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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 145 records · Page 8

Fabrication of chitosan/polyacrylonitrile blend and semi-IPN hydrogel with epichlorohydrin

The present study is focused on the preparation of chitosan (CS)/polyacrylonitrile (PAN) blend and semi-interpenetrating polymer network (sIPN). Blend CS/PAN hydrogel films (HFs) were prepared by solution blending and casting technique. CS in the blend was crosslinked with epichlorohydrin (ECH) to prepare sIPN. The developed CS/PAN blend and sIPN hydrogels were characterized with Field Emission Scanning Electron Microscopy (FE-SEM), Fourier transform infrared spectroscopy (FTIR), Thermagravimetric analysis (TGA), and Differential Scanning Calorimeter (DSC). The result showed good miscibility between CS and PAN and crosslinking of CS in the blend. The swelling of the different blended and sIPN hydrogels samples were examined at room temperature (T{sub r}). Blend (C80/P20) sample showed highest swelling (∼2400%) and fair degree of stability (∼28% until 96 h), whereas sIPN hydrogel exhibited relatively low degree of swelling (∼244%) and high degree of aqueous (∼85 % until 96 h), and thermal (onset temperature 304°C) stabilities.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

The influence of reduced graphene oxide on electrical conductivity of LiFePO{sub 4}-based composite as cathode material

LiFePO{sub 4} is fascinating cathode active materials for Li-ion batteries application because of their high electrochemical performance such as a stable voltage at 3.45 V and high specific capacity at 170 mAh.g{sup −1}. However, their low intrinsic electronic conductivity and low ionic diffusion are still the hindrance for their further application on Li-ion batteries. Therefore, the efforts to improve their conductivity are very important to elevate their prospecting application as cathode materials. Herein, we reported preparation of additional of reduced Graphene Oxide (rGO) into LiFePO{sub 4}-based composite via hydrothermal method and the influence of rGO on electrical conductivity of LiFePO{sub 4}−based composite by varying mass of rGO in composition. Vibration of LiFePO{sub 4}-based composite was detected on Fourier Transform Infrared Spectroscopy (FTIR) spectra, while single phase of LiFePO{sub 4} nanocrystal was observed on X-Ray Diffraction (XRD) pattern, it furthermore, Scanning Electron Microscopy (SEM) images showed that rGO was distributed around LiFePO4-based composite. Finally, the 4-point probe measurement result confirmed that the optimum electrical conductivity is in additional 2 wt% rGO for range 1 to 2 wt% rGO.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Synthesis of gadolinium carbonate-conjugated-poly(ethylene)glycol (Gd{sub 2}(CO{sub 3}){sub 3}@PEG) particles via a modified solvothermal method

PEGylated gadolinium carbonate ((Gd{sub 2}(CO{sub 3}){sub 3})@PEG) powder was successfully synthesized by a modified solvothermal method. The synthesized products were characterized by means of X-ray diffraction (XRD), Fourier Transform Infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and Energy Dispersive X-ray Spectroscopy (EDS). A systematic change in the chemical surface composition, crystallinity and size properties of the Gd{sub 2}(CO{sub 3}){sub 3}@PEG particles was observed by increasing the reaction time at 5 hours, 7 hours, and 8 hours. The corresponding XRD patterns showed that the Gd{sub 2}(CO{sub 3}){sub 3} particles had hexagonal symmetry (JCPDS No. 37-0559) with a crystallite size of 3.5, 2.9, and 4.6 nm. FTIR spectra showed that the Gd{sub 2}(CO{sub 3}){sub 3})@PEG particles were formed with the PEG as carbonyl and hydroxyl group attached to the surface. SEM analysis showed that the Gd{sub 2}(CO{sub 3}){sub 3})@PEG particles had a flake-like morphology of homogeneous sized particles and agglomerates. EDS analysis confirmed the presence of constituent Gd{sub 2}(CO{sub 3}){sub 3} elements.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Preparation of silver-chitosan nanocomposites and coating on bandage for antibacterial wound dressing application

Bandage is a medical device that is essential for wound dressing. To improve the performance of the bandage, it has been coated by silver-chitosan nanocomposites (Ag/Chit) with pad-dry-cure method. The nanocomposites were performed by chemical reduction method at room temperature using glucose as reducing agent, sodium hydroxide (NaOH) as accelerator reagent, silver nitrate (AgNO{sub 3}) as metal precursor and chitosan as stabilizing agent. Localized surface plasmon resonance (LSPR) absorption band of silver nanoparticles was investigated using UV-Vis spectrophotometer. The bandage coated Ag/Chit nanocomposites (B-Ag/Chit) were characterized by fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscope (SEM). In addition, antibacterial activity of the bandage toward Gram positive (Staphylococcus aureus) and Gram negative (Escherichia coli) were also studied. The formation of silver nanoparticles was confirmed by the appearance of LSPR absorption peak at 412.2 – 423.2 nm. Coating of nanocomposite cause increasing rigidity of bandage and decreasing on crystallinity. The bandages of B-Ag/Chit demonstrated good activity against both Gram positive (S. aureus) and Gram negative (E.Coli). Thus the bandages have a potential to be used for antibacterial wound dressing application.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Effect of precursor concentration on the electrical properties of LiFePO{sub 4} prepared by solvothermal method

Lithium iron phosphate (LiFePO{sub 4}) is frequently used for Li-ion battery cathode. LiFePO{sub 4} has the high specific capacity at 170 mAhg{sup −1}, stable voltage at 3.45 V, stable structure, cheap, and low toxicity. The objective of this research is investigating the effect of precursor concentration on the electrical properties of LiFePO{sub 4} prepared by solvothermal method. LiOH, FeSO{sub 4}, H{sub 3}PO{sub 4}, and citric acid were used as the precursors. The LiOH concentration was varied from 0.3 M to 1.8 M. The Fourier Transform Infrared Spectroscopy (FTIR) measurement identified the Fe-O, O-P-O, and P-O bonds which corresponding to LiFePO{sub 4}. The result of 4-point probe measurement shows that, among the prepared samples, the sample from the precursor concentration of 1.8 M has the highest electrical conductivity.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Synthesis and characterization of natural red dye from Caesalpinia sappan linn

The study reports the synthesis and characterization of natural red dye. The dyes were extracted from woods of Caesalpiniasappanlinn at varied temperatures of 70, 80, 90, and 100°C for three hours. The dry wood chips and water at a ratio of 6:1 were immersed in the reactor of 150 liters. The absorbance spectra of the natural red dyes were measured by ultra-violet-visible spectroscopy. Meanwhile, Fourier transform infrared spectroscopy was used to investigate the functional groups of the natural red dyes. In addition, the basic production cost was calculated and the fastness property towards cotton fabrics was investigated according to the Indonesia national standard of 105-C06:2010, 105-B01:2010, and 0288-2008. The results showed that the functional groups found the extracted red dyes indicated the complex bond of brazilein with peak absorbance at a wavelength of 538-540 nm. The extraction temperature also changed the functional group of brazilein. From the color, the absorbance peak, the functional groups, and the main production cost, the best parameter to synthesize the natural red dyes from Caesalpiniasappanlinn was at a temperature of 80°C for two hours. Moreover, the natural red dyes has the fastness to wash resistance, light resistance, and scrub resistance by 4-5, 4, and 3-4, respectively. However, further studies for synthesis the natural red dyes by using a continuous reactor are required to identify the naturally complex compounds in brazilein for improving the fastness properties and for reducing the cost.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Development of metal oxide impregnated stilbite thick film ethanol sensor

This paper presents the study of the sensing efficiency of Titanium oxide/ Stilbite and Copper oxide /Stilbite composites towards detection of hazardous pollutants like ethanol. Stilbite based composites are prepared by physically mixing zeolite with metal oxides namely TiO{sub 2} and CuO with weight ratios of 25:75, 50:50 and 75:25. The resulting sensor materials are characterized by X-ray diffraction and Fourier Transform Infrared Spectroscopy techniques. Composite sensors are fabricated in the form of thick film by using screen printing technique. The effect of metal oxide concentration on various ethanol sensing parameters such as operating temperature, maximum uptake capacity and response/recovery time are investigated. The results indicate that metal oxide impregnated stilbite composites have great potential as low temperature ethanol sensor.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Influence of compositional variation on electrical properties of PANI/SnO{sub 2} nanocomposites

Conducting polyaniline/tin oxide (PANI/SnO{sub 2}) nanocomposites have been successfully synthesized by in-situ polymerization technique. The PANI/SnO{sub 2} nanocomposites of different compositions were prepared by varying weight percentage of SnO{sub 2} nanoparticles such as 10 wt%, 20 wt%, 30 wt%, 40 wt% and 50 wt% into the fixed amount of the aniline monomer. The prepared powder samples were characterized by X-ray diffractometer (XRD), Fourier Transform Infrared spectroscopy (FT-IR) and Scanning electron microscope (SEM). The intensity of diffraction peaks for PANI/SnO{sub 2} composites is increases with increasing SnO{sub 2} wt%. SEM observation showed that the prepared SnO{sub 2} nanoparticles were uniformly dispersed and highly stabilized throughout the macromolecular chain that formed a uniform metal-polymer nanocomposite material. AC electrical conductivity and dielectric properties were studied in the frequency range of 1 KHz -1 MHz. At higher frequencies, the composites exhibit almost zero dielectric loss and maximum value of AC electrical conductivity (σ{sub ac}) of 0.21 S/m is found for a concentration of 30 wt% of SnO{sub 2} in polyaniline.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Luminescence performance of Eu{sup 3+} doped lead free zinc phosphate glasses for red emission

Luminescence performance of zinc phosphate glasses containing Eu{sup 3+} ion with the chemical compositions (60-x)NH{sub 4}H{sub 2}PO{sub 4}-20ZnO-10BaF{sub 2}-10NaF-x Eu{sub 2}O{sub 3} (where x = 0.2, 0.5, 1.0 and 1.5 mol%) has been studied. The Fourier Transform Infrared Spectroscopy (FT-IR) shows several vibrations bands. Luminescence spectra of these glasses exhibit characteristic emission of Eu{sup 3+} ion with an intense and most prominent red emission (614 nm) which is attributed to {sup 5}D{sub 0}→{sup 7}F{sub 2} transition. Judd-Ofelt (Ω{sub 2}, Ω{sub 4}) parameters have been evaluated from the luminescence intensity ratios of {sup 5}D{sub 0}→{sup 7}F{sub J} (where J = 2 and 4) to {sup 5}D{sub 0}→{sup 7}F{sub 1} transition as well as absorption spectra under different constraints. Using J-O parameters and excitation spectra, the radiative parameters are calculated for different Eu{sup 3+} doped glasses.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Effect of grain size on optical properties of iron oxide nanoparticles

In the present paper, iron oxide nanoparticles are successfully synthesized by the sol-gel method. The grain size is varied by sintering the nanoparticles at different temperature 400, 500, 600, 700 and 800 °C. Field emission scanning electron microscope (FESEM) image shows that the grains are uniformly distributed. The grain size increases from 15 nm to 35 nm with increasing the sintering temperature (400-800 °C). Energy dispersive X-ray spectroscopy (EDS) analysis shows that Fe is present in the stoichiometric ratio in all the synthesized samples. Fourier transform infrared spectroscopy (FTIR) spectra show that Fe-O stretching peaks appears at ∼495 cm{sup −1}. The value of energy band gap are found 2.75, 2.67, 2.62, 2.59, and 2.57 eV for the samples sintered at 400, 500, 600, 700 and 800 °C respectively. Therefore, the decrease in band gap with increasing the temperature has been observed. In this paper, the structural and optical properties have been explained on the basis of variation in the grain size with the temperature. The present studied samples more widely used in gas sensors and as catalysts.

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Study of variation in the band gap with concentration of TiO{sub 2}In (LaMnO{sub 3}){sub 1-x} / (TiO{sub 2}){sub x} (where x = 0.0,0.1,0.2,0.3 and 0.4) nanocomposites

In this paper(LaMnO{sub 3}){sub 1−x}/ (TiO{sub 2}) {sub x} (where x = 0.0, 0.1, 0.2, 0.3 and 0.4) nanocomposite are prepared by mixing the LaMnO{sub 3} and TiO{sub 2} (Sigma Chemicals, particle size ∼21 nm) nanoparticle in appropriate ratio. These samples were characterized by using FESEM, EDS and FTIR to study the optical properties. Field Emission Scanning Electron Microscopy (FESEM) image of pure LaMnO{sub 3} sample shows that the uniform particle size distribution is observed. The average particle size of the LaMnO{sub 3} nanoparticles is 43 nm. The crystallite size increases from 16-24 nm with increasing the weight percentage of TiO{sub 2} in LaMnO{sub 3}/TiO{sub 2} nanocomposite up to x = 0.4. The Fourier transform infrared spectroscopy (FTIR) spectra show that the absorption peaks appear at 450 cm{sup −1} and 491 cm{sup −1} which represent the Mn-O bending and Ti-O stretching mode respectively. The broadening of these peaks with increasing the concentration of TiO{sub 2} is also observed. It gives an evidence for the formation of metal oxygen bond. The absorption band at 600 cm{sup −1} corresponds to the stretching mode, which indicates the pervoskite phase present in the sample. The values of band gap are found 2.1, 1.9, 1.5, 1.3 and 1.2 eV for the x = 0.0, 0.1, 0.2, 0.3, and 0.4 respectively. Thus, the decrease in band gap and increase in refractive index with increasing concentration of TiO{sub 2} has been observed. These prepared nanocomposites can be used in the energy applications, to make the electrical devices and as a catalyst for photocatalytic processes e.g. hydrogenation.

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Effect of sintering temperature on the optical properties of BiFeO{sub 3} nanoparticles

BiFeO{sub 3} is a multiferroic material which exhibits excellent optical properties. BiFeO{sub 3} nanoparticles are synthesized by using sol-gel method. The prepared samples are sintered at 500°C, 600°C, 700°C, 800°C and 850°C. In this paper, the effect of sintering temperature on the optical properties in BiFeO{sub 3} nanoparticles is studied. Field emission electron microscopy (FESEM) images show that particles are nearly spherical in shape. It is found that the particles size increases from 37 nm to 51 nm with increasing the sintering temperature. FESEM images also reveal a homogenous size distribution of nanoparticles. All the functional groups are indexed in the Fourier transform infrared spectroscopy (FTIR) spectra. It is found that Fe-O stretching peaks are appeared in the wave number range 447 and 507 cm{sup −1}. The value of energy band gap are found 2.14, 2.26, 2.30, 2.36, and 2.54 eV for the samples sintered at 500°C, 600°C, 700°C, 800°C and 850°C respectively. Thus, the increase in band gap with increasing temperature has been observed. The present samples can be used as photo-catalyst, in non-volatile memories and to make spintronics devices.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Study of structural and optical properties of ZnAlQ{sub 5} (zinc aluminum quinolate) organic phosphor for OLED applications

The various composition of ZnAlQ{sub 5} such as Zn{sub 1.5}A{sub 10.5}Q{sub 5}, Zn{sub 1}Al{sub 1}Q{sub 5}, Zn{sub 0.5}Al{sub 1.5}Q{sub 5} organic phosphors were prepared via simple cost effective co-precipitation method. The FTIR, SEM, photoluminescence analysis of the prepared phosphors were reported. ZnQ{sub 2} and AlQ{sub 3} were also prepared by similar method and their properties were compared with different composition of ZnAlQ{sub 5}. The structural elucidation in the form of stretching frequencies of chemical bonds of the prepared phosphor was carried out using Fourier Transform Infrared Spectroscopy (FTIR). The stretching frequency analysis confirms the formation of prepared phosphor materials. The SEM analysis shows the surface morphological behavior of prepared phosphor materials. Greenish photoluminescence were observed at 505 to 510 nm for the different composition of ZnAlQ{sub 5},in which Zn{sub 1.5}Al{sub 0.5}Q{sub 5} shows maximum luminescence intensity at 505 nm. PL emission of ZnQ{sub 2} was observed at 515 nm, while for AlQ{sub 3} at 520 nm. The blue shift of 10 nm was observed in Zn{sub 1.5}A{sub 10.5}Q{sub 5} due to modification of energy level due to presence of Zn{sup 2+} and Al{sup 3+}. The enhancement in PL intensity was observed in Zn{sub 1.5}A{sub 10.5}Q{sub 5} compared to the other composition due to transfer of energy between Zn{sup 2+} and quinolate complex. Optical properties of the prepared materials were evaluated for possible applications in organic light emitting devices (OLED).

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Effects of Ti doping on the dielectric properties of HfO{sub 2} nanoparticles

We report the effects of Ti doping on the dielectric properties of HfO{sub 2} [Hf{sub 1-x}Ti{sub x}O{sub 2} (x = 0.2-0.8)] nanoparticles at room temperature. The Hf{sub 1-x}Ti{sub x}O{sub 2} nanoparticles were synthesized by a wet chemical process. The structural and morphological properties of the derived samples were analyzed with X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and high resolution transmission electron microscopy (HRTEM). Impedance analysis was performed in pelletized samples in the frequency range of 1 MHz to 1 GHz. The obtained results were analyzed in correlation with microstructure and doping concentration in the derived samples. The average size of the Hf{sub 1-x}Ti{sub x}O{sub 2} nanoparticles is typically in the range of 4-8 nm depending on the processing temperature. The Hf{sub 1−x}Ti{sub x}O{sub 2} nanoparticles show reduction in crystallinity with the increase in Ti doping. The dielectric constants of the derived samples decrease with the increase in frequency. The ac-conductivity in the samples increases with the increase in frequency irrespective of Ti concentration and shows significant drop with the increase in Ti concentration at all frequencies.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Structural and dielectric behavior of Cr{sup 3+} and Gd{sup 3+} substituted Ni-Zn nano ferrites

A series of Gd{sup 3+} doped nano crystalline Ni{sub 0.6}Zn{sub 0.4}Cr{sub 0.5}Gd{sub x}Fe{sub 1.5-x}O{sub 4} (where x=0. 00, 0.02, 0.04, 0.06) were prepared by solution combustion method using oxalyl dehydrazide (ODH) as a fuel. The Structural and dielectric behavior of as synthesized material was characterized through X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR). XRD pattern reveals that the formation of single phase with cubic spinel structure. The average crystallite size and lattice parameter were found to increase with increasing Gd{sup 3+} concentration. The FTIR spectra shows two strong absorption bands at 387 cm{sup −1} and 564 cm{sup −1} both represents tetrahedral and octahedral stretching bonds respectively. The dielectric properties were carried out as a function of frequency and composition with the frequency range 40Hz to 10MHz. All the samples show the collective contribution of n-type and p-type carriers. The permittivity were found to decrease with increasing of Gd{sup 3+} concentration this is due to hopping off electrons and charge transport which is typical characteristic of polar dielectrics. Complex impedance was studied to know the contribution of grains and grain boundary resistance has explained according to the Maxwell Wagener type two layer model.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Synthesis and characterization of a new photoluminescent material (8-hydroxy quinoline) bis (2-2’bipyridine) lanthanum La(Bpy)2q

A new photoluminescence material, (8-hydroxy quinoline) bis (2-2’bipyridine) lanthanum has been synthesized and characterized by different techniques. The prepared material La(Bpy){sub 2}q was characterized for structural, thermal and photoluminescence analysis. Structural analysis of this material was done by Fourier transformed infrared spectroscopy (FTIR) and mass spectroscopy. Thermal analysis of this material was done by thermal gravimetric analysis (TGA) shows the thermal stability up to 190°C.Absorption and emission spectra of the material was measured by UV-visible spectroscopy and photoluminescence spectroscopy. Solution of this material La(Bpy){sub 2}q in ethanol showed absorption peak at 385nm, which may be attributed due to (π – π*) transitions. The photoluminescence spectra of La(Bpy){sub 2}q in ethanol solution showed intense peak at 490 nm.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Fabrication of frequency selective surface for band stop IR-filter

Fabrication and characterization of frequency selective surfaces (FSS) on silicon dioxide/ silicon is reported. Electron beam lithography based techniques are used for the fabrication of periodic slot structure in tungsten layer on silicon dioxide/silicon. The fabrication process consists of growth of SiO{sub 2} on silicon, tungsten deposition, electron beam lithography, and wet etching of tungsten. The optical characterization of the structural pattern was carried out using fourier transform infrared spectroscopy (FTIR). The reflectance spectra clearly show a resonance peak at 9.09 µm in the mid infrared region. This indicates that the patterned surface acts as band stop filter in the mid-infrared region.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Structural and electrical properties of functionalized multiwalled carbon nanotube/epoxy composite

The effect of the functionalization of multiwalled carbon nanotube on the structure and electrical properties of composites was investigated. Samples based on epoxy resin with different weight percentage of MWCNTs were prepared and characterized. The interaction between MWCNT & epoxy resin was noticed by Fourier transform infrared spectroscopy (FTIR). The structure of functionalized multiwalled carbon nanotube (f-MWCNT) reinforced epoxy composite was studied by field emission scanning electron microscope (FESEM). The dispersion of f-MWCNT in epoxy resin was evidenced by high resolution transmission electron microscope (HRTEM). Electrical properties of epoxy/f-MWCNT nanocomposites were measured & the result indicated that the conductivity increased with increasing concentration of f-MWCNTs.

77 NANOSCIENCE AND NANOTECHNOLOGY↗