Ozonation of 1,3,6-naphthalenetrisulphonic acid catalysed by activated carbon in aqueous phase

被引:196
作者
Rivera-Utrilla, J [1 ]
Sánchez-Polo, M [1 ]
机构
[1] Univ Granada, Fac Ciencias, Dept Quim Inorgan, E-18071 Granada, Spain
关键词
ozone; activated carbon; catalysis; 1,3,6-naphthalenetrisulphonic acid;
D O I
10.1016/S0926-3373(02)00117-0
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
This paper presents experimental results of the ozonation of a model aromatic sulphonic compound, 1,3,6-naphthalenetrisulphonic acid (NTS), in the presence of different activated carbons with different physical and chemical surface properties. Carbons used were commercial activated carbons (Ceca AC40, Norit, Merck, Witco, Ceca GAC, Filtrasorb 400, Sorbo) with or without demineralisation pre-treatment. Carbon samples were texturally and chemically characterised using N-2 adsorption isotherms, mercury porosimetry, pH(PZC), selective neutralisation and elemental analysis. Results show that NTS was degraded by ozone at a faster rate in the presence of activated carbon, especially in the case of Sorbo, Ceca GAC and Norit carbons, which display catalytic activity, probably by enhancing ozone decomposition in aqueous phase in highly oxidative species. These catalytic properties seem to be favoured by both the basicity of the carbon surface and the higher macropore volume. Dissolved total organic carbon from the NTS degradation compounds was removed in the presence of activated carbon through both the catalytic activity of activated carbon to mineralise organic matter and the adsorption of these organic compounds on activated carbon. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:319 / 329
页数:11
相关论文
共 33 条
[1]   DECOLORIZATION BY OZONE OF DIRECT DYES IN PRESENCE OF SOME CATALYSTS [J].
ABDO, MSE ;
SHABAN, H ;
BADER, MSH .
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART A-ENVIRONMENTAL SCIENCE AND ENGINEERING & TOXIC AND HAZARDOUS SUBSTANCE CONTROL, 1988, 23 (07) :697-710
[2]   CATALYTIC OZONATION (FE-III/AL2O3) OF PHENOL AND ITS OZONATION BY-PRODUCTS [J].
ALHAYEK, N ;
LEGUBE, B ;
DORE, M .
ENVIRONMENTAL TECHNOLOGY LETTERS, 1989, 10 (04) :415-426
[3]   COMPARATIVE EFFICIENCY OF 3 SYSTEMS (O-3, O-3/H2O2 AND O-3/TIO2) FOR THE OXIDATION OF NATURAL ORGANIC-MATTER IN WATER [J].
ALLEMANE, H ;
DELOUANE, B ;
PAILLARD, H ;
LEGUBE, B .
OZONE-SCIENCE & ENGINEERING, 1993, 15 (05) :419-432
[4]   Advanced oxidation processes (AOP) for water purification and recovery [J].
Andreozzi, R ;
Caprio, V ;
Insola, A ;
Marotta, R .
CATALYSIS TODAY, 1999, 53 (01) :51-59
[5]   THE KINETICS OF MN(II)-CATALYZED OZONATION OF OXALIC-ACID IN AQUEOUS-SOLUTION [J].
ANDREOZZI, R ;
INSOLA, A ;
CAPRIO, V ;
DAMORE, MG .
WATER RESEARCH, 1992, 26 (07) :917-921
[6]   The use of manganese dioxide as a heterogeneous catalyst for oxalic acid ozonation in aqueous solution [J].
Andreozzi, R ;
Insola, A ;
Caprio, V ;
Marotta, R ;
Tufano, V .
APPLIED CATALYSIS A-GENERAL, 1996, 138 (01) :75-81
[7]  
[Anonymous], 1972, WATER AICHE S SERIES
[8]   DETERMINATION OF OZONE IN WATER BY THE INDIGO METHOD [J].
BADER, H ;
HOIGNE, J .
WATER RESEARCH, 1981, 15 (04) :449-456
[9]  
BHAT NN, 1995, P 27 MID IND WAST C, P371
[10]  
Boehm H.P., 1966, CHEM IDENTIFICATION, V16,, P179, DOI [10.1016/S0360-0564(08)60354-5, DOI 10.1016/S0360-0564(08)60354-5]