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.

Plastic handling and manufacturing have recently increased dramatically owing to technological advancements and rising living standards. Consequently, the amount of plastic waste has significantly escalated, seriously pressuring the whole ecosystem. The impacts of waste accumulation in the environment frequently have detrimental effects on living organisms. Sustainable development goals (SDGs) propose balanced and feasible development of entire humanity, protecting natural resources and bringing a clean environment. Poly (ethylene terephthalate) - PET is a common plastic that can seriously threaten the environment if it is not handled appropriately. This review paper tends to show recent trends in the production and recycling of PET polymer on a global scale. The basis of PET chemistry together with possible applications was presented. A target period, from 2020-2024, was used to examine the quantity and main industrial suppliers around the world. Therefore, some sources state that in 2024, nearly 28 Mt of PET was produced and China was the main producer with a global share of 31%. Adequate management of the mentioned polymer is necessary for building an eco-friendly climate for future generations.

Corn processing waste represents an abundant, renewable, and low-cost lignocellulosic resource with considerable potential for environmental remediation applications. Large quantities of residues generated during corn processing, including cobs, husks, bran, and other by-products, are produced annually and can be utilized directly as native biomass or converted through thermochemical processes into hydrochars and biochars. This systematic review provides a comparative analysis of native corn processing biomass, hydrochars produced via hydrothermal carbonization, and biochars obtained through pyrolysis, with a focus on their potential as adsorbents for the removal of organic and inorganic pollutants from soil and water systems. Particular attention is given to the influence of thermochemical conversion processes on the physicochemical properties of the materials, including surface chemistry, porosity, functional groups, and structural characteristics, which govern adsorption mechanisms such as ion exchange, electrostatic interactions, surface complexation, hydrogen bonding, and π–π interactions. Furthermore, the advantages and limitations of each material type are discussed, together with key environmental and techno-economic considerations related to their production and practical application, including indicative production costs (USD per kg of adsorbent) and cost–performance relationships in terms of adsorption capacity. By linking biomass conversion processes, material properties, and adsorption performance, this review aims to provide a comprehensive overview of corn processing waste valorization and to support the development of sustainable adsorbent materials for soil and water remediation. A total of 36 studies were included in the qualitative synthesis following PRISMA guidelines.