Valdés H, Zaror C A
Facultad de Ingeniería, Universidad Católica de la Santísima Concepción, Caupolicán 491, Concepción, Chile.
J Hazard Mater. 2006 Sep 21;137(2):1042-8. doi: 10.1016/j.jhazmat.2006.03.025. Epub 2006 May 2.
The combined or sequential use of ozone and activated carbon to treat toxic effluents has increased in recent years. However, little is known about the influence of carbon surface active sites on ozonation of organic adsorbed pollutants. This paper presents experimental results on the effect of metal oxides and oxygenated surface groups on gaseous ozonation of spent activated carbons. Benzothiazole (BT) was selected as a target organic compound in this study due to its environmental concern. Activated carbons with different chemical surface composition were prepared from a Filtrasorb-400 activated carbon. Pre-treatment included: ozonation, demineralisation, and deoxygenation of activated carbon. Ozonation experiments of BT saturated-activated carbons were conducted in a fixed bed reactor loaded with 2 g of carbon samples. The reactor was fed with an O2/O3 gas mixture (2 dm3/min, 5 g O3/h), for a given exposure time, in the range 10-120 min, at 298 K and 1 atm. Results show that extended gaseous ozonation of activated carbon saturated with BT led to the effective destruction of the adsorbate by oxidation reactions. Oxidation of BT adsorbed on activated carbon seemed to occur via both direct reaction with ozone molecules, and by oxygen radical species generated by catalytic ozone decomposition on metallic surface sites.
近年来,臭氧与活性炭联合或顺序使用以处理有毒废水的情况有所增加。然而,关于碳表面活性位点对有机吸附污染物臭氧化的影响却知之甚少。本文介绍了金属氧化物和含氧表面基团对废活性炭气态臭氧化影响的实验结果。由于苯并噻唑(BT)对环境的影响,本研究选择其作为目标有机化合物。以Filtrasorb - 400活性炭为原料制备了具有不同化学表面组成的活性炭。预处理包括:活性炭的臭氧化、脱矿质和脱氧。在装有2 g碳样品的固定床反应器中进行了BT饱和活性炭的臭氧化实验。在298 K和1 atm条件下,以给定的暴露时间(10 - 120分钟)向反应器中通入O₂/O₃气体混合物(2 dm³/分钟,5 g O₃/小时)。结果表明,对BT饱和的活性炭进行长时间气态臭氧化可通过氧化反应有效破坏吸附质。吸附在活性炭上的BT的氧化似乎既通过与臭氧分子的直接反应,也通过金属表面位点上催化臭氧分解产生的氧自由基物种进行。