Preparation of birnessite-supported Pt nanoparticles and their application in catalytic oxidation of formaldehyde

• Published in: Journal of environmental sciences (China) 2012-06, Vol.24 (6), p.1117-1124
• Main Authors: Liu, Linlin, Tian, Hua, He, Junhui, Wang, Donghui, Yang, Qiaowen
• Format: Article
• Language: English
• Subjects: active sites; Air Pollutants - chemistry; Air Pollution - prevention & control; birnessite; carbon dioxide; Catalysis; Catalysts; Catalytic activity; energy; energy-dispersive X-ray analysis; formaldehyde; Formaldehyde - chemistry; formaldehyde oxidation; manganese oxide; Metal Nanoparticles - chemistry; Metal Nanoparticles - ultrastructure; Microscopy, Electron, Transmission; Nanoparticles; Nanostructure; nitrogen; noble metals; Oxidation; Oxidation-Reduction; Oxides - chemistry; Platinum; Platinum - chemistry; Porosity; Pt催化剂; Pt纳米粒子; Reduction; spectroscopy; Surface Properties; transmission electron microscopy; X-ray diffraction; 催化氧化; 制备; 水钠锰矿; 甲醛; 透射电子显微镜; 铂纳米粒子
• ISSN: 1001-0742; 1878-7320
• DOI: 10.1016/S1001-0742(11)60879-6

Flaky and nanospherical birnessite and birnessite-supported Pt catalysts were successfully prepared and characterized by means of Xray diffraction （XRD）,transmission electron microscopy （TEM）,energy dispersive spectroscopy （EDS） and N2 adsorption-desorption.Effects of the birnessite morphology and Pt reduction method on the catalytic activity for the complete oxidation of formaldehyde （HCHO） were investigated.It was found that flaky birnessite exhibited higher catalytic activity than nanospherical birnessite.The promoting effect of Pt on the birnessite catalyst indicated that the reduction method of the Pt precursor greatly influenced the catalytic performance.Flaky birnessite-supported Pt nanoparticles reduced by KBH 4 showed the highest catalytic activity and could completely oxidize HCHO into CO2 and H2O at 50℃,whereas the sample reduced using H2-plasma showed lower activity for HCHO oxidation.The differences in catalytic activity of these materials were jointly attributed to the effects of pore structure,surface active sites exposed to HCHO and the dispersion of Pt nanoparticles.