Oxidation Of Compounds Research Articles

Physicochemical characterization of thermally oxidized rapeseed oil: An insight into combining acoustic diagnostic technique and chemometrics

This study aimed to apply an ultrasonic pulse-echo system to characterize thermally oxidized rapeseed oil. After 60 h of heating treatment (165 ± 5°C), the physicochemical (density, viscosity, acid value, iodine value and polar compounds) and acoustic properties (velocity, acoustic impedance, maximum amplitude of the first echo, difference in amplitude, and area under the curve) of rapeseed oil were measured. Support vector machine, random forest (RF), and backpropagation neural network algorithms were used to establish quantitative prediction models for viscosity and polar compounds based on the acoustic properties of rapeseed oil. The results indicated significant correlations between acoustic impedance and viscosity (R=0.70), as well as between acoustic impedance and polar compounds (R=0.79). Heating treatment reduced oil unsaturation and led to the formation of oxidative and polymeric compounds, which in turn increased the velocity and impedance, while decreasing the other three acoustic features. The RF model yielded the best performance in predicting viscosity (R2=0.7944) and polar compounds (R2=0.8385). These findings highlight that ultrasonic technology not only accurately predicts key quality parameters, but also provides a rapid, non-destructive, and cost-effective alternative to traditional methods for characterizing thermally oxidized rapeseed oil.

Unveiling BaTiO3-SrTiO3 as Anodes for Highly Efficient and Stable Lithium-Ion Batteries

Amidst the swift expansion of the electric vehicle industry, the imperative for alternative battery technologies that balance economic feasibility with sustainability has reached unprecedented importance. Herein, we utilized Perovskite-based oxide compounds barium titanate (BaTiO3) and strontium titanate (SrTiO3) nanoparticles as anode materials for lithium-ion batteries from straightforward and standard carbonate-based electrolyte with 10% fluoroethylene carbonate (FEC) additive [1M LiPF6 (1:1 EC: DEC) + 10% FEC]. SrTiO3 and BaTiO3 electrodes can deliver a high specific capacity of 80 mA h g−1 at a safe and low average working potential of ≈0.6 V vs. Li/Li+ with excellent high-rate performance with specific capacity of ~90 mA h g−1 at low current density of 20 mA g−1 and specific capacity of ~80 mA h g−1 for over 500 cycles at high current density of 100 mA g−1. Our findings pave the way for the direct utilization of perovskite-type materials as anode materials in Li-ion batteries due to their promising potential for Li+ ion storage. This investigation addresses the escalating market demands in a sustainable manner and opens avenues for the investigation of diverse perovskite oxides as advanced anodes for next-generation metal-ion batteries.

A Comparative Study of Hydrothermally Leached Al3TM and Al3TM-Rh (TM=Zr, V, Ce) Intermetallic Compounds for Catalytic Oxidation of Carbon Monoxide.

Rise of the mute assassin "carbon monoxide (CO)" levels impact all aerobic life. The elevated rates of CO concentration endure climatic and geographical characteristics that exacerbate air pollution. Herein, a simple approach for hydrothermal leaching (HyTL) of Al3TM-Rh0.5 (Target material (TM)=Zr, V, Ce) and Al3TM (TM=Zr, V, Ce) intermetallic compounds produces leached products of ZrO2, VO2, and CeO2 with Rhodium (Rh) as an active component. The characterization result reveals the HyTL process and the presence of the active Rh element that elevated the performance of HyTL-Al3Zr-Rh0.5 towards CO conversion compared to other samples. Further, the cubic ZrO2 phase selectively forms after HyTL at 130 °C even though the formation of the cubic ZrO2 phase takes place at a high temperature. Moreover, the presence of Rh promotes higher catalytic activity in all the cases with low temperatures. The advancement in the present study towards the catalytic oxidation of CO over the hydrothermally leached ZrO2-Rh nanocatalyst guarantees the perspective of the aggregation-activation process.

Metabolic mechanisms of carbon and nitrogen interactions during anaerobic digestion of coal

There was limited research on the impact of nitrogen metabolism in the process of methane production with coal, even if carbon and nitrogen metabolism were closely interconnected. Lignite was the source of carbon and nitrogen in anaerobic digestion system. The relationship between carbon and nitrogen metabolism was systematically discussed during the anaerobic digestion process. The results showed that phenolic carbon or ether carbon (C-O), pyridine-type nitrogen (N-6) and nitrogen oxide compound (N-X) in coal were decomposed under the action of Macellibacteroides, Sphaerochaeta and Trichococcus in the hydrolysis stage, respectively. In the acidogenesis stage, the stress of volatile fatty acids and ammonia produced by dissolved organic matter under the action of Syner-01 and Sphaerochaeta on hydrogenotrophic and acetoclastic methanogens was alleviated during the nitrogen cycle. In the acetogenesis stage, acetic acid produced from the decomposition of organic acids and alcohols by Synergistaceae and Sedimentibacter was competed by denitrifying bacteria and acetogenic methanogens. In the methanogenesis stage, CO2 was reduced by Methanobacterium and Methanoculleus to produce CH4, while acetic acid was decomposed by Methanosaeta to produce CH4. And methyl substances were generated into CH4 by Methanosarcina and Methanofastidiosum. This understanding will provide a basis for strengthening the favorable factors in biomethane production.

Using Celery Powder in a Semi-Dry Fermented Sausage 'Heat-Treated Sucuk': Nitrosamine Formation, Lipid Oxidation, and Volatile Compounds.

This study investigated the effect of using celery powder (CP) as source of pre-converted nitrite (treatments: A: 150 mg/kg NaNO2, B: 100 mg/kg NaNO2 + CP as 50 mg/kg NaNO2 equivalent, C: 50 mg/kg NaNO2 + CP as 100 mg/kg NaNO2 equivalent, D: CP as 150 mg/kg NaNO2 equivalent) on the physicochemical and microbiological properties in heat-treated sucuk (HTS), a kind of semi-dry fermented sausage. The influence of cooking time (CT) on the nitrosamine formation in HTS with and without CP was also determined. The results indicated that the use of CP increased the pH value and decreased the aw value. Micrococcus/Staphylococcus and residual nitrite were not affected by the use of CP. TBARS value varied from 0.78 to 0.90 mg MDA/kg. CP did not affect the abundance of hexanal in HTS, however, it increased the abundance of camphene. The results of PCA showed that treatments A, B, and C had similar volatile compound profiles. CP did not affect both N-nitrosodimethylamine and N-nitrosodiethylamine, but their levels increased as the CT increased. Increased CT also resulted in increased N-nitrosopiperidine (NPIP) in all treatments, but the cooking for 1 min did not cause a significant increase in treatments A, B, and C. CP leads to a significant increase in NPIP content, especially after 3 and 5 min of cooking in HTS.

Genotype-Dependent Variations in Oxidative Stress Markers and Bioactive Proteins in Hereford Bulls: Associations with DGAT1, LEP, and SCD1 Genes.

The objective of this study is to assess the influence of genetic polymorphisms in DGAT1, LEP, and SCD1 on the oxidative stress biomarkers and bioactive protein levels in Hereford bulls. A total of sixty-eight bulls were analyzed at 22 months of age to assess growth metrics and carcass quality, with a focus on polymorphisms in these genes. The key markers of oxidative stress, including malondialdehyde (MDA), and the activities of antioxidant enzymes such as glutathione reductase (GluRed), glutathione peroxidase (GPx), and superoxide dismutase (SOD) were measured, alongside bioactive compounds like taurine, carnosine, and anserine. The results show that the TT genotype of DGAT1 is linked to significantly higher MDA levels, reflecting increased lipid peroxidation, but is also associated with higher GluRed and GPx activities and elevated levels of taurine, carnosine, and anserine, suggesting an adaptive response to oxidative stress. The LEP gene analysis revealed that the CC genotype had the highest MDA levels but also exhibited increased GPx and SOD activities, with the CT genotype showing the highest SOD activity and the TT genotype the highest total antioxidant status (TAS). The SCD1 AA genotype displayed the highest activities of GluRed, GPx, and SOD, indicating a more effective antioxidant defence, while the VA genotype had the highest MDA levels and the VV genotype showed lower MDA levels, suggesting protective effects against oxidative damage. These findings highlight genotype specific variations in the oxidative stress markers and bioactive compound levels, providing insights into the genetic regulation of oxidative stress and antioxidant defences, which could inform breeding strategies for improving oxidative stress resistance in livestock and managing related conditions.

Unveiling the Structural and Chemical Evolution of Layered Oxide Cathode for Na‐Ion Batteries Induced by Water Vapor

AbstractNa‐ion batteries (NIBs) have received considerable attention as promising alternatives to lithium‐ion batteries, particularly for low‐speed electric vehicles and large‐scale energy storage applications. Currently, layered oxide compounds are considered the most important cathode materials for NIBs. However, they suffer from reduced capacity and a shortened lifespan when exposed to water vapor during storage or battery assembly. This article elaborates on the structural and chemical evolution of NaNi1/3Fe1/3Mn1/3O2 (NFM) cathode at the atomic scale in a pure water vapor environment. The Na+/H+ exchange induces the formation of a spinel‐like phase via a multi‐site nucleation mechanism. This transition preferentially occurs either at the cathode surface or along planar defects such as twin boundaries and grain boundaries. Additionally, numerous microcracks perpendicular to <003> direction appear inside NFM grains, further exacerbating the structural deterioration. Upon prolonged exposure to water vapor, NFM grains decompose into a mixture of Na2O and transition metal oxide nanoparticles (FeO, NiO, and MnO), accompanied by the generation of oxygen gas. This research provides a comprehensive atomic‐scale insight into the water vapor instability mechanism of layered oxide cathodes, offering guidance for the design and manufacture of the next generation of water vapor‐tolerant layered oxide cathodes in NIBs.

Ab initio investigation of ZnV2O4, ZnV2S4, and ZnV2Se4 as cathode materials for aqueous zinc-ion batteries

Zinc-ion batteries (ZIBs) employing aqueous electrolytes have emerged as one of the most promising alternatives to lithium-ion batteries (LIBs). Nonetheless, the development of ZIBs is hindered by the scarcity of cathode materials with suitable electrochemical properties. In this work, we investigate the unique properties of zinc vanadate oxide (ZnV2O4, ZVO) and zinc vanadate sulfide (ZnV2S4, ZVS) compounds as cathode materials, focusing on their crystal structures, electrochemical performance, spectroscopic features and potential applications in ZIBs. Additionally, we investigate a new cathode material, zinc vanadate selenide (ZnV2Se4, ZVSe), constructed by replacing sulfur with selenium in the ZVS cubic structure. Our findings reveal that these compounds exhibit distinct electronic and electrochemical properties, although they have similar magnetic properties due to the fact that vanadium has the same oxidation state in all three compounds. On average, ZVS stands out as the most promising candidate for ZIBs cathodes, followed by ZVO. ZVSe, shows lower electrochemical performance and also has the obvious drawback of being more costly than the sulfur- and oxygen-based compounds. Our theoretical results align closely with available experimental data, both for electrochemical properties as well as x-ray and photoelectron spectroscopy, where a comparison can be made.

Reducing the overpotential of overall water spitting by micro-pump-like electrode engineering

Electrolyzing water for hydrogen generation consumes a significant amount of electricity. Minimizing bubble accumulation on the electrodes can reduce the overpotential, thereby enhancing the efficiency of water electrolysis. In this work, Co1.8Mn1.2S4 as the catalyst for oxygen evolution reaction (OER) was optimized from 54 compounds of oxides and sulfides of Ni, Co, and Mn, then designed a three-dimensional electrode with a pump-like function to expel bubbles from the electrodes. Using laser-assisted curing 3D printing technology, a capillary array with side holes was fabricated and utilized as a support structure for the Co1.8Mn1.2S catalyst. During water electrolysis, the electrolyte enters the interior of the capillary through the side holes, and the bubbles inside the capillary are released from both ends of the capillary. The optimized electrode achieved 10 mA cm−2 at an overpotential of 345 mV during the OER, and reached 100 mA cm−2 at an overpotential of 435 mV. In-situ optical microscopy observations and fluid dynamics simulations demonstrated that bubbles were effectively released through the main outlet of the capillary. In overall water splitting, the current density reached 10 mA cm−2 at 1.646 V, without significant current decay after 60 h continuous operation. The electrode design presented holds promise for broader applications in catalytic reactions, such as CO2 reduction, electrochemical ammonia synthesis, and electrochemical treatment of water pollutants.

Photoelectrochemical sensor based on copper tetraamino phthalocyanine graphene oxide covalent compound for sensitive detection of cefazolin sodium

In the present research, a novel photoelectrochemical (PEC) sensor was built to detect cefazolin sodium. A copper tetraamino phthalocyanine (CuTAPc) covalently linked graphene oxide compound (CuTAPc-GO) was fabricated successfully by covalent bonding of CuTAPc with graphene oxide (GO). The novel PEC sensing platform was prepared using CuTAPc-GO as a photoelectric material. The prepared PEC sensor showed a higher PEC efficiency under red light. In the perfect conditions, the PEC sensor exhibited a linear correlation in detecting cefazolin sodium concentrations between 0.25 and 12.5μM, featuring a detection limit at 0.15μM. Furthermore, the manufacturing sensor was employed to detect cefazolin sodium in a real-world sample, demonstrating commendable sensitivity and stability. Thus, our study provides a new method for cefazolin sodium detection.

Study on the microstructure and properties of 35Mn2V steel used in oil pipe by salt bath nitriding

Oil pipe is easy to fail due to wear and corrosion during its service, which seriously affects the normal oil production and causes some unnecessary losses，while salt bath nitriding can form a composite infiltration layer through the composite technology on the surface of the workpiece, which can realize the combination of nitriding and oxidation, to achieve the effect of surface strengthening and modification. In this paper, salt bath nitriding is carried out on oil pipe (35Mn2V steel) with different temperature and time, and metallographic test, loose layer grade evaluation, XRD analysis, SEM observation, corrosion wear test, etc. are conducted to study the effect of salt bath nitriding process on the structure and properties of the permeating layer, comprehensively evaluate the quality of the permeating layer, and explore the wear resistance mechanism. The results show that when 35Mn2V is nitrided at 580℃, the infiltration layer mainly consists of oxide film, porous layer, compound layer and diffusion layer, while when it is nitrided at 630℃, the infiltration layer consists of an additional nitrogenous austenite layer. The thickness of 35Mn2V compound layer increases with the increase of nitriding temperature and the extension of nitriding time, and the influence of changing nitriding temperature on the thickness is greater than that of changing nitriding time. After a short time and low temperature nitriding, the phase composition of the infiltration layer is mainly ε-Fe3N and ε-Fe3O4, after a long time and high temperature nitriding, the phase composition is mainly ε-Fe2N and Fe3O4, in which Fe3O4 is formed in the subsequent oxidation process. The degree of loose layer of the infiltration layer increases with the increase of nitriding temperature and the extension of nitriding time. Most of the loose layer grades of the infiltration layer are level 3, and a few are level 2. The degree of loose layer of the infiltration layer is determined by the process of salt bath nitriding, and the subsequent oxidation, ion stabilization and other processes have little influence on it. When 35Mn2V is subjected to corrosion wear test under small load, the friction coefficient of oxide film is small. When the loose layer is worn, the friction coefficient increases obviously. The compound layer is mainly composed of iron-nitrogen compounds, and its friction coefficient is minimal and relatively stable. When the compound layer is worn through, the friction coefficient of the diffusion layer increases.

Fabrication of a polyoxometalate-based metal-organic compound and its derivative for enhanced photocatalytic, electrocatalytic, and electrochemical sensing properties

A novel polyoxometalate-based metal-organic compound (POMOC), namely [Ag(3-pna)2(H2PW12O40)]n (compound 1, where 3-pna = N-(pyridine-3-yl)nicotinamide), had been successfully synthesized and structurally characterized. The photocatalytic performance of compound 1 for the degradation of gentian violet (GV) and methylene blue (MB) was investigated in detail, which exhibited good cyclic stability as a photocatalyst. In addition, cyclic voltammetry technology was used to verify that compound 1 exhibited excellent electrocatalytic performance towards KBrO3 and H2O2. To improve the degradation of organic dyes and electrochemical sensing performance, a negatively charged oxygen vacancy metal oxide compound 1@C was prepared via pyrolysis using compound 1 as a precursor. Compound 1@C was investigated as an adsorbent, and was found to effectively remove MB and GV from wastewater, with adsorption rates of 824.36 mg/g and 957.02 mg/g, respectively. The performance of compound 1@C/glassy carbon electrode as an electrochemical sensor was studied using differential pulse dissolution voltammetry (DPV). This method proved effective in detecting heavy metal ions Cd2+ and Pb2+ in wastewater with the limits of detection as 4.65 and 1.69 μg/L, respectively. Compound 1@C/GCE showed good anti-interference capabilities and stability in detecting heavy metal ions in wastewater.

Effect of refrigeration and reheating on the lipid oxidation and volatile compounds in silver carp surimi gels.

As unsaturated and saturated aldehydes, ketones are known to be responsible for off-odors in surimi products, and they are mainly derived from lipid oxidation. Because surimi-based products are rich in unsaturated fatty acids, they are prone to producing off-odors during the refrigeration and reheating processes, which are common treatments for leftovers. The present study investigated the color, lipid oxidation productions, fatty acid profiles and volatile components in surimi gels during refrigeration at 4 °C for 3 days with multiple reheating. The results revealed that the accumulation rate of hydroperoxides was higher in the refrigeration stage, whereas the decomposition rate was higher during reheating in surimi gels. Both refrigeration and reheating treatments promoted conjugated diene values, acid values and carbonyl values. Nevertheless, reheating treatment decreased tohiobarbituric acid reactive substances and whiteness. The contents of unsaturated fatty acids, especially α-linolenic acid, arachidonic acid, eicosapentaenoic acid and docosahexaenoic acid, were reduced, whereas the contents of saturated fatty acids increased during refrigeration and multiple reheating. The unsaturated fatty acids were lost as a result of their oxidative deterioration. The volatile components profile showed that the accumulation of volatile components mainly occurred in the refrigeration stage. Multivariate data analysis was utilized to further clarify whether the off-odors in surimi gels were mainly generated in refrigeration. Refrigeration and reheating both contributed to lipid oxidation and the generation of volatile compounds in surimi gels, but the off-odors were mainly generated during refrigeration. This research provides a novel understanding of the formation of food odors in processing. © 2024 Society of Chemical Industry.

The Preparation of MoS2/Metal Nanocomposites Functionalized with N-Oleoylethanolamine: Application as Lubricant Additives

In this study, MoS2 nanosheets have been prepared and treated ultrasonically with silver ammonia solutions. The MoS2/Ag precursor was reduced using dopamine (DA) as reducing and linking agent at room temperature, and it was subjected to a hydrothermal treatment to produce MoS2/Ag nanocomposites (denoted as MoAg). The MoAg samples were functionalized with N-oleoylethanolamine to improve dispersion in the base oil component of additives. Use of the functionalized MoAg (denoted as Fc-MoAg) as a lubricant additive for steel balls resulted in effective friction reduction and anti-wear. This work avoids ion exchange during exfoliation, and the Ag+ has been reduced to nano-silver particles by dopamine to enlarge the layer spaces of MoS2. Taking the case of lubrication with base oil containing Fc-Mo0.6Ag15, the wear scar diameters and coefficients of friction of the steel balls were 0.428 and 0.098 mm, respectively, which were about three-fifths base oil. In addition, MoS2/Cu and MoS2/Ni nanocomposites were synthesized and the tribological properties associated with steel/steel balls assessed. The results demonstrate that all MoS2/metal composites exhibit enhanced tribological behavior in the steel/steel pair tests. Both nanocomposite synergy and the tribofilm containing sulfide, oxide, carbide, and other compounds play important roles in achieving reduced friction and improved anti-wear. The friction and wear properties of base oil containing Fc-MoAg and commercial additives were evaluated using a four-ball wear tester with steel/steel, steel/zirconia and zirconia/zirconia pairs. The base oil containing Fc-MoAg delivered smaller coefficients of friction (COFs) and/or scarring groove depths than those observed with the use of pure base oil and base oil containing commercial additives.

Photoelectrolysis of glucose and fructose containing solution in PGM-free cells for hydrogen and valuable chemicals production

This study investigates the reforming of glucose and fructose by photoelectrolyis, employing TiO2 NTs photoanodes for the selective oxidation of the carbohydrates and Ni foam as cathode. TiO2 NTs with different structural features were grown on Ti felt via anodizing and annealing to promote their crystallization.These electrodes were tested in aqueous solutions at three different pH values (i.e., 2, 7, and 12) both without and with the addition of biomass. When biomass was present, the hydrogen production rate increased, reaching faradic efficiencies (FEs) ∼ 100% in spite of the use of undivided cell, allowing the simultaneous production of valuable partial oxidation compounds, such as gluconic acid (GA) and formic acid (FA), with FEs of 24% and 55% respectively, and overall quantum yields of 5.67% and 4.36% respectively. The photoanodes used demonstrated high mechanical and chemical stability under all the tested conditions, with electrode performance remaining consistent over time, allowing the reuse of the same electrode for a not limited number of runs after a mild cleaning step.The results demonstrated that this photoelectrocatalytic (PEC) process is promising for both biomass valorization and H2 production.

Impact of calcined temperatures on the crystalline parameters, morphological, energy band gap, electrochemical, antimicrobial, antioxidant, and hemolysis behavior of nanocrystalline tin oxide

To construct a battery, the precipitation-synthesized SnO2 products at 450 °C and 650 °C were separately taken and mixed with graphite as the anode and PbO2,V2O5, and graphite materials as cathode materials to make the pellets and examine their open circuit voltage (OCV) values. The microstrain, lattice parameter, and crystallite size values of the above-mentioned tin oxide compounds were obtained through Rietveld refinement-MAUD fit analysis. The microstrain and lattice parameter values of tin oxide were significantly varied at a higher calcined temperature. Surface particle grain growth was increased with the increased calcined temperature from 450 to 650 °C as evidenced by FE-SEM study. Particle size distributions of SnO2 and polycrystalline behavior have been discussed with the aid of TEM analysis. From the UV–visible spectra, optical band gap (Eg) values reduced from 3.73 to 3.69 eV for the SnO2 products with an increase in calcined temperatures from 450 to 650 °C. The antimicrobial responses of the two different calcined SnO2 samples at 450 °C and 650 °C against two different bacterial pathogens (gram-positive-S. aureus and gram-negative-E.coli) were investigated. From the microbicidal assessment, a relatively higher diameter of the zone of inhibition (DZOI) of tin oxide at 650 °C samples was measured to be 19 ± 2 mm and 21 ± 2 mm for S. aureus and E. Coli than the DZOI of SnO2 at 450 °C samples (15 ± 1 mm for S. aureus and 18 ± 1 mm for E. coli. DPPH scavenging activity at 100 μg/ml shows that SnO₂ calcined at 450 °C achieves 68 ± 1 %, while SnO2 calcined at 650 °C exhibits a significantly higher activity of 86 ± 1 %. A slight increase in hemolysis was observed for SnO2 calcined at 650 °C, reaching 1.3 % at higher concentrations, but overall, hemolysis remained below 5 %, indicating high hemocompatibility.

Effect of Powder Reuse on Powder Characteristics and Properties of DED Laser Beam Metal Additive Manufacturing Process with Stellite® 21 and UNS S32750

In this work, the influence of powder reuse up to three times on directed energy deposition (DED) with laser processing has been studied. The work was carried out on two different gas atomized powders: a cobalt-based alloy type Stellite® 21, and a super duplex stainless steel type UNS S32750. One of the main findings is the influence of oxygen content of the reused powder particles on the final quality and densification of the deposited material and the powder catch efficiency of the laser deposition process. There is a direct relationship between a higher surface oxidation of the particles and the presence of oxygen content in the particles and in the as-built materials, as well as oxides, balance of phases (in the case of the super duplex alloy), pores and defects at the micro level in the laser-deposited material, as well as a decrease in the amount of material that actually melts, reducing powder catch efficiency (more than 12% in the worst case scenario) and the initial bead geometry (height and width) that was obtained for the same process parameters when the virgin powder was used (without oxidation and with original morphology of the powder particles). This causes some melting faults, oxides and formation of undesired oxide compounds in the microstructure, and un-balance of phases particularly in the super duplex stainless steel material, reducing the amount of ferrite from 50.1% to 37.4%, affecting in turn material soundness and its mechanical properties, particularly the hardness. However, the Stellite® 21 alloy type can be reused up to three times, while the super duplex can be reused only once without any major influence of the particles’ surface oxidation on the deposited material quality and hardness.

Effects of Pre-Fermentative Treatments with Non-Synthetic Ternary Component Fining Agents Based on Pea Protein on the Volatile Profiles of Aromatic Wines of Tămâioasă Românească

To remove oxidizable polyphenolic compounds from wines, fining treatments with products of various origins are applied before or after fermentation. Seeking alternatives to the treatments with animal proteins or synthetic materials such as polyvinylpolypyrrolidone (PVPP), vegetal and mineral products are tested. One of these alternative agents is pea protein (P), which can be combined with chitosan (K), yeast cell walls (Y), active carbon (C), and/or Ca-bentonite (B). Aside from the proven polyphenol removal effect, these products can also have an impact on aroma. This research evaluates the effect of P and ternary combinations with P on the volatile compounds of aromatic wines from the Tămâioasă românească variety. Several variants of treatments with P and with ternary mixtures involving P were prepared in triplicate with a total dose of 20 g/hL of fining agent applied during the pre-fermentative phase. Volatile profiles were determined using a flash gas chromatograph with two short columns of different polarities. The chromatographic peak areas for the identified ethylic esters, acetates and terpenes were used to compare the fining treatment effects. To test the significant differences between experimental variants, the Analysis of Similarity (ANOSIM) was used. The influences of P used alone and PVPP used alone were both significantly different compared to control (untreated), but based on the dissimilarity index R, PVPP affected the volatile profile about twice as much as P, showing that pea protein is a good alternative for PVPP. The ethyl esters were especially reduced by PVPP, while P especially reduced the terpenes. From all the tested pea protein ternary agents, those containing bentonite (PCB and PYB) showed a significant reducing effect on all classes of compounds and therefore are not recommended. The combinations containing yeast cell walls, PCY and PKY, are the most interesting alternatives to both PVPP and P used independently, PCY being the least aggressive of all treatments on overall aroma, preserving well the aroma compounds of all determined classes, including terpenes.

Hesperetin but not ellagic acid increases myosin heavy chain expression and cell fusion in C2C12 myoblasts in the presence of oxidative stress.

Skeletal muscle regeneration is impaired in elderly. An oxidative stress-induced decrease in differentiation capacity of muscle satellite cells is a key factor in this process. The aim of this study is to investigate whether orange polyphenol hesperetin and pomegranate polyphenol ellagic acid enhance myoblast differentiation in the presence and absence of oxidative stress, and to explore underlying mechanisms. C2C12 myoblasts were proliferated for 24 h and differentiated for 120 h while exposed to hesperetin (5, 20, 50 μM), ellagic acid (0.05, 0.1 μM) or a combination (20 μM hesperetin, 0.05 μM ellagic acid) with and without oxidative stress-inducing compound menadione (9 μM) during 24 h of proliferation and during the first 5 h of differentiation. The number of proliferating cells was assessed using fluorescent labeling of incorporated 5-ethynyl-2'-deoxyuridine. Myosin heavy chain expression was assessed by fluorescence microscopy and cell fusion index was calculated. Furthermore, protein expression of phosphorylated p38 and myomixer were assessed using Western blot. None of the compounds induced effects on cell proliferation. Without menadione, 50 μM hesperetin increased fusion index by 12.6% compared to control (p < 0.01), while ellagic acid did not affect measured parameters of differentiation. Menadione treatment did not change myosin heavy chain expression and fusion index. In combination with menadione, 20 μM hesperetin increased myosin heavy chain expression by 35% (p < 0.01) and fusion index by 7% (p = 0.04) compared to menadione. Furthermore, the combination of menadione with hesperetin and ellagic acid increased myosin heavy chain expression by 35% compared to menadione (p = 0.02). Hesperetin and ellagic acid did not change p38 phosphorylation and myomixer expression compared to control, while treatment with menadione increased p38 phosphorylation (p < 0.01) after 5 h and decreased myomixer expression (p = 0.04) after 72 h of differentiation. Hesperetin increased myosin heavy chain expression in the presence of oxidative stress induced by menadione, and increased cell fusion both in the presence and absence of menadione. Ellagic acid did not affect the measured parameters of myoblast differentiation. Therefore, hesperetin should be considered as nutritional prevention or treatment strategy to maintain muscle function in age-related diseases such as sarcopenia. Future research should focus on underlying mechanisms and translation of these results to clinical practice.

Crystal structure of a tris(2-amino-eth-yl)methane capped carbamoyl-methyl-phosphine oxide compound.

The mol-ecular structure of the tripodal carbamoyl-methyl-phosphine oxide compound diethyl {[(5-[2-(di-eth-oxy-phosphor-yl)acetamido]-3-{2-[2-(di-eth-oxy-phos-phor-yl)acetamido]-eth-yl}pent-yl)carbamo-yl]meth-yl}phospho-nate, C25H52N3O12P3, features six intra-molecular hydrogen-bonding inter-actions. The phospho-nate groups have key bond lengths ranging from 1.4696 (12) to 1.4729 (12) Å (P=O), 1.5681 (11) to 1.5811 (12) Å (P-O) and 1.7881 (16) to 1.7936 (16) Å (P-C). Each amide group adopts a nearly perfect trans geometry, and the geometry around each phophorus atom resembles a slightly distorted tetra-hedron.