Efficient lasing action from Rhodamine-110 (Rh-110) impregnated sol-gel silica samples prepared by dip method

Rhodamine-110/sol-gel samples are prepared by sol-gel technique using dip method. Concentration dependent photophysical studies of these samples have indicated about the least possibility of aggregate formation. The lasing action of Rh-110 in silica samples is studied as a function of dye concentration. An efficient laser emission is observed when the samples are transversely pumped at 337.1 nm and 1.5 Hz repetition rate using a nitrogen laser (400 μJ energy/pulse and 4 ns pulse duration). The maximum of 166% laser efficiency of dye doped sol-gel samples compared to Rhodamine-6G (Rh-6G) in methanol is achieved. The photostability is also measured by using N₂ laser at 1 Hz and it is found nearly 165 pulses. The possible reasons for the photodegradation of the dye molecules are discussed in detail.     

New organic–inorganic hybrid matrices doped with rhodamine 6G as solid-state dye lasers

We report on the laser action of rhodamine 6G (Rh6G) incorporated into new hybrid organic–inorganic monolithic materials. The synthesis of these materials proceeded via the simultaneous sol-gel process of the inorganic part (tetraethoxysilane or tetramethoxysilane) and the free-radical polymerization of an organic monomer part (2-hydroxypropyl methacrylate, 2-hydroxyethyl methacrylate and a 1:1 v/v copolymer of this monomer with methyl methacrylate). The wt. % proportion of the alkoxide was systematically varied in each organic formulation, and the effect of each organic–inorganic composition on the lasing properties of Rh6G was evaluated. The laser samples were transversely pumped and the influence on the laser action of dye concentration, pump wavelength and pump repetition rate was analyzed. Lasing efficiencies of up 26% and good stabilities, with a 90% drop in the initial laser output of up to 12000 pump pulses at 2.5 Hz, were obtained when the samples were pumped at 355 nm with 5.5 mJ/pulse from the third harmonic of a Q-switched Nd:YAG laser. Received: 31 July 2002 / Revised version: 14 October 2002 / Published online: 20 December 2002 RID="*" ID="*"Corresponding author. Fax: +34-91/564-4853, E-mail: ogarcia@ctp.csic.es     

Application of indium tin oxide (ITO) thin film as a low emissivity film on Ni-based alloy at high temperature

Indium tin oxide (ITO) films as the low emissivity coatings of Ni-based alloy at high temperature were studies. ITO films were deposited on the polished surface of alloy K424 by direct current magnetron sputtering. These ITO-coated samples were heat-treated in air at 600–900 °C for 150 h to explore the effect of high temperature environment on the emissivity. The samples were analyzed by X-ray diffraction (XRD), SEM and EDS. The results show that the surface of sample is integrity after heat processing at 700 °C and below it. A small amount of fine crack is observed on the surface of sample heated at 800 °C and Ti oxide appears. There are lots of fine cracks on the sample annealed at 900 °C and a large number of various oxides are detected. The average infrared emissivities at 3–5 μm and 8–14 μm wavebands were tested by an infrared emissivity measurement instrument. The results show the emissivity of the sample after annealed at 600 and 700 °C is still kept at a low value as the sample before annealed. The ITO film can be used as a low emissivity coating of super alloy K424 up to 700 °C.     

Enhancement of conductivity in La2Mo2O9 ceramics fabricated by a novel three-stage thermal processing method

Pure and dense La₂Mo₂O₉ ceramic electrolytes with grain sizes of 1–3 μm were fabricated from nanocrystalline powders by a novel three-stage, one-cycle, pressureless thermal processing method at temperatures as low as 600 °C. Phase formation, microstructure and grain size of the samples were examined using X-ray diffraction and scanning electron microscopy. Density of the sintered samples was determined as in the range of 94–96% of the theoretical density by weight/geometric measurements. Impedance spectroscopy was used to characterize the electrical properties of the sintered samples. The conductivity of the three-stage sintered samples reaches a value of 0.018 S/cm at 600 °C and 0.05 S/cm at 700 °C, much higher than that of the samples fabricated by conventional solid-state reaction method, but similar to that of the samples sintered at 950 °C for 12 h from the same nanocrystalline powders. The high conductivity of these samples was attributed to the co-operation of the excellent performance of nanocrystalline powders and the advantages of the novel three-stage low-temperature thermal processing.     

Thermosonication effect on bioactive compounds,enzymes activity,particle size,microbial load,and sensory properties of almond (Prunus dulcis) milk

The object of this research was to appraise the physicochemical characteristics of almond milk and consumer acceptability after the thermosonication (TS) processing. The almond milk was subjected to TS processing (frequency: 40 kHz; power: 600 W; Temperature: 30, 45, and 60 °C; Time: 10, 20, 30, and 40 min) and pasteurization (for 60 s at 90 °C). After treatments, all samples were analyzed for bioactive compounds, antioxidant activities, microbial, enzymatic, and sensory attributes. The results showed a non-significant difference in total soluble solids and pH while TS processing at 45 and 60 °C significantly increased the cloudiness, viscosity, browning index, and color properties. TS processing increased the bioavailability of total phenolic, flavonols, flavonoids, condensed tannin contents, and antioxidant activity as compared to untreated and pasteurized samples. TS processing also significantly reduced the particle size distribution through acoustic cavitation. Microbial inactivation with TS at 60 °C resulted in ≥ 5 log reduction of total plate count and ≥ 4 log reduction of yeast & mold was achieved. The highest inhibition of lipoxygenase (LOX) and peroxidase (POD) were observed at 60 °C for 30 min. Moreover, the best sensorial properties were observed after TS processing at 60 °C. Thus; TS processing can increase the almond milk quality and safety as a viable substitute for thermal processing.     

Biodiesel production from non-edible Silybum marianum oil using heterogeneous solid base catalyst under ultrasonication

The aim of this study is to investigate modified TiO₂ doped with C₄H₄O₆HK as heterogeneous solid base catalyst for transesterification of non-edible, Silybum marianum oil to biodiesel using methanol under ultrasonication. Upon screening the catalytic performance of modified TiO₂ doped with different K-compounds, 0.7 C₄H₄O₆HK doped on TiO₂ was selected. The preparation of the catalyst was done using incipient wetness impregnation method. Having doped modified TiO₂ with C₄H₄O₆HK, followed by impregnation, drying and calcination at 600 °C for 6 h, the catalyst was characterized by XRD, FTIR, SEM, BET, TGA, UV and the Hammett indicators. The yield of the biodiesel was proportional to the catalyst basicity. The catalyst had granular and porous structures with high basicity and superior performance. Combined conditions of 16:1 molar ratio of methanol to oil, 5 wt.% catalyst amount, 60 °C reaction temperature and 30 min reaction time was enough for maximum yield of 90.1%. The catalyst maintained sustained activity after five cycles of use. The oxidative stability which was the main problem of the biodiesel was improved from 2.0 h to 3.2 h after 30 days using ascorbic acid as antioxidant. The other properties including the flash point, cetane number and the cold flow ones were however, comparable to international standards. The study indicated that Ti-0.7-600-6 is an efficient, economical and environmentally, friendly catalyst under ultrasonication for producing biodiesel from S. marianum oil with a substantial yield.     

Investigation of a Pt–Fe/C catalyst for oxygen reduction reaction in direct ethanol fuel cells

Three cathode catalysts (60% Pt/C, 30% Pt/C and 60% Pt–Fe/C), with a particle size of about 2–3 nm, were prepared to investigate the effect of ethanol cross-over on cathode surfaces. All samples were studied in terms of structure and morphology by using X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses. Their electrocatalytic behavior in terms of oxygen reduction reaction (ORR) was investigated and compared using a rotating disk electrode (RDE). The tolerance of cathode catalysts in the presence of ethanol was evaluated. The Pt–Fe/C catalyst showed both higher ORR activity and tolerance to ethanol cross-over than Pt/C catalysts. Moreover, the more promising catalysts were tested in 5 cm² DEFC single cells at 60 and 80 °C. An improvement in single cell performance was observed in the presence of the Pt–Fe catalyst, due to an enhancement in the oxygen reduction kinetics. The maximum power density was 53 mW cm⁻² at 2 bar rel. cathode pressure and 80 °C.     

XPS investigation of vacuum annealed vertically aligned ultralong ZnO nanowires

The surface properties of vertically aligned ZnO nanowires grown by chemical vapour deposition on GaN using a gold layer as a catalyst are investigated by X-ray Photoelectron Spectroscopy as a function of annealing temperature in ultra high vacuum (UHV). The nanowires are 8.5 μm long and 60 nm wide. 87% of the surface carbon content was removed after annealing at 500 °C in UHV. Analysis of the gold intensity suggests diffusion into the nanowires after annealing at 600 °C. Annealing at 300 °C removes surface water contamination and induces a 0.2 eV upward band bending, indicating that adsorbed water molecules act as surface electron donors. The contaminants re-adsorbed after 10 days in UHV and the surface band bending caused by the water removal was reversed. The UHV experiment also affected the nanowires arrangement causing them to bunch together. These results have clear implications for gas sensing applications with ZnO NWs.     

High-dose high-temperature emission of LiF:Mg,Cu,P: Thermally and radiation induced loss & recovery of its sensitivity

Highly sensitive LiF:Mg,Cu,P (MCP) detectors enable measurements of radiation doses from tens of nanograys up to a few kilograys, where the saturation of the signal of the main dosimetric peak occurs. Thanks to the recently observed high-dose high-temperature emission of MCP detectors heated to temperatures up to 600 °C after exposures to radiation doses ranging from 1 kGy to 1 MGy, a new method of thermoluminescent measurement of radiation doses has been recently developed at the Institute of Nuclear Physics (IFJ). This method can measure doses ranging from micrograys up to a megagray. So far, high dose measurements were performed on fresh MCP samples and each detector was used only once, because as a result of these measurements, the detectors lose their sensitivity to a large extent. In this study, a specific thermal treatment intended to fully restore the loss of MCPs TL sensitivity was sought. We have investigated several annealing procedures, applying different temperatures (from 400 °C up to 700 °C) for different periods of time (10–30 min) in argon atmosphere. In this way we were able to recover MCP sensitivity fully, allowing for reuse of the samples after high-dose irradiation and high-temperature measurement.     

Optical properties of dye-doped zirconia films by spectroscopic ellipsometry

The optical properties of zirconia films doped with rhodamine 6G and oxazine 725 by the sol-gel process were investigated using spectroscopic ellipsometry (SE). Accurate refractive index n and the extinction coefficient k were determined using a three-oscillator classical Lorentz model in the wavelength range of 300-800 nm. The derived refractive index of dye-doped films exhibited anomalous dispersion in the absorption region. Wavelength tunable output lasing action yellow and near-infrared wavelength region was achieved by DFB configuration using zirconia films doped with R6G and oxazine 725.     

Novel utilization of waste marine sponge (Demospongiae) as a catalyst in ultrasound-assisted transesterification of waste cooking oil

This study demonstrates the potential of Na-silica waste sponge as a source of low cost catalyst in the transesterification of waste cooking oil aided by ultrasound. In this work an environmentally friendly and efficient transesterification process using Na-loaded SiO₂ from waste sponge skeletons as a solid catalyst is presented. The results showed that the methyl esters content of 98.4 ± 0.4 wt.% was obtainable in less than an hour (h) of reaction time at 55 °C. Optimization of reaction parameters revealed that MeOH:oil, 9:1; catalyst, 3 wt.% and reaction duration of 30 min as optimum reaction conditions. The catalyst is able to tolerant free fatty acid and moisture content up to 6% and 8%, respectively. In addition, the catalyst can be reused for seven cycles while maintaining the methyl esters content at 86.3%. Ultrasound undoubtedly assisted in achieving this remarkable result in less than 1 h reaction time. For the kinetics study at 50–60 °C, a pseudo first order model was proposed, and the activation energy of the reaction is determined as 33.45 kJ/mol using Arrhenius equation.     

M?ssbauer study of carbon coated iron magnetic nanoparticles produced by simultaneous reduction/pyrolysis

Magnetic iron nanoparticles immersed in a carbon matrix were produced by a combined process of controlled dispersion of Fe^3?+? ions in sucrose, thermal decomposition with simultaneous reduction of iron cores and the formation of the porous carbonaceous matrix. The materials were prepared with iron contents of 1, 4 and 8 in %wt in sucrose and heated at 400, 600 and 800°. The samples were analyzed by XRD, Mössbauer spectroscopy, magnetization measurements, TG, SEM and TEM. The materials prepared at 400° are composed essentially of Fe₃O₄ particles and carbon, while treatments at higher temperatures, e.g. 600 and 800° produced as main phases Fe⁰ and Fe₃C. The Mössbauer spectra of samples heated at 400° showed two sextets characteristic of a magnetite phase and other contributions compatible with Fe^3?+? and Fe^2?+? phases in a carbonaceous matrix. Samples treated at temperatures above 600° showed the presence of metallic iron with concentrations between 16?C43%. The samples heated at 800° produced higher amounts of Fe₃C (between 20% and 58%). SEM showed for the iron 8% sample treated at 600?C800°C particle sizes smaller than 50 nm. Due to the presence of Fe⁰ particles in the carbonaceous porous matrix the materials have great potential for application as magnetic adsorbents.     

Strong temperature effect on X-ray photo-etching of polytetrafluoroethylene using a 10 Hz laser-plasma radiation source based on a gas puff target

The first results of experiments on direct photo-etching of heated PTFE using a 10 Hz X-ray source based on a laser-irradiated gas puff target are presented. X-ray radiation in the wavelength range from 6 to 20 nm was produced as a result of irradiation of a double-stream gas puff target with Nd:YAG laser pulses of energy 0.8 J and time duration 3 ns. The resulting X-ray pulses with energy of about 100–200 mJ were used to irradiate samples of PTFE to create microstructures by direct photo-etching. Strong enhancement of the photo-etching process was observed for samples heated up to 300 °C. PACS 52.38.Ph; 81.65.Cf; 61.82.Pv     

Distributed feedback dye laser holographically induced in improved organic–inorganic photocurable nanocomposites

Distributed feedback (DFB) lasing in permanent volume transmission gratings formed in a laser dye-doped organic–inorganic nanocomposite has been investigated. DFB laser cavities were fabricated using one-step two-beam holographic exposure of Pyrromethene 567 (PM567) doped photopolymerizable acrylate monomers containing inorganic (LaPO₄) nanoparticles. Compared to the formulation previously utilized, the material composition presented provides longer lifetime of the laser. Spectral and polarization properties, input–output and stability characteristics of the laser output have been investigated by varying the material composition and the patterning parameters. DFB lasing emission of the second and the third diffraction orders has been demonstrated. The spectral linewidth of ∼0.08 nm has been observed at a pump energy threshold of about 0.2 μJ/pulse for the second-order DFB lasing when pumped with 532 nm 500 ps laser pulses. Spectral tuning of the lasing output over ∼56 and ∼7 nm was obtained by varying the grating period and the content of inorganic nanoparticles in the polymer matrix, respectively.     

Synthesis of nano onion-like fullerenes by chemical vapor deposition using an iron catalyst supported on sodium chloride

Nano-carbon materials were synthesized by the catalytic decomposition of acetylene at 420 °C using iron supported on sodium chloride as catalyst. The catalysts contain about 0.3, 1.6, 3.3, and 5.2 wt% iron. The samples were examined by scanning and transmission electron microscopy, energy dispersive spectroscopy, and X-ray diffraction. The results show that nano onion-like fullerenes (NOLFs) surrounding an Fe₃C core were obtained using the catalyst containing 0.3 wt% iron. These had a structure of stacked graphitic fragments, with diameters in the range 15–50 nm. When the product was further heat treated under vacuum at 1,100 °C, NOLFs with a clear concentric graphitic layer structure were obtained. The growth mechanism of NOLFs encapsulating metallic cores is suggested to be in accordance with a vapor–solid growth model.     

A comparative study of the luminescence characteristics of polymineral fine grains and coarse-grained K- and Na-rich feldspars

The IRSL and post-IR IRSL (pIRIR) signal characteristics of polymineral fine grains are investigated and compared with those of K- and Na-rich feldspar extracts. TL signal loss after IR and pIRIR stimulations occurs mainly at around 320 °C for polymineral and Na-feldspar samples and around 410 °C for K-feldspar samples, when a preheat temperature of 250 °C for 60 s is used. After preheating to a higher temperature (320 °C for 60 s) all samples show a TL reduction around 410 °C in the blue detection window. Pulse annealing experiments for IRSL and pIRIR signals for preheats between 320 °C and 500 °C indicate that the signal stabilities are similar among the different feldspar types, when a higher preheat temperature (>320 °C) is used. Thermal activation energies for IRSL and pIRIR signals are largest in K-feldspar and smallest in polymineral fine grains, in both blue and UV detection windows for both fast time-resolved (TR) and continuous wave (CW) signals. These results suggest that IRSL and pIRIR signals in polymineral fine grains originate mainly from Na-feldspar grains; these signals are less thermally stable than those from K-feldspar, but a more stable signal (presumably from K-feldspar grains) can be obtained using a higher preheat temperature.     

Pulsed KrF-laser synthesis of single-wall-carbon-nanotubes: effects of catalyst content and furnace temperature on their nanostructure and photoluminescence properties

In this article, we report on the use of a pulsed KrF-laser (248 nm, 20 ns) for the synthesis of single wall carbon nanotubes (SWCNTs) from the ablation of a graphite target loaded with Co/Ni catalyst, under various growth conditions. By varying the Co/Ni catalyst load of the graphite target, from 0 to 2.4 at.%, the laser synthesized SWCNTs, under a furnace temperature (T _f) of 1,100 °C, were found to be decorated by C₆₀ buckyballs, of which the density decreases as the catalyst content is increased. The effect of the catalyst content of the laser-ablated graphite target on the produced carbon nanostructures (C₆₀ vs. SWCNTs) was systematically investigated by means of various characterization techniques, including Raman spectroscopy, thermogravimetry, and SEM/HR-TEM microscopies. A [Co/Ni] ≥ 1.2 at.% was identified as the optimal concentration for the production of SWCNTs without any detectable presence of C₆₀ buckyballs. Thus, under the optimal growth conditions (i.e., [Co/Ni] = 1.2 at.% and T _f = 1,100 °C), the produced SWCNTs were found to be characterized by a very narrow diameter distribution (centered on 1.2 nm) with lengths in excess of 10 μm. By increasing T _f from 900 to 1,150 °C, the diameter of the SWCNTs can be varied from ~0.9 to ~1.3 nm. This nanotube diameter variation was evidenced by Raman and UV–Vis absorption measurements, and its effect on the photoluminescence of the SWCNTs is presented and discussed.     

Using Zn as target to fabricate ZnO coating by thermal oxidation in air on quartz substrate

In this work, ZnO coatings were fabricated by the RF-sputtering method on quartz substrates in an inert gas ambient of Ar followed by a thermal oxidation process in air at different temperatures. The effect of thermal oxidation temperatures on the structures and photoluminescence (PL) properties of the coatings were studied. The structural characteristics of the samples were analyzed by X-ray diffraction (XRD) and atomic force microscope (AFM). The PL spectra were obtained by using a Xe laser as a light source with an excitation wavelength of 325 nm at room temperature. The force-curves were obtained by AFM. The results show that all the prepared ZnO coatings have a compact hexagonal wurtzite structure. With the increasing annealing temperature from 400 °C to 600 °C, the particle size, surface RMS roughness, photoluminescence intensity and adhesion force of the prepared ZnO coatings were increased as well.     

Effect of processing temperature on the superconducting properties of acetone doped MgB2 tapes

Correlation of phase formation, critical transition temperature T_c, microstructure, and critical current density J_c with sintering temperature has been studied for acetone doped MgB₂/Fe tapes. Sintering was performed at 600–850 °C for 1 h in a flowing Ar atmosphere. High boron substitution by carbon was obtained with increasing the sintering temperature; however, the acetone doped samples synthesized at 800 °C contain large size MgB₂ grains and more MgO impurities. Incomplete reaction for the acetone doped samples heated at 600 °C result in bad intergrain connectivity. At 4.2 K, the best J_c value was achieved in the acetone doped sample sintered at 700 °C, which reached 24,000 A/cm² at 10 T and 10,000 A/cm² at 12 T, respectively. Our results indicate that the small grain size and less impurity were also important for the improvement of J_c–B properties besides the substitutions of B by C.     

Passive Q-switching of erbium glass laser by magnesium aluminosilicate sitall with cobalt ions

We have studied the radiation output parameters for an erbium glass laser, lasing at a wavelength of 1.54 μm, with passive Q-switching by means of a cobalt-containing magnesium aluminosilicate sitall compared with a saturable absorber based on a magnesium aluminum spinel crystal with cobalt ions. We have shown that the output characteristics of the laser emission when using sitall are not inferior to the analogous characteristics of a laser based on a spinel crystal, and are practically independent of the temperature of the saturable absorber in the range 0°C–80°C. The duration (energy) of the output pulses was 70 nsec (∼4 mJ), the energy dispersion of the radiation pulse relative to the average value was no greater than 3%, the beam divergence was 2.8 mrad, the laser beam quality factor was M² = 1.2. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 1, pp. 126–131, January–February, 2007.