首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Catalytic hydrodechlorination of chlorinated ethylenes in organic solvents at room temperature and atmospheric pressure
【24h】

Catalytic hydrodechlorination of chlorinated ethylenes in organic solvents at room temperature and atmospheric pressure

机译:室温和大气压下有机溶剂中氯化乙烯的催化加氢脱氯

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

The objectives of this study are to hydrodechlorinate chlorinated ethylenes (ETHs) using noble metal catalysts in organic solvents at 20+-0.5 deg C and atmospheric pressure and to evaluate the competitive degradation of chlorinated ethylenes.Tetrachloroethylene (PCE) was catalytically hydrodechlorinated with 10% Pd/C at 20+-0.5 deg C and atmospheric pressure without accumulation of tetrachloroethane (TTCE) and other chlorinated intermediates.Methanol was the best solvent for the degradation of PCE.NaOH addition clearly increased in degradation rate of PCE.The first order degradation rate constants for PCE,trichloroethylene (TCE),and cis-1,2-dichloroethylene (DCE) were 0.18,0.64,and 2.1 min~(-1),respectively.These values were extremely larger than previous data and organic compounds with less chloride showed larger degradation rate.The degradation rate of PCE significantly decreased by the co-existence of TCE or cis-1,2-DCE.On the other hand,the co-existence of PCE gave little influence on the degradation of TCE and cis-1,2-DCE.These were due to competitive adsorption of chlorinated compounds on active sites on catalyst.The adsorption capacity of Pd/C catalyst for PCE significantly decreased by the co-existence of TCE or cis-1,2-DCE,whereas those of TCE and cis-l,2-DCE were independent from the co-existence of PCE.
机译:这项研究的目的是在有机溶剂中在20 + -0.5摄氏度和大气压下使用贵金属催化剂对氯化乙烯(ETH)进行加氢脱氯,并评估氯化乙烯的竞争性降解。四氯乙烯(PCE)用10%催化加氢脱氯。 Pd / C在20 + -0.5摄氏度和大气压下没有四氯乙烷(TTCE)和其他氯化中间体的积累,甲醇是PCE降解的最佳溶剂.NaOH的添加明显增加了PCE的降解率。 PCE,三氯乙烯(TCE)和顺式1,2-二氯乙烯(DCE)的速率常数分别为0.18、0.64和2.1 min〜(-1)。氯化物表现出更大的降解率.PCE的降解率由于TCE或cis-1,2-DCE的共存而显着降低。另一方面,PCE的共存影响不大TCE和cis-1,2-DCE的降解主要是由于氯化物在催化剂活性位点上的竞争性吸附所致.TCE或cis共存,Pd / C催化剂对PCE的吸附能力大大降低。 -1,2-DCE,而TCE和cis-1,2-DCE则独立于PCE的共存。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号