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用于催化超声降解甲基橙的二氧化锰/二氧化铈

MnO2/CeO2 for catalytic ultrasonic degradation of methyl orange.

作者信息

Zhao He, Zhang Guangming, Zhang Quanling

机构信息

School of Environment & Natural Resource, Renmin University of China, 59 Zhongguancun Street, Beijing 100872, China.

School of Environment & Natural Resource, Renmin University of China, 59 Zhongguancun Street, Beijing 100872, China.

出版信息

Ultrason Sonochem. 2014 May;21(3):991-6. doi: 10.1016/j.ultsonch.2013.12.002. Epub 2013 Dec 13.

Abstract

Catalytic ultrasonic degradation of aqueous methyl orange was studied in this paper. Heterogeneous catalyst MnO2/CeO2 was prepared by impregnation of manganese oxide on cerium oxide. Morphology and specific surface area of MnO2/CeO2 catalyst were characterized and its composition was determined. Results showed big differences between fresh and used catalyst. The removal efficiency of methyl orange by MnO2/CeO2 catalytic ultrasonic process was investigated. Results showed that ultrasonic process could remove 3.5% of methyl orange while catalytic ultrasonic process could remove 85% of methyl orange in 10 min. The effects of free radical scavengers were studied to determine the role of hydroxyl free radical in catalytic ultrasonic process. Results showed that methyl orange degradation efficiency declined after adding free radical scavengers, illustrating that hydroxyl free radical played an important role in degrading methyl orange. Theoretic analysis showed that the resonance size of cavitation bubbles was comparable with the size of catalyst particles. Thus, catalyst particles might act as cavitation nucleus and enhance ultrasonic cavitation effects. Measurement of H2O2 concentration in catalytic ultrasonic process confirmed this hypothesis. Effects of pre-adsorption on catalytic ultrasonic process were examined. Pre-adsorption significantly improved methyl orange removal. The potential explanation was that methyl orange molecules adsorbed on catalysts could enter cavitation bubbles and undergo stronger cavitation.

摘要

本文研究了催化超声降解水溶液中的甲基橙。通过将氧化锰浸渍在氧化铈上制备了非均相催化剂MnO₂/CeO₂。对MnO₂/CeO₂催化剂的形貌和比表面积进行了表征,并确定了其组成。结果表明新鲜催化剂和使用过的催化剂之间存在很大差异。研究了MnO₂/CeO₂催化超声过程对甲基橙的去除效率。结果表明,在10分钟内,超声过程可去除3.5%的甲基橙,而催化超声过程可去除85%的甲基橙。研究了自由基清除剂的作用,以确定羟基自由基在催化超声过程中的作用。结果表明,添加自由基清除剂后甲基橙降解效率下降,说明羟基自由基在降解甲基橙中起重要作用。理论分析表明,空化气泡的共振尺寸与催化剂颗粒的尺寸相当。因此,催化剂颗粒可能充当空化核并增强超声空化效应。催化超声过程中H₂O₂浓度的测量证实了这一假设。考察了预吸附对催化超声过程的影响。预吸附显著提高了甲基橙的去除率。可能的解释是,吸附在催化剂上的甲基橙分子可以进入空化气泡并经历更强的空化作用。

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