Fabrication of WO3 with Macroscopic Structures via CNFs Template

2013 ◽  
Vol 275-277 ◽  
pp. 1798-1801
Author(s):  
Qiang Wu ◽  
Li Zhao

Uniform growth of WO3 with macroscopic structures was successfully achieved by using carbon nanofibers (CNFs) as template. Field emission scanning electron microscopy (FE-SEM), coupled with X-ray diffraction (XRD) analysis confirmed the template effect and the existence of WO3 immobilized on the macroscopic silica fiber.

Molecules ◽  
2019 ◽  
Vol 24 (24) ◽  
pp. 4424 ◽  
Author(s):  
Mehrdad Khatami ◽  
Mina Sarani ◽  
Faride Mosazadeh ◽  
Mohammadreza Rajabalipour ◽  
Alireza Izadi ◽  
...  

Nanoparticles of cerium oxide CeO2 are important nanomaterials with remarkable properties for use in both industrial and non-industrial fields. In a general way, doping of oxide nanometric with transition metals improves the properties of nanoparticles. In this study, nickel- doped cerium oxide nanoparticles were synthesized from Stevia rebaudiana extract. Both doped and non-doped nanoparticles were characterized by X-ray diffraction, Field Emission Scanning Electron Microscopy, Energy Dispersive X-ray, Raman spectroscopy, and Vibrating-Sample Magnetometry analysis. According to X-ray diffraction, Raman and Energy Dispersive X-ray crystalline and single phase of CeO2 and Ni doped CeO2 nanoparticles exhibiting fluorite structure with F2g mode were synthesized. Field Emission Scanning Electron Microscopy shows that CeO2 and Ni doped nanoparticles have spherical shape and sizes ranging of 8 to 10 nm. Ni doping of CeO2 results in an increasing of magnetic properties. The enhancement of ultraviolet protector character via Ni doping of CeO2 is also discussed.


2008 ◽  
Vol 8 (3) ◽  
pp. 1183-1190 ◽  
Author(s):  
Chunxia Li ◽  
Cuikun Lin ◽  
Xiaoming Liu ◽  
Jun Lin

Nanostructured CaWO4, CaWO4:Eu3+, and CaWO4:Tb3+ phosphor particles were synthesized via a facile sonochemical route. X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, photoluminescence, low voltage cathodoluminescence spectra, and photoluminescence lifetimes were used to characterize the as-obtained samples. The X-ray diffraction results indicate that the samples are well crystallized with the scheelite structure of CaWO4. The transmission electron microscopy and field emission scanning electron microscopy images illustrate that the powders consist of spherical particles with sizes from 120 to 160 nm, which are the aggregates of even smaller nanoparticles ranging from 10 to 20 nm. Under UV light or electron beam excitation, the CaWO4 powder exhibited a blue emission band with a maximum at 430 nm originating from the WO2−4 groups, while the CaWO4:Eu3+ powder showed red emission dominated by 613 nm ascribed to the 5D0 → 7F2 of Eu3+, and the CaWO4:Tb3+ powders showed emission at 544 nm, ascribed to the 5D4 → 7F5 transition of Tb3+. The PL excitation and emission spectra suggest that the energy is transferred from WO2−4 to Eu3+CaWO4:Eu3+ and to Tb3+ in CaWO4:Tb3+. Moreover, the energy transfer from WO2−4 to Tb3+ in CaWO4:Tb3+ is more efficient than that from WO2−4 to Eu3+ in CaWO4:Eu3+. This novel and efficient pathway could open new opportunities for further investigating the novel properties of tungstate materials.


2012 ◽  
Vol 531-532 ◽  
pp. 614-617 ◽  
Author(s):  
Gunawan ◽  
I. Sopyan ◽  
A. Naqshbandi ◽  
S. Ramesh

Biphasic calcium phosphate powders doped with zinc (Zn-doped BCP) were synthesized via sol-gel technique. Different concentrations of Zn have been successfully incorporated into biphasic calcium (BCP) phases namely: 1%, 2%, 3%, 5%, 7%, 10% and 15%. The synthesized powders were calcined at temperatures of 700-900°C. The calcined Zn-doped BCP powders were characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), differential and thermogravimetric analysis (TG/DTA) and field-emission scanning electron microscopy (FESEM). X-ray diffraction analysis revealed that the phases present in Zn-doped are hydroxyapatite, β- TCP and parascholzite. Moreover, FTIR analysis of the synthesized powders depicted that the bands of HPO4 increased meanwhile O-H decreased with an increase in the calcination temperature. Field emission scanning electron microscopy (FESEM) results showed the agglomeration of particles into microscale aggregates with size of the agglomerates tending to increase with an increase in the dopant concentration.


RSC Advances ◽  
2016 ◽  
Vol 6 (105) ◽  
pp. 102972-102978 ◽  
Author(s):  
Yu Dong ◽  
Ziting Wang ◽  
Xin Yang ◽  
Meiying Zhu ◽  
Rufen Chen ◽  
...  

Natrojarosite particles were prepared by forced hydrolysis. X-ray diffraction and field-emission scanning electron microscopy were used to characterize the resulting products.


2018 ◽  
Vol 769 ◽  
pp. 29-34 ◽  
Author(s):  
Alexander Thoemmes ◽  
Ivan V. Ivanov ◽  
Adelya A. Kashimbetova

The effect of Nb content on microstructure, mechanical properties and phase formation in annealed and quenched binary Ti-Nb alloys were investigated using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD) analysis. The content of Nb varied in the range 0-37 mass % leading to significant changes in the microstructure. The annealed and furnace-cooled binary Ti-Nb samples exhibited HCP martensitic α` phase at a Nb content below 14 mass % and stable BCC β phase at higher contents of Nb. The structure of the quenched samples changed with increase of Nb content in the following order: coarse primary martensite → fine acicular (α`+α``) martensite → single β phase structure. The mechanical properties of alloys strongly depended on the Nb content and type of the dominating phase.


2016 ◽  
Vol 19 (3) ◽  
pp. 145-150 ◽  
Author(s):  
Meysam Karimi ◽  
Mohammad Rabiee ◽  
Mojgan Abdolrahim ◽  
Mohammadreza Tahriri ◽  
Daryoosh Vashayee ◽  
...  

We present a study of the effect of graphene–PANI nanocomposites on the sensitivity of the urea and glucose multisensory. We used an electroctrochemical multisensor based on two electrodes located in a reservoir with two separate channels. The urease and glu-cose oxidase (GOD) were employed for detecting the urea and glucose, respectively. We characterized the graphene and graphene-PANI samples with X-ray Diffraction (XRD) analysis and scanning electron microscopy (SEM) observations. We further performed the Cyclic voltammetry and Amperometry tests. The collected experimental results revealed that the intensity of the peak significantly increases with the concentration of the urea and glucose.


2012 ◽  
Vol 624 ◽  
pp. 63-66
Author(s):  
Ming Ya Li ◽  
Jian Min Wang ◽  
Jing Guo ◽  
Yue Liu Li ◽  
Xiao Qiang Wang

Highly Ordered arrays of TiO2 nanotubes on Ti wire were prepared by anodic oxidation with ethylene glycol solution of NH4F electrolyte. The phase compositions of the samples were characterized using X-ray diffraction (XRD) analysis using Cu-Kα radiation. The microstructure was observed using scanning electron microscopy (SEM). Experimental results show that at the anode condition of 95V, 50°C, and then themal treatment at 550°C, the highly ordered anatase TiO2 nanotubes arrays arranged on the surface of Ti wire. The length of the nanotube achieved was about 31μm, the internal diameter and outer diameter of the nanotube was 127nm and 170nm, respectively.


2015 ◽  
Vol 1087 ◽  
pp. 452-456
Author(s):  
Khairul Arifah Saharudin ◽  
Srimala Sreekantan

TiO2 nanotubes arrays were prepared by anodization of Ti in EG containing H3PO4 and NH4F electrolyte. The samples were characterized by X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), Energy dispersive X-ray spectroscopy (EDX) and photoluminescence spectra (PL). The as-anodized TiO2 nanotubes were annealed in inert (argon), reducing (nitrogen), or oxidizing (oxygen) atmosphere at 400 °C for 4 hr. XRD analysis revealed that the TiO2 nanotubes were anatase after annealing. In this study, the TiO2 nanotubes annealed in argon exhibited the highest degradation rate of methyl orange (MO) solution under ultraviolet irradiation among the samples. The degradation rate was approximately 98% after 5h, which may be ascribed to the large amount of oxygen vacancies and defects (phosphorus) within the Ar - TiO2 sample that simultaneously increased the degradation rate of MO.


2012 ◽  
Vol 174-177 ◽  
pp. 516-519
Author(s):  
Yong Gang Wang ◽  
Lin Lin Yang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang

The BiFeO3 hollow crystals were successfully prepared at 200oC by a Al3+assisted hydrothermal method. The structures and morphologies of the as-obtained products were characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (SEM). A morphology evolution from irregular shape to square, hollow, and sphere-like was observed as the Al ions concentration varied from 0% to 1.5%. The possible growth mechanism of the BiFeO3hollow crystals was also discussed.


2015 ◽  
Vol 1754 ◽  
pp. 129-134
Author(s):  
Sanjay Kr. Jana ◽  
Saptarsi Ghosh ◽  
Syed Mukulika Dinara ◽  
Apurba Chakraorty ◽  
D. Biswas

AbstractThe work presents a comparative study on GaN/AlGaN type-II heterostructures grown on c-plane Al2O3 and Si (111) substrates by Plasma Assisted Molecular Beam Epitaxy. The in-depth structural characterizations of these samples were performed by High-Resolution X-Ray Diffraction, X-ray Reflectivity and Field Emission Scanning Electron Microscopy. The in-plane and out-of plane strains were determined from measured c- and a-lattice parameters of the epilayers from reciprocal space mapping of both symmetric triple axis (002) and asymmetric grazing incidence (105) double axis mode. The mosaicity parameters like tilt and correlation lengths were also calculated from reciprocal space mapping. Moreover, the twist angle was measured from skew symmetric off axis scan of (102), (103), and (105) planes along with (002) symmetric plane. The defect density were measured from the full width at half maxima of skew symmetric scan of (002) and (102) reflection planes. Also, the strained states of all the layers were analyzed and corresponding Al mole fraction was calculated based on anisotropic elastic theory. The thicknesses of the layers were measured from simulation of the nominal structure by fitting with X-ray Reflectivity experimental curves and also by comparing with cross sectional Field Emission Scanning Electron Microscopy micrographs.


Sign in / Sign up

Export Citation Format

Share Document