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定量离子选择性膜中增塑剂的泄漏 - 纳米海绵方法。

Quantifying plasticizer leakage from ion-selective membranes - a nanosponge approach.

机构信息

Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland.

出版信息

Analyst. 2020 Apr 21;145(8):2966-2974. doi: 10.1039/c9an02621e. Epub 2020 Mar 2.

DOI:10.1039/c9an02621e
PMID:32115595
Abstract

The spontaneous process of release of plasticizers from membranes typically used in ion-selective sensors is an effect which limits the lifetime of sensors and comes with a risk of safety hazards. We use a nanosponge approach to look at the magnitude of this problem, quantifying the resulting contents of the plasticizer in solution. This novel method takes advantage of the spontaneous partition of the plasticizer (released and present in solution) into nanoparticles loaded with a solvatochromic dye. As a result, nanoparticles are transformed into capsules. This process is coupled with the turn-on fluorescence intensity change of the dye embedded in nanostructures, proportional to analyte concentration in the ppm range, providing insight into plasticizer contents in the solution. It was found that the spontaneous release of the plasticizer is dependent on its nature as well as the presence of an ionophore and ion-exchanger. For a typical ion-selective membrane composition the leakage effect results in up to 20 ppm of 2-nitrophenyl octyl ether found in solution after 12 h contact. On the other hand, for a less polar plasticizer - bis(2-ethylhexyl) sebacate, although the presence of an ionophore and ion-exchanger also increases the amount of the compound released from the membrane, its concentration in solution does not exceed 2 ppm after 12 h. The conclusions presented herein can be important not only for designing robust sensors but also for end-user safety. The results obtained for ion-selective membranes were equal within the range of experimental errors with those obtained using a liquid chromatography coupled with mass spectrometry (LC MS) approach, confirming the high analytical potential of the nanosponge approach.

摘要

从通常用于离子选择性传感器的膜中自发释放增塑剂的过程是限制传感器寿命并带来安全隐患的一个问题。我们使用纳米海绵方法来研究这个问题的严重程度,定量分析溶液中增塑剂的含量。这种新方法利用了增塑剂(已释放并存在于溶液中)自发分配到负载溶剂变色染料的纳米颗粒中的原理。结果,纳米颗粒转变为胶囊。这个过程与嵌入纳米结构中的染料的荧光强度变化相关联,其与分析物浓度成正比,可在 ppm 范围内提供溶液中增塑剂含量的信息。结果发现,增塑剂的自发释放取决于其性质以及离子载体和离子交换剂的存在。对于典型的离子选择性膜组成,在 12 小时接触后,溶液中发现高达 20 ppm 的 2-硝基苯辛醚泄漏。另一方面,对于极性较小的增塑剂-双(2-乙基己基)癸二酸酯,尽管离子载体和离子交换剂的存在也会增加从膜中释放的化合物的量,但在 12 小时后,其在溶液中的浓度不超过 2 ppm。本文提出的结论不仅对设计稳健的传感器很重要,而且对最终用户的安全也很重要。使用纳米海绵方法获得的离子选择性膜的结果与使用液相色谱-质谱联用(LC-MS)方法获得的结果在实验误差范围内相等,证实了纳米海绵方法的高分析潜力。

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