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铜铈复合氧化物上石化行业典型VOCs的氧化行为与动力学
摘要点击 1649  全文点击 936  投稿时间:2013-05-15  修订日期:2013-07-23
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中文关键词  挥发性有机化合物    甲苯  正己烷  氧化行为  反应条件  动力学
英文关键词  volatile organic compounds(VOCs)  benzene  toluene  n-hexane  oxidation behavior  reaction conditions  kinetics
作者单位E-mail
陈长伟 中国科学院城市环境研究所, 厦门 361021
武夷学院生态与资源工程学院, 武夷山 354300 
wyucwc@163.com 
于艳科 中国科学院城市环境研究所, 厦门 361021  
陈进生 中国科学院城市环境研究所, 厦门 361021  
何炽 中国科学院城市环境研究所, 厦门 361021 che@iue.ac.cn 
中文摘要
      采用共沉淀法和等体积浸渍法制备了CuCeOx复合催化剂,对材料的物化性质进行了XRD、低温N2吸脱附、H2-TPR和O2-TPD表征. 以石化行业典型VOCs(苯、甲苯和正己烷)为探针污染物,研究了污染物组成与浓度、反应空速、O2浓度、H2O浓度和催化剂种类对其氧化行为的影响,并对反应动力学参数进行了模型拟合. 共沉淀得到的催化剂具有均匀的活性相、好的低温可还原性能和较多的活性表面氧物种. 甲苯氧化率随着污染物浓度升高而降低, 高转化率下苯浓度与其氧化率无相关性,正己烷的氧化率与入口浓度呈正比. 苯能够显著抑制甲苯的氧化,而甲苯加入有利于苯的氧化. 正己烷对苯氧化的影响较小,但能够促进甲苯的转化,苯系物对正己烷氧化有明显的抑制作用. 低空速和高氧浓度都有利于污染物的氧化, 氧浓度的变化对正己烷和苯的氧化影响较小. 水汽对甲苯的氧化有明显的抑制作用,而对 苯和正己烷氧化有明显的促进作用. 共沉淀催化剂具有更好的甲苯和苯氧化性能,而无水条件下浸渍催化剂具有更好的正己烷氧化性能. 拟一级动力学模型能够很好地模拟不同条件下污染物的氧化行为.
英文摘要
      CuCeOx composite catalysts were synthesized via coprecipitation (COP-CuCeOx) and incipient impregnation (IMP-CuCeOx) methods, respectively. The physicochemical properties of the samples were characterized by XRD, low-temperature N2 sorption, H2-TPR and O2-TPD. The influences of reactant composition and concentration, reaction space velocity, O2 content, H2O concentration, and catalyst type on the oxidation behaviors of benzene, toluene, and n-hexane emitted from petrochemical industry were systematically investigated. In addition, the related kinetic parameters were model fitted. Compared with IMP-CuCeOx, COP-CuCeOx had well-dispersed active phase, better low-temperature reducibility, and more active surface oxygen species. The increase of reactant concentration was unfavorable for toluene oxidation, while the opposite phenomenon could be observed in n-hexane oxidation. The inlet concentration of benzene was irrelevant to its conversion under high oxidation rate. The introduction of benzene obviously inhibited the oxidation of toluene and n-hexane, while the presence of toluene had a positive effect on benzene conversion. The presence of n-hexane could promote the oxidation of toluene, while toluene had a negative influence on n-hexane oxidation. Both low space velocity and high oxygen concentration were beneficial for the oxidation process, and the variation of oxygen content had negligible effect on n-hexane and benzene oxidation. The presence of H2O noticeably inhibited the oxidation of toluene, while significantly accelerated the oxidation procedure of benzene and n-hexane. COP-CuCeOx had superior catalytic performance for toluene and benzene oxidation, while IMP-CuCeOx showed higher n-hexane oxidation activity under dry condition. The oxidation behaviors under different conditions could be well fitted and predicted by the pseudo first-order kinetic model.

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