中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Oxalate route for promoting activity of manganese oxide catalysts in total VOCs' oxidation: effect of calcination temperature and preparation method

文献类型:期刊论文

作者Tang, Wenxiang1,3; Wu, Xiaofeng1; Li, Dongyan1,3; Wang, Zhen2; Liu, Gang1,3; Liu, Haidi1; Chen, Yunfa1
刊名JOURNAL OF MATERIALS CHEMISTRY A
出版日期2014
卷号2期号:8页码:2544-2554
关键词volatile organic-compounds benzene combustion lattice oxygen air-pollution ethyl-acetate co oxidation gas-phase toluene removal mnox
ISSN号2050-7488
其他题名J. Mater. Chem. A
中文摘要A novel template-free oxalate route was applied to synthesize mesoporous manganese oxides with high surface area (355 m(2) g(-1)) and well-defined mesopores which can be obtained in large quantities. The physicochemical properties of the materials were characterized by means of TG, XRD, SEM, TEM, H-2-TPR and XPS techniques. All catalysts were tested on catalytic deep oxidation of benzene, and the effects of calcination temperature on the features of catalyst structure and catalytic activity were investigated. Manganese oxides prepared by oxalate route exhibited better catalytic activities for complete oxidation of benzene, toluene and o-xylene as compared with related manganese oxides prepared by other different methods (NaOH route, NH4HCO3 route and nanocasting strategy), and especially the temperature for benzene conversion of 90% on the oxalate-derived manganese oxide catalysts was 209 degrees C, which is 132 degrees C lower than required for the catalyst prepared by NaOH route. The catalytic performance of manganese oxide is correlated with surface area, pore size, low-temperature reducibility and distribution of surface species. The mole ratio of Mn4+/Mn2+ on the samples which performed with better catalytic activity was close to 1.0. This is good for the redox process of Mn4+ <-> Mn3+ <-> Mn2+ which is the key factor in determining the activity on MnOx, further indicating that the oxalate route is good for keeping the distribution of manganese oxidation states at an appropriate degree. A possible process of VOCs' complete oxidation on manganese oxide catalysts is discussed. In addition, the best catalyst was highly stable with prolonged time on stream and was resistant to water vapor.
英文摘要A novel template-free oxalate route was applied to synthesize mesoporous manganese oxides with high surface area (355 m(2) g(-1)) and well-defined mesopores which can be obtained in large quantities. The physicochemical properties of the materials were characterized by means of TG, XRD, SEM, TEM, H-2-TPR and XPS techniques. All catalysts were tested on catalytic deep oxidation of benzene, and the effects of calcination temperature on the features of catalyst structure and catalytic activity were investigated. Manganese oxides prepared by oxalate route exhibited better catalytic activities for complete oxidation of benzene, toluene and o-xylene as compared with related manganese oxides prepared by other different methods (NaOH route, NH4HCO3 route and nanocasting strategy), and especially the temperature for benzene conversion of 90% on the oxalate-derived manganese oxide catalysts was 209 degrees C, which is 132 degrees C lower than required for the catalyst prepared by NaOH route. The catalytic performance of manganese oxide is correlated with surface area, pore size, low-temperature reducibility and distribution of surface species. The mole ratio of Mn4+/Mn2+ on the samples which performed with better catalytic activity was close to 1.0. This is good for the redox process of Mn4+ <-> Mn3+ <-> Mn2+ which is the key factor in determining the activity on MnOx, further indicating that the oxalate route is good for keeping the distribution of manganese oxidation states at an appropriate degree. A possible process of VOCs' complete oxidation on manganese oxide catalysts is discussed. In addition, the best catalyst was highly stable with prolonged time on stream and was resistant to water vapor.
WOS标题词Science & Technology ; Physical Sciences ; Technology
类目[WOS]Chemistry, Physical ; Energy & Fuels ; Materials Science, Multidisciplinary
研究领域[WOS]Chemistry ; Energy & Fuels ; Materials Science
关键词[WOS]VOLATILE ORGANIC-COMPOUNDS ; BENZENE COMBUSTION ; LATTICE OXYGEN ; AIR-POLLUTION ; ETHYL-ACETATE ; CO OXIDATION ; GAS-PHASE ; TOLUENE ; REMOVAL ; MNOX
收录类别SCI
原文出处://WOS:000331247500014
语种英语
WOS记录号WOS:000331247500014
公开日期2014-05-06
版本出版稿
源URL[http://ir.ipe.ac.cn/handle/122111/8157]  
专题过程工程研究所_研究所(批量导入)
作者单位1.Chinese Acad Sci, Inst Proc Engn, Beijing 100190, Peoples R China
2.Natl Ctr Nanosci & Technol, CAS Key Lab Standardizat & Measurement Nanotechno, Beijing 100190, Peoples R China
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Tang, Wenxiang,Wu, Xiaofeng,Li, Dongyan,et al. Oxalate route for promoting activity of manganese oxide catalysts in total VOCs' oxidation: effect of calcination temperature and preparation method[J]. JOURNAL OF MATERIALS CHEMISTRY A,2014,2(8):2544-2554.
APA Tang, Wenxiang.,Wu, Xiaofeng.,Li, Dongyan.,Wang, Zhen.,Liu, Gang.,...&Chen, Yunfa.(2014).Oxalate route for promoting activity of manganese oxide catalysts in total VOCs' oxidation: effect of calcination temperature and preparation method.JOURNAL OF MATERIALS CHEMISTRY A,2(8),2544-2554.
MLA Tang, Wenxiang,et al."Oxalate route for promoting activity of manganese oxide catalysts in total VOCs' oxidation: effect of calcination temperature and preparation method".JOURNAL OF MATERIALS CHEMISTRY A 2.8(2014):2544-2554.

入库方式: OAI收割

来源:过程工程研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。