Synthesis, Characterization of Nano MnO2 and its Adsorption Characteristics Over an Azo Dye

ABSTRACT Nano MnO2 powder was synthesized by low temperature solution combustion method using oxalyl dihydrazide (ODH) fuel. The final product was well characterized by Powder X-ray diffraction (PXRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron microscopy (SEM) for crystallographic purity, phase formation and surface morphology respectively. PXRD results show that pure MnO2 was synthesized at 300 0 C with no other impurities. SEM micrograph shows the product has highly porous structure with large voids, typical of combustion derived material. An adsorption characteristic of the porous MnO2 was studied over direct green dye (DG). The optimum dose of MnO2 for removal of 10 ppm DG azo dye was found to be 0.4 g L -1

Magnetic and Cytotoxicity Properties of La1−xSrxMnO3(0 ≤ x ≤ 0.5) Nanoparticles Prepared by a Simple Thermal Hydro-Decomposition

This study reports the magnetic and cytotoxicity properties of magnetic nanoparticles of La1−xSrxMnO3(LSMO) withx = 0, 0.1, 0.2, 0.3, 0.4, and 0.5 by a simple thermal decomposition method by using acetate salts of La, Sr, and Mn as starting materials in aqueous solution. To obtain the LSMO nanoparticles, thermal decomposition of the precursor was carried out at the temperatures of 600, 700, 800, and 900 °C for 6 h. The synthesized LSMO nanoparticles were characterized by XRD, FT-IR, TEM, and SEM. Structural characterization shows that the prepared particles consist of two phases of LaMnO3(LMO) and LSMO with crystallite sizes ranging from 20 nm to 87 nm. All the prepared samples have a perovskite structure with transformation from cubic to rhombohedral at thermal decomposition temperature higher than 900 °C in LSMO samples ofx ≤ 0.3. Basic magnetic characteristics such as saturated magnetization (MS) and coercive field (HC) were evaluated by vibrating sample magnetometry at room temperature (20 °C). The samples show paramagnetic behavior for all the samples withx = 0 or LMO, and a superparamagnetic behavior for the other samples havingMSvalues of ~20–47 emu/g and theHCvalues of ~10–40 Oe, depending on the crystallite size and thermal decomposition temperature. Cytotoxicity of the synthesized LSMO nanoparticles was also evaluated with NIH 3T3 cells and the result shows that the synthesized nanoparticles were not toxic to the cells as determined from cell viability in response to the liquid extract of LSMO nanoparticles

Transformation of hydrothermally derived nanowire cluster intermediates into CdSiO3 nanobelts

In this communication, we demonstrate that cadmium metasilicate nanobelts could be fabricated via a facile, eco-friendly, low cost hydrothermal treatment in the absence of surfactants and organic additives, followed by calcination. The monoclinic phase formation of the sample is described in detail by powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA) and fourier transform infrared (FT-IR) studies. The field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) measurements of as-formed samples and samples calcined at 600 �C for 3 h indicate that the as-formed CdSiO3 sample consists of entangled nano-wire bundles with diameters ranging from 20 to 80 nm and lengths in the order of several micrometers. The calcined sample consists of nanobelts of slightly increased diameter and increased length compared to the as-formed samples. The selected area electron diffraction (SAED) and high resolution transmission electron microscopy (HRTEM) images reflect the polycrystalline nature of nanobelts. The probable mechanism for the formation of nanobelts is also discussed

Buckling analysis of woven glass epoxy laminated composite plate

Buckling behavior of laminated composite plates subjected to in-plane loads is an important consideration in the preliminary design of aircraft components. The sizing of many structural subcomponents of the aircraft structures is often determined by stability constraints. The objective of the current study is to understand the influence of the length-to-thickness ratio, the aspect ratio, the fiber orientation and the cut-out shapes on the buckling load for the glass epoxy laminated composite plate in clamped-free-clamped-free configuration by FE analysis using MSC Patran/Nastran. Initially, buckling analysis was carried out on aluminum plates, both; experimentally and numerically; for the two different geometric configurations to predict the critical buckling load and the test results were compared with the FEA predictions, to check the validity of the analysis methodology. The same methodology was further followed for analyzing the buckling behavior of the composite plates. The results shows the effect of orientation of fiber, aspect ratio, cut-out shape and length-to-thickness ratio on the buckling of the glass epoxy laminated composite plate

Synthesis,characterization and photoluminescence properties of CaSiO3 :Dy3+ nanophosphors

CaSiO3 : Dy3+ (1-5 mol. %) nanophosphors were synthesized by a simple low-temperature solution combustion method. Powder X-ray diffraction patterns revealed that the phosphors are crystalline and can be indexed to a monoclinic phase. Scanning electron micrographs exhibited faceted plates and angular crystals of different sizes with a porous nature. Photoluminescence properties of the Dy3+-doped CaSiO3 phosphors were observed and analyzed. Emission peaks at 483, 573 and 610 nm corresponding to Dy3+ were assigned as F-4(9/2)-> H-6(15/2), F-4(9/2) -> H-6(13/2) and F-4(9/2) -> H-6(11/2) transitions, respectively, and dominated by the Dy3+ F-4(9/2) -> H-6(13/2) hyperfine transition. Experimental results revealed that the luminescence intensity was affected by both heat treatment and the concentration of Dy3+ (1-5 mol. %) in the CaSiO3 host. Optimal luminescence conditions were achieved when the concentration of Dy3+ was 2 mol. %. UV-visible absorption features an intense band at 240 nm, which corresponds to an O-Si ligand-to-metal charge transfer band in the SiO32- group. The optical energy band gap for the undoped sample was found to be 5.45 eV, whereas in Dy3+-doped phosphors it varies in the range 5.49-5.65 eV. The optical energy gap widens with increase of Dy3+ ion dopant

Effect of Li+-dopant on Photoluminescence of Gd2O3:Eu3+Nanophosphor

Li+-doped Gd2O3:Eu3+ phosphors have been studied as potential red phosphors for application to field emission displays. The Li+-doped and undoped Gd2O3:Eu3+ phosphors were synthesized by low temperature solution combustion method. The enhanced luminescence was regarded as the result of the creation of oxygen vacancies due to the Gd3+ sites occupied by Li+ ions, the alteration of the crystal field surrounding the activator Eu3+ ions owing to the incorporation of Li+ into interstial sites. The result in a remarkable increase on photoluminescence and the strong emission was observed at 612 nm by a factor of 4.1 in comparison with that of undoped sample

Synthesis and characterization of nano CoFe2O4 by low‐temperature combustion synthesis using different fuels

The combustion synthesis has been utilized to prepare nanophased powders of cobalt spinel ferrite using ODH and glycine fuels. The product was characterized by X‐ray diffraction; Fourier transformed spectroscopy, scanning electron microscopy, UV‐Vis absorption etc. The XRD patterns reveal spinal cubic structure. SEM profiles show the product is porous, agglomeration, irregular in shape. The crystallite size was estimated using Scherer’s formula and W‐H plots and show nano in size (13 nm: ODH & 36 nm: Glycine). The UV‐Vis absorption shows at ∼430 nm in both the samples

Synthesis, characterization and photoluminescence properties of CaSiO3: Eu3+ red phosphor

CaSiO3:Eu3+ (1-5 mol%) red emitting phosphors have been synthesized by a low-temperature solution combustion method. The phosphors have been well characterized by powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and optical spectroscopy. PXRD patterns reveal monoclinic CaSiO3 phase can be obtained at 900 degrees C. The SEM micrographs show the crystallites with irregular shape, mostly angular. Upon 254 nm excitation, the phosphor show characteristic fluorescence D-5(0) -> F-7(J) (J = 0, 1, 2, 3, 4) of the Eu3+ ions. The electronic transition located at 614 nm corresponding to D-5(0) -> F-7(2) of Eu3+ ions, which is stronger than the magnetic dipole transition located at 593 nm corresponding to D-5(0) -> F-7(1) of Eu3+ ions. Different pathways involved in emission process have been studied. Concentration quenching has been observed for Eu3+ concentration >4 mol%. UV-visible absorption shows an intense band at 240 nm in undoped and 270 nm in Eu3+ doped CaSiO3 which is attributed to oxygen to silicon (O-Si) ligand-to-metal charge-transfer (LMCT) band in the SiO32- group. The optical energy band gap is widened with increase of Eu3+ ion dopant. (C) 2010 Elsevier B.V. All rights reserved

Thermoluminescence and defect study of MgSiO3 ceramics

Enstatite (MgSiO3) ceramic powders were synthesised by a low-temperature initiated self-propagating, gas-producing solution combustion process. The prepared powders were characterised by powder X-ray diffraction, scanning electron microscopy and Brunauer-Emmer-Teller specific surface area measurements. Defect centres induced by radiation were studied using the techniques of thermoluminescence (TL) and electron spin resonance (ESR). A well-resolved glow with peak at 178 degrees C and a shouldered peak at 120 degrees C were observed. Two defect centres were identified by ESR measurements, which were carried out at room temperature, and these were assigned to an O- ion and F+ centre. The O- ion (hole centre) appears to correlate with the main TL peak at 178 degrees C

Synthesis and characterization of spherical and rod like nanocrystalline Nd2O3 phosphors

Spherical and rod like nanocrystalline Nd2O3 phosphors have been prepared by solution combustion and hydrothermal methods respectively The Powder X-ray diffraction (PXRD) results confirm that hexagonal A-type Nd2O3 has been obtained with calcination at 900 C for 3 h and the lattice parameters have been evaluated by Rietveld refinement Surface morphology of Nd2O3 phosphors show the formation of nanorods in hydrothermal synthesis whereas spherical particles in combustion method TEM results also confirm the same Raman studies show major peaks which are assigned to F-g and combination of A(g) + E-g modes The PL spectrum shows a series of emission bands at similar to 326-373 nm (UV) 421-485 nm (blue) 529-542 nm (green) and 622 nm (red) The UV blue green and red emission in the PL spectrum indicates that Nd2O3 nanocrystals are promising for high performance materials and white light emitting diodes (LEDs) (C) 2010 Elsevier B V All rights reserve