Catalytic reduction of p-nitrophenol over precious metals/highly ordered mesoporous silica

化学 催化作用 介孔材料 介孔二氧化硅 还原剂 金属 粒径 反应速率常数 X射线光电子能谱 4-硝基苯酚 贵金属 柠檬酸钠 无机化学 过渡金属 化学工程 核化学 动力学 物理化学 有机化学 病理 工程类 物理 医学 量子力学
作者
Said M. El‐Sheikh,Adel A. Ismail,Jafar F. Al‐Sharab
出处
期刊:New Journal of Chemistry [The Royal Society of Chemistry]
卷期号:37 (8): 2399-2399 被引量:124
标识
DOI:10.1039/c3nj00138e
摘要

Precious metals, Au, Pt, and Pd, were successfully deposited on highly ordered mesoporous SBA-15. Two different reduction routes were employed to deposit precious metals: (1) under H2 and (2) using sodium citrate. Samples prepared using sodium citrate exhibit a uniform particle size of 10 nm while samples synthesized under H2 show high dispersion with a particle size of 8 and 20 nm for Pt and Pd, respectively. The surface area and pore volume of the mesoporous SBA-15 were significantly reduced due to the impregnation of the precious metals. Detailed TEM and XPS analyses reveal a uniform distribution of particles with a metallic valence state and no evidence of metallic oxides. The prepared catalysts were used to reduce p-nitrophenol (PNP) into p-aminophenol (PAP) where two trends were observed. The catalytic reduction efficiency for PNP reduction using the catalyst prepared with sodium citrate as a reducing agent is in the order of Au > Pt > Pd with a rate constant of 3.24 × 10−1 s−1 for Au/SBA-15. On the other hand, the catalyst prepared with H2 as a reducing agent showed a reverse trend Pd > Pt > Au with a rate constant of 7.15 × 10−1 s−1 for Pd/SBA-15. The highest catalyst efficiency was observed for the case of Pd/SBA-15 synthesized via the H2 route with a rate constant of 7.15 × 10−1 s−1. Also the reaction rate of Pd/SBA-15 synthesized via the H2 route was 2.2 times higher than that of Au/SBA-15 prepared using the sodium citrate route.

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