High Hydroxyl Research Articles

Synthesis and Performance of Epoxy-Terminated Hyperbranched Polymers Based on Epoxidized Soybean Oil

Epoxy-terminated hyperbranched polymers (EHBPs) are a class of macromolecular polymers with a hyperbranched structure containing epoxy groups. They possess characteristics such as low viscosity, high functionality, and thermal stability, which endow them with broad application potential in materials science and chemical engineering. This study uses epoxidized soybean oil (ESO) as the raw material, which undergoes ring-opening reactions with glycerol and is esterified with 2,2-bis(hydroxymethyl)propionic acid (DMPA) to obtain epoxy soybean oil polyol (EGD) with a high hydroxyl value. Subsequently, four types of EHBPs are synthesized by incorporating epichlorohydrin (ECH) in mass ratios of 1:3, 1:4, 1:5, and 1:6 under strong alkaline conditions. The product structure is characterized using FT–IR and GPC. The degree of branching of EGD is calculated using 1H NMR and 13C NMR spectroscopy. The epoxy value of EHBPs is tested using the hydrochloric acid–acetone method, and the water contact angle, adhesion properties, rheological properties, and thermal properties of the EHBPs are also evaluated. The results show that the degree of branching of EGD is 0.45. The epoxy values of the EHBPs are 0.73, 0.79, 0.82, and 0.89 mol/100g, respectively. As the epoxy value and molecular weight of the epoxy hyperbranched polymers (EHBPs) increase, the water contact angle and adhesion strength of the EHBPs rise progressively and the viscosity decreases. Additionally, the glass transition temperature increases with the increase in the epoxy value. These epoxy hyperbranched polymers with low viscosity and high adhesion strength offer a promising approach for modifying surface coatings or formulating adhesives.

A ternary deep eutectic solvent for efficient biomass fractionation and lignin stabilization.

The efficient isolation and lignin stabilization are critical to the fractionation process of lignocellulosic biomass, enabling the subsequent valorization of both carbohydrates and lignin. In this study, a ternary deep eutectic solvent pretreatment system with outstanding reusability has been developed. Under optimal conditions (ChCl: MT: p-TsOH=1:1:0.5, 120°C, 60min), the system efficiently removed 94.66% of hemicellulose and 95.74% of lignin while retaining 84.50% of cellulose. Glucose was obtained from the cellulose-rich solid residue via enzymatic hydrolysis, achieving an 87.12% yield. This DES system inhibits lignin condensation through a dual mechanism of α-etherification and intermolecular forces (π-π stacking and hydrophobic interaction). The recovered lignin exhibits a low molecular weight (922-1049g/mol), high phenolic hydroxyl content (2.57-3.37mmol/g), low polydispersity (1.54-1.61), and high purity (93.02%). Combined with its superior antioxidant activity and UV shielding properties, this lignin represents a promising new resource with potential applications.

Simultaneously reinforce and de-color nanocellulose/lignin composite films by tuning hydroxyl groups with sodium borohydride

Researchers utilized NaBH4 to gently modify alkali lignin, resulting in L-Sx-ty-Pz with high hydroxyl value and decolorization, significantly enhancing the strength of composite films with cellulose nanofibers (CNF). Without strict pH control, the hydroxyl content of the modified lignin reached as high as 9.14 mmol/g. The CF/L-S1-t120-Pu composite film achieved a maximum stress of 45.33 MPa, representing a 116% and 77% increase compared to pure CNF and crude alkali lignin composite films, respectively. The reduction effect of NaBH4 imparted transparency to the film, broadening its applications. Additionally, the film's excellent antibacterial and flame-retardant properties provide strong support for industrial utilization.

Efficient Separation of Poplar Lignin Using a New Carboxylic Acid-Based Deep Eutectic Solvents - Choline Chloride/Malonic Acid.

Separation of lignin by pretreatment is an important step in biomass refining. This study investigated how a novel dicarboxylic acid-based deep eutectic solvent (DES) - choline chloride (ChCl)/malonic acid (MA) - affected the process of separating lignin from poplar. At 140 °C for 3.0 h, with a ChCl: MA molar ratio of 1: 3.5, the ideal pretreatment conditions were met, and 91.8 % lignin was obtained. Even after five DES reuses, the consistent and effective separation efficiency of 77.9 % remains unchanged. The hydrolysate contained 92.4 % of the recovered lignin, with a purity of 94.6 %. Moreover, the regenerated lignin obtained through the new DES pretreatment exhibited a high phenolic hydroxyl content of 1.9 mmol g-1 and a low polydispersity index of 1.4. The results showed efficient and selective separation of lignin using the new binary carboxylic acid-based DES pretreatment was achieved. This research offers a novel approach to effectively separate wood fiber biomass and extract valuable lignin.

Optimized Biomass Production of Probiotic Bacterium Pediococcus acidilactici TMAB26 Using Pineapple Peel: A Response Surface Methodology Approach

Probiotics, being non-pathogenic, offer distinct health advantages tailored to specific species and demonstrate antioxidant properties. Currently, there is a growing interest among people in probiotics due to their therapeutic and health-promoting benefits. The study aimed for utilization of pineapple peel waste as carbon source for biomass production of probiotic bacterial strain Pediococcus acidilactici TMAB26 demonstrating promising avenues for sustainable and efficient production methods. By employing Central Composite Design (CCD) Response Surface Methodology (RSM), the study successfully optimized fermentation conditions, highlighting the significance of pH, temperature, and inoculum size in maximizing biomass yield. The pineapple peel waste was used as complete carbon source that replaced half of the other nutrient componentsof commercial MRS broth. The optimization of medium for biomass production of Pediococcus acidilactici TMAB26 was carried out using Central Composite Design (CCD) in 2 L Erlenmeyer flasks. The findings highlight the pivotal role of the physical parameters in enhancing biomass production, with an optimal combination of 2.5% inoculum, pH 6.5, and temperature 35 °C resulting in a significant biomass yield of 2.56g/100ml. Furthermore, the pineapple peel extract exhibited notable total phenolic content of 262 μg/mL and glucose content of 1.83%, indicating its significance as a valuable nutrient source. Moreover, the probiotic strain TMAB26 showed impressive antioxidant potential, as evidenced by its high hydroxyl radical scavenging activity (92.1 ± 4%) with an IC50 of 24.76 μg/ml.

Electric Field-Induced Synergetic Enhancement of Local Hydroxyl Concentration and Photogenerated Carrier Density for Removal of COads in Electrocatalytic Formic Acid Oxidation.

Direct formic acid fuel cell (DFAFC) is an efficient power generation device, due to its high energy density, low fuel crossover and low emission. However, the anodic reaction of DFAFC, formic acid oxidation (FAOR), inevitably proceeds through an indirect pathway, adsorbing carbon monoxide intermediate (COads), resulting in a rapid decline of activity for FAOR. Therefore, effectively removing COads is the key to the development of DFAFC. In this work, Pd/CeO2 catalyst is synthesized by in situ growth of Pd nanoparticles on the hollow CeO2. Due to the difference of work function between Pd and CeO2, a built-in electric field from Pd side to CeO2 side is formed, which induces a synergistic enhancement of the photogenerated carrier density and the local high hydroxyl concentration at the Pd/CeO2 interface, thus promoting the oxidative removal of COads and significantly improving the stability of FAOR. Therefore, in photo-assisted electrocatalytic FAOR, Pd/CeO2 not only possessed high mass activity (4161.72 mA mg-1 Pd), and its mass activity decreases by only 20.1% after 40000 s chronoamperometry test, which is superior to most Pd-based catalysts. This work provides a new strategy for efficient removal of COads in FAOR through constructing built-in electric fields, which promotes the DFAFC application.

Fabrication of Water-Based Alcoholized Poly(butylene succinate-co-adipate) Submicron Particles as Green Coating Agents for Sustainable Paper Packaging.

This work aims to fabricate the water-based suspension of poly(butylene succinate-co-adipate) (PBSA) particles by an oil-in-water emulsion technique for use as coating agents to enhance paper-based packaging performances and sustainability. A commercial PBSA resin is functionalized by sizing down an approach via microwave-assisted alcoholysis using propylene glycol (PG). The effect of PBSA/PG feed ratio on the structures, properties, and particle formability of the alcoholized (aPBSA) products is examined. 1H NMR results reveal that the average molecular weight of the aPBSA product decreases to half that of neat PBSA when using a ratio of 24:1 and further decreases to a quarter at 6:1. By using small-size aPBSA, the obtained water-based particles show high stability due to high hydroxyl content and poly(vinyl alcohol) assistance. The suspension is then sprayed on a kraft paper substrate and heated at 60 and 100 °C. SEM results reveal that the submicron aPBSA particles penetrate the paper matrix, filling the paper's pores and forming a protective, smooth layer on the paper surfaces. The coated paper shows high water resistance (Cobb60 value of 19.6 g/m2) and water vapor transmission rate (1160 g/(m2 day)). In addition, the aPBSA-coated layers do not impede the paper's repulping and recycling processes, making it a promising solution for improving the sustainability of paper-based packaging.

Solvothermal synthesized mesoporous BiOCl nano-ellipsoids with oxygen vacancies for photocatalytic degradation of low density polyethylene (LDPE) plastic

This study explores mesoporous BiOCl nanoparticles as a promising photocatalyst for low-density polyethylene (LDPE) degradation under visible light for the first time. A solvothermal synthesis yields BiOCl nanoparticles with a high ratio of exposed {010} facets and abundant oxygen vacancies (OVs). These properties, along with the co-existence of Bi³-x and Bi³⁺x defect states, promote a tailored surface chemistry with high surface-bound hydroxyl groups. These properties optimize light absorption by inducing favorable surface states, leading to a red shift in the light absorption edge for efficient utilization of visible light. Additionally, OVs suppress the recombination of photo-generated charge carriers and enhance their transfer rate. Furthermore, the free-standing LDPE/BiOCl nanocomposite films of 50μm, prepared via solution casting technique with varying BiOCl weight percentages (3, 5, and 7 wt.%), exhibit remarkable photocatalytic activity. The analysis of photodegraded LDPE confirms the presence of carbonyl groups (C.I.= 86%), cracks, pores, and hydroxyl radicals (•OH), alongside reduced thermal stability and band gap changes. Through meticulous analysis of the results obtained, we have ascertained that the optimal photocatalytic degradation of LDPE is achieved by incorporating up to 5 wt.% of BiOCl.

Recycling the sediment of cotton spinning effluent for rigid polyurethane foams

Sediment from the effluent of cotton spinning industry was valorized as the renewable bio-based polyols substitute for the rigid polyurethane (RPUFs), targeting to generate the economic and environmental benefits. Before reaction with the isocyanate, the sediment was functionalized by hydroxymethylation, in order to increase the density of the active hydroxyl groups for higher reactivity. The structural characterization results of the functionalized sediment indicated the material exhibited narrow molecular weight distribution, high hydroxyl groups content, and highly aromatic skeleton, which can be qualified as the renewable polyols for the RPUFs. In the crosslinking process, the effect of the polyols substitute rate of the sediments on the physio-chemical properties and the thermo-resistant performances of the resulting RPUFs was investigated. Specifically, in the group with 30 wt% of polyols substitution, the received foam exhibited comprehensive superiorities in compressive strength (0.58 MPa), apparent density (58 kg m−3), and thermo-conductivity (0.032 W m−1 K−1). Attractively, the RPUFs also exhibited good flame retardancy. The burning time can be extended by 30 % compared to the control group that without the sediment's substitution. Moreover, the RPUF also possessed good degradability, allowing for harmless recycling. The current work provided a potential route for the valorization of the hazardous waste effluent from the cotton spinning industry.

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 %).

In vitro antioxidants and anti-inflammatory potentials of high protein-fibre cookies produced from whole wheat, sweet potato, rice bran and peanut composite flour blends

The growing demand for low-cost and functional snacks in many developing nations called for interest in the use of locally grown crops as substitutes for costly imported wheat flour. The amino acid composition, antioxidant and anti-inflammatory properties of the cookies from whole wheat, sweet potato, rice bran and peanut (56.25:18.75:5:20; 37.50:37.50:5:20; 18.75:56.25:5:20% as WPRG 1, WPRG 2, WPRG 3) composite flour blends, respectively, were obtained in this study. The 100% whole wheat and 100% refined flours served as control 1 and 2, respectively. The level of hydrophobic and aromatic amino acids was significantly (p < 0.05) high in WPRG 2 (~ 30 and ~ 10%), respectively when compared to others. However, the branched chain amino acids and Fischer ratio was significantly (p < 0.05) high in WPRG 1 (11.40% and 1.29), respectively, which could have contributed to their improved bioactivities. Notably, the composite cookie samples WPRG 1, 2 and 3 had higher hydroxyl (73.86 − 84.16%), DPPH (76.52 − 84.60%) radical scavenging as well as ferric reducing antioxidant (0.64–0.87 mmolFe2+/mg) properties than the control samples WWF and CWF, respectively. On the contrary, the metal chelating activities of the cookies WPRG 1–3 were not significantly (p > 0.05) different from control samples WWF and CWF. The improved amino acid profile and enhanced antioxidant properties of the composite cookies might have effectively influenced their anti-inflammatory properties (IC50; < 26 μg/ml) when compared to the control samples (IC50; ~ 40 μg/ml), respectively. Hence, the cookies that comprised of antioxidants and anti-inflammatory potentials needed in human health, were acceptable by the consumers.Graphical

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.

In Vitro Inhibitory Mechanism of Polyphenol Extracts from Multi-Frequency Power Ultrasound-Pretreated Rose Flower Against α-Glucosidase.

This paper explored the in vitro inhibitory mechanism of polyphenol-rich rose extracts (REs) from an edible rose flower against α-glucosidase using multispectral and molecular docking techniques. Results showed that REs had an inhibitory effect on α-Glu activity (IC50 of 1.96 μg/mL); specifically, the samples pretreated by tri-frequency ultrasound (20/40/60 kHz) exhibited a significantly (p < 0.05) stronger inhibitory effect on α-Glu activity with an IC50 of 1.33 μg/mL. The Lineweaver-Burk assay indicated that REs were mixed-type inhibitors and could statically quench the endogenous fluorescence of α-Glu. REs increased the chance of polypeptide chain misfolding by altering the microenvironment around tryptophan and tyrosine residues and disrupting the natural conformation of the enzyme. Molecular docking results showed that polyhydroxy phenolics had a high fit to the active site of α-Glu, so REs with high polymerization and numerous phenolic hydroxyl groups had a stronger inhibitory effect. Therefore, this study provides new insights into polyphenol-rich REs as potential α-glucosidase inhibitors.

Application of high-polarity hydroxyl polyacrylate pressure sensitive adhesive in rizatriptan transdermal drug delivery patch

This study aimed to design a rizatriptan (RIZ) transdermal patch by combining of high-polarity hydroxyl pressure sensitive adhesive (PSA) AAOH-45 with an ion-pair strategy and investigate the molecular mechanism of high content hydroxyl PSA to enhance drug-PSA miscibility. RIZ free base, ion-pair complexes and PSAs containing hydroxyl group were prepared and characterized. Formulation factors including counter-ions, PSAs, drug-loading and others were optimized through single-factor studies and evaluated through pharmacokinetic studies and skin irritation tests. The properties of high polarity PSA and molecular mechanism of drug-PSA miscibility were investigated through molecular simulation, FTIR spectra, 13C NMR spectra, DSC, and rheology study. The optimized formulation contained 20 % (w/w) RIZ-OA (Rizatriptan-Oleic acid), 80 % AAOH-45 (w/w) as the matrix, and had a thickness of 90 μm. Compared with the oral group (MRT0-t = 5.96 ± 0.97 h) and the control patch group (MRT0-t = 11.30 ± 1.78 h), the pharmacokinetic behavior of the optimization group demonstrated sustained drug delivery behavior (MRT0-t = 20.21 ± 0.61 h) with no irritation phenomenon. The miscibility of RIZ with PSAs was positively correlated with the mass percentage of 2-HEA. Higher polar similarity, lower flowability, and stronger intermolecular interaction were responsible for the higher compatibility of high hydroxyl PSA with the drug. This study provided a reference for increasing the drug-loading in PSA and developing RIZ patch.

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.

Effect of Ultrahigh Dose Rate on Biomolecular Radiation Damage.

Dose rate is one of the important parameters in radiation-induced biomolecular damage. The effects of dose rate have been known to modify radiation toxicity in biological systems. The rate and extent of sublethal DNA damage (e.g., base damage and single-strand breaks) repair and those of cell proliferation have been manifested by dose rate. However, the recent preclinical application of ultrahigh dose rate [(UHDR) ca. 40 Gy/s and higher] radiation modalities have been shown to lower the type and extent of radiation damage to biological systems. At these UHDR, radiation-induced physicochemical and chemical processes are expected to differ from those observed after irradiation at conventional dose rates (CONV). It is unclear whether these UHDR conditions can affect the quality (type) and quantity (extent) of biomolecular damage such as DNA lesions. Here, we comparatively study the influence of indirect effects of CONV and UHDR on the formation of DNA strand breaks and clustered damage including densely accumulated lesions in an aerated and an anoxic dilute aqueous solution of a plasmid DNA model under low and high hydroxyl radical (•OH) scavenging conditions. Aqueous solutions of purified supercoiled plasmid DNA (pUC19) were prepared in either air- or nitrogen-saturated conditions, with Tris buffer added as the radiation-produced •OH scavenger at low and high scavenging capacities. These DNA samples were irradiated using kV X-ray systems at CONV (0.1 Gy/s) and high dose rate (HDR, 25 Gy/s) as well as UHDR (55 and 125 Gy/s) under different scavenging and environmental conditions. DNA lesions including strand breaks and clustered damage including densely accumulated lesions were quantified by gel electrophoresis and the yields of these lesions were calculated from the dose-response curve. Non-DSB clustered damage including densely accumulated lesions were evaluated by treating DNAs using bacterial endonuclease enzymes (Fpg and Nth) prior to gel electrophoresis. UHDR of 55 and 125 Gy/s induced lower amounts of both isolated strand breaks and clustered DNA damage including densely accumulated lesions at doses >40 Gy in the presence of oxygen, compared to the abundance of these lesions induced by 0.1 and 25 Gy/s irradiation under the same dose conditions. Overall, the strand break and clustered damage including densely accumulated lesions yields decreased by factors of 1.3-3.5 after UHDR. We did not observe these differences either via •OH scavenging or by removing oxygen from the solution. In addition, our results point out that the inter-track recombination reactions did not contribute to the observed dose-rate effects on DNA damage. The effects of dose rate on DNA damage are highly dependent on the total dose, as expected, but also on the •OH scavenging capacity that is employed in the aqueous DNA solutions. These important variables may be relevant in biological systems as well. On a practical level, our in vitro plasmid DNA model, which permits to precisely vary the •OH scavenging capacity and gassing conditions (air saturated vs. N2 saturated) can help to differentiate dose-rate effects on biomolecular damage. Our results indicate that the radical-radical reactions are important in understanding the dose-rate effect on DNA damage.

Regulating the Zn electrode/electrolyte interface with lactose additive for high performance Zn anode

The practical utilization of rechargeable aqueous zinc metal batteries (AZMBs) has been constrained by the formation of zinc dendrites and other associated issues. This article introduces lactose, a compound rich in hydroxyl groups, as an electrolyte additive into the aqueous solution of the electrolyte with the objective of suppressing the harmful growth of zinc dendrites. The lactose additive, with its strong zincophilicity, robust intermolecular hydrogen bonding, and a large number of exposed high electronegativity hydroxyl groups, enables lactose to effectively modulate the electrode/electrolyte interface in a dynamic manner, thereby achieving the stability and reversibility of the zinc anode. The findings presented in this work demonstrate the uniform deposition and stripping of zinc in a 2 M ZnSO4 electrolyte with the addition of lactose, thereby enhancing the cycling performance of Zn||Zn batteries. The alteration of the zinc ion environment on the surface of the zinc electrode, in conjunction with the dynamic modulation of the Gouy-Chapman-Stern (GCS) layer by lactose, increases the nucleation overpotential, thereby facilitating to a uniform deposition morphology in lieu of the formation of large-scale dendrites. Furthermore, the formation of hydrogen bonds serves to prevent the occurrence of side reactions. These factors act in concert to enhance the electrochemical performance of AZMBs. The addition of lactose to the electrolyte has resulted in a significant enhancement in the Coulombic efficiency of the card-type Zn||Cu asymmetric battery, reaching 99.7 %. The biodegradability of lactose and the sustainability of its source make this research conducive to the development of environmentally friendly battery electrolyte additives.

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.

Application of biochar and selenium together at low dose efficiently reduces mercury and methylmercury accumulation in rice grains

Irrespective of cost and ecological risk, literatures have reported that both biochar and selenium (Se) alone at high application rate exhibited positive effects on decreasing rice mercury (Hg) uptake in high Hg contaminated paddy soil. In this study, we investigated whether biochar and Se together at low dose could efficiently reduce the rice grain Hg and MeHg accumulation in the slight Hg-contaminated soil. Compared with control (CK), the Hg concentration of grains in the BC3, Se0.5, and BC3 + Se0.5 treatments decreased by 5.4 %, 38.3 %, and 48.5 %, respectively. Co-application of biochar and Se also decreased the methylmercury (MeHg) concentration in rice grains by 29.1–91.6 %. The decrease of Hg and MeHg level in rice grains for biochar and Se treatments could be attributed to the following mechanisms: (1) high Hg (primarily inorganic Hg) adsorption on biochar through its high hydroxyl groups and large specific surface area; (2) Increased dissolved organic carbon and cysteine contents in pore water after biochar application, which reduced the availability of soil Hg through complexation; (3) Decreased bioavailability of Hg in soil due to the formation of HgSe precipitation which inhibited Hg uptake and translation by rice plant; (4) Both biochar and Se facilitated the reduction of MeHg in soil. Our results indicate that co-application of biochar and Se at low dose is a promising method to effectively mitigate Hg accumulation in rice grains from the slight Hg-contaminated soil.

In situ activation of Sn(OH)4 catalyst for efficient CO2 electroreduction to formate

Electroreduction of CO2 into the highly valuable fuel formic acid (HCOOH) has been considered an ideal method for converting renewable energy and addressing environmental challenges. Herein, we present a straightforward and rapid method for preparing Sn(OH)4 catalysts specifically designed for electroreducing CO2 to formate. The Sn(OH)4 catalyst obtained through in-situ electrochemical reduction transforms from bulk morphology to nanoporous form, featuring numerous grain boundaries and a high hydroxyl content, enhancing its stability and availability of active sites.The resulting electrocatalyst demonstrates a remarkable formate faradaic efficiency (FEformate) exceeding 80 % across a broad potential range (−0.9 to −1.9 V). Notably, a peak FE value of 92 % is achieved for HCOOH production at −1.7 V vs RHE. This study presents a novel and effective method for developing high-performance Sn-based catalysts.