Biosynthesis of MgAl2O4 nanoparticles and their use as photocatalyst for sunlight-driven degradation of Amido-Black

IF 2.4 4区 物理与天体物理 Q3 PHYSICS, CONDENSED MATTER
Wiem Ben Ameur , Bilel Chouchene , Raphaël Schneider , Anouar Hajjaji , Mouldi Zouaoui
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引用次数: 0

Abstract

Magnesium aluminate MgAl2O4, known as spinel, has been the subject of intense research due to its excellent thermal, optical, and dielectric characteristics. In this work, a green synthesis process that is eco-friendly, easy, and of low cost is used to prepare MgAl2O4 nanoparticles. The structural, morphological, and optical properties of the MgAl2O4 spinel were studied by different techniques, such as X-ray diffraction (XRD), transmission electron microscopy (TEM), Brunauer-Emmett-Teller surface area analyzer (BET), UV–visible spectroscopy, and Fourier transform-infrared spectroscopy (FT-IR). The XRD patterns indicate the formation of the MgAl2O4 cubic phase, and the average size of nanoparticles is around 17 nm. TEM images confirmed the pure phase and the nanosize of the particles. The UV–vis absorption spectrum of the MgAl2O4 spinel showed an absorption peak at around 230 nm, and the optical band gap energy was found to be 3.92 eV. Surface analysis was conducted using BET isotherms, demonstrating a specific surface area of 58 m2 g−1 and a 5–10 nm pore size. The dielectric properties of MgAl2O4 spinel were studied using the complex impedance spectroscopy technique over a frequency range from 1 Hz to 13 MHz and a temperature range from 648 to 873 K. The temperature and frequency dependence of the material properties was demonstrated, and the activation energy was also calculated. The photocatalytic activity of MgAl2O4 was investigated for the degradation of the Amido Black 10B dye under sunlight irradiation. The dye was effectively decomposed by ca. 98 % under solar light irradiation within ca. 5 h, with pseudo-first-order rate constants of 7.99 10−3 min−1.
MgAl2O4纳米颗粒的生物合成及其作为光催化剂在日光驱动降解氨基黑中的应用
铝酸镁MgAl2O4,又称尖晶石,由于其优异的热、光学和介电特性,一直是人们研究的热点。本文采用一种环保、简单、低成本的绿色合成方法制备了MgAl2O4纳米颗粒。采用x射线衍射(XRD)、透射电子显微镜(TEM)、布鲁诺尔-埃米特-泰勒表面积分析仪(BET)、紫外可见光谱和傅里叶变换红外光谱(FT-IR)等技术研究了MgAl2O4尖晶石的结构、形态和光学性质。XRD谱图表明MgAl2O4立方相的形成,纳米颗粒的平均尺寸约为17 nm。TEM图像证实了颗粒的纯相和纳米尺寸。MgAl2O4尖晶石的紫外-可见吸收光谱在230 nm附近有一个吸收峰,光学带隙能量为3.92 eV。使用BET等温线进行表面分析,显示比表面积为58 m2 g−1,孔径为5-10 nm。采用复阻抗谱技术研究了MgAl2O4尖晶石在1 Hz ~ 13 MHz频率和648 ~ 873 K温度范围内的介电特性。证明了材料性能与温度和频率的关系,并计算了活化能。研究了MgAl2O4在日光照射下降解氨基黑10B染料的光催化活性。在太阳光照射下,染料在约5 h内有效分解约98%,伪一阶速率常数为7.99 10−3 min−1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Solid State Communications
Solid State Communications 物理-物理:凝聚态物理
CiteScore
3.40
自引率
4.80%
发文量
287
审稿时长
51 days
期刊介绍: Solid State Communications is an international medium for the publication of short communications and original research articles on significant developments in condensed matter science, giving scientists immediate access to important, recently completed work. The journal publishes original experimental and theoretical research on the physical and chemical properties of solids and other condensed systems and also on their preparation. The submission of manuscripts reporting research on the basic physics of materials science and devices, as well as of state-of-the-art microstructures and nanostructures, is encouraged. A coherent quantitative treatment emphasizing new physics is expected rather than a simple accumulation of experimental data. Consistent with these aims, the short communications should be kept concise and short, usually not longer than six printed pages. The number of figures and tables should also be kept to a minimum. Solid State Communications now also welcomes original research articles without length restrictions. The Fast-Track section of Solid State Communications is the venue for very rapid publication of short communications on significant developments in condensed matter science. The goal is to offer the broad condensed matter community quick and immediate access to publish recently completed papers in research areas that are rapidly evolving and in which there are developments with great potential impact.
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