Hydrothermal Carbonization Research Articles

A CASE STUDY OF IMPLEMENTATION OF CIRCULAR ECONOMY PRINCIPLES TO WASTE MANAGEMENT: INTEGRATED TREATMENT OF CHEESE WHEY AND HI-TECH WASTE

In a global context characterized by severe environmental problems and increasing resource scarcity, waste represents both a challenge and an opportunity. This study aims to demonstrate with a real case the potential for optimizing the waste valorization action attainable through the synergic application of different treatments to residues of equally different nature and origin. In particular, bio-chemical (dark fermentation), chemical-physical (selective leaching) and thermo-chemical (hydrothermal carbonization) treatments were applied for the integrated valorization of whey from sheep cheese production and Hi-Tech waste (discarded electrical and electronic equipment). The treatments were applied at a laboratory scale on real samples of these residues. The organic acids used for selective leaching of valuable metals from Hi-Tech waste were obtained by dark fermentation of the cheese whey, while hydrothermal carbonization was used to convert the waste from previous stages into hydrochar feasible as solid fuel or soil improver. The dark fermentation tests have highlighted the possibility of recovering ≈ 100 g of organic acids from 1 L of whey; furthermore, it is also possible to recover bio-hydrogen depending on the operating conditions applied and the type of targeted organic acids. The leaching tests have demonstrated how the organic acids from whey fermentation have selective and quantitative mobilization capacities comparable to those of the same acids available on the market. The carbonization tests produced carbon-enriched hydrochar with promising fuel properties, as well as process waters suitable for anaerobic digestion with methane production. The results of the project led to the filing of an international patent.

The role elucidating of EPS in thermal hydrolysis and nitrogen conversion of sewage sludge during hydrothermal carbonization process, and its effect on hydrochar's properties

Hydrothermal carbonization (HTC) was conducted to observe the effect of extracellular polymeric substances (EPS) structure on the nitrogen migration mechanism during the HTC process. The denitrification efficiency of activated sewage sludge (ASS) decreases with an increase in EPS stripping intensity. Loosely and tightly bound extracellular polymers diminish the denitrification effectiveness by inhibiting the hydrolysis of nitrogen-containing organic compounds and protecting the cell structure, respectively. Intracellular nucleic acids and proteins generate stable N-containing species, such as heterocyclic-N and quaternary-N, which are unfavorable for deep denitrification. In general, nitrogen removal is more effective outside the cell than inside. Deep destruction of EPS eliminated a considerable number of N-containing components, and the N/C value of hydrochar at 180 °C without cell membrane protection was 0.06, which dropped to half that of ASS (0.11). This study revealed the influence of EPS structure on nitrogen migration in hydrothermal environment and provided significant insights for the preparation of clean solid fuels.

Effect of HTC and Water-Leaching of Low-Grade Biomasses on the Release Behavior of Inorganic Constituents in a Calcium Looping Gasification Process at 650 °C.

The release of alkali metals (K, Na) and nonmetals (S, Cl) during a calcium looping (CaL) gasification process of waste derived-hydrochars, water-leached samples, and CaO-biomass blends was investigated. Special attention was paid to biomasses that are not particularly promising for gasification requirements but have a large occurrence in Europe, including Grape Bagasse, Organic Fraction of Municipal Solid Waste (OFMSW), Green Waste, and Out-of-use woods from construction debris and discarded furniture. The release experiments were performed at 650 °C in a flow channel reactor to investigate the behavior of inorganic trace substances. Hot-gas analysis was performed by Molecular Beam Mass Spectrometry (MBMS). Thermodynamic equilibrium calculations via FactSage indicate H2S, carbonyl sulfide (COS), KCl, NaCl, and HCl as the main inorganic impurities. Thus, the focus of the experiments was placed on these species. It was found that the concentrations of trace elements released during gasification at 650 °C, such as H2S, SO2, KCl, and NaCl, are hardly affected by intense water-leaching. In contrast, carbonaceous materials from hydrothermal carbonization exhibit a higher concentration of trace potassium substances (K, KCl, and K2Cl+). When biomass samples are combined with CaO, the total amount of inorganic trace compounds (K, Na, and S compounds) in the resulting syngas could be decreased.

Utilization of papermaking black liquor as liquid phase for hydrothermal carbonization of corn stalks: The unique role of alkali for production of hydrochar

Papermaking black liquor (BL) contains a large amount of organic matter, alkali, and salt, which has high value in industrial and agricultural production. In the present paper, hydrothermal carbonization (HTC) technology has been employed to deal with BL and corn stalk (CS) under various conditions. A variety of analytical technologies, including Fourier Transform Infrared Spectrometer, X-Ray Diffraction, element analyzer, comprehensive thermal analyzer, scanning electron microscope, chromatography/mass spectrometry, TOC analyzer, and density functional theory (DFT), were used to characterize the physicochemical properties of hydrochar and aqueous phase product. The effects of experimental parameters (temperature, solid-liquid ratio, and time) on the HTC of BL and CS were systematically investigated. The higher energy yield and densification of hydrochar prepared by our HTC technology were obtained at 260 ℃ in 30 min with a solid-liquid ratio of 1:3. Mechanism study indicates that NaOH, which comes from the original BL, could effectively facilitate the cleavage of β–O–4 bond in lignin and β–1–4 glycosidic bond in cellulose and hemicellulose molecules. Hemicellulose and cellulose are more susceptible to degradation relevant to the lignin in the presence of NaOH. Elementary analysis shows that the dosage of BL is important for improving energy densification of hydrochar. The combustion characteristics show that hydrochar presents a thermochemical behavior, which is close to bituminous coal. Owing to hydroxyl ion in NaOH ion pair was consumed in the series of dehydrogenation reactions, pH of HTC aqueous phase product significantly decreases from 11 to 13 in original BL to 4.8–5. Such results indicate that a completely change for the components of BL could be obtained by our HTC technology, which provide a novel idea for the treatment of Papermaking BL without concentration.

Elevating clean energy through sludge: A comprehensive study of hydrothermal carbonization and co-gasification technologies

This study explores the recycling challenges of industrial sludge, owing to its non-recyclable properties and associated environmental problems. To promote sustainable energy utilization, a novel approach combining hydrothermal carbonization and co-gasification was employed to facilitate the conversion from waste to energy. The industrial sludge was pretreated in the batch-type hydrothermal treatment unit at 180–220 °C, followed by co-gasification. The experimental results indicate that pretreating the sludge at the hydrothermal temperature of 200 °C maximized its thermal decomposition, leading to a rougher structure with obvious cracks, eventually transforming into numerous fragmented small particles. At 1100 °C with a blending mass ratio of 1:1, the sludge hydrochar at 200 °C significantly enhanced the reactivity of coal char, exhibiting the gasification reactivity index R0.9 of 1.57 times higher than that of untreated char. Using the in-situ technique with the heating stage microscope, it was first observed that the addition of pretreated sludge coal chars underwent gasification in the shrinking core mode, displaying a significant ash melt flow phenomenon. Based on the in-situ X-ray diffraction, it was discovered that more amorphous structures were formed by the reaction of Fe with other minerals in the sludge-coal blended char after hydrothermal carbonization at 200 °C. With pretreatment at the hydrothermal temperature of 200 °C, the sludge can increase the specific surface area of the blended char and facilitate the cracking of carbon crystals during co-gasification. Its specific surface area and the Raman spectroscopic ratio ID1/IG were 1.76 and 1.17 times that of coal char, respectively. Collectively, this study highlights the potential for energy recovery from industrial sludge, contributing to sustainable waste management in the chemical industry.

Role of volatile secondary char on the combustion behavior of cellulose-based hydrochars

Hydrothermal carbonization (HTC) can transform a wide range of biomass into renewable biofuels. Hydrochar, the solid fuel resulting from HTC, has a similar energy density to low-rank coals. Despite an extensive body of literature detailing the thermogravimetric analysis (TGA) of hydrochar under slow pyrolysis and oxidation, there remains a limited understanding of hydrochar's behavior in realistic combustion settings. In this work, we integrate combustion experiments and TGA to understand the combustion characteristics of a model hydrochar fuel. Cellulose-based hydrochars produced at different temperatures along with solvent-extracted chars are tested in a Hencken burner across varying temperatures and oxygen concentrations in the oxidizer gas. Simultaneous CH* chemiluminescence, particle image velocimetry, and two-color pyrometry are used to measure ignition delay time and identify homogeneous/heterogeneous ignition mechanisms and combustion phases. Incorporating TGA with combustion results shows that the ignition mode and combustion processes are strong functions of surrounding gas temperature and oxygen mole fraction. The level of carbonization of the hydrochar dictates the ignition delay time and combustion modes. Further, the presence of a tar-like secondary char on the as-carbonized hydrochars leads to more rapid ignition due to high volatility.

Preparation and characterization of potassium hydroxide activated hydrochar

This paper presents processing and characterization of hydrochar derived from bamboo via hydrothermal carbonization at 200 °C for 4 h followed by activation at 600 °C for 2 h. The hydrochar contains hierarchical pores. The BET surface area of the hydrochar activated by KOH reached 4.5506 m2/g. KOH enhanced pore and nanofiber formation. All the bamboo-derived hydrochars can effectively harvest solar energy to evaporate seawater. The KOH-activated one showed the best performance with the maximum evaporation rate of 3.057 kg/(m2∙h).

Investigation of co-combustion characteristics and kinetics of low-ranked coal and hydrochar derived from cow manure

CO2 emission should be reduced by the effective utilization of low-ranked coal in a coal-based power plant based on co-combustion of coal and biomass. This study investigated the co-combustion behavior of lignite and cow manure using three different kinds of samples: raw lignite coal blended with cow manure (CM-L), raw lignite coal blended with hydrochar derived from cow manure (HCM-L), and co-hydrothermal carbonization (Co-HTC) of lignite coal and cow manure (Co-HCML) using thermogravimetric analysis and a hydrothermal carbonization (HTC) temperature of 200 °C for 60 min. The kinetic parameters were calculated and analyzed using the Flynn-Wall-Ozawa and Kissinger-Akahira-Sunose methods. The combustion characteristics were studied of the various kinds of hydrochar mixed with lignite coal. The results showed that the low-ranked coal improved the fuel properties by increasing carbon content and decreasing sulfur through the HTC processes. The activation energy of Co-HCML was the lowest, which is preferable, and therefore it was recommended as the promising process.

Optimization of traditional market solid waste conversion process into hydrochar using hydrothermal carbonization technology

Abstract In this study, an analysis was carried out to determine the optimum conditions for the hydrothermal carbonization process of traditional market waste using response surface methodology central composite design. The hydrothermal carbonization process was carried out at temperatures (180, 215, 250°C), process times (30, 60, 90 minutes), and a ratio (waste: water media) of 0,5. The results of response surface analysis show that temperature and process time are parameters that significantly affect the quality of hydrochar. Increasing temperature and process time resulted in a decrease in hydrochar weight from 67,01 to 40,77 grams. Furthermore, there was an increasing heating value of hydrochar from 18,87 to 30,5 MJ/Kg. The optimization formulation of the hydrothermal carbonization process of traditional market waste was obtained at a temperature of 181,133°C and a process time of 30 minutes with a prediction value of weight and heating value obtained, namely 61,39 grams and 23 MJ/Kg.

Advanced Waste-to-Energy Technologies: A Review on Pathway to Sustainable Energy Recovery in a Circular Economy

In the face of the rapid rise in global waste production and the pressing need to shift towards sustainable energy options, advanced Waste-to-Energy (WtE) technologies have emerged as a highly promising solution. These innovative technologies effectively utilize waste as a valuable resource, presenting a viable pathway for sustainable energy recovery and making a substantial contribution to the principles of the circular economy paradigm. This review provides a comprehensive overview of advanced WtE technologies, including thermal, biological, and chemical methods, such as gasification, pyrolysis, plasma arc gasification, anaerobic digestion, fermentation, transesterification, and hydrothermal carbonization. The efficiency of these technologies is evaluated based on their energy recovery potential, environmental impact, and economic feasibility. Case studies on successful implementations of advanced WtE technologies are analyzed to highlight their practicality and effectiveness. Finally, the paper addresses technical, regulatory, and policy challenges in this field and provides future perspectives. The objective is to underscore the role of advanced WtE technologies in achieving a sustainable and resource-efficient circular economy.

Optimization conversion of willow biomass derived from phytoremediation into value-added hydrochars: Effects of temperature and medium on Cd/Zn distribution and application potentials

Effective treatment of plant biomass with potentially toxic elements (PTEs) is crucial for phytoremediation. Hydrothermal carbonization (HTC) offers an economical and eco-friendly solution by converting biomass into high-value hydrochar. However, the effects of reaction temperature and medium on the characteristics and metals distribution in hydrochars from PTEs-containing biomass remain unclear. This study explores the effects of different hydrothermal temperature (180–240 °C) and reaction media (H2O, HCl, H2SO4, H3PO4) on the hydrothermal properties of willow biomass containing PTEs, and the distribution and transfer rules of PTEs (Cd and Zn) and the application potential of hydrochar. The results indicated that hydrothermal temperature and acid medium significantly influenced WB conversion, affecting hydrochar properties such as carbonization degree and surface functional groups. Higher hydrothermal temperatures enhanced Cd and Zn fixation in the solid phase, while acid facilitated their migration to the liquid phase. More than 91.08 % of Cd and 88.41 % of Zn in the acid-added system are migrated into the liquid phase at hydrothermal temperature of 180 °C Hydrochar prepared under 180 °C and H3PO4 exhibited excellent adsorption performance for Cd2+ and Cu2+ (2.17 mg/g and 34.38 mg/g, respectively) in aqueous solution. Additionally, hydrochars exhibit high calorific values (20.52–28.01 MJ/kg), suggesting their potential as biofuel. This study provides technical foundation to support the resource processing and safe utilization of forest biomass containing PTEs.

Enhancement of gaseous toluene removal by photocatalysis using hydrothermal synthesis carbon nanodots/TiO2 combined with zeolite ZSM-5

Abstract Many studies have been conducted to produce composite materials that possess the ability to transform volatile organic compounds (VOCs) to other nontoxic forms economically and environmentally by means of photocatalytic method. However, the main drawbacks of these materials include restricted surface area, low affinity towards organic molecules, and wide band gap energy which dramatically inhibit their performance. In this research, a composite material that surpasses the above disadvantages has been successfully synthesized from TiO2 - carbon nanodots (CDs) - zeolite ZSM-5. Particularly, CDs synthesized by bottom-up method were coated on TiO2 before being uniformly distributed on zeolite ZSM-5. The powder samples with varying CDs/TiO2 and zeolite ZSM-5 content were tested for their photocatalytic oxidization capability to determine the appropriate ratio. The results revealed that samples with higher zeolite content improved photocatalytic activity. Under other survey conditions such as low toluene flowrate, high relative humidity as well as high UV intensity, the photocatalytic performance was enhanced notably. The newly produced material has corrected most disadvantages of traditional photocatalysts, however, further researches need to be made to improve the removal stability.

Ti3C2TX MXene/loofah-derived carbon aerogel for high-efficiency adsorption of organic pollutants in wastewater

The contamination of wastewater by organic pollutants significantly impacts human health and the environment due to their carcinogenic nature and various adverse effects. To address this issue, this study offers a high-efficiency and low-cost biomass-based carbon aerogel adsorbent, which was prepared through the hydrothermal carbonization of loofah, followed by Ti3C2TX MXene impregnation. The aerogel features a porous three-dimensional network structure and a substantial specific surface area, facilitating broad-spectrum adsorption capabilities for various dyes and drugs. The aerogel achieved impressive adsorption capacities of 175.29 and 75.73 mg/g for cationic methylene blue and Rhodamine B dyes, and 106.33 and 93.29 mg/g for anionic methyl orange and Congo red dyes, as well as 86.25 mg/g for tetracycline hydrochloride, surpassing other reported biomass-based aerogels. Furthermore, it demonstrated effective decolorization ability for wastewater containing mixed dyes. Notably, it exhibited excellent recycling and regeneration properties, maintaining a high removal rate after multiple cycles of adsorption–desorption. The adsorption process of dye/drug by the aerogel followed Langmuir’s monomolecular layer adsorption model, exhibiting spontaneous, endothermic, and disorder-increasing behavior in alignment with the pseudo-second-order kinetic model. This study presents an efficient biomass-based aerogel for the removal of organic pollutants from wastewater.

Remediation of Arsenic and Heavy Metals and Soil Stabilization by Waste Chitosan based Biochar

Objectives : This study aims to evaluate the feasibility of converting waste chitosan adsorbents, laden with microalgae, into biochar for application as a stabilizing agent to remediate heavy metal-contaminated soil and improve soil quality.Methods : Waste chitosan adsorbents were converted into biochar through two processes: dry thermal carbonization at 400°C to produce pyrochar and hydrothermal carbonization at 200°C to produce hydrochar. The elemental compositions, surface functional groups, morphologies of the biochars were evaluated by elemental analyzer, FT-IR spectrometer, and SEM analysis. The arsenic and heavy metal adsorption characteristics of the produced biochars were assessed. Additionally, the produced biochars were applied as stabilizing agents to arsenic and heavy metal-contaminated soil with varying mixing ratios of 2, 5 and 10 wt%. After a one-week soil stabilization experiment, soil properties and TCLP(Toxicity Characteristic Leaching Procedure) leaching tests were conducted.Results and Discussion : The pyrochar produced from waste chitosan exhibited a porous structure with high pH (pH 10) and minimal surface functional groups. The hydrochar consisted of spherical particles with functional groups such as hydroxyl and amine groups on the surface, exhibiting a slightly acidic pH of 5.8. Pyrochar has a higher adsorption capacity for cationic heavy metals compared to hydrochar due to its porous structure and high pH. On the other hand, when applied to soil, hydrochar demonstrated superior stabilization efficiency for arsenic and heavy metals. This is attributed to the diverse surface functional groups containing oxygen on the hydrochar. The stabilization efficiency was influenced by the biochar mixing ratio, with a 5% hydrochar application resulting in 10-64% stabilization efficiency for all elements.Conclusion : This study confirmed that biochar produced from waste chitosan effectively stabilizes arsenic and heavy metals in soils. Additionally, the quantity of biochar used can impact its effectiveness in stabilization.

Investigation of the Effect of Temperature on the Biofuel Performance of Hydrochar Obtained from Kidney Bean Shell

In this study, hydrochar products were obtained from kidney bean shell (KBS) biomass at different temperatures using the hydrothermal carbonization (HTC) method. Hydrochar products were produced at three different temperatures (200, 220 and 240 C) and a holding time of 90 minutes. Biomass/water ratio was taken as 1:10. Analysis techniques such as Thermogravimetric analysis (TG), Ultimate analysis and Fourier Transform Infrared Spectroscopy (FTIR) were used in the characterization of raw materials and hydrochar products. In addition, the fuel properties (high heating value, energy yield and energy densification ratio) of raw KBS and hydrochar products were also investigated. As the HTC temperature increases, the high heating value of hydrochar products increases. Among hydrochar products, the highest high heating value belongs to the product obtained at 240 C. The combustion behavior of raw and hydrochar a product was examined using the thermogravimetric analysis method and combustion parameters (Ti, Tb and Tm) were determined. As a result, this study has shown that the hydrochar product produced from KBS by hydrothermal carbonization method can be used as a biofuel material.

Development of hydrothermal carbonaceous carbon/NH2-MIL-101(Fe) composite photocatalyst with in-situ production and activation of H2O2 capabilities for effective sterilization

Photocatalytic production of H2O2 has garnered significant attention, but the use of sacrificial reagents in H2O2 photosynthesis and the subsequent limited H2O2 activation efficiency would impede its practical application in water decontamination. In this work, hydrothermal carbonaceous carbon/NH2-MIL-101(Fe) (abbreviated as HTC-cf/NMIL-101(Fe)) heterojunction was fabricated through a solvothermal strategy, and serving as a self-sufficient photo-Fenton-like catalyst to in-situ generate and activate H2O2. Hydrothermal carbonaceous carbon derived from cost-effective waste coffee grounds, serving as a green and sustainable photocatalyst, demonstrated high H2O2 production rate of 612 μmol/g/h without the need for sacrificial reagents or aeration assistance. Moreover, the excellent self-sufficient photo-Fenton activity for HTC-cf/NMIL-101(Fe) can be obtained, which ascribed to the synergistic effect of self-generated H2O2 production as well as the in-situ catalytic H2O2 decomposition of •OH by Fe species in NMIL-101(Fe) and photogenerated electrons. The optimized HTC-cf/NMIL-101(Fe) photocatalyst showed simultaneous improvements in both H2O2 production and activation capabilities. Impressively, the effective circulation of Fe3+/Fe2+ in NMIL-101(Fe), aided by photogenerated electrons, results in a 5-fold increase toward H2O2 decomposition rate constant (Kd) compared to HTC-cf alone under light irradiation in open-air conditions. The enhanced charge separation and appropriate band structure of HTC-cf/NMIL-101(Fe) photocatalyst assured the high selectivity of two-electron O2-reduction to H2O2. HTC-cf/NMIL-101(Fe) displayed excellent photocatalytic sterilization efficiency against E. coli and S. aureus under visible light, and its sterilization application in actual water was also demonstrated. Notably, the adaptability of this system to ambient conditions, including open-air atmosphere, non-sacrificial reagents, and low leaching of Fe ions, highlights the promising practical utility of the HTC-cf/NMIL-101(Fe) photocatalyst.

Simplified Synthesis of Poly(ethyleneimine)-Modified Silica Particles and Their Application in Oligosaccharide Isolation Methods.

There are great challenges in the field of natural product isolation and purification and in the pharmacological study of oligosaccharide monomers. And these isolation and purification processes are still universal problems in the study of natural products (NPs), traditional Chinese medicine (TCM), omics, etc. The same polymer-modified materials designed for the special separation of oligosaccharides, named Sil-epoxy-PEI and Sil-chloropropyl-PEI, were synthesized via two different methods and characterized by scanning electron microscopy combined with energy spectrum analysis, Fourier transform infrared spectroscopy, thermogravimetric analysis, zeta potential as well as surface area analysis, etc. Several nucleotide/nucleoside molecules with different polarities and selectivities were successfully isolated in our laboratory using stainless-steel columns filled with the synthesized material. In addition, the separation of saccharide probes and oligosaccharides mixtures in water extracts of Morinda officinalis were compared in HILIC mode. The results showed that the resolution of separations for the representative analytes of the Sil-epoxy-PEI column was higher than for the Sil-chloropropyl-PEI column, and the developed stationary phase exhibited improved performance compared to hydrothermal carbon, amide columns and other HILIC materials previously reported.

Hydrothermal Carbonization of Soybean Milk Residue (Okara) for Nutrient and Energy Recovery

Hydrothermal Carbonization of Soybean Milk Residue (Okara) for Nutrient and Energy Recovery

Biochar carbon nanodots for catalytic acetalization of biodiesel by-product crude glycerol to solketal: process optimization by RSM and life cycle cost analysis

Carbon-based nanodots have garnered recent interest for their simple synthesis and versatile utility, ranging from biomedical to (opto) electronic applications, evolving into a tunable and biocompatible material. Here, for the first time, a biochar (lotus leaf) derived carbon nanodots was synthesized through hydrothermal carbonization. The synthesized hollow spherical biochar was engineered via functionalization by grafting –SO3H active sites. The attained catalyst was broadly analyzed by XRD, FTIR, TGA, BET, SEM–EDX, TEM, and XPS analysis after which it was applied for the acetalization reaction of crude glycerol (a biodiesel by-product) to form solketal, a potential fuel additive to valorize the large waste stream generated from biodiesel industry. Employing the RSM-CCD methodology, the experimental matrix was executed, and subsequent data were scrutinized through multiple regressions to model a quadratic equation. Under specific reaction parameters—a reaction duration of 14 min, a molar ratio of 7.5:1, and a catalyst loading of 5.7 wt.%, maximum solketal yield (95.7%) was attained through the ultrasonication method. Finally, to conclude, life cycle cost analysis (LCCA) for solketal production was studied here which determined the overall cost of solketal production per kilogram to be 0.719 USD ($), indicating high commercial applicability.

Low-energy thermo-chemical conversion processes of municipal wet waste

Hydrothermal carbonization (HTC) is a low-energy thermochemical process that converts wet biomass into a carbon-rich solid, commonly called hydrochar, for use in a variety of areas, such as soil amendment, biofuels or to produce carbon-based materials. The purpose of this paper is to increase knowledge for the economic valorization of municipal wet waste, considered as a raw material to obtain high value-added products through an HTC process and an additional chemical activation procedure. In the first part of the work, a 4.5-liter batch reactor was designed, built, and used in the HTC experimental campaign by varying the main process parameters, namely reaction time, amount and type of organic waste (e.g. vegetables, fruits, bread, pasta), water concentration, temperature and pressure. In addition, some experiments were conducted by applying the steam explosion technique at the end of the HTC process. The HTC results showed that in biomass with high water content, increasing residence time decreases the hydrochar yield. Considering a dry heterogeneous waste with high carbon content, the yields at the end of the process are much higher. In the second part of this work, the hydrochar samples were treated with a high-temperature activation process based on the use of KOH, obtaining activated carbon. Particularly, the best results were achieved by using high KOH: hydrochar ratios, resulting in high-quality activated carbons with good porosity and a high surface area of 2890 m2/g. Finally, an energy analysis was carried out to evaluate how to make the whole process cost-effective.