Hydroxyl Content Research Articles

Mechanically Induced Green Targeted Conversion of Ammonia Nitrogen to N2: Based on Cavitation Effects and ROS Oxidation.

Addressing the mounting challenge of ammonia nitrogen pollution in aquatic ecosystems necessitates the selective oxidation of ammonia nitrogen to nitrogen gas, a pivotal aspect of eco-friendly nitrogen removal processes. Ultrasound cavitation, renowned for its capacity to generate reactive oxygen species (ROS), has garnered considerable attention in environmental remediation. This study reveals a highly synergistic mechanism in ultrasound coupled stirring (US-ST), establishing optimal coupling conditions through sound field monitoring and quantification of ROS. In comparison to ultrasound treatment alone (US), the sound pressure amplitude significantly increased from ±18 to ±30 kPa in US-ST, markedly reducing the cavitation nucleation threshold and augmenting the steady-state concentration of hydroxyl radicals (HO•) by 13-fold. Further, with appropriate charge transfer conditions enabled by the acoustoelectric characteristics of the passive film on stirring paddles, the concentrations of superoxide (•O2-) and singlet oxygen (1O2) elevated to 9.54 × 10-10 M and 8.43 × 10-13 M, respectively. Under the regulation of 500 rpm stirring vortex, a maximum sonochemical efficiency of 6.5 × 105 mg J-1 was achieved. In the context of domestic wastewater, ammonia nitrogen degradation was achieved through the oxidation and thermal dissociation effects of US-ST. The concentration decreased from 27.5 to 3.4 mg/L after 2 h, with an impressive N2 selectivity of 96.8%. This study elucidates the targeted conversion mechanism of ammonia nitrogen in US-ST, introducing an emerging water treatment technology propelled by mechanical energy.

Synergistic effect of Ca/Zn main stabilizer and maltitol auxiliary stabilizer on the thermal stability, mechanical properties, and transparency of poly(vinyl chloride)

AbstractMaltitol, a natural compound, offers a potentially eco‐friendly alternative to conventional auxiliary thermal stabilizers. Its auxiliary stabilization effect was studied by discoloration tests, Congo red tests, thermogravimetric analysis, and UV–visible spectroscopy. Additionally, x‐ray photoelectron spectroscopy and discoloration tests were used to study the stabilizing mechanisms of maltitol. Compared to dipentaerythritol, commonly used in the PVC industry, maltitol as an auxiliary stabilizer exhibits better improvement in thermal stability. This improvement is related to its melting point, ability to complex with zinc chloride, and content of hydroxyl groups. Furthermore, the addition of maltitol in PVC not only maintains good transparency of PVC basically unchanged but also improves the mechanical properties. Maltitol, as a natural, eco‐friendly, and efficient auxiliary thermal stabilizer, exhibits a promising application prospect in PVC materials.

Glycoside-Mediated Enhancement of Stability in Aluminum Oxyhydroxide Nanoadjuvants during Freeze-Drying.

Aluminum-based adjuvants have been indispensable to vaccine potency. However, their effectiveness is difficult to maintain after freeze-drying, which limits the storage and application of aluminum-adjuvanted vaccines. In this study, the impact of freeze-drying on aluminum oxyhydroxide nanorods (AlOOH NRs) was investigated. Freeze-drying led to aggregation and resulted in the loss of the surface hydroxyl content of aluminum adjuvants. To alleviate freeze-drying-induced damage, the potency of different alkyl glycosides as protectants was further evaluated. It was demonstrated that the structural balance of the head and tail of a glycoside was more conducive to protecting AlOOH NRs from aggregation and loss of surface hydroxyl groups. These results underline the proper selection of protectants to protect adjuvants against functional defects caused by freeze-drying, which is important for the stability and efficacy of vaccines and biopharmaceutical products.

Disassembly of catechyl lignin from castor shells by maleic acid aqueous and production of single catechols

Catechyl lignin (C-lignin) is recognized as a uniform and straight biopolymer that stands out as an exemplary archetype of what is often referred to as "ideal lignin." This difference is due to its unique ability to efficiently depolymerize into a single catechol product. This remarkable property makes C-lignin suitable for further applications and highlights its potential for the production of chemicals. In this study, a protocol utilizing maleic acid aqueous (MAA) was developed for the effective disassembly of coexisting C-lignin and G/S-lignin in castor shells under mild conditions. Thioacidolysis combined with nuclear magnetic resonance (NMR) spectroscopic analyses revealed a significant enrichment of benzodioxane units, without observation of β-O-4 structures from G/S-lignin. The mechanism underlying selective disassembly of coexisting C-lignin and G/S-lignin in castor shells was comprehensive elucidated by analyzing the chemical structure change of benzodioxane and β-O-4 lignin model compounds. Furthermore, the structural characteristics of the disassembled C-lignin were synthetically evaluated, highlighting its narrow molecular weight distribution (Mw = 2432–2763 Da) and high hydroxyl content (aliphatic OH = 7.7–8.4 mmol/g; catechol OH = 5.7–7.5 mmol/g). Compared with the feedstock containing C-lignin and G/S-lignin, the extracted C-lignin sample showed exceptional catalytic activity and selectivity. The results show that the Pd/C-catalyzed hydrogenation reaction mainly produces catechylpropanol compounds (selectivity as high as 97 %).

Insights of Physicochemical Structure Changes of Bituminous Coal with Acidification-assisted Controlled Electric Pulse through SEM, XRD and FTIR

Controlled electric pulse (CEP) cracking coal effectively enhances its permeability, but a high coal breakdown voltage (BV) can result in technical difficulties. To address this problem, the method of using HCl solution to improve the electrical conductivity of coal was proposed. The effects of HCl on coal BV were investigated, and the microstructural changes in coal were analyzed through scanning electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy. Compared with raw coal, the BV of acidified coal decreased significantly. The crushing degree of the coal samples was clearly enhanced with an increasing HCl concentration. Some internal coal minerals were acidified and dissolved, the aromatic layer spacing (d002) increased and the layer sheet stacking height (Lc) decreased, and the crystal structure was damaged. When acidified coal was broken down, numerous internal pores and cracks appeared, active coal groups were shed, the aliphatic hydrocarbons and oxygen-containing functional group contents increased, surface activity was reduced, and the hydroxyl content was reduced, which was conducive to rapid gas desorption. Acidification effectively reduces the BV of coal and improves the cracking and permeability enhancement effect of coal by CEP action.

Significant Biogenic Source of Oxygenated Volatile Organic Compounds and the Impacts on Photochemistry at a Regional Background Site in South China.

Oxygenated volatile organic compounds (OVOCs) significantly modulate atmospheric chemistry, but the sources and air quality impacts of OVOCs in aged urban outflows remain to be elucidated. At a background site in South China, the ozone formation potential of six nonformaldehyde OVOCs studied was equivalent to that of 3.56 ppbv of formaldehyde, more than half of which was contributed by acetaldehyde. Source apportionment incorporating photochemical age revealed that considerable fractions (52.7%-62.6%) of the OVOCs were of biogenic origin, except for ethanol, which was primarily derived from anthropogenic emissions. The oxidation of cis-/trans-2-butene explained 71.1% of the in situ acetaldehyde formation. In contrast, α/β-pinenes and isoprene contributed 73.8% and 28.4% to acetone and methylglyoxal formation, respectively. An average of 12.4% of net in situ ozone (O3) production rate was attributed to the OVOCs studied, where the biogenic fractions accounted for 59%. The changes in the O3 production rate and hydroxyl radical (OH) concentration caused by OVOCs were mainly affected by ozone formation sensitivity. The effects of primary acetaldehyde and acetaldehyde-led O3 on secondary acetaldehyde formation were weak at this background site; however, they cannot be ignored in polluted areas. This study provides a scientific basis for mitigating O3 pollution driven by biogenic emissions and OVOCs.

Effects of Crystal Facets of Quartz on the Formation and Dissociation of Natural Gas Hydrates

Natural gas hydrates are non-stoichiometric crystalline compounds composed of natural gas and water, typically found in the pore spaces constructed by minerals. Mineral crystals exhibit significant variations in surface properties among different crystal facets. Despite the importance of these mineral crystal facets, previous studies have not reported their influence on natural gas hydrates. To address this gap, we focused on quartz, a vital component of hydrate reservoirs, and studied the process of natural gas hydrates formation and dissociation on its distinct crystal facets. In our investigation, we simplified pores as narrow gap spaces between two parallel quartz substrates, and captured the entire process with a microscope. The results indicate that the formation and dissociation of natural gas hydrates are notably influenced by the distinct crystal facets of quartz. The influences of quartz crystal facet on the hydrate formation are primarily attributed to two factors, wettability and hydroxyl concentration of quartz crystal facet. We have also revealed the mechanism of how quartz crystal facet influences the hydrate dissociation. This research provides a fundamental understanding of how mineral crystal facets influence the hydrate formation and dissociation, offering a novel perspective for the design of processes for extracting hydrate.

Fluorine-Free Cycloaliphatic Epoxy-Based Siloxane Nanohybrid Binder with High Polar Hydroxyl Group Content Enabling LiFePO4-Type Battery with High Electrochemical Performance and Stability.

LiFePO4-type (LFP) batteries have attracted significant attention in most battery manufacturing industries due to their long lifespan, high-temperature safety, and low cost of raw materials. However, as an active material, LFP still suffers from several intrinsic drawbacks, including poor conductivity, a low Li+ diffusion coefficient, low capacity, and a lack of electrochemical stability, primarily due to conventional fluorine-based binders. Here, we report a simple yet effective approach to developing a fluorine-free binder based on a robust cycloaliphatic epoxy-based siloxane nanohybrid material (CES) to achieve high electrochemical stability in LFP batteries. The high content of silanol moieties in CES induces a strong affinity for the active material and conductive agent, significantly improving rheological (thixotropy) and mechanical (adhesion and cohesion) properties, which enable the formation of a uniformly coated electrode. As a result, we achieved superior electrochemical performance and stability in CES-applied electrodes compared to those with conventional fluorine-based binders. We investigate the reasons behind the contribution of CES to the electrochemical stability of LFP batteries through various analyses. The high thermal and oxidation stability of CES effectively prevents degradation of LFP-based active materials. Our binder development strategy offers a significant breakthrough in replacing conventional fluorine-based binders, advancing the development of high-performance and stable secondary batteries.

An oxidative depolymerized lignin treated by potassium ferrate and its use in preparation of epoxy resin

AbstractLignin, as an industrial by‐product, can be used as a phenolic substancen. In this study, enzymatic hydrolysis lignin (L) was treated with potassium ferrate and phenol respectively to obtain oxidized lignin (OL) and phenolated lignin (PL). Their phenolic hydroxyl content (PhOH) increased by 29.1% and 40.5%, respectively. Then four kinds of epoxy resins were prepared, namely lignin‐free epoxy resin (LFER), L epoxy resin (LER), PL epoxy resin (PLER), and OL epoxy resin (OLER). Gel permeation chromatography (GPC) and Fourier transform infrared analyses indicated that potassium ferrate oxidation could decline the molecular weight (Mw) and increase the PhOH of L. Mechanical properties test and dynamic mechanical analysis (DMA) results show that cured OLER (OLEN) has higher crosslinking density and better mechanical properties (shear strength increased by 14%, tensile strength increased by 15%) than cured LER (LEN). Thermogravimetric analysis results show that OLEN has better thermal stability than cured LFER (LFEN) and LEN. In addition, scanning electron microscopy images showed that the modified L had better compatibility. This study presents a novel approach for lignin oxidation.

Exploring the relationship between lignin structure and antioxidant property using lignin model compounds

Lignin has a natural polyphenol structure that is expected to replace chemically synthesized antioxidants as a native antioxidant with biodegradable and convenient source characteristics. However, the improvement of the antioxidant property of lignin and its application as an antioxidant are still somewhat limited due to the lack of understanding of the relationship between specific lignin structures and antioxidant property. Therefore, the study of the relationship between lignin structure and antioxidant property is crucial to realize the high-quality application of lignin. In this experiment, the scavenging ability of free 1,1-diphenyl-2-picrylhydrazyl (DPPH·) radicals was determined for different grades of acetylated tannins, typical lignin model compounds and different structural units of milled wood lignin to investigate the relationship between lignin structure and antioxidant property. Based on the experimental results, some structure-activity relationships were proposed and the mechanism of the antioxidant property of lignin was discussed. The number of phenolic hydroxyl groups was linearly and positively correlated with antioxidant property, and the scavenging of DPPH radicals increased significantly with the increase in the number of methoxy groups in the model compounds. Moreover, aldehyde and carboxyl groups had a negative effect on the antioxidant property of lignin, while methoxy, alkyl and alcohol hydroxyl groups played a positive role. The guaiacyl (G) and syringyl (S) units favored the antioxidant property, so the difference in the content of structural units in lignin under certain conditions of phenolic hydroxyl content also affected the antioxidant property. Therefore, the antioxidant property of aspen milled lignin was higher than that of other milled lignin from different wood species. Finally, the mechanism of DPPH free radical scavenging by lignin was revealed to better understand the relationship between lignin structure and antioxidant property.

Skin rash related to the use of wood ash in wound healing, about a case

Abstarct Introduction: The ash of wood plants is part of the ancestral remedies because of its physical and chemical properties. It has detergent, fertilizing, and antiseptic properties, which justifies its many uses. Case report: We report the case of a woman aged 50 years who presented with a generalized rash all over the body with painful macules a burning sensation and a fever. Symptoms appeared after taking wood ash from plants, for three days. The reason for use was the healing of Zona's wound that she contracted and treated before admission. The patient’s general condition was preserved, and the drug treatment allowed a quick healing. Conclusion: Wood ash from plants with a high potassium hydroxyl content may be an irritant and partly explain the reaction observed. Traditional treatments should be used with great care to avoid adverse effects.

Achievement of biochar photocatalytic performance by synergistic oxidation of sulfuric acid/hydrogen peroxide: Towards revealing the mechanism of synergistic oxidation on photocatalytic performance

The oxygen-containing functional groups of biochar have great potential in tailoring photochemical properties, but the content of oxygen-containing functional groups of pristine biochar is insufficient to support photocatalytic reactions. In this study, a synergistic oxidation of H2SO4 and H2O2 was innovatively proposed to prepare biochar photocatalysts (OGPC400). The results showed that the synergistic oxidation of H2SO4 and H2O2 increased the contents of hydroxyl and carboxyl groups of biochar with the degree of oxidation, and the total concentration of acidic functional groups was about 4 mmol/g higher than that of the oxidation with H2SO4 or H2O2 alone, which was attributed to the synergistic oxidation to promote the conversion of CH and C-OH on the benzene ring. The achievement of electron exchange among hydroxyl and carboxyl groups and internal electron transfer within biochar by the benzene ring as a medium resulted in 100 % degradation of rhodamine b (RhB) and 25 times reaction rate constant higher than that of pristine biochar, as compared to only 45 % or 37 % degradation by oxidation with H2SO4 or H2O2 alone. The exciting results confirmed the positive availability of H2SO4 and H2O2 synergistic oxidation on biochar photocatalysts, which is expected to be applied in environmental remediation.

A Low-Hydroxyl Quartz Glass Prepared by Using a Plasma Heat Source as the Flame and High-Purity Quartz Sand as the Raw Material

In this paper, a quartz glass with low hydroxyl groups was prepared by combining the advantages of various processes, using a plasma heat source as the flame and high-purity quartz sand as the raw material. The purity of the quartz sand was 99.997%. The number of air bubbles in the quartz glass prepared using high-purity quartz sand was lower. The hardness and tensile strength of the quartz glass were 737.7–767.1 GPa and 6.88–9.64 MPa, respectively. The hydroxyl content of the sample was only 4.11 ppm, and the hydroxyl content of the homogenized quartz glass was reduced to 2.64 ppm, which was an improvement of about 35%. After homogenization, the fictive temperature (Tf) of the quartz glass was determined to be 1253 cm−1, and the variation of the Tf value along the radial direction was reduced, indicating a more homogeneous glass structure. The stress distribution in the quartz glass was significantly improved. These results indicate that the preparation of quartz glass from high-purity quartz sand using a plasma heat source as the flame opens up new avenues for optical applications.

Excellent facile fabrication of PVA and lignin nanoparticles from wheat straw after novel DES-THF pretreatment

The utilization of environmental friendly and renewable materials has received increasing attention recently. Lignin nanospheres (LNPs) prepared from recovered lignin and residual lignin after DESs and DESs-THF pretreatment were obtained by self-assembly in the present research. Then, films were prepared by incorporating them into polyvinyl alcohol (PVA) solution. The properties of various films were characterized and compared. Results showed that as the LNPs content increased, the UV blocking capacity of the films was gradually enhanced than PVA film. The DES-THF films showed better antioxidant properties up to 69 % due to higher phenolic hydroxyl content. The hydrophobicity of films incorporated with DESs-THF pretreated lignin was consistently better than that of DES pretreated. DES-THF-M films showed a higher Tmax than that of DES-M films, resulting in better thermal stability. Moreover, DES-THF-L films are lighter in color due to a lower degree of condensation, which is favorable to subsequent applications. The incorporation of LNPs improved mechanical and antioxidant properties, thermal stability, and UV shielding ability of PVA films, especially lignin after DES-THF pretreatment. In conclusion, the prepared PVA/LNPs composite films possessed good functional properties that make them potential for packaging materials.

Oxidative stability of chelated Sn(II)(aq) at neutral pH: The critical role of NO3- ions.

Tin(II) compounds are versatile materials with applications across fields such as catalysis, diagnostic imaging, and therapeutic drugs. However, oxidative stabilization of Sn(II) has remained an unresolved challenge as its reactivity with water and dioxygen results in loss of functionality, limiting technological advancement. Approaches to slow Sn(II) oxidation with chelating ligands or sacrificial electron donors have yielded only moderate improvements. We demonstrate here that the addition of nitrate to pyrophosphate-chelated Sn(II)(aq) suppresses Sn(II) oxidation in water across a broad pH range. Evidence of hydroxyl radical concentration reduction and detection of a radical nitrogen species that only forms in the presence of chelated Sn(II) point to a radical-based reaction mechanism. While this chemistry can be broadly applied, we present that this approach maintains Sn(II)'s antibacterial and anti-inflammatory efficacies as an example of sustained oral chemotherapeutic functionality.

Hydrogen enrichment in methanol SI engine at varying injection timing during compression stroke

This study investigates the effect of hydrogen enrichment in a direct-injected methanol-fuelled SI engine, with combustion and emission performance analysed by varying the methanol injection timing from 150° to 60° CA bTDC. A three-dimensional computational fluid dynamic model of the hydrogen-enriched methanol engine was developed to predict the engine performance, in-cylinder, and emission characteristics. The numerical model was solved using three-dimensional Reynolds-Averaged Navier Stokes, the RNG k-epsilon model for turbulence, the O'Rourke and Amsden sub-model for heat transfer, the extended Zeldovich mechanism for nitric oxide emissions, and the Hiroyasu-NSC model for soot emissions. The results indicated that retarding the injection timing resulted in a decrease in the indicated specific CO and soot emissions along with a rise in the indicated specific NOx emissions. Furthermore, hydrogen enrichment with methanol enhanced the hydroxyl radical concentration, reduced the combustion duration, reduced also the indicated specific CO and soot emissions while increasing the indicated specific NOx emissions. The study indicates that hydrogen enrichment could extend the late injection timing limit of methanol by enhancing fuel-air mixing, which improves and controls the combustion process more effectively.

Influences of surface active-groups on the exothermic properties and oxidation of coal molecules

In this study, coal samples' reactive group contents were changed using extractants, and the effects of the reactive group contents spontaneous coal combustion were investigated using infrared spectroscopy, thermogravimetry/derivative thermogravimetry, and differential scanning calorimetry. The results showed that the coal samples' hydroxyl group contents decreased in the order ethylenediamine (3.832 %) > N-methyl-2-pyrollidone mixed solution (2.091 %) > petroleum ether (0.882 %) > toluene (0.495 %) and that the hydroxyl group content was inversely related to the characteristic temperature point. RDG analysis showed that ethylenediamine formed N–H–O hydrogen bonds with hydroxyl-group-bearing molecules, coal molecules formed C–H–O hydrogen bonds with NMP molecules, petroleum ether generated a cumulative dispersive force with aliphatic side chains, and toluene molecules' benzene rings formed a very stable spatial structure with coal molecules' benzene rings. The thermogravimetry/derivative thermogravimetry curves showed that because the characteristic temperature points of the extracted coal samples moved to the high-temperature region from T5 onward, the coal samples had to be heated to a higher temperature to reach the energy required for the reaction. From the DSC thermograms, the exergy decreased in the order toluene (110.68 J/g) > NMP (110.52 J/g) > ethylenediamine (78.29 J/g) > petroleum ether (65.45 J/g). With increasing temperature from T1 to T6, the Pearson correlation coefficients of the alcoholic and phenolic hydroxyl groups were calculated at −0.7, −0.72, −0.93, −0.84, −0.8, −0.8, and −0.93 and −0.72, −0.91, −0.83, −0.79, −0.815, and −0.91, respectively, indicating that the hydroxyl group content influenced the coal's spontaneous combustion more than the other groups' contents.

Optimizing biosurfactant structure: Experimental and theoretical investigation of the influence of hydroxyl groups on sour corrosion mitigation

Oil and natural gas remain crucial for meeting global energy demands, but their extraction and processing face significant challenges due to sour corrosion. This study explores the influence of hydroxyl groups on the performance of biosurfactants, specifically sorbitol oleate (SOCI) and pentaerythritol oleate (POCI), in sour environments. This study reveals that the presence of more hydroxyl groups in inhibitor molecules significantly enhances their effectiveness against sour corrosion. A weight loss study showed that the corrosion rates dropped to 0.033 mm/y for POCI and 0.005 mm/y for SOCI from an initial rate of 0.490 mm/y in the blank solution, indicating the superior inhibition efficiency of SOCI (98.9 %) compared to POCI (93.3 %) at 24 × 10−4 M. Electrochemical measurements corroborated these findings, demonstrating increased corrosion resistance and reduced current densities in the presence of both inhibitors, with SOCI exhibiting better performance. The inhibition mechanism involves a combination of physical and chemical adsorption. Density functional theory calculations indicated the role of hydroxyl groups in enhancing adsorption and corrosion inhibition efficiency, with SOCI exhibiting a smaller energy gap, lower hardness, and higher softness compared to POCI. MD simulations confirmed the stable adsorption of both inhibitors on the Fe (110) surface, with SOCI showing a more favorable orientation and stronger interaction due to its higher number of hydroxyl groups. This facilitates stronger adsorption on the CS surface and the formation of a more robust protective film. The combined experimental and computational findings highlight the importance of molecular structure, film-forming ability, and hydroxyl content for the design and development of next-generation hydroxyl-rich biosurfactants for mitigating sour corrosion in the oil and gas industry.

A Nd-doped silica glass with high doping concentration, low hydroxyl content, and 900 nm fluorescence emission fabricated by laser additive manufacturing

The 900 nm wavelength laser is effective for atmospheric detection and various other applications.The frequency-doubled 450 nm deep blue laser can be used in maritime military, quantum optics, biomedicine, laser storage, laser display, and deep ultraviolet laser fields, among others. Although Nd3+ is considered the optimal medium for generating 900 nm lasers, competition with the 1060 nm emission wavelength must be addressed. In Nd-doped silica glass, without the introduction of aluminum, the emission intensity of the three-level transition is higher than that of the four-level transition. However, it can cause a concentration quenching between Nd3+, but co-doping with Al can effectively suppress it. As the Al/Nd ratio increases, the emission intensity at 1060 nm increases relative to that at 900 nm. By precisely adjusting the Al/Nd ratio, it is possible to suppress the 1060 nm emission while also inhibiting concentration quenching caused by Nd3+.

Designed synthesis of demethylated-hydroxymethylated lignin-based adsorbent for removal of Cr(VI) ions from wastewater

Lignin-based adsorbents for the removal of Cr(VI) ions have attracted intensive attention due to the advantages of renewability, biodegradablity, low cost and environmental friendliness. However, there are still a lot of challenges such as poor adsorption capacity, low lignin content in adsorbents, and harsh preparation conditions. Here, a tandem hydroxymethylation-demethylation method is proposed for preparing an excellent lignin-based Cr(VI) adsorbent (DHKL), which features with high lignin content (>85 wt%) and high hydroxyl content (up to 6.26 mmol/g) under milder conditions. The prepared DHKL exhibits an adsorption capacity reaching up to 1040.9 mg/g and can maintain this capacity even in the presence of other metal ions in the solution. Model analyses indicate that chemisorption occurring in a monolayer is the main process, which is spontaneous and endothermic. Structural changes of DHKL before and after adsorption indicated that Cr(VI) ions are mainly reduced to Cr(III) ions by hydroxyl groups with some of the absorbed Cr ions dispersed into the inner part of DHKL. Based on these results, the detailed possible adsorption mechanism is deduced, providing guidance for designing, producing and utilizing lignin-based adsorbents.