Acid Molar Research Articles

Achieving Ultra-Low-Sulfur Model Diesel Through Defective Keggin-Type Heteropolyoxometalate Catalysts

Various Keggin-type heteropolyoxometalate catalysts with structural defects and surface acidity were synthesized by immobilizing 12-phosphotungstic acid (HPW) on mesoporous SBA−15, to produce near-zero-sulfur diesel fuel. As the calcination temperature increased, the W=O and the corner-shared W–O–W bonds in the Keggin unit partially broke, creating oxygen defects, as evidenced by the Rietveld refinement and in situ FTIR characterization. All the catalysts contained Lewis (L) and Brønsted (B) acid sites, with L acidity predominant. The relative intensity of the IR band (I980) of W=O bond inversely correlated with the number of L acid sites as the calcination temperature varied, suggesting that oxygen defects contributed to the Lewis acid sites formation. In the oxidation of dibenzothiophene (DBT) in a model diesel within a biphasic system, DBT conversion exceeded 99% under the optimal reaction conditions (reaction temperature 70 °C, reaction time 60 min, H2O2/sulfur molar ratio 8, H2O2/formic acid molar ratio 1.5, catalyst concentration 2 mg/mL). The influence of fuel composition and addition of indole and 4,6-DMDBT on DBT oxidation were also evaluated. Indole and cyclohexene negatively impacted the DBT oxidative removal. Oxygen defects served as active centers for competitive adsorption of sulfur compound and oxidant. Both L and B acid sites were involved in transferring O atom from peroxophosphotungstate complex to sulfur in DBT, resulting in DBTO2 sulfone, which was immediately extracted by polar acetonitrile. This study confirms that structural defects and surface acidity are crucial in the deep oxidative desulfurization (ODS) reaction, and in enabling the simultaneous oxidation and separation of refractory organosulfur compounds in a highly efficient model diesel.

COMPARISON OF BIODIESEL PRODUCTION FROM OLEIC ACID IN BATCH REACTOR AND MEMBRANE REACTOR

This study examines the production of biodiesel by the esterification reaction between oleic acid and ethanol. Conversions between reactions carried out with batch reactors and membrane reactors are compared and the advantages of membrane reactors are stated. The parameters examined in the study are catalyst concentration (2%, 4%, 6%), ethanol/oleic acid molar ratio (3,6,9) and temperature (between 45-65°C). The effect of these parameters on oleic acid conversion was evaluated and the reactions were carried out under the conditions determined because of the optimization. The highest conversion value in the batch reactor was obtained as 85.5% at 65°C, with an alcohol: acid molar feed ratio of 6:1 and a catalyst concentration of 4%. In addition, 50% conversion was achieved in the batch reactor with an ethanol/oleic acid molar ratio of 3, temperature 55°C and 4% catalyst ratio, while 75% conversion was achieved in the membrane reactor. These results show that the acid conversion achieved in the membrane reactor is 26% higher compared to batch reactors under the same operating conditions.

Understanding the role of alloying elements Cr, Ni in erosion–corrosion process of nuclear grade austenitic stainless steel 304 L by total reflection X-ray fluorescence

Stainless steel (SS) has gained an indispensable position as one of the most widely used industrial material. In nuclear industry, it is one of the technologically most important structural materials used in pressure tube, containment vessel and reprocessing-related applications. In fact, SS 304 L is the workhorse material of the reprocessing plant which faces the hostile conditions of acid, temperature as well as high radiation dose. These conditions can affect the erosion-corrosion behavior of the material and can lead to poor mechanical properties. This also affects the life of the reactor components. In the present study, a systematic work has been carried out to develop an in-depth understanding of the Corrosion Rates (CRs) with respect to the loss of major and minor elements from SS into the corrosive nitric acid medium using Total reflection X-Ray Fluorescence (TXRF). The effect of acid molarity as well as temperature, on the erosion-corrosion behavior of SS304L was studied. The TXRF studies have revealed that the CR was maximum in 2 M HNO3 and minimum in 8 M, showing that as the nitric acid molarity has an important role to play in the corrosion and as the molarity increases, the passivation of SS 304 L also increases. This observation was further corroborated with the concentrations of Fe, Cr and Ni, which had leached into the nitric acid medium. The role of alloying elements, Cr and Ni, in the passivation of SS was also studied. The effect of temperature showed that at 45 °C, the rate of corrosion was minimum, as compared to at 25 °C and 90 °C which reveals that the formation of chromium oxide passive layer was thermodynamically most favorable at this temperature.

Optimization of Eugenol Extraction From Piper betle Leaves Using Natural Deep Eutectic Solvents and Ultrasound‐Assisted Extraction

ABSTRACTPiper betle L. (Piperaceae) is a herbal plant used in Thai traditional medicine for its antifungal and antiallergic properties, particularly through topical application. This study aimed to optimize the extraction of Piper betle leaves using natural deep eutectic solvents to enhance the extraction efficiency of eugenol, the active compound in Piper betle leaves. Various types of hydrogen bond donors—including glycolic acid, lactic acid, malic acid, tartaric acid, ascorbic acid, and citric acid—were combined with a hydrogen bond acceptor, choline chloride, to prepare natural deep eutectic solvents. The results indicated that lactic acid was the most effective hydrogen bond donor for eugenol extraction. Subsequently, the choline chloride:lactic acid molar ratios, the natural deep eutectic solvent:water mass ratios, and ultrasonication times were varied. Results showed that the optimal conditions based on one‐factor‐at‐a‐time approach were a choline chloride:lactic acid molar ratio of 1:5, a natural deep eutectic solvent:water mass ratio of 2:1, and an ultrasonication time of 30 min. Under these conditions, the eugenol concentration reached 457.22 ± 21.68 µg/mL, compared to 224.76 ± 6.99 µg/mL when ethanol was used. In conclusion, this study successfully optimized the extraction of eugenol from Piper betle leaves using natural deep eutectic solvents. These findings suggest that natural deep eutectic solvents could be a more effective solvent for the extraction of eugenol.

Preparation and Properties of Crosslinked Quaternized Chitosan-Based Hydrogel Films Ionically Bonded with Acetylsalicylic Acid for Biomedical Materials.

The aim of the current study is to develop chitosan-based biomaterials which can sustainably release acetylsalicylic acid while presenting significant biological activity. Herein, an innovative ionic bonding strategy between hydroxypropyl trimethyl ammonium chloride chitosan (HACC) and acetylsalicylic acid (AA) was proposed, skillfully utilizing the electrostatic attraction of the ionic bond to achieve the controlled release of drugs. Based on this point, six crosslinked N-[(2-hydroxy-3-trimethylammonium)propyl]chitosan acetylsalicylic acid salt (CHACAA) hydrogel films with varying acetylsalicylic acid contents were prepared by a crosslinking reaction. The results of 1H nuclear magnetic resonance spectroscopy (1H NMR) and scanning electron morphology (SEM) confirmed the crosslinked structure, while the obtained hydrogel films possessed favorable thermal stability, mechanical properties, and swelling ability. In addition, the drug release behavior of the hydrogel films was also investigated. As expected, the prepared hydrogel films demonstrated the capability for the sustainable release of acetylsalicylic acid due to ion pair attraction dynamics. Furthermore, the bioactivities of CHACAA-3 and CHACAA-4 hydrogel films with acetylsalicylic acid molar equivalents of 1.25 and 1.5 times those of HACC were particularly pronounced, which not only exhibited an excellent drug sustained-release ability and antibacterial effect, but also had a higher potential for binding and scavenging inflammatory factors, including NO and TNF-α. These findings suggest that CHACAA-3 and CHACAA-4 hydrogel films hold great potential for applications in wound dressing, tissue engineering scaffolds, and drug carriers.

EXTRACTION OF PURE ALUMINA FROM KAOLIN: A REVIEW

This study demonstrated that high-purity alumina can be generated from kaolin using various methods. It examined different leaching techniques, considering the size and percentage recovery of alumina by weight in selected kaolin samples, the calcination temperature, and the molar concentration of acids over time. Additionally, it analyzed the characteristics of several kaolin sources in Nigeria with the aim of extracting alumina. The research indicates that Nigerian kaolinite clay typically contains 22–40% alumina by weight. However, leaching kaolin yielded alumina with a purity of 60–97 wt%, with particle sizes ranging from 16 to 177 nm. Alumina derived from kaolin is deemed beneficial for manufacturing refractory materials, water purification, and biomedical applications.

Yogurt acid whey powder dietary inclusion level modulates broiler cecal microbiota composition and metabolic activity

All over the world, the increasing demand for Greek yogurt generates vast quantities of acid whey as a by-product. The large volume and nutrient composition of yogurt acid whey makes it worthwhile to investigate potential uses in animal nutrition. This study aimed to investigate the inclusion of yogurt acid whey powder (YAWP) in four dietary levels on broiler performance, cecal microbiota composition and metabolic activity. A total of 300 male one-day-old male Ross broiler chickens were randomly assigned into 4 treatments of 5 replicates each. Broilers were fed maize-soybean meal basal diets following a 2-phase feeding program. Depending on the YAWP inclusion level (g kg-1 diet), treatments were no YAWP addition (W0), YAWP at 25 g kg-1 (W25), YAWP at 50 g kg-1 (W50) and YAWP at 100 g kg-1 (W100). Overall body weight gain, feed intake and feed conversion ratio were not affected by YAWP addition. In the ceca, a linear decrease in total bacteria counts and a linear increase in Lactobacillus spp. was noted with increasing YAWP dietary level. A linear reduction of Clostridium cluster I and E. coli species was noted with increasing YAWP dietary level. A linear increase in total volatile fatty acids concentration, acetic acid and butyric acid molar ratios was shown with increasing YAWP level. In conclusion, the addition of YAWP did not affect overall performance but positively modulated the cecal microbiota and metabolic activity of 42-day-old broiler chickens.

Dispersive liquid–liquid microextraction using tailor-made hydrophobic deep eutectic solvents for parabens analysis in mouthwash samples

Hydrophobic deep eutectic solvents (DESs), formulated with menthol and medium-chain fatty acids, exhibit restricted sensitivity for paraben extraction through liquid–liquid microextraction. Consequently, to enhance the effectiveness of the DES-based dispersive liquid–liquid microextraction (DES-DLLME) technique, we aimed to explore the effects of varying fatty acid chain lengths and refining the menthol-to-fatty acid molar ratios. In this study, an optimized DES-based DLLME strategy was developed to extract four parabens, methylparaben, ethylparaben, propylparaben, and butylparaben, which were subsequently analyzed using high-performance liquid chromatography with diode array detection (HPLC-DAD). After optimization, the developed DES-DLLME demonstrated good linearity in the concentration range of 0.497 ng mL−1 to 3.2 μg mL−1 for MP, 0.467 ng mL−1 to 3.2 μg mL−1 for EP, 0.416 ng mL−1 to 3.2 μg mL−1 for PP and 0.402 ng mL−1 to 3.2 μg mL−1 for BP. The limits of detection and quantification were in the ranges of 0.121–0.149 ng mL−1 and 0.402–0.497 ng mL−1, respectively. Good reproducibility (RSD < 4.92%, n = 6) and precision (RSD < 3.32%, n = 5) were obtained. This method exhibited promising application potential in the analysis of the four parabens in both labeled and unlabeled mouthwash samples, with good recoveries in the range of 85.01 ± 3.17% to 104.42 ± 2.36%. The proposed DES-DLLME method is eco-friendly, simple, low-cost, rapid for extraction (50 s), and utilizes a small volume of the extracting solvent (900 µL). The optimized DES-DLLME method provided an efficient and sustainable solution for the analysis of parabens in mouthwashes, highlighting its applicability in eco-friendly analytical practices.

Effect of maltodextrin and Persian gum as wall materials and tannic acid as copigment on some properties of encapsulated sour cherry anthocyanin microcapsules

Due to the instability of anthocyanins, their application as natural colorants is limited. To improve their stability, anthocyanins extracted from sour cherry were copigmented with tannic acid at varying molar ratios. The optimal anthocyanin:copigment molar ratio was determined to be 1:0.25. Subsequently, both non-copigmented and copigmented anthocyanins (using the optimal tannic acid molarity) were spray-dried with either maltodextrin alone (T1 and T2) or a combination of maltodextrin and Persian gum (T3 and T4). The anthocyanin retention in T2 and T4 was approximately 53 % and 38 %, respectively, which were higher than in the non-copigmented samples. All powders demonstrated high encapsulation efficiency (>90.37 %). Stability tests on the anthocyanins conducted over 28 days indicated that light exposure had no effect on the reduction of anthocyanin content when maltodextrin was used. Thus, the copigmentation of anthocyanins with tannic acid, combined with encapsulation in maltodextrin, presents a promising method for producing a stable natural colorant.

A salt/salt aqueous two-phase system based on pH-switchable deep eutectic solvent for the extraction and separation of mulberry polysaccharides

With the aim of expanding the potential application scope of mulberries, eleven pH-switchable deep eutectic solvents were screened for the ultrasonic-assisted extraction of mulberry polysaccharides, and a salt/salt aqueous two-phase system was constructed for the efficient separation of mulberry polysaccharides by regulating the system pH. DES-9 (tetraethylammonium chloride: octanoic acid molar ratio = 1: 2) with a critical response pH value of approximately 6.1 was concluded to be the best extraction solvent for extracting mulberry polysaccharides. A maximum polysaccharide extraction yield of 270.71 mg/g was obtained under the optimal conditions. The maximum polysaccharide extraction efficiency was 78.09 % for the pH-driven tetraethylammonium chloride/K2HPO4 aqueous two-phase system. An acidic β-pyran mulberry polysaccharide with a low-molecular weight of 9.26 kDa and a confirmed monosaccharide composition were obtained. This efficient and environmentally friendly polysaccharide separation method offers a new approach for the efficient extraction and utilization of other plant polysaccharides.

Enhancing phase and morphology control of vanadium oxide films for resistive memory applications: A water-assisted chemical approach

This study explores the influence of precursor solution composition and solvent selection on the synthesis of vanadium oxide (VO2) thin films tailored for resistive memory applications. The vanadium pentoxide and oxalic acid molar ratio and the dispersing medium (ethanol, water, and their mixture) were varied. Water content significantly influenced the VO2 phase, morphology, and film thickness. Ethanol yielded mixed vanadium oxide phases VO2 − Tetragonal, V2O5 − Orthorhombic, and Monoclinic) and a film with minor imperfections. Conversely, the active layer prepared using an aqueous medium showed a predominant VO2 − Monoclinic phase, albeit with a non-uniform film. An ethanol–water mixture produced the most uniform morphology and a mixture of vanadium oxide phases (VO2 − Tetragonal, V2O5- Orthorhombic). All devices displayed resistive switching behavior. VO2-containing devices exhibited a more pronounced transition from an ohmic conduction state to a space-charge-limited conduction mechanism. ON-state currents remained consistent, while OFF-state currents varied notably.

Novel approach on the evaluation of enzyme-aided alkaline extraction of polysaccharide from Hordeum vulgare husk and molecular insight on the multifunctional scaffold

Hordeum vulgare husk, a cereal grain, is rich in dietary fiber and prebiotics beneficial for the gut microbiota and host organism. This study investigates the effects of barley husk-derived water-soluble xylan (BH-WSX) on gut homeostasis and the microbiome. We enzymatically extracted BH-WSX and evaluated its prebiotic and antioxidant properties. A 40.0 % (w/v) xylan yield was achieved, with the extracted xylan having a molecular mass of 212.0885 and a xylose to glucuronic acid molar ratio of 6:1. Specialized optical rotation research indicated that the isolated xylan is composed of monomeric sugars such as D-xylose, glucose, and arabinose. Fourier Transform Infrared (FTIR) spectroscopy revealed that the xylan comprises β (1 → 4) linked xylose units, randomly substituted with glucose residues, α-arabinofuranose, and acetyl groups. Nuclear Magnetic Resonance (NMR) analysis showed that the barley husk extract's backbone is substituted with 4-O-methyl glucuronic acid at the O2 position. Thermogravimetric analysis indicated that WSX exhibits a single sharp peak at 266 °C on the Differential Thermal Gravimetry (DTG) curve. Furthermore, a combination of in vitro, in vivo models, and molecular docking analysis elaborated on the anti-adhesion properties of BH-WSX. This study presents a novel approach to utilizing barley husk as an efficient source of functional polysaccharides for food-related industrial applications.

The interaction of light with oxygen-vacancy-rich W18O49 nanoparticles synthesized using different acid molarities for acidic and neutral water treatments

Toxic industrial compounds as a global difficulty can adversely impact people's health and the environment which motivates studies on the interaction of light and metal oxide nanoparticles to treat the water through adsorption or photocatalysis mechanism by nanoparticles. In the paper, oxygen-vacancy-rich W18O49 nanorods are successfully synthesized by a facile one-pot hydrothermal method using different molarities of hydrochloric acid (HCl) (2–12 M) as proposed candidates to treat the wastewater and solve the global difficulty related to treating the acidic water. The results declare that the change in acid molarity leads to noteworthy changes in the characteristic properties of the produced W18O49 nanorods, and the lowest acid molarity (2 M) causes the formation of uniform and pure monoclinic W18O49 nanorods with the high specific surface area (SSA) of 51.33 m2/g. Furthermore, the nanorods exhibit indirect and direct band gap energies in the range of 2.52–2.68 eV and 2.54–3.08 eV, respectively, as influenced by varying acid molarities (2–12 M). Furthermore, the impressive effects of acid molarity on the methylene blue removal efficiency of the nanorods under ultraviolet (UV) light are observed. The highest efficiency is obtained for W18O49 nanorods synthesized using the acid molarity of 2 M which can be explained by its high SSA, small band gap energy, generation of a large number of electron-hole pairs, and its efficient charge separation. The efficiencies of water treatment reach up to 99 % and 99.5 % at pH of 7 and 5, respectively, which is an excellent achievement and leads to proposing the mentioned W18O49 nanorods as an excellent candidate for treating wastewater and acid factory effluent which represents an appreciable breakthrough in addressing the issue.

Catalytic performance of hexagonal boron Nitride@ APTS-SO3H as heterogeneous nanocatalyst for biodiesel production

In this study, the synthesis of a new stable hexagonal boron nitride (h-BN) is reported via the combustion of boric acid and urea using a pyrolysis method. The surface of hBN particles was modified and the physical/chemical properties of h-BN-APTS-SO3H were examined by different characterization, confirming the modification of h-BN. The effects of methanol/acid molar ratio, temperature, and amount of catalyst were investigated. The results showed that the optimal conditions for the esterification of palmitic acid were as follows: methanol to a palmitic acid molar ratio of 30:1, a temperature of 50 °C, a catalyst of 300 mg for 5 h, and a maximum yield of biodiesel of 90 % was achieved. Furthermore, the quality parameters of the biodiesel were made according to ASTM methods [ASTM D445: Kinematic viscosity, ASTM D445: Flash-point, ASTM D92: Ash content, ASTM D6751: Density]. Tests indicate that the quality parameters of the prepared biodiesel were within ASTM standards. Significantly, the h-BN@APTS-SO3H(1) catalyst showed excellent stability on repeated reuse and can be recycled several times without much activity loss.

Surface Engineering of Superparamagnetic Graphene Oxide Nanosheet as a Chemically Tunable Platform for Facial Biofuel Production by Lipase.

In this research, we utilized an efficient approach to synthesize superparamagnetic graphene oxide (SPGO) rapidly in a one-pot method using microwave irradiation of graphene oxide (GO), urea, and Fe(III) ion. Tannic acid (TA) was introduced to the surface of SPGO through a straightforward and eco-friendly process. Methods were devised to furnish GO nanosheets and modify their surfaces with TA in an environmentally friendly manner. Two series of nanosheets, namely, SPGO/TA-COOH and SPGO/TA-IM, were engineered on the surface and used for immobilizing lipase enzyme. Through various analytical tools, the unique biocatalysts SPGO/TA-COOH/L and SPGO/TA-IM/L were confirmed. These biocatalysts exhibited enhanced stability at high temperatures and pH levels compared with free lipase. They also demonstrated prolonged storage stability and reusability over four months and seven cycles, respectively. Furthermore, the catalytic activity of immobilized lipase showed minimal impairment based on kinetic behavior analysis. The kinetic constants of SPGO/TA-IM/L were determined as Vmax = 0.24 mM min-1, Km = 0.224 mM, and kcat = 0.8 s-1. Additionally, the efficiency of biocatalysts for biodiesel production from palmitic acid was studied, focusing on various reaction parameters, such as temperature, alcohol to palmitic acid molar ratio, water content, and lipase quantity. The esterification reaction of palmitic acid with methanol, ethanol, and isopropanol was tested in the presence of SPGO/TA-COOH/L and SPGO/TA-IM/L, and the corresponding esters were obtained with a yield of 30.6-91.6%.

Characteristics of whole wheat steamed bread production by two-stage fermentation procedure with Jiaozi as starter

Given the beneficial role of biological acidification in improving the quality of cereal-based products, this study evaluated the applicability of Jiaozi as a starter for whole wheat dough fermentation and steamed bread quality improvement. During the first 12 h of dough fermentation, yeast and lactic acid bacteria (LAB) populations increased significantly, resulting in rapid carbohydrate consumption and acidification of the dough. The lactic/acetic acid molar ratio was approximately 3.3, which was within the recommended fermentation quotient (FQ). Compared with the unfermented dough and the dough fermented for 12 h, the dough fermented for 6 h had an improved protein network structure, and the steamed bread made from it also showed the best quality. At a low leavening temperature of 28 °C, satisfactory specific volume and height/diameter ratio were obtained. The dough with an inoculation amount of 50% of the fully fermented dough showed the highest CO2 production capacity. Compared with yeast, the whole wheat steamed bread produced by Jiaozi using the two-stage fermentation process showed higher specific volume, resistant starch (RS) content and protein digestibility. The results showed that the use of Jiaozi as a starter has great potential for application in improving the quality of whole wheat steamed bread.

Esterification catalytic over Imidazolium Ionic Liquid Modified salt of phosphotungstic Acid catalyst

A solid acid was prepared by the reaction of phosphotungstic acid (HPW)with 1-methy- limidazolium sulfobutyrolactone (MIMSB) and characterized by the methods of X-ray powder diffraction, FT-IR, potentiometric titration and SEM. Then the solid acid was employed for esterification to evaluate its acid-catalytic activity. Various reaction parameters, including catalyst dosage, reaction time, n-butanel/butyric acid molar ratio and reaction temperature were systematically examined. These results indicated that the prepared catalyst maintained the Keggin structure of the raw HPW, and had high acidity. The catalyst exhibited excellent catalytic activity in esterification of n-butyric acid and n-butanol.93. 4% conversion of n-butyric acid was obtained under the optimized reaction conditions. The catalyst also had good stability.

Efficient extraction of metals (Fe, Zn, Pb) from hazardous jarosite using ionic liquid and waste-derived solvents.

The present study evaluated a solvo-metallurgical technique for metal extraction from industrial solid waste (jarosite) using ionic liquids (ILs) and waste-derived solvents. The jarosite contains a considerable amount of metal ions, namely iron, zinc, and lead. The jarosite was characterized by XRF, XRD, SEM, and FTIR techniques. The parameters affecting metal extraction, such as stirring time, acid molarity, and temperature, have been examined. Aliquat 336 was used to extract metals from fresh and roasted jarosite after equilibration with HCl. The response surface methodology (RSM) was used to optimize the parameters for the maximum metal extraction using [A336] [Cl]. Maximum extraction of iron (86.75%), zinc (51.96%), and lead (94.38%) from roasted jarosite was achieved at optimum conditions (125-min stirring time, 5M acid molarity, and 20ml/g liquid-to-solid ratio). Furthermore, the metal extraction was investigated using waste-derived solvents. The results show that waste-derived solvents, such as biomass and plastic pyrolysis oil, can effectively extract metals from fresh and roasted jarosite. Biomass pyrolysis oil achieved the highest extraction at 50°C for 90min, while plastic pyrolysis oil achieved the highest extraction at 50°C for 60min from roasted jarosite. These solvents are also cost-effective because they are made from waste plastic and biomass.

Relationship between Rumen Microbial Differences and Phenotype Traits among Hu Sheep and Crossbred Offspring Sheep.

This experiment was conducted to investigate the effect of three-way hybrid sheep and Hu sheep on serum indicators, rumen fermentation, rumen enzyme activity, and microorganisms in sheep. Healthy and similar birth weights from three groups (Hu, n = 11; Charolais × Australian White × Hu, CAH, n = 11; Charolais × Dorper × Hu, CDH, n = 11) were selected to be fed by the ewes until 45 days of age. Subsequently, they were weaned intensively and underwent short-term fattening for 3 months along with selected male lambs fed intensively. During this period, they were fed and watered ad libitum. Blood and rumen fluid were collected and analyzed for serum indicators and rumen fluid microorganisms, enzyme activity, and VFA, respectively, at the end of the fattening period. Compared with Hu lamb, the offspring of the three-way hybrid lamb showed significant improvements in body weight, serum lactate dehydrogenase, and creatinine content. However, there was no significant effect on serum immunity and antioxidant indices. In addition, the rumen fluid volatile fatty acid (VFA) molar concentration and microcrystalline cellulose and lipase content were significantly lower in the three-way hybrid lamb compared to Hu lamb, but β-glucosidase, amylase, pepsin, and VFA molar ratio were not significantly affected. Subsequently, 16S rRNA sequencing diversity analysis revealed that three-way hybrid lamb significantly increased rumen microbial ACE and Chao1 indices compared to Hu lamb. Meanwhile, the abundance of Verrucomicrobiota and Synergistota significantly increased at the phylum level. Correlation analysis showed that Prevotella had the highest proportion, while Rikenellaceae_RC9_gut_group correlated most closely with others genus. The microbial communities isovaleric acid molar concentration and proportion were strongly correlated. In addition, there were significant differences in correlations between microbial communities and isobutyric acid, butyric acid and valeric acid content, and their molar proportion, but they were not significantly correlated with digestive enzymes. From the functional enrichment analysis, it was found that hybrid progeny were mainly enriched in the pyruvate metabolism, microbial metabolism in diverse environments, carbon metabolism, and quorum sensing pathways. In contrast, the Hu sheep were primarily enriched in the cysteine and methionine, amino sugar and nucleotide sugar, and biosynthesis of secondary metabolite pathways. These results suggest that hybridization can play a role in regulating organismal metabolism and improve animal production performance by influencing the structure and characteristics of microbial communities.

Extraction of ofloxacin from water using hydrophobic eutectic solvents

Wastewater treatment plants do not cope well with emerging micropollutants, such as pharmaceuticals, because they are not effective to remove them. Therefore, this work aims to develop a process for the extraction of ofloxacin (OFX) based on a liquid-liquid extraction using hydrophobic eutectic solvents (HES), coupled with the Conductor-like Screening Model for Real Solvent (COSMO-RS) for solvent screening. First, COSMO-RS was used to predict the partition coefficient of OFX for four HES families: L-menthol: fatty acid, L-menthol: fatty alcohol, fatty acid: fatty acid and fatty acid: fatty alcohols, at three different molar ratios (2:1, 1:1, and 1:2). These results showed that HES formed by fatty acids, especially those with a longer alkyl chain and a higher fatty acid molar ratio, were the most suitable solvents for OFX extraction. Then, the most promising HES to extract OFX was evaluated experimentally. The HES decanoic acid: dodecanoic acid (C10 acid: C12 acid) in a molar ratio of 2:1 being the system with best extraction results of OFX was selected to optimize the extraction conditions of OFX, namely pH, HES: water ratio (v/v), and OFX concentration, using a response surface methodology (RSM). The results obtained showed that at a pH of 5.2, HES-water ratio (v/v) of 1.3, and 2.5 mg/ml of OFX that an extraction efficiency of OFX of (98.8 ± 0.9)% could be achieved. The results show that one-step OFX extraction is possible, but is significantly influenced by both the extraction parameters and the hydrophobic properties of the HES.