In-situ study on thermal decomposition of 1,3-disilabutane to silicon carbide on Si(1 0 0) surface

The intermediates of thermal decomposition of 1,3-disilabutane (SiH₃CH₂SiH₂CH₃, DSB) to form SiC on Si(1 0 0) surface were in situ investigated by reactive ion scattering (RIS), temperature programmed reactive ion scattering (TPRIS), temperature programmed desorption (TPD), and auger electron spectroscopy (AES). DSB as a single molecular precursor was exposed on Si(1 0 0) surface at a low temperature less than 100 K, and then the substrate was heated up to 1000 K. RIS, TPD, and AES investigations showed that DSB adsorbed molecularly and decomposed to SiC via some intermediates on Si(1 0 0) surface as substrate temperature increasing. Between 117 and 150 K molecularly adsorbed DSB desorbed partially and decomposed to CH₄Si₂, which is the first observation on Si(1 0 0) surface, and further decomposed to CH₄Si between 150 and 900 K. CH₄Si lost hydrogen and formed SiC over 900 K.     

Electrochemical and surface behavior of hydyroxyapatite/Ti film on nanotubular Ti-35Nb-xZr alloys

In this paper, we investigated the electrochemical and surface behavior of hydroxyapatite (HA)/Ti films on the nanotubular Ti-35Nb-xZr alloy. The Ti-35Nb-xZr ternary alloys with 3-10 wt.% Zr content were made by an arc melting method. The nanotubular oxide layers were developed on the Ti-35Nb-xZr alloys by an anodic oxidation method in 1 M H₃PO₄ electrolyte containing 0.8 wt% NaF at room temperature. The HA/Ti composite films on the nanotubular oxide surfaces were deposited by a magnetron sputtering method. Their surface characteristics were analyzed by field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS) and an X-ray diffractometer (XRD). The corrosion behavior of the specimens was examined through potentiodynamic and AC impedance tests in 0.9% NaCl solution. From the results, the Ti-35Nb-xZr alloys showed a solely β phase microstructure that resulted from the addition of Zr. The nanotubular structure formed with a diameter of about 200 nm, and the HA/Ti thin film was deposited on the nanotubular structure. The HA/Ti thin film-coated nanotubular Ti-35Nb-xZr alloys showed good corrosion resistance in 0.9% NaCl solution.     

Gradient HPLC-DAD stability indicating determination of miconazole nitrate and lidocaine hydrochloride in their combined oral gel dosage form

The pharmaceutical combination of miconazole nitrate (MZ) and lidocaine hydrochloride (LD) is used in the curative and prophylactic therapy of the oral and gastro-intestinal infections caused by Candida albicans. To the best of our knowledge, no attempts have yet been made to assay this combination by any analytical method. A simple and selective high-performance liquid chromatography-diode array detection (HPLC-DAD) stability-indicating method was developed for the simultaneous determination of MZ and LD in their combined formulation. Effective chromatographic separation was achieved using a Zorbax SB-C8 column with gradient elution of the mobile phase composed of 0.05 M phosphoric acid and acetonitrile. The gradient elution started with 25% (by volume) acetonitrile, ramped up linearly to 65% in 6 min, then kept constant until the end of the run. The mobile phase was pumped at a flow rate of 1 mL/min. The multiple wavelength detector was set at 215 nm and analytes were quantified by measuring their peak areas. The retention times for LD and MZ were approximately 4.1 and 8.4 min, respectively. The reliability and analytical performance of the proposed HPLC procedure were statistically validated with respect to linearity, ranges, precision, accuracy, selectivity, robustness, detection and quantification limits. Calibration curves were linear in the ranges of 5-100 μg/ml for both drugs with correlation coefficients > 0.999. Both drugs were subjected to stress conditions of hydrolysis, oxidation, photolysis and thermal degradation. The proposed method proved to be stability-indicating by the resolution of the two analytes from the related substance and potential impurity (2,6-dimethylaniline) and from the forced-degradation products. The validated HPLC method was applied to the analysis of MZ and LD in the combined oral gel preparation, in which the two analytes were successfully quantified and resolved from the pharmaceutical additives. The proposed method made use of DAD as a tool for peak identity and purity confirmation.     

Direct Metallization of Gold Nanoparticles on a Polystyrene Bead Surface using Cationic Gold Ligands

Gold nanoparticles are formed to cover the surface of sulfonated‐polystyrene (PS) beads by the in‐situ ion‐exchange and chemical reduction of a stable cationic gold ligand, which makes it different from the physical adsorption or multiple electroless metallization methods. PS beads are synthesized by dispersion polymerization with a diameter of 2.7 µm, and their surface is modified by introducing sulfonic acid groups (SO) to give an ion exchange capacity of up to 2.25 mequiv. · g⁻¹, which provides 1.289 × 10¹⁰ SO per bead. Subsequently, the anionic surface of the PS beads is incorporated with a cationic gold ligand, dichlorophenanthrolinegold(III) chloride ([AuCl₂(phen)]Cl), through an electrostatic interaction in the liquid phase to give gold nanoparticles (ca. 1–4 nm in diameter) formed on the PS surface. Assuming that approximately three SO groups interact with one [AuCl₂(phen)]⁺ ion in the ion‐exchange process, the gold coverage on a PS bead is estimated as 12.0 wt.‐%, which compares well with the 16.8 wt.‐% of gold loading measured by inductively coupled plasma–mass spectrometry. Because of the adjustable IEC values of the polymer surface and the in‐situ metallization of Au in the presence of S atoms, both of which are of a soft nature, the developed methodology could provide a simple and controllable route to synthesize a robust metal coating on the polymer bead surface.

     

Thom polynomials, symmetries and incidences of singularities

As an application of the generalized Pontryagin-Thom construction [RSz] here we introduce a new method to compute cohomological obstructions of removing singularities — i.e. Thom polynomials [T]. With the aid of this method we compute some sample results, such as the Thom polynomials associated to all stable singularities of codimension ≤8 between equal dimensional manifolds, and some other Thom polynomials associated to singularities of maps N ⁿ ?P ^n+k for k>0. We also give an application by reproving a weak form of the multiple point formulas of Herbert and Ronga ([H], [Ro2]). As a byproduct of the theory we define the incidence class of singularities, which — the author believes — may turn to be an interesting, useful and simple tool to study incidences of singularities. Oblatum 4-II-1999 & 19-VII-2000?Published online: 30 October 2000     

Efficient Ultraviolet Nanosources Based on Third-Harmonic Generation in Dielectric–Metal Composite Nanodisks

Dielectric materials with high indices have recently attracted much attention in the community of nanophotonics. Severe optical losses in visible–ultraviolet (UV) region, however, limit their applications. This article proposes dielectric–metal nanocomposites as alternative high-index materials for Mie-resonance-based applications. Such composite materials have high indices in the range of wavelength longer than plasmon resonance of inclusion metal nanoparticles, while they have much lower losses in the range from blue-violet down to near-UV compared with commonly used high-index materials such as silicon, enabling near-UV generation with high efficiency based on third-harmonic generation (THG). The numerical results show that ZnO nanodisk containing silver nanoparticles can generate near-UV radiation at 351.3 nm via THG with an efficiency about 20 times higher compared with silicon nanodisk under same pumping condition. Significantly high THG efficiency of 0.015% has been predicted with such a composite nanodisk supported by aluminum substrate under pumping with a peak intensity of 20 GW cm⁻², a spot size of 0.8 $\mu \mathrm{m}$, a duration of 50 fs at 1054 nm, respectively.     

A Tetrairon Dication Featuring Tetraethynylbenzene Bridging Ligand: A Molecular Prototype of Quantum Dot Cellular Automata

The unprecedented tetrairon dication [{Cp*(dppe)FeC≡C-}₄-μ-(1,2,4,5-C₆H₂)](PF₆)₂ ( 1 ) was obtained through a sequence of three reactions from 1,2,4,5-tetraethynylbenzene, Cp*(dppe)FeCl (Cp*=C₅Me₅, dppe=1,2-bis(diphenylphosphino)-ethane), KOtBu, and ferrocenium hexafluorophosphate. The cyclic voltammogram of the target molecule, isolated in 77 % yield, exhibits four well separated and reversible redox events showing that 1 is thermodynamically stable with respect to disproportionation (Kc>10⁶). The tetranuclear dication 1 was characterized by XRD on single crystal, IR and NMR spectroscopies and Mössbauer spectrometry. The experimental data show that 1 behaves as a class II mixed-valence complex with the positive charges preferentially disposed on antipodal positions. This new molecule can be regarded as a potential molecular prototype of quantum dot cellular automata.     

Five‐coordinate dinuclar cobalt (II), copper (II), zinc (II) and cadmium (II) complexes with 4‐bromo‐N‐(2‐pyridinylmethylene)benzenamine: Synthesis,characterisation and methyl methacrylate polymerization

A series of late transition metal complexes, [(bpma)Co(μ – Cl)Cl] ₂ , [(bpma)Cu(μ – Cl)Cl] ₂ , [(bpma)Zn(μ – Cl)Cl] ₂ and [(bpma)Cd(μ – Br)Br] ₂ (where bpma is 4‐bromo‐N‐((pyridin‐2‐yl)methylene)benzenamine) have been synthesized and structurally characterized. The X‐ray structures of dimeric complexes [(bpma)M(μ – X)X] ₂ (M = Co, Cu and Zn, X = Cl; M = Cd, X = Br) showed a distorted 5‐coordinate trigonal bipyramidal geometry involving two nitrogen atoms of N,N‐bidentate ligand, two bridged and one terminal halogen atoms. The complex [(bpma)Cu(μ – Cl)Cl] ₂ revealed the highest catalytic activity for the polymerisation of methyl methacrylate in the presence of modified methylaluminoxane with an activity of 9.14 × 10⁴ g PMMA/mol·Cu·h at 60 °C and afforded syndiotactic poly (methylmethacrylate) (rr = 0.69).     

C0-semigroups on a locally convex space

A necessary and sufficient condition that a densely defined linear operator A in a sequentially complete locally convex space X be the infinitesimal generator of a quasi-equicontinuous C₀-semigroup on X is that there exist a real number β ? 0 such that, for each λ > β, the resolvent (λI ? A)^?1 exists and the family {(λ ? β)^k(λI ? A)^?k; λ > β, k = 0, 1, 2,…} is equicontinuous. In this case all resolvents (λI ? A)^?1, λ > β, of the given operator A and all exponentials exp(tA), t ? 0, of the operator A belong to a Banach algebra $\text{B}{}_{\mathrm{г}}\text{(X)}$ which is a subspace of the space L(X) of all continuous linear operators on X, and, for each t ? 0 and for each x?X, one has lim_{k → z} (I ? k^?1tA)^?kx = exp(tA) x. A perturbation theorem for the infinitesimal generator of a quasi-equicontinuous C₀-semigroup by an operator which is an element of $\text{B}{}_{\mathrm{г}}\text{(X)}$ is obtained.