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首页> 外文期刊>Applied clay science >Memory effect-enhanced catalytic ozonation of aqueous phenol and oxalic acid over supported Cu catalysts derived from hydrotalcite
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Memory effect-enhanced catalytic ozonation of aqueous phenol and oxalic acid over supported Cu catalysts derived from hydrotalcite

机译:水滑石衍生的负载型Cu催化剂上苯酚和草酸水溶液的记忆效应增强催化臭氧化反应

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摘要

Mg/Al supported metal (Fe, Co, Ni and Cu) oxide catalysts were prepared by co-precipitation of hydrotalcite-like clay materials as precursors, calcined, and used for the ozonation reaction of phenol and oxalic acid. The reaction was carried out using the catalyst and aqueous solution of phenol or oxalic acid in an O_3/O_2 mixed gas-flow at 20℃. In the ozonation of phenol, the combination of ozone and supported metal oxide catalysts was effective for the removal of total organic carbon (TOC). Also in the ozonation of oxalic acid as the main TOC component, Cu/Mg/Al catalysts showed the highest activity, followed by Ni/Mg/Al catalyst, while both Fe/Mg/Al and Co/Mg/Al catalysts were not active. Leaching of Cu and Ni, probably due to the chelation of metals by oxalic acid, was significantly observed at the beginning of the reaction. However the metal leaching disappeared at the end of the reaction possibly due to the entire consumption of oxalic acid during the reaction. The best result of oxalic acid mineralization was observed over Cu/Mg/Al catalyst calcined at 600℃, on which least leaching of the metal was detected. Moreover, a "memory effect" of hydrotalcite accelerated the mineralization of oxalic acid over the Cu/Mg/Al catalyst; oxalate anions were captured and decomposed in the reconstituted hydrotalcite interlayer space on the surface of the Cu/Mg/Al catalyst, resulting in a remarkable enhancement in the catalytic activity of the ozonation.
机译:Mg / Al负载的金属(Fe,Co,Ni和Cu)氧化物催化剂是通过将类似水滑石的粘土材料作为前体共沉淀而制备的,经煅烧后可用于苯酚和草酸的臭氧化反应。使用催化剂和苯酚或草酸的水溶液在20℃的O_3 / O_2混合气流中进行反应。在苯酚的臭氧化中,臭氧和负载型金属氧化物催化剂的组合可有效去除总有机碳(TOC)。同样在草酸作为主要TOC组分的臭氧化反应中,Cu / Mg / Al催化剂表现出最高的活性,其次是Ni / Mg / Al催化剂,而Fe / Mg / Al和Co / Mg / Al催化剂均不活跃。在反应开始时,明显观察到了铜和镍的浸出,这可能是由于草酸与金属的螯合所致。然而,金属浸出在反应结束时消失了,这可能是由于反应期间草酸的全部消耗。草酸矿化的最佳结果是在600℃煅烧的Cu / Mg / Al催化剂上观察到的,其中金属的浸出最少。此外,水滑石的“记忆效应”促进了草酸在Cu / Mg / Al催化剂上的矿化。草酸盐阴离子被捕获并在Cu / Mg / Al催化剂表面的水滑石中间层空间中分解,从而显着提高了臭氧化反应的催化活性。

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