首页 | 本学科首页   官方微博 | 高级检索  
     

页岩油泥催化热解研究
引用本文:孙佰仲,马奔腾. 页岩油泥催化热解研究[J]. 东北电力学院学报, 2013, 0(5): 6-9
作者姓名:孙佰仲  马奔腾
作者单位:[1]中国大唐集团公司科学技术研究院,北京100032 [2]东北电力大学能源与动力工程学院,吉林吉林132012
摘    要:在管式反应器上,考察了页岩油泥在不同催化剂( Al2 O3、K2 CO3、Fe2 O3)及比例(质量比为13、15、110)下的热解行为,着重研究了催化剂对产油率和热解油馏程的影响。结果表明:油泥催化热解效果良好,碳酸钾在15时,产油率达到44.08%,氧化铝在13时,产油率达到45.42%,与无催化剂相比,分别提高了28.97%和32.89%。对馏程的促进方面,氧化铁表现突出,在15和110时,均使得重、柴油含量下降,汽油含量上涨。催化热解是按碳正离子机理进行的,重质油发生裂化反应,烷烃出现聚合反应,均提高轻质油的产量。

关 键 词:页岩油泥  催化剂  产油率  馏程

Study on Catalytic Pyrolysis of Oil Shale Sludge
SUN Bai-zhong,MA Ben-teng. Study on Catalytic Pyrolysis of Oil Shale Sludge[J]. Journal of Northeast China Institute of Electric Power Engineering, 2013, 0(5): 6-9
Authors:SUN Bai-zhong  MA Ben-teng
Affiliation:1. China Datang Corporation Science and Technology Research Institute , China Datang Corporation , Beijing 100032 ;2. En- ergy and Power Engineering College, Northeast Dianli University, Jilin Jilin 132012)
Abstract:Aimed at studying on the relationship between catalysts and oil yield and boiling ranges,pyrolysis of oil shale sludge was carried out in a tubular electric furnace with different catalysts ( Al2 O3、K2 CO3 and Fe2 O3 ) and mixing ratios ( 1 3、1 5、1 10 ) . The results showed that the effect of catalytic pyrolysis of oil shale sludge was good,the addition of K2 CO3 at 1:5 leaded to the increase of the total oil yield up to 44. 08%, when the mass fraction of Al2 O3 in oil sludge was 33%,the yield of shale oil increased to 45. 42%. Compared with Catalyst-free,the oil yield respectively increased by 28. 97% and 32. 89%. In the aspect of catalysts im-proving the quality of shale oil,Fe2 O3 appeared stronger catalytic role than other metal oxides. When the mass fraction of Fe2 O3 in oil shale sludge was 10~20%,the yield of gasoline increased sharply. Catalytic pyrolysis is abide by carbocations mechanism. Both the cracking of heavy oil and polymerization of paraffin could im-prove the yield of gasolene.
Keywords:Oil shale sludge  Catalyst  Oil yield  Boiling ranges
本文献已被 维普 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