利用阳起石果皮提取物制造的银纳米粒子的催化降解功效

4区 材料科学 Q2 Materials Science
Maya Kassem Agha, Batoul Maatouk, Rami Mhanna, Mohammad H. El-Dakdouki
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引用次数: 0

摘要

利用绿色合成方法制备金属纳米粒子,并将其应用于高效降解对环境有害的染料,是目前所采用方法的一种有吸引力的替代方法。本报告采用猕猴桃果皮水提取物作为生物还原剂,在优化合成条件下成功实现了银纳米粒子(AgNPs)的绿色合成。实验参数包括反应物比例、反应温度和反应时间。生物纳米粒子在 λmax 480 nm 处显示出 SPR 吸收带。透射电子显微镜(TEM)和扫描电子显微镜(SEM)图像显示出直径为 36 nm 的类球形单分散纳米粒子。通过动态光散射法测定,纳米颗粒的流体力学直径为 106 nm,高负ζ电位(-34 mV)支持其卓越的胶体稳定性。能量色散 X 射线证实银是纳米颗粒的主要成分。X 射线衍射(XRD)衍射图证实了纳米粒子的结晶度及其面心立方(fcc)晶格结构。傅立叶变换红外光谱(FTIR)鉴定了植物中促进还原 Ag+ 离子和稳定所形成的 AgNPs 的植物化学物质的官能团。具体而言,傅立叶变换红外光谱中 3 412、1 618、1 419 和 1 237 cm-1 处的条带表明存在酚类化合物。通过比色法进行的植物化学分析显示,猕猴桃皮提取物中含有丰富的酚类化合物。在对有机染料的催化降解进行评估时,当使用 1.6 毫克的纳米颗粒时,生物合成的 AgNPs 能诱导亚甲基蓝染料瞬间完全褪色。使用较低剂量的 AgNPs(0.4 毫克)时,处理 3 小时后染料降解了 80%。降解反应遵循二阶动力学,速率常数为 0.01083 mM-1s-1。目前的研究凸显了所制备的纳米粒子作为高效催化剂降解亚甲基蓝等有害有机染料的巨大潜力,并为研究生物源 AgNPs 催化降解其他结构不同的染料污染物的效率提供了令人感兴趣的论据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catalytic Degradation Efficacy of Silver Nanoparticles Fabricated Using Actinidia deliciosa Peel Extract
The preparation of metallic nanoparticles using green synthetic approaches and its application toward the efficient degradation of environmentally hazardous dyes constitutes an attractive alternative to currently employed methods. In the current report, the green synthesis of silver nanoparticles (AgNPs) was successfully achieved using Actinidia deliciosa (kiwifruit) peel aqueous extract as a bioreducing agent under optimized synthesis conditions. The experimental parameters were optimized in terms of reactant ratio, reaction temperature, and reaction time. The biogenic nanoparticles exhibited SPR absorption band at λmax 480 nm. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) images revealed quasispherical monodisperse nanoparticles which were 36 nm in diameter. The hydrodynamic diameter of the nanoparticles was 106 nm as determined by dynamic light scattering, and the highly negative ζ-potential (−34 mV) supported its superior colloidal stability. Energy dispersive X-ray confirmed that silver is a major constituent of the nanoparticles. X-ray diffraction (XRD) diffractograms confirmed the crystallinity of the nanoparticles and its face-centered cubic (fcc) lattice structure. The functional groups in the plant’s phytochemicals facilitating the reduction of Ag+ ions and stabilization of the formed AgNPs were identified by fourier transform infrared (FTIR) spectroscopy. In specific, the bands in the FTIR spectra at 3,412, 1,618, 1,419, and 1,237 cm−1 suggested the presence of phenolic compounds. Phytochemical analysis by colorimetric assays revealed that the kiwifruit peel extract was rich in phenolic compounds. When evaluated in the catalytic degradation of organic dyes, the biosynthesized AgNPs induced instant and complete discoloration of the methylene blue dye when 1.6 mg of nanoparticles was used. At a lower dose of AgNPs (0.4 mg), 80% degradation of the dye occurred after 3 hr of treatment. The degradation reaction followed second-order kinetics with a rate constant of 0.01083 mM−1s−1. The current study highlights the immense potential of the prepared nanoparticles as efficient catalysts for the degradation of hazardous organic dyes such as methylene blue and presents an intriguing argument for investigating the catalytic efficiency of the biogenic AgNPs for the degradation of other structurally different dye pollutants.
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来源期刊
Journal of Nanomaterials
Journal of Nanomaterials 工程技术-材料科学:综合
CiteScore
6.10
自引率
0.00%
发文量
577
审稿时长
2.3 months
期刊介绍: The overall aim of the Journal of Nanomaterials is to bring science and applications together on nanoscale and nanostructured materials with emphasis on synthesis, processing, characterization, and applications of materials containing true nanosize dimensions or nanostructures that enable novel/enhanced properties or functions. It is directed at both academic researchers and practicing engineers. Journal of Nanomaterials will highlight the continued growth and new challenges in nanomaterials science, engineering, and nanotechnology, both for application development and for basic research.
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