Ozonation of activated carbons:: Effect on the adsorption of selected phenolic compounds from aqueous solutions

被引:151
作者
Alvarez, PM [1 ]
García-Araya, JF
Beltrán, FJ
Masa, FJ
Medina, F
机构
[1] Univ Extremadura, Dept Ingn Quim & Energet, Badajoz 06071, Spain
[2] Univ Rovira & Virgili, ETSEQ, Dept Engn Quim, Tarragona 430070, Spain
关键词
activated carbon; phenol; p-chlorophenol; p-nitrophenol; ozone; adsorption; surface chemistry;
D O I
10.1016/j.jcis.2004.09.014
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
The impact of ozonation on textural and chemical surface characteristics of two granular activated carbons (GAC), namely F400 and AQ40, and their ability to adsorb phenol (P), p-nitrophenol (PNP), and p-chlorophenol (PCP) from aqueous solutions have been studied. The porous structure of the ozone-treated carbons remained practically unchanged with regard to the virgin GAC. However, important modifications of the chemical surface and hydrophobicity were observed from FTIR spectroscopy, pH titrations, and determination of pH(PZC). As a rule, the ozone treatment at either room temperature (i.e., about 25 degreesC) or 100 degreesC gave rise to acidic surface oxygen groups (SOG). At 25 degreesC primarily carboxylic acids were formed while a more homogeneous distribution of carboxylic, lactonic, hydroxyl, and carbonyl groups was obtained at 100 degreesC. The experimental isotherms for phenolic compounds on both GAC were analyzed using the Langmuir model. Dispersive pi electrons of the ring of the aromatics and those of the carbon basal planes were thought to be the primary forces interactions between, responsible for the physical adsorption whereas oxidative coupling of phenolic compounds catalyzed by basic SOG was a major cause of irreversible adsorption. The exposure of both GAC to ozone at room temperature decreased their ability to adsorb P, PNP, and PCP. However, when ozone was applied at 100 degreesC adsorption was not prevented but in some cases (P and PNP on F400) the adsorption process was even enhanced. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:503 / 512
页数:10
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