Notes

[Effect associated with CDK1 Inhibits the Regulation of PLK1, Aurora N and TRF1 around the Growth involving The leukemia disease Cells].
The need for replacing conventional sources of energy with renewable ones has been on a swift rise since the last couple of decades. In this context, the progress in third-generation solar cells has taken a good leap in the last couple of years with increasing prospects of high efficiency, stability, and lifetime. Quite recently, a new form of carbon has been discovered accidentally in the form of carbon quantum dots (C QD), which is being pursued actively owing to its chemical stability and luminescent properties. In the current work, we report highly luminescent C QD prepared via a simple hydrothermal route. Transmission electron microscopy revealed an average particle size of 3.4 nm. The prepared C QD were used in a co-sensitized solar cell, where an improvement in the device characteristics was observed. The enhancement in the device characteristics is supported by impedance and electron life-time analysis. Further, the time-dependent analysis of the current and voltage revealed the functioning of the solar cell in real-time condition.Herein we report high strength composites prepared by reaction of sulfur, plant oils (either canola oil or sunflower oil) and brown grease. Brown grease is a high-volume, low value animal fat rendering coproduct that represents one of the most underutilized products of agricultural animal processing. Chemically, brown grease is primarily comprised of triglycerides and fatty acids. The inverse vulcanization of the unsaturated units in triglycerides/fatty acids upon their reaction with sulfur yields CanBG x or SunBG x (x = wt% sulfur, varied from 85-90%). These composites were characterized by infrared spectroscopy, dynamic mechanical analysis (DMA), mechanical test stand analysis, elemental analysis, and powder X-ray diffraction. CanBG x and SunBG x composites exhibit impressive compressive strengths (28.7-35.9 MPa) when compared to other materials such as Portland cement, for which a compressive strength of ≥17 MPa is required for residential building. Stress-strain analysis revealed high flexural strengths of 6.5-8.5 MPa for CanBG x and SunBG x composites as well, again exceeding the range of ∼2-5 MPa for ordinary Portland cements. The thermal properties of the composites were assessed by thermogravimetric analysis, revealing decomposition temperatures ranging from 223-226 °C, and by differential scanning calorimetry. These composites represent a promising new application for low value animal coproducts having limited value to be used as organic crosslinkers in the atom-efficient inverse vulcanization process to yield high sulfur-content materials that have impressive mechanical properties.A green, simple and efficient method is developed for the synthesis of quinazolin-4(3H)-ones via visible light-induced condensation cyclization of 2-aminobenzamides and aldehydes under visible light irradiation. The reaction proceeds using fluorescein as a photocatalyst in the presence of TBHP without the need for a metal catalyst. In addition, this reaction tolerates a broad scope of substrates and could afford a variety of desirable products in good to excellent yields. Thus, the present synthetic method provides a straightforward strategy for the synthesis of quinazolin-4(3H)-ones.In this work, a series of colloidal gold nanoparticles with controllable sizes were anchored on carbon nanotubes (CNT) for the aerobic oxidation of benzyl alcohol. The intrinsic influence of Au particles on the catalytic behavior was unraveled based on different nanoscale-gold systems. 7-Ketocholesterol HMG-CoA Reductase inhibitor The Au/CNT-A sample with smaller Au sizes deserved a faster reaction rate, mainly resulting from the higher dispersion degree (23.5%) of Au with the available exposed sites contributed by small gold particles. However, monometallic Au/CNT samples lacked long-term stability. CeO2 was herein decorated to regulate the chemical and surface structure of the Au/CNT. An appropriate CeO2 content tuned the sizes and chemical states of Au by electron delivery with better metal dispersion. Small CeO2 crystals that were preferentially neighboring the Au particles facilitated the generation of Au-CeO2 interfaces, and benefited the continuous supplementation of oxygen species. The collaborative functions between the size effect and surface chemistry accounted for the higher benzaldehyde yield and sustainably stepped-up reaction rates by Au-Ce5/CNT with 5 wt% CeO2.Activated-hydrochar (AHC) derived from sugarcane bagasse was synthesized by hydrothermal carbonization (HTC) using phosphoric acid and sodium hydroxide (NaOH) as activators. The properties of AHC were systematically characterized by elemental analysis, BET, SEM, FTIR, XPS and zeta potential, and applied to evaluate the adsorption ability of methylene blue (MB) by batch adsorption tests. The MB adsorption isotherm and kinetics of AHC were well described by the Langmuir model and pseudo-second-order kinetic model. Characteristic analysis suggested electrostatic attraction, hydrogen bonding and π-π interactions were the main contributors to MB adsorption. Analysis of mass transfer mechanisms demonstrated the adsorption process towards MB by AHC involved intra-particle diffusion to some extent. Thermodynamic studies indicated MB adsorption was an endothermic, spontaneous process associated with a disorder increase at the solid-liquid interface. The maximum adsorption capacity of AHC for MB was 357.14 mg g-1 at 303 K. Thus, the combination of HTC in phosphoric acid and NaOH activation offered a facile, green and economical alternative for conversion of sugarcane bagasse into efficient adsorbents used in wastewater treatment.In this work, l-tryptophan functionalized silica-coated magnetic nanoparticles were readily prepared and evaluated as a recyclable magnetic nanocatalyst for the synthesis of spiro[indene-2,2'-naphthalene]-4'-carbonitrile derivatives through the one-pot four-component reaction of malononitrile, cyclohexanone, aromatic aldehydes, and 1,3-indandione. This novel magnetic nanocatalyst was confirmed to be effective and provide products in moderate to excellent yields under reflux conditions. The structure of obtained nanoparticles was characterized using FT-IR, XRD, VSM, EDX, elemental mapping, FE-SEM, and TGA. This synthetic protocol provides several benefits such as excellent yields in short reaction times (64-91%), saving costs, reusability of the catalyst using an external magnet (seven runs), and low catalyst loading.Kitchen sea salt or table salt is used every day by cooks as a food seasoning. Here, it is introduced into a gel polymer (poly(vinyl) alcohol (PVA)-table salt) for use as an electrolyte, and an electrode was constructed from graphene nanosheets for use as symmetrical solid-state supercapacitors. The graphene sheets are prepared by a pulse control plasma method and used as an electrode material, and were studied by X-ray diffraction (XRD), Raman spectroscopy, as well as scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). A specific capacitance of 117.6 F g-1 at 5 mV s-1 was obtained in a three electrode system with table sea salt as an aqueous electrolyte. For a symmetrical solid-state supercapacitor graphene/PVA-table sea salt/graphene gave a good specific capacitance of 31.67 F g-1 at 0.25 A g-1 with an energy density of 6.33 W h kg-1 at a power density of 600 W kg-1, with good charge-discharge stability, which was 87% after 8000 cycles. Thus, the development of table sea salt as an environmentally friendly electrolyte has a good potential for use in energy storage applications.Prior experimental work showed that Bi2Se3, as a sister compound of the best room-temperature thermoelectric material Bi2Te3, has remarkably improved thermoelectric performance by Sb-Br codoping. But the relationship between its crystalline structure and thermoelectric properties is still unclear to date. Here, we use first-principles calculations to explore the possible reasons for such improvement. The electronic structures of Bi2-x Sb x (Se1-y Br y )3 (x = 0, 1, 2; y = 0, 0.08) are systematically investigated. Significant effects of 8% Br codoping in BiSbSe3 are found. First, the Br atom acts as an electron donor, thus greatly increasing the carrier concentration. Second, similar to the effect of Sb doping, Br codoping further improves greatly the degeneracy of the conduction band edge, which leads to a remarkably increased density-of-states effective mass without deterioration of the carrier mobility, and simultaneously preserves a large Seebeck coefficient of ∼-254 μV K-1 at 800 K. In addition, the Br codoping softens the chemical bonds, which enhances anharmonic scattering and further reduces the lattice thermal conductivity. We predict that the maximum zT of BiSb(Se0.92Br0.08)3 at 800 K can reach 0.96 with the carrier concentration of 9.22 × 1019 cm-3. This study rationalizes a potential strategy to improve the thermoelectric performance of Bi2Se3-based thermoelectric materials.Dual-functional catalysis indicates that an organic p-n bilayer induces the catalytic oxidation involved in downhill reactions, not only under illumination but also in the dark. When the organo-bilayer is composed of a perylene derivative (3,4,9,10-perylenetetracarboxylic-bis-benzimidazole (PTCBI), n-type) and cobalt phthalocyanine (CoPc, p-type), only the photocatalytic oxidation of hydrazine (N2H4) occurs. However, the loading of Ag co-catalyst onto the CoPc surface in the PTCBI/CoPc bilayer successfully led to dual catalysis in terms of the oxidation of N2H4 to N2. To develop the present dual catalysis Ag loading was essential to achieve the catalysis performance particularly without irradiation.In this study, we focus on the biomimetic development of small molecules and their biological sensing with DNA. The binding of herring sperm deoxyribonucleic acid (hs-DNA) with naturally occurring bioactive small molecule α-amyrin acetate (α-AA), a biomimetic - isolated from the leaves of Ficus (F.) arnottiana is investigated. Collective information from various imaging, spectroscopic and biophysical experiments provides evidence that α-AA is a minor groove sensor of hs-DNA and preferentially binds to the A-T-rich regions. Interactions of different concentrations of small molecule α-AA with hsDNA were evaluated via various analytical techniques such as UV-Vis, circular dichroism (CD) and fluorescence emission spectroscopy. Fluorescence emission spectroscopy results suggest that α-AA decreases the emission level of hsDNA. DNA minor groove sensor Hoechst 33258 and intercalative sensor EB, melting transition analysis (T M) and viscosity analysis clarified that α-AA binds to hs-DNA via a groove site. Biophysical chemistry and molecular docking studies show that hydrophobic interactions play a major role in this binding. The present research deals with a natural product biosynthesis-linked chemical-biology interface sensor as a biological probe for α-AA hs-DNA.Carbon steel is widely used as the piping of the primary heat transport system (PHT) in pressurized heavy water reactors (PHWR). Effects of zinc/aluminum treatment and simultaneous injection of zinc and aluminum on corrosion behavior and semiconductor properties of oxide films formed on carbon steels were characterized by the gravimetric method, potentiodynamic polarization scan, EIS, Mott-Schottky test, SEM, EDS mapping, XPS analysis and photocurrent response measurement. The results showed that all the metal cation ions treatment can improve the corrosion resistance of oxide films in varying degrees. 20 ppb Zn2+ had the greatest enhancement in corrosion resistance, followed by 20 ppb Zn2+ + 20 ppb Al3+. ZnFe2O4, FeAl2O4 and ZnAl2O4 were detected to be new spinel phases generated in oxide films. The oxide films on the surface of carbon steel all demonstrated n-type semiconductor properties. It was worth noting that the total content of manganese and zinc in the oxide film played an important role in the corrosion resistance of carbon steel.
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