Tunable Emissive Lanthanidomesogen Derived from a Room‐Temperature Liquid‐Crystalline Schiff‐Base Ligand

A novel photoluminescent room‐temperature liquid‐crystalline salicylaldimine Schiff base with a short alkoxy substituent and a series of lanthanide(III) complexes of the type [Ln(LH)₃(NO₃)₃] (Ln=La, Pr, Sm, Gd, Tb, Dy; LH=(E)‐5‐(hexyloxy)‐2‐ [{2‐(2‐hydroxyethylamino)ethylimino]methyl}phenol) have been synthesized and characterized by FTIR, ¹H and ¹³C NMR, UV/Vis, and FAB‐MS analyses. The ligand coordinates to the metal ions in its zwitterionic form. The thermal behavior of the compounds was investigated by polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). The ligand exhibits an enantiotropic hexagonal columnar (Col_h) mesophase at room temperature and the complexes show an enantiotropic lamellar columnar (Col_L) phase at around 120 °C with high thermal stability. Based on XRD results, different space‐filling models have been proposed for the ligand and complexes to account for the columnar mesomorphism. The ligand exhibits intense blue emission both in solution and in the condensed state. The most intense emissions were observed for the samarium and terbium complexes, with the samarium complex glowing with a bright‐orange light (ca. 560–644 nm) and the terbium complex emitting green light (ca. 490–622 nm) upon UV irradiation. DFT calculations performed by using the DMol3 program at the BLYP/DNP level of theory revealed a nine‐coordinate structure for the lanthanide complexes.     

Multi-wavelength Brillouin fiber laser using dual-cavity configuration

A simple technique for achieving multi-wavelength tunable multi-wavelength Brillouin fiber laser (BFL) based on dual-pass configuration is demonstrated. The BFL uses a piece of 10 km long non-zero dispersion shifted fiber (NZ-DSF) as a Brillouin gain medium to obtain odd-order Brillouin Stokes waves as an output with the line spacing of 0.16 nm (20 GHz) between each two consecutive waves by employing even-order Brillouin Stokes to improve output performance of the laser. With a BP of 15.3 dBm, at least 15 odd-order Brillouin Stokes and anti-Stokes lines are generated. The laser is room temperature stable, tunable over 50 nm wavelength range and has an optical signal to noise ratio of more than 30 dB at 1560 nm region. This Brillouin fiber laser can operate at any wavelength depending on the Brillouin pump (BP) wavelength used.     

Investigation of dispersion characteristic in tapered fiber

A dispersion characteristic of a tapered fiber is investigated using temporal interferometer by employing a broadband amplified spontaneous emission (ASE) source to generate an interference pattern. The dispersion characteristic of the tapered fiber is acquired from a Fourier transform of the interference pattern. The second and third order dispersions of β₂ and β₃ are obtained at 1544.1 nm for −600 ps²/km and −2 ps³/km, respectively. The β₂ value obtained is observed to be more than 300 times higher than that of a non-tapered single mode fiber. The high dispersion characteristic is due to tapering process that changes the birefringence characteristic due to the reduction in the fiber’s size and structure.     

Compact fiber laser at L-band region using Erbium-doped Zirconia fiber

A compact Erbium-doped fiber laser (EDFL) operating in L-band region is demonstrated using a fabricated Erbium-doped Zirconia fiber (EDZF) for the first time. The fiber is fabricated by combining Zr and Al to achieve the maximum Erbium ion concentration of 4320 wt ppm. By using a fiber Bragg grating (FBG) in a ring configuration, the laser operates at 1579.6 nm with a slope efficiency of 13.6% and the threshold pump power of 25.1 mW. The lasing wavelength is obtained at Bragg wavelength with an output power of 13 dBm and a 3 dB spectral width of 0.02 nm using a piece of 2 m long EDZF in conjunction with 120 mW of 1480 nm pump power.     

Dual Role of Silver Moieties Coupled with Ordered Mesoporous Cobalt Oxide towards Electrocatalytic Oxygen Evolution Reaction

Herein, we show that the performance of mesostructured cobalt oxide electrocatalyst for oxygen evolution reaction (OER) can be significantly enhanced by coupling of silver species. Various analysis techniques including pair distribution function and Rietveld refinement, X‐ray absorption spectroscopy at synchrotron as well as advanced electron microscopy revealed that silver exists as metallic Ag particles and well‐dispersed Ag₂O nanoclusters within the mesostructure. The benefits of this synergy are twofold for OER: highly conductive metallic Ag improves the charge transfer ability of the electrocatalysts while ultra‐small Ag₂O clusters provide the centers that can uptake Fe impurities from KOH electrolyte and boost the catalytic efficiency of Co–Ag oxides. The current density of mesostructured Co₃O₄ at 1.7 V_RHE is increased from 102 to 211 mA cm^?2 with incorporation of silver spices. This work presents the dual role of silver moieties and demonstrates a simple method to increase the OER activity of Co₃O₄.     

Electrical conductivity studies on PVA/PVP-KOH alkaline solid polymer blend electrolyte

A series of conducting thin-film solid electrolytes based on poly (vinyl alcohol)/ poly (vinyl pyrrolidone) (PVA/PVP) polymer blend was prepared by the solution casting technique. PVA and PVP were mixed in various weight percent ratios and dissolved in 20 ml of distilled water. The samples were analyzed by using impedance spectroscopy in the frequency range between 100 Hz and 1 MHz. The PVA/PVP system with a composition of 80% PVA and 20 wt.% PVP exhibits the highest conductivity of (2.2±1.4) × 10⁻⁷ Scm⁻¹. The highest conducting PVA/PVP blend was then further studied by adding different amounts of potassium hydroxide (KOH) ionic dopant. Water has been used as solvent to prepare PVA/PVP-KOH based alkaline solid polymer blend electrolyte films. The conductivity was enhanced to (1.5 ± 1.1) × 10⁻⁴ Scm⁻¹ when 40 wt.% KOH was added. Paper presented at the International Conference on Functional Materials and Devices 2005, Kuala Lumpur, Malaysia, June 6 – 8, 2005.     

Efficient enrichment of alpha,beta-unsaturated bovine insulins-(C12)n using tweezing adsorptive bubble separation (TABS) with bovine serum albumin

Alkyl-substituted insulin molecules are depository preparations used in the treatment of diabetes. The isolation and purification of these active compounds is performed on the hand of several complicated separation steps. In this work, nonmodified and new synthesized alpha,beta-unsaturated bovine insulins-(C12)(n) were selectively isolated from aqueous solution using tweezing adsorptive bubble separation (TABS) with BSA, which enabled reversible binding with the unpolar side chains of bovine insulin and its derivates. The bovine insulin/serum albumin complex could be efficiently transferred into the foam phase at pH 8 with an enrichment factor of 2.6 and a recovery of 89.7%. Experiments with alkylated alpha,beta-unsaturated bovine insulins-(C12)(n) performed at pH 9 enriched even quantitatively the complex under equal experimental conditions, accompanied with an enrichment factor of 3.3. Additionally performed radio immunoassay tests revealed that the immunological activity of alpha,beta-unsaturated bovine insulins-(C12)(n) remained unchanged after foaming.     

Enantioseparation of (R,S)-ketoprofen using Candida antarctica lipase B in an enzymatic membrane reactor

An enzymatic membrane reactor (EMR) for enantioseparation of (R,S)-ketoprofen via Candida antarctica lipase B (CALB) as biocatalyst was investigated. A comparative study of free and immobilized CALB was further conducted. The catalytic behaviour of CALB in an EMR was affected by the process parameters of enzyme load, substrate concentration, substrate molar ratio, lipase solution pH, reaction temperature, and substrate flow rate. Immobilization of CALB in the EMR was able to reduce the amount of enzyme required for the enantioseparation of (R,S)-ketoprofen. Immobilized CALB in the EMR assured higher reaction capacity, better thermal stability, and reusability. It was also found to be more cost effective and practical than free CALB in a batch reactor.     

Treatment of metal-plating waste water by modified direct contact membrane distillation

In this study, the treatability of metal-plating waste water by modified direct contact membrane distillation (DCMD) at different temperature differences (ΔT = 30°C, 40°C, 50°C, and 55°C was investigated. Two different hydrophobic membranes made of poly(tetrafluoroethylene) (PTFE) and poly(vinylidene fluoride) (PVDF) having different pore sizes (0.22 μm and 0.45 μm) were used. The results indicated that conductivity, COD, sulphate, copper, and nickel could be successfully removed by modified DCMD. The rejection efficiencies for conductivity, COD, and sulphate were 99%, 86%, and 99%, respectively. Copper rejection was effective with both membranes while nickel concentration was below the limit of detection in the effluent. It was found that the pollutant rejection efficiency was affected by the raw water characteristics, membrane properties, and influent heating temperatures. In addition to the water quality parameters, the flux was measured to evaluate membrane performance. A high flux was obtained at 65°C (ΔT = 55°C) with 0.45 μm pore size PTFE membrane (24.1 L m^?2 h^?1) and with PVDF membrane (17.1 L m^?2 h^?1). The flux was mainly affected by temperature and membrane properties. As a result, modified DCMD and all the membranes used in this study were effective for the treatment of metal-plating waste water.