首页 | 本学科首页   官方微博 | 高级检索  
     

重瓦斯油及其窄馏分加氢反应性能考察
引用本文:段爱军. 重瓦斯油及其窄馏分加氢反应性能考察[J]. 中国石油大学学报(自然科学版), 2003, 27(6)
作者姓名:段爱军
作者单位:石油大学重质油国家重点实验室,北京,102249
摘    要:对Athabasca油砂沥青重瓦斯油以及不同馏程范围的窄馏分的物化性质进行了考察。结果显示 ,随着馏分沸程的增加 ,硫、氮等杂原子含量以及碱性氮和非碱性氮含量的增加。各种不同馏程范围馏分以及窄馏分的加氢精制反应性能表明 ,馏分中的氮化物含量 ,尤其是非碱性氮化物的含量 ,与其脱氮反应性能有密切关系。随着馏分终馏点的增加或者随着窄馏分馏程的变重 ,加氢脱硫和加氢脱氮转化率以及碱性氮和非碱性氮转化率均有所降低 ,其中非碱性氮的转化率下降幅度较大。由窄馏分的加氢反应性能考察可知 ,各类化合物的易脱除顺序为 :含硫化合物 ,碱性氮化物 ,非碱性氮化物

关 键 词:重瓦斯油  加氢精制  窄馏分  加氢脱硫  加氢脱氮  转化率

Investigation of physiochemical properties of different boiling fractions
DUAN Ai-jun. State Key Laboratory of Heavy Oil Processing in the University of Petroleum,China,Beijing. Investigation of physiochemical properties of different boiling fractions[J]. Journal of China University of Petroleum (Edition of Natural Sciences), 2003, 27(6)
Authors:DUAN Ai-jun. State Key Laboratory of Heavy Oil Processing in the University of Petroleum  China  Beijing
Affiliation:DUAN Ai-jun. State Key Laboratory of Heavy Oil Processing in the University of Petroleum,China,Beijing 102249
Abstract:The physiochemical properties of different boiling fractions derived from Athabasca bitumen heavy gas oil were investigated and tested in high-pressure microhydrotreator over a commercial Ni-Mo/Al-2O-3 catalyst. The results showed that the amounts of sulfur, total nitrogen, basic nitrogen and non-basic nitrogen increased with the fraction boiling ranges. The reaction mechanisms of these distillates and narrow cuts were studied under different conditions. As the boiling range increased, the conversion rates of total sulfur, total nitrogen, basic and non-basic nitrogen decreased, which shows a relationship between the amount of non-basic nitrogen and the reactivity of reactant. The removal of sulfur compounds was comparatively easier than that of nitrogen compounds, and the removal of non-basic compounds was the most difficult.
Keywords:heavy gas oil  hydrofining  distillation  narrow fraction  hydrodesulphurization  hydrodenitrification  conversion rate
本文献已被 CNKI 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