Selective adsorption and photodegradation of salicylic acid by a novel magnetic molecularly imprinted mesoporous TiO2 co-doped with silver nanoparticles and carbon nanotubes (Fe3O4@mTiO2-Ag-CNTs-MIPs) under visible light

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2024-10-05 DOI:10.1016/j.jphotochem.2024.116071
Yuan Wang , Ying Liu , Jiao Jiao , Qing-Yan Gai , Yu-Jie Fu , Run-Ze Cao
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Abstract

A novel magnetic molecularly imprinted mesoporous TiO2 co-doped with silver nanoparticles and carbon nanotubes (Fe3O4@mTiO2-Ag-CNTs-MIPs), was successfully prepared for the selective adsorption and photodegradation of salicylic acid (SA). The morphological and physicochemical properties of the prepared composite were characterized by SEM, FT-IR, XRD, VSM, UV–Vis DRS, EIS and XPS. The adsorption and photodegradation performance of Fe3O4@mTiO2-Ag-CNTs-MIPs towards SA was investigated. The results showed that Fe3O4@mTiO2-Ag-CNTs-MIPs could achieve the specific adsorption of SA with the selectivity coefficient higher than 2. Compared with Fe3O4@mTiO2, the photodegradation efficiency of Fe3O4@mTiO2-Ag-CNTs-MIPs for SA under visible light was significantly improved, indicating that the doping of CNTs and Ag together with the loading of MIPs could enhance the photocatalytic performance of the prepared composite. Under the irradiation of visible light (300 W) for 150 min, the degradation rate of SA (5 mg/L) in 50 mL of solution (pH 3) by Fe3O4@mTiO2-Ag-CNTs-MIPs (15 mg) was up to 98.41 %. Moreover, the degradation rate of the recovered Fe3O4@mTiO2-Ag-CNTs-MIPs for SA was still 87.12 % after five cycles. The primary active species for the photodegradation of SA by Fe3O4@mTiO2-Ag-CNTs-MIPs were O2- and h+, and the potential degradation pathways of SA were elucidated by high-resolution UPLC-MS. Overall, this study constructed a promising photocatalyst Fe3O4@mTiO2-Ag-CNTs-MIPs, which was expected to effectively degrade the pollutant SA in wastewater treatment.

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掺杂银纳米颗粒和碳纳米管的新型磁性分子印迹介孔二氧化钛(Fe3O4@mTiO2-Ag-CNTs-MIPs)在可见光下对水杨酸的选择性吸附和光降解
成功制备了掺杂银纳米粒子和碳纳米管的新型磁性分子印迹介孔二氧化钛(Fe3O4@mTiO2-Ag-CNTs-MIPs),用于水杨酸(SA)的选择性吸附和光降解。通过扫描电镜、傅立叶变换红外光谱、XRD、VSM、紫外-可见DRS、EIS和XPS对制备的复合材料的形貌和理化性质进行了表征。研究了 Fe3O4@mTiO2-Ag-CNTs-MIPs 对 SA 的吸附和光降解性能。结果表明,Fe3O4@mTiO2-Ag-CNTs-MIPs 可实现对 SA 的特定吸附,选择性系数大于 2。与 Fe3O4@mTiO2 相比,Fe3O4@mTiO2-Ag-CNTs-MIPs 在可见光下对 SA 的光降解效率显著提高,表明 CNTs 和 Ag 的掺杂以及 MIPs 的负载可以提高所制备复合材料的光催化性能。在可见光(300 W)照射 150 分钟的条件下,Fe3O4@mTiO2-Ag-CNTs-MIPs(15 mg)对 50 mL 溶液(pH 3)中 SA(5 mg/L)的降解率高达 98.41%。此外,经过五个循环后,回收的 Fe3O4@mTiO2-Ag-CNTs-MIPs 对 SA 的降解率仍为 87.12%。Fe3O4@mTiO2-Ag-CNTs-MIPs光降解 SA 的主要活性物种为 O2∙- 和 h+,并通过高分辨率 UPLC-MS 阐明了 SA 的潜在降解途径。总之,本研究构建了一种前景良好的光催化剂 Fe3O4@mTiO2-Ag-CNTs-MIPs,有望在废水处理中有效降解污染物 SA。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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