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A method for extracting the substrate-independent stress–strain curves of thin films was developed using spherical nanoindentation to investigate the yield behavior of diamond-like carbon (DLC) thin films with Young’s moduli of ∼73 GPa and ∼76 GPa. The resulting stress–strain curves showed that these films commence yielding at ∼13 GPa and ∼14 GPa, respectively. These yield strength values agree with the critical pressure necessary to initiate the transformation of sp2-bonded carbon into significantly harder sp3-bonded carbon, indicating that the yielding of the materials is associated with the sp2-to-sp3 phase transition. The ability of a DLC film to accommodate a progressively increasing contact stress with strain beyond the yield point while dissipating part of the accumulated strain energy, as evidenced in this work, implies a unique mechanism of the brittle material for passively mitigating contact deformation and fracture in tribological applications.
Drug delivery systems (DDSs) have been developed to target tumor cells by releasing active biomolecules at the specific site of infection, thus eliminating the side effects of anticancer drugs. However, DDSs are generally limited by high drug dosage, biobarriers, poor target recognition, etc. To address these deficiencies, we propose a new noninvasive method consisting of exposing the cancer cells to a combination of low-intensity pulsed ultrasound (LIPUS) and static magnetic field (SMF). This combined treatment found to negatively regulate colon cancer cell (HCT116) activities in vitro by altering their cell membrane potential and permeability thus increased the DDS efficacy by 40%. The treated cancer cell membrane became hyperpolarized leading to cancer cell death. The combination treatment (LIPUS + SMF) restricted the cancer cell proliferation to 16 and 5% in the presence of bare anticancer drug and DDS, respectively, in 72 h, which is almost 40% higher than that observed without the treatment. The acceleration of cancer cellular inhibition was confirmed by the significant increase in the apoptosis of the cell exposed to the LIPUS + SMF treatment. The observed improvement is believed to be due to changes in the cell membrane stability/permeability as a result of mechanical (20–22 kPa) and electrical (19–23 µV/cm) stimuli generated during the LIPUS + SMF treatment.
The self-learning kinetic Monte Carlo method has been shown to be suitable for examining the temporal and spatial evolution of adatom islands on the (111) surface of several fcc metals, unbiased by diffusion processes chosen a priori. A pattern-recognition scheme and a diffusion path finder scheme enable collection of a large database of diffusion processes and their energetics. A variety of mechanisms involving single and multiple atoms, and concerted island motion are uncovered in long-time simulations. In this contribution, after reviewing the methodology, we present results comparing the diffusion kinetics of two sets of homo-epitaxial and hetero-epitaxial systems: small (2–8 atom) Pd and Ag islands on the respective (111) surfaces and small Cu islands on Ni(111) and Ni islands on Cu(111). We trace the dominance of concerted motion in Pd/Pd(111) and Ni/Cu(111) and competition among concerted, multiatom and single-atom processes in Ag/Ag(111) and Cu/Ni(111) to the strength of the lateral interaction among adatoms in these systems.
Titania nanoparticles (anatase or anatase + rutile) with enhanced photocatalytic activity were successfully produced by treating titanyl sulfate with various peroxo compounds (hydrogen peroxide, ammonium persulfate, and urea hydrogen peroxide) with further annealing. Transformation of titanyl sulfate to titanium dioxide was investigated by X-ray diffraction, electron microscopy, X-ray microanalysis, IR, Raman, X-ray photoelectron, and UV/vis spectroscopy. The peroxo compound and annealing temperature play an important role in phase composition and properties of the samples. Correlations between phase composition, oxygen content, band gaps, and constant rates for methyl orange (MO) discoloration were found. The [TiOx(O2)2−x(H2O)m] phase, which forms on the first stage of the reaction, contains nanoparticles with small crystallites (1–2 nm) and promotes formation of titanium dioxide with the anatase structure. Thermal decomposition of the peroxo-containing phase results in formation of titanium dioxide. Oxygen excess prevents transformation of anatase to rutile, decreases band gap, and increases activity of titanium dioxide (anatase or anatase + rutile) in the model reaction of MO destruction.
Cation doping is a practical way of engineering the optical properties of one-dimensional semiconductor nanomaterials, such as their band gap. We have grown zinc oxide (ZnO) nanorods doped with sodium cations (Na+) using a hydrothermal method at temperatures as low as 60 °C. We have investigated the effect of different concentrations of Na+ on structural and optical properties and morphology of the ZnO nanostructures. We have also simulated and discussed the chemical route of formation of doped and undoped ZnO nanorods. We found that, for low-temperature hydrothermal doping of ZnO nanorods with Na+, the optimum concentration ratio of zinc to sodium precursors is 1:10.
Molten vanadate-induced hot corrosion is the major cause of failure of superalloys which are generally used at higher temperatures (such as in internal combustion engines, gas turbines, high temperature tooling and dies, and petrochemical industries and marines). This effect can be minimized by applying thermally stable coatings over the superalloy. In this aspect, the current work investigates the effect of nanostructured aluminum chromium nitride (AlCrN) and titanium aluminum nitride (TiAlN) coatings on the hot corrosion behavior of Co-based superalloy, Superco-605, in an aggressive environment of Na2SO4–60% V2O5 (ratio by weight) at 700 °C up to 80 cycles. Each cycle consisted of 1 h heating at 700 °C followed by 20 min cooling in an ambient temperature. Hot corrosion kinetics was studied using the thermogravimetric technique and found to follow the parabolic rate law. The corrosion surface morphology and phases formed during hot corrosion were studied using field emission scanning electron microscopy equipped with energy dispersive spectroscopy and X-ray diffraction techniques. It was found that AlCrN coating had a better hot corrosion resistance than TiAlN coating.
Powder X-ray diffraction has become a routine procedure for the quantification of phases in mixtures. The most common method for this measurement is the Rietveld method, which generally returns the relative weight percentages of the crystalline components within the mixture. However, in many instances, it is also desirable to obtain an estimate of the amorphous content of a sample. There are several methods that may be used for this measurement and their accuracy has been assessed previously with a number of ideal, synthetic mixtures. Many samples, especially in the mineralogy sphere, are far from ideal and contain multiple phases of varying absorption contrast. This creates a microabsorption problem which affects the accuracy of the determination of both the crystalline and amorphous components. This paper assesses commonly used methods of amorphous determination with a series of synthetic samples designed to create a considerable microabsorption problem.
The triplite LiFeSO4F displays both the highest potential ever reported for an Fe-based compound, as well as a comparable specific energy with that of popular LiFePO4. The synthesis is still a challenge because the present approaches are connected with long time, special equipments or organic reagents, etc. In this work, the triplite LiFeSO4F powder was synthesized through an ambient two-step solid-state route. The reaction process and phase purity were analyzed, coupled with structure refinement and electrochemical test.
The Schiff base N1,N2-di(2-hydroxy)benzylidenebenzene-1,2-di-imine was prepared from salicylaldehyde and 1,2-diaminobenzene by reflux in ethanol for 6 h obtaining an orange crystalline solid. The Schiff base solid was separated by filtration and washed with ethanol and ethylic ether, and finally, it was dried in a vacuum system for 2 h. The X-ray powder diffraction pattern for this new compound showed that the crystalline compound belongs to the monoclinic system and space group P21/c (No. 14) with refined unit-cell parameters a = 5.9672 (7) Å, b = 16.561 (1) Å, c = 16.337 (2) Å, β = 91.41° (1). The volume of the unit cell is V = 1614.1 (2) Å3.
The fire-retardant and water-repellent bio-structural panels (BISPs) were successfully developed using cellulose nanofibrils, corn starch, boric acid, and n-dodecenyl succinic anhydride with adhesive-free character. Its performance properties were evaluated and compared with other well-known products on the market. The BISP's density (0.1 g/cm3) and permeance value [41.81 g/day/m2 with 5.76% coefficient of variation (CV)] were found higher than compared competitor products. The BISPs' contact angle was found 132.13° (1.59% CV) for BISP. The BISP was the only fire-retardant product, and the only one developed almost no smoke 2.20%.
Estradiol valerate (brand name: Delestrogen) is used as a hormone replacement therapy for menopause symptoms and for treating advanced prostate cancer. Commercial estradiol 17β valerate crystallizes in the monoclinic space group P21 with a = 7.36787(3), b = 19.84900(6), c = 13.99395(10) Å, β = 90.6845(5)°, V = 2046.398(18) Å3, and Z = 4.