scholarly journals Synthesis and Optical Manifestation of NiO-Silica Nanocomposite

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
S. Chakrabarty ◽  
K. Chatterjee

NiO-silica nanocomposites with average diameter ranging from 2–40 nm were prepared by sol-gel method followed by the heat treatment varying from 400°C to 1000°C. The details of morphology and crystalline nature of all the as prepared samples were characterized by TEM, HRTEM, and XRD analysis. The planes obtained from SAED pattern supports the planes originated from XRD study. From the optical absorption study, it is revealed that the band gap energy of NiO can extensively be manipulated by composite formation with silica and the size variation of that nanocomposite. Absorption peak position varies almost linearly with the oxidation temperature of the samples. Photoluminescence spectroscopy reveals that NiO-silica nanocomposite, prepared at 600°C and below, shows strong emission at 3.62 eV, but the nanocomposites with bigger size greatly hinder the effect of selective emissivity.

Author(s):  
James E. Mark ◽  
Dale W. Schaefer ◽  
Gui Lin

A relatively new area that involves silicon-containing materials is the synthesis of “ultrastructure” materials (i.e., materials in which structure can be controlled at the level of 100 Å). An example is the “sol-gel” hydrolysis of alkoxysilanes (organosilicates) to give silica, SiO2. The reaction is complicated, involving polymerization and branching, but the overall reaction may be written . . . Si(OR4 + 2H2O → SiO2 + 4ROH (9.1) . . . where the Si(OR)4 organometallic species is typically tetraethoxysilane such as tetraethylorthosilicate (TEOS, with R being C2H5). In this application, the precursor compound is hydrolyzed and then condensed to yield branched polymers. Eventually a continuous swollen gel is formed. The gel is dried at moderately low temperatures to remove volatile species, and then it is fired into a porous ceramic object that can then be densified and machined into a final ceramic part. The production of ceramics by this novel route triggered interest in the ceramics community because of advantages over the conventional powder-processing approach to ceramics. Advantages include (i) the higher purity of the starting materials, (ii) the relatively low temperatures required, (iii) the possibility of controlling the ultrastructure to reduce the microscopic flaws that lead to failure, (iv) the ease with which ceramic coatings can be formed, and (v) the ease with which ceramic alloys can be prepared (e.g., by hydrolyzing solutions of both silicates and titanates). The sol-gel approach has been used to form ceramic-like phases in a variety of polymers. Poly(dimethylsiloxane) (PDMS) is the most popular. PDMS is relatively weak and stands to benefit most from reinforcement. PDMS is easily absorbs the precursor materials generally used in the solgel process. Nearly monodisperse silica microparticles can be obtained using siloxane elastomer mixtures. In some cases, the PDMS has been part of a copolymer, with ureas, imides, amideimides, and dianilines. In other approaches, the particle surface is modified, for example, with a polysiloxane. Siloxane/silica nanocomposites have also been used as “culture-stone-protective materials.” Sol-gel hydrolysis and condensation can be carried out within a polymeric matrix to generate particles of the ceramic material, typically with an average diameter of a few hundred angstroms.


2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Sibongile C. Nkabinde ◽  
Makwena J. Moloto ◽  
Kgabo P. Matabola

Polyacrylonitrile (PAN), cellulose acetate (CA), PAN-TiO2, and CA-TiO2 nanofibers were prepared using the electrospinning technique under varying the loading of the TiO2 nanoparticles. The latter TiO2 nanoparticles were prepared using the sol-gel method by varying the calcination temperatures. The absorption and emission spectra illustrated the formation of TiO2 nanoparticles with an increase in absorption band edges with smaller particles. The TEM results showed the spherical morphology of the nanoparticles calcined at 500°C with an average diameter of 12.2±3.3 nm. XRD analysis revealed anatase phase as the dominant crystalline phase of the nanoparticles. TiO2 nanoparticle loadings of 0.2 and 0.4 wt% were incorporated into 16 wt% CA solutions while 1, 2, and 3 wt% of TiO2 nanoparticles were incorporated into 10 wt% PAN solutions. The SEM results illustrated the lowering in diameter and morphology of the nanofibers upon incorporation of nanoparticles. Their respective average diameters are 220, 338, 181, and 250 nm for PAN, CA, PAN-TiO2, and CA-TiO2 polymer fibers, respectively. The morphology of the nanofibers improved while the diameter increased with an increase in polymer concentration. Different loadings of TiO2 nanoparticles improved the electrospinnability and morphology and further decreased the size of the nanofibers. FTIR spectroscopy signifies the formation of nanocomposites and the presence of TiO2 nanoparticles which corresponded to the Ti-O stretching and Ti-O-Ti bands on the FTIR spectra.


2019 ◽  
Vol 19 (4) ◽  
pp. 827
Author(s):  
Yudha Ramanda ◽  
Nuryono Nuryono ◽  
Eko Sri Kunarti

This study focuses on the synthesis and application of a Fe3O4/SiO2/TiO2 nanocomposite as a photocatalyst in CO2 indirect reduction. The synthesis was started by preparation of magnetite (Fe3O4) followed by silica (SiO2) coating and titania (TiO2) deposition. Magnetite was prepared by the sono-coprecipitation method, then the coating of SiO2 and deposition of TiO2 were performed by the sol-gel method under ultrasonic irradiation. All the material products were characterized by an X-ray diffractometer (XRD), Fourier-transform infrared spectrophotometer (FTIR), and transmission electron microscope (TEM). The final material product was also analyzed by a specular reflectance UV-Visible spectrometer (SR-UV-Vis) and the turbidimetry method. The product of the indirect reduction was analyzed by a gas chromatography-mass spectrometer (GC-MS). The XRD diffractograms and FTIR spectra confirmed the presence of Fe3O4, SiO2, and the anatase phase of TiO2. The TEM images revealed the presence of a core-shell nanocomposite with an average diameter of 19.22 ± 1.25 nm. The SR-UV-Vis spectrum was used to determine the band gap energy of the photocatalyst, with the result being 3.22 eV. Turbidimetry aimed to measure the magnetic recoverability of the final material, and the result was that it had better recoverability compared to a non-magnetic photocatalyst composite. The GC chromatogram of the indirect reduction product indicated four majorfractions; the MS spectra showed these to be methanol, formaldehyde, formic acid, and CO2. The GC-MS results revealed that CO2 indirect reduction achieved 73.91% conversion of CO2 and 55.01% selective to methanol.


2005 ◽  
Vol 876 ◽  
Author(s):  
Jeanne E. Panels ◽  
Yong L. Joo

AbstractFor the first time, silica nanofiber mats containing vanadium pentoxide crystals have been made via a sol-gel/electrospinning technique without using any polymer binder. XRD analysis after calcination of the fibers indicates the presence of vanadium pentoxide crystals. The average diameter of 20mol%V fibers after calcination at 800°C is 420nm. SEM and TEM images demonstrate crystal growth on the surface of the fibers after calcination at 800°C. XPS analysis also indicates the growth of V2O5 crystals at high enough temperatures. Physisorption of 20mol%V fibers after calcination at 800°C gave a BET surface area of 1.9 m2/g and an average pore diameter of 6 nm.


Author(s):  
Nurul Diyana Zainal ◽  
Hadi Nur ◽  
Lee Siew Ling

Modification of sol-gel method was used to synthesize homogeneous particle size nitrogen-doped titania (N-TiO2) nanomaterials using tetraethyl ammonium hydroxide (TEAOH) as N source. XRD analysis showed that these N-TiO2 (1-5 % N concentration) crystallined in anatase structure. The crystallinity of the samples decreased with increasing of N content. The calculation using Scherrer equation showed that the particle size of the synthesized N-TiO2 ranged 15.02 - 26.85 nm, strongly suggesting attainment of nanomaterials. DR UV-Vis results indicated that the band gap energy of 5% N doped TiO2 was only 2.58 eV, implying the sample could be a potential photocatalyst under visible light irradiation.  Homogeneous particle size of the synthesized nanomaterials was evidenced through FESEM images. Meanwhile, the EDX analysis confirmed the homogenous distribution of elements Ti, N and O in 5% N doped titania sample. 


2012 ◽  
Vol 545 ◽  
pp. 137-142 ◽  
Author(s):  
Mohd Sufri Mastuli ◽  
Rusdi Roshidah ◽  
Annie Maria Mahat ◽  
Norazira Saat ◽  
Norlida Kamarulzaman

A sol-gel method was used to synthesize a highly stable form of MgO from magnesium oxalate dihydrate. The sol-gel products were characterized using simultaneous thermogravimetric analysis (STA), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and UV-Visible light spectroscopy (UV-Vis). From the XRD analysis, all the MgO samples showed a single face-centered cubic phase. FESEM micrographs showed a crystallite size ranging from 10 nm to 59 nm. The size of the MgO crystallites increased with increasing temperatures. The crystallite size of the MgO is still relatively small, that is, below 100 nm even when the precursor was calcined at a higher temperature of 950 °C and a longer time of 36 h. Such results indicated that the growth of the crystallites is slow for this route of synthesis. The morphologies of the MgO samples are varied from the all spherical of the lower temperature to the more cubic shape with less agglomeration of the higher calcined samples. The band gap energy of the MgO samples also increased with temperature.


2018 ◽  
Vol 9 (1) ◽  
pp. 133-139
Author(s):  
Waleed S. Mohammed ◽  
Ahmed H. El-Shazly ◽  
Marwa F. Elkady ◽  
Masahiro Ohshima

Introduction: The utilization of biodiesel as an alternative fuel is turning out to be progressively famous these days because of worldwide energy deficiency. The enthusiasm for utilizing Jatropha as a non-edible oil feedstock is quickly developing. The performance of the base catalyzed methanolysis reaction could be improved by a continuous process through a microreactor in view of the high mass transfer coefficient of this technique. Materials & Methods: Nanozirconium tungstovanadate, which was synthetized using sol-gel preparation method, was utilized in a complementary step for biodiesel production process. The prepared material has an average diameter of 0.066 &µm. Results: First, the NaOH catalyzed methanolysis of Jatropha oil was investigated in a continuous microreactor, and the efficient mixing over different mixers and its impact on the biodiesel yield were studied under varied conditions. Second, the effect of adding the nanocatalyst as a second stage was investigated. Conclusion: The maximum percentage of produced methyl esters from Jatropha oil was 98.1% using a methanol/Jatropha oil molar ratio of 11 within 94 s using 1% NaOH at 60 &°C. The same maximum conversion ratio was recorded with the nanocatalyst via only 0.3% NaOH.


Author(s):  
Atefeh Nazari Setayesh ◽  
Hassan Sedghi

Background: In this work, CdS thin films were synthesized by sol-gel method (spin coating technique) on glass substrates to investigate the optical behavior of the film. Methods: Different substrate spin coating speeds of 2400, 3000, 3600 rpm and different Ni dopant concentrations of 0 wt.%, 2.5 wt.%, 5 wt.%) were investigated. The optical properties of thin films such as refraction index, extinction coefficient, dielectric constant and optical band gap energy of the layers were discussed using spectroscopic ellipsometry method in the wavelength range of 300 to 900 nm. Results: It can be deduced that substrate rotation speed and dopant concentration has influenced the optical properties of thin films. By decreasing rotation speed of the substrate which results in films with more thicknesses, more optical interferences were appeared in the results. Conclusion: The samples doped with Ni comparing to pure ones have had more optical band gap energy.


Planta Medica ◽  
2021 ◽  
Author(s):  
Sandra Alves de Sousa Garcia ◽  
Priscila Bianca Rodrigues da Rocha ◽  
Bruno dos Santos Souza ◽  
Andressa Tuane Santana Paz ◽  
Ana Luiza Caetano Negris ◽  
...  

AbstractPunicalagin, the principal ellagitannin of Lafoensia pacari leaves, has proven antioxidant activity, and standardized extracts of L. pacari can be topically used for skin aging management. We hypothesized that Pluronic nanomicelles or vesicles could solubilize sufficiently large amounts of the standardized extracts of L. pacari and provide chemical stability to punicalagin. The standardized extracts of L. pacari were obtained with an optimized extraction procedure, and the antioxidant activity was characterized. Formulations containing Pluronic at 25% and 35% were obtained with or without Span 80. They were characterized by average diameter, polydispersity index, punicalagin content, physicochemical stability, and rheology. A release and skin permeation study was carried out in vertical diffusion cells. The extraction procedure allowed quantifying high punicalagin content (i.e., 141.61 ± 3.87 mg/g). The standardized extracts of L. pacari showed antioxidant activity for all evaluated methods. Pluronic at 25 and Pluronic at 35 with standardized extracts of L. pacari showed an average diameter of about 25 nm. The addition of Span 80 significantly increased the mean diameter by 15-fold (p < 0.05), indicating the spontaneous formation of vesicles. Pluronic formulations significantly protected punicalagin from chemical degradation (p < 0.05). Pluronic at 25 formulations presented as free-flowing liquid-like systems, while Pluronic at 35 resulted in an increase of about 44-fold in |ƞ*|. The addition of Span 80 significantly reduced the Pluronic sol-gel transition temperature (p < 0.05), indicating the formation of vesicles. Formulations with Span 80 significantly enhanced punicalagin skin permeation compared to formulations without Span 80 (p < 0.05). Formulations with Span 80 were demonstrated to be the most promising formulations, as they allowed significant permeation of punicalagin (about 80 to 315 µg/cm2), which has been shown to have antioxidant activity.


Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1554
Author(s):  
Justinas Januskevicius ◽  
Zivile Stankeviciute ◽  
Dalis Baltrunas ◽  
Kęstutis Mažeika ◽  
Aldona Beganskiene ◽  
...  

In this study, an aqueous sol-gel synthesis method and subsequent dip-coating technique were applied for the preparation of yttrium iron garnet (YIG), yttrium iron perovskite (YIP), and terbium iron perovskite (TIP) bulk and thin films. The monophasic highly crystalline different iron ferrite powders have been synthesized using this simple aqueous sol-gel process displaying the suitability of the method. In the next step, the same sol-gel solution was used for the fabrication of coatings on monocrystalline silicon (100) using a dip-coating procedure. This resulted, likely due to substrate surface influence, in all coatings having mixed phases of both garnet and perovskite. Thermogravimetric (TG) analysis of the precursor gels was carried out. All the samples were investigated by X-ray powder diffraction (XRD) analysis. The coatings were also investigated by scanning electron microscopy (SEM), atomic force microscopy (AFM) and Mössbauer spectroscopy. Magnetic measurements were also carried out.


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