Various Characterization Techniques (various + characterization_techniques)

Distribution by Scientific Domains


Selected Abstracts


Synthesis and properties of mesogen-jacketed liquid crystalline polymers containing bistolane mesogen

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 21 2010
Zhen Lin Zhang
Abstract On the basis of the concept of mesogen-jacketed liquid crystalline polymers, a series of new methacrylate monomers, (2,5- bis[2-(4,-alkoxyphenyl) ethynyl] benzyl methacrylate (MACn, n = 4, 6, 8, 10, and 12) and 2,5- bis[2-(6,-decanoxynaphthyl) ethynyl] benzyl methacrylate (MANC10), and their polymers, PMACn (n = 4, 6, 8, 10, and 12) and PMANC10 were synthesized. The bistolane mesogen with large ,-electron conjugation were side-attached to the polymer backbone via short linkages. Various characterization techniques such as differential scanning calorimetry, wide-angle X-ray diffraction, and polarized light microscopy were used to study their mesomorphic phase behavior. The polymer PMACn with shorter flexible substituents (n = 4) forms the columnar nematic (,N) phase, but other polymers with longer flexible tails (n = 6, 8, 10, and 12) can develop into a smetic A (SA) phase instead of a ,N phase. The PMANC10 containing naphthyl can also form a well-defined SA phase. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 [source]


Effect of pH on the Carbonate Incorporation into the Hydroxyapatite Prepared by an Oxidative Decomposition of Calcium,EDTA Chelate

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2008
Yusuf Yusufoglu
In this study, the carbonate incorporation into the hydroxyapatite (HAp) lattice under various pH conditions was investigated. Crystalline-sodium and carbonate-containing calcium HAp (NaCO3HAp) powders were prepared using an oxidative decomposition of calcium,EDTA chelates in a sodium phosphate solution with hydrogen peroxide. The powders obtained were characterized by X-ray diffraction, infrared spectroscopy, thermal gravimetric analysis, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and elemental analysis. Depending on pH, spherical particles approximately 3.5 ,m in diameter or hexagonal prismatic particles measuring 3,9 ,m in length were obtained. Various characterization techniques showed that the precipitates were a single-phase NaCO3HAp. The carbonate content and the lattice parameters of the HAp were a function of solution pH. Maximum carbonate incorporated into the HAp lattice was at pH=10, corresponding to lattice parameters of a=0.93880 nm and c=0.69070 nm. Furthermore, spectroscopic analyses indicate that the as-prepared samples are B-type carbonated HAp, in which carbonate ions occupy the phosphate sites. After heat treatment at 965°C, most of the carbonate is removed from the HAp lattice. [source]


Microwave-Assisted Combustion Synthesis of Tantalum Nitride in a Fluidized Bed

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2003
Akhil Jain
Combustion synthesis experiments in a fluidized bed have been conducted using nitrogen as the fluidizing gas for the formation of transition-metal nitrides that are potential replacements for traditional hydrodenitrogenation and hydrodesulfurization catalysts. The microwave-assisted ignition of reaction has been investigated for its potential to produce nitride overlayers on two different sizes of tantalum particle substrates. Various characterization techniques,X-ray diffractometry, energy dispersive spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy,have been used to study the presence of nitride overlayers. The results indicate that microwave assistance can permit controlled formation of tantalum nitride (Ta2N) overlayers. [source]


Preparation and characterization of ultrafine electrospun polyacrylonitrile fibers and their subsequent pyrolysis to carbon fibers

POLYMER INTERNATIONAL, Issue 8 2006
Juthawan Sutasinpromprae
Abstract The present contribution reports the fabrication and characterization of ultrafine polyacrylonitrile (PAN) fibers by electrospinning and further development of the as-spun PAN fibers into ultrafine carbon fibers. The effects of solution conditions (i.e., solution concentration, viscosity, conductivity, and surface tension) and process parameters (i.e., applied electrostatic field strength, emitting electrode polarity, nozzle diameter, and take-up speed of a rotating-drum collector) on morphological appearance and average diameter of the as-spun PAN fibers were investigated by optical scanning (OS) and scanning electron microscopy (SEM). The concentration, and hence the viscosity, of the spinning solutions significantly affected the morphology and diameters of the as-spun PAN fibers. The applied electrostatic field strength and nozzle diameter slightly affected the diameters of the as-spun fibers, while the emitting electrode polarity did not show any influence over the morphology and size of the as-spun fibers. Utilization of the rotating-drum collector enhanced the alignment of the as-spun fibers. Within the investigated concentration range, the average diameter of the fibers ranged between 80 and 725 nm. Finally, heat treatment of the as-spun fibers with their average diameter of about 450 nm was carried out at 230 and 1000 °C, respectively. Various characterization techniques revealed successful conversion into carbon fibers with an average diameter of about 250 nm. Copyright © 2006 Society of Chemical Industry [source]


Vibrational, optical and microhardness studies of trimethoprim DL -malate

CRYSTAL RESEARCH AND TECHNOLOGY, Issue 12 2009
S. Franklin
Abstract Trimethoprim malate, an organic crystal, has been synthesized using slow evaporation method from its aqueous solution. Structural, optical and the mechanical properties of the grown crystal have been investigated by various characterization techniques which include FTIR spectra, single crystal XRD, UV-Vis spectra and Vickers microhardness testing. The structure of the compound predicted by analysing the recorded FTIR spectrum compliments the structure determined using single crystal X-ray diffraction. Single crystal X-ray diffraction study reveals that the crystals are monoclinic [P21/c, a=12.9850 Å, b=9.3038 Å, c=15.6815 Å and ,=111.065°]. The UV-Vis spectrum exhibits maximum transparency (98%) for a wide range suggesting the suitability of the title compound for optical applications. The optical constants have been calculated and illustrated graphically. Microhardness tests have been performed on the cystal under study and the Vicker hardness number has been calculated. The work hardening coefficient is found to be 2.85 which suggest that the crystal belongs to the family of soft materials. (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Transesterification of dimethyl oxalate with phenol over TiO2/SiO2: Catalyst screening and reaction optimization

AICHE JOURNAL, Issue 12 2008
Xia Yang
Abstract Physicochemical properties of silica-supported titanium oxide catalysts as well as their performances for transesterification of dimethyl oxalate (DMO) with phenol to methyl phenyl oxalate (MPO) and diphenyl oxalate (DPO) have been investigated systematically. Various wt % of TiO2 were loaded on SiO2 by a two-step wet impregnation method. The surface properties of TiO2/SiO2 catalysts were explored by various characterization techniques (BET, SEM, ICP, XPS, XRD, FTIR of pyridine adsorption, and NH3 -TPD). Catalytic performances of TiO2/SiO2 catalysts were found to be strongly dependent on TiO2 dispersion and surface acidity. Monolayer dispersion capacity of TiO2 on silica was estimated to be about 4.0 TiO2 molecules per nm2 (SiO2) and no crystalline TiO2 was detected at TiO2 loading less than 12 wt %. FTIR and TPD analysis suggested that weak Lewis acid sites on the surface of TiO2/SiO2 were responsible for their unique selectivity to the target products, MPO and DPO. An optimization of reaction conditions for the transesterification of DMO with phenol was performed over 12 wt % TiO2/SiO2 calcined at 550°C. In addition, we studied the disproportionation reaction from MPO to DPO via a catalytic distillation process, which is highly efficient to promote formation of the desired DPO. © 2008 American Institute of Chemical Engineers AIChE J, 2008 [source]


GaN/AlN super-lattice structures on vicinal sapphire (0001) substrates grown by rf-MBE

PHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 7 2005
X.Q. Shen
Abstract GaN/AlN super-lattice structures (SLs) grown on the vicinal sapphire (0001) substrates by rf-MBE are investigated using various characterization techniques. The satellite XRD diffraction peaks originating from the SLs are clearly observed, which indicate an abrupt interface and good periodicity of the SLs. Cross-sectional TEM observations show differnet features of SLs grown on the various vicinal substrates, depending on whether macro-steps form on the surface or not. DUV-Raman measurements show unique spectra from the SLs, which are different from the usual GaN and AlN films. The usage of a proper vicinal substrate angle shows a great merit to obtain high quality GaN/AlN SLs. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Experimental and Theoretical Investigation of the Room-Temperature Photoluminescence of Amorphized Pb(Zr,Ti)O3

CHEMPHYSCHEM, Issue 8 2005
Emmanuelle Orhan Dr.
Abstract Ultrafine PbZr0.20Ti0.80O3 was amorphized through high-energy mechanical milling. The structural evolution through the amorphization process was accompanied by various characterization techniques, such as X-ray diffraction, Fourier-transformed IR spectroscopy (FTIR), high-resolution transmission electron microscopy (HR-TEM), and Raman spectroscopy. A strong photoluminescence was measured at room temperature for amorphized PbZr0.20Ti0.80O3, and interpreted by means of high-level quantum mechanical calculations in the density functional theory framework. Three periodic models were used to represent the crystalline and amorphized PbZr0.20Ti0.80O3, and they allowed the calculation of electronic properties that are consistent with the experimental data and that explain the appearance of photoluminescence. [source]