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首页> 外文期刊>Applied Surface Science >Nitric acid-treated birnessite-type MnO_2: An efficient and hydrophobic material for humid ozone decomposition
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Nitric acid-treated birnessite-type MnO_2: An efficient and hydrophobic material for humid ozone decomposition

机译:硝酸处理的水钠锰矿型MnO_2:一种有效的疏水材料,用于湿臭氧分解

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摘要

MnO2 catalysts are important for low-temperature removal of air pollutants. Sometimes the unavoidable moisture is not conductive to the desired reactions, therefore, water-resistant materials are desirable. However, the reported methods are not easily fulfilled for practical applications and the underlying mechanism for the improved hydrophobicity has not been clarified. In this study, highly water-resistant birnessite-type MnO2 was designed for humid ozone (O-3) decomposition, which is important for alleviating global O-3 pollution. The sample treated by nitric acid (H-MnO2) exhibited stable O-3 conversion of similar to 50% within 24 h under 50% of relative humidity (115 ppm of O-3, 600 L.g(-1).h(-1) of space velocity, 25 degrees C). However, the pristine MnO2 was quickly deactivated with O-3 conversion dropping to similar to 10% within 30 min. Detailed characterizations show that higher amount of acid sites and oxygen vacancies together with their improved water-resistant properties facilitates adsorption and subsequent decomposition of humid O-3 over the H-MnO2. DFT calculations demonstrate that compared with the pristine MnO2, oxygen vacancies were more easily formed over the H-MnO2, and the surface of the H-MnO2 was more hydrophobic and more attractive to O-3 adsorption. Finally, a mechanism involving acid sites and oxygen vacancies for gaseous O-3 decomposition was proposed. (C) 2018 Elsevier B.V. All rights reserved.
机译:MnO2催化剂对于低温去除空气污染物很重要。有时不可避免的水分不能引导所需的反应,因此,需要防水材料。然而,所报道的方法在实际应用中不容易实现,并且改善疏水性的基本机理还不清楚。在这项研究中,高度耐水的水钠锰矿型MnO2被设计用于湿臭氧(O-3)的分解,这对于减轻全球O-3污染很重要。用硝酸(H-MnO2)处理的样品在50%的相对湿度(115 ppm的O-3、600 Lg(-1).h(-1)下,在24小时内显示稳定的O-3转化率,类似于50% ),即25摄氏度)。但是,原始的MnO2迅速失活,O-3转化率在30分钟内下降到接近10%。详细的特征表明,较高的酸位和氧空位,以及其改进的耐水性能,促进了潮湿的O-3在H-MnO2上的吸附和随后的分解。 DFT计算表明,与原始MnO2相比,H-MnO2上更容易形成氧空位,并且H-MnO2的表面更疏水并且对O-3吸附更具吸引力。最后,提出了一种涉及酸位和氧空位的O-3气态分解机理。 (C)2018 Elsevier B.V.保留所有权利。

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