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用于低温下甲醛完全氧化的贵金属促进水钠锰矿催化剂的制备与性能

Fabrication and Performance of Noble Metal Promoted Birnessite Catalysts for Complete Oxidation of Formaldehyde at Low Temperatures.

作者信息

Liu Linlin, Tian Hua, He Junhui, Wang Donghui, Ma Chunyan, Yang Qiaowen

出版信息

J Nanosci Nanotechnol. 2015 Apr;15(4):2887-95. doi: 10.1166/jnn.2015.9163.

Abstract

Noble metal (Au, Ag, Pd and Pt) promoted birnessite (Bir) catalysts were successfully prepared and tested for catalytic oxidation of formaldehyde (HCHO). The catalysts were characterized by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), hydrogen temperature programmed reduction (H2-TPR), inductively coupled plasma atomic emission spectroscopy (ICP-AES) and N2 adsorption-desorption. The activities of noble metal (Au, Ag, Pd and Pt) promoted birnessite catalysts follow the order of 1.0Pt/Bir > 1.0Pd/Bir > Bir > 1.0Ag/Bir > 1.0Au/Bir, revealing that the loading of Pd and Pt improves the catalytic activity of birnessite, but the loading of Ag and Au slightly decreases the catalytic activity of birnessite. Effects of the Pt loading amount were also investigated on the activity of Pt/Bir catalysts for HCHO oxidation. Pt/Bir with a Pt loading of 1.5 wt% (1.5 Pt/Bir), which has the best reduction properties, was found to be the most efficient catalyst. Over this catalyst, HCHO could be completely oxidized into CO2 and H2O at 70°. 1.5 Pt/Bir also shows good catalytic stability under the HCHO oxidation atmosphere. The differences in the catalytic activity of these materials are largely attributed to their reducibility as well as the dispersion of metal nanoparticles, but are not directly related to their specific surface areas.

摘要

成功制备了贵金属(金、银、钯和铂)促进的水钠锰矿(Bir)催化剂,并对其进行了甲醛(HCHO)催化氧化测试。通过X射线衍射(XRD)、透射电子显微镜(TEM)、氢气程序升温还原(H2-TPR)、电感耦合等离子体原子发射光谱(ICP-AES)和N2吸附-脱附对催化剂进行了表征。贵金属(金、银、钯和铂)促进的水钠锰矿催化剂的活性顺序为1.0Pt/Bir > 1.0Pd/Bir > Bir > 1.0Ag/Bir > 1.0Au/Bir,这表明钯和铂的负载提高了水钠锰矿的催化活性,但银和金的负载略微降低了水钠锰矿的催化活性。还研究了铂负载量对Pt/Bir催化剂HCHO氧化活性的影响。发现铂负载量为1.5 wt%的Pt/Bir(1.5 Pt/Bir)具有最佳的还原性能,是最有效的催化剂。在该催化剂上,HCHO在70°时可完全氧化为CO2和H2O。1.5 Pt/Bir在HCHO氧化气氛下也表现出良好的催化稳定性。这些材料催化活性的差异很大程度上归因于它们的还原性以及金属纳米颗粒的分散性,但与它们的比表面积没有直接关系。

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