Dehydrogenation of homocyclic liquid organic hydrogen carriers (LOHCs) over Pt supported on an ordered pore structure of 3-D cubic mesoporous KIT-6 silica

Chang-Il Ahn, Yeonsu Kwak, Ah-Reum Kim, Munjeong Jang, Arash Badakhsh, Junyoung Cha, Yongmin Kim, Young Suk Jo, Hyangsoo Jeong, Sun Hee Choi, Suk Woo Nam, Chang Won Yoon*, Hyuntae Sohn

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

27 Citations (Scopus)
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Abstract

Pt supported on ordered mesoporous silica (KIT-6) catalyst was examined for the dehydrogenation of homocyclic liquid organic hydrogen carriers (LOHCs, 1: MCH, 2: hydrogenated biphenyl-based eutectic mixture (H-BPDM)) conditions. The longer pore-residence time of the MCH molecules in the 3D bicontinuous pore structure of the Pt/KIT-6 catalyst strongly affected the catalytic activity because a higher MCH concentration was achieved in the vicinity of the Pt active sites. Pt/KIT-6 catalyst exhibited a higher surface area, pore volume, and Pt dispersion with narrower particle size distribution (average Pt particle size: ~1.3 nm). Therefore, higher LOHC conversion with faster hydrogen production occurred, with a higher hydrogen selectivity over Pt/KIT-6 compared with Pt/SiO2 and Pt/Al2O3. Long-term experiment results indicated that the Pt/KIT-6 catalytic activity was stable over the reaction time than that of the other catalysts. No significant structural collapse occurred in KIT-6 during the dehydrogenation. Carbon coking was observed for all three samples.

Original languageEnglish
Article number121169
Number of pages13
JournalApplied Catalysis B: Environmental
Volume307
Early online date15 Feb 2022
DOIs
Publication statusPublished - 15 Jun 2022

Keywords

  • dehydrogenation
  • KIT-6
  • liquid organic hydrogen carriers
  • methylcyclohexane
  • ordered mesoporous silica

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