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零价铁与乙二胺四乙酸在低温常压下对苯酚及芳香族化合物的去除作用

Elimination of phenol and aromatic compounds by zero valent iron and EDTA at low temperature and atmospheric pressure.

作者信息

Sanchez Irama, Stüber Frank, Font Josep, Fortuny Agustí, Fabregat Azael, Bengoa Christophe

机构信息

Departament d'Enginyeria Química, Escola Tècnica Superior d'Enginyeria Química, Universitat Rovira i Virgili, Av. Països Catalans 26, 43007 Tarragona, Catalonia, Spain.

出版信息

Chemosphere. 2007 Jun;68(2):338-44. doi: 10.1016/j.chemosphere.2006.12.059. Epub 2007 Feb 14.

Abstract

This work deals with a new abiotic oxidation process designed as a suitable pre-treatment step within a biological depuration of wastewater containing phenol or its derivatives (o-cresol, 2-chlorophenol and p-nitrophenol) or aniline. The reaction was carried out in a stirred tank reactor at 20 degrees C and atmospheric pressure in presence of the organic compound, 150mgl(-1), zero valent iron particles (10g), ethylenediamine tetraacetic acid (EDTA, 101mgl(-1)) and air. The experimental results show that 85% of phenol conversion can be achieved after 360min. 2-Chlorophenol was found to be more easily degradable and it is completely eliminated after 300min. The oxidation of o-cresol and aniline behaved more closely to phenol obtaining after 360min 70% and 68% of conversion respectively. p-Nitrophenol was a very refractory compound, giving only 28% of conversion after 360min. Moreover, the influence of some operating variables was studied over the following ranges: temperature from 20 to 50 degrees C, initial phenol concentration from 150 to 1000mgl(-1), EDTA concentration from 50 to 200mgl(-1) and iron particles from 5 to 20g. As expected, temperature strongly enhances phenol conversion. Also, an increase of the catalyst to phenol ratio or the iron or EDTA to phenol ratio improves the reaction rate. A preliminary kinetic analysis of the data shown that the rate of phenol disappearance is not first order with respect to the phenol.

摘要

本研究涉及一种新的非生物氧化过程,该过程被设计为一种合适的预处理步骤,用于对含有苯酚或其衍生物(邻甲酚、2-氯苯酚和对硝基苯酚)或苯胺的废水进行生物净化。反应在搅拌釜式反应器中于20℃和大气压下进行,反应体系中存在150mg/L的有机化合物、10g零价铁颗粒、乙二胺四乙酸(EDTA,101mg/L)和空气。实验结果表明,360分钟后苯酚转化率可达85%。发现2-氯苯酚更易降解,300分钟后可完全去除。邻甲酚和苯胺的氧化行为与苯酚更为相似,360分钟后转化率分别为70%和68%。对硝基苯酚是一种非常难降解的化合物,360分钟后转化率仅为28%。此外,还研究了一些操作变量在以下范围内的影响:温度从20℃到50℃,初始苯酚浓度从150mg/L到1000mg/L,EDTA浓度从50mg/L到200mg/L,铁颗粒从5g到20g。正如预期的那样,温度显著提高了苯酚转化率。此外,催化剂与苯酚的比例或铁或EDTA与苯酚的比例增加也提高了反应速率。对数据的初步动力学分析表明,苯酚消失速率对苯酚而言不是一级反应。

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