Free Hydroxyl Research Articles

Fully bio-sourced catalyst-free covalent adaptable networks from epoxidized soybean oil and L-tartaric acid

Epoxidized vegetable oil (EVO)-based epoxy systems offer a promising avenue for replacing non-recyclable petroleum-based thermoset elastomers. Looking towards future prospects, they also hold potential to evolve into sustainable covalent adaptable networks (CANs). Typically, transesterification-based CANs require catalysts to achieve crosslinked structures that are reprocessable at relatively high temperatures (T ≥ 150 °C). In this study, epoxidized soybean oil (ESBO) was cross-linked with a eutectic hardener composed of L-tartaric acid (TAR) and ethyl lactate (in an aqueous solution), resulting in the development of a fully bio-based 3D covalent network capable of reprocessing without the need for an exogenous catalyst. In addition, it was demonstrated that the peculiar structure of L-tartaric acid, with –OH groups linked to its backbone, plays a prominent role in the reactivity of the system. These free hydroxyl functions facilitate both the ring-opening of epoxides and transesterification reactions, thus enhancing both curing and covalent exchange kinetics.

Physicochemical and antioxidant properties of pectin fractions extracted from lemon (Citrus Eureka) peels

Pectin, a natural polysaccharide, holds versatile applications in food and pharmaceuticals. However, there is a need for further exploration into extracting novel functional fractions and characterizing them thoroughly. In this study, a sequential extraction approach was used to obtain three distinct lemon pectin (LP) fractions from lemon peels (Citrus Eureka): LP extracted with sodium acetate (LP-SA), LP extracted with ethylenediaminetetraacetic acid (LP-EDTA), and LP extracted with sodium carbonate and sodium borohydride (LP-SS). Comprehensive analysis revealed low methyl-esterification in all fractions. LP-SA and LP-SS displayed characteristics of rhamnogalacturonan-I type pectin, while LP-EDTA mainly consisted of homogalacturonan pectin. Notably, LP-SA formed self-aggregated particles with rough surfaces, LP-EDTA showed interlocking linear structures with smooth planes, and LP-SS exhibited branch chain structures with smooth surfaces. Bioactivity analysis indicated that LP-SA had significant apparent viscosity and ABTS radical scavenging activity, while both LP-EDTA and LP-SS showed excellent thermal stability according to thermogravimetric analysis (TGA). Furthermore, LP-SS exhibited remarkable gel-forming ability and significant hydroxyl free radicals scavenging activity. In conclusion, this study presents a novel method for extracting various lemon pectin fractions with unique structural and bioactive properties, contributing insights for advanced applications in the food and pharmaceutical sectors.

Extraction of Anthocyanins from Red Amaranth and Their Antioxidant Activities in Vitro

Amaranth is rich in anthocyanins and has significant antioxidant activity. This paper reviewed the content, extraction methods and antioxidant mechanism of anthocyanins in amaranth. it was found that amaranth not only has a good price, but also has a strong scavenging capacity for superoxide free radicals, DPPH free radicals and hydroxyl free radicals, showing potential medical value. However, the current extraction methods and conditions still need to be further studied and optimized to improve the extraction rate and purity of anthocyanins in amaranth. Therefore, it is suggested that future research should focus on the impact of different extraction methods on extraction efficiency and quality, and further compare the content, cost and quality of anthocyanins in amaranth with those commonly used today, so as to promote the sustainable development of food industry and drug development.

Facile and Bioinspired Approach from Gallic Acid for the Synthesis of Biobased Flame Retardant Coatings of Basalt Fibers.

A sustainable, bioinspired approach to functionalize basalt fibers with an innovative gallic acid (GA)-iron phenyl phosphonate complex (BF-GA-FeP), for the purpose of improving the flame retardancy in composite materials, is developed. BFs were at first pretreated with O3, obtaining surface free hydroxyl groups that allowed the subsequent covalent immobilization of biosourced GA units on the fiber through ester linkages. Phenolic -OH groups of the GA units were then exploited for the complexation of iron phenyl phosphonate, resulting in the target-complex-coated BF fiber (BF-GA-FeP). Microwave plasma atomic emission spectroscopy and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy analyses of BF-GA-FeP highlighted an increase in iron content, modification of fiber morphology, and occurrence of phosphorus, respectively. BFs, modified with a low amount of the developed complex, were used to reinforce a poly(lactic acid) (PLA) matrix in the production of a biocomposite (PLA/BF-FeP). PLA/BF-FeP showed a higher thermal stability than neat PLA and PLA reinforced with untreated BFs (PLA/BF), as confirmed by thermogravimetric analysis. The cone calorimeter test highlighted several advantages for PLA/BF-FeP, including a prolonged time to ignition, a reduced time to flame out, an 8% decrease in the peak heat release rate, and a 15% reduced fire propagating index compared to PLA/BF.

Dissolved oxygen enhanced piezo-photocatalytic performance in Ag dots-modified BaTiO3 nanoparticles for efficient degradation of multiple organic pollutants

Piezoelectric nanomaterials have attracted much attention due to their ability to modulate photo-excited carrier separation and migration under strain. Perovskite-structured BaTiO3 (BT) is a promising piezo-photocatalytic material due to its high piezoelectric coefficient and special phase structure. In this work, a series of x wt.% Ag/BT composites prepared by a two-step approach were developed for piezo-photocatalysis applications. The 0.8 wt.% Ag/BT showed an excellent piezo-photocatalytic performance for degrading 75.8 % Rhodamine B (RhB) in 60 min. Especially, the catalytic performances were strongly correlated with the atmosphere conditions of the catalyst. The piezo-photodegradation rate of RhB by 0.8 wt.% Ag/BT under O2 atmosphere reached 95.7 % in 40 min, and the first order kinetic rate constant (k) reached 0.06759 min−1, which was 9.9 and 2.4 times that of N2 and air condition, respectively. The Density functional theory (DFT) calculations further revealed that dissolved oxygen could enhance the material's adsorption of RhB. Compared with hydroxyl free radicals (OH) and holes (h+), superoxide radicals (O2–) play an indispensable role in the catalytic process through the trapping experiments and ESR analyses. Furthermore, the RhB degradation pathway and potential ecotoxicity were also proposed. This work is hoped to provide an understanding the mechanism of piezo-photocatalysis and bring new ideas for the development of piezo-photocatalysis catalysis for multifunctional environmental applications.

Ameliorative role of melatonin against adrenaline induced oxidative stress mediated cardiac and hepatic tissue injuries through preserving pyridoxine metabolism in male Wistar rats: A mechanistic insight

Adrenaline (AD) is a naturally occurring catecholamine, synthesised in the adrenal medulla to prepare the organisms for a "fight or flight" response. Under stressful circumstances, the circulatory catecholamine undergoes auto-oxidation, resulting in the formation of free radicals. Chronic stress results in the depletion of micronutrient stores in the body. Pyridoxine, often known as vitamin B6, is an essential water-soluble vitamin that acts as a coenzyme in many metabolic processes. Therefore, our current investigation has prioritized the regulation of pyridoxine metabolism during the period of chronic stress and the precise role of melatonin, as a natural antioxidant, in preventing the alterations generated by adrenaline in cardiac and hepatic tissues. Adrenaline augmented the oxidative stress indices, leading to an imbalance in the antioxidative state resulting in changes in the levels of certain organ-specific serum markers, modifications in the levels of PL (pyridoxal), PLP (pyridoxal-5-phosphate), and the enzymes responsible for their metabolism and breakdown. The foregoing results were corroborated by the histochemical and histological examinations. Melatonin efficiently counteracted all these harmful changes. Besides, the current study demonstrates that both PLP and melatonin show efficacy in scavenging free radicals, including superoxide anion free radicals and hydroxyl radicals, in the chemical system. However, the in vitro studies demonstrated that when administered together, melatonin and PLP more effectively mitigate free radical generation than the individual molecule. These findings were further confirmed by the ITC binding study. These results suggest that a combination of melatonin and PLP could be a better therapeutic approach for the amelioration of stress induced oxidative damages in cardiac and hepatic tissues with an improved pyridoxine metabolism.

Synthesis of zeolite X from fly ash in an impinging stream reactor and its mechanisms

The conventional hydrothermal method with magnetic stirring for the synthesis of zeolite X from fly ash has some problems, such as low micromixing efficiency, low mass transfer rate, and long synthesis time. In this study, impinging stream reactor is used to improve the mass transfer and micromixing and the mechanism how the nucleation and crystallization of zeolite is accelerated is explored. The results show that premixing in the impinging stream reactor can reduce the stirring and aging time from 4 h to 20 min because the hydroxyl free radicals resulting from the cavitation effect can accelerate the crystallization of zeolite. After collision, the viscosity of the system is increased from 0.22 Pa·s to 3 Pa·s, which can increase the residence time of cavitation bubbles in the gel solution and effectively inhibit the aggregation of crystal nuclei. As a result, the crystal nuclei in the system are well dispersed. The impinging stream reactor can also accelerate the mass transfer between liquid and solid phases and improve the micromixing of raw materials, so that the polymerization between Si and Al is increased and the nucleation of zeolite X is accelerated. The degree of order of zeolite X samples obtained by premixing in the impinging stream reactor is much higher than that obtained by magnetic stirring. The relative crystallinity after crystallization for 12 h (100 %) is higher than that obtained by magnetic stirring (94.93 %); and the n(Si/Al) is lower than that obtained by magnetic stirring. It is concluded that premixing in the impinging stream reactor can improve the polymerization of aluminosilicate and accelerate the nucleation and crystallization of zeolite X. Under the same conditions, zeolite X synthesized by premixing in the impinging stream reactor has better CO2 adsorption capacity than those synthesized by magnetic stirring and industrial synthesis.

Responsive Anionophores with AND Logic Multi-Stimuli Activation.

Artificial ion transport systems have emerged as an important class of compounds that promise applications in chemotherapeutics as anticancer agents or to treat channelopathies. Stimulus-responsive systems that offer spatiotemporally controlled activity for targeted applications remain rare. Here we utilize dynamic hydrogen bonding interactions of a 4,6-dihydroxy-isophthalamide core to generate a modular platform enabling access to stimuli-responsive ion transporters that can be activated in response to a wide variety of external stimuli, including light, redox, and enzymes, with excellent OFF-ON activation profiles. Alkylation of the two free hydroxyl groups with stimulus-responsive moieties locks the amide bonds through intramolecular hydrogen bonding and hence makes them unavailable for anion binding and transport. Triggering using a particular stimulus to cleave both cages reverses the hydrogen bonding arrangement, to generate a highly preorganized anion binding cavity for efficient transmembrane transport. Integration of two cages that are responsive to orthogonal stimuli enables multi-stimuli activation, where both stimuli are required to trigger transport in an AND logic process. Importantly, the strategy provides a facile method to post-functionalize the highly active transporter core with a variety of stimulus-responsive moieties for targeted activation with multiple triggers.

Responsive Anionophores with AND Logic Multi‐Stimuli Activation

AbstractArtificial ion transport systems have emerged as an important class of compounds that promise applications in chemotherapeutics as anticancer agents or to treat channelopathies. Stimulus‐responsive systems that offer spatiotemporally controlled activity for targeted applications remain rare. Here we utilize dynamic hydrogen bonding interactions of a 4,6‐dihydroxy‐isophthalamide core to generate a modular platform enabling access to stimuli‐responsive ion transporters that can be activated in response to a wide variety of external stimuli, including light, redox, and enzymes, with excellent OFF‐ON activation profiles. Alkylation of the two free hydroxyl groups with stimulus‐responsive moieties locks the amide bonds through intramolecular hydrogen bonding and hence makes them unavailable for anion binding and transport. Triggering using a particular stimulus to cleave both cages reverses the hydrogen bonding arrangement, to generate a highly preorganized anion binding cavity for efficient transmembrane transport. Integration of two cages that are responsive to orthogonal stimuli enables multi‐stimuli activation, where both stimuli are required to trigger transport in an AND logic process. Importantly, the strategy provides a facile method to post‐functionalize the highly active transporter core with a variety of stimulus‐responsive moieties for targeted activation with multiple triggers.

Glucose Oxidase Energized Osmium with Dual-Active Centers and Triple Enzyme Activities for Infected Diabetic Wound Management.

Diabetic wounds are susceptible to bacterial infections, largely linked to high blood glucose levels (hyperglycemia). To treat such wounds, enzymes like glucose oxidase (GOx) can be combined with nanozymes (nanomaterials mimic enzymes) to use glucose effectively for purposes. However, there is still room for improvement in these systems, particularly in terms of process simplification, enzyme activity regulation, and treatment effects. Herein, the approach utilizes GOx to directly facilitate the biomineralized growth of osmium (Os) nanozyme (GOx-OsNCs), leading to dual-active centers and remarkable triple enzyme activities. Initially, GOx-OsNCs use vicinal dual-active centers, enabling a self-cascaded mechanism that significantly enhances glucose sensing performance compared to step-by-step reactions, surpassing the capabilities of other metal sources such as gold and platinum. In addition, GOx-OsNCs are integrated into a glucose-sensing gel, enabling instantaneous visual feedback. In the treatment of infected diabetic wounds, GOx-OsNCs exhibit multifaceted benefits by lowering blood glucose levels and exhibiting antibacterial properties through the generation of hydroxyl free radicals, thereby expediting healing by fostering a favorable microenvironment. Furthermore, the catalase-like activity of GOx-OsNCs aids in reducing oxidative stress, inflammation, and hypoxia, culminating in improved healing outcomes. Overall, this synergistic enzyme-nanozyme blend is user-friendly and holds considerable promise for diverse applications.

Surface modification of polyester fabrics using choline hydroxide-catalysed glycolysis

This study explores the surface modification of polyethene terephthalate (PET) fabric via glycolysis, employing choline hydroxide as an eco-friendly catalyst. A range of chemicals was evaluated for catalysing the glycolysis reaction. Among them, choline hydroxide demonstrated notable enhancements in surface hydrophilicity, moisture regain, wicking properties, and water contact angle, surpassing other catalysts. Scanning Electron Microscopy (SEM) revealed a marked increase in surface roughness and irregularities following glycolysis in the presence of this ionic liquid. The surface modification technique employed in this investigation resulted in a decrease of less than 20% in the breaking force of the fabric. Fourier Transform Infrared (FT-IR) spectroscopy and the methylene blue staining method confirmed the emergence of free hydroxyl groups on the modified fabric's surface. These findings suggest that glycolysis catalysed by choline hydroxide is a promising approach for enhancing the surface characteristics of polyester fabrics, which may lead to improved functional properties in textile applications.

Generation Mechanism of Hydroxyl Free Radicals in Micro–Nanobubbles Water and Its Prospect in Drinking Water

Micro–nanobubbles (MNBs) can generate ·OH in situ, which provides a new idea for the safe and efficient removal of pollutants in water supply systems. However, due to the difficulty in obtaining stable MNBs, the generation efficiency of ·OH is low, and the removal efficiency of pollutants cannot be guaranteed. This paper reviews the application research of MNB technology in water security from three aspects: the generation process of MNBs in water, the generation rule of ·OH during MNB collapse, and the control mechanisms of MNBs on pollutants and biofilms. We found that MNB generation methods are divided into chemical and mechanical (about 10 kinds) categories, and the instability of the bubble size restricts the application of MNB technology. The generation of ·OH by MNBs is affected by the pH, gas source, bubble size, temperature, and external stimulation. And the pH and external stimulus have more influence on ·OH generation in situ than the other factors. Adjusting the pH to alkaline or acidic conditions and selecting ozone or oxygen as the gas source can promote ·OH generation. MNB collapse also releases a large amount of energy, during which the temperature and pressure can reach 3000 K and 5 Gpa, respectively, making it efficient to remove ≈90% of pollutants (i.e., trichloroethylene, benzene, and chlorobenzene). The biofilm can also be removed by physical, chemical, and thermal effects. MNB technology also has great application potential in drinking water, which can be applied to improve water quality, optimize household water purifiers, and enhance the taste of bottled water. Under the premise of safety, after letting people of different ages taste water samples, we found that compared with ordinary drinking water, 85.7% of people think MNB water is softer, and 73.3% of people think MNB water is sweeter. This further proves that MNB water has a great prospect in drinking water applications. This review provides innovative theoretical support for solving the problem of drinking water safety.

Characteristic volatile components analysis of Camelina sativa (L.) Crantz by GC-MS and their antibacterial and antioxidant activities

Camelina sativa (L.) Crantz is an oilseed plant common in Europe and Asia. This study used the gas chromatography–mass spectrometry (GC-MS) to examine the differences in the aroma on the basis of extraction method such as water distillation extraction (CSPW), Solid-phase microextraction (CSPM) and subcritical extraction (CSPS). Antibacterial test was evaluated by the microdilution method against Salmonella typhimurium, Streptococcus pneumoniae, Escherichia coli, Strepococcus pyogenens, Staphylococcus aureus, and antioxidant activity was determined through DPPH free radical, hydroxyl free radical, and superoxide anion radical scavenging capacity activity. The result revealed that three extraction methods were distinct from each other based on their volatile compounds. Sixty-one volatiles of diverse chemical nature were identified and quantified. The volatile components contain thioether, aldehydes, alcohols, ketones, acids, esters, alkene, alkanes, amide, and furan compounds. The volatile components of Camelina sativa (L.) Crantz have good antibacterial and antioxidant activities. Furthermore, this work provides reference methods for detecting novel volatile organic compounds in plants and products.

Structure–activity relationship and biofilm formation-related gene targets of oleanolic acid-type saponins from Pulsatilla chinensis against Candida albicans

In the course of our investigations of antifungal natural products, the structure–activity relationship and antifungal activities of oleanolic acid-type saponins (1–28) from Pulsatilla chinensis against human and plant pathogenic fungi were elucidated. The analysis of structure–activity relationship of oleanolic acid-type saponins showed that the free carboxyl at C-28 was essential for their antifungal activities; the free hydroxyl group at the C-23 site of oleanolic acid-type saponins played a crucial role in their antifungal activities; the oligosaccharide chain at C-3 oleanolic acid-type saponins showed significant effects on antifungal efficacy and a disaccharide or trisaccharide moiety at position C-3 displayed optimal antifungal activity. The typical saponin pulchinenoside B3 (16, PB3) displayed satisfactory antifungal activity against human and plant pathogenic fungi, especially, C. albicans with an MIC value of 12.5 μg/mL. Furthermore, PB3 could inhibit the biofilm formation of C. albicans through downregulating the expression of the integrated network of biofilm formation-associated transcription factors (Bcr1 Efg1, Ndt80, Brg1, Rob1 and Tec1) and adhesion-related target genes (HWP1, ALS1, and ALS3). Meanwhile, we found that PB3 could effectively destroy the mature biofilm of C. albicans by the oxidative damage and inducing mitochondria-mediated apoptosis in cells.

Comparative study of reactive oxygen species and tetracycline degradation pathways in catalytic peroxodisulfate activation by asymmetric mesoporous TiO2 and the corresponding controlled-release materials

The removal of trace amounts of antibiotics from water environments while simultaneously avoiding potential environmental hazards during the treatment is still a challenge. In this work, green, harmless, and novel asymmetric mesoporous TiO2 (A-mTiO2) was combined with peroxodisulfate (PDS) as active components in a controlled-release material (CRM) system for the degradation of tetracycline (TC) in the dark. The formation of reactive oxygen species (ROS) and the degradation pathways of TC during catalytic PDS activation by A-mTiO2 powder catalysts and the CRMs were thoroughly studied. Due to its asymmetric mesoporous structure, there were abundant Ti3+/Ti4+ couples and oxygen vacancies in A-mTiO2, resulting in excellent activity in the activation of PDS for TC degradation, with a mineralization rate of 78.6%. In CRMs, ROS could first form during PDS activation by A-mTiO2 and subsequently dissolve from the CRMs to degrade TC in groundwater. Due to the excellent performance and good stability of A-mTiO2, the resulting constructed CRMs could effectively degrade TC in simulated groundwater over a long period (more than 20 days). From electron paramagnetic resonance analysis and TC degradation experiments, it was interesting to find that the ROS formed during PDS activation by A-mTiO2 powder catalysts and CRMs were different, but the degradation pathways for TC were indeed similar in the two systems. In PDS activation by A-mTiO2, besides the free hydroxyl radical (·OH), singlet oxygen (1O2) worked as a major ROS participating in TC degradation. For CRMs, the immobilization of A-mTiO2 inside CRMs made it difficult to capture superoxide radicals (·O2−), and continuously generate 1O2. In addition, the formation of sulfate radicals (·SO4−), and ·OH during the release process of CRMs was consistent with PDS activation by the A-mTiO2 powder catalyst. The eco-friendly CRMs had a promising potential for practical application in the remediation of organic pollutants from groundwater.

Role of Nb2O5 Crystal Phases on the Photocatalytic Conversion of Lignin Model Molecules and Selectivity for Value-Added Products.

The photocatalytic conversion in aqueous media of phenol and guaiacol as a lignin model compound using Nb2O5 with different crystal phases was studied. Nb2O5 particles were synthesized using hydrothermal methods, where it was observed that changes in the solvent control their morphology and crystal phase. Different photocatalytic behavior of Nb2O5 was observed with the selected model compounds, indicating that its selection directly impacts the resulting conversion and selectivity rates as well as the reaction pathway, highlighting the relevance of model molecule selection. Photocatalytic conversion of phenol showed conversion rate (C%) up to 25 % after 2 h irradiation and high selectivity (S%) to pyrogallol (up to 50 %). Orthorhombic Nb2O5 spheres favored conversion through free hydroxyl radicals while monoclinic rods did not convert phenol. Guaiacol photocatalytic oxidation showed high conversion rate but lower selectivity. Orthorhombic and monoclinic Nb2O5 favored the formation of resorcinol with S % ~0.43 % (C % ~33 %) and ~13 % (C % ~27 %) respectively. The mixture of both phases enhanced the guaiacol conversion rate to ~55 % with ~17 % of selectivity to salicylaldehyde. The use of radical scavengers provided information to elucidate the reaction pathway for these model compounds, showing that different reaction pathways may be obtained for the same photocatalyst if the model compound is changed.

Alkaline earth metal modified La-Fe based perovskite enhances hydroxyl radicals for efficient coke cleaning

The low conversion rate of coke during online coke cleaning is due to the stable structure of graphite carbon, which makes it difficult to react with steam. Therefore, there is an urgent need to design a catalyst for catalytic graphite carbon conversion to achieve efficient in situ coke cleaning. Alkaline earth metal Sr modified La-Fe based perovskite LSF-x (x = 0, 0.2, 0.4, 0.6, 0.8, 1) were prepared by hydrothermal method. DFT and experimental results indicate that doping Sr at the A-site reduces the adsorption energy barrier of water molecules, promotes the decomposition of water molecules to produce absorbed and free hydroxyl radicals, and thereby enhances the conversion of graphite carbon. At 900 °C, a catalytic coke conversion of 97.32% in the presence of La0.2Sr0.8FeO3 was achieved, which was 2.09 times the value without a catalyst. The research results provide a certain theoretical basis for catalytic heterogeneous reactions.

Phytochemical composition and in vitro antioxidant and antimicrobial activities of Bersama abyssinica F. seed extracts

Medicinal plants can be potential sources of therapeutic agents. Traditional healers use a medicinal plant from Ethiopia, Bersama abyssinica Fresen, to treat various diseases. This study aimed to investigate the phytochemical components and antioxidant and antimicrobial activities of B. abyssinica seed extracts (BASE). Gas chromatography coupled to mass spectroscopy (GC–MS) analysis was used to determine the phytochemical compositions of BASE. The antioxidant activities were assessed by using 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay, thiobarbituric acid-reactive species (TBARS) assay, ferric chloride reducing assay and hydroxyl scavenging capacity assay. Antimicrobial activity was investigated using the agar well diffusion method. Phytochemical screening showed the presence of saponins, glycosides, tannins, steroids, phenols, flavonoids, terpenoids, and alkaloids. GC–MS analysis revealed the presence of 30 volatile compounds; α-pinene (23.85%), eucalyptol (20.74%), β-pinene (5.75%), d-limonene (4.05%), and o-cymene (5.02%). DPPH-induced free radical scavenging (IC50 = 8.78), TBARS (IC50 = 0.55 µg/mL), and hydroxyl radicals’ scavenging capacities assays (IC50 = 329.23) demonstrated high antioxidant effects of BASE. Reducing power was determined based on Fe3+–Fe2+ transformation in the presence of extract. BASE was found to show promising antibacterial activity against S. aureus, E. coli, and P. aeruginosa (zone of inhibition 15.7 ± 2.5 mm, 16.0 ± 0.0 mm, and 16.7 ± 1.5 mm, respectively), but excellent antifungal activities against C. albican and M. furfur (zone of inhibition 22.0 ± 2.0 mm and 22.0 ± 4.0 mm, respectively). The seeds of B. abyssinica grown in Ethiopia possess high antioxidant potential, promising antibacterial and superior antifungal activity. Therefore, seeds of B. abyssinica provide a potential source for drug discovery.

Effects of Aqueous Solution and Immersion Duration on Spontaneous Combustion Characteristics of Weakly Caking Coal

ABSTRACT Coal spontaneous combustion (CSC) severely affects the development of the coal industry and threatens the safety of coal miners. This study investigated how immersing coal in aqueous solution affects the CSC risk and evaluated the effect of the immersion duration. Fourier transform infrared spectrometry and thermogravimetric−differential scanning calorimetry analysis were performed. Coal samples were immersed in water from an underground coalmine or in distilled water for 30 or 60 days. Changes in microscopic functional groups and thermokinetic behaviors were determined. Immersion in distilled water for 60 days led to 4.41%, 2.26%, and 6.25% smaller masses of C=O, –CH3, and free hydroxyl groups, respectively, relative to their levels in raw coal. Additionally, the characteristic temperatures T 4 , T 5 , and T 6 were 8.8%, 9.0%, and 9.2% lower, respectively, and the average apparent activation energy was 15.67% lower. Immersion in water from an underground coalmine for 60 days led to 5.68%, 2.58%, and 6.54% higher masses of C=O, –CH3, and free hydroxyl groups, respectively, and 12.8%, 13.0%, and 13.5% higher characteristic temperature, respectively; the average apparent activation energy was 20.43% lower. These findings suggest that the coal immersed in water from an underground coalmine was the most susceptible to CSC.

OPTIMIZATION OF THE METHOD OF QUANTITATIVE DEFINITIONS OF FLAVONOIDS IN THE RAW MATERIALS OF "MENYANTHIDIS TRIFOLIATAE LEAVES"

The aim of the study is to optimize the methodology of quantitative determination of flavonoids in the leaves of Menyanthidis trifoliatae. In official medicine, the leaves of Menyanthidis trifoliatae are used for anorexia and dyspeptic disorders.
 In the current regulatory documentation (State Pharmacopoeia of the Russian Federation), it is proposed to evaluate the quality of raw materials by the content of the amount of flavonoids in terms of rutin using spectrophotometry. This technique is based on the ability of flavonoids containing free aromatic hydroxyl groups to form colored products with diazotized sulfanilic acid. The disadvantage of this technique is the long and time-consuming stage of cleaning raw materials from certain groups of lipophilic substances, which can also react with diazotized sulfanilic acid to form colored products.
 We have proposed a selective method for the quantitative determination of flavonoids in the herb trifoliate by the method of spectrophotometry in terms of rutin. The technique is based on the ability of flavonoids to form stable colored complexes with aluminum chloride. We have selected the optimal conditions for extraction and complexation reaction of aluminum chloride with flavonoids of M. trifoliatae extract. The proposed method has been validated and is suitable for use in an analytical laboratory.