首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
Recent developments and trends of sol–gel auto-combustion method for spinel ferrite nanomaterial synthesis are briefly discussed and critically analyzed. The analysis of various parameters of reaction which could be used for better understanding of synthesis process and control of microstructure and property of spinel ferrite nanopowder products was the main objective of this review article. Special attention was paid to variety of particle size and phase purity. For these purposes the correlation between complexant, oxygen balance and combustion process chemical additives, as well as heating mechanism and atmosphere, was established. These results are relevant from standpoints of both application and processing of ferrites.  相似文献   

2.
Sol–gel autocombustion is confirmed to be an efficient method in the synthesis of Co–Ni alloy powder. Addition of adequate amount of ethanol can make the reduction reaction thorough and increase the purity of the samples. X-ray diffraction measurement indicates that the obtained samples consist of a single phase with bcc structure. Transmission electron microscopy study shows the grain size is about 10 nm. The magnetic measurements show that the samples are a soft magnetic material with the coercive field smaller than 100 Oe and the saturation magnetization about 95% of the theoretical value.  相似文献   

3.
Investigations of the electronic structures of substituted strontium apatites were carried out by using X-ray photo electron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction technique (XRD) has been used to determine the structural parameters. Electron microprobe microanalysis technique was used to estimate the elemental concentrations in each substituted apatite material. The present work aims at studying the changes in the electronic structure of Sr5(PO4)3OH (Sr-HAP) upon isomorphic substitution by F and Cl at the OH site of apatite and Sr by Na at trans Sr-HAP. The ion exchange between Na+ in sodium alginate and aqueous Ca2+ was important for the preparation of calcium hydroxyapatite. In contrast, the reaction of sodium alginate with the mixture of Na4P2O7 and aqueous Sr2+ afforded strontium hydroxyapatite at the specific ratio. The structure of calcium and strontium phosphates prepared from the sol–gel process evidently depended on the amount of sodium alginate introduced into the mixture of Na4P2O7 and the corresponding divalent cations. The findings have ensured that substitution of Sr-HAP by Na enhances the binding energy of O and Sr core levels. It was also noticed that the same substitution decreases the binding energy of P 2s-level. These observations point out to a decrease in the electron density at P and an increase in the electron density at O in Sr atoms.  相似文献   

4.
Silica gel supported titanium dioxide particles (TiO2–SiO2) prepared by sol–gel method was as photocatalyst in the degradation of β-naphthol in water under UV-illumination. The prepared sample has been characterized by powder X-ray diffraction (XRD), infrared spectroscopy (IR) and scanning electron microscopy (SEM). The supported catalyst had large surface area and good sedimentation ability. The photodegradation rate of β-naphthol under UV-irradiation depended strongly on adsorption capacity of the catalyst, and the photoactivity of the supported catalyst was much higher than that of the pure titanium dioxides. The experiments were measured by high performance liquid chromatography (HPLC). The photodegradation rate of β-naphthol using 60% TiO2–SiO2 particles was faster than that using TiO2 “Degussa P-25”, TiO2 “PC-50” and TiO2 “Aldrich” as photocatalyst by 2.7, 4 and 7.8 times, respectively. The kinetics of photocatalytic β-naphthol degradation was found to follow a pseudo-first-order rate law. The effect of the TiO2 loading on the photoactivity of TiO2–SiO2 particles was also discussed. With good photocatalytic activity under UV-irradiation and the ability to be readily separated from the reaction system, this novel kind of catalyst exhibited the potential effective in the treatment of organic pollutants in aqueous systems.  相似文献   

5.
Vanadium pentoxide (V2O5) nanoparticles were synthesized at moderate reaction temperatures by hydrolysis of VO[OCH(CH3)2]3 in two different air- and water-stable ionic liquids with the same anion: 1-butyl-1-methyl pyrrolidinium bis(trifluoromethylsulfonyl)amide ([Py1,4]Tf2N) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide ([EMIM]Tf2N) via the sol–gel method using acetone and isopropanol either as refluxing solvents or as co-solvents. The cation type of the ionic liquid affects the crystallinity, morphology, and surface area of the produced nanoparticles: [Py1,4]Tf2N gave products with higher crystallinity especially with acetone as a refluxing and co-solvent, while [EMIM]Tf2N gave a clear mesoporous morphology with isopropanol as a refluxing solvent. Ionic liquids affect the key factors (morphology and surface area) that make V2O5 an attractive material as catalyst and/or cathodic material for lithium ion batteries.  相似文献   

6.
Mesoporous yttria-stabilized zirconia (YSZ) membranes can be used for liquid phase applications in harsh environments and as supports for ultra-thin dense ceramic, carbonate, or metallic membranes. This article reports on the synthesis and characterization of three-layer mesoporous ceramic membranes consisting of a mesoporous YSZ layer, a macroporous YSZ intermediate layer, and macroporous α-alumina support. The macroporous YSZ intermediate layer was coated on the alumina support using a suspension of submicron-sized YSZ powders, and the mesoporous YSZ layer was obtained by dip-coating with diluted zirconia sol doped with yttrium nitrate. The mesoporous YSZ layer has desired cubic phase structure. Crack-free mesoporous YSZ membranes could be obtained by multiple dip-coating, drying, and calcination using a dilute YSZ sol at a concentration of 0.014 M with the help of using a drying control chemical additive. The 5 times dip-coated mesoporous YSZ membranes were about 1 μm in thickness with an average pore diameter of 3 nm. The mesoporous YSZ membranes exhibited Knudsen separation factor. The characteristics of the dip-coating process for the mesoporous YSZ membranes on the macroporous YSZ support are similar to those on the macroporous alumina support.  相似文献   

7.
《Materials Letters》2004,58(17-18):2302-2305
Ultrafine Ba0.5Sr0.5TiO3 powders were prepared by using barium nitrate, strontium nitrate, tetrabutyl titanate, and ammonia via citrate–nitrate combustion process at low temperature (500 °C), along with the X-ray diffraction (XRD), differential scanning calorimetry (DSC)/thermogravimetry analysis (TGA) and scanning electron microscopy (SEM) analytic reports. Spark plasma sintering was carried out to obtain the ultrafine crystalline BST and to improve the dielectric properity. It was found that the sintered BST showed ultrafine crystalline microstructure. At 25 °C, the dielectric constant and dissipation factor of the sintered sample were 1533 and 0.0063 at 10 kHz.  相似文献   

8.
ZnO microstructures of different morphologies were synthesized by the sol–gel assisted hydrothermal method using Zn(NO3)2, citric acid and NaOH as raw materials. Twining-hexagonal prism, twining-hexagonal disk, sphere and flower-like ZnO microstructures could be synthesized only through controlling the pH of the hydrothermal reaction mixture at 11, 12, 13 and 14, respectively. The as-synthesized samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM). Optical properties were examined by UV–Vis absorption/diffuse reflectance spectroscopy and room-temperature photoluminescence measurements (PL). Photocatalytic activities of the samples were evaluated by degradation of Reactive Blue 14 (KGL). The results indicated that the flower-like ZnO composed of nanosheets possessed superior photocatalytic activity to other ZnO microstructures and commercial ZnO, which could be attributed to the morphology, surface defects, band gap and surface area. The formation mechanisms of different ZnO morphologies were also investigated based on the experimental results.  相似文献   

9.
10.
11.
Template-based growth has been demonstrated as an attractive method for the synthesis of oxide nanorod arrays. In this paper, TiO2 nanorod arrays in anodic alumina membranes have successfully been synthesized by an improved sol–gel template method. TiO2 nanorods were obtained to injection of prepared TiO2-sol from the sol–gel process and then the samples were immediately immersed into boiling TiO2-sol solutions. Aligned TiO2 nanorod arrays were polycrystalline anatase-phase after annealing at 400 °C for 2 h with diameters about 160–250, 80–130 and 40–70. A lateral shrinkage approximately 15–20% was found in TiO2 nanorods with respect to the template pore diameter. This size difference is likely due to the volume shrinkage caused by removing residual materials and densification during annealing.  相似文献   

12.
13.
Carbon nanotubes used as fillers in composite materials are more and more appreciated for the outstanding range of accessible properties and functionalities they generate in numerous domains of nanotechnologies. In the framework of biological and medical sciences, and particularly for orthopedic applications and devices (prostheses, implants, surgical instruments, …), titanium substrates covered by tantalum oxide/carbon nanotube composite coatings have proved to constitute interesting and successful platforms for the conception of solid and biocompatible biomaterials inducing the osseous regeneration processes (hydroxyapatite growth, osteoblasts attachment). This paper describes an original strategy for the conception of resistant and homogeneous tantalum oxide/carbon nanotubes layers on titanium through the introduction of carbon nanotubes functionalized by phosphonic acid moieties (P(O)(OH)2). Strong covalent CP bonds are specifically inserted on their external sidewalls with a ratio of two phosphonic groups per anchoring point. Experimental results highlight the stronger “tantalum capture agent” effect of phosphonic-modified nanotubes during the sol–gel formation process of the deposits compared to nanotubes bearing oxidized functions (OH, CO, C(O)OH). Particular attention is also paid to the relative impact of the rate of functionalization and the dispersion degree of the carbon nanotubes in the coatings, as well as their wrapping level by the tantalum oxide matrix material. The resulting effect on the in vitro growth of hydroxyapatite is also evaluated to confirm the primary osseous bioactivity of those materials. Chemical, structural and morphological features of the different composite deposits described herein are assessed by X-ray photoelectron spectroscopy (XPS), scanning (SEM) and transmission (TEM) electronic microscopies, energy dispersive X-rays analysis (EDX) and peeling tests.  相似文献   

14.
A method has been developed to cast novel organic/inorganic polymer hybrids from multicomponent solutions containing tetramethyl orthosilicate, calcium nitrate tetrahydrate, polycaprolactone, water, and methylethyketone via sol-gel process. The existence of the hydrogen bonds between organic and inorganic components of the hybrid and hydroxyapatite formation on the surface was proved by Fourier transform infrared analysis. The morphology of the hybrid material was studied by scanning electron microscopy. The structure of a molecular level dispersion was disclosed by atomic force microscopy, pore size distribution, and surface measurements. The infrared spectra of the hybrid relative to sample soaked in a fluid simulating the composition of human blood plasma suggests that polycaprolactone/CaO * SiO(2) hybrid material synthesised via sol-gel process is bioactive as well as the CaO * SiO(2) gel glass.  相似文献   

15.

In this study, Si porous pyramids nanostructures were synthesized by the metal-assisted chemical etching technique. Different KOH concentrations were used to develop high surface area Si porous pyramids for application as supercapacitor electrodes. Field-emission scanning electron microscope (FE-SEM) studies showed that 5% KOH solution will lead to high surface area Si pyramids with a specific capacitance of 90.3 F/cm2. Silicon carbide (SiC) thin film was coated on Si pyramids (SiC@Si) using a facile sol–gel method followed by a carbothermal reduction process. Tetraethylorthosilicate and sugar were used as carbon sources. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR) and FE-SEM analysis were used to characterize the developed SiC@Si samples. The developed SiC@ Si electrode exhibited a high specific capacitance of 135.5 F/cm2 at a scan rate of 10 mV/s (in 1 M NaOH electrolyte). The supercapacitor capability of this SiC@Si structure is significantly higher than classical materials. Because of its facile, controllable and efficient synthesis technique, this novel SiC@Si can be considered a very promising candidate for power sources applications.

  相似文献   

16.
17.
18.
High lithium ion conductive garnet-type barium lanthanum lithium tantalate, Li6BaLa2Ta2O12 (LLBTO), was prepared by a modified sol–gel Pechini method from the appropriate mixtures of lithium carbonate, lanthanum oxide, barium carbonate and tantalum ethoxide. The thermal decomposition of the precursor powder was investigated by TG/DTA analysis. The LLBTO precursor powders were annealed at various temperatures between 923 and 1123 K for 6 h in air. The transformation process from precursor powder to crystalline garnet-like phase was analyzed by X-ray powder diffraction (XRPD). The morphology of the powders annealed at various temperatures was investigated by scanning electron microscopy (SEM). The resultant pelletized Li6BaLa2Ta2O12, prepared by sol–gel synthesis method, shows a total Li-ion conductivity of 1.69 × 10?5 S/cm at 298 K and an activation energy is 0.40 eV. The ionic conductivities reported in this study are slightly higher than those reported for LLBTO sample synthesized by conventional solid state synthesis route.  相似文献   

19.
Poly(є-caprolactone) (PCL 6, 12 and 24 wt%) and zirconium (ZrO2) organic–inorganic hybrid materials have been synthesized by the sol–gel method from a multicomponent solution containing zirconium propoxide [Zr(OC2H7)4], poly(ε-caprolactone) (PCL), water, chloroform (CHCl3). Sodium ampicillin was incorporate in the hybrid materials to verify the effect as local controlled drug delivery system. The structure of interpenetrating network is realized by hydrogen bonds between Zr-OH group (H donator) in the sol–gel intermediate species and carboxylic group (H-acceptor) in the repeating units of the polymer. The presence of hydrogen bonds between organic/inorganic components of the hybrid material was proved by FTIR analysis. The morphology of the hybrid material was studied by scanning electron microscope (SEM). The structure of a molecular level dispersion has been disclosed by atomic force microscope (AFM), pore size distribution and surface measurements. The bioactivity of the synthesized hybrid material has been showed by the formation of a layer of hydroxyapatite on the surface of PCL/ZrO2 samples soaked in a fluid simulating the composition of the human blood plasma. Release kinetics in a simulate body fluid (SBF) have been subsequently investigate. The amount of sodium ampicillin released has been detected by UV–VIS spectroscopy and SEM. The release kinetics seems to occur in more than one stage. HPLC analysis has also been taken to ensure the integrity of ampicillin after the synthetic treatment.  相似文献   

20.
An aqueous sol–gel chemistry approach for the preparation of Sr-substituted perovskite gadolinium cobaltates Gd1−xSrxCoO3−δ (x = 0.0, 0.25, 0.5 and 0.75) has been applied. The metal ions, generated by dissolving starting materials in diluted acetic acid were complexed by EDTA to obtain the precursors for non-substituted and Sr-substituted GdCoO3. However, only two single-phase cobaltate samples with x = 0.0 and 0.25 have been obtained by the suggested sol–gel method. The influences of synthesis temperature and the amount of substituent on the phase purity of Gd1−xSrxCoO3−δ were investigated. The evolution of the gels during heating, composition and micro-structural features in the polycrystalline samples was studied by thermal analysis (TG/DSC), infrared spectroscopy (IR), powder X-ray diffraction analysis (XRD) and scanning electron microscopy (SEM).  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号