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Batch removal of Pb (ΙΙ) ions from aqueous medium using gamma-Al2O3 nanoparticles/ethyl cellulose adsorbent fabricated via electrospinning method: An equilibrium isotherm and characterization study

. Chem . 54 (1982) 2201–2218. DOI: 10.1351/pac198557040603. 49. Liu, D., Que, G.H., Wang, Z.X., Yan, Z.F. In situ FT-IR study of CO and H 2 adsorption on a Pt/Al2O 3 catalyst, Catal. Today. 68 (2001) 155–160. DOI: 10.1016/S0920-5861(01)00306-6. 50. Alvar, E.N., Rezaei, M. & Alvar, H.N. Synthesis of mesoporous nanocrystalline MgAl 2 O 4 spinel via surfactant assisted precipitation route. Powder Technol. 198 (2010) 275–278. DOI: 10.1016/j.powtec.2009.11.019. 51. Kao, L.H. & Hsu, T.C. Silica template synthesis of ordered mesoporous carbon thick films

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Synthesis and phosphorescent properties of the copolymers of N-vinylcarbazole, methyl methacrylate and iridium complex

Abstract

The copolymers containing carbazole unit and iridium complexes, such as (Ir(bpy)2Cl, Ir(mbpy)2Cl and Ir(Brbpy)2Cl, were synthesized via radical copolymerization of N-vinylcarbazole, methyl methacrylate and iridium complex. The synthesized copolymers were characterized by FT-IR, UV-Vis absorption spectroscopy and photoluminescence (PL) spectroscopy, respectively. According to the results, the copolymers (Ir(Brbpy)2Cl/PVK and Ir(mbpy)2Cl/PVK) exhibit yellow phosphorescence with an emission peak at around 553 nm under UV-visible light in the solid state. The results also reveal almost complete energy transfer from the host carbazole segments to the guest Ir complex in the copolymer film when the Ir content reaches 1.0 wt.%. The synthesized copolymers are good candidates as blue or yellow phosphorescent materials for PLED applications.

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Investigation on room temperature photoluminescence of pure and aluminum doped zinc oxide nanoparticles

Abstract

Pure and aluminum doped zinc oxide nanoparticles were prepared by soft chemical method. The prepared nanoparticles were characterized by XRD, SEM-EDAX, UV-Vis, PL and FT-IR studies. XRD patterns revealed that the nanoparticles were crystallized in hexagonal wurtzite structure with an average particle size of 19 nm to 26 nm. The surface morphology was explored using SEM micrographs. The incorporation of aluminum was confirmed by EDAX and FT-IR studies. The band gaps of the particles were found from 3.48 eV to 3.53 eV through UV-Vis spectral studies. The defect related mechanism was investigated using PL measurements. The chemical functional groups in FT-IR spectra proved the formation of pure and aluminum doped zinc oxide nanoparticles.

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Thermal behaviour of light lanthanide(III) complexes with 2,3-pyridinedicarboxylic acid

Abstract

The lanthanide(III) complexes with 2,3-pyridinedicarboxylate ligand (PDC) were obtained as crystalline compounds from the water solutions. These compounds form the series of Ln2(PDC)3 ・ nH2O. All compounds are stable in air and insoluble in both water and common organic solvents. The hydrated complexes have been characterized by elemental analysis, thermal analysis (TG/DSC/DTA, and TG−FT-IR), FT-IR spectroscopy and X-ray analysis. 2,3-pyridinedicarboxylates of lanthanides(III) are stable in air below 313−323 K. Upon heating, hydrated complexes lose crystallization and lattice water in two steps. The values of dehydration enthalpy complexes are calculated from the DSC curves. The anhydrous compounds are stable at the temperature from 473 K to about 623 K and when heated they decompose to lanthanide oxides. Thermal and spectroscopic studies are essential for further studies and classification of compounds as MOF-like structures.

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Effect of fabrication technique on the crystalline phase and electrical properties of PVDF films

Abstract

The effect of different fabrication techniques on the formation of electroactive β-phase polyvinylidene fluoride (PVDF) has been investigated. Films with varying concentration of PVDF and solvent - dimethyl formamide (DMF) were synthesized by tape casting and solvent casting techniques. The piezoelectric β-phase as well as non polar β-phase were observed for both the tape cast and solvent cast films from X-ray diffraction (XRD) micrographs and Fourier transform infra-red spectroscopy (FT-IR) spectra. A maximum percentage (80 %) of β-phase was obtained from FT-IR analysis for a solvent cast PVDF film. The surface morphology of the PVDF films was analyzed by FESEM imaging. The dielectric properties as a function of temperature and frequency and the ferroelectric hysteresis loop as a function of voltage were measured. An enhancement in the value of the dielectric constant and polarization was obtained in solvent cast films.

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Synthesis and characterization of indium tin oxide nanoparticles via reflux method

Abstract

Synthesis of indium tin oxide (ITO) nanoparticles by reflux method without chlorine contamination at different pHs, temperatures, solvents and concentrations has been studied. Indium chloride, tin chloride, water, ethanol and Triton X-100 were used as starting materials. Structure, size, surface morphology and transparency of indium tin oxide nanoparticles were studied by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and UV-Vis spectrophotometry. XRD patterns showed that 400 °C is the lowest temperature for synthesis of ITO nanoparticles because metal hydroxide does not transform to metal oxide in lower temperature. FT-IR results showed the transformation of hydroxyl groups to oxide. SEM images showed that pH is the most important factor affecting the nanoparticles size. The smallest nanoparticles (40 nm) were obtained at pH = 8.8. The size of crystallites was decreased by lowering of concentration (0.025 M).

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Synthesis of maghemite (γ-Fe2O3) nanoparticles by thermal-decomposition of magnetite (Fe3O4) nanoparticles

Abstract

In this research work, we prepared γ-Fe2O3 nanoparticles by thermal-decomposition of Fe3O4. The Fe3O4 nanoparticles were synthesized via co-precipitation method at room temperature. This simple, soft and cheap method is suitable for preparation of iron oxide nanoparticles (γ-Fe2O3; Fe3O4). The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer and differential scanning calorimeter (DSC). The XRD and FT-IR results indicated the formation of γ-Fe2O3 and Fe3O4 nanoparticles. The TEM images showed that the γ-Fe2O3 and Fe3O4 were spherical, and their size was 18 and 22 nm respectively. Magnetic properties have been measured by VSM at room temperature. Hysteresis loops showed that the γ-Fe2O3 and Fe3O4 nanoparticles were super-paramagnetic.

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Evaluation of the acid properties of aluminossilicate MCM-22 material synthesized under static conditions

Abstract

The hydrothermal synthesis of MCM-22 zeolite was carried out using silica, sodium aluminate and hexamethyleneimine, under static conditions at 150 °C for a period of 10 days, followed by washing with deionized water, drying overnight and calcination at 650 °C. The obtained material was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). The XRD analysis evidenced that MCM-22 presented a well defined MWW structure. The FT-IR spectrum confirmed the efficiency of the hexamethyleneimine as an organic template used to direct the structure of the MCM-22 zeolite under static conditions. The SEM image indicated that the particles are spherical in shape, with a diameter of ca. 10 μm. The acid properties of the MCM-22 zeolite, as determined by n-buthylamine adsorption, were investigated in the temperature ranges of 105 to 300 °C and 300 to 525 °C, relative to medium and strong acid sites, respectively.

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Evaluation of the biomedical properties of hydroxyapatite obtained from bone waste

Evaluation of the biomedical properties of hydroxyapatite obtained from bone waste

The method of obtaining hydroxyapatite by thermal treatment of deproteinised and defatted bone pulp called bone sludge was presented. The products of the calcining process were characterized with X-ray diffraction (XRD) and Fourier transformed infrared spectroscopy (FT-IR). The calcium content was determined with titration, whereas the contents of total phosphorus - with a spectrophotomertric method. X-ray investigations confirmed that hydroxyapatite was the main component of the calcining products in the calcining process. The FT-IR spectra confirmed that all organic substances were removed during the calcining process. On the basis of the research into physiological liquids the propensity to resorption of hydroxyapatite bioceramic was evaluated.

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Study of damage extent to glass fibre in glass-fibre fabric reinforcement during exposure simulating concrete pore solution

Abstract

The paper evaluates extent of corrosion damage to composite glass-fibre fabric reinforcement in environment simulating concrete pore solutions (pH 12.6, 13.0, 13.5) and carbonated concrete contaminated with chlorides (pH 8.1 + Cl-) using the FT-IR and SEM/EDS techniques. Also, the effect of corrosion damage on tensile strength of segmented glass fibre as well as the presence of specific protective organic coating on glass fibre were studied. The results demonstrate local corrosion damage of samples at pH 13.5 and on the other hand high stability in environment simulating carbonated concrete and carbonated concrete contaminated with chlorides. The study also suggests unevenness of organic coating with occurrence of localized porosity which is related to aforementioned corrosion damage. Corrosion damage in FT-IR spectra manifests by changes in peaks signalling hydrolysis of protective organic coating and occurrence of peaks suggesting presence of Ca2+ rich corrosion products.

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