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A deep eutectic solvent (DES) composed of sulfamic acid and glycerol allowed for the sustainable preparation of cellulose nanofibrils (CNF) with simultaneous sulfation. The reaction time and the levels of sulfamic acid demonstrated that fibers could be swelled and sulfated simultaneously by a sulfamic acid-glycerol-based DES and swelling also promoted sulfation with a high degree of substitution (0.12). The DES-pretreated fibers were further nanofibrillated by a grinder producing CNF with diameters from 10 nm to 25 nm. The crystallinity ranged from 53-62%, and CNF maintained the original crystal structure. DES pretreatment facilitated cellulose nano-fibrillation and reduced the energy consumption with a maximum reduction of 35%. The films prepared from polyvinyl alcohol (PVA) and CNF showed good UV resistance ability and mechanical properties. This facile and efficient method provided a more sustainable strategy for the swelling, functionalization and nano-fibrillation of cellulose, expanding its application to UV-blocking materials and related fields.Urine is the main source of nitrogen pollution, while urea is a hydrogen-enriched carrier that has been ignored. Decomposition of urea to H2 and N2 is of great significance. Unfortunately, direct urea oxidation suffers from sluggish kinetics, and needs strong alkaline condition. Herein, we developed a self-driving nano photoelectrocatalytic (PEC) system to efficiently produce hydrogen and remove total nitrogen (TN) for urine treatment under neutral pH conditions. TiO2/WO3 nanosheets were used as photoanode to generate chlorine radicals (Cl•) to convert urea-nitrogen to N2, which can promote hydrogen generation, due to the kinetic advantage of Cl-/Cl• cyclic catalysis. Copper nanowire electrodes (Cu NWs/CF) were employed as the cathode to produce hydrogen and simultaneously eliminate the over-oxidized nitrate-nitrogen. The self-driving was achieved based on a self-bias photoanode, consisting of confronted TiO2/WO3 nanosheets and a rear Si photovoltaic cell (Si PVC). The experiment results showed that hydrogen generation with Cl• is 2.03 times higher than in urine treatment without Cl•, generating hydrogen at 66.71 μmol h-1. At the same time, this system achieved a decomposition rate of 98.33% for urea in 2 h, with a reaction rate constant of 0.0359 min-1. The removal rate of total nitrogen and total organic carbon (TOC) reached 75.3% and 48.4% in 2 h, respectively. This study proposes an efficient and potential urine treatment and energy recovery method in neutral solution.The efficiency of thin-film chalcogenide solar cells is dependent on their window layer thickness. However, the application of an ultrathin window layer is difficult because of the limited capability of the deposition process. This paper reports the use of atomic layer deposition (ALD) processes for fabrication of thin window layers for Cu(Inx,Ga1-x)Se2 (CIGS) thin-film solar cells, replacing conventional sputtering techniques. We fabricated a viable ultrathin 12 nm window layer on a CdS buffer layer from the uniform conformal coating provided by ALD. CIGS solar cells with an ALD ZnO window layer exhibited superior photovoltaic performances to those of cells with a sputtered intrinsic ZnO (i-ZnO) window layer. The short-circuit current of the former solar cells improved with the reduction in light loss caused by using a thinner ZnO window layer with a wider band gap. Ultrathin uniform A-ZnO window layers also proved more effective than sputtered i-ZnO layers at improving the open-circuit voltage of the CIGS solar cells, because of the additional buffering effect caused by their semiconducting nature. In addition, because of the precise control of the material structure provided by ALD, CIGS solar cells with A-ZnO window layers exhibited a narrow deviation of photovoltaic properties, advantageous for large-scale mass production purposes.The development of microelectronics is always driven by reducing transistor size and increasing integration, from the initial micron-scale to the current few nanometers. The photolithography technique for manufacturing the transistor needs to reduce the wavelength of the optical wave, from ultraviolet to the extreme ultraviolet radiation. One approach toward decreasing the working wavelength is using lithography based on beyond extreme ultraviolet radiation (BEUV) with a wavelength around 7 nm. The BEUV lithography relies on advanced reflective optics such as periodic multilayer film X-ray mirrors (PMMs). PMMs are artificial Bragg crystals having alternate layers of "light" and "heavy" materials. The periodicity of such a structure is relatively half of the working wavelength. Because a BEUV lithographical system contains at least 10 mirrors, the optics' reflectivity becomes a crucial point. The increasing of a single mirror's reflectivity by 10% will increase the system's overall throughput six-fold. In this work, the properties and development status of PMMs, particularly for BEUV lithography, were reviewed to gain a better understanding of their advantages and limitations. Emphasis was given to materials, design concepts, structure, deposition method, and optical characteristics of these coatings.Automotive waste represents both a global waste challenge and the loss of valuable embedded resources. This study provides a sustainable solution to utilise the mixed plastics of automotive waste residue (ASR) as a resource that will curtail the landfilling of hazardous waste and its adverse consequences to the environment. In this research, the selective thermal transformation has been utilised to produce nano silicon carbide (SiC) using mixed plastics and glass from automotive waste as raw materials. The composition and formation mechanisms of SiC nanoparticles have been investigated by X-ray diffraction (XRD), X-ray-Photoelectron Spectroscopy (XPS) and Transmission Electron Microscopy (TEM). The as synthesised SiC nanoparticles at 1500 °C has uniform spherical shapes with the diameters of the fixed edges of about 50-100 nm with a porous structure. This facile way of synthesising SiC nanomaterials would lay the foundations for transforming complex wastes into value-added, high-performing materials, delivering significant economic and environmental benefits.Metal-supported catalyst with high activity and relatively simple preparation method is given priority to industrial production. In this work, this study reported an easily accessible synthesis strategy to prepare Mott-Schottky-type N-doped carbon encapsulated metallic Co (Co@Np+gC) catalyst by high-temperature pyrolysis method in which carbon nitride (g-C3N4) and dopamine were used as support and nitrogen source. The prepared Co@Np+gC presented a Mott-Schottky effect; that is, a strong electronic interaction of metallic Co and N-doped carbon shell was constructed to lead to the generation of Mott-Schottky contact. The metallic Co, due to high work function as compared to that of N-doped carbon, transferred electrons to the N-doped outer shell, forming a new contact interface. In this interface area, the positive and negative charges were redistributed, and the catalytic hydrogenation mainly occurred in the area of active charges. The Co@Np+gC catalyst showed excellent catalytic activity in the hydrogenation of phenylacetylene to styrene, and the selectivity of styrene reached 82.4%, much higher than those of reference catalysts. The reason for the promoted semi-hydrogenation of phenylacetylene was attributed to the electron transfer of metallic Co, as it was caused by N doping on carbon.In this study, graphene oxide (GO) was synthesized using Hummers method. The synthesized GO was characterized using field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Fourier transformed infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) nitrogen adsorption. The analyses confirmed the presence of oxygen functional groups (C=O and C-O-C) on the GO surface. These oxygen functional groups act as active sites in the adsorption Sr (II). The BET analysis revealed the surface area of GO of 232 m2/g with a pore volume of 0.40 cm3/g. The synthesized GO was used as an adsorbent for removing Sr (II) from aqueous solutions. The adsorption equilibrium and kinetic results were consistent with the Langmuir isotherm model and the pseudo-second-order kinetic model. A maximum strontium adsorption capacity of 131.4 mg/g was achieved. The results show that the GO has an excellent adsorption capability for removing Sr (II) from aqueous solutions and potential use in wastewater treatment applications.There is an urgent need to develop systems for nucleic acid delivery, especially for the creation of effective therapeutics against various diseases. We have previously shown the feasibility of efficient delivery of small interfering RNA by means of gold nanoparticle-based multilayer nanoconstructs (MLNCs) for suppressing reporter protein synthesis. The present work is aimed at improving the quality of preparations of desired MLNCs, and for this purpose, optimal conditions for their multistep fabrication were found. All steps of this process and MLNC purification were verified using dynamic light scattering, transmission electron microscopy, and UV-Vis spectroscopy. Factors influencing the efficiency of nanocomposite assembly, colloidal stability, and purification quality were identified. These data made it possible to optimize the fabrication of target MLNCs bearing small interfering RNA and to substantially improve end product quality via an increase in its homogeneity and a decrease in the amount of incomplete nanoconstructs. We believe that the proposed approaches and methods will be useful for researchers working with lipid nanoconstructs.We present a terahertz spherical aberration-corrected metalens that uses the dynamic phase to achieve polarization multiplexed imaging. The designed metalens has polarization-dependent imaging efficiencies and polarization extinction ratios that exceed 50% and 101, respectively. Furthermore, opposite gradient phases can be applied to orthogonal polarizations to shift the imaging of the two polarized sources in the longitudinal and transverse directions. find more Indeed, we find that the metalens has a smaller depth-of-focus than a traditional metalens when imaging point sources with limited objective lengths. These results provide a new approach for achieving multifunctional beam steering, tomographic imaging and chiroptical detection.In recent times, an increasing number of applications in different fields need gas sensors that are miniaturized but also capable of distinguishing different gases and volatiles. Thermal electronic noses are new devices that meet this need, but their performance is still under study. In this work, we compare the performance of two thermal electronic noses based on SnO2 and ZnO nanowires. Using five different target gases (acetone, ammonia, ethanol, hydrogen and nitrogen dioxide), we investigated the ability of the systems to distinguish individual gases and estimate their concentration. SnO2 nanowires proved to be more suitable for this purpose with a detection limit of 32 parts per billion, an always correct classification (100%) and a mean absolute error of 7 parts per million.

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