Haycowan2392

The effects of five domestic thawing methods, including air thawing (AIR), water thawing with bags (W + B), water thawing without bags (W - B), refrigerator thawing (REF), and microwave thawing (MIC), on the main health-promoting compounds and antioxidant capacity in both unblanched and blanched baby mustard were investigated in this study. The results showed that different thawing methods markedly affected the health-promoting compounds and antioxidant capacity of baby mustard. MIC better retained the overall nutritional quality of frozen baby mustard compared with the four other treatments. AIR led to significant decreases in the glucosinolate contents in unblanched and blanched baby mustard. W + B led to significant decreases in the total phenols contents and antioxidant capacity levels in unblanched and blanched baby mustard, as well as the ascorbic acid content in unblanched baby mustard. W + B led to a significant decrease in the FRAP level in unblanched baby mustard, as well as the glucosinolate and ascorbic acid contents and ABTS level in blanched baby mustard. REF led to significant decreases in glucosinolates and proanthocyanidins contents in unblanched baby mustard, as well as the ascorbic acid content in blanched baby mustard. Furthermore, the thawing time was greatly shortened by MIC (only approximately 1 min). Thus, MIC was the optimal thawing method for frozen baby mustard regardless of whether it was blanched, as MIC best preserved nutritional quality and reduced the thawing time.High-temperature arsenic resistance catalysts of CeLa0.5Fe x /Ti (x = 0, 0.1, 0.2, 0.3, 0.4, 0.5) series were prepared and measured under a simulation condition of arsenic poisoning. The as-prepared catalysts were characterized by XRD, SEM, TEM, and XPS. The specific surface area and pore size of the catalysts were measured. At x = 0.2, the catalyst shows the best arsenic resistance and catalytic performance. The active temperature range of the CeLa0.5Fe0.2/Ti catalyst is 345-520 °C when the gas hourly space velocity is up to 225 000 mL g-1 h-1. Compared with commercial vanadium-based catalysts, CeLa0.5Fe0.2/Ti shows much better catalytic performance. The introduction of Fe will improve the dispersion of CeO2 and increase the concentration of Ce3+ and unsaturated active oxygen on the surface. The NH3-TPD and H2-TPR results show that the CeLa0.5Fe0.2/Ti catalyst has more acidic sites and more excellent redox performance than CeLa0.5Fe0/Ti. The CeLa0.5Fe0.2/Ti catalyst might have application prospects in the field of selective catalytic reduction of NO x with NH3.In a previous study, we demonstrated that conductive Au nanosheets can be prepared by UV irradiation of an Au nanoparticle monolayer spreading on water. In this study, we applied this UV irradiation technique to inexpensive Ag nanoparticles (NPs) to expand their versatility. UV irradiation of Ag NPs on water resulted in the formation of large Ag NPs and was ineffective for preparing conductive Ag films. The solubilization of additives in the water phase, however, resulted in the conversion of the large Ag NPs into a nanosheet, and the solubilization method was highly effective for preparing transparent conductive Ag films with an optical transmittance of above 70%.Investigations regarding AgBr-based photocatalysts came to the center of attention due to their high photosensitivity. The present research focuses on the systematic investigation regarding the effect of different alkali metal cation radii and surfactants/capping agents applied during the synthesis of silver-halides. Their morpho-structural and optical properties were determined via X-ray diffractometry, diffuse reflectance spectroscopy, scanning electron microscopy, infrared spectroscopy, and contact angle measurements. The semiconductors' photocatalytic activities were investigated using methyl orange as the model contaminant under visible light irradiation. The correlation between the photocatalytic activity and the obtained optical and morpho-structural properties was analyzed using generalized linear models. Moreover, since the (photo)stability of Ag-based photoactive materials is a crucial issue, the stability of catalysts was also investigated after the degradation process. It was concluded that (i) the photoactivity of the samples could be fine-tuned using different precursors and surfactants, (ii) the as-obtained AgBr microcrystals were transformed into other Ag-containing composites during/after the degradation, and (iii) elemental bromide did not form during the degradation process. Thus, the proposed mechanisms in the literature (for the degradation of MO using AgBr) must be reconsidered.The influence of temperature and solvent on the solid-liquid ternary phase diagrams of the 2HNIW·HMX cocrystal has been investigated. Ternary phase diagrams were constructed for the 2HNIW·HMX cocrystal in acetonitrile and ethyl acetate at 15 °C and 25 °C. HMX and HNIW showed inconsistent dissolution behavior and congruent dissolution behavior in acetonitrile and ethyl acetate, respectively. In the HMX-HNIW-acetonitrile system, the 2HNIW·HMX cocrystal has a narrow thermodynamically stable region at both temperatures. The cocrystal exhibits a wider thermodynamically stable region in the HMX-HNIW-ethyl acetate system. The results show that the choice of solvent has a crucial influence on the dissolution behavior of the cocrystal and the size and position of each region in the phase diagram, while the temperature has no apparent effect on the overall appearance of the phase diagram. By properly selecting the ratios, the 2HNIW·HMX cocrystal could be prepared by the isothermal slurry conversion crystallization method.Janus-type structures were obtained from gold nanoparticles grafted with two types of chemically incompatible mesogenic ligands with a strong tendency for nano-segregation. A lamellar arrangement, in which metallic nanoparticle-rich sublayers are separated by organic ligand-rich sublayers of various composition, was formed due to the ligand segregation process. The layers could be easily aligned by mechanical shearing; for most materials the layer normal was parallel to the shearing direction but perpendicular to the shearing gradient, such transverse mode is only rarely observed for lamellar materials. Reversible changes of layer thickness under UV light were observed due to the presence of an azo-moiety in the organic ligand molecules.Illuminated gapped-gold-nanorod dimers hold surface plasmon polaritons (SPPs) that can be engineered, by an appropriate choice of geometrical parameters, to enhance the electromagnetic field at the gap, allowing applications in molecular detection via surface-enhanced Raman spectroscopy (SERS). Envisioning hybrid devices in which the SERS spectroscopy of molecules in the gap is complemented by electrical measurements, it arises the question of designing efficient geometries to contact the nanorods without decreasing the enhancement factor (EF) of the nanoantenna, i.e., the figure of merit for SERS spectroscopy. Within this framework we theoretically study the feasibility to fabricate designs based on covering with gold the far-from-the-gap areas of the dimer. We show that by tuning the geometrical parameters of the designs these systems can reach enhancement factors larger than the best achieved in the uncovered dimer this supremacy survives even in the presence of dimer asymmetries and vacancies at the interfaces between the nanorods and the covering layers. Our results show that geometrical modifications away from the gap can improve the optical response at the gap, thus enabling the use of these devices both for hybrid and optical applications.Here, we report the synthesis of five novel seven-membered carbasugar analogs. We adopted a chiral-pool strategy starting from the cheap and readily available d-mannitol to synthesize these ring-expanded carbasugars. Apart from several regioselective protecting group manipulations, these syntheses involved Wittig olefination and ring-closing metathesis as the key steps. We observed an unprecedented deoxygenation reaction of an allylic benzyl ether upon treatment with H2/Pd during the synthesis. Preliminary biological evaluation of the carbasugars revealed that these ring expanded carbasugars act as inhibitors of various glycosidases. This study highlights the importance of the synthesis of novel ring expanded carbasugars and their biological exploration.Despite the pharmacological potential of the pyrazolo[3,4-c]pyrazoles, only a few methods of preparation and direct functionalization of this moiety have been described. Etomoxir CPT inhibitor We report herein a convenient design of new pyrazolo[3,4-c]pyrazoles with a high therapeutic impact. The effective chosen strategy consists of hydrazine condensations and C-N Ullmann-type cross-coupling reactions with microwave activation. Moreover, chemoselective bromination of the newly formed bipyrazoles followed by Suzuki-Miyaura cross-coupling reactions allowed the synthesis of a variety of modulated heterobicycles.The experimental reactivity of isomeric (Z)- and (E)-β-nitrostyrenes participating in [3+2] cycloaddition (32CA) reactions has been analysed on the basis of molecular electron density theory (MEDT) at the HF/6-311G(d,p), B3LYP/6-311G(d,p) and ωB97X-D/6-311G(d,p) computational levels. It was found that the polar zw-type 32CA reactions with 5,5-dimethylpyrroline-N-oxide proceed via a one-step mechanism, characterised by the attack of the nucleophilic oxygen centre of the nitrone on the electrophilically activated β-position of these nitrostyrenes. This behaviour is completely understood by means of the analysis of the conceptual DFT reactivity indices. These 32CA reactions present low activation enthalpies of 4.4 (Z) and 5.0 (E) kcal mol-1, and are exo (Z) and endo (E) stereoselective (B3LYP), as well as completely meta regioselective (ωB97X-D, B3LYP). The less stable (Z)-β-nitrostyrene is more reactive than the (E)-one (HF). ELF and AIM topological analyses of the reagents and TSs show the great similitude between their electronic structures. Finally, NCI allows explaining the exo stereoselectivity found in the reaction of (Z)-β-nitrostyrene. The present MEDT study explains the different reactivity, selectivity and competitiveness in the title reactions.The lithium/sulfuryl chloride battery has been used as a primary power source because of its high energy/power density and level of safety. However, disadvantages regarding the sluggish kinetics of the electrode materials have limited its further energy related applications. Herein, we report an efficient approach to prepare nitrogen-doped graphene nanocages with high surface roughness to overcome this issue. The combination of a porous wrinkled surface and hollow structure can properly accommodate the volume-change, promote charge transfer, and enhance structural stability. The designed composite electrode can deliver an initial voltage as high as 3.58 V, an advanced discharge time of 840 s, and an outstanding relative capacity (63.20 mA h) and rate capability (29.36%). This unique structure engineering strategy also provides a potentially cost-effective way for synthesizing other carbon materials and their application in various electrochemical energy storage devices.