Collagen network as the scaffold for spontaneously distributed optical resonators

The idea behind this work was to acquire one dimensional lasing in the Rhodamine 6G dye doped collagen fibers with the control of random lasing phenomenon properties by changing the dye molecular arrangement. We show that a simple manipulation of the dye concentration in biopolymeric fibril matrix bulk and an additional use of α-cyclodextrin (α-CD) molecules determine formation of specific dye aggregates and as a consequence the shift of the random lasing emission wavelength in the desired direction. The analysis of the light transport mean free path in function of the dye and (α-CD) concentration was done with the use of coherent back scattering technique.     

α-溴化芳香酮合成方法的改进

在氧化铜存在的条件下,以单质溴为溴源,芳香酮可有效地转化成相应的α-溴代酮,所有产物结构都通过了核磁共振氢谱的表征。     

FUZZY REASONING USING POSITIONAL INFORMATION

Abstract

The paper argues in favour of reasoning methods that process positional information, i.e. information about the position of the input with respect to the class prototype, and thus achieve a better specification of the corresponding output class. It is shown that such an approach leads to reducing or cancelling unwanted nonlinearities (of input-output characteristic) imposed by reasoning methods, nonlinearities that alter the dependence expressed in the knowledge base. Two methods which use positional information are presented: (a) the mapping of o-cut borders (MACB) (Stoica, 1993, Proc. Fifth IFSA World Congress, pp. 1266-1269), inspired from a particular interpretation of the representation theorem and (b) the Left/Right Centre of Gravity (L/R COG) (Ghanayem, 1995, Proc. IEA/AIE, pp. 41 -45). The methods are tested in implementing a power system stabiliser (PSS) Simulation results show better performance of methods that use positional information, as compared with classic Mamdani (Mamdani, 1975, International Journal of Man-Machine Studies, 7, 1-13) reasoning. Reflections on a “best” reasoning method conclude the paper.     

Sonochemical fabrication and catalytic properties of α-Fe2O3 nanoparticles

In this study, α-Fe₂O₃ (hematite) nanoparticles were synthesised by a sonochemical method. The influence of different factors such as chemical composition of the precursors, atmosphere of the reactions and type of the sonicator on the chemical formula, crystallinity, morphology and size of the obtained products were investigated. Powder X-ray diffraction, scanning electron microscopy and IR spectroscopy, were used to characterise the nanostructures. The catalytic tests were performed in the reaction of methyl phenyl sulphide oxidation. The results exhibit the good catalytic performance of the as-prepared α-Fe₂O₃ nanoparticles.     

Facile Synthesis and Proposed Mechanism of α,ω‐Oxetanyl-Telechelic Poly(3-nitratomethyl-3-methyl oxetane) by an SN2(i) Nitrato Displacement Method in Basic Media

The synthesis of a novel heterocyclic–telechelic polymer, α,ω-oxetanyl-telechelic poly(3-nitratomethyl-3-methyl oxetane), is described. Infrared spectroscopy (IR), gel permeation chromatography (GPC), and nuclear magnetic resonance (NMR) spectroscopy have been used to confirm the successful synthesis, demonstrating the presence of the telechelic-oxetanyl moieties. Synthesis of the terminal functionalities has been achieved via displacement of nitrato groups, in a manner similar to that employed with other leaving groups such as azido, bromo, and nitro, initiated by nucleophiles. In the present case, displacement occurs on the ends of a nitrato-functionalized polymer driven by the formation of sodium nitrate, which is supported by the polar aprotic solvent N,N-dimethyl formamide. The formation of an alkoxide at the polymer chain ends is favored and allows internal back-biting to the nearest carbon bearing the nitrato group, intrinsically in an S_N2(i) reaction, leading to α,ω-oxetanyl functionalization. The telechelic-oxetanyl moieties have the potential to be cross-linked by chemical (e.g., acidic) or radiative (e.g., ultraviolet) curing methods without the use of high temperatures, usually below 100°C. This type of material was designed for future use as a contraband simulant, whereby it would form the predominant constituent of elastomeric composites comprising rubbery polymer with small quantities of solids, typically crystals of contraband substances, such as explosives or narcotics. This method also provides an alternative approach to ring closure and synthesis of heterocycles.     

Influence of Composition on Self-toughening and Oxidation Properties of Y-α-Sialons

Y-α-sialon ceramics with different compositions were hot-press sintered. Varying the m or n value in theα-Sialon general formula, both the α-sialon grain morphology and phase assemblages present diversification, therefore, affecting the toughness and hardness. Meanwhile, varying the compositional parameters also influenced the composition and structure of the intergranular glass phase, as well as its oxidation behavior at 1100-1200 ℃. The oxidation of the intergranular phase Mt in the Y-α-sialon ceramics was significantly enhanced with further rising the oxidation temperature to 1300 ℃.     

Intensification of Freeze-Drying Rate of Bacillus subtilis MTCC 2396 Using Tungsten Halogen Radiation: Optimization of Moisture Content and α-Amylase Activity

A novel freeze-drying protocol has been explored to render fast and cost-effective freeze drying of hyperamylase producing Bacillus subtilis MTCC2396 employing a tungsten halogen lamp radiator (THLR) as a heat source. Response surface methodology assessed the maximum reduction in moisture content (96.07%) and minimum reduction in α-amylase (EC 3.2.1.1) activity (1.02%) in 4 h drying time at 42.5°C radiation temperature. α-amylase activity (0.046 U) and final moisture content (3.93%) of the optimally freeze-dried bacterial strain appeared satisfactory. The freeze-drying time using THLR (4 h) is remarkably lower compared to that under a conventional conductive plate heater (CPH) (10 h) at otherwise identical conditions. The higher effective moisture diffusivity of 0.0052 to 0.0078 m ²/s under THLR compared to 0.00084 to 0.0015 m ²/s under CPH (corresponding to 20–50°C) advocated the superiority of the THLR heating protocol. The higher efficacy of THLR was also evidenced through lower activation energy (8.42 kJ/mol) of moisture diffusion compared to that (12.051 kJ/mol) of CPH. The optimally freeze-dried bacteria demonstrated the same growth rate in addition to exhibiting excellent retention of bioremedial (Hg²⁺ removal) activity to that of the control.     

Development of α-Tocopherol Acetate Nanoparticles: Influence of Preparative Processes

We studied different methods of preparing α-tocopherol acetate (ATA) nanoparticles, which are to be used in targeting the lungs as aerosols in order to prevent cigarette smoke toxicity. Poly-(lactide) nanoparticles were prepared using nanoprecipitation and solvent evaporation techniques, which produced, respectively, too small and too large nanoparticles to be aerosolized. The emulsification-diffusion method produced 2 months stable nanoparticles with a size between (500–700 nm). Increasing ATA concentration (1–7 mg/mL) induced a decrease in the association rate (97–93%) and in the adsorbed ATA rate (7–4.5%), which was associated with variations of Zeta potentials (?27.5 to ?24.3 mV) and decrease in polymeric wall thickness and density.     

Synthesis and characterization of α/β-Bi2O3 with enhanced photocatalytic activity for 17α-ethynylestradiol

The α/β-Bi₂O₃ photocatalyst was successfully synthesized by a novel solvothermal-calcination method. The physical and chemical properties of as-prepared samples were characterized based on XRD, XPS, SEM, TEM, EDS, BET, UV–vis DRS and PL techniques. The synthesized α/β-Bi₂O₃ photocatalyst exhibited enhanced photocatalytic activity for 17α-ethinylestradiol (EE2), and 96.9% of EE2 was degraded after only 24 min of visible-light irradiation using α/β-Bi₂O₃ as photocatalyst. The reaction rate constant over α/β-Bi₂O₃ photocatalyst was 1.42, 2.23, 9.22 and 54.1 times higher than pure β-Bi₂O₃, α-Bi₂O₃+β-Bi₂O₃, α-Bi₂O₃ and P25 respectively. Effect of catalyst dosage and pH value was investigated. The possible photocatalytic mechanism has been discussed on the basis of the theoretical calculation and the experimental results. α/β-Bi₂O₃ was a fairly stable and efficient photocatalyst under the studied experimental conditions, proving that the α/β-Bi₂O₃ photocatalyst was a promising photocatalyst for the practical application.