The concept of a bio-based economy has been adopted by many advanced countries around the world, and thermochemical conversion of waste biomass is recognized as the most effective approach to achieve this objective. Recent studies indicate that hydrothermal carbonization (HTC) is a promising method for the conversion of waste biomass towards novel carbonaceous materials known as hydrochars. This cost-effective and eco-friendly process operates at moderate temperatures (180–280 °C) and uses water as a reaction medium. HTC has been successfully applied to a wide range of waste materials, including lignocellulose biomass, sewage sludge, algae, and municipal solid waste, generating desirable carbonaceous products. This review provides an overview of the key HTC process parameters, as well as the physical and chemical properties of the obtained hydrochar. It also explores potential applications of produced materials and highlights the modification and functionalization techniques that can transform these materials into game-changing solutions for a sustainable future.

In this study, hydrothermal carbonization (HTC) at five temperatures (180, 200, 220, 240, and 260 °C) was applied to transform Paulownia leaves (PL) into a carbonaceous sorbent of Pb(II) from aqueous solutions. To enhance the adsorption efficiency of the obtained hydrochar (PH), subsequent alkali activation was performed using NaOH. Preliminary results of the Pb(II) adsorption (C_Pb = 200 mg/L) showed removal coefficients after 48 h of 73.44 mg/g, 82.37 mg/g, and 110.9 mg/g for PL, PH-220, and MPH-220, respectively. The selected hydrochar (PH-220) and modified hydrochar (MPH-220) were further investigated by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The results revealed that alkali treatment changed the hydrochar structure and, thus, improved its adsorption performance. The kinetic parameters showed that the Pb(II) sorption onto MPH-220 followed a pseudo-second-order model, while the intra-particle diffusion went through two simultaneous stages. The Langmuir isotherm model best described the experimental data and indicated the value of 174.75 mg Pb(II)/g as the maximum adsorption capacity. The two possible mechanisms of Pb(II) binding were complexation and/or Pb-π electron interaction. The obtained results indicate the great potential of MPH-220 for Pb(II) removal from aqueous media and its potential utilization as an effective adsorbent for wastewater purification.

This study used widely available waste biomass, corn cob (CC), to remove Pb ions from aqueous solutions. A two-step conversion of this material was carried out to improve its adsorption characteristics. Firstly, CC was prepared by hydrothermal carbonization; afterward, the obtained hydrochar was doped by MgCl₂ and pyrolyzed. The synthesized hydro-pyrochar (HCC-Mg) was used for adsorption experiments in a batch system. The surface and structural properties of HCC-Mg were characterized by SEM-EDX and FTIR analysis before and after Pb adsorption. Kinetic and isotherm models were applied to the experimental results. It was confirmed that Pb adsorption on HCC-Mg occurred rapidly, with a maximum adsorption capacity of 87.08 mg/g. The pseudo-second-order model best described the adsorption process, while the best fit of the experimental data was observed with the Sips isotherm model. The results of this study showed that the capacity of the synthesized HCC-Mg material had increased more than 14 times compared with raw CC. In addition, the synthesized material had the potential to be reused for at least five cycles with minimal loss of adsorption capacity and efficiency. Moreover, the results confirmed that HCC-Mg can be used as an efficient, sustainable adsorbent of Pb from polluted water.

This study explores the utilization of waste grape pomace-derived hydrochar as an efficient adsorbent for lead (Pb²⁺) removal from aqueous solutions. Hydrochar was produced via hydrothermal carbonization (HTC) at 220 °C, followed by doping with magnesium and iron salts, and subsequent pyrolysis at 300 °C to obtain Fe/Mg-pyro-hydrochar (FeMg-PHC). The material’s structural and morphological changes after Pb²⁺ adsorption were examined using FTIR. FTIR revealed chemisorption and ion exchange as key mechanisms, shown by decreased hydroxyl, carbonyl, and metal–oxygen peaks after Pb²⁺ adsorption. Adsorption tests under varying pH, contact time, and initial Pb²⁺ concentrations revealed optimal removal at pH 5. Kinetic modeling indicated that the process follows a pseudo-second-order model, suggesting chemisorption as the dominant mechanism. Isotherm analysis showed that the Sips model best describes the equilibrium, with a maximum theoretical adsorption capacity of 157.24 mg/g. Overall, the simple two-step synthesis—HTC followed by pyrolysis—combined with metal doping yields a highly effective and sustainable adsorbent for Pb²⁺ ion removal from wastewater.

In recent decades, massive exploitation of fossil fuels caused a growing demand for the production of energies from renewable sources. Hydrochar obtained from waste biomass via hydrothermal carbonization (HTC) possesses good potentials as a biofuel. Therefore, we performed HTC of corn cob, paulownia leaves, and olive pomace at different temperatures (180, 220, and 260oC). The main goal of this study was to comparatively evaluate the influence of HTC conditions on the structure and fuel characteristics of the obtained solids. The results showed that the yields of hydrochar decrease significantly with increasing temperature in all samples. The carbon content and higher heating value increased and reached the highest values in hydrochars obtained at 260?C, while the content of volatile matter decreased. Furthermore, the Van Krevelen diagram reveals that the transformation of feedstock to lignite-like products upon HTC was achieved. In this study, the results showed that processes of dehydration and decarboxylation during HTC provoke intensive biomass transformation and that hydrochars obtained at higher temperatures have significantly enhanced fuel properties and fewer volatiles compared to the feedstock.