Valdés Héctor, Zaror Claudio A
Facultad de Ingeniería, Universidad Católica de la Santísima Concepción, Caupolicán 491, Concepción, Chile.
Chemosphere. 2006 Nov;65(7):1131-6. doi: 10.1016/j.chemosphere.2006.04.027. Epub 2006 Jun 13.
Ozone oxidation combined with activated carbon adsorption (O(3)/AC) has recently started to be developed as a single process for water and wastewater treatment. While a number of aspects of aqueous ozone decomposition are well understood, the importance and relationship between aqueous ozone decomposition and organic contaminant degradation in the presence of activated carbon is still not clear. This study focuses on determining the contribution of homogeneous and heterogeneous reactions to organic contaminants removal in O(3)/AC system. Benzothiazole (BT) was selected as a target organic pollutant due to its environmental concern. A reactor system based on a differential circular flow reactor composed by a 19 cm(3) activated carbon fixed bed column and 1 dm(3) storage tank was used. Ozone was produced from pure and dry oxygen using an Ozocav ozone generator rated at 5 g O(3)h(-1). Experimental results show that BT removal rate was proportional to activated carbon dosage. Activated carbon surface contribution to BT oxidation reactions with ozone, increased with pH in absence of radical scavengers. The radical reaction contribution within the pH range 2-11 accounted for 67-83% for BT removal in O(3)/AC simultaneous treatment. Results suggest that at pH higher than the pH of the point of zero charge of the activated carbon dissociated acid groups such as carboxylic acid anhydrides and carboxylic acids present on activated carbon surface could be responsible for the observed increase in the ozone decomposition reaction rate. A simplified mechanism and a kinetic scheme representing the contribution of homogeneous and heterogeneous reactions on BT ozonation in the presence of activated carbon is proposed.
臭氧氧化与活性炭吸附相结合(O(3)/AC)最近开始作为一种单一工艺用于水和废水处理。虽然水相中臭氧分解的许多方面已得到充分理解,但在活性炭存在下,水相中臭氧分解与有机污染物降解之间的重要性和关系仍不明确。本研究重点在于确定均相和非均相反应对O(3)/AC体系中有机污染物去除的贡献。由于苯并噻唑(BT)对环境的影响,将其选为目标有机污染物。使用了一种基于差分式循环反应器的系统,该反应器由一个19 cm(3)的活性炭固定床柱和1 dm(3)的储存罐组成。使用额定产率为5 g O(3)h(-1)的Ozocav臭氧发生器由纯干燥氧气产生臭氧。实验结果表明,BT去除率与活性炭用量成正比。在没有自由基清除剂时,活性炭表面对BT与臭氧氧化反应的贡献随pH升高而增加。在pH值为2 - 11的范围内,自由基反应对O(3)/AC同时处理中BT去除的贡献占67 - 83%。结果表明,在高于活性炭解离酸基团零电荷点的pH值下,活性炭表面存在的羧酸酐和羧酸等解离酸基团可能是观察到的臭氧分解反应速率增加的原因。提出了一个简化的机理和动力学方案,以表示在活性炭存在下均相和非均相反应对BT臭氧化的贡献。