Light energy utilization and microbial catalysis for enhanced biohydrogen: Ternary coupling system of triethanolamine-mediated Fe@C-Rhodobacter sphaeroides.

This study investigated the mediating effect of Triethanolamine on Fe@C-Rhodobacter sphaeroides hybrid photosynthetic system to achieve efficient biohydrogen production. The biocompatible Fe@C generates excited electrons upon exposure to light, releasing ferrum for nitrogenase synthesis, and regulating the pH of the fermentation environment. Triethanolamine was introduced to optimize the electron transfer chain, thereby improving system stability, prolonging electron lifespan, and facilitating ferrum corrosion. This, in turn, stimulated the lactic acid synthetic metabolic pathway of Rhodobacter sphaeroides, resulting in increased reducing power in the biohybrid system. The ternary coupling system was analyzed through the regulation of concentration, initial pH, and light intensity. The system achieved the highest total H2 production of 5410.9 mL/L, 1.29 times higher than the control (2360.5 mL/L). This research provides a valuable strategy for constructing ferrum-carbon-based composite-cellular biohybrid systems for photo-fermentation H2 production.

The Adsorption of Pb(II) from Aqueous Solution Using KOH-Modified Banana Peel Hydrothermal Carbon: Adsorption Properties and Mechanistic Studies.

Adopting banana peel as a raw material, the adsorption properties of banana peel hydrothermal carbon modified with a KOH solution for lead ions in aqueous solution were studied. The surface structure and functional groups of the modified hydrothermal carbon were analyzed by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared (FT-IR) spectroscopy, the Brunner-Emmet-Teller (BET) method, element analysis, and Raman spectroscopy. The results showed that an adsorption capacity of 42.92 mg/g and a removal rate of 86.84% were achieved when the banana peel hydrothermal carbon was modified with a KOH solution of 0.5 mol/L, with a pH of 6 and a solid-liquid ratio of 1 g/L. The equilibrium adsorption time for lead ions in solution being adsorbed using KOH-modified hydrothermal carbon was 240 min, the adsorption process satisfied the quasi-second-order kinetic model and the Redlich-Peterson isotherm equation, and the equilibrium removal efficiency was 88.62%. The adsorption of lead ions using KOH-modified hydrothermal carbon is mainly chemical-physical adsorption.

Nutrient-rich hydrothermal carbon production by exogenous nutrients combined with seaweed internal water.

As a product of hydrothermal carbonization (HTC) technology, hydrothermal carbon has shown excellent application potential in soil improvement, greenhouse gas reduction and pollution remediation. Since a large amount of water and biomass are directly used as reaction media, hydrothermal carbon produced by traditional HTC possesses poor nutrient properties and accompanied by the generation of toxic and hazardous wastewater. Here, a versatile and easily scalable strategy has been demonstrated for the one-step production of industrial nutrient-rich hydrothermal carbon (NRHC) by combining the exogenous nutrients with seaweed internal water. During the reaction process, exogenous nutrients (NH4H2PO3, KNO3, CO(NH2)2) participated in the HTC reaction and were uniformly distributed on the surface of hydrothermal carbon through surface complexation precipitation, ion exchange, and electrostatic interactions. Simulations based on density functional theory revealed that NRHC produced in presence of exogenous nutrients possessed more active sites and surface charges. Moreover, the adsorbent and adsorbate were simultaneously affected by intermolecular forces, electrostatic forces, and internal energy of the system, and the thermodynamics of adsorption process was more stable. Compared with no exogenous nutrient involvement, NRHC produced by exogenous nutrients showed 2.12, 18.56, and 25.69 times increase in the N, P, and K content. The length of the seed germination root system increased by 4.3-5.9 times, which met the standards set for agricultural fertilizer. Due to increased yield per unit volume and reduced wastewater generation, the cost of NRHC production reduced by 47.83-58.23 per cent and profit enhanced by 1.56-1.68 times, as compared to traditional HTC. This low-cost streamlined process provides a new strategy for large-scale production and direct application of hydrothermal carbon.

Novel heterogeneous Fenton catalysts for promoting carbon iron electron transfer by one-step hydrothermal synthesization.

Carbon materials play a crucial role in promoting the Fe(III)/Fe(II) redox cycle in heterogeneous Fenton reactions. However, the electron transfer efficiency between carbon and iron is typically low. In this study, we prepared a novel heterogeneous Fenton catalyst, humboldtine/hydrothermal carbon (Hum/HTC), using a one-step hydrothermal method and achieved about 100 % reduction in Fe(III) during synthesis. Moreover, the HTC continuously provided electrons to promote Fe(II) regeneration during the Fenton reaction. Electron paramagnetic resonance (EPR) and quenching experiments showed that Hum/HTC completely oxidized As(III) to As(V) via free radical and non-free radical pathways. Attenuated total reflectance Fourier-transform infrared (ATR-FTIR) and two-dimensional correlation spectroscopy (2D-COS) analyses revealed that monodentate mononuclear (MM) and bidentate binuclear (BB) structures were the dominant bonding methods for As(V) immobilization. 40 %Hum/HTC exhibited a maximum As(III) adsorption capacity of 167 mg/g, which was higher than that of most reported adsorbents. This study provides a novel strategy for the efficient reduction of Fe(III) during catalyst synthesis and demonstrates that HTC can continuously accelerate Fe(II) regeneration in heterogeneous Fenton reactions.

Hydrothermal Carbon Coating of an Activated Carbon-A New Adsorbent.

A new adsorbent material was prepared by coating an activated carbon with hydrothermal carbon obtained from sucrose. The material obtained has different properties from the sum of the properties of the activated carbon and the hydrothermal carbon, which shows that a new material was obtained. It has a high specific surface area (1051.9 m2 g-1) and is slightly more acidic than the starting activated carbon (p.z.c.-point of zero charge 8.71 vs. 9.09). The adsorptive properties of a commercial carbon (Norit RX-3 Extra) were improved over a wide pH and temperature range. The capacity values of the monolayer according to Langmuir's model reached 588 mg g-1 for the commercial product and 769 mg g-1 for the new adsorbent.

Hydrothermal carbon microspheres and their iron salt modification for enhancing biohydrogen production.

Dark fermentation (DF) for hydrogen (H2) evolution is often limited to industrial application due to its low H2 yield. In this work, hydrothermal carbon microspheres (HCM) and iron modified HCM (Fe-HCM) were prepared by hydrothermal process using waste corn cob. Subsequently, HCM and Fe-HCM were used in DF for more H2. The highest H2 yields amended with HCM and Fe-HCM at 600 mg/L were achieved to be 119 and 154 mL/g glucose (0.87 and 1.2 mol H2/mol glucose), respectively, being 24% and 59% higher than that of control yield. Soluble metabolites revealed HCM and Fe-HCM promoted butyric acid-based DF. Microbial composition depicted that HCM and Fe-HCM improved the abundance level of Firmicutes from 35% to 41% and 56%, while the abundance level of Clostridium_sensu_stricto_1 rose from 25% to 38% and 51%, respectively. This provides valuable guidance for hydrothermal carbon used in biofuel production.

Cellulose-based slow-release nitrogen fertilizers: Synthesis, properties, and effects on pakchoi growth.

The application of most slow-release fertilizers is limited by complex preparation processes and short slow-release periods. In this study, carbon spheres (CSs) were prepared by a hydrothermal method using cellulose as the raw material. Using CSs as the fertilizer carrier, three new carbon-based slow-release nitrogen fertilizers were prepared using direct mixing (SRF-M), water-soluble immersion adsorption (SRFS), and co-pyrolysis (SRFP) methods, respectively. Examination of the CSs revealed regular and ordered surface morphology, enrichment of functional groups on the surfaces, and good thermal stability. Elemental analysis showed that SRF-M was rich in nitrogen (total nitrogen content of 19.66 %). Soil-leaching tests showed that the total cumulative nitrogen release of SRF-M and SRF-S was 55.78 % and 62.98 %, respectively, which greatly slowed down the release of nitrogen. Pot experiment results revealed that SRF-M significantly promoted the growth of pakchoi and improved crop quality. Thus, SRF-M was more effective in practical applications than the other two slow-release fertilizers. Mechanistic studies showed that CN, -COOR, pyridine-N and pyrrolic-N participated in nitrogen release. This study thus provides a simple, effective, and economical method for the preparation of slow-release fertilizers, providing new directions for further research and the develop of new slow-release fertilizers.

Selective adsorption of uranium (VI) from wastewater using a UiO-66/calcium alginate/hydrothermal carbon composite material.

Uranium mining, smelting, and nuclear industries generate a considerable amount of wastewater containing uranium. To treat this wastewater effectively and inexpensively, a novel hydrogel material (cUiO-66/CA) was developed by co-immobilizing UiO-66 with calcium alginate and hydrothermal carbon. Batch tests were conducted to determine the optimal adsorption conditions for uranium using cUiO-66/CA, and the adsorption behavior was spontaneous and endothermic, confirming the quasi-second-order dynamics model and the Langmuir model. At a temperature of 308.15 K and pH = 4, the maximum adsorption capacity of uranium was 337.77 mg g-1. The surface appearance and interior structure of the material were analyzed using SEM, FTIR, XPS, BET, and XRD techniques. The results indicated two possible uranium adsorption processes of cUiO-66/CA: (1) Ca2+ and UO22+ ion exchange process and (2) coordination of uranyl ions with hydroxyl and carboxyl ions to form complexes. cUiO-66/CA exhibited strong selectivity for U (VI) in a multicomponent mixed solution and uranium-containing wastewater, with uranium removal rates of 99.03 % and 81.45 %, respectively. The hydrogel material demonstrated excellent acid resistance, and the uranium adsorption rate exceeded 98 % in the pH range of 3-8. Therefore, this study suggests that cUiO-66/CA has the potential to treat uranium-containing wastewater in a broad pH range.

Effective removal of Rhodamine B using the hydrothermal carbonization and citric acid modification of furfural industrial processing waste.

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.

Reduction of Hexavalent Chromium from Soil of the Relocated Factory Area with Rice Straw Hydrothermal Carbon Modified by Nano Zero-Valent Iron (nZVI).

In order to reduce the content of Cr(VI) in the soil of the relocated chromium salt factory, the rice straw-derived hydrothermal carbon was prepared by hydrothermal method and loaded with nano zero-valent iron generated by liquid phase reduction, which effectively alleviated the self-aggregation problem of nano zero-valent iron (nZVI) in the treatment of Cr(VI) and improved the Cr(VI) reduction rate without changing the soil structure. The reduction effect of Cr(VI) in soil by key influencing factors such as carbon-iron ratio, initial pH value, and initial temperature was investigated. The results showed that nZVI modified hydro-thermal carbon composite (named RC-nZVI) had a good reduction effect on Cr(VI). Scanning electron microscope (SEM) and energy spectrum analysis showed that nZVI was evenly distributed on the surface of hydrothermal carbon, which effectively reduced the agglomeration of iron. Under the conditions of C/Fe = 1:2, 60 °C, with pH of 2, the average Cr(VI) content in soil decreased from 182.9 mg kg-1 to 21.6 mg kg-1. Adsorption kinetics of Cr(VI) by RC-nZVI fit well with the pseudo-second-order model, and the kinetic velocity constant revealed that Cr(VI) reduction rate decreased with increasing initial Cr(VI) concentration. Cr(VI) reduction by RC-nZVI was mainly dominated by chemical adsorption.

Biomass-Based Hydrothermal Carbons for the Contaminants Removal of Wastewater: A Mini-Review.

The preparation of adsorbents with eco-friendly and high-efficiency characteristics is an important approach for pollutant removal, and can relieve the pressure of water shortage and environmental pollution. In recent studies, much attention has been paid to the potential of hydrothermal carbonization (HTC) from biomass, such as cellulose, hemicellulose, lignin, and agricultural waste for the preparation of adsorbents. Hereby, this paper summarizes the state of research on carbon adsorbents developed from various sources with HTC. The reaction mechanism of HTC, the different products, the modification of hydrochar to obtain activated carbon, and the treatment of heavy metal pollution and organic dyes from wastewater are reviewed. The maximum adsorption capacity of carbon from different biomass sources was also evaluated.

Platinum/carbon dots nanocomposites from palm bunch hydrothermal synthesis as highly efficient peroxidase mimics for ultra-low H2O2 sensing platform through dual mode of colorimetric and fluorescent detection.

Detection of hydrogen peroxide and glucose in nanomolar level is crucial for point-of-care medical diagnosis. It has been reported that human's central nervous system diseases such as Alzheimer's disease, Parkinson's disease, and even amyotrophic lateral sclerosis, are presumably caused H2O2 or reactive radical species (ROS). Sensing of H2O2 released from human biofluids, tissues, organ from metabolism disorder at ultra-low concentration assists for early identification of severe diabetis mellitus related to glucose, and heart attack, as well as stroke related to cholesterol. In this work, carbon dots (CDs) having an average diameter at 6.99 nm with highly photoluminescence performance were successfully synthesized from palm empty fruit bunch (EFB) using green and environmentally friendly process via hydrothermal condition. CDs acted well on peroxidase-like activity for H2O2 detection at room temperature, however their sensitivity on ultra-low H2O2 concentration needed to be improved. To enhance their reactivity on H2O2 nanozyme activity at room temperature, synthesis of hybrid metal nanoparticles (AgNPs and PtNPs) on CDs surface was established. The findings exhibited that CDs/PtNPs was the most suitable nanozyme achieving highly efficient peroxidase mimic for dual mode of colorimetric and fluorescent H2O2 sensing platform at very low limit of detection of 0.01 mM (10 nM) H2O2.

Multi-walled carbon nanotube-modified hydrothermal carbon: A potent carbon material for efficient remediation of cadmium-contaminated soil in coal gangue piling site.

Coal gangue contains numerous metal ions. After rainwater leaching, the metal ions in coal gangue migrate into the surrounding soil, posing significant threats to human health and ecosystems. To remove Cd from contaminated soil surrounding a coal gangue pile area, loofah, oak chips, and corn stalks were used as raw materials to prepare loofah hydrothermal carbon (LH), oak chip hydrothermal carbon (OH), corn stalk hydrothermal carbon (CH). Next, LH, OH, and CH were modified using multiwalled carbon nanotubes (MWCNTs) to obtain loofah-, oak-chip-, and corn-stalk-MWCNTs hydrothermal carbon composites (LMH, OMH, and CMH). The loofah hydrothermal carbon with excellent pore structure, specific surface area and pore capacity was selected, and the loading of MWCNTs was varied to give it better adsorption performance. The N2 adsorption-desorption experiments showed that the specific surface area and pore volume of LMH, OMH and CMH were significantly higher than those of LH, OH and CH, respectively. The specific surface area and pore volume of LMH are 101.948 m2 g-1 and 6.226 cm3 g-1, respectively. By EDS analysis and infrared spectroscopy, it can be seen that LMH has more o-containing functional groups than OMH and CMH. Remediation experiments were carried out on the actual contaminated soil obtained from Chaili Coal Mine. It was found that the mass fractions of Cd in the acid-soluble state in the soil samples that were treated with LH and LMH decreased by 18.54% and 26.3%, respectively, after 20 d. Therefore, LMH significantly affected Cd fixation and promoted Cd pollution remediation in the coal gangue pile area.

Adsorption of estrone, 17ß-estradiol, and 17α-ethinylestradiol from water onto modified multi-walled carbon nanotubes, carbon cryogel, and carbonized hydrothermal carbon.

Carbon materials of different structural and textural properties (multi-walled carbon nanotubes, carbon cryogel, and carbonized hydrothermal carbon) were used as adsorbents for the removal of estrone, 17ß-estradiol, and 17α-ethinylestradiol from aqueous solutions. Chemical modification and/or activation were applied to alter surface characteristics and to increase the adsorption and desorption efficiency of carbon materials. Surfaces of treated and untreated carbon materials were characterized through the examination of the textural properties, the nature of surface functional groups, and surface acidity. It was found that the adsorption capacity of tested carbon materials is not directly proportional to the specific surface area and the content of surface oxygen groups. However, a high ratio of surface mesoporosity affected the adsorption process most prominently, by increasing adsorption capacity and the rate of the adsorption process. Adsorption of estrone, 17ß-estradiol, and 17α-ethinylestradiol followed pseudo-second-order kinetic model, while the equilibrium adsorption data were best fitted with the Langmuir isotherm model. Calculated mean adsorption energy values, along with the thermodynamic parameters, indicated that removal of selected hormones was dominated by the physisorption mechanism. High values of adsorption efficiency (88-100 %) and Langmuir adsorption capacities (29.45-194.7 mg/g) imply that examined materials, especially mesoporous carbon cryogel and multi-walled carbon nanotubes, can be used as powerful adsorbents for relatively fast removal of estrogen hormones from water.

Hydrothermal Carbon as Reactive Fillers to Produce Sustainable Biocomposites with Aromatic Bio-Based Epoxy Resins.

Thiswork is focused on the development of sustainable biocomposites based on epoxy bioresin reinforced with a natural porous material (hydrochar, HC) that is the product of spruce bark wastes subjected to hydrothermal decomposition. To identify the influence of hydrochar as a reinforcing material on the designed composites, seven formulations were prepared and tested. An aromatic epoxy monomer derived from wood biomass was used to generate the polymeric matrix, and the formulations were prepared varying the filler concentration from 0 to 30 wt %. The reactivity of these formulations, together with the structural, thermal, and mechanical properties of bio-based resin and biocomposites, are investigated. Surprisingly, the reactivity study performed by differential scanning calorimetry (DSC) revealed that HC has a strong impact on polymerization, leading to an important increase in reaction enthalpy and to a decrease of temperature range. The Fourier Transform Infrared Spectroscopy (FT-IR) investigations confirmed the chemical bonding between the resin and the HC, while the dynamic mechanical analysis (DMA) showed increased values of crosslink density and of storage moduli in the biocomposites products compared to the neat bioresin. Thermogravimetric analysis (TGA) points out that the addition of hydrochar led to an improvement of the thermal stability of the biocomposites compared with the neat resorcinol diglycidyl ether (RDGE)-based resin (T5% = 337 °C) by ≈2-7 °C. Significantly, the biocomposites with 15-20 wt % hydrochar showed a higher stiffness value compared to neat epoxy resin, 92SD vs. 82SD, respectively.

Strong and thermostable hydrothermal carbon coated 3D needled carbon fiber reinforced silicon-boron carbonitride composites with broadband and tunable high-performance microwave absorption.

Excellent electromagnetic wave (EMW) absorbing materials with high-temperature stable and superior mechanical properties are among the most promising candidates for practical application. Here, novel hydrothermal carbon coated three-dimensional (3D) needled carbon fiber reinforced silicon-boron carbonitride (HC-CF/SiBCN) composites with a hierarchical A (CF)/B (HC)/C (SiBCN) structure were constructed and prepared for the first time by combining hydrothermal transformation and precursor infiltration and pyrolysis (PIP) process. The thickness of the HC coating controlled by the glucose concentration played a crucial role in tailoring the EMW capacity of the composite. The incorporation of SiBCN could not only effectively improve the oxidation resistance but also actively enhance the mechanical properties of the HC coated CF structure. Compared to the weak high-temperature oxidation resistance and mechanical properties of pristine 3D needled CF felt, the composites after the introduction of HC and SiBCN were thermostable in air atmosphere beyond 1000 °C to about above 70% weight retention, and the maximum flexural and compression strength of the composites could reach to 23.51 ± 1.37 and 12.22 ± 1.12 MPa, respectively. A substantial enhancement of EMW absorption ability was achieved through incorporation of HC and SiBCN, which could be attributed to the matched characteristic impedance and enhanced loss ability, whose optimization EMW absorption performance was the minimum reflection loss (RLmin) of -52.08 dB and effective absorption bandwidth (EAB) of 7.64 GHz for the composite obtained by two PIP cycles with 24 wt% glucose solution, demonstrating that the HC-CF/SiBCN composites with high-temperature stable, excellent mechanical and superior EMW absorption properties could be considered as a promising candidate for the applications in harsh environments.

Norfloxacin adsorption on montmorillonite and carbon/montmorillonite hybrids: pH effects on the adsorption mechanism, and column assays.

The presence of norfloxacin antibiotic (NFX) in drinking water raises significant scientific concern due to the health and environmental problems that may cause. This study aimed to evaluate the NFX removal: 1) in batch adsorption at different pH values on montmorillonite (M) and montmorillonite-carbon hybrids (M-HC); 2) in continuous columns experiments, to assess the technological application of these hybrids as domestic filters, using one M-HC as adsorbent material ranging from 1% to 5%. Batch experiments showed that adsorption occurred in all the samples, being M the material with the highest adsorption capacity (95% of adsorption for cationic NFX). For the M-HC the adsorption seemed to be not strongly dependent of the pH (20%- 41% of adsorption). The characterization of adsorbents and NFX adsorption products (FTIR, XRD, and zeta potential analysis) disclosed that adsorption occurs at both the external surface and the interlayer space of M. For the M-HC synthesized without activation, the interlayer space seemed to be predominantly responsible; while for the activated M-HC the adsorption occurred at the external surface (its interlayer was destroyed). The column experiments revealed that the best adsorption capacity and highest flow were attained using 1% of adsorbent material in the column packing.

Antibacterial composite paper with corn stalk-based carbon spheres immobilized AgNPs.

Silver nanoparticles (AgNPs) have been widely used for sterilization due to their broad-spectrum bactericidal properties. However, there exist the problems of premature releasing and accumulative toxicity when free AgNPs are applied. This study proposed a one-pot hydrothermal strategy to synthesize carbon spheres immobilized silver nanoparticles (AgNPs@CS). The synthesis involves with silver ammonia solution as Ag precursor, and corn stalk as green reducing agent and carbon precursor. Furthermore, AgNPs@CS was anchored by cellulose nanofibers (CNF) to obtain the antibacterial composite paper. The obtained CNF/AgNPs@CS paper exhibited superior antibacterial properties against E. coli and S. aureus. Notably, the accumulative release rate of AgNPs from AgNPs@CS was 10.2% in 9 days, while that from CNF/AgNPs@CS paper was only 6.7% due to the anchoring effect of both CS and CNF, which was low for avoiding the cumulative toxicity problem. In addition, the mechanical and barrier properties of CNF/AgNPs@CS paper were also improved by 29.4% (tensile index), 2.7% (tear index), 7.4% (burst index), 10% (folding endurance), 0.8% (water vapor transmission) and 9.4% (oxygen transmission rate), respectively. Therefore, the composite paper has potential application as a medical antibacterial material.

Adsorption of Lead (II) from Aqueous Solution with High Efficiency by Hydrothermal Biochar Derived from Honey.

A novel natural honey hydrothermal biochar (HHTB) was prepared using natural honey as raw material. The as-prepared adsorbent was applied to adsorb Pb2+ from aqueous solution and characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy to investigate the structure and morphology change of the adsorbent before and after Pb2+ adsorption. The influence of the pH, initial Pb2+ concentration, temperature, and contact time on the adsorption of Pb2+ was systematically investigated. The results revealed that the adsorption capacity for Pb2+ is up to 133.2 mg·g-1 at initial pH of 5.0 and adsorption temperature of 298 K. Meanwhile, the adsorption of Pb2+ on HHTB can be well fitted by the pseudo-second-order model and Langmuir isotherm model. The adsorbent had great selectivity for Pb2+ from the aqueous solution containing coexisting ions including Cd2+, Co2+, Cr3+, Cu2+, Ni2+ and Zn2+. Furthermore, the adsorption of Pb2+ on HHTB was attributed to complexation coordination, where it involved hydroxyl and carboxylic groups on HHTB in the process of adsorption of Pb2+.

[Research progress in hydrothermal carbon materials for separation and analysis].

Hydrothermal carbon materials are new functional materials prepared by the hydrothermal reaction of sugars or carbonaceous organic compounds. They have many advantages such as abundant resources of raw materials, environmental-friendliness, hydrophilicity, and easy of modify and so on. These carbon materials have been widely used as catalyst carriers, energy electrode materials, environmental adsorbents, etc. Among these, the application of hydrothermal carbon materials as absorbents reveals their ability to show strong interactions with specific molecules. In recent years, the application of these materials has been gradually extended to the field of chromatography, as stationary phases for solid-phase separation as well as for the enrichment of complex biological samples. In this paper, the recent applications of hydrothermal carbon materials for the analysis of ionic compounds, polar compounds, phosphorylated peptides, and glycopeptides are presented. Finally, the future scope of these materials in separation and enrichment is also discussed.