Enhanced one-pot selective conversion of cellulose to ethylene glycol over NaZSM-5 supported metal catalysts
| Title | Enhanced one-pot selective conversion of cellulose to ethylene glycol over NaZSM-5 supported metal catalysts |
| Publication Type | Journal Article |
| Year of Publication | 2021 |
| Authors | Sreekantan, S, Kirali, AArunima, Marimuthu, B |
| Journal | New Journal of Chemistry |
| Volume | 45 |
| Issue | 41 |
| Pagination | 19244-19254 |
| Date Published | OCT |
| Type of Article | Article |
| ISSN | 1144-0546 |
| Abstract | The mesopores interconnected with microporous NaZSM-5 was synthesised by sol-gel method. Reactions involving cellulose using different bimetallic and trimetallic combinations of nickel, aluminium, and tungsten metals supported on NaZSM-5 have been carried out. Different weight percentages (wt%) of Al, Ni, and W were loaded onto the NaZSM-5 support via a wet impregnation method. The prepared catalysts were characterized using PXRD, FE-SEM, HR-TEM, BET, and XPS studies to investigate the presence of mesopores, the textural properties, the metal loading, and the active oxidation states. The catalytic activities of the xAl-yNi-zW/NaZSM-5 (where x, y, and z are the wt% values of Al, Ni, and W, respectively) supported catalysts were studied during the one-pot conversion of cellulose into ethylene glycol at 220 degrees C and with a pressure of 70 bar H-2 (at the reaction temperature) in water (as a solvent). The 5%Al-8%Ni-25%W/NaZSM-5 catalyst exhibited the highest cellulose conversion of 100%, with an ethylene glycol yield as high as 89% (C mol%) under moderate reaction conditions being reported for the first time. Al3+ in the catalyst hydrolyzed cellulose, and W5+ species acted as acid centres that facilitated the retro-aldol condensation reaction and eventually led to an increased EG yield in the presence of Ni. The catalyst was moderately stable after four consecutive runs for 6 h at 220 degrees C and at a H-2 reaction pressure of 70 bar, though a 12 h reaction resulted in the highest EG yield. The high yields under moderate reaction conditions promise an energy-efficient and economically feasible process. |
| DOI | 10.1039/d1nj03257g |
| Type of Journal (Indian or Foreign) | Foreign |
| Impact Factor (IF) | 3.591 |
Divison category:
Catalysis and Inorganic Chemistry
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