Methanol Concentration Research Articles

Phytochemical screening, antioxidant and anti-inflammatory activities of Rosmarinus officinalis medicinal plant from Algeria

This study aims to investigate phytochemical screening, total polyphenol, flavonoids and tannins content, antioxidant activities, and anti-infalammatory effects of methanol, water and ethyl acetate extracts of R.officinalis L growing in Mascara region (Algeria). The extracts were screened for their possible antioxidant activity was determined by DPPH free radical-scavenging and reducing power assay, in vitro anti-inflammatory activity was evaluated by membrane stabilization method using sodium diclofenac as a reference drug. Phytochemical screening of the extracts revealed a presence of tannins (total and gallic), flavonoids, phenols, quinones, coumarins, saponosides, teranoids. and Reducing sugar.. The results showed that methanolic extract significantly (P˂ 0.05) antioxidant than the aqueous and ethyl acetate extract with IC50 values of (5.032 ± 1.003 μg/ml). Furthemore, the ethyl acetate extract showed significantly (P˂ 0.05) inhibition of hypotonicity induced haemolysis 94.36 % at concentration of 250 μg/ml compared to 50 % for sodium diclofenac at 100 μg/ml. The results obtained confirm the traditional therapeutic effects and these plants can be a potential source of anti-inflammatory drug.

Antimicrobial Potential of Tinospora Cordfolia (Willd.) Miers (Menispermaceae) Against Disease-Causing Clinical Bacterial Pathogens

Tinospora cordifolia is an important plant growth herb belonging to the family Menispermaceae. It is a climbing deciduous and succulent shrub considered traditional medicine in Ayurveda. It has various sources of bioactive compounds and medicinal properties that produce great varieties of secondary metabolites with a broad spectrum of biological activities. It is well known for its nutraceutical food that provides health benefits mainly due to the phytochemicals present in the plant such as alkaloids, flavonoids, proteins, and carbohydrates. It has a wide application in pharmacological research such as antitumor, antiinflammatory, Cerebro-protective, cardio-protective, immunoregulatory, Vasorelaxation, and anxiolytic. Tinospora cordifolia showed antimicrobial activity against a few pathogenic bacteria and pathogenic fungi but not many clinical bacterial pathogens and hospital-acquired infections. In this study, the author focused on the antimicrobial activity of Tinospora cordifolia against eight clinical pathogenic bacteria (Escherichia coli, Klebsiella pneumoniae, MRSA, Proteus mirabilis, Salmonella typhi, Shigella sonnei, Pseudomonas aeruginosa, Acinetobacter baumanii) isolated mainly from patient’s sample. T. cordifolia was extracted from two different solvents, methanol and water. The antimicrobial activity was determined using an agar well diffusion assay. T. cordifolia extract has antibacterial activity against all tested clinical bacterial pathogens and has the highest antibacterial activity against Salmonella typhi in all ratios of methanol concentrations (47.5μg/ml). The Minimum Inhibitory Concentration (MIC) of Tinospora cordifolia methanol extract was found at 100μg/ml. Methanol solvent concentration with the most active antibacterial activity of the extract was of different concentrations as 300μg/ml followed by 450μg/ml and 500μg/ml.

Cyclic Removal and Destruction of Per- and Polyfluoroalkyl Substances from Water Using Ion Exchange, Resin Regeneration, and UV/Sulfite Reduction

Ion exchange (IX) can effectively remove per- and poly-fluoroalkyl substances (PFAS) from drinking water sources at ng/L to µg/L levels. However, adsorbed PFAS on spent resins should be further destructed for detoxification. Traditional resin incineration or landfilling may cause secondary pollution to the surrounding environment and cannot achieve resin reuse. This study explored three variations of a PFAS treatment train, aiming to completely defluorinate PFAS with different chain lengths and functional groups at environmentally relevant levels (ng/L) and to reuse the resins and solvents. The optimized treatment train includes IX, resin regeneration with 5wt% NaCl and 60% v/v methanol, distillation of waste regenerant, and advanced reduction by hydrated electrons (eaq−) generated during the ultraviolet/sulfite (UV/sulfite) treatment of still bottoms. Such a treatment train achieved nearly 100% PFAS removal from surface water and groundwater using either PFAS-specific or generic resins, and almost 100% defluorination of PFAS except a few short-chain fluorinated sulfonates and ethers. Regenerated resins had comparable PFAS removal to the pristine resins over three cycles. The generic resins (e.g., Dupont AmberLite™ IRA910) are easier to regenerate and thus are recommended for the treatment train over PFAS-selective resins (e.g., Purofine® PFA694E). Direct heterogenous defluorination on resins loaded with perfluorooctane sulfonate (PFOS) was ineffective, potentially due to the consumption of UV light/eaq− by the resins and insufficient contact between the UV light/eaq− with PFOS on the resin surface. Distillation of the waste regenerant successfully concentrated PFAS in the still bottoms, reduced the waste volume, and removed excess methanol, all essential for effective UV/sulfite treatment. Meanwhile, the produced condensate with high methanol contents and low PFAS levels can be reused for the next regeneration cycle. Findings from this study provide a timely and sustainable solution to the stringent and evolving regulations on PFAS and the resultant production of PFAS-laden resins as hazardous wastes.

A simple, rapid, and low-cost approach for colloidal nanoparticle-based surface enhanced Raman Scattering detection of endosulfan pesticide at trace levels

Abstract Surface Enhanced Raman Spectroscopy (SERS) is a highly specific, sensitive, and portable technique with great potential for on-site pesticide detection and monitoring. Endosulfan, an organochlorine pesticide known for its high toxicity, slow degradation, and bioaccumulation, has poor affinity for metallic SERS substrates. This study presents a label-free SERS detection method for endosulfan, using aggregating agents like potassium chloride (KCl), potassium hydroxide (KOH), potassium bromide (KBr), and sodium hydroxide (NaOH) to modify the behavior of Ag colloidal nanoparticles (NPs) and enhance the SERS signal of endosulfan molecules trapped within formed hot-spots. We analyzed the UV–Vis spectra, the hydrodynamic diameter, and zeta-potential of Ag NPs with the addition of these agents and endosulfan. Successful detection of both α- and ß- endosulfan isomers at μM concentrations in both ethanol and methanol was achieved with KOH-treated Ag NPs. The method was also applied to detect endosulfan in real water samples, along with simultaneous detection of λ-cyhalothrin, showcasing its capability to identify multiple analytes. The selectivity and specificity were confirmed using a mixture of endosulfan and thiabendazole, highlighting the crucial role of selecting the appropriate aggregating agent for each analyte. Overall, the findings emphasize the potential of aggregating agents to mediate the SERS enhancement of endosulfan, facilitating simple and rapid protocols for environmental pollutant detection, while shedding light on the intricate interplay between NP behavior, surface chemistry, and analyte interaction.

Copper-based nanozyme-linked immunosorbent assay for quantitative detection of fumonisin B1

Fumonisin B1 (FB1) is a Group 2B carcinogen. It is vital to develop an ultra-sensitive, low-cost, and rapid screening method for FB1 for food safety risk control. In this study, a novel copper-based nanozyme was synthesized. The anti-FB1 monoclonal antibody (mAb) was conjugated with copper-based nanozyme through physical adsorption to probe construction. The probe could compete with the limited antigen and trigger a color change when employing the 3,3’,5,5’-tetramethylbenzidine (TMB) as chromogenic substrate in the presence of H2O2. Several experimental conditions were optimized, including the concentration of coating antigen, the concentration of mAb coupled to the nanozyme, incubation time, and methanol concentration. Under optimal conditions, a direct competitive nanozyme-linked immunosorbent assay (NLISA) has been established with a limit of detection (LOD) of 6.52 pg/mL. The developed method presented good accuracy and precision. The spiked recoveries ranged from 97.368 % to 120.916 %, with coefficient of variation (CV) below 10 %. In addition, there was a high consistency (R2=0.9820 for corn; R2=0.9936 for wheat) between the developed detection method and the reference method, liquid chromatography/mass spectrometry (LC-MS/MS). This research can expand the application areas of copper-based nanozymes and improve the sensitivity and efficiency of FB1 monitoring.

A comparison of extraction methods for preparation of glucosinolate-containing extracts from Brassica juncea antagonistic toward Ditylenchus dipsaci

Summary The stem and bulb nematode, a globally distributed pest, primarily affects onions and garlic, causing significant yield losses. Chemical treatments are a practical and effective method for controlling plant-parasitic nematodes to protect high-value crops. However, to minimise environmental damage, chemicals of natural origin need to be investigated. Brown mustard (Brassica juncea) plant is an annual plant in the Brassicaceae family, which is rich in bioactive compounds called glucosinolates. These bioactive compounds play a major role in the defence of Brassica plants against biotic stress factors in nature. Based on this point, efforts to develop plant protection products from the brown mustard plant are ongoing. In this study, the most suitable pre-extraction and extraction conditions were determined to ensure the maximum preservation of glucosinolate content and biological activity, to process brown mustard on an industrial scale. For this purpose, steam treatment was applied before extraction at 3 bar (=3 × 105 Pa) pressure for 1 and 3 min. Four different temperatures (room temperature, 40, 55 and 70°C) and two different methanol concentrations (70% and 80%) were tested to optimise glucosinolates extraction from brown mustard. It was found that sinigrin was the most abundant glucosinolate, with extraction yields 1184.4 ± 14.4 mg kg−1 at 55°C for 3 min, and 2624.2 ± 98.5 mg kg−1 at 70°C/70% MeOH for 1 min. However, nematode immobility was higher at 55°C/70% MeOH for 3 min. It was determined that the application of hot steam for 3 min at 3 bar pressure as a pre-extraction process provided optimal conditions for methanolic extraction. The results may contribute significantly to the development of potential plant protection products with further studies.

Molecular diffusion in aqueous methanol solutions: The combined influence of hydrogen bonding and hydrophobic ends.

Although the nonmonotonic variation in the diffusion coefficients of alcohol and water with changing alcohol concentrations in aqueous solutions has been reported for many years, the underlying physical mechanisms remain unclear. Using molecular dynamics simulations, we investigated the molecular diffusion mechanisms in aqueous methanol solutions. Our findings reveal that the molecular diffusion is co-influenced by hydrogen bonding and the hydrophobic ends of methanol molecules. A stronger hydrogen bond (HB) network and a higher concentration of hydrophobic ends of methanol molecules both enhance molecular correlations, thereby slowing molecular diffusion in the solution. As methanol concentration increases, the HB network weakens, facilitating molecular diffusion. However, the increased concentration of hydrophobic ends counteracts this effect. Consequently, the diffusion coefficients of water and methanol molecules exhibit nonmonotonic changes. Previous studies have only focused on the role of HB networks. For the first time, we have identified the impact of the hydrophobic ends of alcohol on molecular diffusion in aqueous alcohol solutions. Our research contributes to a better understanding and manipulation of the properties of aqueous alcohol solutions and even liquids with complex compositions.

Enhanced Production of Furfural via Methanolysis of Wood Biomass with HCl Gas.

This study explores the production of furfural, xylose and methylxylosides through the methanolysis of wood flour using anhydrous HCl gas. The process involves methanolysis of wood flour with HCl gas under pressure to generate methylxylosides, which are subsequently converted to xylose and furfural via autohydrolysis in a Parr batch reactor system. The methanolysis was conducted in temperature-controlled HCl gas reactor employing 24 h reaction time and 50 % methanol content in wood flour. During the methanolysis step with HCl gas, 65 % of the available xylan in wood flour was converted to water-soluble methylxylosides, xylose, xylooligosaccharides (XO) and water-soluble methyl xylooligosaccharides (MXO). Methanolysis filtrates were then autohydrolyzed with Parr 50 mL batch reactor system to xylose and furfural in two different pH values at 180 °C. The highest furfural yield of 91 % from methanolysis filtrate was achieved with pH 1.2 and 25 min reaction time.

Increasing capacitive desalination stability of active carbon by forming methanol layer on its surface

Capacitive deionization (CDI) based on active carbon is a promising technology for desalinating brackish water, but its desalination performance usually decreases after multiple adsorption/desorption cycles, which seriously hinders its practical application. To explore a solution method, study was conducted on regulating cyclic stability of active carbon electrode by utilizing methanol in NaCl solution. When the methanol content of the solution was 2 vol%, the active carbon electrode displayed 82% desalination capacity retention after the 12th cycle, which was 64% higher than the value reached when the methanol content was 0 vol%. This enhancement in stability was due to the formation of protective methanol layer on electrode surface, which retarded contact of carbon with water and thus oxidation of positive electrode. To put this finding into use, methanol was employed to improve stability of flowing electrode of a flowing CDI (FCDI) device, which does not need continuous addition of methanol into NaCl solution. The capacity retention of the flowing electrode after the 9th cycle was also markedly increased (94%＞80%) by methanol. This study provided a new route for improving cyclic stability of active carbons, which was suitable for application in FCDI.

Controlling strategies of methanol generation in fermented fruit wine: Pathways, advances, and applications.

Methanol is widely existed in fermented fruit wines (FFWs), and the concentration is excessive at times due to inappropriate fermentation conditions. Methanol is neurotoxic, and its metabolites of formaldehyde and formic acid can cause organic lesions and central respiratory system disorders. FFWs with unspecified methanol limits are often produced with reference to grape wine standards (250/400mg/L). To clarify the causes of methanol production in FFWs and minimize the methanol content, this study summarizes the current process methods commonly applied for methanol reduction in FFWs and proposes novel potential controlling strategies from the perspective of raw materials (pectin, pectinase, and yeast), which are mainly the low esterification modification and removal of pectin, passivation of the pectinase activity, and the gene editing of yeast to target the secretion of pectinases and modulation of the glycine metabolic pathway. The modified raw materials combined with optimized fermentation processes will hopefully be able to improve the current situation of high methanol content in FFWs. Methanol detection technologies have been outlined and combined with machine learning that will potentially guide the production of low-methanol FFWs and the setting of methanol limits for specific FFW.

Assessing the potential for upscaling the continuous production of lignin oils through reductive catalytic depolymerization

Lignin represents up to one third of lignocellulosic biomass and is a sustainable carbon source available at a sufficient scale to replace an impactful amount of fossil resources when converted into materials and chemicals. The molecular structure of lignin renders it ideal to obtain renewable aromatic building blocks for the polymer industry. Nevertheless, in polymeric form, lignin poses serious challenges for material applications and chemical conversion, namely poor solubility, and low reactivity. This problem can be circumvented by depolymerization of isolated lignins. To meet the demand for renewable aromatic building blocks, it is crucial to utilize technical lignin streams generated on large scale. This will eventually allow the development of continuous, high-throughput processes which are required for viable industrial-scale operations. Our work demonstrates for the first time that “technical grade” hydrolysis lignin from an operating biorefinery can be successfully subjected to continuous reductive catalytic depolymerization (RCD) in a packed bed reactor using a commercially available Pd/Al2O3 catalyst. The impact of catalyst amount, feed concentration (in methanol), and temperature with regards to process stability and product quality was investigated. The product was characterized by NMR, GPC, and GC-FID. Feed concentrations up to 7 wt% could be continuously processed for 77 h at 200 °C whereas at 225 °C, the operation time was restricted to 21 h. In all cases, a stable output was obtained over time in terms of molar mass, OH-group distributions, and monomer content. At 200 °C, carbon yields above 90 % of the soluble lignin fraction were feasible.

A simple and low-cost method for determination of methanol in alcoholic solutions

Methanol poisoning can occur through consumption of methanol-containing alcohols, especially in areas where production, distribution, sale and consumption of alcohol is lawfully prohibited. Due to its toxic potency, determination of methanol in alcoholic solutions is important. The aim of the present study was to develop a rapid, simple and inexpensive method for quantification of methanol in alcoholic solutions that uses minimal equipment available in most laboratories. The method developed is based microdistillation and chromotropic acid, which can be conducted without sophisticated instruments or personal. The system consists of a micro-tube suspended in a falcon tube to function as a collector. Methanol is separated from wine by microdistillation at 90°C in water bath and converted to formaldehyde in the collector. The collector contains an acidic permanganate solution that converts methanol to formaldehyde. Formaldehyde was then quantified by use of chromotropic acid in concentrated sulfuric acid. Experimental variables were optimized by using central composite design (CCD). Method detection and quantification limits were 183 mg L−1 and 584 mg L−1, respectively. The percent relative standard deviation (RSD%) were between 6.4 and 7.9. Accuracies were between 89.6 % and 92.4 %. Concentrations of methanol in five alcoholic solutions were between 2.9×104 and 3.0×104, mg/L, v/v (ppm). Due to its simplicity and cost effectiveness, this method can be used for routine, real-time determination of methanol in alcoholic solutions.

Multianalyte Detection with Metasurface-Based Midinfrared Microspectrometer.

Midinfrared (2.5-25 μm) spectroscopy is an ideal tool for identifying chemicals in a nondestructive manner. The traditional platform is a Fourier transform infrared (FTIR) spectrometer, but this is too bulky, expensive, and power-hungry for many applications. There is therefore a growing demand for small, lightweight, and cost-effective microspectrometers for use in the field. One emerging platform is the filter-array detector-array microspectrometer. It pairs a broadband detector array with a thin and rigid array of spectral filters to offer a robust, compact platform for real-time in situ sensing. However, most demonstrations have only focused on identifying a single chemical against a null sample, even though many applications would involve multianalyte detection. In this work, we show a rare attempt at simultaneously tracking multiple analytes with a metasurface filter-array microspectrometer. The metasurface consists of periodic lattices of subwavelength circular apertures in an aluminum layer to create an array of bandpass filters. The filter array is imaged with an off-the-shelf microbolometer via a reverse-lens imaging setup to simultaneously monitor the concentration of ethanol and methanol in gasoline. This represents an important application of fuel quality monitoring. Chemometric models (PLS and SVR) are trained and tested on gasoline blends with ethanol and methanol contents, both ranging from 0% to 20% v/v. A support vector machine regression (SVR) model with a cubic kernel was found to have the lowest combined prediction errors. The root-mean-square-error of prediction (RMSEP) for ethanol and methanol are 1.23% and 1.84% v/v; the corresponding pseudounivariate limit of detection is found to be 4.22% and 6.86% v/v, respectively. This work takes the emerging field of metasurface-based mid-infrared spectrometers from single- to multianalyte detection, thereby considerably expanding their range of potential applications.

Tuning Perovskite Nanocrystal Synthesis via Amphiphilic Block Copolymer Templates and Solvent Interactions.

Amphiphilic block copolymer (a-BCP) micelles offer morphological diversity and dimensional tunability, making them suitable for the fabrication of perovskite nanocrystals. However, precise control over the nucleation and growth of perovskite nanocrystals using a-BCP colloidal templates remains underexplored. This study investigates the effects of toluene, methanol, and polystyrene-block-poly(2-vinylpyridine) (PS-b-P2VP) on the formation of cesium lead bromide (CsPbBr3) nanocrystals. The process involves four stages: (i) PS-b-P2VP micellization, (ii) PbBr2 complexation, (iii) coordination interaction with P2VP, and (iv) burst nucleation of CsPbBr3 nanocrystals. Toluene, a good solvent for PS but a nonsolvent for P2VP, PbBr2, and CsBr, facilitates the formation of PS-b-P2VP spherical micelles. Adding PbBr2 to these micelles in toluene results in multiple emulsion, dispersing PbBr2 microstructures (microemulsion) and forming [PbBr3]- complexes encapsulated by the micelles (nanoemulsion). Prolonged stirring enhances this nanoemulsion. CsBr, insoluble in toluene, must be dissolved in methanol before being mixed with micelle-encapsulated complexes, promoting quick crystal nucleation. However, excess methanol weakens micellization, leading to the formation of fused micelles and irregular nanocrystals. At a high methanol content, [PbBr4]2- complexes also form, driving CsPbBr3 to CsPb2Br5 transformation via Ostwald ripening, resulting in large CsPb2Br5 microcrystals that precipitate due to gravitational forces overcoming Brownian motion, destabilizing their dispersion in the solution.

Maximization of Biodiesel production from oil that produced during salmon smoking process with high amount of omega-3 by using homogenous catalyst.

The escalating global demand for oil, coupled with declining fossil fuel production, prompts the urgent exploration of renewable alternatives. To address this challenge, researchers are actively seeking environmentally friendly fuels like biodiesel. Among potential feedstocks, oil that is produced from salmon smoking process during industry emerges as a promising option. Smoked salmon oil could be a challenge when producing biodiesel due to its high content of omega-3 compounds. Using homogenous commercial catalyst from alkali to achieve the highest yield from salmon smoking oil was the aim of the current study. A Box-Behnken design and response surface methodology in Design Expert software (version 13) was used to study the effect of four main factors on the biodiesel yield from salmon smoking oil. The optimum biodiesel values were 70°C, 90 min, 0.753 wt.%, and 20 wt.% for temperature, reaction time, sodium hydroxide concentration, and methanol concentration, respectively. At these optimum values, the highest biodiesel production was 92.0% with fatty acid methyl ester contents of 83.4% and conversion efficiency of 77%. Thin-layer chromatography and thermal gravimetric analysis confirmed the successful production of biodiesel at optimized conditions. Using Aspen Plus simulation software confirmed the cost-effectiveness of the homogenous catalyst used for enhancing biodiesel production from salmon smoking oil.

High-efficiency expression of alginate lyase in Pichia pastoris facilitated by Vitreoscilla hemoglobin

Vitreoscilla hemoglobin (VHb) can enhance the ability of recombinant strains to express heterologous proteins under low-oxygen conditions. However, its mechanism of action in the Pichia pastoris expression system remains unclear. In this study, three VHb construction strategies were designed to elucidate the mechanisms by which VHb promotes heterologous protein expression in P. pastoris. Notably, the co-expression pattern involving the sequential expression of the 102C300C gene followed by the Vgb gene significantly improved enzyme activity in the recombinant strain X33-102C300C-Vgb. The enzyme activity was 203.4 ± 0.57 U/mL at 180 h of fermentation in the 5-L system, which was 20.7 % higher than that of the starting strain X33-102C300C. Fluorescent labeling experiments revealed for the first time that a dual-transcription unit approach achieved superior VHb expression, indicating its potential for further development. Furthermore, transcriptomic and metabolomic analyses demonstrated that VHb enhanced the growth of recombinant yeast colonies by improving respiration-related metabolism under low-oxygen conditions. This, in turn, alleviated the repression of the expression alcohol oxidase (AOX) at high methanol concentrations, resulting in increased alginate lyase activity. This study provides a theoretical foundation for improving the target protein expression in recombinant P. pastoris during high-density fermentation.

Development of a gradient method for sulfamethoxazole, trimethoprim, isoniazid, and pyridoxine hydrochloride in rabbit plasma through QbD-driven investigation

The current study developed a method for quantifying four drugs—Sulfamethoxazole, Trimethoprim, Isoniazid, and Pyridoxine—in rabbit plasma. The method uses gradient liquid chromatography based on analytical quality by design. To achieve separation, a Eclip Plus C18 (250 mm × 5 mm, 4.6 µm) column with L1 packing was used, and analytes were detected at 254 nm at ambient temperature. The optimized mobile phase consisted of 50 mM potassium dihydrogen phosphate buffer (pH 6.5) and Methanol. The concentration of Methanol was 3% (0–5 min), 15% (5–15 min), 55% (15–27 min), and 3% Methanol until the end of the 30-min runtime, and the flow rate was set at 0.95 mL/min. Control Noise Experimentation was used to screen studies, revealing that flow rate, pH, and Methanol concentration significantly affected the analytical attributes. The study identified critical attributes (resolution and asymmetric factor) and developed a quality target method profile. A central composition design was used to optimize the essential parameters. The method developed for the drugs showed peaks at retention times of 6.990 min for Isoniazid, 7.880 min for Pyridoxine, 15.530 min for Sulfamethoxazole, and 26.890 min for Trimethoprim, respectively. The method was validated with linearity in the range of 10–640 ng ml−1, with R2 of 0.9993, 0.9987, 0.9993, and 0.9992 for Sulfamethoxazole, Trimethoprim, Isoniazid, and Pyridoxine, respectively.

Methanol Equilibrium Curves of Power Transformer Oil–Paper Insulation

To eliminate the problem of the aging of cellulose insulation in the manufacturing stage, a new drying method is being developed based on the use of methanol vapors. Previous studies have shown that the complete removal of methanol from the cellulose insulation after the drying process is very difficult. Therefore, it is necessary to check how the remaining methanol after drying affects the properties of both the cellulose materials and mineral oil. To conduct such studies, it is necessary to know the methanol content in oil that can be expected depending on its initial content in the cellulose materials and the temperature of the insulation system. Therefore, the main goal of this work is to develop methanol equilibrium curves for oil–paper insulation. To achieve the assumed goal, three-stage studies were conducted. A gas chromatograph equipped with a flame ionization detector was used in all stages of these studies. The gas partition coefficient between oil and air was determined for a temperature of 70 °C. The key experimental finding was the development of methanol equilibrium curves for oil–paper insulation. Thanks to this achievement, it is possible to estimate the methanol content in cellulose materials and mineral oil depending on the insulation temperature. Such data are necessary, among others, to plan appropriate studies aimed at assessing the impact of methanol content on the dielectric and physicochemical properties of these materials, important from the point of view of the operation of power transformers.

Evaluation of the Physico-chemical and Biological Properties of Fermented Nipa (Nypa fruticans) Sap Under Closed and Open Vessel Fermentation System for Bioethanol Production

Background The potential of Nipa (Nypa fruticans) sap in the Cagayan Region, Philippines, for bioethanol production remains largely underexplored despite its vast expanse. Methods This study investigates the key physico-chemical properties of Nipa sap from Aparri, Cagayan, with a focus on fermentation dynamics and storage conditions to optimize ethanol production. Two fermentation treatments closed and open vessel conditions, were compared to determine the optimal conditions for maximum ethanol yield. Over a 7-day fermentation period, the acetic acid production, yeast activity, sugar content, and ethanol concentration of closed vessel fermented sap (CVFS) and open vessel fermented sap (OVFS) were monitored. Results CVFS demonstrated a higher ethanol yield (7.56%v/v at peak day), characterized by minimized acetic acid accumulation and stable yeast activity. In contrast, OVFS exhibited significant fluctuations in acetic acid and ethanol levels, indicating a lower fermentation efficiency. Conclusion The presence of methanol and high acetic acid content in open-vessel fermentation systems highlights the importance of fermentation conditions to prevent impurities. This study provides valuable insights into optimizing ethanol production from fermenting Nipa sap by employing closed vessel fermentation, which is crucial for sustainable bioethanol production in the Cagayan region.

Effect of Ionic Surfactants on Kinetics and Mechanism of the Bi(III) Ion Electroreduction in the Mixed Aqueous-Organic Solutions of Supporting Electrolytes.

This work presents the results of a study on the effect of ionic surfactants: cationic hexadecyltriammonium bromide (CTAB) and anionic sodium salt of sulfonic acid (1OSASS) on the Bi(III) electroreduction process in mixed aqueous-organic supporting electrolyte solutions containing methanol. This study showed that the composition of the supporting electrolyte solution, particularly the methanol and surfactant concentrations, significantly affects the mechanism and rate of the Bi(III) ion electroreduction. Analysis of the influence of the indicated factors on the mechanisms and kinetics of metal ion electroreduction can contribute not only to the optimization of industrial electrochemical processes but also to the development of innovative technological solutions, such as advanced electrochemical materials and novel sensors. In these experiments, an innovative electrode made of cyclic renewable liquid silver amalgam (R-AgLAFE) was used as a working electrode, which stands out among classic mercury electrodes (HMDE type) due to the significant reduction in mercury consumption while maintaining similar performance.