Comparative study on the support properties in the total oxidation of dichloromethane over Pt catalysts

被引:48
作者
El Assal, Zouhair [1 ,2 ,3 ]
Ojala, Satu [1 ]
Pitkaaho, Satu [1 ]
Pirault-Roy, Laurence [4 ]
Darif, Bouchra [1 ,3 ]
Comparot, Jean-Dominique [4 ]
Bensitel, Mohammed [3 ]
Keiski, Riitta L. [1 ]
Brahmi, Rachid [3 ]
机构
[1] Univ Oulu, Fac Technol, Environm & Chem Engn, POB 4300, FI-90014 Oulu, Finland
[2] Univ Oulu, Thule Inst, POB 7300, FI-90014 Oulu, Finland
[3] Univ Chouaib Doukkali, Fac Sci El Jadida, Dept Chem, LCCM, BP 20, El Jadida 24000, Morocco
[4] Univ Poitiers, Inst Chem Poitiers Mat & Nat Resources, UMR 7285 IC2MP, B27,4 Rue Michel Brunet,TSA 51106, F-86073 Poitiers, France
关键词
Bronsted acidity; Catalytic oxidation; CVOC abatement; Dichloromethane; Lewis acidity; Methyl chloride; CHLORINATED HYDROCARBONS; ACID SITES; PLATINUM; MECHANISM; CERIA; NANOCRYSTALLINE; GAMMA-AL2O3; ALUMINA; CH2CL2; VOCS;
D O I
10.1016/j.cej.2016.10.139
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The aim of this work was to study the influence of the support oxide properties on the total oxidation of dichloromethane in moist conditions. The support materials gamma-Al2O3, TiO2, CeO2 and MgO were synthesized by a sol-gel method followed by wet impregnation of Pt and characterized by different physicochemical techniques. The conversion of DCM was higher than 90% at 500 degrees C over impregnated and non-impregnated Al2O3, TiO2 and CeO2, even at high GHSV. CO, CH3CI and CH2O were the major byproducts observed and their amounts decreased after Pt impregnation. The CH3CI formation was higher when Lewis acid sites were present while the existence of Bronsted sites promoted the CH2O formation. The complete conversion of DCM was achieved at around 450 degrees C over the Al2O3 and Pt/Al2O3 and at 500 degrees C for Pt/TiO2. These two catalysts exhibited the highest total acidities among the materials tested. The activity of Pt/Al2O3 remained the same also after 55 h of testing, however, increase in Pt particle size and decrease in acidity were observed. Pt/CeO2 while being less active showed smallest amount of byproduct formation during the whole temperature range used in light-off tests. This is most probably due to its easy reduction ability. The textural parameters of the supports did not appear to be the key parameters when considering the activity and selectivity of the catalysts. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1010 / 1022
页数:13
相关论文
共 51 条
[1]   Performance, structure, and mechanism of CeO2 in HCl oxidation to Cl2 [J].
Amrute, Amol P. ;
Mondelli, Cecilia ;
Moser, Maximilian ;
Novell-Leruth, Gerard ;
Lopez, Nuria ;
Rosenthal, Dirk ;
Farra, Ramzi ;
Schuster, Manfred E. ;
Teschner, Detre ;
Schmidt, Timm ;
Perez-Ramirez, Javier .
JOURNAL OF CATALYSIS, 2012, 286 :287-297
[2]   Study of MgO and Pt/MgO systems by XRD, TPR, and 1H MAS NMR [J].
Aramendía, MA ;
Benítez, JA ;
Borau, V ;
Jiménez, C ;
Marinas, JM ;
Ruiz, JR ;
Urbano, F .
LANGMUIR, 1999, 15 (04) :1192-1197
[3]   Effect of support on the deep oxidation of propane and propylene on Pt-based catalysts [J].
Avila, M. S. ;
Vignatti, C. I. ;
Apesteguia, C. R. ;
Garetto, T. F. .
CHEMICAL ENGINEERING JOURNAL, 2014, 241 :52-59
[4]   Study of Pt-CeO2 interaction and the effect in the selective hydrodechlorination of trichloroethylene [J].
Barrabes, N. ;
Foettinger, K. ;
Dafinov, A. ;
Medina, F. ;
Rupprechter, G. ;
Llorca, J. ;
Sueiras, J. E. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2009, 87 (1-2) :84-91
[5]  
Berteau P., 1989, CATAL TODAY, V5, P121, DOI DOI 10.1016/0920-5861(89)80020-3
[6]   FCC gasoline sulfur reduction additives:: Mechanism and active sites [J].
Can, F. ;
Travert, A. ;
Ruaux, V. ;
Gilson, J.-P. ;
Mauge, F. ;
Hu, R. ;
Wormsbecher, R. F. .
JOURNAL OF CATALYSIS, 2007, 249 (01) :79-92
[7]   Catalyst performance and mechanism of catalytic combustion of dichloromethane (CH2Cl2) over Ce doped TiO2 [J].
Cao, Shuang ;
Wang, Haiqiang ;
Yu, Feixiang ;
Shi, Mengpa ;
Chen, Shuang ;
Weng, Xiaole ;
Liu, Yue ;
Wu, Zhongbiao .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2016, 463 :233-241
[8]   Catalytic oxidation of dichloromethane over Pt/CeO2-Al2O3 catalysts [J].
Chen, Qiu-Yan ;
Li, Na ;
Luo, Meng-Fei ;
Lu, Ji-Qing .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2012, 127 :159-166
[9]   On the selection of the catalyst among the commercial platinum-based ones for total oxidation of some chlorinated hydrocarbons [J].
Corella, J ;
Toledo, JM ;
Padilla, AM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2000, 27 (04) :243-256
[10]   Total Oxidation of Dichloromethane Over Metal Oxide Catalysts [J].
El Assal, Zouhair ;
Pitkaaho, Satu ;
Ojala, Satu ;
Maache, Rhizlane ;
Bensitel, Mohamed ;
Pirault-Roy, Laurence ;
Brahmi, Rachid ;
Keiski, Riitta L. .
TOPICS IN CATALYSIS, 2013, 56 (9-10) :679-687