Activated carbon as catalyst in wet oxidation of phenol:: Effect of the oxidation reaction on the catalyst properties and stability

被引:37
作者
Cordero, T. [1 ]
Rodriguez-Mirasol, J. [1 ]
Bedia, J. [1 ]
Gomis, S. [2 ]
Yustos, P. [2 ]
Garcia-Ochoa, F. [2 ]
Santos, A. [2 ]
机构
[1] Univ Malaga, Dept Chem Engn, ETSI Ind, E-29071 Malaga, Spain
[2] Univ Complutense Madrid, Dept Chem Engn, Fac CC Quim, Madrid 28048, Spain
关键词
catalytic wet oxidation; activated carbon; phenol;
D O I
10.1016/j.apcatb.2007.12.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Catalytic wet oxidation (CWO) of phenol has been carried out in a continuous three-phase reactor by using a commercial activated carbon (AC) as catalyst, feeding oxygen as gas phase and an aqueous solution 1000 ppm in phenol to the reactor. A stable catalyst under operation conditions is one of the main difficulties to pass up in the catalytic wet oxidation process, so the stability of the activated carbon with the time on stream (TOS) was investigated. To do this the phenol conversion change was analyzed with TOS and results were contrasted to the change of the physicochemical properties of the AC with the TOS. Gas adsorption/desorption, TPD, XPS and SEM measurements were applied to the AC taken from the reactor after several TOS values. A significant reduction of the micro-pore volume and BET surface area of the catalyst was observed with TOS. However, as reaction proceeded the external surface area and the total amount of oxygen surface group increased. Moreover, regeneration of the initial catalyst properties was done by washing with water saturated in oxygen, at the reaction conditions or by heating in N-2 atmosphere at 450, 700 and 900 degrees C. The total micro-pore volume and internal surface area of the catalyst were not recovered by the regeneration process, probably due to blockage of the narrow micropores by pyrolytic carbon produced during the first step of the wet oxidation process. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 131
页数:10
相关论文
共 59 条
[21]   METHOD FOR THE CALCULATION OF EFFECTIVE PORE-SIZE DISTRIBUTION IN MOLECULAR-SIEVE CARBON [J].
HORVATH, G ;
KAWAZOE, K .
JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 1983, 16 (06) :470-475
[22]   Catalytic and noncatalytic wet oxidation [J].
Imamura, S .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1999, 38 (05) :1743-1753
[23]   WET OXIDATION CATALYZED BY RUTHENIUM SUPPORTED ON CERIUM(IV) OXIDES [J].
IMAMURA, S ;
FUKUDA, I ;
ISHIDA, S .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1988, 27 (04) :718-721
[24]   Wet air oxidation: a review of process technologies and aspects in reactor design [J].
Kolaczkowski, ST ;
Plucinski, P ;
Beltran, FJ ;
Rivas, FJ ;
McLurgh, DB .
CHEMICAL ENGINEERING JOURNAL, 1999, 73 (02) :143-160
[25]   Oxidation of primary alcohols with air on carbon-supported platinum catalysts for the synthesis of aldehydes or acids [J].
Korovchenko, Pavel ;
Donze, Cecile ;
Gallezot, Pierre ;
Besson, Michele .
CATALYSIS TODAY, 2007, 121 (1-2) :13-21
[26]   STUDIES ON PORE SYSTEMS IN CATALYSTS .V. T METHOD [J].
LIPPENS, BC ;
DEBOER, JH .
JOURNAL OF CATALYSIS, 1965, 4 (03) :319-&
[27]   Wet air oxidation: past, present and future [J].
Luck, F .
CATALYSIS TODAY, 1999, 53 (01) :81-91
[28]   PHENOL ADSORPTION ON ACTIVATED CARBONS - APPLICATION TO THE REGENERATION OF ACTIVATED CARBONS POLLUTED WITH PHENOL [J].
MAGNE, P ;
WALKER, PL .
CARBON, 1986, 24 (02) :101-107
[29]   Catalytic wet oxidation of p-coumaric acid: Partial oxidation intermediates, reaction pathways and catalyst leaching [J].
Mantzavinos, D ;
Hellenbrand, R ;
Livingston, AG ;
Metcalfe, IS .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1996, 7 (3-4) :379-396
[30]   Platinum catalysed wet oxidation of phenol in a stirred slurry reactor - A practical operation window [J].
Masende, ZPG ;
Kuster, BFM ;
Ptasinski, KJ ;
Janssen, FJJG ;
Katima, JHY ;
Schouten, JC .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 41 (03) :247-267