Biochar is attracting attention as an alternative carbon/fuel source to coal in the process industry and energy sector. However, it is prone to self-heating and often leads to spontaneous ignition and thermal runaway during storage, resulting in production loss and health risks. This study investigates biochar self-heating upon its contact with O₂ at low temperatures, i.e., 50–300 °C. First, kinetic parameters of O₂ adsorption and CO₂ release were measured in a thermogravimetric analyzer using biochar produced from a pilot-scale pyrolysis process. Then, specific heat capacity and heat of reactions were measured in a differential scanning calorimeter. Finally, a one-dimensional transient model was developed to simulate self-heating in containers and gain insight into the influences of major parameters. The model showed a good agreement with experimental measurement in a closed metal container. It was observed that char temperature slowly increased from the initial temperature due to heat released during O₂ adsorption. Thermal runaway, i.e., self-ignition, was observed in some cases even at the initial biochar temperature of ca. 200 °C. However, if O₂ is not permeable through the container materials, the temperature starts decreasing after the consumption of O₂ in the container. The simulation model was also applied to examine important factors related to self-heating. The results suggested that self-heating can be somewhat mitigated by decreasing the void fraction, reducing storage volume, and lowering the initial char temperature. This study demonstrated a robust way to estimate the cooling demands required in the biochar production process.

In this paper, the interaction between caking bituminous coal (HC) and two types of biomass, namely sunflower husks (SFHs) and walnut shells (WSs), was studied via lab-scale fixed-bed reactor experiments and thermogravimetric analysis (TGA). The dynamics of volatile matter composition and weight loss changes were analyzed for the initial biomass types and their 1:1 blends with HC during co-pyrolysis. Derivative thermogravimetry (DTG) revealed that during the co-pyrolysis of HC with biomass, the number of reaction stages increased to four, compared to three during individual pyrolysis, indicating synergistic thermal behavior. The apparent activation energy (E_a) of the blends was higher (62.8 kJ/mol for SFH/HC and 61.8 kJ/mol for WS/HC) than that of the individual HC (55.1 kJ/mol), SFHs (43.8 kJ/mol), and WSs (52.4 kJ/mol), confirming intensified reaction complexity. Co-pyrolysis resulted in higher methane (CH₄) production, with the CH₄:HAc (acetic acid) ratio increasing from 1.2 (WSs) and 1.7 (SFHs) to 1.9 (WS/HC) and 3.3 (SFH/HC). The non-additive behavior of blends is established, indicating the interactions between biomass and HC during co-pyrolysis. These findings support a more resilient and sustainable approach to producing fuels and reducing agents, particularly through the utilization of agricultural residues and waste biomass.

As the iron and steel industry needs to cut its CO₂ emissions drastically, much effort has been put into establishing new—less greenhouse-gas-intensive—production lines fueled by hydrogen and electricity. Blast furnaces, as a central element of hot iron production, are expected to lose importance, at least in European production strategies. Yet, blast furnaces could play a significant role in the transitional phase, as they allow for the implementation of another CO₂-reducing fuel, carbonized wood reducing agents, as a substitute for coal in auxiliary injection systems, which are currently widely used. Wood carbonization yields vastly differing fuel types depending on the severity of the treatment process, mainly its peak temperature. The goal of this study is to define the lowest treatment temperature, i.e., torrefaction temperature, which results in a biogenic reducing agent readily employable in existing coal injection systems, focusing on their conveying properties. Samples of different treatment temperatures ranging from 285 to 340 °C were produced and compared to injection coal regarding their chemical and mechanical properties. The critical conveyability in a standard dense-phase pneumatic conveying system was demonstrated with a sample of pilot-scale high-temperature torrefaction.