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April 12, 2026Carbon Reports0 citationsOpen Access

Evolution of pore structure in cypress-derived carbon during hydrothermal treatment and subsequent carbonization

JHJun’ichi HAYASHIIHIsao HasegawaKNKiyoharu Nakagawa

Key Points

  • The research aims to understand how temperature influences pore formation in cypress hydrochar during hydrothermal carbonization and subsequent carbonization.
  • Conducted hydrothermal carbonization at temperatures of 170–240 °C.
  • Characterized hydrochars using nitrogen adsorption and thermogravimetric analysis.
  • Performed carbonization at 900 °C to enhance porosity.
  • Samples at 170 and 200 °C showed minimal porosity.
  • Hydrochar produced at 240 °C had significant mesopore volume, despite low surface area.
  • Carbonization led to increased microporosity and a hierarchical pore structure.

Abstract

Hydrothermal carbonization (HTC) is a promising method for converting wet biomass into carbon materials; however, the mechanisms underlying pore formation during HTC remain poorly understood. This study examined how reaction temperature affects pore development in cypress hydrochar. Hydrochars were prepared at 170–240 °C and characterized by nitrogen adsorption and thermogravimetric analysis. While samples prepared at 170 and 200 °C showed almost no porosity, the hydrochar produced at 240 °C exhibited a significant increase in mesopore volume despite a low surface area, indicating the formation of relatively large pores (~50 nm). Thermogravimetric analysis revealed extensive hydrolysis of hemicellulose and cellulose at 240 °C, yielding a thermally stable structure enriched in lignin-derived components. To further develop the pore structure, the hydrochar was carbonized at 900 °C. This carbonization greatly increased microporosity while partially maintaining larger pores, creating a hierarchical pore structure. In contrast, raw cypress char exhibited mainly microporosity, with little mesoporosity. These findings suggest that higher HTC temperatures play a key role in mesopore formation, likely through enhanced hydrolysis and heterogeneous solid formation, offering insights into the design of biomass-derived porous carbon materials.

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Cite This Study

HAYASHI et al. (2026) studied this question.

synapsesocial.com/papers/69db36a04fe01fead37c4921https://doi.org/10.7209/carbon.050205
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