Preparation and properties of nanocrystal SmBO_3 by nitrate-citrate sol-gel combustion method

Nanocrystal SmBO3 powders were synthesized by nitrate-citrate sol-gel combustion method. The phase evolution, morphologies and absorbency of the synthesized powders were characterized by X-ray diffraction （XRD）, Field emission scanning electronic microscope （FESEM）, Fourier transform infrared spectroscopy （FFIR） and UV-3101PC spectrophotometer （UVPC）, respectively. XRD and FESEM results showed that pure SmBO3 phase was obtained at 750 ℃, with an average original particle size of about 100 nm. FTIR showed that there were apparently concentrated absorbent peaks between 500 and 1400 cm^-1. Moreover, the reflectivity of the powders apparently decreased at the wavelength between 1.05 and 1.15 μm. Therefore, SmBO3 might be a kind of absorbent material for infrared laser.

Characterization and luminescence of Eu/Sm-coactivated CaYAl_3O_7 phosphor synthesized by using a combustion method

A novel red-emitting phosphor, CaYA1307： Eu^3＋, Sm^3＋, is synthesized by a combustion method at a low temperature （850 ℃）, and the single phase of CaYA1307 is confirmed by powder X-ray diffraction measurements. The photoluminescence property results reveal that the red emission intensity of Eu^3＋ is strongly dependent on the Sm^3＋ concentration. Only the Eu^3＋ luminescence is detected in the Eu^3＋-Sm^3＋ co-doped CaYA1307 phosphor with 393 nm excitation. However, under the characteristic excitation （402 nm） of Sm^3＋, not only the Sm^3＋ emission but also the Eu^3＋ emission are observed. A possible mechanism of the energy transfer between Sm^3＋ and Eu3＋ is investigated in detail.

Nanostructured Yb:GGG polycrystalline powders via gel combustion method

Gadolinium gallium gamet （GGG） nanopowders doped with ytterbium ions （Yb：GGG） were synthesized with citric acid as a fuel via gel combustion method. The optimized conditions for preparing yb^3＋：Gd3Ga5O12 nanopowders were discussed. The heat behavior, structure and morphology of powders were analyzed with thermal analysis （TG-DTA）, X-ray diffraction （XRD）, infrared spectra OR） and transmission electron microscope （TEM）. TG-DTA analysis revealed that the weight loss of the precursor occured below 800 ℃ and its crystallization temperature was 830.6℃. XRD and IR analysis showed that the precursor converted directly into pure GGG at a relatively lower temperature （900 ℃） without any other intermediate phase. The lattice constant was 1.2377 calculated by extrapolation method. TEM results indicated that the spherical powders showed good dispersity and had a relatively narrow size distribution with average particle size of approximately 40-50 ran, which was favorable for good sinterability of Yb：GGG laser ceramic.

Structural and Optical Properties of Cu2+ + Ce3+ Co-Doped ZnO by Solution Combustion Method

In this work, ZnO, Ce3+ doped ZnO (ZnO/Ce3+) and Cu2+ + Ce3+ co-doped ZnO (ZnO/Cu2+ + Ce3+ ) solid solutions powders were synthesized by a solution combustion method maintaining the Ce3+ ion concentration constant in 3%Wt while the Cu2+ ion concentration was varied in 1, 2, 3, 10 and 20%Wt. After its synthesis, all the samples were annealed at 900?C by 24 h. The ZnO, ZnO/Ce3+ and ZnO/Cu2+ + Ce3+ powders were structurally characterized using X-ray diffraction (XRD) technique, and the XRD patterns showed that for pure ZnO, Cu2+ undoped ZnO/Ce3+ and ZnO/Ce3+ doped with the Cu2+ ion, the three samples exhibited the hexagonal wurtzite ZnO crystalline structure. However, the morphology and particle size of both samples were observed by means of a scanning electron microscopy (SEM);from SEM image, it is observed that the crystallites of both samples are agglomerated forming bigger amorphous particles with an approximate average size of 1 μm. In addition, the photoluminescence of the ZnO, Ce3+ doped ZnO and Cu2+ + Ce3+ doped ZnO samples was measurement under an illumination of 209 nm wavelength (UV region): for the ZnO/Ce3+ sample, your emission spectrum is in the visible region from blue color until red color;the UV band of the ZnO is suppressed. The multicolor emission visible is attributed to the Ce3+ ion photoluminescence, while for the ZnO/Cu2+ + Ce3+, its emission PL spectrum is quenching by the Cu2+ ion, present in the ZnO crystalline.

Effect of Bi3+ Ion Substitution on Magnetic Properties of Cobalt Nano Ferrites Prepared by Sol-Gel Combustion Method

Bismuth substituted cobalt nano ferrites with the chemical composition Co Bix Fe2-x O4 (x = 0.00, 0.05, 0.10, 0.15, 0.20 & 0.25) were prepared by sol-gel combustion method. The phase identification of prepared samples is characterised by X-ray powder diffraction (XRD) method, which confirms the formation of a single phase fcc spinal structure. The mean crystallite sizes of all prepared samples were obtained within the range of 21 (±5) nm. Transmission Electron Microscopy (TEM) images also confirmed the crystallite size of all the synthesised samples was in nano range. With the effect of Bi3+ ion substitution on spinal cobalt ferrite, the magnetic properties were investigated by using Vibration Sample Magnetometer (VSM). The obtained hysteresis (M-H) curves of all the samples were analysed under the applied magnetic field of range ± 10 K Oe at 300 K. The magnetic properties such as saturation magnetisation (Ms), remnant magnetization (Mr) and coercivity (Hc) values are tabulated, which show a decrease in trend as the bismuth ion concentration increases. This is due to the addition of Bi3+ ion in the place of Fe3+ ion (octahedral site) and hence the Bi3+-Fe3+ ion interaction predominates as compared with the Fe2+-Fe3+ ion interaction. The data obtained from magnetic studies, the variation among the magnetic properties have been investigated for all the prepared samples.

Effect of co-doped metal caions on the properties of Y_2O_3:Eu^(3+) phosphors synthesized by gel-combustion method

Y2O3：Eu3＋ phosphors co-doped with different metal cations （Li＋, Na＋, K＋, Mg2＋, Ca2＋） are prepared by the gel- combustion method with Y2O3：Eu3＋, and R（NO3）x （R = Li, Na, K, Mg, Ca） serving as raw materials and glycine as fuel, calcined at 1000 ℃ for 2 h. The synthesized Y203 ：Eu3＋ phosphors doped with different metal cations and doping ratios are characterized by x-ray diffractometry （XRD）, fluorescence and phosphorescent spectrophotometer. The co-doping metal cations are advantageous to the development of Y203：Eu3＋ lattice. All the samples can emit red light peaked at 611 nm under 254-nm excited. The luminescence intensities of co-doping samples are increased because the cations increase the electron transition probability of Eu3＋ from 5D0 level to 7F level. The fluorescence lifetime of Eu3＋ （SD0 --＋7F2） is increased by doping metal cations.

A modified solution combustion method to superfine Gd_2O_3:Eu^(3+) phosphor:preparation,phase transformation and optical properties

Cubic and monoclinic Gd2O3:Eu3+ phosphors in the range of nano-scale and submicron-scale were prepared by a modified solution combustion method.Coexistence of cubic and monoclinic phases was found in the highest luminescent sample synthesized at 600 oC.In relation to commercial sample,the relative luminescence intensity was 49.8%.The shape of emission spectrum of the sample thus changed and the charge-transfer-state band of excitation spectrum slightly shift toward higher energies.With increasing the anneal...

CaTiO_(3)-Sm_(0.9)Nd_(0.1)AlO_(3) ceramics with a moderate dielectric constant and a high quality factor prepared by sol-gel auto combustion method

CaTiO_(3)-LnAlO_(3)(Ln=La,Nd,Sm) is a perovskite-type microwave material system characterized by a moderate dielectric constant εr,a high quality factor Q×f,and a small temperature coefficient of resonant frequency τf,making this system promising for microwave devices.However,its high synthesis temperature and sintering temperature limit its industrial applications.In our work,single phase0.7 CaTiO_(3)-0.3 Sm_(0.9)Nd_(0.1)AlO_(3)(7 CT-3 SNA) was synthesized via the sol-gel auto combustion method using citric acid as fuel at a relatively low temperature.After being calcined at 600℃ for 2 h,wellcrystallized 7 CT-3 SNA powders with 30-50 nm average particle size were achieved,suggesting good sintering activity.The new and narrow order band at about 800 cm^(-1) in the Raman spectra indicates a high ordering degree in the B site of 7 CT-3 SNA solid solution.Compared with the solid-state reaction method and co-precipitation method,the 0.7 CT-0.3 SNA ceramics fabricated by the current method possess a much lower calcination temperature,a similar εr value,and an improved Q × f value.The optimum microwave dielectric properties of εr=43.54,Q×f=54375 GHz,and τf=-6.3 ×10^(-6)/℃ are obtained for the CTSA ceramics derived from the sol-gel auto combustion process.Therefore,the 7 CT-3 SNA ceramics prepared in this study are potential dielectric materials for microwave applications,indicating that the sol-gel auto combustion method is a good alternative strategy for the fabrication of CaTiO_(3)-LnAlO_(3) ceramics.

Characterization and photoluminescence of Lu_2O_3-Eu^(3+) nano-phosphor prepared by modified solution combustion method

Nanoscale Lu2O3：Eu3＋ phosphor was prepared by a modified solution combustion method using urea and acrylamide monomer.The particle sizes and photoluminescent properties of nano-phosphor were closely related to the molar ratio of urea-to-RE nitrates and acrylamide monomer-to-RE nitrates.The as-prepared samples with the sizes of 9.6-11.6 nm were characterized by X-ray diffraction,scanning electron microscopy,transmission electron microscopy and energy dispersive spectrometer.Lu2O3：Eu3＋ nano-phosphor that depicted high photoluminescence in the size around 10 nm was reported.Compared with the sample prepared by solid state reaction,the photoluminescence of sample was increased sufficiently to be 45.1%.The emission spectra of the samples presented the typical emission from 5D0 level to 7FJ（J=0,1,2,3,4） level of the Eu3＋ ion.

Electrical,Magnetic and Catalytic Investigations on Some Manganite Perovskites Prepared by Combustion Method

AMnO3 （A=Sr, Sm and Nd） manganites with perovskite structure, prepared by combustion method were characterized by X-ray diffraction （XRD）, infra-red spectroscopy, Brunauer-Emmett-Teller （BET） surface area analyzer and scanning electron microscopy （SEM）. The solid state and spectroscopic studies such as electrical resistivity, magnetic susceptibility, electron spin resonance （ESR） and diffuse reflectance spectroscopy were carried out and attempted to correlate with the catalytic activities of the compounds. To evaluate the catalytic activity, a model reaction of CO oxidation over these compounds was undertaken. An attempt was made to understand the effect of A-site change by different metal cations in the manganite perovskites on solid state and catalytic properties.

Structure properties and sintering densification of Gd_2Zr_2O_7 nanoparticles prepared via different acid combustion methods

Gadolinium zirconate（Gd2Zr2O7） nanocrystals were prepared via two different combustion methods： citric acid combustion（CAC） and stearic acid combustion（SAC）. The effects of the different preparation methods on the phase composition, microtopography, and sintering densification of the resulting Gd2Zr2O7 nanopowders were investigated by thermal-gravimetric and differential thermal analysis（TG-DTA）, Fourier transform infrared spectroscopy（FTIR）, X-ray diffraction（XRD）, and transmission electron microscopy（TEM） techniques. The results indicated that both methods could produce Gd2Zr2O7 nanopowders with an excellent defective fluorite structure. The reaction time was reduced by the SAC method, compared with the CAC method. The nanopowders synthesized by the two methods were different in grain size distribution. The resulting nanoparticle diameter was about 50 nm for CAC and 10 nm for SAC. After vacuum sintering, the sintered bodies also had a different relative density of about 93% and 98%, respectively. Thus the preparation of Gd2Zr2O7 nanopowders by SAC was the first choice to achieve the desired sintering densification.

SYNTHESIS OF STRONTIUM-AND MAGNESIUM-DOPED LANTHANUM GALLATE BY GLYCINE-NITRATE COMBUSTION METHOD

Sr- and Mg-doped lanthanum gallate powders with the composition of La0.55Sr0.15Ga0.85Mg0.15O2.85were synthesized by a glycine-nitrate combustion method. Powders prepared under different fuel combustion conditions were investigated by XRD and TEM. The results show that, under slightly rich fuel condition, the product powders contain less impurity phases, and powders prepared by the glycine-nitrate combustion contain far less impurity phases and have smaller particle sizes than those prepared by solid-state reaction method or acrylamide polymerization technique.

Photoluminescence studies of Eu^(2+)-Yb^(3+) co-doped BaMgAl_(10)O_(17) phosphor synthesized by the combustion method

BaMgAl10Ol7：Eu^2＋,Yb^3＋ was investigated as a possible quantum cutting system to enhance solar cells efficiency. Phosphors were synthesized by combustion method and composed of nanorods. Photoluminescence spectra showed that Eu in the sample was reduced to bivalence while Yb remained trivalence. Through a cooperative energy transfer process, the obtained powders exhibited both blue emission of Eu^2＋ （around 450 nm） and near infrared emission of Yb^3＋ （around 1020 nm） under broad band excitation （250-410 nm） originating from 4f→5d transition of Eu2＋. Energy transfer phenomenon between the sensitizer Eu2＋ and the activator Yb3＋ was investigated via the luminescent spectra and the decay curves of Eu2＋ with different Yb3＋ concentrations. Results indicated that energy transfer efficiency from Eu2＋ to Yb3＋ was not high. The poor efficiency can be explained by the long distance between rare earth ions.

The synthesis of B,N-carbon dots by a combustion method and the application of fluorescence detection for Cu^2+

Heteroatom doping is an efficient approach to regulate the fluorescence properties of carbon dots.Using aminophenylboronic acid as the raw material,a combustion method was developed for the synthesis of boron,nitrogen-doped carbon dots（B,N-carbon dots）.The B,N-carbon dots emitted green fluorescence and displayed high resistance to both photo bleaching and ionic strength.A facile fluorescence sensing approach for Cu^2＋ was fabricated via static fluorescence quenching.Under optimal conditions,a rapid detection of Cu^2＋ could be completed in 2 min with a linearity ranging from 1 μmol/L to 25 μmol/L and a detection limit of 0.3 μmol/L Furthermore,the proposed method showed potential applications for the detection of Cu^2＋ in natural water samples.

Effects of calcination temperature and time on the Ca3Co4O9 purity when synthesized using starch-assisted sol-gel combustion method

Ca3Co4O9 is a p-type semiconducting material that is well-known for its thermoelectric(TE),magnetic,electronic,and electro-optic properties.In this study,sol–gel autoignition was used to prepare Ca3Co4O9 at different calcination temperatures(773,873,973,and 1073 K)and time(4,6,8,10,12,and 14 h)using starch as a fuel.The phase and microstructure of the prepared Ca3Co4O9 powder were investigated.Thermogravimetry–differential thermal analysis(TGA)confirms that the final weight loss occurred at 1073 K to form Ca3Co4O9 stable powder.The variable-pressure scanning electron microscopy(VP-SEM)images show that the size of powder particles increases from 1.15 to 1.47μm as calcination time increases from 4 to 12 h,and the size remains almost constant thereafter.A similar pattern is also observed on the increment of the crystallite size and percentage of crystallinity with X-ray diffraction(XRD)analysis.The highest crystallinity is found about 92.9%when the powder was calcinated at 1073 K for 12 and 14 h with 458 and 460Åcrystallite size,respectively.Energy dispersive X-ray spectroscopy(EDS)analysis demonstrates that the calcinated powder has a high intensity of Ca,Co,and O with uniform distribution.High-resolution transmission electron microscopy(HRTEM)images prove that there is no distinct lattice distortion defect on the crystal structure.

Chemical Analysis Method for Carbon Bearing Refractory Products——Determination of the Total Carbon by Combustion Gravimetric Method

GB/T 13245-91 1 Theme and Scope This standard specifies the method abstract, reagents, apparatus, specimen, analyzing procedure, result calculation and permissible tolerance used for determination of the total carbon with combustion gravimetric method.

Combustion Synthesis and Luminescent Properties of CaO: Eu^(3+), M^+ (M=Li, Na, K) Phosphor

Li ^＋ , Na^ ＋ , or K ^＋ co-doped CaO： Eu^3＋ phosphors were prepared by the combustion synthesis method and characterized by X-ray diffraction （XRD）, photoluminescence and photolumi-nescence excitation （PL-PLE） spectra. The experimental results show that, upon excitation with 250 nm xenon light, the emission spectrum of the CaO： Eu^3＋ consists of 4f-4f emission transitions from the 5D0 excited level to the 7FJ （J=1, 2, 3） levels with the mainly electric dipole transition 5D0→7F2 of Eu3＋, indicating that the Eu^3＋ occupies a low symmetry. The charge-transfer band （CTB） shows somewhat red shift with the decreasing ionic radii of co-doped alkali metal ions. The PL and PLE intensities are significantly enhanced, especially the strongest intensity of luminescent is CaO： Eu^3＋, Li ＋ phosphor, when alkali metal ions are incorporated. The strongest peak of emission is slightly shifted from 614 to 593 nm, indicating that the Eu^3＋ ion locates in a symmetric position （Oh） when alkali metal ions are incorporated.

Luminescence Characterization and Synthesis of γ-LiAlO_2:Eu^(3+) by Gel Combustion

γ-LiAlO2：Eu3＋（Eu3＋：LAO） phosphor was obtained by gel combustion method using LiNO3,Al（NO3）3·9H2O,Eu（NO3）3·6H2O and citric acid as raw materials.The structure,morphology and luminescence were characterized by means of X-ray diffraction （XRD）,scanning electron microscopy （SEM）,photoluminescence （PL）.The results demonstrated that the phosphor was pure-phase of flaky tetragonal crystal system with a mean size of around 1 μm.The strongest excitation peak was at 254 nm,belonging to the broadband excitation and the maximum emission peak was at 613 nm,corresponding to the 5D0→7F2 transition of Eu3＋.Luminous intensity is closely related to the calcination temperature and doping concentration of Eu3＋.

Mechanism of Combustion Synthesis of TiC-Ti Cermet

In order to investigate the mechanism of combustion synthesis of TiC-Ti cermet, a mixture of Ti and C was used for a combustion front quenching test, and the microstructural evolution in the quenched sample was analyzed by scanning electron microscopy （SEM） and energy dispersive X-ray （EDX）. Also, a temperature-time profile of the combustion reaction was measured. Based on the experimental results, a reaction-dissolution-precipitation mechanism of the combustion synthesis of TiC-Ti was proposed.