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Highly ordered Nanomaterial Functionalized Copper Schiff Base Framework: Synthesis, Characterization, and Hydrogen Peroxide Decomposition Performance

机译:高度有序的纳米材料功能化铜席夫碱骨架:合成,表征和过氧化氢分解性能

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摘要

An immobilized copper Schiff base tridentate complex was prepared in three steps from SBA-15 supports. The immobilized copper nanocatalyst (heterogeneous catalyst) was characterized by Fourier transform infrared spectroscopy (FT-IR), cross polarization magic angle spinning (CP-MAS), 13-carbon nuclear magnetic resonance (13C-NMR), atomic absorption spectroscopy (AAS), thermogravimetric analysis (TGA), and N2-physisorption. Moreover, morphological and structural features of the immobilized nanocatalyst were analyzed using transmission electron microscopy (TEM) and X-ray powder diffraction spectrometry (PXRD). After characterizing the nanocatalyst, the catalytic activity was determined in hydrogen peroxide (H2O2) decomposition. The high decomposition yield of H2O2 was obtained for low-loaded copper content materials at pH 7 and at room temperature. Furthermore, the nanocatalyst exhibited high activity and stability under the investigated conditions, and could be recovered and reused for at least five consecutive times without any significant loss in activity. No copper leaching was detected during the reaction by AAS measurements.
机译:从SBA-15载体分三步制备了固定的Schiff碱基铜三齿复合物。通过傅立叶变换红外光谱(FT-IR),交叉极化幻角旋转(CP-MAS),13碳核磁共振(13C-NMR),原子吸收光谱(AAS)对固定化的铜纳米催化剂(非均相催化剂)进行了表征。 ,热重分析(TGA)和N2物理吸附。此外,使用透射电子显微镜(TEM)和X射线粉末衍射光谱(PXRD)分析了固定化纳米催化剂的形态和结构特征。表征纳米催化剂后,测定过氧化氢(H2O2)分解的催化活性。对于pH 7和室温下的低载铜含量材料,H2O2的分解产率很高。此外,纳米催化剂在所研究的条件下表现出高活性和稳定性,并且可以连续至少五次被回收和再利用而活性没有任何显着损失。在反应过程中通过AAS测量未检测到铜浸出。

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