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| Content Provider | Springer Nature Link |
|---|---|
| Author | Echaroj, Snunkheam Santikunaporn, Malee Chavadej, Sumaeth |
| Copyright Year | 2014 |
| Abstract | The mechanisms of the dehydration reaction of 1-decanol to 1-decene over precipitated gamma-alumina (γ-Al$_{2}$O$_{3}$) by means of the micro-kinetic modeling approach were investigated. Experimental data were collected in the reaction temperature range of 533–608 K, while the retention time was varied from 0.029 to 0.15 h. The γ-Al$_{2}$O$_{3}$ catalyst was synthesized using a traditional precipitation method. The yield of both internal olefins and 1-decene increased with increasing reaction temperature. Conversely, the yield of di-n-decyl ether decreased with increasing temperature. An increase in retention time increased the yield of 1-decene and internal olefins. These experimental data correlated well with the rate equation that assumes the formation of 1-decene to be reversible and a dual-site reaction. It is reasonable to state that internal isomerization is reversible with a single-site reaction. The apparent activation energy for the dehydration reaction of 1-decanol to 1-decene, obtained from the Arrhenius plot data, was 102 ± 2 kJ/mol. |
| Starting Page | 75 |
| Ending Page | 91 |
| Page Count | 17 |
| File Format | |
| ISSN | 18785190 |
| Journal | Reaction Kinetics and Catalysis Letters |
| Volume Number | 114 |
| Issue Number | 1 |
| e-ISSN | 18785204 |
| Language | English |
| Publisher | Springer Netherlands |
| Publisher Date | 2014-10-01 |
| Publisher Place | Dordrecht |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Dehydration 1-Decanol 1-Decene Internal isomerization Precipitation Gamma-alumina Catalysis Physical Chemistry Industrial Chemistry/Chemical Engineering |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physical and Theoretical Chemistry Catalysis |
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