration by robust ionic liquid-based dispersive liquid-liquid microextraction
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Simultaneous multicomponent spectrophotometric monitoring of methyl and propyl parabens using multivariate statistical methods after their preconcentration by robust ionic liquid-based dispersive liquid-liquid microextraction

机译:健壮的基于离子液体的分散液-液微萃取预浓缩后,使用多元统计方法同时对羟基苯甲酸甲酯和对羟基苯甲酸甲酯进行多组分分光光度监控

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摘要

A powerful and efficient signal-preprocessing technique that combines local and multiscale properties of the wavelet prism with the global filtering capability of orthogonal signal correction (OSC) is applied for pretreatment of spectroscopic data of parabens as model compounds after their preconcentration by robust ionic liquid-based dispersive liquid-liquid microextraction method (IL-DLLME). In the proposed technique, a mixture of a water-immiscible ionic liquid (as extraction solvent) [Hmim][PF6] and disperser solvent is injected into an aqueous sample solution containing one of the IL's ions, NaPF6, as extraction solvent and common ion source. After preconcentration, the absorbance of the extracted compounds was measured in the wavelength range of 200-700 nm. The wavelet orthogonal signal correction with partial least squares (WOSC-PLS) method was then applied for simultaneous determination of each individual compound. Effective parameters, such as amount of IL, volume of the disperser solvent and amount of NaPF6, were inspected by central composite design to identify the most important parameters and their interactions. The effect of pH on the sensitivity and selectivity was studied according to the net analyte signal (NAS) for each component. Under optimum conditions, enrichment factors of the studied compounds were 75 for methyl paraben (MP) and 71 for propyl paraben (PP). Limits of detection for MP and PP were 4.2 and 4.8 ng mL~(-1), respectively. The root mean square errors of prediction for MP and PP were 0.1046 and 0.1275 lgmL~(-1), respectively. The practical applicability of the developed method was examined using hygienic, cosmetic, pharmaceutical and natural water samples.
机译:强大而有效的信号预处理技术将小波棱镜的局部和多尺度特性与正交信号校正(OSC)的全局滤波功能结合在一起,用于对苯甲酸酯作为模型化合物的光谱数据进行预处理,然后通过强力离子液体对其进行预浓缩。分散液-液微萃取法(IL-DLLME)。在提出的技术中,将与水不混溶的离子液体(作为萃取溶剂)[Hmim] [PF6]和分散剂的混合物注入到包含IL离子之一NaPF6作为萃取溶剂和普通离子的水溶液中资源。预浓缩后,在200-700 nm的波长范围内测量提取化合物的吸光度。然后,采用偏最小二乘的小波正交信号校正(WOSC-PLS)方法同时测定每种化合物。通过中央复合设计检查了有效参数,例如IL的量,分散剂溶剂的量和NaPF6的量,以确定最重要的参数及其相互作用。根据每种组分的净分析物信号(NAS)研究了pH对灵敏度和选择性的影响。在最佳条件下,所研究化合物的富集系数为对羟基苯甲酸甲酯(MP)为75,对羟基苯甲酸丙酯(PP)为71。 MP和PP的检出限分别为4.2和4.8 ng mL〜(-1)。 MP和PP的预测均方根误差分别为0.1046和0.1275 lgmL〜(-1)。使用卫生,化妆品,药​​品和天然水样品检查了所开发方法的实际适用性。

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