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1.
Phase equilibria established in the PbO - BiVO4 system over the whole component concentration range up to 1000°C have been investigated. A phase diagram has been constructed
using DTA and XRD.
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2.
Meysam Soleymani Ahmad Moheb Ezatolah Joudaki 《Central European Journal of Chemistry》2009,7(4):809-817
Single phase nanocrystalline La0.6Ca0.4MnO3 powder was synthesized by both the usual and a modified citrate gel precursor method, and the effects on the formation of
homogeneous nano-sized powder with a perovskite structure were investigated. In the modified method, single phase La0.6Ca0.4MnO3 powder with an average particle size of 17.2 nm was obtained when the powder was pyrolyzed at 520°C for 2 h. Its specific
surface area was 40.7 m2 g−1, about 4-fold larger than that of powder made by the usual citrate gel method.
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3.
The effect of calcium substitution on the afterglow of tetrastrontium aluminate phosphors (Sr4Al14O25:Eu2+, Dy3+) was investigated. A series of (Sr1-xCax)O⊎nAl2O3:Eu2+(1%), Dy3+(0.5%), with variation of calcium content (x = 0 − 1), were synthesized by a high temperature solid state reaction in a reducing
atmosphere. The photoluminescence, persistent luminescence (afterglow), and lumen equivalents of these materials were studied
and compared. It turned out that the afterglow properties of the phosphors were strongly dependent on the Sr/Ca ratio. As
the Ca content increased, a phase transition and blue shift in emission spectra were observed.
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4.
The triplet excited state properties and photosensitization mechanisms of indigo were investigated based on density functional
theory calculations. The solvent effects on the photosensitization mechanisms of indigo have also been considered. The thermodynamic
feasibility of the possible 1O2 and O2·−-photogeneration pathways by triplet excited state indigo in different solvents was explored, in order to gain some deeper
insights into the photosensitization characters of the dye.
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5.
Giedre Nenartaviciene Ramunas Skaudzius Rimantas Raudonis Aivaras Kareiva 《Central European Journal of Chemistry》2009,7(3):362-368
The aqueous sol-gel synthesis technique for the preparation of (Pb,Sr)Sr2(Y,Ca)Cu2O7±x (Pb-1212) and (Pb2,Cu)Sr2(Y,Ca)Cu2O8±x (Pb-3212) superconductors using two different complexing agents, namely 1,2-ethanediol and tartaric acid was studied. The
phase transformations, composition and micro-structural features in the polycrystalline samples were studied by powder X-ray
diffraction analysis (XRD), infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). XRD analysis of the ceramic
samples obtained by calcination of Pb-Sr-Y-Ca-Cu-O acetate-glycolate precursor gels in air, for 10 hours at 800°C and at 825°C,
showed the presence of homogeneous Pb-1212 and Pb-3212 crystallites as major phases. The XRD patterns of the ceramics obtained
from Pb-Sr-Y-Ca-Cu-O acetate-tartrate precursor gels, however, showed multiphasic character. The critical temperature of superconductivity
(TC (onset)) observed by resistivity measurements were found to be 91 K and 75 K for Pb-1212 and Pb-3212 samples, respectively.
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6.
Yordanka Y. Ivanova Tsvetelina I. Gerganova M. Helena V. Fernandes Isabel M. Miranda Salvado 《Central European Journal of Chemistry》2009,7(1):42-46
Nanostructured hybrid materials containing Al2O3 were synthesized via a sol-gel method through hydrolysis and co-condensation reactions using trimethylsilyl isocyanate (TMSI) as a new silica
source in the presence of tetramethoxysilane (TMOS) and three different quantities (10, 20 and 30 wt.%) of aluminum sec-butoxide
(Al(OBusec)3 as a modifying agent. The xerogel nanostructured materials are pyrolyzed in nitrogen atmosphere in the temperature range
from 400°C to 1100°C. The transformation of the xerogel hybrid networks into Al-Si oxycarbonitride materials has been investigated
by XRD, FTIR, SEM, AFM, and 29Si MAS-NMR. To the best of our knowledge, the work reported here is the first synthesis of porous di-urethanesils modified
with aluminum and one of the few examples of alumosilica oxycarbonitride materials
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7.
Anna Blonska-Tabero 《Central European Journal of Chemistry》2009,7(2):252-258
Phase diagrams in the subsolidus area of the systems FeVO4 - CdO and FeVO4 - Cd2V2O7 have been deduced using the results of XRD and DTA analyses. On the basis of these diagrams and some additional verifying
research, a projection of the subsolidus area of the CdO - V2O5 - Fe2O3 system onto the plane that comprises the components’ concentration triangle has been presented. The H-type phase is the only
phase formed in this system. It co-exists at equilibrium with other phases in six subsidiary subsystems.
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8.
Ghasem Rezanejade Bardajee Farnaz Jafarpour Hamid Samareh Afsari 《Central European Journal of Chemistry》2010,8(2):370-374
In this report, a rapid, efficient and environmental friendly synthesis of 3-carboxycoumarins under ultrasound irradiation
in water media is described. The Knoevenagel condensation of Meldrum’s acid with substituted benzaldehydes in the presence
of zirconium oxide chloride (ZrOCl2·8H2O) and ultrasonic irradiation in water gave the corresponding 3-carboxycoumarins in good to excellent yields.
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9.
Abdülhadi Baykal Yüksel Köseoğlu Mehmet Şenel 《Central European Journal of Chemistry》2007,5(1):169-176
Heating hydrous manganese (II) hydroxide gel at 85 °C for 12 hours produces Mn3O4 nanoparticles. They were characterized by X-ray powder diffraction (XRD) and infrared spectroscopy (FTIR). The particle size
estimated from the SEM and X-ray peak broadening is approximately 32 nm, showing them to be nanocrystalline. EPR measurements
confirm a typical Mn2+signal with a highly resolved hyperfine structure.
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10.
A novel hydroxyamino phosphane was synthesised through the reaction of 2-imidazolidinone with ClPPh2 and subsequently reaction
of the resulting bisphosphino derivative with the Grignard reagent BrMgC5H11. The interaction of the pentyl substituent with one of the two phosphino groups and the structure in solution is shown by
multinuclear NMR-spectroscopy..
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11.
Zehra Durmus Hüseyin Kavas Abdulhadi Baykal Muhammet S. Toprak 《Central European Journal of Chemistry》2009,7(3):555-559
A novel environmental friendly, room temperature route using an ionic liquid 1-n-butyl-3-methylimidazolium hydroxide ([BMIM]OH)
for the synthesis of Mn3O4 nanoparticles is presented. The product was characterized using Fourier transform infrared spectroscopy, X-ray powder diffraction,
and transmission electron microscopy. Phase purity was confirmed by XRD, and X-ray line profile fitting determined a crystallite
size of 42 ± 11 nm. TEM analysis revealed various morphologies. EPR measurements have indicated the existence of long-range
interactions, due to the wide range of particle sizes and morphologies observed.
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12.
Ágnes Zsigmond Suhsen Undrala Ferenc Notheisz Áron Szöllősy József Bakos 《Central European Journal of Chemistry》2008,6(4):549-554
Using a modified Augustine’s method variously substituted Rh complexes were anchored on Al2O3 support. The prepared catalysts were characterized by spectroscopic methods and were applied in the hydrogenation of several
acetophenone derivatives (p-CF3-acetophenone, acetophenone, p-NH2-acetophenone). Enantioselective C=O hydrogenations were observed with reasonable activity and selectivity on all heterogenized
complexes, e.e. up to 80%. At the same time the immobilized samples showed the advantages of the heterogeneous systems: easy handling and
recyclability.
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13.
Lachezar Radev Vladimir Hristov Irena Michailova Bisserka Samuneva 《Central European Journal of Chemistry》2009,7(3):317-321
In this work we present experimental results about synthesis, structure evolution and in vitro bioactivity of new calcium phosphate silicate/wollastonite (CPS/W) glass-ceramics. The samples obtained were synthesized
via polystep sol-gel process with different Ca/P+Si molar ratio (R). The structure of the materials obtained was studied by
XRD, FTIR spectroscopy and SEM. XRD showed the presence of Ca15(PO4)2(SiO4)6, β-CaSiO3 and α-CaSiO3 for the sample with R=1.89 after thermal treatment at 1200°C/2h. The XRD results are in good agreement with FTIR analysis.
SEM denotes that apatite formation can be observed after soaking in simulated body fluid (SBF).
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14.
Lachezar Radev Vladimir Hristov Irena Michailova Bisserka Samuneva 《Central European Journal of Chemistry》2009,7(3):322-327
Ceramics, with basic composition based on the CaO-SiO2-P2O5-MgO system with different Ca+ Mg/P+Si molar ratio (R), were prepared via polystep sol-gel technique. The structure of the
obtained ceramic materials has been studied by XRD, FTIR spectroscopy, and SEM. X-ray diffraction showed the presence of akermanite
and HA for the sample with R = 1.68 and Mg substituted β-TCP and silicocarnotite for the sample with R = 2.16, after thermal
treatment at 1200°C/2 h. The obtained results are in good agreement with FTIR. In vitro test for bioactivity in static condition
proved that the carbonate containing hydroxyapatite (CO3HA) can be formed on the surface of the synthesized samples. CO3HA consisted of both A- and B-type CO32− ions. SEM micrographs depicted different forms of HA particles, precipitated on the surface after soaking in 1.5 simulated
body fluid (SBF).
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15.
Nadezhda Rangelova Lachezar Radev Sanchi Nenkova Isabel M. Miranda Salvado Maria H. Vas Fernandes Michael Herzog 《Central European Journal of Chemistry》2011,9(1):112-118
Methylcellulose (MC) / SiO2 organic / inorganic hybrid materials have been prepared from MC and methyltriethoxysilane or ethyltrimethoxysilane, and characterized
by XRD, FTIR and AFM. XRD showed peak shifts. FTIR shows intermolecular hydrogen bonding between MC and SiO2. AFM depicts surface roughness which depends on the silica precursor and MC content.
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16.
The reaction mechanism between AlX and HX (X = Br, Cl, and F) have been characterized in detail using DFT as well as the ab initio method. The reaction yielding AlX3 and molecular hydrogen was calculated to be highly exothermic. The present calculations also show that the possible routes
to the trihalides species start more favorable with the primary insertion product AlX2H than with the biadduct AlX(HX)2 one.
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17.
Petr Bělina Petra Šulcová Miroslav Trojan Pavel Mazurek 《Central European Journal of Chemistry》2007,5(3):706-714
New binary lanthanum-aluminum triphosphates were synthesized by thermal-condensation method from H3PO4, La2O3 and Al(OH)3. These pigments could be potentially used as special inorganic pigments; their corrosion-inhibition properties were widely
studied. Synthesis conditions were determined on the basis of DTA and TG measurements. The products were also characterized
by X-ray diffraction analysis. Physical properties — density by pycnometric method, particle size distribution, oil number
and critical pigment volume concentration (CPVC), pH and specific conductivity of their aqueous extracts were also determined.
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18.
Abbas Tarassoli Tahereh Sedaghat Hamid-Reza Goudarzi 《Central European Journal of Chemistry》2009,7(1):130-133
Aminolysis of N3P3CI6 by an oxodiamine, bis-(2-ortho-aminophenoxyethyl) ether, has been carried out under various experimental conditions and new
products with different architectures have been obtained. The reaction in diethyl ether when using a Na2CO3-water interface process gives the mono-BINO as major product. Reaction on Al2O3/KOH leads to the spirocyclic compound, while, when the reaction is carried out in toluene in the presence of NEt3, a mixture of mono- and di-BINO products are obtained. These new products have been characterized by IR, 1H and 31P NMR spectroscopy.
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19.
Carla Ferragina Romolo Di Rocco Pasquale Patrono Lucantonio Petrilli 《Central European Journal of Chemistry》2009,7(1):31-34
Layered compounds with CdS particles supported on the ion-exchanger, γ-titanium dihydrogen phosphate, were prepared by the
stepwise reaction of the ion-exchanger and cadmium solution, followed by reaction with H2S gas. The CdS content on the ion-exchanger is dependent on the timeframe of the H2S gas flow. The materials obtained were layered, as shown by the X-ray measurements that exhibit both precursor and CdS diffraction
peaks. The thermal treatment of the material obtained gives evidence of its stability (≤ 320°C) before the CdS decomposition,
which occurs in a single step.
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20.
Mónica Díaz-Pérez Manuel Aboal-Somoza Pilar Bermejo-Barrera Adela Bermejo-Barrera 《Central European Journal of Chemistry》2008,6(4):520-525
Preliminary results of development of a direct and fast method of determination of antimony in samples of tap water using
GFAAS are presented. The found levels of antimony were lower than permitted for human consumption. A mixture of Pd and Mg(NO3)2 (concentrations in the injected solution: 8.6 μg mL−1 and 5.8 μg mL−1 respectively) was used as the chemical modifier. The pyrolysis and atomization temperatures were 1000 and 1700°C, respectively
and the mean analytical recovery 98.2%.
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