化工学报 ›› 2009, Vol. 60 ›› Issue (5): 1254-1259.

• 能源和环境工程 • 上一篇    下一篇

金属化合物催化多环芳烃合成二噁英的机理

严密,李晓东,张晓翔,刘科,严建华,岑可法   

  1. 能源清洁利用国家重点实验室(浙江大学)
  • 出版日期:2009-05-05 发布日期:2009-05-05

Mechanism of PCDD/Fs formation from PAHs catalyzed by metal compounds

YAN Mi, LI Xiaodong, ZHANG Xiaoxiang, LIU Ke, YAN Jianhua, CEN Kefa   

  • Online:2009-05-05 Published:2009-05-05

摘要:

为研究飞灰中金属化合物催化多环芳烃合成二噁英的机理,进行了不同催化剂和苊的燃烧试验,同时进行了X射线衍射试验(XRD)和热重试验(TGA)。根据试验结果分析得到:多环芳烃主要以de novo反应合成二噁英, PCDFs占主要成分;在无氯气氛下,CuCl2绝大部分还原生成CuCl,金属氯化物主要通过金属配位体提供氯源;CuCl2和FeCl3对催化裂解氧化苊的作用相似;CuCl2在150~200℃就可以和苊催化反应生成二噁英或氯代有机物。

关键词:

二噁英, 苊, 金属化合物, 催化剂

Abstract:

In order to understand the effect of different metal compounds on polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) formation from polycyclic aromatic hydrocarbons (PAHs), a series of experiments were conducted with different metal compounds as catalysts and acenaphthylene (AcPy) on a fixed-bed reactor.X-ray diffraction and thermogravimetry were made to monitor the reaction.The experimental results revealed that PCDD/Fs from PAHs were mainly formed by de novo synthesis.Without the presence of Cl2, most of cupric chloride were reduced to cuprous chloride.Metal chloride offered chlorine through metal complex.CuCl2 and FeCl3 played a similar role in activating the formation of organic chlorinated compounds.AcPy could form dioxins or other chlorinated compounds catalyzed by CuCl2 at 150—200℃.

Key words:

二噁英, 苊, 金属化合物, 催化剂