Hydrothermal Carbonization as a Process to Facilitate the Disposal of Bioplastics

Bioplastics are steadily replacing fossil-based plastics due to their renewable origin and biodegradability. However, their end-of-life can be problematic: they are often collected with the organic fraction of municipal solid waste (OFMSW) but can be not satisfactorily biodegradable in plants that treat it, leading to their rejection at the entrance. This work focuses on five different commercial bioplastics employed in the eyewear industry: two based on cellulose acetate, one on galalithe, one on corn starch and one on polyamide. The aim was to assess their treatability via hydrothermal carbonization (HTC), which was never reported in the literature for these materials. Under HTC at 180 and 220 °C for 1 h, four of the tested bioplastics show significant degrees of degradation, leading to the formation of different solid and liquid products, which were respectively characterised according to their elemental composition and pH. The interesting different behaviours may be ascribed to the different compositions and structures of the materials. HTC appears as a viable route to facilitate the degradation of these recalcitrant materials and may be followed by a material recovery or an energetic valorisation through anaerobic digestion or thermochemical pathways, depending on the purity of the waste stream

Thermal Analysis and Kinetic Modeling of Pyrolysis and Oxidation of Hydrochars

This study examines the kinetics of pyrolysis and oxidation of hydrochars through thermal analysis. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) techniques were used to investigate the decomposition profiles and develop two distributed activation energy models (DAEM) of hydrochars derived from the hydrothermal carbonization of grape seeds produced at different temperatures (180, 220, and 250 °C). Data were collected at 1, 3, and 10 °C/min between 30 and 700 °C. TGA data highlighted a decomposition profile similar to that of the raw biomass for hydrochars obtained at 180 and 220 °C (with a clear distinction between oil, cellulosic, hemicellulosic, and lignin-like compounds), while presenting a more stable profile for the 250 °C hydrochar. DSC showed a certain exothermic behavior during pyrolysis of hydrochars, an aspect also investigated through thermodynamic simulations in Aspen Plus. Regarding the DAEM, according to a Gaussian model, the severity of the treatment slightly affects kinetic parameters, with average activation energies between 193 and 220 kJ/mol. Meanwhile, the Miura–Maki model highlights the distributions of the activation energy and the pre-exponential factor during the decomposition