Two-stage fast pyrolysis and catalytic steam reforming of corn waste bio-oil for hydrogen production: Screening and optimization of Ni Fe catalysts supported on porous clay heterostructures
Converting agricultural residues into hydrogen offers a promising route toward low-carbon energy. This study presents a two-stage process combining fast pyrolysis of con waste bio-oil followed by catalytic steam reforming (CSR) using Ni Fe catalysts supported on porous clay heterostructures (PCH). Fast pyrolysis at 500 °C for 1 h produced 41.4 wt% bio-oil rich in lignin-derived phenolics. Catalyst screening during reforming at 800 °C identified 0.8Ni–0.2Fe/PCH as the optimal formulation, delivering 58.8% H 2 yield and 87.3% feedstock conversion with 7.2 mmol/g cat carbon deposition after 1 h. Relative to monometallic counterparts, Ni Fe synergy improved reforming performance while reducing carbon deposition by up to 38.9%. Under autothermal reforming (ATR), optimizing temperature (700–900 °C) and O 2 /C ratios (0.15–0.45) improved H 2 selectivity by balancing reforming and oxidation reactions. Importantly, the 0.8Ni–0.2Fe/PCH remained highly stable over 170 h, sustaining >80% H 2 yield and >90% conversion with minimal carbon deposition. Characterization (BET, SEM–EDX, XRD, FTIR) confirmed well-dispersed Ni Fe species anchored within the PCH framework, consistent with enhanced stability and resistance to carbon deposition. These results highlighted the Ni–Fe/PCH as efficient and promising catalyst platform for hydrogen production from corn waste bio-oil. • Green hydrogen was produced from corn waste via two-stage fast pyrolysis and catalytic reforming. • 0.8Ni–0.2Fe/PCH exhibited the highest H 2 reforming performance and conversion at 800 °C in both 1 and 18 h tests. • A higher Ni/Fe ratio enhanced Ni–Fe synergy, reducing carbon up to 38.9% compared with monometallic Ni or Fe. • Optimizing temperature (700–900 °C) and O 2 /C under ATR operation enhanced H 2 selectivity and reduced carbon deposition. • Long-term operation (170 h) at 800 °C and O 2 /C 0.30 maintained high H 2 yield/conversion with low carbon (∼1.2 mmol/g cat ).
Authors
- Chatchai Veranitisagul (ORCID: https://orcid.org/0000-0002-9280-1352)
- Wanwitoo Wanmolee (ORCID: https://orcid.org/0000-0003-0681-4067)
- Khatiya Weerasai (ORCID: https://orcid.org/0000-0001-5975-2248)
- Punjarat Khongchamnan
- Pornlada Daorattanachai (ORCID: https://orcid.org/0000-0001-5071-1036)
- Navadol Laosiripojana (ORCID: https://orcid.org/0000-0001-5290-4229)
- Thanapat Chomchatwarl
- Apirat Laobuthee
Institutions
- Université Claude Bernard Lyon 1 (FR)
- Rajamangala University of Technology (TH)
- Centre National de la Recherche Scientifique (FR)
- National Science and Technology Development Agency (TH)
- Joint Graduate School of Energy and Environment (TH)
- Kasetsart University (TH)
- National Nanotechnology Center (TH)
- Institut de Recherches sur la Catalyse et l'Environnement de Lyon (FR)
- King Mongkut's University of Technology Thonburi (TH)
- King Mongkut's University of Technology North Bangkok (TH)
- National Center for Genetic Engineering and Biotechnology (TH)
Publication Details
- Journal
- Fuel Processing Technology
- Published
- 2026-02-03
- DOI
- https://doi.org/10.1016/j.fuproc.2026.108411
- Citations
- 1
- Primary Topic
- Catalysts for Methane Reforming
- Type
- article
- Field-Weighted Citation Impact
- 12.85