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A dissolvable hierarchical layered double hydroxide templated from porous zeolitic imidazolate framework-67 for dispersive solid phase extraction of bisphenol A

机译:从多孔沸石咪唑酯框架-67涂上双酚A的分散固相萃取的可溶性分层层状双氢氧化物。

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摘要

This is the first time that the in situ preparation of advanced extraction media based on a hierarchical layered double hydroxide (HLDH) has been reported in a study. The sorbent was obtained through surfactant-assisted self-assembly of Co(ii)/imidazolate (ZIF-67), followed by in situ conversion of the ZIF-67 into the final HLDH sorbent. The obtained Ni-Co LDH was used for dispersive solid-phase extraction (DSPE) of bisphenol A (BPA) as a model compound from different water samples and a PC baby bottle sample. After the extraction process, elution was accomplished by dissolving the HLDH containing the extracted analytes by changing the solution pH. The applied method didn't use any organic solvents for the extraction and desorption steps and eliminated the problems related to the memory effect of the sorbent in the DSPE method. The extracted analyte was then quantified using high-performance liquid chromatography (HPLC). An optimization strategy based on response surface methodology (RSM) was combined with chromatography analysis. Plackett-Burman design was utilized to screen the experimental factors. The effective factors were then optimized using Central Composite Design (CCD). Under optimum conditions, the linearity range of the method was 0.5-200 mu g L-1. Relative standard deviations (RSDs) were between 4.3% and 5.2%, respectively. The limit of detection (LOD) and limit of quantification (LOQ) were 0.12 mu g L-1 and 0.4 mu g L-1, respectively. Relative recoveries higher than 92% were achieved in analysis of different environmental water samples.
机译:这是第一次在研究中据报道了基于等级分层双氢氧化物(HLDH)的先进提取介质的原位制备。通过Co(II)/咪唑酯(ZIF-67)的表面活性剂辅助自组装获得吸附剂,然后将ZIF-67的原位转化为最终的HLDH吸附剂。所得Ni-Co LDH用于双酚A(BPA)的分散固相萃取(DSPE),为来自不同水样和PC婴儿瓶样品的模型化合物。在提取过程之后,通过溶解含有提取的分析物的HLDH通过改变溶液pH来完成洗脱。应用方法没有使用任何有机溶剂来提取和解吸步骤,并消除了DSPE方法中吸附剂的记忆效应相关的问题。然后使用高效液相色谱(HPLC)定量提取的分析物。基于响应面方法(RSM)的优化策略与色谱分析相结合。 Plackett-Burman设计用于筛选实验因素。然后使用中央复合设计(CCD)优化有效因素。在最佳条件下,该方法的线性范围为0.5-200μmgl-1。相对标准偏差(RSD)分别为4.3%和5.2%。检测极限(LOD)和定量限制(LOQ)分别为0.12μg1-1和0.4μg1-1。在分析不同环境水样中,实现了高于92%的相对回收。

著录项

  • 来源
    《Analytical methods》 |2019年第32期|共6页
  • 作者

    Ghani Milad;

  • 作者单位

    Univ Mazandaran Fac Chem Dept Analyt Chem Babol Sar Iran;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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