Abstract
Formate received significant attention for storing H2 in chemical bonds using the concept of H2 carriers. In this report, hydrogen generation from formate was optimized systematically by varying reaction variables. Initial mass activity with a turnover frequency of 3200 molH2 molPd-1 h-1 and 92% H2 yield were obtained in sodium formate (7 M 2.0 mL) dehydrogenation over Pd(3 wt %)/C at 80 °C. Influence of formate cations (Na, K, and NH4) on dehydrogenation was also elucidated, presenting that the fastest initial reaction kinetics was achieved with ammonium formate, whereas the highest H2 yield was obtained with potassium formate (PF) in multiple catalyst recycle tests. Finally, an on-site power generation system was integrated, where a proton exchange membrane fuel cell (PEMFC) was operated in conjunction with H2 produced from the custom developed semibatch dehydrogenation reactors. The system operation was demonstrated with continuous feeding of PF to generate H2 and power on demand without an external heat source by utilizing waste heat produced from the PEMFC in a highly efficient manner.
| Original language | English |
|---|---|
| Pages (from-to) | 9846-9856 |
| Number of pages | 11 |
| Journal | ACS Sustainable Chemistry and Engineering |
| Volume | 8 |
| Issue number | 26 |
| DOIs | |
| Publication status | Published - 6 Jul 2020 |
Bibliographical note
Publisher Copyright:Copyright © 2020 American Chemical Society.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- formate dehydrogenation
- heat integrated dehydrogenation system
- on-site power generation
- optimization of reaction condition
- palladium nanocatalyst
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