标题: | 臭氧结合活性碳增进2-氯酚水溶液之处理效能 Enhancement of Aqueous 2-Chlorophenol Degradation by Ozone and GAC Processes |
作者: | 金艾棣 Ai-Ti Chin 陈重男 Dr. Jong-Nan Chen 环境工程系所 |
关键字: | 活性碳;2-氯酚;臭氧;石墨;异相反应;动力模;GAC;Ozone;Graphite;2-Chlorophenol;Heterogeneous reaction;Kinetics |
公开日期: | 2001 |
摘要: | 臭氧对2-氯酚有良好的分解作用,但其分解后的有毒中间产物及低矿化效果一直是臭氧实际应用的瓶颈。应用活性碳作为异相触媒,其强大的吸附能力可增加被吸附的臭氧与其反应的机会,同时能去除臭氧化后有毒的中间产物。本研究以一套臭氧与颗粒状活性碳结合之程序(O3/GAC)来处理实验室所合成的目标污染物2-氯酚水溶液,藉由系统中异相活性碳的同时作用,探讨臭氧、污染物及活性碳的三相反应,并评估污染物氧化及矿化的效能,依此建立臭氧与活性碳结合的反应动力式,最后以连续流式的操作来检验系统的长时效性与模式可信度。再者,以不同前处理之活性碳及成分相近的石墨比较其处理效能之差异。 实验结果显示,在臭氧系统中加入活性碳触媒,发现活性碳会与臭氧反应造成其表面官能基及元素的改变,同时加速臭氧分解的速率,此反应系统可以增进去除污染物及矿化的效果。其次在活性碳加入剂量为1 g/L时,无论pH值为何,TOC去除率皆大幅增加,尤以低pH值时去除率由8.9%增加到47.6%,增进效率有四倍余。在臭氧消耗率方面,一样是在低pH值的环境下臭氧节省率最佳,每去除一单位的TOC可节省2.75倍的臭氧剂量。在有机物的去除率及生物毒性降低方面,效果皆随着活性碳剂量的增加而增加,但在剂量超过2 g/L时,臭氧与污染物竞争吸附越显着,反而使臭氧大量消耗。 在连续流的实验中得知,臭氧结合活性碳比单独使用活性碳(1 g/L)时,活性碳使用时效增长50%以上,臭氧有对活性碳现场再生的功能。最后由半批次实验所建立的动力方程式应用于连续流的模拟,发现模拟值与实验值的误差小于3%,显示模拟效果佳。 Ozone exhibits a high competence on 2-Chlorophenol degradation , but the toxic intermediates after decompotion and low efficiency of mineralization are the bottleneck of practical ozone application. Applying granular activated carbon (GAC) that has powerful adsorbability to be a heterogeneous catalyst can increase the probability of the reaction between absorbed ozone and itself , and meantime this process can remove the toxic intermediates . This study use the Ozone/GAC combination (O3/GAC)to treat our pollutant 2-Chlorophenol aqueous solution . With the heterogeneous GAC reacting simultaneously , we discuss the tri-phases reaction of ozone , pollutant and GAC . Furthermore , the efficiency of pollutants’ oxidization and mineralization will be estimated . Thus , we can establish the Kinetics . Finally , the efficacy and reliability of model can be checked by continuous flow operation . Moreover , the difference of efficiency from other pretreatment GAC and graphite similar to GAC can be compared . The experiments employing GAC as a catalyst show that GAC has reactions with ozone that makes changes of surface functional group and elements , and meanwhile it speeds up the rate of ozone decomposition . The system can improve the effect of pollutant removal and mineralization . Moreover , no mater what the pH value is , the TOC removal rate raises considerably with GAC 1 g/L dosage . Particularly in the low pH value environment , the TOC removal rate increases from 8.9% to 47.6% , the efficiency increases more than four times , and ozone consumption also decreases more obviously at a low pH value . 2.75 times Ozone dosage can be saved while one unit of TOC is removed , the organic matter removal rate and the reduction of toxicity increase with GAC dosage , but the competition of adsorption among ozone and pollutants becomes critical , thus , making the ozone consumed enormously . In the continuous flow system , it shows the effective lifetime of GAC increased over 50% by combining Ozone/GAC than GAC only . Besides , ozone has the ability to regenerate GAC on the spot . The model value and the experimental value is compared by applying the models established from semi-batch in the continuous flow system , the inaccuracy between the model value and experimental value is less than 3% . It shows the accuracy of the model . |
URI: | http://140.113.39.130/cdrfb3/record/nctu/#NT900515018 http://hdl.handle.net/11536/69363 |
显示于类别: | Thesis |