Methyl Isobutyl Ketone Research Articles

Investigation of ferulic acid recovery from enzymatic hydrolysate of wheat bran using various solvents and liquid-liquid extraction assisted by membrane contactor

Ferulic acid (FA) is the main phenolic compound in wheat bran. Its antioxidant and antibacterial properties make it a valuable product in various field. This study investigates the recovery of FA from an enzymatic hydrolysate of wheat bran via a liquid–liquid extraction (LLE) assisted by membrane contactor (MC). Initially, three alcohols (oleyl alcohol, octan-1-ol, decan-1-ol), two esters (1-octyl acetate and ethyl acetate), and one ketone (methyl isobutyl ketone) were examined for FA recovery from a binary solution with varying pH and initial FA concentrations. Subsequently, the LLE assisted by MC from the enzymatic hydrolysate at both natural pH (5.5) and adjusted pH (4) was studied. The findings indicate that, at pH 4, all the solvents extract over 88–97 % of FA. At pH 5, 6, and 7, only oleyl alcohol and 1-octyl acetate achieve extractions exceeding 82–89 %. The examination of the initial FA concentration ranging from 50 to 250 mg/L showed no significant impact on FA recovery, as all solvents permitted extraction of more than 92 %. The results of the LLE assisted by MC of FA from the enzymatic hydrolysate have shown that initial pH and solvent viscosity play a crucial role in both the kinetics and the maximum recovery yield of FA. Specifically, at pH 4, extraction kinetics are significantly faster, resulting in a potential yield in excess of 97 %. However, higher solvent viscosity decreases extraction kinetics, reducing the mass transfer coefficient. The use of MC proves advantageous in preventing the formation of emulsions, particularly when long-chain alcohols and esters are involved in the process. The obtained results enabled proposing a comprehensive solution to recover FA from biomass, a crucial step in optimizing the utilization of natural phenolic compounds for potential applications across various industries.

Comparison between Electrooxidation of 1-Naphthol and 2-Naphthol in Different Non-Aqueous Solvents and Suppression of Layer Growth of Polymers

The two naphthol isomers were investigated in different organic solvents by taking cyclic voltammograms, and fouling took place on a platinum electrode surface, except for dimethyl sulfoxide and dimethyl formamide. Studies in allyl alcohol rarely used in electrochemical investigations pointed to the importance of the carbon–carbon double bond as electrode deactivation was remarkably faster compared with its saturated analog solvent. Similarly, the use of the other unsaturated solvent mesityl oxide in the electropolymerization of naphthols resulted in different findings compared with methyl isobutyl ketone. As dimethyl formamide was the best choice concerning the solubility of products, it was successfully tested in electrode renewal after deactivation in an aqueous solution. The increase in dimethyl formamide content led to more and more improved reproducibility of the currents of the outlined aromatic compounds. Naphthol isomers were assessed in the suppression of layer growth originating from the electrooxidation of another monomer phloroglucinol. Its simultaneous electrooxidation with naphthol monomers had a dramatic effect on layer morphology and it was found that instead of a coherent organic layer originating from the homopolymerization of phloroglucinol, the copolymerization with naphthols led to the development of more porous and rougher deposits. The suppressed electropolymerization thus increased sensitivity towards a chosen redox active compound, 4-methoxyphenol.

Removal of acrylic acid from aqueous solution utilizing tri-n-octyl amine or tributyl-phosphate in edible oils through reactive extraction

The separation of acrylic acid from its aqueous solutions with edible oils by reactive extraction method was investigated. Walnut oil, hazelnut oil, sesame oil, and safflower oil were used to prepare a relatively environmentally friendly and low-toxic organic phase. Tributyl phosphate (TBP) and tri-n-octyl amine (TOA) were chosen as extractants. In addition, a modifier (octanol, decanol, octyl acetate, methyl isobutyl ketone, 2-octanone, dimethyl phthalate) was added to the organic phase, and its effect on the extraction was investigated. The temperature effect (25, 45, and 65 °C), one of the parameters affecting the extraction process, was investigated. The results were presented as distribution coefficient (D), extraction efficiency (E%), and loading factor (Z). In the physical extraction experiments performed with edible oils, the extraction efficiency ranged between 14 and 21%, while it reached around 70% with TBP and above 90% with TOA in the reactive extraction. It was observed that the highest efficiency among the oils was obtained with safflower oil (71.88% for TBP and 92.68 % for TOA) for both extractants used. Moreover, using octanol as a modifier in the organic phase had a positive effect on the removal of acrylic acid from aqueous media by reactive extraction.

A Closed-Loop Biorefinery Approach for the Valorization of Winery Waste: The Production of Iron-Sulfonated Magnetic Biochar Catalysts and 5-Hydroxymethyl Furfural from Grape Pomace and Stalks

In this work, a closed-loop strategy for the management and valorization of winery waste was proposed. The exhausted pomace and grape stalks that are typically obtained from white wine industries were used as a source of simple sugars, namely, glucose and fructose, and of lignocellulosic feedstock for the preparation of selective catalysts for the 5-hydroxymethylfurfural (5-HMF) production from fructose. A novel synthetic procedure was developed for the synthesis of iron-sulfonated magnetic biochar catalysts (Fe-SMBCs). Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), BET surface area, porous structure analysis and determination of total amount of acid sites were performed in order to characterize the physico-chemical properties of the synthesized systems. Then, these heterogeneous catalysts were successfully tested via the dehydration of simple sugars into 5-HMF by using methyl isobutyl ketone (MIBK) and gamma valerolactone (GVL) as co-solvents. The optimum 5-HMF yield of 40.9 ± 1.1%mol with a selectivity of 59.8 ± 2.6%mol was achieved by adopting the following optimized conditions: 0.1 g of catalyst, volume ratio of GVL to H2O = 2 to 1, 403 K, 6 h. In addition, the catalyst was easily recycled using an external magnetic field and used for at least five reaction cycles without significant loss of catalytic activity.

Development of an Extraction Column using Machine Learning for the Prediction of Feed and Solvent to Obtain the Desired Extraction

The phrase "Industry 4.0" describes the fourth industrial revolution, which is characterized by the usage of digital technology to improve automation, connectivity, and efficiency across various industrial processes. The optimal column designs, suitable solvent selection, and extraction yield prediction are all aided by artificial intelligence (AI). Integration of AI technology with extraction columns is a significant step forward for industrial processes, bringing in a new era of intelligent systems that drive previously unheard-of increases in quality, efficiency, and environmental responsibility. The choice of acetone and water as the input solvents and Methyl Isobutyl Ketone (MIBK) as the extracting solvent results in an ideal configuration for the machine-learning design of an extraction column. With acetone's enhanced solubility and miscibility properties and water's versatility as a solvent, the two work well together. The extraction column was created using Python and concepts and methods based on chemical properties as well as machine learning. The intended extraction column may be implemented with the help of the Python code that is supplied. Based on parameters entered by the user, including extract temperature, raffinate temperature, extract mass flow rate, and extract temperature, it forecasts the temperatures and mass flow rates of acetone and water. By considering the properties of mass flow rates and temperatures, the projections ensure physical feasibility. Utilizing controlled data for training, the model applies a linear regression approach. The findings include the mass flow rate of acetone, the temperature of the water, and the water mass flow rate. The integration of state-of-the-art machine-learning techniques and Industry 4.0 is made possible in this work. This holds the promise of increased process optimization and efficiency in chemical extraction processes.

Experimental and computational studies on isolation of cardanol from cashew nut shell liquid using diethanolamine‐based deep eutectic solvent at different molar ratios

AbstractBACKGROUNDAmine‐based deep eutectic mixtures composed of choline chloride and a DEA‐based hydrogen‐bond donor (HBD) can be used in various molar ratios such as 1:2, 1:3, 1:4, 1:5, 1:6 and 1:7 for isolation of cardanol from cashew nut shell liquid (CNSL).RESULTSIn this study, green techniques were created to extract cardanol from CNSL by utilizing a deep eutectic solvent (DES) based on diethanolamine with various molar ratios [hydrogen‐bond acceptor (HBA): HBD] of 1:2, 1:3,1:4,1:5, 1:6 and 1:7. To enhance cardanol's solubility in DES, promote phase separation, and increase cardanol yield, ethyl acetate (EA) and isobutyl methyl ketone (IBMK) could be utilized as co‐solvents. At temperatures ranging from 293 to 343.15 K and 1 atm, the density of various molar ratios of DES was determined. Additionally, the prepared DES pH behaviour as well as the relationship between pH and temperature were investigated. All investigated DES temperature increases caused a decrease in pH value. By using thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC), similar molar ratios of amine‐based DESs were studied for their thermal stability in terms of decomposition temperature, mass loss and melting temperature. The melting temperature and thermal stability were both increased when the HBD increased. The thermal stability of DES, which mostly depends on intermolecular interactions, is greatly influenced by HBD. Finally, at T = 298.15 K and 1 atm, cardanol was extracted from 50 mL CNSL using different volumes of various molar ratios of DES (100 mL, 75 mL, 50 mL and 25 mL) together with 25 mL IBMK and 25 mL EA. The extracted cardanol was evaluated using Fourier transform infrared spectroscopy and gas chromatography–mass spectrometry.CONCLUSIONIt was observed that the yields of cardanol from each prepared molar ratios ratio of 100 mL DES were 96.57%, 95.38% and 92.87%, respectively. In this study, the sigma potential and sigma profile of chosen HBA and HBD were determined using conductor‐like screening model for real solvents (COSMO‐RS), and the interactions between the molecules during the extraction process were analyzed. The findings demonstrated the viability of using the chosen DESs for the polyphenol extraction process. © 2024 Society of Chemical Industry (SCI).

DEWAXING OF DISTILLATE OIL FRACTION (400- 500 ºC) USING UREA

De-waxing of lubricating oil distillate (400-500 ºC) by using urea was investigated in the present study. Lubricating oil distillate produced by vacuum distillation and refined by furfural extraction was taken from Al-Daura refinery. This oil distillate has a pour point of 34 ºC. Two solvents were used to dilute the oil distillate, these are methyl isobutyl ketone and methylene chloride. The operating conditions of the urea adduct formation with n-paraffins in the presence of methyl isobutyl ketone were studied in details, these are solvent to oil volume ratio within the range of 0 to 2, mixer speed 0 to 2000 rpm, urea to wax weight ratio 0 to 6.3, time of adduction 0 to 71 min and temperature 30-70 ºC). Pour point of de-waxed oil and yield of wax produced were determined to show the effect of these operating conditions. The most favorable operating conditions were solvent to oil volume ratio of 1, mixer speed of 1500 rpm, urea to wax weight ratio of 5, time of adduction of 13 min and temperature of 30-52 ºC.

Extraction of 5-Hydroxymethylfurfural and Furfural in Aqueous Biphasic Systems: A COSMO-RS Guided Approach to Greener Solvent Selection.

5-Hydroxymethylfurfural (HMF) and furfural (Fur) are promising biobased platform chemicals, derived from the dehydration of carbohydrate feedstocks, normally conducted in an aqueous phase. Plagued by side-reactions in such phase, such as the rehydration to levulinic acid (LA) and formic acid (FA) or self-condensation to humins, HMF and Fur necessitates diversification from monophasic aqueous reaction systems toward biphasic systems to mitigate undesired side-reactions. Here, a methodology based on the COnductor-like Screening MOdel for Real Solvents (COSMO-RS) method was used to screen solvent candidates based on the predicted partition coefficients (Ki). Hansen solubility parameters in conjunction with excess thermodynamic quantities determined by COSMO-RS were employed to assess solvent compatibility. Experimental validation of the COSMO-RS values highlighted only minor deviations from the predictions with root-mean-square-error (RMSE) values of HMF and Fur at 0.76 and 5.32, respectively, at 298 K. The combined effort suggested cyclohexanone, isophorone, and methyl isobutyl ketone (MIBK) as the best candidates. Finally, extraction solvent reuse demonstrated cyclohexanone suitability for HMF extraction with KHMF of 3.66 and MIBK for Fur with KFur 7.80 with consistent partitioning across four total runs. Both solvents are classified as recommended by the CHEM21 solvent selection guide, hence adding to the sustainability of the process.

Heteropoly acid catalysis in the valorization of bio-renewables: Acetylation of 1,4-cineole and 1,8-cineole (eucalyptol) in green solvents

In this work, a novel synthesis of monoterpenic acetate esters potentially valuable as flavoring agents was developed. It involves the reactions of 1,4-cineole and 1,8-cineole with acetic anhydride giving the desired products in 80–88 % total yields. The process is performed under ambient conditions in green solvents such as methyl isobutyl ketone, methyl ethyl ketone, dimethyl carbonate or diethyl carbonate in the presence of acidic cesium salt of phosphotungstic acid, Cs2.5H0.5PW12O40, as an efficient solid acid catalyst. The catalyst is stable toward leaching in the reaction system and can be reused. The process produces mixtures of acetate esters with different flavor bouquets which can be used directly as ingredients in fragrance compositions without separating individual compounds.

Biomass characterization and solvent extraction as tools to promote phenol production from urban pruning

Nowadays, leaves, bark, and branches are generated from the tree-pruning process in urban places, where their management is a problem because of the necessity of disposal. These wastes are lignocellulosic biomasses with poor properties for use in biofuel production, but with interesting projections for building block products such as phenol compounds. Therefore, extensive biomass characterization of urban pruning from Liquidambar styraciflua L. was developed to evaluate its composition as a tool for phenol production through thermal processing, in which solvent extraction is a complementary tool for selectivity improvement. The results showed high lignin content in bark and leaves at 45 and 28 %, respectively, compared with that in branches (14 %). Additionally, high extractives in leaves (14 %) could be an additional source of phenols. The lignin units were analyzed by Raman dispersion, revealing p–hydroxyphenyl (H) units in the bark, guaiacyl (G) units in the bark and leaves, and syringyl (S) units only in the branches. Furthermore, the micropyrolysis coupled with gas chromatography/mass spectrometry assay realized at 600 °C showed high presence of phenolic compounds in the three biomass investigated, where a high phenol concentration was identified in leaves, probably due to the S unit degradation during pyrolysis. With these results, an assay for bio-oil production was performed in a low-temperature pyrolysis reactor using leaves as feedstock, reaching a low bio-oil yield with high water content favored for the high inorganic content of leaves (13 %). The produced bio-oil was used for liquid–liquid extraction evaluation, where 1-octanol and methyl isobutyl ketone were identified as interesting solvents for catechol and phenol extraction, respectively. This article presents the challenge of characterizing each part of urban trees, which could be a tool to promote the use of urban pruning by studying the thermal degradation mechanism to implement processes for high-value products, such as phenols produced from L. styraciflua L.

Predictive modeling for VOC adsorption on TiO2 filters: Implications for enhanced photocatalytic oxidation in indoor air quality management

Adsorption of volatile organic compounds (VOCs) onto the surface of a TiO2 filter is essential for initiating photocatalytic oxidation (PCO). This study investigated the adsorption coefficients (K) of 14 VOCs under different relative humidities (RH) and explored the influence of different air velocities on the adsorption of Methyl isobutyl ketone (MIBK). Consequently, a polyparameter linear free energy relationship (pp-LFER) model was established to predict lnK at 35 % RH (lnK35%). Moreover, the study found that lnK has a linear relationship with RH, represented as lnK=αRH+β. The parameters ′α′ and ′β′ can be accurately predicted using the Henry’s Law constant (K°OH) and lnK35%, respectively. By combining the pp-LFER model with regression equations for ′α′ and ′β′, it is possible to predict lnK for VOCs across various RH levels. The study also revealed that the adsorption coefficient of increases with escalating air velocities (0.04 – 0.34 m/s), primarily due to mass transfer. The observed low adsorption performance for aldehydes, commonly seen as by-products in the PCO process, suggests cautious usage of the PCO filtration system in practice before the by-products are eliminated downstream. This study offers valuable insights for the practical application of PCO technologies in the comprehensive removal of indoor VOCs.

Gut microbiota functional profiling in autism spectrum disorders: bacterial VOCs and related metabolic pathways acting as disease biomarkers and predictors.

Autism spectrum disorder (ASD) is a multifactorial neurodevelopmental disorder. Major interplays between the gastrointestinal (GI) tract and the central nervous system (CNS) seem to be driven by gut microbiota (GM). Herein, we provide a GM functional characterization, based on GM metabolomics, mapping of bacterial biochemical pathways, and anamnestic, clinical, and nutritional patient metadata. Fecal samples collected from children with ASD and neurotypical children were analyzed by gas-chromatography mass spectrometry coupled with solid phase microextraction (GC-MS/SPME) to determine volatile organic compounds (VOCs) associated with the metataxonomic approach by 16S rRNA gene sequencing. Multivariate and univariate statistical analyses assessed differential VOC profiles and relationships with ASD anamnestic and clinical features for biomarker discovery. Multiple web-based and machine learning (ML) models identified metabolic predictors of disease and network analyses correlated GM ecological and metabolic patterns. The GM core volatilome for all ASD patients was characterized by a high concentration of 1-pentanol, 1-butanol, phenyl ethyl alcohol; benzeneacetaldehyde, octadecanal, tetradecanal; methyl isobutyl ketone, 2-hexanone, acetone; acetic, propanoic, 3-methyl-butanoic and 2-methyl-propanoic acids; indole and skatole; and o-cymene. Patients were stratified based on age, GI symptoms, and ASD severity symptoms. Disease risk prediction allowed us to associate butanoic acid with subjects older than 5 years, indole with the absence of GI symptoms and low disease severity, propanoic acid with the ASD risk group, and p-cymene with ASD symptoms, all based on the predictive CBCL-EXT scale. The HistGradientBoostingClassifier model classified ASD patients vs. CTRLs by an accuracy of 89%, based on methyl isobutyl ketone, benzeneacetaldehyde, phenyl ethyl alcohol, ethanol, butanoic acid, octadecane, acetic acid, skatole, and tetradecanal features. LogisticRegression models corroborated methyl isobutyl ketone, benzeneacetaldehyde, phenyl ethyl alcohol, skatole, and acetic acid as ASD predictors. Our results will aid the development of advanced clinical decision support systems (CDSSs), assisted by ML models, for advanced ASD-personalized medicine, based on omics data integrated into electronic health/medical records. Furthermore, new ASD screening strategies based on GM-related predictors could be used to improve ASD risk assessment by uncovering novel ASD onset and risk predictors.

Hierarchically porous silica particles: One-pot synthesis, tunable hydrophilic/hydrophobic properties, prospects for selective oil adsorption

Submicron spherical silica particles were synthesized via base hydrolysis of tetraethoxysilane (TEOS) and phenyltriethoxysilane (PTEOS) in a presence of cetyltrimethylammonium bromide. It was shown that the replacement of a part of TEOS with PTEOS in the reaction mixture led to formation of particles containing hierarchical micro-mesoporous structure with specific surface area of up to ∼ 1170 m2 g−1. The amount of PTEOS leads to the increase of water contact angle of the particles from 10° to 155° which causes a gradual change in their surface properties from hydrophilic to superhydrophobic. The static adsorption capacity of the particles was measured for water, toluene and methyl isobutyl ketone and was found to be affected by both the amount of OH- or C6H5-groups on the surface and the characteristics of porosity. In particular, the adsorption capacity for non-polar volatile organics increases with the increase of the hydrophobicity of particles. It was found that synthesized superhydrophobic silica particles efficiently and quickly absorb oil from water surface and then can be easily removed mechanically.

Electrical and water resistance properties of conductive paste based on gold/silver composites

This study aimed to investigate the effects of a corrosive environment on both the electrical and the water resistance properties of conductive paste based on gold/silver composites. The conductive paste was prepared by incorporating silver and gold powders, polyvinyl acetate, polyvinyl chloride as adhesive components, and methyl isobutyl ketone as a diluent. The gold/silver composite powder was prepared with different mass ratios of gold and silver. The paste was coated on a substrate and heated at 80℃ to form the conductive paste film. Characterizations of conductive paste were performed by using FT-IR spectroscopy, electrometry, cyclic voltammetry, and contact angle measurements. Thus, the conductive paste films were tested under two conditions: the absence and the presence of exposure to nitric acid vapor. The results showed that the resistance and the contact angle of the conductive paste were more stable after exposure to nitric acid vapor, particularly in samples of higher gold content. Furthermore, the electrochemical behavior of the conductive paste with gold content remains unchanged after exposure to nitric acid vapor. Results suggest that gold has properties in terms of stability, resistance to oxidation, and maintaining surface characteristics, making it a preferable component for applications requiring resistance to corrosive environments.

Electrical and mechanical response of spin-coated PVDF-TrFE formed from MIBK and DMSO solvents under external excitations

Flexible polymer piezoelectric materials are of interest in electro-mechanical applications; however, the mechanical and electrical properties of these materials can be affected by their formation. In this study vibrational analysis was performed to explore the mechanical and electrical properties of piezoelectric PVDF-TrFE polymer using external excitations. Frequency response study of cantilever cantilevers was used to explore the natural mechanical response of a flexible KAPTON cantilever coated with PVDF-TrFE of different concentrations, and with different solvent formations. It is found that the mechanical response of the PVDF-TrFE coated KAPTON cantilever has reduced vibration amplitude when a combined Methyl Isobutyl Ketone (MIBK) and Dimethyl Sulfoxide (DMSO) is used, but it is not affected with only MIBK is used. When using a combined MIBK and DMSO solvent, the 1.25%w/v PVDF-TrFE material was easily mixed, and it possessed a higher piezoelectric electrical response to the MIBK solutions. The piezoelectrical coefficients were also calculated by applying a dynamic force to the cantilevers and found that q31 of cantilever coated with the PVDF formed using the mixture of DMSO and MIBK solution is higher than that formed using MIBK.

ИЗУЧЕНИЕ ПРОЦЕССА ГИДРИРОВАНИЯ КАРБОНИЛЬНЫХ СОЕДИНЕНИЙ В ПРИСУТСТВИИ НАНОСТРУКТУРИРОВАННЫХ НИКЕЛЕВЫХ КАТАЛИЗАТОРОВ

The influence of the catalyst preparation method on the process of hydrogenation of carbonyl compounds in the presence of nickel catalysts obtained by the deposition-precipitation method using urea as a precipitant was studied. It has been shown that an increase in the content of nickel and modifiers helps to increase the substrate conversion using the example of the methyl isobutyl ketone (MIBK) hydrogenation reaction.

A continuous flow polyurethane foam solid phase microextraction lab-in-syringe platform for the automatic determination of toxic metals

A novel fully automatic continuous flow polyurethane foam solid phase microextraction lab-in-syringe system for on-line sample preconcentration/separation has been developed as a front-end to flame atomic absorption spectrometry. For the first time lab-in-syringe in continuous flow has been adopted for the determination of toxic metals. The microextraction procedure was performed after on-line metal complexation with ammonium pyrrolidine dithiocarbamate, while the elution was conducted by 400 μL of methyl isobutyl ketone. The main chemical and hydrodynamic factors that affected the performance of the method were optimized using Cd and Pb as model analytes. For 90 s preconcentration time, the limits of the detection were 0.20 and 1.7 μg L−1 for Cd and Pb, respectively, while the enhancement factors were 79 for Cd and 150 for Pb. The relative standard deviation% values were lower than 2.8 % for all analytes. As a proof-of-concept the proposed system was used for environmental water analysis, providing relative recoveries within the range of 94.0 and 104.4 %. The Green Analytical Procedure Index and Blue Applicability Grade Index proved reduced environmental impact and high practicality for the proposed method.

Palmitic acid and trans-4-hydroxy-3-methoxycinnamate, the active ingredients of Yaobishu formula, reduce inflammation and pain by regulating gut microbiota and metabolic changes after lumbar disc herniation to activate autophagy and the Wnt/β-catenin pathway

The imbalance in gut microbiota triggers an inflammatory response that spreads from the gut to the discs and is associated with lumbar disc herniation (LDH). In this study, we investigated the mechanism of palmitic acid (PA) and trans-4-hydroxy-3-methoxycinnamic acid (THMC) on microbiota, metabolic homeostasis, and autophagy after LDH. The LDH rat model was established by puncturing the exposed intervertebral disc. 16S rDNA was used to assess the gut microbiome composition. The microbial metabolites were analyzed by UPLC–MS. The mechanism of PA and THMC in LDH was explored by fecal microbiota transplantation (FMT). We found that Yaobishu, PA, THMC, and the positive control drug Celebrex attenuated intervertebral disc damage in LDH rats and downregulated TRPV1, IL-1β, and IL-18 expression. In addition, Yaobishu reduced Oscillospirales and Ruminococcaceae abundances after LDH. PA increased Bacilli's abundance while decreasing Negativicutes and Ruminococcaceae abundances. Metabolomics showed that Yaobishu increased 2-hexanone, methyl isobutyl ketone, 2-methylpentan-3-one, and nonadecanoic acid levels but decreased pantetheine and urocanate levels. PA and THMC reduced uridine and urocanate levels. Yaobishu, PA, and THMC activated autophagy and the Wnt/β-catenin pathway in LDH rats. Moreover, antibiotics abrogated these effects. FMT-PA and FMT-THMC activated autophagy and decreased IL-1β, IL-18, Wnt1, β-catenin, and TRPV1 expression. FMT-PA and FMT-THMC partially reversed the effects of 3-MA. Taken together, our data suggest that Yaobishu, PA, and THMC relieve inflammation and pain by remodeling the gut microbiota and restoring metabolic homeostasis after LDH to activate autophagy and the Wnt/β-catenin pathway, which provide a new therapeutic target for LDH in the clinic.

Experimental investigation of reactive extraction of p-hydroxybenzoic acid using TOA in toluene, petroleum ether and MIBK

ABSTRACT p-hydroxybenzoic acid (p-HBA) remains present in various industrial effluents, it has various industrial applications and excellent medicinal properties, on the contrary, it degrades the fertility of soil if discharged in atmosphere hence, retrieval of p-HBA from effluent is a mandate. In past decades, reactive extraction has arisen as an efficient and attractive separation technique. Therefore, in the present study, the reactive extraction of p-HBA, using Tri-n-octylamine diluted in toluene, petroleum ether, and methyl isobutyl ketone, has been investigated. The results have been reported in terms of efficiency, distribution coefficient, equilibrium complexation constant, and loading ratio. The order of diluents, with respect to extraction given, is MIBK (93.43%) > toluene (92.57%)> petroleum ether (91.43%). The relative basicity model is used to for the interpretation and is found suitable for explaining the results. The diffusion coefficient was also found using Reddy Doraiswamy equation and Wilke Chang equation. Further, minimum number of stages of counter current extraction column and solvent to feed ratio were also calculated to investigate the feasibility of the process.

Extraction of the Food Additive Tartaric Acid Using Octanol, Methyl Isobutyl Ketone, Kerosene, Mustard Oil, And Groundnut Oil

Tartaric acid (TA) is a dicarboxylic acid found in bananas, grapes, apples, papaya, cherries, pineapple, pears, mangoes, and tamarind. Due to its widespread use in the food, cosmetic and pharmaceutical industries, it is an essential carboxylic acid. Tartaric acid is produced commercially from wine-industry byproducts and is also present in the industry's effluent. Separating tartaric acid from wastewater is challenging. In this research, tartaric acid was separated from the aqueous phase using chemical and organic solvents such as groundnut oil, mustard oil, kerosene, octanol, and methyl isobutyl ketone (MIBK). Experiments were conducted at 298 K to determine the extraction efficiency (E%) and distribution coefficient (KD). The maximum extraction efficiencies of tartaric acid were found to be 49.01, 25.62, 16.73, 15.89 and 14.29% when using MIBK, octanol, kerosene, mustard oil and groundnut oil, respectively. The results demonstrate the significance of solvent choice in the extraction of tartaric acid with solvents such as MIBK and octanol being more effective at extracting TA from aqueous solutions. On the other hand, the sustainability of the method for separating tartaric acid was highlighted when organic solvents were applied.