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

板状镍催化剂上氨分解和氨部分氧化制氮氢气的研究
引用本文:邱发礼,吕绍洁.板状镍催化剂上氨分解和氨部分氧化制氮氢气的研究[J].应用化学,1988,0(5):39-43.
作者姓名:邱发礼  吕绍洁
作者单位:中国科学院成都有机化学研究所
摘    要:研制了一种 Ni/Al2O3多孔板状催化剂.该催化剂在反应温度高于750℃,氨分解率高于99.5%时,允许反应空速达10000—40000h-1.用该催化板组装的反应器可采用内加热形式,和一般的外加热反应器相比可节约能耗约30%.在催化板上氨分解的经验动力学方程是γ=kp2NH3,表观活化能为153.0kJ/mol.将该催化剂用于氨部分氧化时,在空气和氨比为1.0—1.7,680—750℃,氨空速10000—40000h-1条件下,在氨点火后无外加能源情况下,能制得含氢30~43%,残氧小于0.1%的氮氢混合气,氨的转化率>99.5%,连续250小时反应表明,催化剂活性稳定.宏观动力学研究得出,反应对氨呈零级,表观活化能为37.2kJ/mol.

关 键 词:氨分解  氨部分氧化  镍催化剂  动力学  
收稿时间:1987-04-03
修稿时间:1987-07-27

STUDY ON THE DECOMPOSITION AND PARTIAL OXIDATION OF AMMONIA ON POROUS Ni/Al_2O_3 CATALYST PLATE
Qiu Fali,L? Shoujie.STUDY ON THE DECOMPOSITION AND PARTIAL OXIDATION OF AMMONIA ON POROUS Ni/Al_2O_3 CATALYST PLATE[J].Chinese Journal of Applied Chemistry,1988,0(5):39-43.
Authors:Qiu Fali  L? Shoujie
Institution:Chengdu Institute of Organic Chemistry, Academia Sinica
Abstract:A porous Ni/Al2O3 catalyst plate was prepared.It gives NH3 conversion more than 99.5% at 750℃ and space velocity of NH3 10000-40000h-1.An internal heating type was adopted Which saves 30% energy in comparison with the external heating type.The results of reaction kinetics showed that the rate equation of ammonia decomposition on the catalyst plate is γ=kP2NH3 and the apparent activation energy is 153.0kJ/mol. The partial oxidation of ammonia on the catalyst plate was also investigated at the conditions of 680—750℃,air/NH3=1.7-1.0 and space velocity 10000-40000h-1.The results showed that a gas mixture containing 30-43% of H2 and less 0.1% of O2 was obtained without external heating after NH3 combustion.A duration test for 250h indicated that NH3 conversion was over 99.5%.The reaction kinetics showed that the rate equation of partial oxidation of ammonia was of zero order and the apparent activation energy obtained was 37.2kJ/mol.
Keywords:NH_3-Decomposition  of ammonia  NH_3-Partial  Oxidation of ammonia Ni catalyst  Kinetics  
本文献已被 CNKI 等数据库收录!
点击此处可从《应用化学》浏览原始摘要信息
点击此处可从《应用化学》下载免费的PDF全文
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