Free Hydroxyl Research Articles

The role of BaTiO3 nanoparticles as photocatalysts in the synthesis and characterization of novel fruit dyes is investigated.

In the present work, the photocatalytic activity against the natural dye extracted from the novel fruits has been studied by the BaTiO3 nanoparticles (NPs) under a ultra-violet (UV) light source. The large concentrations of an essential phenolic agent present in this phytochemical extract superimposed with cloths fibers make strong stain and degrade into another form of toxic, which is excluded from the many textiles industries as the colorful waste waters without recycling and removal of that dye pigments have been investigated using both photodegradation and photoluminescence techniques. The entitled nanoparticles (NPs) were prepared using the soft chemical root-modified solvothermal synthesis combo method and exposure to heat treatment such that the annealing process has been done for different temperatures ranging from 100°C to 250°C. As for as concern the characterization, as a start, structural and morphology studies have been reported here that highly crystalline oriented peaks data using powder x-ray diffraction techniques (PXRD) as well as the surface morphology including the size, shape, and mass distribution using the field emission scanning electron microscopy (FESEM) techniques, which purely belong to rutile tetragonal structure of the crystal system and circular and noncircular flakes like rough surface morphology materials respectively. The lattice dissociation constant 'ε' value of the BaTiO3 NPs has determined to be ~2.71 × 10-3 using the Williamson-Hall (W-H plot) analysis of crystallographic data. In the UV visible spectroscopy findings, since the extreme quantum confinement of BaTiO3 nanoflakes/nanodisc, the optical energy bandgap has been estimated to be a range of 1.98 to 2.67 eV (~2.48 eV) found from the Tauc plot analysis, which contributes to the significantly owing to the enhanced photocatalytic efficiency with excellent performance along exciton formation, superoxide ions, and hydroxyl free radicals generations under UV-vis light irradiation resulting in efficient degradation of typical novel fruit organic dye. Photoluminescence spectra observed at room temperature and low temperature have been observed for the BaTiO3 nanoflakes, which exhibit the blue emission due to the crystalline defects such as the appearance of Ba vacancies leads to the conceivable beginning of p-type conductivity and the origination of free exciton emission reveals the direct bandgap transition nature of nanoflakes. RESEARCH HIGHLIGHTS: According to our findings, 89.71% of the natural syzygium cumin is degraded by photocatalysis reaction. As a plausible mechanism for the destruction of natural dyes under solar light, photocatalytic destruction has been proposed. The reaction between these reactive free radical species leads to high efficiency photodegradation with a short decay time. In addition to water treatment and environmental cleaning applications, the excellent performance of this photocatalyst makes it a promising candidate for other applications. Hence, the synthesized BaTiO3 nanoflakes showcase a highly significant advancement towards the development of a textiles dye recycling method.

Proximate, Mineral, Amino Acid Composition, and Bioactive Properties of Dough Meals Supplemented with African Walnut Flour

This study investigated the impact of African walnut flour supplementation on the nutritional and bioactive properties of dough meals formulated with varying proportions of plantain flour. The proximate composition, mineral content, amino acid profile, color characteristics, antioxidant and anti-diabetic properties were analyzed for five different formulations: 100% plantain flour (P100), 95% plantain flour with 5% African walnut flour (PAW95), 90% plantain flour with 10% African walnut flour (PAW90), 85% plantain flour with 15% African walnut flour (PAW85), and 80% plantain flour with 20% African walnut flour (PAW80). The proximate analysis revealed significant variations, with moisture content ranging from 53.71% to 71.89%, ash content from 0.77% to 1.28%, and protein content from 3.38% to 11.14%. Notably, PAW80 showed the highest protein content. Mineral analysis showed that calcium, potassium, and magnesium levels varied significantly across the samples, with the highest calcium content observed in PAW80 (32.55 mg/kg) and the highest potassium content in PAW95 (47.80 mg/kg). Amino acid analysis indicated that essential amino acids, particularly leucine, valine, and lysine, were present in higher concentrations in the supplemented samples compared to P100. Antioxidant assays indicated that PAW80 had the highest 2,2-diphenyl-1-picrylhydrazyl (DPPH) (67.22%) and hydroxyl (73.66%) free radical scavenging activities. The in vitro anti-diabetic assays revealed that α-amylase and α-glucosidase inhibitory activities were enhanced with higher walnut flour supplementation. These findings suggest that African walnut flour can significantly enhance the nutritional quality and bioactive properties of plantain-based dough meals, and thus make it a functional food with potential health benefits.

Effect of vildagliptin conjugated monometallic nanoparticles and bimetallic nanocomposites on diabetes-induced cognitive deficit

Oxidative stress is one of the major causes of different metabolic disorders, including diabetes, cardiovascular diseases, neurodegenerative diseases and cancers. Some metabolic disorders like diabetes mellitus leads to secondary complications after micro and macrovascular complications. Some of the most prevalent neurodegenerative diseases, like cognitive impairment and Alzheimer's disease, are found in chronic diabetic patients. The present study is designed to understand the mechanism of interconnection between diabetes mellitus and cognitive deficit using the alloxan model of diabetes-induced cognitive deficit in the rat model. The alloxan monohydrate produces reactive oxygen species, producing superoxide free radicals, hydrogen peroxide and hydroxyl radicals. The hydroxyl radicals ultimately cause the death of beta cells, causing diabetes. Hence, the correlation of oxidative stress and neurodegeneration in cognitive impairment is the trigger for this study. In the present study, we investigate the ameliorative effect of vildagliptin (VLD) and its conjugated nanoparticles against alloxan-associated brain damage due to oxidative stress. The gold (Au), selenium (Se) nanoparticles, and bimetallic (Se@Au) nanocomposites of VLD are synthesized and assessed for improvement in their brain availability. The in-vitro antioxidant evaluation of the VLD and nanoparticles is done using DPPH, ABTS, and FRAP assay. The memory-related neurobehavioral studies, in-vivo antioxidant studies, in-vivo biochemical studies, and histopathological examinations are evaluated in rat brains. The VLD and its nanoformulations exhibited in-vitro and in-vivo antioxidant properties significantly (p < 0.01). They reduced the activity of AChE and nitrite in the alloxan diabetic rats. The bimetallic Se@Au VLDNCs displayed a more protective effect than VLD, VLD–AuNPs, and VLD–SeNPs.

Differential Cytoprotective Effect of Resveratrol and Its Derivatives: Focus on Antioxidant and Autophagy-Inducing Effects

Numerous beneficial effects of resveratrol were reported; however, its pharmacological profile is contradictious. Previously, we have demonstrated that resveratrol has a dose-dependent cytoprotective effect and the essential role of autophagy induction was demonstrated. Resveratrol suffers from unfavorable pharmacokinetics, hindering its clinical use. Our aim was to study the cytoprotective effect of resveratrol derivatives to better understand structure–activity relationships that may facilitate the development of compounds with better druglike characteristics. Serum-deprivation-induced caspase activation, free radical generation, mitochondrial membrane depolarization and autophagy were detected in the presence of resveratrol analogs with different oxidation states on mouse embryonal fibroblasts. Distinct cytoprotective mechanisms of the examined compounds were revealed. Monomethyl resveratrol had similar potency to resveratrol (EC50: 85.3 vs. 84.2 μM); however, autophagy induction was not essential for its cytoprotective effect. Oxyresveratrol was found to be a strong antioxidant that can induce direct cytoprotection rather than autophagy. Trimethyl-resveratrol, lacking free hydroxyl groups, induced damage that was too significant and hardly compensated by the activation of cytoprotective machineries, and caspase activation was reduced by only 24.5%. Based on our results, methylation of resveratrol reduces its antioxidant activity, while autophagy induction can still contribute to its cytoprotective effect. The introduction of an additional hydroxyl group, however, augments the antioxidant properties, inducing cytoprotection without autophagy induction.

Investigation on mechanism of mechanical activation and chemical reactions in CMP of diamond assisted by hydroxyl free radicals

Chemical mechanical polishing (CMP) is a crucial manufacturing process for diamond substrate applications. However, due to the extremely high hardness and chemical stability of diamond, its CMP efficiency is extremely low. This study aims to achieve microscopic simulation of atomic oxidation removal at the three-phase interface between diamond abrasive particle, diamond substrate, and hydroxyl free radicals (∙OH) aqueous solution. The mechanical activation behavior, microscopic mechanism, and feasibility of elementary reactions in the ∙OH aqueous solution environment was studied using various perspectives of radial distribution function, central atomic coordination state, atomic bonding and removal forms, energy, electron orbitals, and density functional theory (DFT). The simulation results indicate that during the process of diamond atomic oxidation removal, the atomic density at the first adjacent position centered on one atom decreases, and the stable covalent bond structure is disrupted, resulting in an amorphous phase transition. The chemical adsorption reaction generates C-O and C–H bonds. The C atoms mainly separate from the diamond substrate by the forming products such as carbon monoxide (CO), carbon dioxide (CO2), and carbon chains. The mechanical activation behavior indirectly reduces the activation energy of chemical reactions, while increasing the absolute value of adsorption energy and improving the ability of chemical adsorption solution atoms H and O, as well as ∙OH groups. Based on DFT, it has been verified that the intrusion process of ∙OH groups in the elementary reactions involving the typical product C*O2 is an exothermic reaction that can occur spontaneously, and the energy barrier needs to be overcome by the mechanical action of abrasive particles. At the same time, the energetics of the oxidation of diamond C atoms to generate C*O2 have successfully confirmed that the combined action of ∙OH and diamond abrasive particles is expected to achieve efficient oxidation removal and finishing polishing of diamond atoms.

Polymeric phenylpropanoid derivatives crosslinked by hydroxyl fatty acids form the core structure of rape sporopollenin.

Sporopollenin, a critical innovation in the evolution of terrestrial plants, is the core building brick for the outer wall of land-plant spores and pollen. Despite its significance, the basic structure of sporopollenin remains elusive due to its extreme chemical inertness. In this study, we used ethanolamine to completely dissolve rape sporopollenin and successfully identified a total of 22 components, including fatty acids, p-coumaric acid, sterols and polymeric phenylpropanoid derivatives. After that, using NaOH treatment and partial dissolution, alongside Arabidopsis mutants analysis and spectroscopic methods, we determined that polymeric phenylpropanoid derivatives crosslinked by hydroxyl fatty acids serve as the core structure of sporopollenin. The free hydroxyl groups and carboxyl groups of the polymeric phenylpropanoid derivatives can be modified by other fatty acids (C16:0, C18:0 and C18:3) as well as alcohols/phenols (for example, naringenin, β-sitosterol), resulting in a structure that protects pollen from terrestrial stresses. This discovery provides a basis for further exploration of sporopollenin's role in plant reproduction and evolution.

Heterogeneous Activation of Persulfate by Petal-Shaped Co3O4@BiOI to Degrade Bisphenol AF

In catalytic tests, the results have shown that almost all the BPAF was removed within 30 min when the dosage of Co3O4@BiOI and sodium persulfate (PS) was 0.15 g and 0.1 mM, respectively. Acid conditions inhibited BPAF degradation, but the inclusion of a precise concentration of bicarbonate ions (HCO3−) promoted degradation. The presence of chloride (Cl−), sulfate ions (SO42−), and a high concentration of HCO3− inhibited the degradation process, whereas the addition of nitrate ions (NO3−) had a minor effect on the catalytic process. The presence of free radicals (sulfate (SO4•−), hydroxyl (•OH), and superoxide (O2•−)) and the non-free radical singlet oxygen (1O2) in the Co3O4@BiOI/PS system was determined by electron paramagnetic resonance (EPR) and quenching tests. We propose that the Co(II)/Co(III) and Bi(III)/Bi(V) redox pairs simultaneously activate PS where the Co3O4 and BiOI components work synergistically to promote the rapid oxidative degradation of BPAF in water.

Divergent Sc(OTf)3‐Catalyzed Tandem Cyclization of o‐Hydroxyphenyl Enaminones with 1,3,5‐Triazinanes: Access to C3‐Aminomethyl Chromones and Tetrahydropyrimidines

A Sc(OTf)3‐catalyzed tandem cyclization reaction of o‐hydroxyphenyl enaminones with 1,3,5‐triazinanes has been developed to generate two distinct annulated products in moderate to good yields, which is dominated by the electronic characteristics of the 1,3,5‐triazinanes. The 1,3,5‐triaryl‐1,3,5‐triazinane was treated as C–N synthon to produce C3‐aminomethyl chromone, while the 1,3,5‐trialkyl‐1,3,5‐triazinane acted as C–N–C–N synthons to deliver N,N‐dialkyl tetrahydropyrimidine with a free hydroxyl group.

Unveiling the apoptotic potential of antioxidant-rich Bangladeshi medicinal plant extractives and computational modeling to identify antitumor compounds

Nowadays, there has been a significant surge in the exploration of anticancer compounds derived from medicinal plants due to their perceived safety and efficacy. Therefore, our objective was to investigate the antioxidant and antiproliferative properties, along with the phytoconstituents, of methanol extracts from various parts of 15 selected Bangladeshi medicinal plants. Standard spectrophotometric methods and confocal microscopy were utilized to assess the antioxidant and antiproliferative potential of these extracts. Additionally, phytochemical profiling was executed through gas chromatography-mass spectrometry (GC-MS) analysis. Among the extractives, Bombax ceiba bark exhibited the highest scavenging capacity against DPPH (IC50: 10.3 ± 0.7 μg/mL) and hydroxyl (IC50: 3.9 ± 0.1 μg/mL) free radicals. Furthermore, the total antioxidants, reducing power, and polyphenols of B. ceiba bark were higher than those of other extracts. B. ceiba bark also showed significant antiproliferative capacity against MCF-7 cells (86.67 %) in the MTT assay, followed by Cocos nucifera roots (83.92 %), Bixa orellana leaves (44.09 %), and Leea macrophylla roots (25 %). Moreover, B. ceiba bark, L. macrophylla roots, C. nucifera roots, and B. orellana leaves-treated Ehrlich ascites carcinoma (EAC) cells demonstrated growth inhibition rates of 87.27 %, 80.45 %, 42.9 %, and 37.27 %, respectively. Fluorescence microscopic analysis of EAC cells treated with these extracts revealed apoptotic features such as condensed chromatin, cell shrinkage, nucleus fragmentation, and membrane blebbing compared to untreated EAC cells. The GC-MS analysis of B. ceiba bark identified 18 compounds, including various alcohols, alkenes, and esters. Additionally, a molecular docking study revealed oxalic acid, cyclohexyl dodecyl ester as the most potent compound (−6.5) active against breast cancer. In summary, our results demonstrate that B. ceiba bark possesses robust antioxidant and antiproliferative properties, along with potent antitumor compounds, which could be utilized in the treatment of carcinoma.

Synergistic catalytic degradation of Methotrexate using Ce-based high-entropy metal oxides: Insights from DFT calculations and CWPO performance

Methotrexate (MTX), a widely used anticancer drug, is a refractory organic pollutant posing serious threats to ecosystems and human health. This study focuses on the development of a novel catalyst composed of Ce-based high-entropy metal oxides (NHEMO) supported on nepheline for the catalytic wet peroxide oxidation (CWPO) process, targeting MTX degradation in simulated wastewater. The NHEMO catalyst exhibited a unique high-entropy structure that enhances catalytic performance by facilitating diverse electronic interactions, which was confirmed through X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses showing a well-defined crystal structure and uniform dispersion of metal oxides. Additionally, X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray spectroscopy (EDS) revealed a stable metal composition and high oxidation states of active metal sites. At a reaction temperature of 160 °C, with a residence time of 150 s and an oxidation coefficient of 5, the catalyst achieved a MTX removal rate of 93.49 % and a chemical oxygen demand (COD) removal of 99.95 %. Density Functional Theory (DFT) calculations further demonstrated that H2O2 decomposes into both adsorbed (surface-bound) and free (solution-phase) hydroxyl radicals (·OH). These radicals synergistically degrade MTX through both radical and non-radical pathways, ensuring comprehensive pollutant breakdown. The catalyst also showed excellent stability and a very low metal dissolution rate during the reaction, maintaining high catalytic activity after repeated recycling. This catalyst offers high cost-effectiveness, activity, and stability, providing a promising solution for treating refractory organic pollutants in pharmaceutical wastewater.

A novel and sustainable approach to efficiently modify cotton material via a physical flash-explosion with sub- or SCF-CO2 as medium.

A novel and eco-friendly approach to modify natural cotton fiber by flash-explosion with a sub- or supercritical fluid of carbon dioxide (sub- or SCF-CO2) for improving its structure and properties was constructed for the first time. The achieved results demonstrate that remarkable improvements in the coloration performance of cotton fiber by 71.1% and the water retention by 1001.2% against the control could be readily available by employing the flashily-explosion method at a recommended condition with 4-cycle explosion in sub- or SCF-CO2, and system temperature, fluid treatment duration and explosion number exhibited much more pronounced positive influences among all parameters. Additionally, minimal influences from the supercritical explosion on cotton fiber micronaire value, thermal property and tensile breaking strength were also observed. The scanning electron microscopy (SEM) and porosity investigations clearly show that plenty of micropores and/or strip fissures were formed on the fiber surfaces and their inner phases, and notably improved fiber surface area, pore volume and size were also obtained after a subsupercritical flash-explosion. Nuclear magnetic resonance hydrogen spectroscopy (1H NMR) and Fourier transform infrared spectroscopy (FT-IR) analysis disclose that numbers of hydrogen bonds between the fiber macrochains and/or from their intramolecular chains were broken by generating numerous free hydroxyl groups, which reasonably supported the improvements of the dye uptake behaviors and water retention properties, etc. The Energy-dispersive X-ray spectroscopy (EDS) analysis on the fiber cross-sections further confirms that a loosening of the inner aggregation structure of the cotton fiber was achieved after a flash explosion by significantly enhancing its coloration performance, etc. This innovative approach provides a promising idea and possibility as an alternative to chemical methods via mechanically and physically modifying fiber or other materials with sub- or SCF-CO2 fluid in an eco-friendly and sustainable manner.

Catechol- and Phenolic Hydroxyl-Functionalized Partially Bio-Based (Co)poly(ether sulfone)s with Multifarious Applicability

A largely bio-based new bisphenol, namely, 4,4′-((3,4-dimethoxyphenyl)methylene)-bis(2-methoxyphenol) (DMBM) was synthesized by the reaction of veratraldehyde with guaiacol. DMBM and varying compositions of DMBM and bisphenol A were polycondensed with bis(4-fluorophenyl) sulfone to afford reasonably high molecular weight film-forming (co)poly(ether sulfone)s possessing built-in methoxyl groups. T10 and Tg values of (co)poly(ether sulfone)s were in the range 382–478 °C and 171–187 °C, respectively indicating their good thermal stability and the values decreased with increase in mol % incorporation of DMBM. The methoxyl groups present in (co)poly (ether sulfone)s were quantitatively de-blocked resulting in the formation of corresponding polymers possessing pendant catechol moieties and free phenolic hydroxyl groups. By virtue of the presence of these functional moieties, (co)poly(ether sulfone)s are amenable for post-polymerization modifications, and exhibited properties such as antimicrobial (23 mm against Staphylococcus aureus and 18 mm against Escherichia coli)), antioxidant (72 % scavenger of free radicals), adhesive (2.24 MPa lap shear strength) and usefulness as redox-active agent in zinc-ion batteries. These data underscore the promise of DMBM as a versatile monomer of wider utility for the synthesis of functional (co)poly(ether sulfone)s capable of expanding their applicability beyond the conventional ones.

Enhanced nanocellulose extraction from date palm waste: green solvent hydrolysis with transition metal complex

This study presents a novel method for nanocellulose production using [Bmim]Cl as a green solvent, with enhanced hydrolysis efficiency achieved through the addition of a transition metal complex as a catalyst. The redox capability of the transition metal complex to break the glycosidic bonds in cellulose is amplified by the addition of an oxidizing agent. This protocol represents the latest innovation in the field of nanocellulose production, resulting in improved yield and reduced particle size. Nanocellulose (NC) was extracted from date seeds using 1-butyl-3-methylimidazolium chloride [Bmim]Cl coupled with a transition metal complex comprising copper metal and pyridine as a ligand along with H2O2\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\ ext{H}}_{2}{\ ext{O}}_{2}$$\\end{document} as an oxidizing agent. Unlike conventional [Bmim]Cl hydrolysis, which typically yields only microcrystalline cellulose (MCC), this approach resulted in a 25% higher yield of NC than that of MCC. Dynamic light scattering analysis showed a substantial reduction in hydrodiameter from 1200 nm for MCC to 128.7 nm for NC, highlighting the remarkable efficiency of this process. Thermal analysis demonstrated the high stability of NC, which showed a Tonset\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${T}_{onset}$$\\end{document} of 286 °C and an activation energy (Ea\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${E}_{a}$$\\end{document}) of 220.41 kJ/mol. X-ray diffraction analysis indicated that NC possessed a high degree of crystallinity (Crl=\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${C}_{rl}=$$\\end{document} 70.28%). Furthermore, NC underwent modification with 3-aminopropyltriethoxysilane to replace free hydroxyl groups (–OH), making it redispersal and suitable for various applications. This modification was confirmed through Fourier transform infrared spectroscopy, which showed the presence of characteristic functional groups, and energy-dispersive X-ray spectroscopy, which verified the elemental composition. Zeta potential measurements revealed surface charge differences, with MCC at − 27.87 mV, NC at − 27.28 mV, and modified NC at − 44.72 mV, indicating improved colloidal stability after modification. These findings highlight the protocol's effectiveness and its potential impact on the NC production industry, offering improved yields and the production of nanosized fibers using green solvents.

Exopolysaccharide (EPS) Produced by Leuconostoc mesenteroides SJC113: Characterization of Functional and Technological Properties and Application in Fat-Free Cheese

A Leuconostoc mesenteroides strain (SJC113) isolated from cheese curd was found to produce large amounts of a mucoid exopolysaccharide (EPS). An analysis revealed the glucan nature of the EPS with 84.5% (1→6)-linked α-d-glucose units and 5.6% (1,3→6)-linked α-d-glucose units as branching points. The EPS showed 52% dextranase resistance and a yield of 7.4 ± 0.9 g/L from MRS medium supplemented with 10% sucrose within 48 h. Ln. mesenteroides SJC113 was also characterized and tested for the production of EPS as a fat substitute in fresh cheese. Strain SJC113 showed high tolerance to a wide range of NaCl concentrations (2, 5 and 10%), high β-galactosidase activity (2368 ± 24 Miller units), cholesterol-reducing ability (14.8 ± 4.1%), free radical scavenging activity (11.7 ± 0.7%) and hydroxyl scavenging activity (15.7 ± 0.4%). The strain had no virulence genes and was sensitive to clinically important antibiotics such as ampicillin, tetracycline and chloramphenicol. Ln. mesenteroides SJC113 produced highly viscous EPS during storage at 8 °C in skim milk with 5% sucrose. Therefore, these conditions were used for EPS production in skim milk before incorporation into fresh cheese. Four types of fresh cheese were produced: full-fat cheese (FF) made from pasteurized whole milk, non-fat cheese (NF) made from pasteurized skim milk, non-fat cheese made from skim milk fermented with Ln. mesenteroides without added sugar (NFLn0) and non-fat cheese made from skim milk fermented with Ln. mesenteroides with 5% sucrose (NFLn5). While the NF cheeses had the highest viscosity and hardness, the NFLn5 cheeses showed lower firmness and viscosity, higher water-holding capacity and lower weight loss during storage. Overall, the NFLn5 cheeses had similar rheological properties to full-fat cheeses with a low degree of syneresis. It was thus shown that the glucan-type EPS produced by Ln. mesenteroides SJC113 can successfully replace fat without altering the texture of fresh cheese.

A water stable cobalt-bipyridine based hydrogen bonding double layered network for catalytic degradation of tetracycline

Reaction of Co(NO3)2∙6H2O, 2, 2′-bipyridine (bipy) and 1, 4-benzene dicarboxylic acid (H2BDC) by a two-step hydrothermal process, a stable inorganic-organic hybrid compound, [Co(bipy)(H2O)4]BDC (1), was obtained, which structure was characterized by X-ray single crystal diffraction analysis. Acted as catalyst, its photocatalysis-peroxymonosulfate (PMS) activation for tetracycline (TC) degradation was explored under solar light. The critical experimental factors in tetracycline decomposition were investigated, including the pH, [Co(bipy)(H2O)4]BDC dosage, tetracycline concentration, PMS dose, and temperature. [Co(bipy)(H2O)4]BDC has fast degradation performance, sufficient stability and reusability, that degradation rate were 97.5 % and 88.8 % after five cycles within 60 min. Furthermore, the sulfate radical (SO4•−, superoxide (O2•−), hydroxyl (•OH) free radicals and singlet oxygen (1O2) were confirmed as the key oxidation factors in the 1/PMS/SL system for tetracycline degradation.

Effects of ultrasonic degradation on physicochemical and antioxidant properties of Gleditsia sinensis seed polysaccharides

In this study, two degraded polysaccharides from Gleditsia sinensis seed were obtained under ultrasonic power treatments of 300 and 450 W. The physicochemical properties, structural characteristics, and antioxidant activities of the degraded and undegraded polysaccharides were studied and compared. Ion exchange chromatography and methylation analysis showed that the polysaccharides had similar basic structural features and were composed of the same monosaccharide units before and after degradation, but the ultrasonic treatment increased the total monosaccharide content and changed the Mannose/Galactose value. Furthermore, with the increase in the ultrasonic power, the molecular weight and intrinsic viscosity of polysaccharides decreased, and the micromorphology became looser. The scavenging capacities for 1,1-diphenyl-2-picrylhydrazyl and hydroxyl free radicals and the reducing ability were significantly increased by the ultrasonic treatment. In conclusion, ultrasonic treatment may be an effective way to improve the antioxidant activities of polysaccharides from G. sinensis seed, and further studies on its antioxidant mechanism are still needed.

Influence of imidazole-based ionic liquid surfactants on the wetting effect of long-flame coals

In order to study the wetting effect of C12MImBF4, C12MImBr and C12MImCl on long-flame coal, and their mechanism of action on coal-water bonding, physical experiments, molecular dynamics simulation and DFT theoretical calculation were combined in this work. It is confirmed that the imidazole ionic liquid surfactant optimizes the wetting effect by forming hydrogen bonds, reducing the surface tension of water, and increasing the number of free hydroxyl groups in coal. After the wettability test, the concentration of 4 g/L of the three ionic liquid surfactants had the best wetting effect on long-flame coal, and the contact angle at this concentration was reduced by more than 40 % compared with water within 0.2 s after dripping on the coal. Due to the difference in the anionic head group of the three surfactants, there are differences in the number and strength of hydrogen bonds formed between the three surfactants and water molecules, the results of wettability C12MImBF4 > C12MImCl > C12MImBr were presented. Combined with these characteristics of imidazole ionic liquids on long-flame coal, the reasonable application in the wet dust removal process of actual coal mine production can optimize the efficiency of droplet capture of coal particles, so as to effectively improve the dust removal capacity.

Extraction of polyphenols from Apocynum venetum leaves using customized deep eutectic solvents: Process optimization and antioxidant evaluation

To encourage the commercial utilization of A. venetum polyphenols as bio-colorant on textile, five different combinations of deep eutectic solvents (DESs) were evaluated using a single-factor approach and the extraction of polyphenols from A. venetum leaves by ultrasound-assisted DESs was optimized. At the same time, the antioxidant activity of polyphenols prepared were investigated. The DESs composed of choline chloride and glycerol with a molar ratio of 1:2 and a water content of 20 % showed higher extraction performance than other DESs and traditional solvents (water, 60 % ethanol and 60 % methanol). With the most effective solvent the maximum yield 8.24 % of polyphenols was obtained under the optimal extraction conditions were as follows: the ratio of liquid volume (mL) to solid mass (g) is 49:1, extraction temperature of 77 ℃, and extraction time of 55 min. In addition, the polyphenols that have been separated and purified from the DESs extract exhibited antioxidant activities in three kinds of assays including 2,2-diphenyl-1-picrylhydrazyl stable free radical (DPPH), 2,2’-azino-bis-(3-ethylbenzothiazoline-6-sulfonic) acid free radicals (ABTS) and hydroxyl radical (•OH) scavenging activity. Therefore, this paper demonstrates that DESs are effective and environmentally friendly solvents extraction of antioxidant polyphenols pigments from the leaves of A. venetum.

Use of modified chitosan as bitumen modifier and its impact on rheological properties in bitumen modification.

Conventional bitumen is a viscoelastic material composed of asphaltene and maltene. It is prepared by air-blowing, but this approach makes the bitumen more brittle and susceptible to temperatures. To decrease the temperature susceptibility, synthetic polymers or additives are used to make polymer-modified bitumens. Polymer-modified bitumens have poor storage stability and phase separation and are costly. Chitosan has free amino and hydroxyl groups. Some studies showed that chitosan can be used as a bitumen emulsifier, increasing emulsion viscosity. This study describes the synthesis of O-carboxymethyl chitosan (OCMC) from chitosan, and the same was blended in base bitumen VG10 and VG30 to improve its constitutive properties. VG10 and VG30 grade bitumen were characterized for penetration, softening point, kinematic and absolute viscosity, and ductility. OCMC-modified bitumens were also characterized by their rheological and mechanical properties. OCMC was used in the concentration range of 0.5 to 4.5 wt%. The study revealed that using sulfur increases the ductility and penetration of modified bitumen with 1.5 wt% of OCMC and meets the specification of VG40-modified bitumen as per BIS specification IS:73:2013. The study showed that blending 1.5 wt% of OCMC in VG30 base bitumen enhances the complex modulus to 76,517Pa (at 42°C) with a minimum phase angle of 68.58° and meets the VG40 bitumen specification. Simultaneously, blending 1.5 wt% of OCMC in VG10 base bitumen enhances the complex modulus to 64,454Pa with a minimum phase angle of 77.39° (at 42°C) and meets the VG30 bitumen specification. Studies showed that using SBS in a small amount of 0.25 wt% along with modified chitosan improves the rutting resistance and shear modulus by more than 67°C at 1.1kPa.

Preparation and Characterization of Multi-Network Crosslinked Gels for Preventing Spontaneous Combustion of Coal

ABSTRACT In order to improve the inhibition performance of a retardant in various stages of coal spontaneous combustion, this study selected guar gum (guar) mixed with sodium tetraborate to form a multi-web gel. Then, polyethylene glycol (PEG) was added for the insertion and modification to improve the physical inhibition effect. Furthermore, we compounded the composite guar/PEG with the chemical retardant 2-hydroxyphosphonoacetic acid (HPAA) to prepare a composite retardant with the effect of full-stage inhibition. Multi-web gel composite inhibitor with a full-stage inhibition effect was prepared. Response surface analysis was used to determine the optimal solution. Scanning electron microscopy tests revealed that the surface folds of PEG/guar increased and the water retention capacity was greatly enhanced. The plugging wind experiment results show that the limiting air pressure of the gel material is 249 Pa, which can match the downhole plugging wind work. Using XRD experiments, the diffraction angle of PEG/guar was narrowed from 18.20° to 17.64°, the crystal layer spacing was increased from 4.8685 nm to 5.0218 nm, and PEG was successfully intercalated into the guar. Using Fourier-transform infrared spectroscopy, it was found that the content of free hydroxyl groups and aliphatic groups became lower, and the content of carbonyl groups and ether bonds increased, which greatly enhanced the antioxidant capacity of coal. Using thermogravimetric analysis, the characteristic temperature points of single and composite inhibitors were examined macroscopically. The results showed that the inhibition treatment could obviously chelate the transition metal ions in the coal samples, which greatly inhibited the process of coal oxidation and achieved the purpose of inhibiting the spontaneous combustion of coal.