首页 | 本学科首页   官方微博 | 高级检索  
     检索      

由N-羟乙基乙二胺合成哌嗪
引用本文:吴刚健,严之光.由N-羟乙基乙二胺合成哌嗪[J].华东理工大学学报(自然科学版),2001,27(1):30-33,37.
作者姓名:吴刚健  严之光
作者单位:华东理工大学化学工程系,
摘    要:研究了以N-羟乙基乙二胺(HDEA)为原料,经催化脱水环化全盛哌嗪(PIP)的过程;考察了不同的催化剂,催化剂用量,反应时间、温度、压力,溶剂配比等对转化率和哌唪选择性的影响。结果表明,较好的催化剂为Raney Ni(C),在180℃,3MPa,溶剂与原粒配比6:1(mol:mol),催化剂用量ω=0.10,反应时间3h时,得到的转化率为89.2%,选择性85.0%,收率75.8%。小试数据能在放大试验中重复,精馏分离得到的产品哌嗪纯度>98.0%。

关 键 词:N-羟乙基乙二胺  哌嗪  催化脱水  合成  溶剂配比  催化剂  转化率  选择性
文章编号:1006-3080(2001)01-0030-04

Synthesis of Piperazine from N-Hydroxyethylethylenediamine
WU Gang-jian,YAN Zhi-guang.Synthesis of Piperazine from N-Hydroxyethylethylenediamine[J].Journal of East China University of Science and Technology,2001,27(1):30-33,37.
Authors:WU Gang-jian  YAN Zhi-guang
Abstract:A catalytic dehydrolysis process for synthesis of piperazine (PIP) from N-hydroxyethylethylenediamine (HDEA) has been studied. Various kinds of catalysts, such as acid catalysts, metal oxide supported on γ-Al2O3 and Raney Ni have shown certain activities on this reaction. In this case, the suitable catalyst is Raney Ni, especially the Raney Ni (C) which is prepared by adding some copper. The effect of content of metal copper on the reaction results has also been observed, it shows that the optinum wCu is 0.07~0.10. The optimal reaction conditions for Raney Ni (C) are 180°C, 3MPa, H2O∶HDEA=6∶1(mol∶mol), catalyst amount wcat=0.10 and reaction time 3h. Under these conditions the conversion and selectivity are 89.2% and 75.8% respectively. The results of scale-up experiment are comparable to these of the laboratory test. The SEM micrographs of fresh and used catalyst showed that the used catalyst has been covered by some substance, and the skeleton structure can not be distinguished clearly. So the conversion and selectivity of the product decrease with the used times. After fractional distillation, the purity of the product PIP is higher than 95%.
Keywords:N    hydroxyethylethylenediamine  piperazine  heteropolyacid  Raney Ni  dehydrolys
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号