Optical Coherence Tomography Implemented by Photonic Crystal Fiber

We report a photonic crystal fiber (PCF)-based optical coherence tomography (OCT) system, in which conventional single-mode fiber for the transmission line and the fiber coupler for the beam splitter/combiner are replaced with PCF and PCF coupler. The PCF coupler fabricated using the fused biconical tapered (FBT) method showed a nearly flat coupling ratio over a broad spectral bandwidth of 400 nm, which provided an axial resolution of 3-μm for OCT imaging. With a white-light source, the 8-μm thick air gap between two stacked cover glasses was measured, and with a conventional superluminecent diode (SLD) source, the in vitro images of rat eye and Misgurnus mizolepis skin were successfully obtained. The PCF and PCF coupler might enable a white-light as the source for the cost effective and high-resolution OCT system.     

Photophysical properties of near-infrared-emitting Ln(III) complexes with 1-(9-Anthryl)-4,4,4-trifluoro-1,3-butandione (Ln = Nd and Er)

We report the synthesis and photophysical properties of Nd(III) and Er(III) complexes with 1-(9-anthryl)-4,4,4-trifluoro-1,3-butandione (9-ATFB). The complexes of [Nd(9-ATFB)4]- and [Er(9-ATFB)4]- produced sensitized near-infrared (NIR) luminescence via the excitation of anthracene. This suggests that the intramolecular energy transfer occurred from the singlet excited state of anthracene to the resonance levels of the metal ions, since the phosphorescence of anthracene is forbidden under normal conditions. The observed quantum yield of the visible luminescence showed that the energy transfer is more efficient for [Nd(9-ATFB)4]- than for [Er(9-ATFB)4]-. The lifetimes of the NIR luminescence of the complexes were in the microsecond range. The quantum yields of the sensitized NIR of the complexes were estimated using the lifetime and the energy-transfer quantum yield.     

Design of organic supercapacitors with high performances using pore size controlled active materials

In this study, we thoroughly investigate the required properties of active materials for organic supercapacitors with high performances. In this regard, we synthesize carbon xerogels with different physical properties, including specific surface area and pore size. The carbon xerogels are prepared via the sol-gel reaction of resorcinol and formaldehyde under different gelation temperature conditions. Through Fourier-transform infrared, nitrogen adsorption–desorption, and scanning electron microscopy analysis, we can confirm that carbon xerogels with different physical properties can be successfully synthesized. We apply the prepared carbon xerogels to organic supercapacitor electrodes. As a result of electrochemical experiments, carbon xerogels with high surface area exhibit high electrochemical performances at low-rate charge?discharge processes. However, as the charge–discharge rate increases, carbon xerogels with low surface area and high conductivity exhibit higher performances. Therefore, the surface area of active materials is a key factor for supercapacitors with high performances at low-rate charge–discharge processes. However, the effects of conductivity can be more crucial as compared with those of surface area as the charge–discharge rates increase. In addition, we suggest that the physical properties of active materials should be differently optimized as the charge–discharge rate is employed.     

Tailoring the porous texture of activated carbons by CO<Subscript>2</Subscript> reactivation to produce electrodes for organic electrolyte-based EDLCs

Highly microporous carbon obtained by KOH etching of carbohydrates exhibited enhanced specific capacitance due to the increased adsorption of electrolyte ions on its large surface, which renders it a promising electrode material. However, the KOH-activated carbon electrode did not achieve its optimum charge capacity in organic electrolytes due to the limited accessibility of the electrolyte ions to the micropores, which hindered the adsorption of ions. The electrode performance was enhanced by enlarging the micropores of KOH-activated carbon to mesopores via reactivation in a stream of CO₂, which allowed the mesopore/micropore ratio to be increased without compromising the originally high specific surface area. The extended amount of mesopores increased the charge capacity of the electrode by enabling the large organic electrolyte ions to access the porous surface, as compared to untreated KOH-activated carbon.     

Spray dried calcium gelled arabinoxylan microspheres: A novel carrier for extended drug delivery

Arabinoxylan (AX) microspheres were formulated by ionotropic gelation for extended drug delivery. AX from Plantago ovata was tested for gelation with aluminium, barium, calcium, magnesium, and iron(III) chloride. Only calcium was found to lead to weak gelation with AX. The conventional needle extrusion produced fragile AX beads with calcium and hence the spray drying process was adopted for the preparation of metronidazole hydrochloride (MH) loaded AX microspheres. MH loading in AX microspheres was 30.8 mass %, 31.9 mass %, and 29.3 mass % in formulations gelled with 0.05 g, 0.1 g, and 0.15 g of calcium chloride per 100 mL of solution, respectively. Scanning electron microscopy revealed the crystallinity reduction of MH in microspheres. The surface of drug loaded calcium gelled AX microsphere was rougher than that of an ungelled one. Interactions of calcium with AX and the amorphous nature of the drug in the microspheres were evidenced by infrared spectroscopy and X-ray diffraction studies. Calcium-induced gelation can extend the drug release to over 90 min in 0.1 M HCl despite the hydrophilic nature of AX and the high solubility of metronidazole.     

Preparation and characterization of a polyimide nanofoam through grafting of labile poly(propylene glycol) oligomer

Preparation of a polyimide nanofoam (PI‐F) for microelectronic applications was carried out using a polyimide precursor synthesized from poly[(amic acid)‐co‐(amic ester)] and grafted with a labile poly(propylene glycol) (PPG) oligomer. Polyimide precursor was synthesized by partial esterification of poly(amic acid) (PAA) derived from pyromellitic dianhydride (PMDA) and 4,4′‐oxydianiline (ODA). The precursor was then grafted with bromide‐terminated poly(propylene glycol) in the presence of K₂CO₃ in hexamethylphosphoramide and N‐methylpyrrolidone, imidized at 200°C in nitrogen and the product was subsequently decomposed in air at 300°C to eliminate the labile PPG oligomer to produce PMDA/ODA polyimide nanofoam. Nuclear magnetic resonance spectroscopy (¹H‐NMR) and Fourier transform infrared spectroscopy (FT‐IR) techniques were used to characterize the formation of polyimide precursor and extent of grafting of PPG with polyimide. The results of thermogravimetric analysis (TGA) showed three step decomposition of nanofoam with the removal of PPG at 350°C and decomposition of polyimide at around 600°C. The polyimide nanofoams were also characterized by small angle X‐ray scattering (SAXS), field‐emission scanning electron microscopy (FE‐SEM) and transmission electron microscopy (TEM). The morphology showed nanophase‐separated structures with uniformly distributed and non‐interconnected pores of 20–40 nm in size. Dynamic mechanical analysis (DMA) indicated higher storage modulus for the foamed structure compared to the pure PI with reduction in loss tangent for the former system. Copyright © 2004 John Wiley & Sons, Ltd.     

Influence of surface characteristics of carbon blacks on cure and mechanical behaviors of rubber matrix compoundings

In this work, the effect of chemical modification on the surface energetics and cure kinetics of carbon blacks (CBs) modified with KOH and C6H6 was investigated by contact angle and rheometer measurements, respectively. Also, the resulting mechanical properties of the CBs/styrene-butadiene composites were studied in terms of tensile and dynamic mechanical analysis. As experimental results, the polar basic and nonpolar chemical treatments showed an increase of the London dispersive component (gamma(S)(L)) of gamma(S) of the CBs without significantly changing the surface properties and microstructures that resulted from the deaggregation of microstructures and decrease of the swollen weight of the sample in the equilibrium state. Also, it was clearly revealed that the increase of gamma(S) of the CBs could largely affect the vulcanization and mechanical properties of the composites, resulting from the increase in gamma(S)(L) of the CBs. These results were evident that the mechanical properties of the composites were controlled more by the gamma(S)(L) of gamma(S) than by the specific (or polar) component (gamma(S)(SP)), including electron acceptor and donor parameters on CB surfaces in an organic matrix composite system.     

The Incompressible Limits of Viscous Polytropic Fluids with Zero Thermal Conductivity Coefficient

ABSTRACT

We study the singular limit of viscous polytropic fluids without thermal conductivity as the Mach number tends to zero. A uniform existence result for the Cauchy problem in R ³ is proved under the assumption that the initial data belongs uniformly to H ^k (R ³) with k = 2, 3 and is well-prepared in H ¹ (R ³).