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通过用膦酸对ZrO纳米颗粒进行表面功能化设计杂化PAH纳米吸附剂

Design of Hybrid PAH Nanoadsorbents by Surface Functionalization of ZrO Nanoparticles with Phosphonic Acids.

作者信息

Bou Orm Nadine, Gréa Thomas, Hamandi Marwa, Lambert Alexandre, Lafay Florent, Vulliet Emmanuelle, Daniele Stéphane

机构信息

College of Natural and Health Sciences, Zayed University, P. O. Box 144534 Abu Dhabi, United Arab Emirates.

CP2M-ESCPE Lyon, CNRS-UMR 5128, Université Claude Bernard Lyon 1, 43 Bd du 11 Novembre 1918, 69616 Villeurbanne, France.

出版信息

Nanomaterials (Basel). 2021 Apr 8;11(4):952. doi: 10.3390/nano11040952.

DOI:10.3390/nano11040952
PMID:33917895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8068232/
Abstract

This study focuses on the preparation of innovative nanocomposite materials based on surface modification of commercial nano-ZrO optimized from Brønsted acid-base surface reactions. This surface modification was carried out by direct grafting of suitable phosphonic acids bearing a vinylic or phenylic substituent in aqueous solution. Different loading quantities of the anchoring organophosphorus compounds were applied for each materials synthesis. The resulting nanohybrids were thoroughly characterized by infrared spectroscopy (DRIFT), solid-state nuclear magnetic resonance (NMR), nitrogen adsorption-desorption (BET), thermogravimetric analysis (TG), and X-ray photoelectron spectroscopy (XPS), demonstrating the reliability and efficient tunability of the surface functionalization based on the starting Zr/P ratio. Our nanocomposite materials exhibited a high specific surface area as well as complex porosity networks with well-defined meso-pore. The as-prepared materials were investigated for the adsorption of a mixture of 16 polycyclic aromatic hydrocarbons (PAHs) at 200 ng·mL in an aqueous solution. Adsorption kinetics experiments of each individual material were carried out on the prepared PAHs standard solution for a contact time of up to 6 h. Pretreatments of the adsorption test samples were performed by solid-phase extraction (SPE), and the resulting samples were analyzed using an ultrasensitive GC-orbitrap-MS system. The pseudo-first-order and the pseudo-second-order models were used to determine the kinetic data. The adsorption kinetics were best described and fitted by the pseudo-second-order kinetic model. The correlation between the nature of the substituent (vinylic or phenylic) and the parameters characterizing the adsorption process were found. In addition, an increase of PAHs adsorption rates with phosphonic acid loading was observed.

摘要

本研究聚焦于基于布朗斯特酸碱表面反应优化的商用纳米ZrO进行表面改性来制备创新型纳米复合材料。这种表面改性是通过在水溶液中直接接枝带有乙烯基或苯基取代基的合适膦酸来实现的。每种材料合成时都应用了不同负载量的锚定有机磷化合物。通过红外光谱(DRIFT)、固态核磁共振(NMR)、氮吸附-脱附(BET)、热重分析(TG)和X射线光电子能谱(XPS)对所得纳米杂化物进行了全面表征,证明了基于起始Zr/P比的表面功能化的可靠性和有效可调性。我们的纳米复合材料表现出高比表面积以及具有明确中孔的复杂孔隙网络。对所制备的材料在水溶液中对16种多环芳烃(PAHs)混合物(浓度为200 ng·mL)的吸附性能进行了研究。在制备的PAHs标准溶液上对每种材料进行吸附动力学实验,接触时间长达6小时。吸附测试样品通过固相萃取(SPE)进行预处理,所得样品使用超灵敏气相色谱-轨道阱质谱系统进行分析。采用伪一级和伪二级模型来确定动力学数据。吸附动力学最好用伪二级动力学模型来描述和拟合。发现了取代基(乙烯基或苯基)的性质与表征吸附过程的参数之间的相关性。此外,观察到随着膦酸负载量的增加,PAHs的吸附速率提高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/b867104db6c8/nanomaterials-11-00952-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/daa1d225f405/nanomaterials-11-00952-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/70a2267d7d59/nanomaterials-11-00952-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/4460c030b479/nanomaterials-11-00952-g0A3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/338292a12043/nanomaterials-11-00952-g0A4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/88cbe6081b64/nanomaterials-11-00952-g0A5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/3f71eddbbead/nanomaterials-11-00952-g0A6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/fc2c1ff38b88/nanomaterials-11-00952-g0A7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/1cb0d5e6a556/nanomaterials-11-00952-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/b867104db6c8/nanomaterials-11-00952-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/daa1d225f405/nanomaterials-11-00952-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/70a2267d7d59/nanomaterials-11-00952-g0A2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/4460c030b479/nanomaterials-11-00952-g0A3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/338292a12043/nanomaterials-11-00952-g0A4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/88cbe6081b64/nanomaterials-11-00952-g0A5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/3f71eddbbead/nanomaterials-11-00952-g0A6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/fc2c1ff38b88/nanomaterials-11-00952-g0A7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/1cb0d5e6a556/nanomaterials-11-00952-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e273/8068232/b867104db6c8/nanomaterials-11-00952-g003.jpg

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