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超声辅助芬顿反应法制备氧化铜(II)的催化活性。

Catalytic activity of copper (II) oxide prepared via ultrasound assisted Fenton-like reaction.

机构信息

Department of Chemistry, Koç University, Rumeli Feneri Yolu, Sarıyer, 34450 Istanbul, Turkey.

出版信息

Ultrason Sonochem. 2014 Mar;21(2):854-9. doi: 10.1016/j.ultsonch.2013.09.006. Epub 2013 Sep 15.

Abstract

Copper (II) oxide nanoparticles were synthesized in an ultrasound assisted Fenton-like aqueous reaction between copper (II) cations and hydrogen peroxide. The reactions were initiated with the degradation of hydrogen peroxide by ultrasound induced cavitations at 0 °C or 5 °C and subsequent generation of the OH radical. The radical was converted into hydroxide anion in Fenton-like reactions and copper hydroxides were readily converted to oxides without the need of post annealing or aging of the samples. The products were characterized with X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and Brunauer-Emmett-Teller (BET) surface area analysis. Catalytic activity of the nanoparticles for the hydrogen peroxide assisted degradation of polycyclic aromatic hydrocarbons in the dark was tested by UV-visible spectroscopy with methylene blue as the model compound. The rate of the reaction was first order, however the rate constants changed after the initial hour. Initial rate constants as high as 0.030 min(-1) were associated with the high values of surface area, i.e. 70 m(2)/g. Annealing of the products at 150 °C under vacuum resulted in the decrease of the catalytic activity, underlying the significance of the cavitation induced surface defects in the catalytic process.

摘要

在超声辅助芬顿类似的水溶液反应中,用铜(II)阳离子和过氧化氢合成了氧化铜(II)纳米粒子。反应是通过在 0°C 或 5°C 下超声诱导空化使过氧化氢降解,随后生成 OH 自由基引发的。在芬顿类似的反应中,自由基转化为氢氧根阴离子,而铜氢氧化物无需对样品进行后退火或老化即可很容易地转化为氧化物。采用 X 射线衍射(XRD)、扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)和 Brunauer-Emmett-Teller(BET)表面积分析对产物进行了表征。通过用亚甲基蓝作为模型化合物的紫外可见光谱法测试了纳米粒子在黑暗中对多环芳烃的过氧化氢辅助降解的催化活性。反应速率为一级反应,但初始小时后速率常数发生变化。初始速率常数高达 0.030 min(-1),与高表面积值(即 70 m(2)/g)相关。在 150°C 下真空退火会降低催化活性,这表明空化诱导的表面缺陷在催化过程中具有重要意义。

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