教授 博士生导师 硕士生导师
性别: 男
毕业院校: 大连理工大学
学位: 博士
所在单位: 化工学院
学科: 工业催化. 物理化学
办公地点: 大连理工大学 西部校区 化工实验楼B521
联系方式: 0411-84986120
电子邮箱: hongchenguo@dlut.edu.cn
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论文类型: 期刊论文
发表时间: 2003-07-01
发表刊物: Xiandai Huagong/Modern Chemical Industry
收录刊物: Scopus、EI、PKU、ISTIC
卷号: 23
期号: SUPPL.
页面范围: 193-197
ISSN号: 02534320
关键字: Catalysis; Organic chemicals; Synthesis (chemical); Zeolites, High silicious zeolite; Monoethanolamine; Selective synthesis; Triethylenediamine, Industrial chemicals
摘要: The performance of TEDAMAX-01, a kind of catalyst with the topological structure of high silicious zeolite MFI, in catalyzing the reaction of monoethanolamine (MEOA) to triethylenediamine (TEDA) has been evaluated by a small fixed-bed reactor under the ambient pressure and carrier gas free conditions. In order to avoid forming morpholinium compounds as well as pipe-blocking by TEDA, MEOA was co-fed by 18% (wt) of ammonia and 50% (wt) of water. Results show that the activity and the selectivity of TEDAMAX-01 increase notably at reaction temperature in the range of 330-380 C, meanwhile keep stable with weight-hourly-space-velocity (WHSV) of reactant mixture in the range of 1-4 h-1. Under conditions of 370 C and WHSV = 2 h-1, TED AM AX-01 can give approximately 99% conversion under MEOA and more than 97% selectivity to TEDA. During a period of 266 h of continuous operation under these conditions, the conversion of MEOA does not decrease, the selectivity of TEDA decreases slowly before 100 hrs but keeps around 90% thereafter. The recycling of separative mother liquor as the source of feeding ammonia and feeding water, and repetitious regeneration of coked catalyst by the high-temperature calcination for four times seem to have no obvious influence on the activity, selectivity and durability of TEDAMAX-01 catalyst. It is therefore reasonable to expect a promising foreground of commercialization for TEDAMAX-01 catalyst.