Zachohead8400

2 kJ/mol.Four antioxidant peptides (Ile-Tyr, Leu-Tyr, Val-Tyr, and Tyr-Leu-Ala), identified from brown rice protein hydrolysates, showed strong ROO· and ABTS·+ scavenging activities. Changes in the antioxidant activity of peptides and GSH (control) under different processing conditions, namely, NaCl, temperature, pH, and gastrointestinal proteases, were evaluated by the oxygen radical absorbance capacity assay and the Trolox equivalent antioxidant capacity assay. Results indicated that with the increase in NaCl concentration, temperature, and pH (beyond neutral), the antioxidant activity of the peptides decreased, while the decrease was lower than that of GSH. The antioxidant activity of the four antioxidant peptides changed slightly after in vitro digestion, indicating a relatively high digestion resistance. The protective effect on the oxidative damage model of 2,2-azobis (2-methylpropionamide)-dihydrochloride-induced human red blood cells was also studied. Leu-Tyr and Tyr-Leu-Ala could alleviate but not totally inhibit oxidative damage in red blood cells, and their protective effects were dependent on concentration.Along with the development of motor vehicle industry technology at this time, the fuel demand is also increasing while the supply is running low. Thus, alternative fuels are needed to meet these energy needs. This study aims to explain the physical and chemical characteristics of a fuel mixture (MF) between palm sap bioethanol with premium fuel. The results showed that the higher the bioethanol concentration of the palm sap, the higher the MF's viscosity, but the lower the heat of the fuel. This decrease is caused by differences in the heating value of the two fuels. The MF's high heat burn value is blue, while the low heat value of the flame is reddish yellow. The results of this study are very important as a basis for the development of bioethanol from palm sap as an environmentally friendly vehicle-fuel substitute material.An improved density functional theory-based H coverage-dependent electrochemical model with explicit solvent effect is proposed for Cu(111), which is used to identify potential-dependent initial competitive CO2 electroreduction pathways considering HER. We find that a chemisorbed CO2 molecule at the present electrode/aqueous interface can be spontaneously formed and the overpotentials can affect its coordination pattern. The Eley-Rideal mechanism may be more favorable during the initial CO2 electroreduction into CO, whereas chemisorbed CO2 reacting with adsorbed H into HCOO- via the Langmuir-Hinshelwood mechanism is more facile to occur. The analyses of energetics suggest that the low overpotentials have a negligible influence on CO and HCOO- formation, and HCOO- species with monodentate and bidentate configurations may also parallelly form with the surmountable barriers at room temperature. However, the high potentials have an interruptive effect on initial CO2 electroreduction because of the significantly increased barriers, indicating that the chemisorbed CO2 can be stabilized by imposing more negative potentials and thus going against initial CO2 electroreduction. By analyzing the competing HER with initial CO2 electroreduction into CO, we find that HER is competitive with initial CO formation because of the required lower overpotentials. Simultaneously, the present study shows that the blocked Cu surface by adsorbed H and CO can explain why the initial CO formation pathway is unfavorable at the high overpotentials. Our present conclusions can also confirm the previous experimental report on initial formation of CO and HCOO-.Water flooding is widely used for recovering crude oil from unconventional reservoirs due to its economic feasibility. At reservoir conditions, the injected water is usually imbibed into fractured rocks, so-called spontaneous imbibition, providing a considerable driving force for enhancing oil recovery. In this work, spontaneous imbibition on a rock surface is investigated at high-pressure conditions, and its influence on tight oil recovery is revealed from a pore-scale perspective. Specifically, three typical core samples are selected and characterized to obtain their pore-size distribution by applying the NMR technique. These core samples are then saturated with crude oil and are submerged in formation water, which is filled in a high-pressure vessel. Oil recovery efficiency as well as the imbibition rate is consequently calculated for specific pores during spontaneous imbibition. Test results indicate that oil recovery from spontaneous imbibition is different in different pores depending on the petrophysical properties of the tight cores. That is, the difference in imbibition efficiency between small and large pores decreases as permeability and porosity increase in the core samples. In addition, as for core samples #1 and #2, the imbibition rate usually reaches a maximum at the initial imbibition stage. However, as for core sample #3, the maximum imbibition rate is far delayed due to high capillarity. selleck inhibitor This work may reveal the fundamental mechanism of the influence of spontaneous imbibition on a rock surface at high-pressure conditions on tight oil recovery from a pore-scale perspective.Sol-gel-derived bioactive glass nanoparticles have attracted special interest due to their potential as novel therapeutic and regenerative agents. Significant challenges are yet to be addressed. The fabrication of sol-gel-derived nanoparticles in binary and ternary systems with an actual composition that meets the nominal has to be achieved. This work addresses this challenge and delivers nanoparticles in a ternary system with tailored composition and particle size. It also studies how specific steps in the fabrication process can affect the incorporation of the metallic ions, nanoparticle size, and mesoporosity. Sol-gel-derived bioactive glass nanoparticles in the 62 SiO2-34.5 CaO-3.2 P2O5 (mol %) system have been fabricated and characterized for their structural, morphological, and elemental characteristics using Fourier transform infrared spectroscopy, X-ray diffraction analysis, scanning electron microscopy associated with elemental analysis, transmission electron microscopy, and solid-state nuclear magnetic resonance.