Study of Catalytic Cracking of Asphaltene in Near-Critical Water

Article Preview

Abstract:

The method of solvent division is adopted to separate asphaltene from Shengli heavy oil by n-heptane. 1HNMR and 13CNMR spectrum of asphaltene were determined with a Bruker Avance 400 NMR spectrometer. Combining with the elemental analysis results, the aromatic-ring structure is main structural composition in the asphaltene. Asphaltene was catalyzed and cracked with naphthenate nickel as catalytic cracking catalyst in near-critical water. The suitable reactional condition was obtained by orthogonal experiment method, reaction temperature 300°C, the mass fraction of catalyst used 0.6%, reaction time 24h. By testing element content of cracked asphaltene, carbon element content had reduced 0.06%~0.80%; hydrogen element content had reduced by 0.74%~3.41%; oxygen element content had reduced by 3.12%~27.1%; nitrogen element content had reduced by 0.40%~13.47%; sulfur element content had reduced by 9.85%~31.26%.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 860-863)

Pages:

1021-1025

Citation:

Online since:

December 2013

Authors:

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2014 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] QIN Kuang-zong, GUO Shao-hui. Petroleum asphaltenes[M]. Beijing: Petroleum Industry Press, 2002: 140-141.

Google Scholar

[2] FAN Hong-fu, LIU Yong-jian, ZHAO Xiao-fei, ZHONG Li-guo. Studys on effect of metal ions on aquathermolysis reaction of liaohe heavy oils under steam treatment[J]. Journal of Fuel Chemistry and Technology, 2001, 29(5): 430-432.

Google Scholar

[3] CHEN Er-yue, LIU Yong-jian, Ge Hong-jiang, WEN Shou-bin. Study on the degradation of the asphaltene in Liaohe heavy oil during catalytic aquathermolysis reaction[J]. Journal of Daqing Petroleum Institute, 2005, 29(5): 9-11.

Google Scholar

[4] JIA Wang-lu. Molecular structure and its applieation study of 0il as phaltenes from Lunnan area, Tarim basin[D] Guangzhou Institute of Geochemitry, Chinese Academy of Sciences, (2004).

Google Scholar

[5] SISKIN M, KATRITZKY A R. Reactivity oforganic compounds in hot water: geochemical and technological implications[J]. Science, 1991, 254(11): 231-237.

DOI: 10.1126/science.254.5029.231

Google Scholar

[6] DONG Xi-gui, LEI Qun-fang, YU Qing-sen. NMR determination of petroleum asphaltenes and their model molecules evaluation[J]. Journal of Fuel Chemistry and Technology, 2004, 36(6): 668-670.

Google Scholar

[7] TAKEGAMI Y, WATANABE Y, SUZUKI T, et al. Structural investigation on column chromatographed vacuum residues of various prtroleum crudes by 13C nuclear magnetic resonance spectroscopy[J]. Fuel, 1980, 59(4): 253-259.

DOI: 10.1016/0016-2361(80)90144-1

Google Scholar

[8] CLARK P D, HYNE J B. Studies on the Chemical Reactions of Heavy Oils under Steam Stimulation Condition[J]. AOSTRA J Reactor, 1990, 6(1): 29-395.

Google Scholar