Abstract
Chemocatalytic conversion of biomass-based saccharides to lactic acid (LA) is one of the prospective routes for biomass valorization, but generally suffers from harsh reaction conditions with relatively low selectivity toward C[sbnd]C bond cleavage. Herein, a novel ternary heterostructure g-C3N4/N-TiO2/NiFe-LDH (NTCN/LDH) photocatalyst prepared by a simple wet-chemical method was demonstrated to be high-performance for cascade upgrading of various biomass sugars to LA (up to 99.0 % yield) in H2O at 60 °C under visible-light irradiation for a short time (≥15 min). A relay photo/thermal catalytic mechanism was mainly responsible for the superior performance of NTCN/LDH in LA production, as elucidated by DFT calculations, in which NTCN/LDH provided suitable Lewis acid sites (i.e., adsorption sites) for thermocatalytic sugar isomerization (e.g., glucose-to-fructose conversion), while the constructed double type-II heterojunction could regulate the type and count of the formed reactive oxygen species (dominantly ·O2−) to achieve precise photocatalytic C3-C4 bond breaking. The scale-up test could still maintain 92 % LA yield of the first-time experiment, indicating the eximious industrialization potential of the versatile NTCN/LDH catalyst. In addition, the life cycle assessment illustrated that the entire system has less impact on the environment than the current industrial LA production process.
| Original language | English |
|---|---|
| Article number | 139687 |
| Journal | Chemical Engineering Journal |
| Volume | 452 |
| DOIs | |
| State | Published - 15 Jan 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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SDG 12 Responsible Consumption and Production
Keywords
- Biomass conversion
- Lactic acid
- Life cycle assessment
- Photocatalysis
- Reaction mechanism
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