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A novel and efficient protocol for the microwave‐assisted synthesis of diversely substituted 2,2′‐bisbenzimidazol‐5,6′‐dicarboxylic acid (BIMCA) from the reaction of 3,4‐diaminobenzoic acid with oxalic acid has been developed, which proceeds through sequential nucleophilic addition and electrophilic substitution in accordance with the Philips method. The synthetic utility of this strategy was demonstrated by the concise, one‐pot synthesis of (BIMCA) and metal complexes. (BIMCA) with a [{Fe(salen)}2O] Schiff base ligand complex and new benzimidazole coordination compounds with double oxygen [(BIMCA){Fe(salen)}2] ligand complexes were obtained. The resulting [(BIMCA){Fe(salen)}2] ligand complex was then synthesized from Co(CH3COO)2.4H2O, Ni(CH3COO)2.4H2O and Cu(CH3COO)2.H2O heteronuclear complexes. The condensations proceed with good yield to give products that, in certain instances, are not readily attainable by conventional condensation techniques. The structures of the compounds were identified by Fourier‐transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance (1H NMR), elemental analysis and magnetic susceptibility. The mutagenic potential of the synthesized chemicals was evaluated by the Ames test towards mutant Salmonella typhimurium strains TA98 and TA100. It was recorded that these chemicals had no mutagenic action. Also, antimicrobial activities were screened by broth microdilution test. It was seen that the minimum inhibitory concentration (MIC) against Klebsiella pneumoniae, Staphylococcus aureus and Staphylococcus epidermidis was 0.195 mg/mL, followed by a MIC value of 0.390 mg/mL against Escherichia coli and Salmonella typhimurium. [(BIMCA){Fe(salen)}2Co(II)] demonstrated significant antimicrobial activity against Proteus mirabilis and Staphylococcus aureus, with an MIC of 0.195 mg/mL, followed by an MIC of 0.390 mg/mL against Pseudomonas aeruginosa, K. pneumonia and Salmonella typhimurium. The antioxidant properties were examined using various chemical assays, and [(BIMCA){Fe(salen)}2O] and (BIMCA) exhibited greater 2,2'‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulfonic acid) (ABTS) and 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) radical scavenging ability, when compared with other compounds. Enzyme inhibitory effects were tested against acetylcholinesterase (AChE), amylase, butyrylcholinesterase (BChE) and tyrosinase. [(BIMCA){Fe(salen)}2Cu(II)] displayed the best AChE (IC50 0.51 mg/mL), BChE (IC50 0.51 mg/mL) and tyrosinase (IC50 1.52 mg/mL) inhibitory effects. Furthermore, molecular docking calculations were performed to gain insights into the interaction between [(BIMCA){Fe(salen)}2] and AChE, and between [(BIMCA){Fe(salen)}2Cu(II)] and amylase. Both compounds showed the potential inhibition of the protein targets. [ABSTRACT FROM AUTHOR]

The reaction between cadmium nitrate tetrahydrate and N,N′-bis(pyridin-3-ylmethyl)oxalamide (L) in a 1:3 molar ratio in a water/acetonitrile (1:6 v/v) mixture afforded single crystals of compound 1 suitable for X-ray diffraction analysis. Compound 1 consists of the coordination polymer (CP) [[Cd(L)2(OH2)2](NO3)2·4H2O]∞, in which CdII ions are bridged by neutral L antiperiplanar N-ligands in a wavy ribbon fashion developed along the c-axis. Two trans-disposed water molecules complete the pseudo-octahedral coordination geometry of the metal ion. The crystal packing of 1 revealed the interplay between π–π stacking interactions and an intricate hydrogen-bonded network involving oxalamides, nitrates, and water molecules. The donor properties of L and the intermolecular interactions in compound 1 are interpreted based on hybrid-DFT calculations. [ABSTRACT FROM AUTHOR]

The possibility of catalysis by VO2+, Cr3+, Cr2O72–, Mn2+, MnO4–, Fe3+, Co2+, Ni2+, Cu2+, Ce3+, BrO3–, or IO3– ions of oxalic acid oxidation reaction with ozone in strongly acidic aqueous solutions at pH 0.3–1.7 has been studied. The final product of the oxidation is carbon dioxide. The kinetic regularities of the reaction have been determined from the rates of ozone consumption and carbon dioxide release. Without a catalyst, oxalic acid does not interact with ozone. It has been found that Mn2+, MnO4– and Co2+ ions are effective catalysts, while the catalytic effect of VO2+, Cr3+, Cr2O72–, Fe3+, Ni2+, Cu2+, Ce3+, BrO3–, or IO3– is weak or does not manifest itself at all. The effects of acidity and concentrations of the catalyst in solution and ozone in the gas phase on the kinetics of the process have been studied. Kinetic schemes of catalytic reactions and leading intermediates are proposed. The data obtained will help in choosing the optimal conditions for the process of oxidative mineralization of oxalic acid under the action of ozone in strongly acidic media. [ABSTRACT FROM AUTHOR]

In this study, we show that the use of a mixture of melamine and oxalic acid during the synthesis of acid-treated crystalline graphitic carbon nitride samples significantly enhances its photocatalytic activity in VOCs destruction processes. The rate of photocatalytic ethanol destruction with the participation of modified crystalline graphitic carbon nitride obtained under optimal conditions is 67.1 μmol h−1, which is almost twice higher than sample synthesized in the absence of oxalic acid, and is two orders of magnitude higher than the activity of bulk g–C3N4. The synthesized materials were characterized using XRD, FT-IR, UV–Vis, PL, SEM, and EDXA methods. The high activity of the modified carbon nitride samples is attributed to increased light absorption in the visible region of the spectrum and better crystallinity, which can lead to more efficient separation and transport of photogenerated charges. To our knowledge, the effect of the simultaneous use of melamine and oxalic acid for obtaining acid-treated crystalline graphitic carbon nitride is, shown for the first time. [ABSTRACT FROM AUTHOR]

Owing to the low energy consumption and few by-products, toluene alkylation is regarded as a promising way to produce p-xylene. The zeolites with the characteristics of 10-MR were usually employed to catalyze the toluene alkylation after being modified. However, the catalyst activity is liable to sharp decrease by common modifying strategies. In this study, the alkylation of toluene with dimethyl carbonate was catalyzed by the MCM-22 zeolites with selective dealumination and silanization treatment. The Al sites on the MCM-22 external surface were first eliminated by oxalic acid, and then trimethylsilyl groups were grafted at the external surface of MCM-22 by bonding with Si–OH formed from dealumination. This modification strategy can not only reduce the Brønsted acid sites on the external surface and narrow the pore entrance size but also retain more internal active sites, leading to improving PX selectivity without a significant decrease in activity. Compared to parent MCM-22, the PX selectivity was doubled, and the toluene conversion only decreased from 39 to 34% over 200-DeMCM-22 catalyst at 400 °C. [ABSTRACT FROM AUTHOR]

Dicarboxylic acids (DCAs) are major players in the formation of secondary organic aerosols (SOAs) and climate change. DCAs have potential impact on human health and environmental issues ranging from local scale to global scale participate mainly in the cloud condensation. In this context, oxalic acid (OA) and malonic acid (MA) are the most dominant DCAs in the atmosphere. A full atmospheric degradation mechanism of OA and MA with the most reactive tropospheric oxidants, namely, OH, Cl and NO3 radicals, were studied using M06‐2X, ωB97XD/cc‐pVTZ and 6‐311++G(2df,2p) level of theories. To evaluate the atmospheric influence, this study enables us to deep investigation of fate of OA and MA with respect to the mentioned radicals and their subsequent secondary reactions. The latter result in the formation of carbon dioxide (CO2), formic acid (HCOOH), which contributes to the formation of SOA and climate change. The reaction mechanism in this study was initiated through H‐abstraction reaction, followed by dehydrogenation and decarboxylation reaction of both DCAs. The rate coefficients of OA, MA with OH, Cl and NO3 radicals are determined theoretically using variational transition state theory (VTST) with Eckart tunnelling method in the temperature range of 278–1000 K. At 298 K, the rate coefficient of OA with OH, Cl and NO3 are 2.48 × 10−15, 2.37 × 10−20, 6.16 × 10−23 in cm3 molecule−1 s−1, whereas MA with OH, Cl and NO3 are 9.76 × 10−14, 1.01 × 10−12 and 5.89 × 10−18 in cm3 molecule−1 s−1, respectively. Our present results shed light on the atmospheric implications of two DCAs and provide the significant insight for the atmospheric pathways. [ABSTRACT FROM AUTHOR]

Gluconic acid and sorbitol are among the value-added chemicals that can be derived from biomass. Nowadays, these compounds are typically produced through biotechnological processes, but electrochemical methods offer numerous advantages over alternative approaches. While studies have extensively explored metals like copper, palladium, gold, and platinum, nickel has received relatively limited attention in this context. Notably, nickel exhibits electrochemical activity suitable for organic electrosynthesis. This work has been achieved with 5-h long-term electrolysis, glucose as a reactant, utilizing modified nickel electrodes in a KOH solution. While these studies achieved substantial conversion rates, the selectivities and Faraday efficiencies toward gluconic acid and sorbitol remained comparatively low. The long-term electrolysis of glucose using modified nickel electrodes resulted in the identification of various side products. These include formic acid, oxalic acid, glycolic acid, tartronic acid, glyceric acid, and arabinose. [ABSTRACT FROM AUTHOR]

BACKGROUND: The excessive salt intake associated with Douchi has become a topic of controversy. Addressing this concern and enhancing its market competitiveness necessitates the application of salt reduction fermentation in Douchi. Therefore, to promote the application of salt reduction fermentation in Douchi, a comprehensive study was undertaken aiming to investigate the differences in biogenic amines, volatile compounds and non‐volatile compounds in Douchi with varying salt content. RESULTS: The findings unequivocally demonstrate that salt hampers the formation of metabolites in Douchi. As the salt content increased, there was a significant decrease (P < 0.05) in the levels of total acid, amino‐type nitrogen and free amino acids in Douchi. Notably, when the salt content exceeded 80 g kg−1, there was a substantial reduction (P < 0.05) in putrescine, lactic acid and malic acid levels. Similarly, when the salt content surpassed 40 g kg−1, β‐phenethylamine and oxalic acid levels exhibited a significant decline (P < 0.05). Furthermore, the results of E‐nose and principal component analysis based on headspace solid phase microextraction gas chromatography–mass spectrometry revealed notable discrepancies in the volatile compound content between Douchi samples with relatively low salt content (40 and 80 g kg−1) and those with relatively high salt content (120, 160 and 200 g kg−1) (P < 0.05). By employing partial least squares discriminant analysis, eight distinct volatile compounds, including o‐xylene, benzaldehyde and 1‐octen‐one, were identified. These compounds exhibited higher concentrations in Douchi samples with relatively low salt content (40 and 80 g kg−1). The sensory results showed that Douchi samples with lower salt content exhibited higher scores in the soy sauce‐like and Douchi aroma attributes. CONCLUSION: In conclusion, this study significantly enhances our understanding of the impact of salt on metabolites in Douchi and provides invaluable insights for the development of salt reduction fermentation in this context. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Bis-[2-(3,4-dihydroxyphenyl)-4,5-diphenyl-1H-imidazol-3-ium] Oxalate ethanol solvate crystal has been isolated from slow solvent evaporation method and the structure was characterized by FT-IR, NMR and Single crystal XRD. The compound crystallizes in the triclinic space group P 1 ¯ with a = 7.7925(16), b = 10.716(3), c = 13.952(3), α = 106.545(5), β = 97.514(5), γ = 110.152(5), V = 1014.0(4) Å3 and Z = 1. The single crystal X-ray data of the compound confirms two proton transfers from an oxalic acid to the pyrimidine-type-nitrogen of two separate imidazole rings. The structure and symmetry of the Imidazolium Oxalate is dictated by N–H⋯O and O–H⋯O hydrogen bonding interactions and are confirmed by hydrogen bonding analysis and hirshfeld surface analysis. The partial double bond character in the imidazolium ring confirms delocalization across the molecular framework. The partial double bond character of the C–O bonds also confirms delocalization in the oxalate anion. The crystal is 3-dimensional structure, with crystal growth in all the crystallographic axis. Computational analysis [DFT, B3LYP/6-311G(d,p)] reveals close correlation of the constrained optimized structure with the experimental data. Imidazolium oxalate crystal form by the protonation of Imidazole compound and complex formation with oxalate ion. [ABSTRACT FROM AUTHOR]

The effect of introducing oxalic acid into the mother gel of TS-1 zeolite on the crystallization behavior and physiochemical properties was investigated. The addition of oxalic acid with a buffering action significantly accelerated the crystallization process of TS-1 while simultaneously inhibiting the formation of anatase. The resultant TS-1 zeolites displayed enhanced performance in catalyzing the epoxidation of 1-hexene with H2O2 as an oxidant. [ABSTRACT FROM AUTHOR]

The article explores the perception of aroma and flavor and their relationship with food preferences, appetite and satiety, and emotional well-being. Topics discussed include phytonutrition, phytoaromatherapy, epigenetics, mental health phytonutrition, gut-brain axis, role of gastrointestinal mechanisms in appetite, relationship of retronasal olfaction, satiation and food consumption, role of neurogastronomy and gastrophysics in facilitating awareness of flavor creation, and elements of flavor.

Chromium-contaminated soil is a serious environmental problem that threatens human health and the environment. Electrokinetic technology is used as a promising solution to treat these soils, as it relies on applying an electric field to remove pollutants from the soil. In this study, four experiments were conducted, where experiments have shown that the use of wheat straw as an available, cheap, economical and efficient adsorbent material to prevent the occurrence of reverse osmosis. The results showed that the percentage of removal increased with the increase in the acidity of the medium, that is, as the pH decreased. This is due to an increase in the movement of pollutants as the soil particles become more positively charged, which enhances Attract negative heavy metal ions. This leads to increased movement of heavy metal ions into soil pores, making them more susceptible to transport under the influence of an electric field. The results proved that when using a disinfection solution with a pH of 2, it gave a higher result compared to pH 7 and 12, where the percentage of removal was 78.3%, 62.6 %, and 51.9% respectively. The dissolution of these metals can be enhanced by adding oxalic acid at a constant voltage gradient 1.2 v/cm and an initial concentration of 200 mg/kg. It was noted after the end of the experiment that the percentage of removal reached 81.9%, as the concentration of metals on the cathode side was higher than on the cathode side. The anode, and this is due to the migration of metals under the influence of electromigration to the cathode side, where the chromium concentration was 47 mg/kg at the cathode side, 27 mg/kg at the anode side. [ABSTRACT FROM AUTHOR]

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This study investigates the effectiveness of blast furnace slags (BFSs) as catalysts in the ozonation process to degrade complex contaminants such as bezafibrate (BFZ) at different pH levels. The findings reveal that the presence of BFS enhances degradation efficiency, achieving a 10% improvement at pH 10 and a 30% improvement at pH 5.5 compared to simple ozonation. The highest degradation efficiency was observed in the Ozonation–BFS system at pH 10, with 90% decomposition of BFZ. These results were corroborated through ozone consumption analysis, BOD5 measurements, and the identification of oxalic acid as the final decomposition product. Due to the complexity of the reaction system, kinetic characterization was performed using non-parametric modeling based on differential neural networks. The model indicated that the observed reaction rate for BFZ degradation in the presence of ozone and BFS was 4.12 times higher at pH 5.0 and 1.08 times higher at pH 10.0 compared to simple ozonation. These results underscore the potential of using BFS in catalytic ozonation processes for the effective treatment of recalcitrant contaminants in wastewater. [ABSTRACT FROM AUTHOR]

Simple Summary: Economically, Varroa destructor is the most important parasite to honey bees. There are many ways to deal with it, including pharmaceutical and biotechnological treatments. However, the mite has become resistant to many synthetic pesticides. There is little research on its response to organic acids. This report examines the question of whether it could become resistant to oxalic acid. The review uses literature from the past 30 years, and calculates and reviews the annual median efficacy for different application methods. If an efficacy of 70% or more is achieved, it can be concluded that the organism is not resistant. There is no evidence of resistance development, despite some outliers, which can be explained by the studies. Further tests are required to confirm the results. As Varroa destructor is one of the most important pathogens of Apis mellifera, there are numerous treatment methods, including pharmaceutical and biotechnological approaches. However, the rapid development of resistance to synthetic acaricides by Varroa destructor has become a significant concern. To date, there have been no investigations into the development of resistance to organic acids. This review examines the potential risk of oxalic acid resistance development by evaluating literature sources from the past 30 years following the PRISMA 2020 guidelines. Median annual efficacies are calculated and reviewed over time for several application methods. An efficacy higher than 70% is determined as not resistant. Independent of the method of application, no resistance development can be observed, although there are some outliers of the annual median. These outliers can be explained by brood status or study setting. However, the result is limited by the low number of efficacy values, and further standardised studies are needed. [ABSTRACT FROM AUTHOR]

Sewage sludge biochar (SSB) exhibits higher phosphorus (P) concentrations than the original sewage sludge (SS) and can be used as a P fertilizer. However, SSB-associated P is strongly retained in chemical compounds, which hinders its release and subsequent plant uptake. The use of organic acids facilitates P solubilization from SSB. Herein, we evaluated the effect of oxalic acid on P release from SSB applied to soil over time. Biochar was produced at 300 °C (SSB300) and 500 °C (SSB500). P release from SSB increased with an increasing concentration of oxalic acid in the SSB incubation solution and in SSB-treated soil. P speciation in SSB showed that P was predominantly inorganic (Pi), which represented 81% and 92% of the total P in SSB300 and SSB500, respectively. Pi in SSB consisted mainly of non-apatite P, accounting for 91% and 96% of all Pi in SSB300 and SSB500, respectively. Because SSB is predominantly insoluble in water, oxalic acid is crucial for the release of P from SSB. Oxalic acid increased P release from SSB300 and SSB500 by 103- and 600-fold, respectively, compared to the control, from which P was extracted with water. Oxalic acid enhancement of P release from SSB increases the possibility of using SSB as a sustainable source of P for agriculture. [ABSTRACT FROM AUTHOR]

Oxalic acid is one of the important acids that is used in many fields. It is of medical, industrial and agricultural importance and is used as an acid in foods, building and construction, pharmacy, and others. This acid is produced in multiple ways, and the biogenic method is the best method because it is safe and cheap. Hence, this study came about, where reliance was placed on wheat bran in preparing nutrient medium to produce oxalic acid from Candida albicans and Aspergillus niger yeast isolated from environmental and pathogenic sources. The study aimed to use wheat bran as an alternative medium for growing fungi and yeasts that produce oxalic acid, and to compare the productivity of this medium with standard media. One hundred fungal isolates were isolated from different environmental and clinical sources, and grown in Sabouraud Dextrose Agar medium (SDA) and Potato dextrose agar to obtain pure isolates of A. niger and C. albicans. Thirty seven isolates of C. albicans and thirty two isolates of A. niger were isolated. Thirty one contaminated samples were discarded. The isolates were grown in standard (SDB, PDB) and alternative (wheat bran WB) media. The amount of acid was estimated by mulching against potassium permanganate The results showed that wheat bran (WB) medium was the most efficient in producing oxalic acid with a rate of 26.2% for A. niger and 25.3% for Candida albicans, compared to standard media. The best temperature for acid production was 32°C with a production rate of 19.1% for A. niger and 22.7% for C. albicans. The best pH was 6.5 for A. niger with a production rate of 20.2% and 5.5 for C. albicans with a production rate of 23.3%. The study conclude from the above that the fungus A. niger is the best compared to C. albicans, as well as the medium of wheat bran is a promising and effective medium in the production of oxalic acid in an environmentally friendly way.

Chromium-contaminated soil is a serious environmental problem that threatens human health and the environment. Electrokinetic technology is used as a promising solution to treat these soils, as it relies on applying an electric field to remove pollutants from the soil. In this study, four experiments were conducted, where experiments have shown that the use of wheat straw as an available, cheap, economical and efficient adsorbent material to prevent the occurrence of reverse osmosis. The results showed that the percentage of removal increased with the increase in the acidity of the medium, that is, as the pH decreased. This is due to an increase in the movement of pollutants as the soil particles become more positively charged, which enhances Attract negative heavy metal ions. This leads to increased movement of heavy metal ions into soil pores, making them more susceptible to transport under the influence of an electric field. The results proved that when using a disinfection solution with a pH of 2, it gave a higher result compared to pH 7 and 12, where the percentage of removal was 78.3%, 62.6 %, and 51.9% respectively. The dissolution of these metals can be enhanced by adding oxalic acid at a constant voltage gradient 1.2 v/cm and an initial concentration of 200 mg/kg. It was noted after the end of the experiment that the percentage of removal reached 81.9%, as the concentration of metals on the cathode side was higher than on the cathode side. The anode, and this is due to the migration of metals under the influence of electromigration to the cathode side, where the chromium concentration was 47 mg/kg at the cathode side, 27 mg/kg at the anode side.

The extraction of organic pollutants from environmental samples using green solvents has received a lot of interest recently. Simply said, this is due to their extremely low toxicity and volatility when compared to the common organic solvents. Therefore, many extraction exercises now include ionic solvents, as well as the more current deep eutectic solvents (DES). Hence, the current study reports on 1) the synthesis and characterisation of choline chloride/oxalic acid (1:1) and choline chloride/urea (1:2) deep eutectic solvents and 2) their application in liquid-liquid and solid-liquid assisted extraction of 14 targeted OPFRs from landfill leachate and sediment samples. The densities, refractive indices and melting points of the DES measured were 1.11 ± 0.15 g/mL, 1.14 ± 0.10 g/mL; 1.50 ± 0.12, 1.45 ± 0.20; and 12 ± 0.05°C, 35 ± 0.06–55 ± 0.05°C for choline chloride/urea (1:2) and choline chloride/oxalic acid (1:1) respectively. Choline chloride/urea (1:2) and choline chloride/oxalic acid (1:1) viscosities were 87.0 ± 0.20 kg·m −1·s −1 and 13.5 ± 0.14 kg·m −1·s −1 respectively. 1H NMR and FTIR confirmed the structures of the two DES. Recoveries using internal standards dTPP, dTBP, dTPrP and 13C18MTPP ranged from 59.9 ± 7.41–103 ± 5.32%; whereas the percent recoveries using CRM ranged from 85.7–117%. In the leachate (510–1433 ng/L) and sediment (725–1224 ng/g dw) samples from each landfill, 14 and 13 targeted OPFRs, respectively, were detected. The high recoveries and extraction of OPFRs demonstrated by the two DES imply that these could replace conventional organic solvents used to extract OPFRs from environmental media. [ABSTRACT FROM AUTHOR]

Hexavalent chromium (Cr(VI)) has attracted great considerations due to their high toxicity, teratogenicity, and carcinogenicity. In this study, four Zr‐MOFs were synthesized and used to comparative study their catalytic performances of oxalic acid (OA) for Cr(VI) removal. Results showed that the removal efficiency for Cr(VI) was reached 65.91%, 78.64%, 53.58%, and 96.32% by MOF‐525, MOF‐525(Co), MOF‐525(Zn), and MOF‐525(Fe) in the presence of OA when the initial Cr(VI) concentration was 100 mg·L−1, respectively. The single‐factor experiments for further improving the Cr(VI) removal by MOF‐525(Fe)/OA demonstrated that the optimal conditions were OA dosage of 790 mg·L−1, and MOF‐525(Fe) dosage of 500 mg·L−1 and pH of 2.0, and the MOF‐525(Fe)/OA system could be used to treat Cr(VI)‐containing wastewater at concentrations below 50 mg·L−1. Ionic strength studies indicated that Na+, K+, Mg2+, Cl−, and SO42− had little effect on the catalytic reduction of Cr(VI), while high concentrations of Ca2+ (0.10 and 0.25 mol·L−1), NO3− (0.25 mol·L−1), and PO43− (0.25 mol·L−1) had significant inhibition effects. The reusability experiments showed that the stability of MOF‐525(Fe) was excellent, and it could be used for potential applications. Based on the results of Fourier transform infrared spectroscopy (FTIR), X‐ray photoelectron spectroscopy (XPS), and Electron Paramagnetic Resonance spectrometer (EPR), the possible reduction mechanism of Cr(VI) by MOF‐525(Fe)/OA system was proposed as follows: The complexation of OA with Fe3+ was first complexed to produce Fe2+ and CO2•−, then Cr(VI) was combined with Zr–O and Fe–O clusters in MOF‐525(Fe) to obtain activation energy, and the reduction ability was enhanced at the same time; finally, Cr(VI) obtained electrons from CO2•− and was sequentially reduced as Cr(V) and Cr(III). [ABSTRACT FROM AUTHOR]

The exploitation of deep-eutectic solvents (DESs) offered a potential substitute for water-based solutions when it came to leaching REEs from phosphogypsum (PG). The REEs leachate from PG obtained by DES which comprised choline chloride (ChCl) and diglycolic acid (DGA) or lactic acid (LA). The data offered a successful method for REEs leaching by DES ChCl:LA. The optimal leaching conditions included 150 min, 70°C, ChCl:LA 1:2 molar ratio of 800 rpm, a 15:1 L/S ratio, and 15% additional water. Cyanex 923 was used to assess REEs extraction from DES leachate. The best parameters were 900 rpm, 0.8 M Cyanex/toluene at 25°C, with 15 min extraction time and 1/1 A/O ratio. The REEs were stripped from the REEs/Cyanex after equilibrating for 20 minutes using 0.7 M citric acid, 1/2 A/O ratio, and 1000 rpm at 25°C. The RE ions precipitated from the obtained stripping solution by 30% oxalic acid and pH 1. The RE oxalate was precipitated and then burned at 700°C to gain RE oxide. The RE oxide powder was subjected to analysis to determine the REEs; it was possible to determine that the REEs were 80.98% in RE oxide concentrate, resulting in a purity of 94.76%. [ABSTRACT FROM AUTHOR]

Abstract Objective Germanium, an important component of electronics, is considered by many global economies as a critical raw material. Therefore, investigating its potential new sources is crucial for prospective technology development. This paper presents the investigation results on the leaching of liquation-feeding furnace dross using sulfuric and oxalic acid solutions. Results The dross contained mostly zinc (68.0% wt.) but also elevated germanium concentration (0.68% wt.). The influence of temperature, time, initial acid concentration, and liquid-to-solid phase ratio (L:S) was examined. It was found that germanium availability via leaching is limited—maximum leaching yields using aqueous solutions of sulfuric and oxalic acids were 60% (80 °C, 2 h, 15% wt. H2SO4, L:S 25:1) and 57% (80 °C, 3 h, 12.5% wt. H2C2O4, L:S 10:1), respectively.

Ethnomedicinal plants are thought to have better prospects of harboring endophytes that produce natural products with pharmacological activities. This study aimed to investigate the antiplasmodial and anticancer properties of secondary metabolites of endophytic fungi from three medicinal plants. The endophytic fungi included Lasiodiplodia theobromae isolated from Cola acuminata, Curvularia lunata Bv4 isolated from Bambusa vulgaris, and Curvularia lunata Eg7 isolated from Elaeis guineensis. The identification of the fungi was based on the internal transcribed spacer (ITS-rDNA) sequence. The fungi were subjected to solid-state fermentation and the secondary metabolites were extracted with ethyl acetate. In vitro antiplasmodial screening of extracts was performed using the SYBR green I-based fluorescence assay on the chloroquine-resistant Plasmodium falciparum strain DD2. The cytotoxicity of the extracts on human red blood cells and Jurkat (leukemia) cells was assessed using the tetrazolium-based colorimetric MTT assay. Gas chromatography-mass spectrometry (GC–MS) analysis was used to identify the constituents of the fungal extracts. The extract of L. theobromae showed the best antiplasmodial activity against chloroquine-resistant P. falciparum (IC50 = 5.4 µg/mL) and was not harmful to erythrocytes (CC50 > 100 µg/mL). All three fungal extracts showed a weak cytotoxic effect against Jukart cell lines (CC50 > 100 µg/mL). GC–MS analysis of the three endophytic fungal extracts revealed the presence of forty major bioactive compounds, including: oxalic acid, isobutyl nonyl ester, 2,4-di-tert-butylphenol, and hexadecanoic acid, among others. The endophytic fungi from the medicinal plants in this study were promising sources of bioactive compounds that could be further evaluated as novel drugs for the treatment of malaria caused by P. falciparum-resistant strains. [ABSTRACT FROM AUTHOR]

Fire and mechanical performances of a bio‐based flax/furan resin composite are evaluated and, in order to assess their commercial potential, compared with those of conventional carbon/glass fiber‐reinforced composites. Fire retardant (FR) variants of flax/furan were obtained by adding FRs to the resin and using (i) flax or (ii) FR‐treated flax fabrics. With (i), the fire hazard of the composite could be reduced to minimum, without detrimental effect on the mechanical properties. However, use of FR‐flax fabric (ii) led to impairment of mechanical properties. This indicated that for optimized fire and mechanical properties, use of a FR in the resin matrix suffices; there is no advantage in using a FR‐treated flax fabric. Natural aging of the samples for 10 years followed by water aging indicated that water absorption in flax/furan composites was much higher than in comparable carbon/epoxy composites. While there was evidence of released acidic components such as acetic acid, oxalic acid, and so forth, in flax/furan composites, mainly from oxidative degradation of furan resin, there was no evidence of leaching of FR additives from the matrix. However, FR treatment of flax fabric affected the fiber–matrix interfacial adhesion, leading to considerable water absorption during aging and disintegration of the reinforcement. Highlights: Furan resins are naturally fire retardant, burn only under forced combustion.FR flax/furan composites obtained by adding FRs to the resin or the flax fabric.FR treatment of the flax impairs mechanical properties and water tolerance.FRs in the resin neither affect mechanical properties nor leach out in water. [ABSTRACT FROM AUTHOR]

Pretreatment facilitates cost-effective operations on lignocellulosic biomass ranging from densification to deconstruction and bioproduct development. However, determining molecular-level mechanisms behind pretreatment and their effects has remained elusive. Here, we combine computational simulation and experiment to investigate the effects on wheat straw agricultural residue densification of an emerging pretreatment solvent, namely, a deep eutectic solvent (DES) consisting of choline chloride (ChCl) and oxalic acid (OA). Ab initio molecular dynamics indicates that dissociation of lignin from cellulose in lignin–carbohydrate complexes, which does not occur to a significant extent in aqueous solution, is favorable in the DES and occurs via cleavage of the guaiacyl : xylose ether bond linkage by OA. The ensuing hemicellulose removal exposes lignin to the DES which, molecular dynamics simulation indicates, leads to lignin expansion. The resulting changes in wheat straw fiber structure, lignin distribution, and functional group modifications upon DES treatment by scanning electron and fluorescence microscopy along with Fourier-transform infrared spectroscopy. The molecular expansion of lignin enhances inter-particle binding in wheat straw, leading to denser structures under pelletization. The resulting high mechanical stability and combustion properties make the wheat straw a suitable precursor of high-quality densified solids (e.g., solid biofuel). Overall, we shed light on the molecular-level mechanisms involved in DES pretreatment for biomass densification, demonstrated here in the development of a solid biofuel. The approach here illuminates the rational design from first chemical principles of methods to convert lignocellulosic resources into advanced materials. [ABSTRACT FROM AUTHOR]

Metals such as nickel, cobalt, lithium, and manganese are widely used in lithium-ion batteries (LIBs) in electronic devices and electric vehicles. It is forecast that there will be a strong increase in the number of electronic devices and electric vehicles in the coming years. (1) Background: In this paper, the application of ultrasound waves on improving Li, Co, Mn, and Ni leaching efficiency from mixed active cathode materials from different types of LIBs is presented. (2) Methods: Environmentally friendly, low-concentrated (0.75 M) organic acids (oxalic acid, citric acid) and, additionally, sulfuric acid, were used in sonochemical and chemical leaching (stirring process) at a temperature of 60 °C. (3) Results: The results showed significantly higher leaching efficiency of metals with ultrasound-assisted treatment, especially when using organic acids. An average of 50% better leaching results were obtained for Li in oxalic acid (99.6%) and for Co (93.1%) in citric acid during sonochemical leaching. (4) Conclusions: Based on the theory of hydrogen peroxide formation during ultrasound wave transition in solutions, the role of H2O2 as one of the most effective reductants used to enhance cobalt, manganese, and nickel leaching from LIBs is indicated. [ABSTRACT FROM AUTHOR]

This study investigated the catalytic CO2 methanation using nickel oxide (NiO) nanoparticles and nickel oxalate (NiC2O4) as catalysts. The NiC2O4 precursor was synthesized through a chemical precipitation reaction between nickel (II) nitrate hexahydrate (Ni(NO3)2.6H2O) and oxalic acid (H2C2O4.2H2O). Nickel oxide (NiO) nanoparticles were synthesized through thermal decomposition of NiC2O4 precursor at 450 °C in air. The samples were characterized by XRD, FTIR, BET, SEM, and EDX. The XRD and FTIR analyses revealed that the NiO nanoparticles were well‐crystallized having size 17.30 nm. The BET analysis of the NiO sample revealed mesoporous NiO nanoparticles with a specific surface area (SBET) of 29.08 m2/g and a narrow distribution of pore sizes. The catalytic performance of NiO and NiC2O4 catalysts studied for the CO2 methanation in tubular packed bed reactor at 150–550 °C and 1 atm. The reduced NiO nanoparticles exhibited more catalytic activity than the decomposed NiC2O4 catalyst. At 380 °C, 1 atm, and gas hourly space velocity (GHSV) of 9000 mL g−1 h−1, the reduced NiO nanoparticle catalyst showed high catalytic activity, with a maximum CO2 conversion of 85.54 %, 99 % CH4 selectivity, and 84.69 % CH4 yield. Furthermore, the NiO nanoparticle catalyst demonstrated excellent stability after 12 h of streaming at 380 °C. [ABSTRACT FROM AUTHOR]

This article explores the synthesis of β-N-oxalyl-l-α,β-diaminopropionic acid (β-ODAP) in grass pea, a legume commonly grown in Asia and Africa. The authors present conflicting findings regarding the enzymes responsible for β-ODAP synthesis. They challenge a previous study's claim that the enzyme LsAAE3 is involved, instead proposing that LsBOS is responsible. The authors provide evidence supporting their own two-step mechanism for β-ODAP synthesis and refute the claim that LsAAE3 has evolved to repurpose its activity. Understanding the production of β-ODAP is crucial for developing grass pea cultivars without the neurotoxic compound. [Extracted from the article]

Varroa destructor is a dangerous pest directly for beekeeping and indirectly for crops that require insect pollination. In recent years, the application of chemical pesticides has led to the occurrence of mite resistance and contamination of hive products. Plant extracts are considered as a suitable alternative to chemical acaricides for the Varroa mite control. Therefore, the present study aimed to investigate the acaricidal and insecticidal activity of extract of Prangos ferulacea plant against the Varroa mite and its host in the honey bee colonies in the climatic conditions of Kurdistan province from 2022 to 2024. The P. ferulacea plant was collected in June 2022 from different regions of Kurdistan province in the flowering stage, extracted and then its chemical compounds were identified using GC-MS. The present study was conducted in the form of a factorial experiment based on a completely random basic design with four treatments and seven replications. Before conducting the bioassay experiments, the experimental colonies were homogenized in terms of queen age, population (adults and brood), and honey storage. Also, the initial infestation rate of colonies with Varroa mites was evaluated for adult and brood. The results showed that the extract of 50% of P. ferulacea was relatively favorable acaricidal properties. So that, there was no significant difference with oxalic acid and Apistan treatments in terms of mite mortality percentage in the first time of spraying. Also, the result showed that the bee's mortality percentage was not more than 7% in any of the times of spraying with the 50% extract of the P. ferulacea, and there was observed a significant difference compared to the oxalic acid and Apistan treatments in terms of bee's mortality percentage (P<0.01). The queen superseding was not observed in any of the experimental treatments. According to the findings of the present research, the concentration of 50% of the extract P. ferulaceous can be suggested as a suitable alternative to synthetic acaricides and organic acids to control the Varroa mite in honey bee colonies. [ABSTRACT FROM AUTHOR]

Analytical methods with wide field range and high spatial resolution are required to observe the distribution of the crystal structure in micro‐regions undergoing macroscopic chemical reactions. A recent X‐ray diffraction (XRD) imaging method combines XRD with an X‐ray optical device such as a glass polycapillary consisting of a bundle of numerous monocapillaries. The former provides the crystal structure, while the latter controls the shape of the incident or diffracted X‐rays and retains the positional information of the sample. Although reducing the monocapillary pore size should improve the spatial resolution, manufacturing technology challenges must be overcome. Here, an anodic aluminium oxide (AAO) film, which forms self‐ordered porous nanostructures by anodic oxidation in an electrolyte, is applied as an X‐ray optical device. The AAO film (pore diameter: 110 nm; size of the disc: 11 mm; and thickness: 620 µm) was fabricated by anodization in a mixture of oxalic acid and ethylene glycol. The film was incorporated into a laboratory XRD instrument. Compared with using a glass polycapillary alone, using a combination of a glass polycapillary and the AAO film improved the spatial resolution of the XRD imaging method by 40%. This XRD imaging method should not only provide practical analysis in a laboratory environment but also support various observations of the crystal structure distribution. [ABSTRACT FROM AUTHOR]

• Nanosilicon was synthesized and characterized for size, shape, stability and functional group analysis. • Metabolomics elucidated differential metabolites of PEG-induced water stress and nanosilicon-treated leaves. • Volcano plot demonstrated differential metabolites recognized significantly in tolerant vs. susceptible group. • Enrichment analysis explains drought-responsive metabolites and novel pathways inclined by nanosilicon. Chickpea (Cicer arietinum L.) is a crucial agricultural crop, facing challenges in yield due to environmental stresses, particularly drought. The potential of nanosilicon (NS) in improving drought tolerance in crops remains unclear. This study efforts on synthesizing and characterizing silicon nanoparticles using sodium silicate, examining properties such as size, shape, stability, and functional groups before assessing their potential biological effects. Two chickpea varieties, drought-tolerant (GJG-6) and drought-susceptible (GJG-3), were selected based on previous research exploring biochemical and physiological changes under polyethylene glycol (PEG)-induced osmotic stress. Gas chromatography and mass spectrometry were employed to elucidate the metabolomic profile of chickpea leaves under PEG-induced osmotic stress, with and without NS treatment, at 23 days after sowing. Heatmap analysis depicted the intensity gradient of identified metabolites induced by NS treatment under osmotic stress. Fold change and volcano plot analyses revealed significantly differential metabolites between tolerant (T) and susceptible (S) groups. Metabolites such as l -tryptophan, d -fucitol, beta- d -(+) talopyranose, alloxanic acid, and azelaic acid were significantly upregulated in the tolerant group (T/S). Remarkably, metabolites like oxalic acid, 5-methyluridine, l -histidine, lactic acid, l -asparagine, and mannonic acid exhibited higher fold changes in the NS-treated tolerant variety compared to the susceptible one under drought influence (T_PEGNS/S_PEGNS). NS-treated tolerant variety revealed vital drought-responsive metabolites like l -asparagine, behenic acid, alanine, stearic acid, and d -mannose. This study unveils novel metabolites responsive to drought stress and induced by NS treatments, emphasizing their roles in antioxidants and signal transduction pathways that mitigate the effects of drought in chickpea. [Display omitted] [ABSTRACT FROM AUTHOR]

Medicago sativa is a high-quality legume forage that is widely cultivated around the world. However, low phosphorus (LP) stress is one of the main limiting factors for its yield and quality. Currently, it is unclear how various alfalfa root types respond to LP stress. Thus, the creeping-rooted M. varia 'Gannong No. 4' (or GN), tap-rooted M. sativa 'Longdong' (or LD), and rhizomatous-rooted M. sativa 'Qingshui' (or QS) were selected to detect changes in growth, metabolites, phytohormones, and organic acids after 34 days of LP stress treatment (0.01 mmol·L−1 KH2PO4). We observed LP stress significantly inhibited plant growth, and 123, 73, and 42 considerably upregulated differential metabolites were categorized into 33, 26, and 20 metabolic pathways in GN, LD, and QS under LP stress, respectively. Amino acids, plant growth regulators, and organic acids are the main metabolites. After 34 d of LP treatment, the plant height, total surface area, leaf length, ground biomass, leaf width, total volume, leaf area, and ZT content of different root types of alfalfa significantly decreased, while the contents of malic acid, citric acid, oxalic acid, IAA, ABA, and GA3 significantly increased. The plant height, leaf length, leaf width, leaf area, total surface area, total volume, ground biomass, root biomass, the number of different metabolites, and the contents of malic, citric, and oxalic acid, and IAA of GN were significantly higher than those of QS and LD under LP stress. From this point of view, GN was more tolerant than LD and QS under the LP condition. [ABSTRACT FROM AUTHOR]

Adsorptive–photocatalytic composites based on activated carbon (AC) and α-ferrous oxalate dihydrate (α-FOD) were synthesized by an original two-step method and subsequently used for the removal of phenol from aqueous solutions. To obtain the composites, ferrotitaniferous black mineral sands (0.6FeTiO3·0.4Fe2O3) were first dissolved in an oxalic acid solution at ambient pressure, and further treated under hydrothermal conditions to precipitate α-FOD on the AC surface. The ratio of oxalic acid to the mineral sand precursor was tuned to obtain composites with 8.3 and 42.7 wt.% of α-FOD on the AC surface. These materials were characterized by X-ray powder diffraction, scanning electron microscopy, and the nitrogen adsorption–desorption method. The phenol removal efficiency of the composites was determined during 24 h of adsorption under dark conditions, followed by 24 h of adsorption–photocatalysis under visible light irradiation. AC/α-FOD composites with 8.3 and 42.7 wt.% of α-FOD adsorbed 60% and 51% of phenol in 24 h and reached a 90% and 96% removal efficiency after 12 h of irradiation, respectively. Given its higher photocatalytic response, the 42.7 wt.% α-FOD composite was also tested during successive cycles of adsorption and adsorption–photocatalysis. This composite exhibited a reasonable level of cyclability (~99% removal after four alternated dark/irradiated cycles of 24 h and ~68% removal after three simultaneous adsorption–photocatalysis cycles of 24 h). The promising performance of the as-prepared composites opens several opportunities for their application in the effective removal of organic micropollutants from water. [ABSTRACT FROM AUTHOR]

Lignin, the second most abundant natural polymer, is a by-product of the biorefinery and pulp and paper industries. This study was undertaken to evaluate the properties and estimate the prospects of using lignin as a by-product of the pretreatment of common reed straw (Phragmites australis) with deep eutectic solvents (DESs) of various compositions: choline chloride/oxalic acid (ChCl/OA), choline chloride/lactic acid (ChCl/LA), and choline chloride/monoethanol amine (ChCl/EA). The lignin samples, hereinafter referred to as Lig-OA, Lig-LA, and Lig-EA, were obtained as by-products after optimizing the conditions of reed straw pretreatment with DESs in order to improve the efficiency of subsequent enzymatic hydrolysis. The lignin was studied using gel penetration chromatography, UV-vis, ATR-FTIR, and 1H and 13C NMR spectroscopy; its antioxidant activity was assessed, and the UV-shielding properties of lignin/polyvinyl alcohol composite films were estimated. The DES composition had a significant impact on the structure and properties of the extracted lignin. The lignin's ability to scavenge ABTS+• and DPPH• radicals, as well as the efficiency of UV radiation shielding, decreased as follows: Lig-OA > Lig-LA > Lig-EA. The PVA/Lig-OA and PVA/Lig-LA films with a lignin content of 4% of the weight of PVA block UV radiation in the UVA range by 96% and 87%, respectively, and completely block UV radiation in the UVB range. [ABSTRACT FROM AUTHOR]

In vegetable fermentation, pellicle is a common quality deterioration phenomenon. This study investigates the characteristics of glucose, organic acids, amino acids, and biogenic amines during the pellicle occurrence and disappearance of paocai. The results revealed a slight increase in pH of the fermentation system after pellicle occurred, and glucose was the main carbohydrate that microbial activity primary relied on. The microorganisms responsible for pellicle formation consumed organic acids in brine, but the lactic acid in paocai gradually increased and exceeded 25 mg/g. The appearance of pellicle caused a decrease in total free amino acids from 200.390 mg/100 g to 172.079 when pellicle occurred, whereas its impact on biogenic amines was not apparent. Through Kyoto Encyclopedia of Genes and Genomes pathway enrichment of metagenomics sequencing data, screening, and sorting of the key enzymes involved in organic acid metabolism, it was observed that the composition and species of the key microorganisms capable of metabolizing organic acids were more abundant before the appearance of pellicle. When pellicle occurred, lactic acid may be metabolized by Lactobacillus plantarum; in contrast, Lactobacillus and Pichia were associated with citric acid metabolism, and Lactobacillus, Pichia, Saccharomycodes, and Kazachstania were linked to malic acid metabolism. Moreover, Prevotella, Kazachstania, Lactobacillus, Vibrio, and Siphonobacter were implicated in succinic acid metabolism. Additionally, the production of tartaric acid and oxalic acid in paocai and brine resulted from abiotic effects. This knowledge offers a theoretical basis for precise control of paocai fermentation process. Practical Application: Our study revealed the specific situation of the metabolites produced by the microorganisms during the pollution and recovery process of pellicle in paocai fermentation, especially the effect of pellicle on the key process of organic acid metabolism. These research results provided theoretical basis for precise control of paocai fermentation. [ABSTRACT FROM AUTHOR]

Aluminum alloy forms a protective layer of aluminum oxide when exposed to air, which gives it corrosion resistance. But, the layer can be easily damaged, causing metal corrosion. The hard anodizing method is used to solve this issue. Determining the appropriate anodizing parameters, including current density, process time, and electrolyte concentration, is crucial for attaining the desired thickness and hardness of the anodized layer. An experimental design approach utilizing the response surface method (RSM) was employed to investigate the effects of these variables. Quadratic models were presented to predict the hardness and thickness of the layer with an average error of 2.84% and 3.89%, respectively. The models were verified through analysis of variance (ANOVA) to assess the effect of each parameter and their interactions. Oxalic acid concentration, the interaction between process time and oxalic acid concentration, and the square of current density and process time have a significant impact on hardness. Layer thickness is mainly influenced by current density, process time, and the interaction between process time and oxalic acid concentration. Optimization results show that a current density of 1.19 A / dm 2 , a process time of 160 min, sulfuric and oxalic acid concentrations of 26.25 g r / l i t and 36.88 g r / l i t , respectively, leads to hardness of 434 HV and thickness of 93.6 µm. A scanning electron microscope (SEM) image under optimal conditions shows that aluminum porous arrays created by an anodizing process in mixed sulfuric acid and oxalic acid electrolyte, with a hexagonal shape observed across a wide range of grain domains. [ABSTRACT FROM AUTHOR]

Delayed graft function (DGF) after kidney transplantation heralds a worse prognosis. In patients with hyperoxaluria, the incidence of DGF is high. Oxalic acid is a waste product that accumulates when kidney function decreases. We hypothesize that residual diuresis and accumulated waste products influence the DGF incidence. Patients transplanted between 2018-2022 participated in the prospective cohort study. Pre-transplant concentrations of oxalic acid and its precursors were determined. Data on residual diuresis and other recipient, donor or transplant related variables were collected. 496 patients were included, 154 were not on dialysis. Oxalic acid, and glyoxylic acid, were above upper normal concentrations in 98.8%, and 100% of patients. Residual diuresis was ≤150 mL/min in 24% of patients. DGF occurred in 157 patients. Multivariable binary logistic regression analysis demonstrated a significant influence of dialysis type, recipient BMI, donor type, age, and serum creatinine on the DGF risk. Residual diuresis and glycolic acid concentration were inversely proportionally related to this risk, glyoxylic acid directly proportionally. Results in the dialysis population showed the same results, but glyoxylic acid lacked significance. In conclusion, low residual diuresis is associated with increased DGF incidence. Possibly accumulated waste products also play a role. Pre-emptive transplantation may decrease the incidence of DGF. [ABSTRACT FROM AUTHOR]

Objectives: This study assessed the efficacy of different combinations of oxalic acid, 35% hydrogen peroxide, and 5.25% sodium hypochlorite (NaOCl) for bleaching of tooth discolorations caused by hemoglobin. Materials and Methods: In this in vitro study, 40 sound extracted human premolars were disinfected and decoronated. Their primary color parameters were measured (T1). The teeth were then centrifuged with human blood for 3 days, rinsed, polished, and their color parameters were measured again (T2). They were randomly divided into 4 groups (N=10) and treated as follows: Group A: in-office bleaching with Pola-Office Plus followed by 30 seconds of light-curing, group B: 0.24 M oxalic acid for 5 minutes followed by in-office bleaching, group C: 5.25% NaOCl for 5 minutes followed by in-office bleaching, and group D: 0.24 M oxalic acid (5 minutes) followed by 5.25% NaOCl (5 minutes) and subsequent application of in-office bleaching gel. The color parameters of the teeth were measured again (T3). Data were analyzed by one-way ANOVA and paired sample t-test (alpha=0.05). Results: T2-T3 ΔE in groups B and D was significantly higher than that in group A (P<0.05); the difference between groups B and D was not significant. The mean ΔE and ΔL in group C were not significantly different from those in group A (P>0.05). ΔL significantly and equally increased in groups B and D after bleaching. Conclusion: Application of oxalic acid followed by in-office bleaching gel is more effective than the bleaching gel alone for correction of tooth discolorations caused by hemoglobin. [ABSTRACT FROM AUTHOR]

Textile industry effluents contain several hazardous substances, such as dye-containing effluents, which pose environmental and aesthetic challenges. Presently, the microbial-based remediation process is in use. This study investigated the application of ferrous–ferric oxide (Fe3O4) nanoparticles, a readily formulated nanoadsorbent, to remove scattered dye molecules from industrial effluents. The ferrous–ferric oxide nanoparticles were prepared using a chemical co-precipitation method. The nanoparticles had 26.93 emu g−1 magnetization, with sizes smaller than 20 nm, and possessed a highly purified cubic spinel crystallite structure. The catalytic activity of the iron oxide depended on the dose, photocatalytic enhancer, i.e., H2O2 level, pH of the reaction medium, and dye concentration. We optimized the Fenton-like reaction to work best using 1.0 g/L of ferrous–ferric oxide nanoparticles, 60 mM oxalic acid at pH 7.0, and 60 ppm of dye. Iron oxides act as photocatalysts, and oxalic acid generates electron–hole pairs. Consequently, higher amounts of super-radicals cause the rapid degradation of dye and pseudo-first-order reactions. Liquid chromatography–mass spectrometry (LC-MS) analysis revealed the ferrous–ferric oxide nanoparticles decolorized and destroyed Disperse Red 277 in 180 min under visible light. Hence, complete demineralization is observed using a photo-Fenton-like reaction within 3 h under visible light. These high-capacity, easy-to-separate next-generation adsorption systems are suggested to be suitable for industrial-scale use. Ferrous–ferric oxide nanoparticles with increased adsorption and magnetic properties could be utilized to clean environmental pollution. [ABSTRACT FROM AUTHOR]

Plutonium oxalate supernatant requires a treatment step for further recovery of the residual Pu. As the oxalate ion present in the solution poses problems during the recovery of Pu, it needs to be destroyed. In the present work, Mn2+ based catalytic destruction of oxalate ion was studied in detail, as it could minimize the generation of secondary radioactive waste compared to the conventional process. The effect of various parameters, namely concentrations of HNO3, catalyst, oxalic acid and effect of the metal ion has been studied. Moreover, the robustness of the catalytic destruction method along with the kinetics of oxalate destruction reaction has been investigated. The process was also demonstrated with Pu supernatant generated from CORAL at 1 L scale. [ABSTRACT FROM AUTHOR]

Oxalic acid (OA) is a predominant constituent in kidney stones, contributing to 70–80% of all cases. Rapid detection of OA is vital for the early diagnosis and treatment of kidney stone conditions. This work introduces a novel electrochemical sensing approach for OA, leveraging vanadium disulfide (VS2) nanoflowers synthesized via hydrothermal synthesis. These VS2 nanoflowers, known for their excellent electrocatalytic properties and large surface area, are used to modify glassy carbon electrodes for enhanced OA sensing. The proposed OA sensor exhibits high sensitivity and selectivity across a wide linear detection range of 0.2–20 μM, with an impressively low detection limit of 0.188 μM. The practicality of this sensor was validated through interference studies, offering a promising tool for the early diagnosis and monitoring of kidney stone diseases. [ABSTRACT FROM AUTHOR]

In order to inhibit the corrosion of ADC12 aluminum alloy caused oxalic acid in engine coolant, corrosion inhibitor technology is usually used because of its simple operation, low cost, no impact on metal heat dissipation, and effectively suppressing metal corrosion at a lower concentration. In this paper, the corrosion inhibition, long-term and adsorption mechanisms of humic acid (HA) on ADC12 aluminum alloy were studied using electrochemical testing, surface analysis techniques, and theoretical calculations. The results showed that HA was a mixed corrosion inhibitor that followed the Langmuir adsorption model and belonged to physical chemical mixed adsorption. The corrosion inhibition efficiency of HA was the highest at a concentration of 1500 ppm and enhanced with the extension of soaking time. After soaking for 72 h, the corrosion inhibition efficiency of HA reached its maximum (92.7%), indicating that HA had a good long-term corrosion inhibition effect. HA had a high adsorption energy on the surface of ADC12 aluminum alloy, and HA molecules adsorbed on its surface through the carboxyl groups linked to N atom to form a protective corrosion inhibitor film, effectively inhibiting its corrosion. [ABSTRACT FROM AUTHOR]

Background and aims: Root-knot nematodes (RKN; Meloidogyne spp.) are among the highly prevalent and significantly detrimental pathogens that cause severe economic and yield losses in crops. Currently, control of RKN primarily relies on the application of chemical nematicides but it has environmental and public health concerns, which open new doors for alternative methods in the form of biological control. Methods: In this study, we investigated the nematicidal and attractive activities of an endophytic strain WF01 against Meloidogyne incognita in concentration-dependent experiments. The active nematicidal metabolite was extracted in the WF01 crude extract through the Sephadex column, and its structure was identified by nuclear magnetic resonance and mass spectrometry data. Results: The strain WF01 was identified as Aspergillus tubingensis based on morphological and molecular characteristics. The nematicidal and attractive metabolite of A. tubingensis WF01 was identified as oxalic acid (OA), which showed solid nematicidal activity against M. incognita, having LC50 of 27.48 μg ml–1. The Nsy-1 of AWC and Odr-7 of AWA were the primary neuron genes for Caenorhabditis elegans to detect OA. Under greenhouse, WF01 broth and 200 μg ml–1 OA could effectively suppress the disease caused by M. incognita on tomatoes respectively with control efficiency (CE) of 62.5% and 70.83%, and promote plant growth. In the field, WF01-WP and 8% OA-WP formulations showed moderate CEs of 51.25%–61.47% against RKN in tomato and tobacco. The combined application of WF01 and OA resulted in excellent CEs of 66.83% and 69.34% toward RKN in tomato and tobacco, respectively. Furthermore, the application of WF01 broth or OA significantly suppressed the infection of J2s in tomatoes by upregulating the expression levels of the genes (PAL, C4H, HCT, and F5H) related to lignin synthesis, and strengthened root lignification. Conclusion: Altogether, our results demonstrated that A. tubingensis WF01 exhibited multiple weapons to control RKN mediated by producing OA to lure and kill RKN in a concentration-dependent manner and strengthen root lignification. This fungus could serve as an environmental bio-nematicide for managing the diseases caused by RKN. [ABSTRACT FROM AUTHOR]

Aliphatic‐aromatic copolyesters offer a promising solution to mitigate plastic pollution, but high content of aliphatic units (>40 %) often suffer from diminished comprehensive performances. Poly(butylene oxalate‐co‐furandicarboxylate) (PBOF) copolyesters were synthesized by precisely controlling the oxalic acid content from 10 % to 60 %. Compared with commercial PBAT, the barrier properties of PBOF for H2O and O2 increased by more than 6 and 26 times, respectively. The introduction of the oxalic acid units allowed the water contact angle to be reduced from 82.5° to 62.9°. Superior hydrophilicity gave PBOF an excellent degradation performance within a 35‐day hydrolysis. Interestingly, PBO20F and PBO30F also displayed obvious decrease of molecular weight during hydrolysis, with elastic modulus >1 GPa and tensile strength between 35–54 MPa. PBOF achieved the highest hydrolysis rates among the reported PBF‐based copolyesters. The hydrolytic mechanism was further explored based on Fukui function analysis and density functional theory (DFT) calculation. Noncovalent analysis indicated that the water molecules formed hydrogen bonding interaction with adjacent ester groups and thus improved the reactivity of carbonyl carbon. PBOF not only meet the requirements of the high‐performance packaging market but can quickly degrade after the end of their usage cycles, providing a new choice for green and environmental protection. [ABSTRACT FROM AUTHOR]

Quantification of oxalate salts in soil clay minerals is necessary to study oxalate biogeochemistry, but existing analytical techniques are expensive and time-consuming. We aim to develop an efficient attenuated total reflectance mid-infrared (MIR) spectroscopic technique to quantify oxalate salts in a clay mineral matrix. We calibrated MIR models for analysis of oxalate anion concentrations in standard solutions (0–0.01 M) by using a partial least-squares regression algorithm. MIR models were also developed for analysis of sodium oxalate (NaOx) and calcium oxalate (CaOx) content in clay mineral mixtures with composition like soils of a semi-arid region and with contrasting concentrations (0–1.0 g g−1 for both oxalate salts) to test sensitivity of analyses. Validation plots (true vs predicted values) showed excellent model fit (R2 $ \ge $ ≥ 0.96) and accuracy (normalized root mean squared error of prediction $ \le $ ≤ 0.06) for CaOx, NaOx and oxalic acid components. Once predictive models are stored in analytical software, MIR spectroscopic analyses of samples are much more efficient than chemical techniques. Our MIR spectral-based models are suitable for direct quantification of oxalate salts in clay mineral mixtures for samples like those used for model calibration. [ABSTRACT FROM AUTHOR]

Anodization is a method to fabricate a tunable nanoporosity and thickness of alumina coating. This research is devoted to large-area hard anodization (HA), ultrahard anodization (UHA), and transitional modes. The phenomenon and challenges of UHA and the transition from HA are studied on large-area samples using linear-sweep voltammetry. The findings indicate that a uniform large-area thick coating can be achieved by utilizing pre-UHA modes. The study's results indicate that UHA leads only to coatings with non-uniform thickness in large-area anodization. The peculiarities of pre-UHA are studied using different temperatures (0, 5, 10, and 15 °C) and processing times (1, 2, 4, 6, and 12 h) in a 0.3 M oxalic acid electrolyte. The current study shows the possibility for the fast growth of thick nanoporous alumina up to 235 ± 4 µm for only 12 h. [ABSTRACT FROM AUTHOR]

Olive leaves (OLLs) are an exceptional bioresource of natural polyphenols with proven antioxidant activity, yet the applicability of OLL extracts is constrained by the relatively high polarity of the major polyphenols, which occur as glycosides. To overcome this limitation, OLLs were subjected to both hydrothermal and ethanol organosolv treatments, fostered by acid catalysis to solicit in parallel increased polyphenol recovery and polyphenol modification into simpler, lower-polarity substances. After an initial screening of natural organic acids, oxalic acid (OxAc) was found to be the highest-performing catalyst. The extraction behavior using OxAc-catalyzed hydrothermal and ethanol organosolv treatments was appraised using kinetics, while treatment optimization was accomplished by deploying response-surface methodology. The comparative assessment of the composition extracts produced under optimal conditions of residence time and temperature was performed with liquid chromatography–tandem mass spectrometry and revealed that OLLs treated with 50% ethanol/1.5% HCl suffered extensive oleuropein and flavone glycoside hydrolysis, affording almost 23.4 mg hydroxytyrosol and 2 mg luteolin per g dry weight. On the other hand, hydrothermal treatment with 5% OxAc provided 20.2 and 0.12 mg of hydroxytyrosol and luteolin, respectively. Apigenin was in all cases a minor extract constituent. The study presented herein demonstrated for the first time the usefulness of using a natural, food-grade organic acid to perform such a task, yet further investigation is needed to maximize the desired effect. [ABSTRACT FROM AUTHOR]

Since the global invasion of the ectoparasitic mite Varroa destructor (Anderson and Trueman), selection of mite-resistant honey bee (Apis mellifera L.) colonies appears challenging and has to date not broadly reduced colony mortality. The low published estimated heritability values for mite infestation levels could explain the limited genetic progresses obtained so far. We hypothesize that intercolonial horizontal mite transmission could differentially affect the single colonies located in a given apiary and therefore invisibly bias colony infestation phenotypes. This bias may be lower in regions with lower colony density, providing suitable conditions to set up evaluation apiaries. To verify these hypotheses, we monitored mite infestation and reinvasion in experimental colonies, as well as infestation in neighboring colonies belonging to beekeepers in three areas with variable colony densities in the canton of Bern, Switzerland during three consecutive beekeeping seasons. Mite immigration fluctuated between apiaries and years and significantly contributed to colony infestation level. Depending on apiary and year, 17–48% of the mites present in the experimental colonies at the time of the summer oxalic acid final treatment potentially derived from mite immigration that had occurred since mid-spring. Mite immigration was not linked to local colony density or the infestation levels of beekeepers' colonies located within 2 km. Our results do not prove that apiaries for colony evaluation should necessarily be established in areas with low colony density. However, they highlight the high impact of beekeeping management practices on mite colony infestation levels. [ABSTRACT FROM AUTHOR]

The excellent physical and chemical properties of deep eutectic solvents, especially the ability of some of them to dissolve biomass, make them broadly applicable in biomass pretreatment. In this study, oat straw was pretreated with deep eutectic solvents composed of choline chloride and an acid (formic, lactic, or oxalic acid). The highest reducing sugar yield was obtained for the formic acid/choline chloride mixture. Using a pretreatment temperature of 110 °C, a reaction time of 2 h, and a solid-liquid ratio of 1:20, the reducing sugar yield obtained by cellulase hydrolysis was 23.5%, the degradation rate of cellulose reached 76.9%, and hemicellulose was completely degraded. The pretreated oat straw was then analyzed by scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray diffraction. The changes in its crystallinity and lignin content compared to the untreated specimen were determined. A preliminary mechanism for the pretreatment of oat straw with formic acid/choline chloride was revealed. The study could provide an opportunity to expand the application in biochemicals or biological feed processes. [ABSTRACT FROM AUTHOR]