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The urgent need for sustainable waste management strategies has led to the exploration of innovative approaches for the valorization of waste. In this study, a method is proposed for carbonizing waste biomass materials, particularly paper mill waste sludges (primary and biological) and knots, to produce porous carbonaceous supports. Through an initial hydrothermal carbonization followed by carbonization with nitrogen flow, porous carbon materials are successfully generated. The findings of this investigation validate the successful generation of effective carbonaceous supports utilizing waste biomass materials. These materials are then evaluated for their effectiveness as porous supports in the ionic liquid‐catalyzed cycloaddition reaction of CO2 to styrene oxide, achieving a remarkable conversion rate of up to 98% and an impressive selectivity exceeding 99%. Additionally, the results underscore the significant impact of the selected IL on the overall conversion process. Overall, this study presents a promising pathway for the valorization of paper mill waste sludge through the production of porous carbon materials with potential applications in catalysis and beyond. [ABSTRACT FROM AUTHOR]

In this study, the removal of RhB from water by furfural residue (FR) biochar was prepared by hydrothermal carbonization (HTC) and citric acid (CA) modification and named this biochar as CHFR (C refers to citric acid, H refers to hydrothermal carbonization and FR is furfural residue). The CHFR were characterized by SEM, FT-IR and XPS, and CHFR was investigated by the effects of initial concentration, adsorbent dosage, pH, and contact time on the removal of RhB, and the experimental data were analyzed using the adsorption isotherm models, the adsorption kinetic models and thermodynamics, et al. The results showed that CHFR has strong adsorption performance, and the theoretical maximum adsorption capacity of RhB was 39.46 mg·g−1 under the reaction conditions of pH3, the dosage of 1.5 g·L−1, and 120 min contact time, with a removal efficiency close to 100%. the adsorption of RhB by CHFR is spontaneous and endothermic, which is consistent with the Freundlich adsorption, and the isotherm model fits well with the pseudo-second-order model, and the adsorption rate could still be as high as 92.74% after five regenerations, therefore, CHFR is an environmentally friendly and efficient adsorbent with excellent adsorption regeneration performance. [ABSTRACT FROM AUTHOR]

The application of hydrochar as a cost-effective solution has received much attention for the remediation of contaminated water. An economical and environmental approach to enhancing the physicochemical and adsorption performance of hydrochar is essential. In this study, the green technology of ball-milling was firstly employed to improve the adsorption capacity of hydrochar for the typical antibiotics norfloxacin. Aqueous batch adsorption experiment using both pristine and ball milled hydrochar derived from water hyacinth, prepared by hydrothermal carbonization at three temperatures (180, 200, 220 °C) was conducted. The results showed that ball-milling decreased the specific surface area of hydrochar, but still greatly enhanced their performance on the adsorption of norfloxacin. Surface functional groups, aromatization degree, and hydrophobicity of hydrochar were increased after ball-milling, as evidenced by measurements of Boehm titration, Raman spectra, and contact angle, respectively. With these changes, all the ball-milled water hyacinth hydrochar exhibited a better performance on the adsorption of norfloxacin than pristine hydrochar. Ball-milled 220 °C water hyacinth hydrochar showed the greatest norfloxacin adsorption (68.53 mg g−1) compared to unmilled hydrochar (24.29 mg g−1), and the enhancement was effective in a wide pH range (5–9) in aqueous solutions. The thermodynamics study indicated that the norfloxacin adsorption on ball-milled hydrochar was both physically spontaneous and exothermic. Combined physicochemical characterization of hydrochar and batch experiment results suggest that the enhanced adsorption capacity was owing to boosting H-bonds, π-π electron-donor–acceptor, and hydrophobic interaction. This study suggested that ball-milling can be served as a facile, green, and cost-effective method to obtain modified hydrochar for the removal of pollutants in water. Highlights: • Surface functional groups and hydrophobicity of hydrochar were increased after ball-milling. • Ball-milling was firstly used to modify hydrochar (BMHC) to remove antibiotics. • BMHC had a high adsorption capacity of 68.53 mg g-1 for norfloxacin (NOR). • NOR adsorption on BMHC was enhanced by increased H-bonds, π-π EDA, and hydrophobic interaction. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) technology transforms organic biomass components, such as cellulose and lignin, into valuable carbon materials, gases and inorganic salts through hydrolysis, degradation and polymerization, with significant advantages over traditional methods by reducing energy consumption, lowering pollutant emissions and enhancing carbonization efficiency. In the context of global climate change, HTC plays a critical role in water environment management by addressing industrial, agricultural, and domestic wastewater challenges. The application of HTC extends to wastewater treatment, where hydrochar effectively adsorbs heavy metals, organic compounds, and anions, thereby improving water quality. However, challenges remain, such as optimizing the process for diverse raw materials, managing economic costs, and addressing environmental and social impacts. Future research and policy support are essential for advancing HTC technology. By enhancing reaction mechanisms, developing catalysts, and promoting international cooperation, HTC can significantly contribute towards achieving carbon neutrality goals and fostering sustainable development. [ABSTRACT FROM AUTHOR]

This study explores the hydrothermal carbonization (HTC) process applied to the exhausted chestnut produced by the tannin extraction industry, utilizing process water recirculation to enhance the efficiency and sustainability of the conversion process. Tannin extraction from wood typically involves hot water treatment, leaving behind residual wood biomass known as exhausted wood. These by-products maintain their renewable properties because they have only been exposed to hot water under a high pressure, which is unlikely to cause major alterations in their structural components. Hydrothermal treatment was carried out at temperatures of 220 °C and 270 °C for 1 h, with process water being recirculated four times. This investigation focused on analyzing the effects of recirculation on the yield and fuel properties of hydrochar, as well as characterizing the combustion behavior of the obtained hydrochar. The results indicated that recirculation of process water led to improvements in both the mass and energy yields of hydrochar. The mass yield of the hydrochar samples increased by 5–6%, and the ERE of the hydrochar samples increased by 5–8% compared to the HTC reference sample. However, alterations in the combustion characteristics were observed, including decreases in ignition temperature and combustion reactivity. The results indicate that, with PW recirculations, the combustion index decreased by about 14% and 18% for 220 °C and 270 °C, respectively. Overall, this research demonstrates the potential of utilizing HTC on chestnut tannin residue with process water recirculation to produce stable solid fuel and provides insights into the combustion behavior of the resulting hydrochar. [ABSTRACT FROM AUTHOR]

Herein we study the economic performance of hydrochar and synthetic natural gas co-production from olive tree pruning. The process entails a combination of hydrothermal carbonization and methanation. In a previous work, we evidenced that standalone hydrochar production via HTC results unprofitable. Hence, we propose a step forward on the process design by implementing a methanation, adding value to the gas effluent in an attempt to boost the overall process techno-economic aspects. Three different plant capacities were analyzed (312.5, 625 and 1250 kg/hr). The baseline scenarios showed that, under the current circumstances, our circular economy strategy in unprofitable. An analysis of the revenues shows that hydrochar selling price have a high impact on NPV and subsidies for renewable coal production could help to boost the profitability of the process. On the contrary, the analysis for natural gas prices reveals that prices 8 times higher than the current ones in Spain must be achieved to reach profitability. This seems unlikely even under the presence of a strong subsidy scheme. The costs analysis suggests that a remarkable electricity cost reduction or electricity consumption of the HTC stage could be a potential strategy to reach profitability scenarios. Furthermore, significant reduction of green hydrogen production costs is deemed instrumental to improve the economic performance of the process. These results show the formidable techno-economic challenge that our society faces in the path towards circular economy societies. [ABSTRACT FROM AUTHOR]

Hydrochar, a carbonaceous material produced through hydrothermal carbonization of lignocellulosic biomass, has gained significant attention due to its versatile applications in agriculture, energy, and environmental protection. This review extensively explores hydrochar production by hydrothermal carbonization, specifically microwave and supercritical water treatment. These innovative approaches hold substantial promises in enhancing the efficiency and sustainability of hydrochar synthesis. The review commences with an in-depth analysis of the fundamental principles governing hydrochar production, emphasizing the distinct mechanisms of microwave and supercritical water treatment. Insightful discussions on the influence of critical process parameters, such as temperature, pressure, and residence time, underscore these factors' pivotal role in tailoring hydrochar characteristics. Drawing on a wide array of research findings, the review evaluates the impact of different lignocellulosic biomass feedstocks on hydrochar properties, which is crucial for optimizing hydrochar production. The comparative assessment of microwave and supercritical water treatment sheds light on their unique advantages and challenges, guiding researchers toward informed decision-making in selection of methods. Furthermore, the review delves into the myriad applications of hydrochar, spanning soil amendment, carbon sequestration, and renewable energy. Environmental considerations and life cycle assessments associated with microwave and supercritical water treatment are also explored, providing a holistic perspective on the sustainability of hydrochar production. In conclusion, this comprehensive review synthesizes current knowledge on hydrochar production from diverse lignocellulosic biomass sources, emphasizing the efficacy of microwave and supercritical water methods. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) converts wet biomass into hydrochar and a process liquid, but aromatic compounds in the products have been reported as a roadblock for soil applications as they can inhibit germination, plant growth, and soil microbial activity. Here, we compared HTC and hydrothermal humification (HTH) of cow manure digestate while varying the initial alkaline content by adding KOH. HTH converted 37.5 wt% of the feedstock to artificial humic acids (A-HAs) found in both solid and liquid, twice that of HTC. HTH reduced phenolic and furanic aromatic compounds by over 70% in solids and 90% in liquids. The A-HAs in HTH resemble natural humic acids (N-HA), based on FTIR, UV–vis spectra, and CHN and XRD analysis. The HTH liquid possesses 60% higher total organic carbon (TOC) than HTC. Although one-third of TOC can be precipitated as A-HA, a high TOC concentration remains in the liquid, which is shown to be mainly organic acids. Therefore, we also evaluated the HTC and HTH liquids for anaerobic biomethane production, and found that compared to the original cow manure digestate, the HTH liquids increased methane yield by 110.3 to 158.6%, a significant enhancement relative to the 17.2% increase seen with HTC liquid. The strong reduction in organic acids during biogas production from HTH liquid indicates the potential for converting soluble byproducts into methane, while maintaining high A-HAs levels in the solid product. Highlights: Hydrothermal humification of the digestate feedstock created about 37.5 wt% artificial humic acids in both solid and liquid phases. Increasing the alkaline content of the reaction media significantly decreased the aromatic content in the process liquid while increasing the concentration of organic acids and sugars. There was little to no gas production observed in the HTH process at higher alkaline contents, indicating carbon preservation in the liquid and solid phases. Anaerobic processing of the hydrothermal humification (HTH) process liquid resulted in a 158.6% increase in methane production compared to the primary biomass. The organic acid concentrations decreased after the anaerobic fermentation, while the main HTH product, artificial humic acids, remained nearly unchanged. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) has emerged as a pivotal technology in the battle against climate change and fosters circular economies. Operating within a unique reaction environment characterized by water as a solvent and moderate temperatures at self-generated pressures, HTC efficiently converts biomass residues into valuable bio-based products. Despite HTC's potential—from the management of challenging biomass wastes to the synthesis of advanced carbons and the implementation of biorefineries—it encounters hurdles transitioning from academic exploration to industrial implementation. Gaps persist, from a general comprehension of reaction intricacies to the difficulty of large-scale integration with wastewater treatments, to the management of process water, to the absence of standardized assessment techniques for HTC products. Addressing these challenges demands collaboration to bridge the many scientific sectors touched by HTC. Thus, this article reviews the current state of some hot topics considered crucial for HTC development: It emphasizes the role of HTC as a cornerstone for waste management and biorefineries, highlighting potentialities and challenges for its development. In particular, it surveys fundamental research aspects, delving into reaction pathways, predictive models, analytical techniques, and HTC modifications while exploring HTC's crucial technological applications and challenges, with a peculiar focus on combined HTC, wastewater integration, and plant energy efficiency. [ABSTRACT FROM AUTHOR]

Recently, bi-functional electrocatalytic materials have the potential for both the hydrogen evaluation reaction (HER) and oxygen evaluation reaction (OER) in the alkaline medium. In the present investigation, the cobalt sulfide/cobalt oxide hanged on the nitrogen-doped activated carbon nanosheets (CoS/CoO@NAC) as nanocomposites were synthesized through the hydrothermal and then the carbonization processes. The X-ray diffraction peaks observed in the CoS/CoO@NAC nanocomposites revealed the presence of CoS, CoO, and N-doped activated carbon nanosheets which confirmed the formation of binary nanocomposites. The BET analysis of CoS/CoO@NAC nanocomposites resulted an enhancement of the surface area of about 1038.57 m2/g along with the pore size and pore volume of 3.23 nm and 0.442 cc/g, respectively. The CoS/CoO@NAC, nanocomposites were used for bi-functional catalysis which divulged the low over potential for both HER and OER analyses at about −0.266 V and 0.199 V vs. RHE, respectively at 10 mA/cm2 current density in the alkaline medium. [Display omitted] • CoS/CoO@NAC nanocomposites synthesized by hydrothermal and carbonization processes. • CoS/CoO@NAC nanocomposites showed an enhancement of surface area of 1038.57 m2/g. • HER analysis of CoS/CoO@NAC shows an overpotential of −0.266 V. • OER analysis of CoS/CoO@NAC shows an overpotential of 0.2654 V. • CoS/CoO/NAC suitable for the bi-functional electrocatalyst in an alkaline medium. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) has recently emerged as a promising technology for converting diverse forms of waste with a high moisture content into value-added products such as biofuel, biochar, and activated carbon. With an increasing demand for sustainable and carbon-neutral energy sources, HTC has attracted considerable attention in the literature. However, a successful transition from laboratory-scale to large-scale industrial applications entails notable challenges. This review critically assesses the upscaling of hydrothermal carbonization processes, emphasizing the challenges, innovations, and environmental implications associated with this transition. The challenges inherent in upscaling HTC are comprehensively discussed, including aspects such as reactor design, process optimization, and the current treatment technology for process water. This review presents recent innovations and technological advancements that address these challenges and explores integrated solutions to enhancing hydrothermal carbonization's scalability. Additionally, this review highlights key companies that have developed and implemented HTC plants for commercial purposes. By overcoming the obstacles and achieving advancements in the upscaling of hydrothermal carbonization, this review contributes to the ongoing efforts to realize the full potential of HTC as a sustainable and scalable biomass conversion technology and proposes future directions. [ABSTRACT FROM AUTHOR]

[Display omitted] • Carbon-rich and low-ash hydrochars is prepared innovatively from sewage sludge. • Hydrochar produced from sludge alkaline hydrolysate showed nanoparticle structure. • Multilayer microsphere structure was formed from sludge alkali-thermal hydrolysate. • Hydrochar with carbon content over 70% and ash content less than 5% was realized. • Hydrolysis temperature is an important factor to influence the hydrochar formation. The production of carbon-rich and low-ash hydrochar from sewage sludge is attracting interest due to its great application prospect in high value-added carbon materials fields, but which is impossible through direct hydrothermal carbonization. In this study, alkali-thermal hydrolysis followed by acid-assisted hydrothermal carbonization was thus proposed. Thermal hydrolysis at strong alkaline environment was more effective than acid one to promote the dissolution of organic matters and restrain the release of inorganic matters from sludge, which created a favorable condition for hydrochar formation in a carbon-rich and low-ash way. Alkali-thermal hydrolysis began to show a positive effect on the dissolution of organics in sludge when temperature exceeded the threshold of 90 °C, and an increase of 9.77 % was found at 150 °C when compared to 30 °C. Acid-assisted hydrothermal carbonization of alkali-thermal hydrolysate (ATH) at pH 1.0 strongly promoted condensation polymerization of dissolved organics to form hydrochar and meanwhile inhibited introduction of dissolved inorganics. The nanosized microparticulate hydrochar derived from ATH-30 had a carbon and ash content of 50.98–61.31 % and 10.76–12.09 %, while the micro-sized microspheric hydrochar with multiple deposition layers formed from ATH-150 showed a better performance in carbon-rich and low-ash aspect where a carbon and ash content of 58.24–70.07 % and 0.40–3.24 % was realized, both of which were obviously superior to the direct hydrochar (carbon 34.86 % and ash 46.11 %). The condensation of dissolved organics during alkali-thermal hydrolysis stage is important to the carbonization degree of hydrochar. This study provides a new perspective in sludge disposal and production of advanced carbon materials. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) has developed considerably over the last 15 years and offers a viable alternative for the utilization of municipal and industrial organic waste such as sewage sludge. However, the technology has yet to establish itself as a valorization process for waste biomasses (2024) and is not yet a recognized state of the art. Nevertheless, the HTC technology could gain greater relevance in the future, especially as an alternative valorization pathway for sewage sludge. During HTC, significant amounts of HTC process water (PW) are produced as a byproduct. The process water is inorganically and organically polluted and has to be treated, as it would be a burden on water bodies and thus on the environment if left untreated. In the EU and specifically Germany, industrial wastewater producers like HTC-plant operators are obliged to treat their industrial wastewater before discharging it into the environment. In addition to a large amount of PW and its treatment to the required limits, the organic load and possible persistent and toxic substances pose major challenges for plant operators. Many proven processes from industrial wastewater treatment were transferred for the treatment of PW. Treatment of the PW in a manner that is industrially viable, economically viable, and efficient is crucial for the effective commercialization of HTC technology. In this, the challenges and opportunities of PW composition, management, and treatment, including legal aspects, are mainly discussed. Therefore, the legal framework in the European Union and specifically for Germany will be elaborated. Furthermore, different treatment pathways are also highlighted. [ABSTRACT FROM AUTHOR]

[Display omitted] • The effect of thermal hydrolysis on sludge hydrochar properties was investigated. • The nitrogen and sulfur content in hydrochars decreased significantly. • Hydrochar thermal decomposition stability was improved. • The driving mechanism of thermal hydrolysis was elucidated. Hydrothermal carbonization of waste activated sludge suffers from a low degree of carbonization caused by limited hydrolysis of carbohydrates and proteins, resulting in a high nitrogen content in hydrochar. Thus, it is hypothesized that thermal hydrolysis could destroy the stable floc structure of waste activated sludge, leading to higher degree of carbonization and high quality hydrochar with low nitrogen content by improving the solubilization and hydrolysis of organic matter. In the current study, thermal hydrolysis at 90 °C, 125 °C, and 155 °C was performed prior to hydrothermal carbonization to obtain low-nitrogen-content hydrochar. Thermal hydrolysis greatly improved the hydrolysis of sewage sludge. The nitrogen and sulfur content in hydrochars obtained after thermal hydrolysis decreased to 1.5–1.6 % from 1.7 %, and to 0.4 % from 0.5 %, respectively, depending on the hydrolysis conditions. Thermal decomposition stability of hydrochars obtained after thermal hydrolysis were also improved. Thermal hydrolysis at 90 °C and 125 °C promoted hydrolysis, dehydration, and the Diels-Alder reaction during hydrothermal carbonization, resulting in lower hydrochar yield but higher H/C and O/C atomic ratio. The Maillard reaction occurred during thermal hydrolysis at 155 °C, leading to the formation of large molecular refractory compounds that were retained in the hydrochar and increased the hydrochar yield. Furthermore, thermal hydrolysis can accelerate pyrolysis reaction of hydrochars, resulting in reduced energy consumption. The newly established thermal hydrolysis-hydrothermal carbonization process using sewage sludge as the feedstock has the potential to contribute to the development of the hydrothermal carbonization industry. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) is a thermochemical conversion technology to produce hydrochar from wet biomass without drying, but it is time-consuming and expensive to experimentally determine the optimal HTC operational conditions of specific biomass to produce desired hydrochar. Therefore, a machine learning (ML) approach was used to predict and optimize hydrochar properties. Specifically, biochemical components (proteins, lipids, and carbohydrates) of biomass were predicted and analyzed first via elementary composition. Then, accurate single-biomass (no mixture) based ML multi-target models (average R2 = 0.93 and RMSE = 2.36) were built to predict and optimize the hydrochar properties (yield, elemental composition, elemental atomic ratio, and higher heating value). Biomass composition (elemental and biochemical), proximate analyses, and HTC conditions were inputs herein. Interpretation of the model results showed that ash, temperature, and the N and C content of biomass were the most critical factors affecting the hydrochar properties, and that the relative importance of biochemical composition (25%) for the hydrochar was higher than that of operating conditions (19%). Finally, an intelligent system was constructed based on a multi-target model, verified by applying it to predict the atomic ratios (N/C, O/C, and H/C). It could also be extended to optimize hydrochar production from the HTC of single-biomass samples with experimental validation and to predict hydrochar from the co-HTC of mixed biomass samples reported in the literature. This study advances the field by integrating predictive modeling, intelligent systems, and mechanistic insights, offering a holistic approach to the precise control and optimization of hydrochar production through HTC. Highlights: Biochemical components of biomass were first predicted by elemental composition. The multi-target ML model accurately predicted hydrochar with R2 = 0.93. The ash, T, N, and C were the most critical factors affecting hydrochar properties. An online intelligent system based on optimal models was posted and verified. [ABSTRACT FROM AUTHOR]

[Display omitted] • Solvent recirculation is a feasible strategy to valorize the HTC aqueous waste. • HTC moderate temperatures favor additional hydrochar formation during recirculation. • HTC of blended biomasses enhances hydrochar recovery at 180 °C. • Process water recirculation promotes dehydration and decarboxylation reactions. • A significantly higher energy recovery is achieved by process water recirculation. This study aims at valorizing the residual aqueous phase from hydrothermal carbonization (HTC) of Sicilian agro-wastes in order to enhance the hydrochar recovery, positively affecting the process energy balance. Process waters (PW) obtained from HTC and co-HTC using orange peel waste and fennel plant residues were used as recycled solvent in experiments carried out at the temperatures of 180 and 230 °C. The results showed that an additional hydrochar formation was promoted during recirculation of solvent, leading to average increments of solid mass yield of 10.5 wt% for tests conducted at 180 °C and 3.9 wt% for 230 °C. After five consecutive recirculation phases in co-HTC runs, the hydrochar yield increased up to 18.2 wt%. The low H/C and O/C atomic ratios values, found after recirculation, indicate that organic acids, accumulated in the PW, may catalyze the process and promote the biomass deoxygenation by boosting dehydration and decarboxylation. The recovered PWs from conversion steps with deionized water were also carbonized in absence of the solid feedstock in order to quantify their contribution in hydrochar formation during recirculation and thus the synergistic interactions. After recirculation, energy recovery averagely augmented by more than threefold, showing that the proposed strategy could significantly improve the sustainability of HTC. [ABSTRACT FROM AUTHOR]

[Display omitted] • A new strategy for using waste cork. • PC4-800 exhibits excellent pore structure and abundant N-containing groups. • PC4-800 has ultra-high toluene capture of 867.03 mg/g. • Pores with sizes of 1.71–2.28 nm are most effective for adsorption. • N-6 had the strongest affinity for toluene through Gaussian imitating. Converting waste resources into porous carbon for pollutants capture is an effective strategy to achieve the environmental goal of "treating waste with waste". Cork is an ideal precursor of porous carbons due to its ordered honeycomb-like cell structure and layered composition distribution. Herein, N-doped porous carbons (PCs) were prepared via two steps of urea-assisted hydrothermal carbonization and chemical activation to mitigate volatile organic compounds (VOCs) pollution. Results indicated that the obtained PC4-800 exhibited remarkable features for adsorption including high total pore volume (0.97 cm3/g) and specific surface area (1864.89 m2/g), as well as abundant N-containing functional groups. The excellent pore structure was primarily owing to the corrosion of the carbon matrix by the gas produced from the reaction of K 2 CO 3 and N-containing functional groups. The adsorption results showed that the PC4-800 have an outstanding toluene adsorption capacity (867.03 mg/g) that outperforming majority of adsorbents previously reported. There are substantial pores in N-doped PCs with a pore width of 1.71–2.28 nm, which is 3 to 4 times the molecular dynamic diameter of toluene, and plays a crucial role in the absorption process. Moreover, the promotional influence of N-functional groups on the toluene adsorption process was verified through DFT calculation by Gaussian imitating, where N-6 generated π-electron enrichment sites on the surface of N-doped PCs, facilitating π-π dispersion with the benzene ring in toluene. This study provides a new strategy to convert waste cork into high-performance adsorbents for VOCs removal. [ABSTRACT FROM AUTHOR]

The present study aims to test several conditions of the thermochemical pretreatment of torrefaction and carbonization to improve the physical and combustible properties of the Portuguese RDF. Therefore, two different types of RDF were submitted alone or mixed in 25%, 50%, and 75% proportions to dry carbonization processes in a range of temperatures between 250 to 350 °C and residence time between 15 and 60 min. Hydrothermal carbonization was also carried out with RDF samples and their 50% mixture at temperatures of 250 and 300 °C for 30 min. The properties of the 51 chars and hydrochars produced were analyzed. Mass yield, apparent density, proximate and elemental analysis, ash mineral composition, and higher heating value (HHV), among others, were determined to evaluate the combustion behavior improvement of the chars. The results show that after carbonization, the homogeneity and apparent density of the chars were increased compared to the raw RDF wastes. The chars and hydrochars produced present higher HHV and lower moisture and chlorine content. In the case of chars, a washing step seems to be essential to reduce the chlorine content to allow them to be used as an alternative fuel. In conclusion, both dry and wet carbonization demonstrated to be important pretreatments of the RDF to produce chars with improved physical and combustion properties. [ABSTRACT FROM AUTHOR]

The removal of lead metals from wastewater was carried out with carbon microspheres (CMs) prepared from date palm leaflets using a hydrothermal carbonization process (HTC). The prepared CMs were subsequently activated with phosphoric acid using the incipient wetness impregnation method. The prepared sample had a low Brunauer–Emmet–Teller (BET) surface area of 2.21 m2·g−1, which increased substantially to 808 m2·g−1 after the activation process. Various characterization techniques, such as scanning electron microscopy, BET analysis, Fourier transform infrared, and elemental analysis (CHNS), were used to evaluate the morphological structure and physico-chemical properties of the CMs before and after activation. The increase in surface area is an indicator of the activation process, which enhances the absorption properties of the material. The results demonstrated that the activated CMs had a notable adsorption capacity, with a maximum adsorption capacity of 136 mg·g−1 for lead (II) ions. This finding suggests that the activated CMs are highly effective in removing lead pollutants from water. This research underscores the promise of utilizing activated carbon materials extracted from palm leaflets as an eco-friendly method with high potential for water purification, specifically in eliminating heavy metal pollutants, particularly lead (II), contributing to sustainability through biomass reuse. [ABSTRACT FROM AUTHOR]

Four deciduous woody feedstocks (Casuarina equisetifolia L., Eucalyptus globulus, Wrightia tinctoria, and Neolamarika cadamba) were subjected to the Hydrothermal Carbonization (HTC) process inside a 50 mL stainless steel hydrothermal reactor at varying temperatures (180°C, 215°C, and 250°C), while keeping water-to-feedstock ratio (6:1 v/w%) and residence time (1.5 h) constant. The mass yield and energy yield of the resulting biomass were calculated as parameters for energy intensification. Characterization of the biomass, biochar, and bio-oil was conducted using elemental analysis, SEM, and GC-MS. Interestingly, the mass yield of biochar decreased with increasing temperature, but it significantly improved the energy densification ratio, with a minimum of 1.06 observed for Neolamarika cadamba biomass at 180°C and a maximum of 1.23 observed for Eucalyptus globulus biomass at 250°C. Moreover, detailed analysis of the bio-oil obtained at 250°C using GC-MS revealed the presence of a diverse range of fine chemicals, including benzyl, carboxylic acid, ester, methyl, phenol, pyrrole, nitro, and aliphatic hydrocarbons. These findings suggest that the HTC process can be optimized to tailor the production of specific value-added chemicals from lignocellulosic woody biomass. [ABSTRACT FROM AUTHOR]

A key factor restricting the application of biochar in the steel industry is its high-quality upgrading. This paper evaluated the characteristics of hydrochar produced by HTC (hydrothermal carbonization) process of corncob to be used as a solid fuel. HTC temperatures (240–300 °C) and HTC water-reused times (1–3 times) were examined for their effects on hydrochar yield, physicochemical characteristics, and combustion properties. The results showed hydrochar yields, O/C, and H/C parameters decreased as HTC temperature and water-reused times increased, while its high heating value increased. Due to dehydration and decarboxylation, hydrochar showed similar characteristics to those in bituminous coal. The removal efficiency of alkali metal K reached 99% after HTC treatment. Carbonaceous hydrochar had become more compact, orderly, and stable with increasing amounts of aromatic functional groups, C = C, and C = O. Hydrochar, as a biofuel, has higher ignition energy and is more stable than corncob due to its high carbonaceous order degree. To calculate combustion kinetic parameters, the Kissinger–Akahira–Sunose (KAS) and Flynn–Wall–Ozawa (FWO) methods were applied. The results revealed that Eα (average activation energy) was quite similar between the two models. HC-300 had an Eα of 262 kJ/mol. HTC could be an efficient way to reutilize corncob biomass into clean biofuels with high calorific value. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) solid and liquid products may inhibit seed germination, necessitating post-treatment. The hydrothermal humification (HTH) method addresses this drawback by transforming inhibitory compounds, such as aromatics, into artificial humic acids (AHAs) and artificial fulvic acids (AFAs). This study introduces a novel approach by investigating the substitution of the commonly used alkaline agent in HTH, KOH, with hydrated lime to develop cost-effective hydrothermal fertilizers from sugar beet pulp, enriching them with AHAs. It assesses the effects of lime on AHA production and soluble organic compounds compared to KOH. The results indicate that lime significantly reduces furans (from 560 to 3.15 mg/kg DM in solid and from 344 to 3.86 mg/L in process liquid) and boosts sugars and organic acids, especially lactic acid (from 4.70 to 65.82 g/kg DM in solid and from 4.05 to 22.89 mg/L in process liquid), increasing hydrochar yield (68.8% with lime vs. 27.4% with KOH). Despite the lower AHA production with lime compared to KOH (3.47% vs. 15.50%), lime-treated hydrothermal products are abundant in calcium and magnesium, boasting a pH of 7. This property presents a safer and more efficient alternative to hydrothermal fertilizers. The characterization of AHAs aligns with standard and natural humic substances, while lime-assisted HTH products, applied at a level of 0.01% w/w, could significantly enhance wheat growth and nutrient uptake compared to the control group. Importantly, these products show no toxicity on Daphnia magna, underscoring their potential for sustainable agriculture. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) of sawdust for producing hydrochar was optimized using response surface methodology (RSM). After optimization, the combustion behaviour and other relevant fuel properties of hydrochar that was obtained at the optimized conditions were studied. Additionally, the aqueous phase obtained at the optimized conditions was recycled as the reaction medium for producing hydrochar and the influence of the aqueous phase recycling on the hydrochar yield and properties was evaluated. The results indicated that the highest hydrochar yield of 84.23 wt.% under the predicted optimum conditions of temperature of 162.23°C, 2.51 h, feedstock loading of 10.71 wt.%, and catalyst loading of 7.99 wt.%. Furthermore, it was found that the use of recycled aqueous phase as the reaction medium led to an increase in the hydrochar yield, higher heating value (HHV), and energy yield, and difference in combustion behaviour was minor. Overall, this study filled the gap in HTC literature regarding the effect of catalyst on hydrochar production and provided a practical solution to treat the aqueous phase. [ABSTRACT FROM AUTHOR]

• Microalgae and sewage sludge were converted into hydrochars at three temperatures. • High addition of sewage sludge affected formation and composition of secondary char. • Less sewage sludge led to higher C retainment and fixed C in hydrochars. • Presence of toxic compounds in microalgae may limit potential utilization. The role of microalgae cultivation in wastewater treatment and reclamation has been studied extensively, as has the potential utility of the resulting algal biomass. Most methods for processing such biomass generate solid residues that must be properly managed to comply with current sustainable resource utilization requirements. Hydrothermal carbonization (HTC) can be used to process both individual wet feedstocks and mixed feedstocks (i.e., co-HTC). Here, we investigate co-HTC using microalgae and digested sewage sludge as feedstocks. The objectives were to (i) study the material's partitioning into solid and liquid products, and (ii) characterize the products' physicochemical properties. Co-HTC experiments were conducted at 180–250°C using mixed microalgae/sewage sludge feedstocks with the proportion of sewage sludge ranging from 0 to 100 %. Analyses of the hydrochar composition and the formation and composition of secondary char revealed that the content of carbonized material in the product decreased as the proportion of sewage sludge in the feedstock increased under fixed carbonization conditions. The properties of the hydrochars and the partitioning of material between the liquid phase and the hydrochar correlated linearly with the proportion of microalgae in mixed feedstocks, indicating that adding sewage sludge to microalgae had weak or non-existent synergistic effects on co-HTC outcomes. However, the proportion of sewage sludge in the feedstock did affect the secondary char. For example, adding sewage sludge reduced the abundance of carboxylic acids and ketones as well as the concentrations of higher molecular weight cholesterols. Such changes may alter the viable applications of the hydrochar. [ABSTRACT FROM AUTHOR]

• In-situ formation of MgFe 2 O 4 enhancing the dehydration and decarboxylation of SM. • Stabilization of HMs was obviously increased after MgFe 2 O 4 modified HTC. • P retention rate reached 88% due to the decrease of soluble and exchangeable P. • MFHCs exhibited high Pb(II) and Cu(II) adsorption capacity without any HMs leaching. Hydrothermal carbonization is an efficient technique for the disposal of livestock manure, enabling its harmless treatment, quantity reduction, and resourceful utilization. Co-hydrothermal of modified materials facilitates the production of more valuable carbonaceous materials. However, further exploration is needed to understand their potential impact on the environmental risks associated with livestock manure disposal and the application of products derived from it. Therefore, the carbonization degree, heavy metals stabilization, and phosphorus retention during the hydrothermal treatment of swine manure were systematically investigated in this study under the influence of in-situ formed MgFe 2 O 4. The results revealed that the in-situ formation of MgFe 2 O 4 improved the dehydration and decarboxylation of organic components in swine manure, thereby improving its carbonization degree. Furthermore, both hydrothermal carbonization and MgFe 2 O 4 modified hydrothermal carbonization resulted in an enhanced stabilization of heavy metals, leading to a significant reduction in their soluble/exchangeable fraction and reducible fraction. Phosphorus was predominantly retained in the hydrochars, with the highest retention rate reaching 88%, attributed to the significant decrease in soluble and exchangeable phosphorus fractions facilitated by the in-situ formation of MgFe 2 O 4. Moreover, MgFe 2 O 4 modified hydrochars exhibited remarkable adsorption capacity for Pb(II) and Cu(II) without any leaching of heavy metals. Overall, the findings indicated that the in-situ formation of MgFe 2 O 4 positively influenced the hydrothermal of swine manure, improving certain economic benefits in its practical application. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) is a thermochemical conversion method to upgrade the raw biomass into carbon-rich material, which is known as hydrochar. This commentary will focus on the applications of hydrochar in wastewater treatment. Hydrochar has been widely used as an adsorbent for the removal of water pollutants; however, owing to its poor porous texture and small surface area, it is usually converted through an activation process, which yields an activated carbon with superior physicochemical properties and adsorption capacities. While HTC is proven to be beneficial, the current limitations of HTC as a pretreatment prior to activated carbon production are also incorporated to provide insight into its usage during the activation process. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) is a proven cost-effective and energy-efficient method for waste management and value-added product recovery. There are, however, several issues that require further improvement or research. Identifying the strengths and weaknesses of HTC in comparison to traditional pyrolysis is crucial for scientists to choose between them or use both (complementary) to achieve specific product properties. Additionally, sharing information on diverse modeling approaches and scales is crucial to enhance the robustness and universality of HTC process models. In addition, the study on the applicability of hydrochars on target applications such as soil amendment is crucial to give back nutrients to soils and face the dependence on finite specific feedstocks in this field. Also, proper management of the process by-products, especially process water, must be addressed to improve the carbon and hydric footprint of the process. Reviewing the suitability of HTC to treat specific challenging wastes, whose strength is not related to their calorific value but to their nutrient composition (i.e., manures), is also an appealing topic for HTC research. This paper aims to tackle the above-mentioned issues through an updated review and discussion of research gaps that require further investigation. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) has the potential to be a sustainable and environmentally beneficial approach for organic waste treatment. It is likely that HTC product use will dictate the viability of large-scale HTC facilities; therefore, understanding the viability and environmental implications associated with HTC product valorization pathways is critical. The overall goal of this review is to gain an understanding of how HTC product valorization is currently being modeled in life cycle assessment studies, and to use such information to assess current research and/or data needs associated with product valorization. To accomplish this, a review of existing HTC literature was conducted and used to assess the current state of knowledge surrounding the environmental implications of HTC product use. From this review of the literature, it is clear that potential exists for HTC product valorization. To realize this potential in a full-scale application, research gaps and data needs were identified that included a system-level integration to evaluate location-specific information as well as more extensive characterization of the impact of HTC product properties on valorization impacts. [ABSTRACT FROM AUTHOR]

Novel copper-carbon dots doped magnetic biochar (CDMBC) was synthesized and applied for the remediation of congo red (CR) dye from an aqueous system. Copper doped carbon dots (Cu@CDs) were prepared by hydrothermal carbonization at 180 °C for 8 h using Ascorbic acid, urea, and copper chloride as precursors, and biochar was synthesized through pyrolysis of rice husk at 600 °C. The synthesized biochar was doped with Cu@CDs using the hydrothermal route at 150 °C for 4 h. The surface functionality and morphology of the as-synthesized CDMBC were analyzed using FESEM, XRD, RAMAN, FTIR, BET, and EDS studies. The as-synthesized CDMBC showed good adsorptive ability for the removal of CR dye in the shortest time of 10 min. The adsorption experiments were performed at different catalyst dosages, pH, initial concentrations, temperature, and contact time to determine the effect of different parameters on the removal rate. The kinetic and isothermal studies were evaluated at 20 mg L−1 of CR concentration, 10 min contact time, pH-6.0, and 27 °C of temperature with 100 mg of catalyst dosage. The reaction followed second-order kinetics with an R2 value of 0.992. The maximum adsorption capacity was observed to be 437.4 mg g−1 at 100 mg of catalytic dose for the removal of 20 mg L−1 of CR dye. The CDMBC exhibited excellent regeneration ability up to 5 cycles when treated with 0.1 M NaOH, showing removal of 90.1% after 5 cycles. These findings indicated that the CDMBC can be used as a potential catalyst in the removal of dyes from contaminated water. Highlights: Synthesis of copper carbon dots (Cu@CDs) through hydrothermal route and doping of Cu@CDs on magnetic biochar for the synthesis of copper carbon dots doped magnetic biochar (CDMBC). Morphological and surface functionalization of CDMBC using FESEM, EDS, Raman, XRD, FTIR, and BET studies. Kinetic and isothermal studies for the removal of CR dye. Regeneration studies and proposed mechanism for the removal of CR dye. [ABSTRACT FROM AUTHOR]

Anaerobic digestion is the mainstream method for energy conversion of food waste, but dewatering and resource utilization of its digestate is the downstream technical obstacle. In this study, an energy and resource utilization scheme via the integrated process of anaerobic digestion and hydrothermal carbonization of food waste is proposed, among which the hydrothermal carbonization not only is used to remove water from digestate in a non-phase change manner with low energy consumption but also convert digestate into hydrochar. Moreover, the scheme has the least environmental impact compared to the anaerobic digestion and composting treatment by life cycle assessment. In particular, it has a lower impact potential (−141.46 kg CO 2 eq) than anaerobic digestion (−38.87 kg CO 2 eq) for the global warming category, indicating that the addition of hydrothermal carbonization can bring better environmental benefits. This study provides a reference for the development of disposal technology for food waste. • An energy and resource utilization scheme of food waste is proposed. • Hydrothermal carbonization converts the digestate into hydrochar. • The treatment scheme has a lower global warming potential (−141.46 kg CO 2 eq). • Shortening transportation distance can reduce the environmental burden. [ABSTRACT FROM AUTHOR]

[Display omitted] • Theoretical assessment of HTC integration to a biogas plant treating sewage sludge. • HTC as efficient dewatering technology more than halves the solid product volume. • HTC integration replaces hygienization without major increase in energy consumption. • Integration improves ammonium nitrogen, phosphorous and carbon recovery. In recent years, extensive experimental research on hydrothermal carbonization (HTC) of sewage sludge has been performed, to study the effects of process conditions on hydrochar characteristics and nutrient, carbon, and energy recovery from sewage sludge. To promote the implementation of HTC, this study assessed HTC (230 °C, 30 min) integration into an advanced centralized biogas plant by analyzing its theoretical effects on the fates of sewage sludge solids, nitrogen, phosphorus, and carbon. The study used the mass and nutrient flows and concentrations obtained from laboratory studies, and the studied biogas plant had an original layout that employed hygienization. HTC integration decreased the solid product volume by up to 56 % and, increased the recovery of ammonium in ammonia water by 33 % and methane by 1.4 %, while increasing the biogas plant energy demand by 4 %. The changes in the nutrient and solids flows and their recovery potentials show the need to consider the rearrangements of the liquid and gas flows in the biogas plant and the re-dimensioning of stripping process. [ABSTRACT FROM AUTHOR]

The objective of this project was to develop a new bioproduct that will utilize agricultural waste and modify the product to increase its present adsorption capacity. After the hydrothermal carbonization of corn silk, a novel hydrochar was generated and treated using sulfuric acid to boost its adsorption capacity. FT‐IR, SEM–EDX, TGA, and BET surface analysis studies were used to analyze the structure of the produced biosorbents. According to the EDX analysis results, there are C, H, and N elements in the hydrochar structure, and the treated hydrochar contains S in addition to these elements. While the presence of several functional groups was indicated by FT‐IR data, post‐adsorption EDX analysis proved that Cr ions were adhering to hydrochar. The proper parameters for the adsorption processes for both biosorbents were established. By analyzing the outcomes of kinetics tests at various concentrations and isotherm experiments, the adsorption procedure was identified. The pseudo‐second‐order kinetic model was shown to be consistent with the kinetic pathways of adsorptions. Although the results of the isotherm experiments also suited the Langmuir isotherm, the Freundlich isotherm had higher R2 values and was more consistent with the results. The outcomes demonstrated that sulfuric acid‐modified hydrochar offered greater Cr(VI) adsorption capacity. qm values defining the maximum adsorption capacities of HC and THC at a temperature of 333 K were estimated to be 263.16 and 294.12 mg g−1, in that order. Based on the qm values, the adsorption capabilities of HC and THC were compared with those of a few other adsorbents. THC (29.11 m2 g−1) had a 29% larger surface area than HC (22.57 m2 g−1), according to the surface area of BET test results. [ABSTRACT FROM AUTHOR]

Currently, heavy metal pollution is a challenge that needs to be solved urgently, and there is a broad prospect for food waste(FW) utilization. In this paper, activated hydrochar (AHC) made from FW according to actual proportion was produced by hydrothermal carbonization (HTC) and activated with K2CO3. The effects of the AHC on Cu(II) adsorption were investigated using static adsorption experiments. The results indicated that the sample fabricated at 160°C (FW-160) for 6 h had the best adsorption performance with the maximum adsorption amount of Cu(II) (36.77 mg/g). The oxygenated functional group on the surface of FW-160 was observed. The pseudo-second-order kinetic model fitted the experimental results better, which proved that chemisorption was the main adsorption mechanism, and the surface complexations, including oxygenated functional groups, were the predominant factors in hydrochar(HC) sorption for Cu(II). The adsorption amount of the sample simulating rotten FW with Aspergillus niger (FW-160A) was 24.82 mg/g. Through the HTC process, the rotten FW can be made into heavy metal absorbents which can be stored for long term, and finally realize the reduction of volume and cost of storage. [ABSTRACT FROM AUTHOR]

In this study, we have successfully synthesized a high surface area of activated carbons (ACs) from cocoa pod husk (CPH) by using a combination of hydrothermal carbonization (HTC) and chemical activation in the presence of ZnCl2 as both of catalyst as well as activating agent. During HTC, the effect of HTC temperature (200 and 225℃) and ZnCl2 to biomass mass ratio (1:1, 2:1, 3:1) as a catalyst to the characteristics of the obtained hydrochar (HC) and ACs were investigated. The obtained hydrochar (HCs) was then processed by using ZnCl2 chemical activation with a fixed HC to ZnCl2 mass ratio of 1:4 and the mixture was pyrolyzed at 600 ℃ for 1 h under an inert atmosphere. The results showed that the addition of catalyst during HTC presented different AC morphology, where the carbon samples were decorated with carbon microspheres. An increase of surface area was observed, where the ACs synthesized from catalyzed HC at biomass to ZnCl2 ratio of 1:3 at temperature 200 ℃ gave a higher surface area of 1954 m2/g compared to that of without catalyst (1165 m²/g). The catalysis effect was more profound at the HTC temperature of 200 ℃ compared to 225 ℃, as reflected in the significant increase of AC surface area. The addition of a catalyst creates ACs with narrow pore distribution compared to that of synthesized in the absence of a catalyst. It was also observed that the ACs from catalyzed hydrochar possessed higher oxygenated functional groups (OFG) than those without catalysts. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Napier grass is a herbaceous biomass that can be used as biofuel; however, its high ash, potassium, sulfur and chlorine content may cause problems when combusted. Napier grass was submitted to vapothermal carbonization (VTC) and hydrothermal carbonization (HTC) processes at 190 and 220 °C to compare their ability to enhance its fuel properties. The different water distribution between phases in the two processes was verified: up to 14.5% of the water vaporized to steam in the VTC ran at 220 °C, while over 99% of the water remained in the liquid state and in contact with the solids during all HTC runs. Both processes improved the calorific value of the Napier grass (up to 20.6% for VTC220 and up to 29.8% for HTC220) due to the higher C content in the chars. Both processes reduced the sulfur content, removing up to 15.3% of it with VTC190 and 28.5% of it with HTC190 compared to that of Napier grass. In contrast, the two processes had different effects on the ash and chlorine content. While HTC removed both ash and Cl from the Napier grass, VTC concentrated it in the chars (ash: 5.6%wt. Napier grass, 3.3%wt. HTC chars, 7.1%wt. VTC; chlorine: 1.08%wt. Napier grass, 0.19%wt. HTC chars, 1.24%wt. VTC). Only the HTC process leached high percentages of Cl (up to 80%), S (up to 70%), sodium (Na, up to 80%) and potassium (K, up to 90%) into the process water. This may prevent fouling and slagging problems when burning HTC char. The biofuel qualities of the raw Napier grass, VTC, and HTC chars were evaluated using two standards: the international standard for solid biofuels, EN ISO 17225, and the Korean regulation for biomass solid recovered fuels (Bio-SRF). Napier grass and VTC chars presented problems regarding Cl content thresholds for both EN ISO 17225 and Bio-SRF. Both VTC and HTC chars along with the Napier grass fulfilled the requirements for heavy metals (Pb, Ni, Cr, and Cd) except for copper. The choice of process in practical applications will depend on the goal; HTC improves fuel quality and VTC has higher high solid, carbon and energy yields. [ABSTRACT FROM AUTHOR]

Disposal of sewage sludge (SS) is one of the problems in treatment plants; however, SS has a high-water volume and lacks some compounds and can be mixed with other biomass. The present study analyzed co-hydrothermal carbonization of sewage sludge with sawdust and corn stalk. This research aimed to optimize the process parameters, the temperature in the range of 180–300 °C, the reaction time in the range of 30–60 min, and pH in the range of 5–9 on the mass yield, energy yield, and high heat value (HHV) to increase the quality of hydrochar, and to analyze the effect of hydrothermal carbonization (HTC) on the characteristics of raw materials and hydrochar. The response surface method and Benken's box model were conducted using Design Expert 10 software. The optimal conditions for HHV, mass yield, and energy yield were 15.802 MJ/kg, 63.754%, and 67.415% respectively which occurred in the 205.358 °C, 30 min reaction time, and pH of 5. The temperature was the most influential parameter. The morphological, physicochemical, thermal, and crystalline properties of the hydrochar with the maximum HHV, mass yield and energy yield were evaluated as well. These results demonstrate that HTC is a suitable process to produce hydrochar, which can be used as a direct solid fuel. Highlights : • Hydrothermal carbonization of sewage sludge with sawdust and cornstalk was investigated. • Response surface optimization hydrothermal carbonization process was studied. • The morphological, physicochemical, thermal, and crystalline properties of the hydrochar are reported. • The optimal HHV was 15.802 MJ/kg. • The process can produce hydrochar which can be used for direct combustion or activated carbon. [ABSTRACT FROM AUTHOR]

Hydrochar is considered to be a good adsorbent for the separation of metal ions from aqueous solutions. However, the yield of hydrochar from raw straw is generally low, because the hydrothermal carbonization occurs via dehydration, polymerization, and carbonization. In this work, various hydrochar samples were prepared from rice straw with nitrogen and phosphorus salt; moreover, toilet sewage was used instead of nitrogen, and phosphorus salt and water were used to promote the polymerization and carbonization process. The modified carbon was characterized using XRD, XPS, SEM, and FTIR, and the adsorption capacity was investigated. A significant increase in hydrochar yield was observed when toilet sewage was used as the solvent in the hydrothermal carbonization process. The adsorption capacity of N/P-doped rice straw hydrochar for Cd2+ and Zn2+ metal ions was 1.1–1.4 times higher than that those using the rice straw hydrochar. The Langmuir models and pseudo-second-order models described the metal adsorption processes in both the single and binary-metal systems well. The characterization results showed the contribution of the surface complexation, the electrostatic interaction, the hydrogen bond, and the ion exchange to the extraction of Cd2+ and Zn2+ using N/P-doped rice straw hydrochar. [ABSTRACT FROM AUTHOR]

Hydrothermal carbonization (HTC) of rice husk was optimized in terms of the adsorption capacity at equilibrium (qe) and hydrochar mass yield (MY). The studied variables were reaction temperature, residence time, and biomass-to-water ratio by means of response surface methodology. In both cases, reaction temperature resulted the most significant parameter promoting high qe values at higher temperatures when treating methylene blue (MB) as the target pollutant. Nevertheless, MY was low (~40%) when focusing on a possible industrial application. Hence, maximizing qe and MY simultaneously by optimization of multiple responses emerges as a promising solution to improve MY values (>60%) with no significant differences regarding the qe response. Furthermore, additional activation was conducted on optimal hydrochars to further investigate the enhancement of qe. As a result, no statistical differences between non-modified and activated hydrochars were observed for qe; however, the pseudo-second-order constant (k2) seemed to be increased after alkali activation, mainly due to a larger surface area. Non-modified and activated hydrochars were characterized via SEM, FTIR, XRD, and BET, resulting in two significant effects contributing to MB adsorption: increased surface area and functionalized hydrochar surface. Consequently, this work provides valuable insights on subsequent application of this HTC optimization scheme at an industrial scale. [ABSTRACT FROM AUTHOR]

With the increase of organic emissions in production and human life, the pollution control of organic is now an urgent problem in the environmental field. In this study, hydrothermal carbonization rice husk-loaded Al-modified biochar (Al-BC) was synthesized, and the results of scanning electron microscopy could be used to determine that Al oxide composite was loaded on the surface of the material. The specific surface area was 57.049 m2 g−1, pore volume was 0.254 cm3 g−1, and average pore diameter was 8.922 nm for BC and 109.617 m2 g−1, 0.215 cm3 g−1, and 3.969 nm for Al-BC, respectively. The control effects of these two adsorption materials on organic pollutant ibuprofen (IBU) under different pH conditions were also investigated. The research results show that the adsorption capacity of Al-BC (30.24–1.48 mg g−1) is better than BC (19.98–0.92 mg g−1) at pH from 2 to 11. Solution pH plays a crucial role in IBU adsorption from organic solution. The Langmuir fitting results show that at pH = 7, the saturated adsorption capacity of IBU on BC could reach up to 18.68 mg g−1; the adsorption capacity on Al-BC was 60.49 mg g−1. The thermodynamic parameters indicate that the adsorption is spontaneous, endothermic, and increased disorder. The adsorption material prepared in this study could provide a reference for organic pollution control in water. [ABSTRACT FROM AUTHOR]

Date palm stones are regarded as possible alternatives to activated carbon (AC) precursors with high potential for various environmental applications. In this research study, date palm stones derived activated carbon (DPSAC) was used as adsorbent for removing toxic remazol brilliant blue R (RBBR). The synthesis of DPSAC involved a chemical treatment using KOH and NaOH (1:1). Characterization of DPSAC revealed that it exhibited a BET surface area of 715.30 m2/g, Langmuir surface area of 1061.93 m2/g, total pore volume of 0.39 cm3/g, and average pore diameter of 2.15 nm. Adsorption uptake of RBBR increased (from 24.54 to 248.54 mg/g), whereas the removal percentage decreased (from 98.16 to 82.85%) when the initial RBBR concentration increased (from 25 to 300 mg/L). The adsorption process performed best under acidic conditions (pH 3), with an RBBR uptake of 98.33 mg/g. Because of the high R2 values (0.9906 and 0.9779) and low average errors (6.24 and 13.95%), this adsorption process followed the Freundlich isotherm and pseudo-first-order (PFO) models, respectively. The Langmuir adsorption capacity (Qm) was 319.63 mg/g. Thermodynamic parameters were − 11.34 kJ/mol for ∆H° (exothermic in nature), 0.05 kJ/mol K for ∆S° (increasing randomness level at solid–liquid interface), − 27.37 kJ/mol for ∆G° (spontaneous), and 6.84 kJ/mol for Ea (controlled by physisorption). [ABSTRACT FROM AUTHOR]

In the wake of economic and population growth, increased wastewater production poses a challenge related to sewage sludge treatment, which is problematic given its high moisture content, amount, and hazardous characteristics. This study focuses on the hydrothermal carbonization of sewage sludge to produce carbonous material–hydrochar, which may be an alternative to fossil fuels. The effect of process parameters, namely, temperature (180, 240, 300 °C) and duration time (30, 90, 180 min), on hydrochar properties (proximate and ultimate analysis, heating values) and process performance were studied. Obtained results indicate and confirm that hydrothermal carbonization, especially temperature increase, improves the fuel properties of carbonized sewage sludge. The highest low heating value was obtained for hydrochar derived at 300 °C in 180 min (~23 MJ × kg−1). The highest energy gain was noted for hydrochar derived at 240 °C in 180 min (~23%). As well as relatively high mass and energy yield in comparison to other hydrochars, these parameters are considered the most favorable for sewage sludge hydrothermal carbonization. However, high energy consumption (over 1300 kJ × g−1) suggests that more research on the process's economical efficacy is required. [ABSTRACT FROM AUTHOR]

Chlorinated organic pollutants have been recognized as one of the major problems in the field of environmental engineering. In this work, 1,2-dichloroethane (DCE) waste liquid was used as feedstock to produce carbon adsorbent through the hydrothermal carbonization process. And the effects of nonylphenol ethoxylate (NP-10)/DCE mixing ratio, sulfuric acid initial concentration, and reaction time on the adsorption capacity of hydrochars at 180°C were investigated. Properties of the NP-10/DCE blended hydrochars were assessed by scanning electron microscopy, Brunauer-Emmett-Teller, and Fourier-transform infrared spectroscopy analysis. Experimental results show that the hydrochar obtained by using 50% DCE and 50% NP-10 with 71 wt.% sulfuric acid at 5 h demonstrated the best surface area (567.61 m2·g-1) and abundant functional groups. The methylene blue adsorption experiments indicated that the maximum adsorption capacity of the hydrochar was 440.49 mg·g-1, which was higher than that of commercial activated carbon (261.74 mg·g-1). This study provides a novel approach for the disposal of chlorinated organic waste liquids. [ABSTRACT FROM AUTHOR]

This study presents novel life cycle assessment (LCA) findings on hydrochar production from Saudi-Arabia-based date palm fronds biomass waste using hydrothermal carbonization (HTC). The LCA procedure incorporated normalization, weighting, and improvement assessment. The system boundary encompassed water consumption and energy requirements within a lab setting representing a gate-to-gate process. The OpenLCA 1.11.0 software with the European Life Cycle Database 3.2 (ELCD 3.2) was utilized for the study and we employed the ReCiPe Midpoint (H) 2016 and Environmental Footprint 3.0 (EF 3.0) impact assessment methods. The results indicated that fossil fuel usage represented the most significant impact category with the HTC and drying processes identified as major contributors. It was also observed that the HTC process exerted far greater detrimental impacts on the environment than the biomass grinding process. The overwhelming impact of fossil fuel resources could be mitigated by optimizing the batches of biomass or hydrochar samples in each operation, which could alleviate fossil fuel consumption by up to 94%. The findings emphasize the need for targeted interventions to mitigate the environmental burden and contribute to sustainable hydrochar production. [ABSTRACT FROM AUTHOR]