This study aims to investigate how the morphology of cellulose influences the hydrolysis and carbonization during hydrothermal treatment at temperatures between 180 and 240 °C. The morphology of cellulose, especially different crystallinities and degrees of polymerization, is represented by microcrystalline cellulose and α-cellulose. Kinetic analysis is considered a tool to allow the determination of the mechanisms of the two types of cellulose during the hydrothermal process. A kinetic model, in which cellulose is assumed to be hydrolyzed to a limited extent, is proposed. Five scenarios are used as models for pyrolysis of nonhydrolyzed cellulose that forms primary char, along with reaction pathways of hydrolyzable cellulose and its derivatives that latterly form secondary char. The morphologies of solid products are in good agreement with the results of the proposed model.

The effect of Brønsted acids on the hydrothermal dehydration of fructose to 5-hydroxymethylfurfural (HMF), a promising platform chemical from renewable resources, exceeds the sole donation of catalytically active protons.

This study investigates the production of bio-based carbon materials for energy storage and conversion devices based on two different vineyard residues (pruning, pomace) and cellulose as a model biomass. Three different char categories were produced via pyrolysis at 900 °C for 2 h (biochars, BC), hydrothermal carbonization (HTC) (at 220, 240 or 260 °C) with different reaction times (60, 120 or 300 min) (hydrochars, HC), or HTC plus pyrolysis (pyrolyzed hydrochars, PHC). Physicochemical, structural, and electrical properties of the chars were assessed by elemental and proximate analysis, gas adsorption surface analysis with N₂ and CO₂, compression ratio, bulk density, and electrical conductivity (EC) measurements. Thermogravimetric analysis allowed conclusions to be made about the thermochemical conversion processes. Taking into consideration the required material properties for the application in electrochemical double-layer capacitors (EDLC) or in a direct carbon fuel cell (DCFC), the suitability of the obtained materials for each application is discussed. Promising materials with surface areas up to 711 m² g⁻¹ and presence of microporosity have been produced. It is shown that HTC plus pyrolysis from cellulose and pruning leads to better properties regarding aromatic carbon structures, carbon content (>90 wt.%), EC (up to 179 S m⁻¹), and porosity compared to one-step treatments, resulting in suitable materials for an EDLC application. The one-step pyrolysis process and the resulting chars with lower carbon contents and low EC values between 51 and 56 S m⁻¹ are preferred for DCFC applications. To conclude, biomass potentials can be exploited by producing tailored biomass-derived carbon materials via different carbonization processes for a wide range of applications in the field of energy storage and conversion.