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| Content Provider | Springer Nature Link |
|---|---|
| Author | Kweon, Hyukmin Nguyen Huy, Chinh Kim, Hanna Lee, Youngil Shin, Eun Woo |
| Copyright Year | 2014 |
| Abstract | In this study, we performed the hydrocracking of vacuum residue (VR) in an autoclave reactor using a Ni–Mo/Al$_{2}$O$_{3}$ catalyst at 450 and 500 °C under 150 bar of pressure and characterized coke structure generated over the catalyst during the reaction in order to understand the coking behavior in the hydrocracking of vacuum residue. The insoluble coke generated during VR hydrocracking was characterized by N$_{2}$ sorption, TGA, XRD, FE-SEM (EDX), EPMA, FT-IR, Raman, and $^{13}$C CP/MAS–NMR techniques. In the absence of catalyst, dominant thermal hydrocracking at 500 °C produced pregraphite coke containing sulfur compounds since sulfur components in the feed could not be removed by thermal hydrocracking. With catalyst, the coke structures generated during a reaction depended on the reaction temperature. The NMR, Raman, XRD, TPO, and FT-IR spectra showed that amorphous coke containing highly branched oligomers and polycyclic aromatics were generated during hydrocracking at 450 °C, whereas hydrocracking at 500 °C mainly produced pregraphite coke. The presence of the catalyst in hydrocracking of VR played an important role in increasing decomposition of VR and decreasing coke deposition. |
| Starting Page | 133 |
| Ending Page | 147 |
| Page Count | 15 |
| File Format | |
| ISSN | 18785190 |
| Journal | Reaction Kinetics and Catalysis Letters |
| Volume Number | 113 |
| Issue Number | 1 |
| e-ISSN | 18785204 |
| Language | English |
| Publisher | Springer Netherlands |
| Publisher Date | 2014-06-10 |
| Publisher Place | Dordrecht |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Hydrocracking Vacuum residue Ni–Mo/Al$_{2}$O$_{3}$ Catalyst Coke structure Deactivation Catalysis Physical Chemistry Industrial Chemistry/Chemical Engineering |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physical and Theoretical Chemistry Catalysis |
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