Aqueous phase reforming and hydrodeoxygenation of ethylene glycol on Pt/SiO2-Al2O3: Effects of surface acidity on product distribution

Seongho Jeon, Hyun Seog Roh, Dong Ju Moon, Jong Wook Bae

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11 Citations (Scopus)


Aqueous-phase reforming (APR) and aqueous-phase hydrodeoxygenation (APH) reactions of ethylene glycol (EG) were investigated using platinum supported solid-acid SiO2-Al2O3 catalysts with different Si/Al molar ratios. The molar ratio of Si/Al on the SiO2-Al2O3 mixed metal oxides largely altered the surface area due to changes to the acidity, as well as changing the reduction behavior of the supported platinum nanoparticles. The Pt/SiO2-Al2O3 catalysts with a Si/Al molar ratio of 0.1 showed a higher activity for APR as well as APH. Among the various properties of Pt/SiO2-Al2O3, the amount of acid sites on the SiO2-Al2O3 supports changed the EG conversion and production distribution with different coke depositions. The acidic property was a more dominant factor for the catalytic activity than the affects of the platinum crystallite size on the reduction behavior. The easy and simultaneous cleavages of C-C as well as the C-O bonds in EG on the Bronsted acid sites of Pt/SiO2-Al2O3 catalysts were responsible for a higher EG conversion and hydrocarbon formation. A larger number of weak acid sites was also related to the formation of larger hydrocarbons and a lower coke deposition. Compared with Pt/Al2O3, improved catalytic acidity with a low coke deposition was observed for Pt/SiO2-Al2O3 at a Si/Al molar ratio of 0.1. This can mainly be attributed to the easy control of weak and strong acid sites with a high dispersion of platinum crystallites by simply changing the Si/Al molar ratio of the SiO2-Al2O3 mixed metal oxides.

Original languageEnglish
Pages (from-to)68433-68444
Number of pages12
JournalRSC Advances
Issue number72
Publication statusPublished - 2016

Bibliographical note

Funding Information:
This work was supported by the Korea Institute of Energy Tech-nology Evaluation and Planning (KETEP) with Project the number 20132010201750. The authors would like to acknowledge the financial support from the National Research Foundation of Korea (NRF) grant funded by the Korea government (NRF-2014R1A1A2A16055557 and NRF-2016M3D3A1A01913253). This work was supported by an institutional program Grant (2E26570-16-037) from Korean Institute of Science and Technology.

Publisher Copyright:
© The Royal Society of Chemistry 2016.

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Chemical Engineering(all)


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