Wang Hou Chuan, Chang Shu Hao, Hung Pao Chang, Hwang Jyh Feng, Chang Moo Been
Graduate Institute of Environmental Engineering, National Central University, Chungli, Taiwan.
J Hazard Mater. 2009 May 30;164(2-3):1452-9. doi: 10.1016/j.jhazmat.2008.09.093. Epub 2008 Oct 1.
Catalytic oxidations of PCDD/Fs (polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans) with ozone on the transition metal oxides (iron oxide or manganese oxide) at the temperature range of 120-180 degrees C were investigated. These two catalysts were prepared by precipitation methods. Iron oxide has a higher surface area (330 m(2)/g) than manganese oxide (53 m(2)/g). In the absence of ozone, the removal efficiencies of PCDD/Fs achieved with iron oxide or manganese oxide were between 83% and 85%, while the destruction efficiencies were only between 20% and 25% at 180 degrees C. It indicates that adsorption was the main removal mechanism of PCDD/Fs over these two catalysts. On the other hand, ozone addition greatly enhanced the catalytic activity of iron oxide or manganese oxide catalysts on the oxidation of gaseous PCDD/Fs. At 180 degrees C, the destruction efficiencies of gaseous PCDD/Fs achieved with iron oxide or manganese oxide with 100 ppm O(3) exceeded 90%. It indicates that catalytic ozonation achieved with iron oxide or manganese oxide is effective in decomposing PCDD/Fs and the application of ozone lowers the reaction temperature of PCDD/F oxidation below 200 degrees C. Furthermore, the synergistic effect of iron oxide and ozone is superior to that of manganese oxide due to the fact that the surface of iron oxide has more hydroxyl groups, which easily form hydrogen bonds with ozone and decompose to form atomic oxygen for the further reaction with dioxin molecules.
研究了在120-180摄氏度温度范围内,多氯代二苯并对二噁英和多氯代二苯并呋喃(PCDD/Fs)在过渡金属氧化物(氧化铁或氧化锰)上与臭氧的催化氧化反应。这两种催化剂通过沉淀法制备。氧化铁的比表面积(330平方米/克)高于氧化锰(53平方米/克)。在没有臭氧的情况下,氧化铁或氧化锰对PCDD/Fs的去除效率在83%至85%之间,而在180摄氏度时破坏效率仅在20%至25%之间。这表明吸附是PCDD/Fs在这两种催化剂上的主要去除机制。另一方面,添加臭氧极大地增强了氧化铁或氧化锰催化剂对气态PCDD/Fs的氧化催化活性。在180摄氏度时,添加100 ppm O₃的氧化铁或氧化锰对气态PCDD/Fs的破坏效率超过90%。这表明用氧化铁或氧化锰进行催化臭氧化对分解PCDD/Fs是有效的,并且臭氧的应用将PCDD/F氧化的反应温度降低到200摄氏度以下。此外,氧化铁和臭氧的协同效应优于氧化锰,因为氧化铁表面有更多的羟基,这些羟基容易与臭氧形成氢键并分解形成原子氧,用于与二噁英分子进一步反应。