EDTA assisted synthesis of HA nanoparticles and Cobalt-HA nanocomposites

2020 ◽  
Vol 3 (3) ◽  
Author(s):  
Sri Devi P ◽  
Sahana L
Keyword(s):  
Sol Gel ◽  
Stoichiometric Composition ◽  
Xrd Analysis ◽  
Living System ◽  
Mineral Phase ◽  
Bone Substitute Material ◽  
Edax Analysis ◽  
Permanent Implants ◽  
Regenerative Therapies ◽  
Sem Morphology

Nano biomaterials such as polymers, ceramics and metals are widely used in bone for regenerative therapies, bone grafts and tissue engineering as well as for temporary or permanent implants to stabilize fractures and replace joints. Bioceramics are specifically developed to replace parts of living system due to its biocompatibility. Hydroxyapatite (HA)Ca10(PO4)6(OH)2 used as a bone substitute material with stoichiometric composition i.e.,Ca/P(ratio) 1.67, which is similar to the mineral phase of the human bone. In this present work, (EDTA) ethylene diamine tetra acetic acid assisted as a capping agent for the synthesis of nano hydroxyapatite and cobalt substituted hydroxyapatite nanocomposites by sol gel method. The synthesized nano-HA powder and Co-HA nanocomposites are further characterized by using FTIR, XRD, SEM, EDAX and anti-bacterial activity. XRD analysis of HA Nanoparticles and Co-HA Nanocomposites, shows the strongest 2θ values at 32.1°,25.91°and at 32.1°, 10.1°, 16.6° respectively. SEM morphology predicts an elongated spherical morphology for HA Nanoparticles and Co-HA Nanocomposites. The elemental composition was confirmed with EDAX analysis and the FTIR spectrum indicates the functional groups of the synthesized compounds. The antibacterial activity was analyzed for both the gram-positive and the gram-negative bacteria’s.

Fabrication and Characterization of Porous Mullite Coating on Porous Silicon Carbide Support

2007 ◽  
Vol 280-283 ◽  
pp. 1301-1304 ◽  
Author(s):  
Ning Wang ◽  
Xiao Zhan Yang ◽  
Jian Bao Li ◽  
Hong Lin ◽  
Bo Chi
Keyword(s):  
Silicon Carbide ◽  
Porous Silicon ◽  
Sol Gel ◽  
Stoichiometric Composition ◽  
Xrd Analysis ◽  
Dip Coating ◽  
Average Pore ◽  
Porous Silicon Carbide ◽  
Mullite Coating ◽  
Porous Mullite

Mullite powders of stoichiometric composition were synthesized by sol-gel process with TEOS and Al(NO3)3·9H2O as silicon and aluminum source. Homogeneous mullite powders were used as the starting materials to prepare the porous mullite coating on the porous silicon carbide support by repeated dip-coating method. XRD analysis revealed that the mullite precursor gels almost completely transformed to orthorhombic crystalline mullite at 1200°C. The average pore diameter and porosity of the porous mullite coating were about 4.5µm and 52.3%, respectively.

scholarly journals Aqueous Sol-Gel Synthesis of Different Iron Ferrites: From 3D to 2D

Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1554
Author(s):  
Justinas Januskevicius ◽  
Zivile Stankeviciute ◽  
Dalis Baltrunas ◽  
Kęstutis Mažeika ◽  
Aldona Beganskiene ◽  
...  
Keyword(s):  
Magnetic Measurements ◽  
Substrate Surface ◽  
Sol Gel ◽  
Synthesis Method ◽  
Xrd Analysis ◽  
Dip Coating ◽  
Yttrium Iron ◽  
Iron Garnet ◽  
Dip Coating Technique ◽  
Sol Gel Synthesis

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.

scholarly journals Hard Coating Materials Based on Photo-Reactive Silsesquioxane for Flexible Application: Improvement of Flexible and Hardness Properties by High Molecular Weight

Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1564
Author(s):  
Jong Tae Leem ◽  
Woong Cheol Seok ◽  
Ji Beom Yoo ◽  
Sangkug Lee ◽  
Ho Jun Song
Keyword(s):  
Molecular Weight ◽  
Surface Morphology ◽  
High Molecular Weight ◽  
Sol Gel ◽  
Xrd Analysis ◽  
Polyhedral Oligomeric Silsesquioxanes ◽  
Coating Materials ◽  
Pencil Hardness ◽  
Coated Film ◽  
Flexible Application

EPOSS of polyhedral oligomeric silsesquioxanes (POSS) mixture structure and LPSQ of ladder-like polysilsesquioxane (LPSQ) structure were synthesized via sol–gel reaction. EPSQ had a high molecular weight due to polycondensation by potassium carbonate. The EPSQ film showed uniform surface morphology due to regular double-stranded structure. In contrast, the EPOSS-coated film showed nonuniform surface morphology due to strong aggregation. Due to the aggregation, the EPOSS film had shorter d-spacing (d1) than the EPSQ film in XRD analysis. In pencil hardness and nanoindentation analysis, EPSQ film showed higher hardness than the EPOSS film due to regular double-stranded structure. In addition, in the in-folding (r = 0.5 mm) and out-folding (r = 5 mm) tests, the EPSQ film did not crack unlike the EPOSS coated film.

Synthesis of Cu Loaded TiO2 Nanoparticles for the Improved Photocatalytic Degradation of Rhodamine B

2016 ◽  
Vol 15 (05n06) ◽  
pp. 1660002 ◽  
Author(s):  
V. Kavitha ◽  
P. S. Ramesh ◽  
D. Geetha
Keyword(s):  
Titanium Dioxide ◽  
Rhodamine B ◽  
Sol Gel ◽  
Average Particle Size ◽  
Visible Spectrum ◽  
Xrd Analysis ◽  
Bandgap Energy ◽  
Average Particle ◽  
Titanium Tetraisopropoxide ◽  
Photoexcited Electron

Copper doped Titanium dioxide TiO2 nanoparticles were synthesized by sol–gel method using titanium tetraisopropoxide and copper sulfate as precursors. The synthesized nanoparticles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), UV-Visible spectroscopy (UV-Vis), Photoluminesce spectroscopy (PL) and atomic force microscopy (AFM). XRD analysis confirms the formation of anatase titanium dioxide and average particle size was 35[Formula: see text]nm. Cu– TiO2 exhibits a shift in the absorption edge toward visible spectrum. The rate of recombination and transfer behavior of the photoexcited electron–hole pairs in the semiconductors was recorded by photoluminescence. From SEM spherical shaped nanoparticles was observed. Comparing with pure TiO2 nanoparticles, Cu doped TiO2 photocatalyst exhibited enhanced photocatalytic activity under natural sunlight irradiation in the decomposition of rhodamine B aqueous solution. The maximum 97% of degradation efficiency of Rhodamine B was observed at 0.6% Cu–TiO2 within 180[Formula: see text]min. The photocatalytic efficiency of Rhodamine B of Cu doped TiO2 nanoparticle was higher than the pure TiO2, which could be attributed to the small crystallinity intense light absorption in Sunlight and narrow bandgap energy of Copper.

PREPARATION AND FERROELECTRIC PROPERTY OF (100)-ORIENTED Ca0.4Sr0.6Bi4Ti4O15 THIN FILM ON Pt/Ti/SiO2/Si SUBSTRATE

2010 ◽  
Vol 17 (05n06) ◽  
pp. 445-449 ◽  
Author(s):  
SUHUA FAN ◽  
QUANDE CHE ◽  
FENGQING ZHANG
Keyword(s):  
Thin Film ◽  
Thin Films ◽  
Ferroelectric Property ◽  
Remanent Polarization ◽  
Sol Gel ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Si Substrate ◽  
Degree Of Orientation ◽  
Equiaxed Grains

The (100)-oriented Ca0.4Sr0.6Bi4Ti4O15(C0.4S0.6BTi ) thin film was successfully prepared by a sol-gel method on Pt/Ti/SiO2/Si substrate. The orientation and formation of thin films under different annealing schedules were studied using XRD and SEM. XRD analysis indicated that (100)-oriented C0.4S0.6BTi thin film with degree of orientation of I(200)/I(119) = 1.60 was prepared by preannealing the film at 400°C for 3 min followed by rapid thermal annealing at 800°C for 5 min. SEM analysis further indicated that the (100)-oriented C0.4S0.6BTi thin film with a thickness of about 800 nm was mainly composed of equiaxed grains. The remanent polarization and coercive field of the film were 16.1 μC/cm2 and 85 kV/cm, respectively.

Structural, Magnetic and Dielectric Analysis of Higher Magnetic Mn Doped Zn-Cr Oxide Nanoparticles

2021 ◽  
Vol 9 (VI) ◽  
pp. 95-102
Author(s):  
S. D. Balsure
Keyword(s):  
Type Strain ◽  
Sol Gel ◽  
Hexagonal Wurtzite Structure ◽  
Xrd Analysis ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
Microstructural Parameters ◽  
Auto Combustion ◽  
Mn Doped ◽  
Combustion Technique

Higher magnetic Mn doped Zn-Cr oxide nanoparticles with general compositional formula MxZn0.95-xCr0.05O have been synthesized by using sol-gel auto combustion technique. Room temperature X-ray diffraction (XRD) technique has been employed to study the structural and microstructural parameters of the as-prepared samples. XRD analysis confirms the phase purity and hexagonal wurtzite structure of all the samples. Replacement of Zn2+ ions by Mn2+ ions shifts peak positions slightly towards the lower angles which in turn expands the lattice lengths ‘a’ from 3.2487 to 3.2528 Å and ‘c’ from 5.2043 to 5.2118 Å. Crystallite size obtained from Scherrer equation was confirmed by Williamson – Hall (W-H) and size – strain plot methods (SSP). Both W-H and SSP methods reveals the tensile type strain for undoped sample and comprehensive type strain for Mn2+ doped samples. Magnetic properties were investigated by using vibrating sample magnetometer. Diluted ferromagnetic behaviour is observed for all the samples and saturation magnetization (MS) increases from 0.0514 to 0.1163 emu/gm. Two-probe technique was employed to understand the dielectric behaviour of the samples as a function of frequency. At lower frequency region, both dielectric constant () and dielectric loss tangent (tan ) shows higher values and decreases with the increasing applied frequency.

scholarly journals Effect of the sintering temperature on the fabrication of alumina beads

2019 ◽  
Vol 16 (2) ◽  
pp. 125-135
Author(s):  
Ayse KALEMTAS
Keyword(s):  
Sintering Temperature ◽  
Sol Gel ◽  
Xrd Analysis ◽  
Liquid Phase Sintering ◽  
Sintered Ceramic ◽  
Mullite Phase ◽  
Commercial Grade ◽  
Composite Beads ◽  
Sintering Additive ◽  
Dta Analysis

In this study, kaolin bonded alumina-alginate composite beads were fabricated via a facile one-step sol-gel process by using sodium alginate. In order to achieve sintering of the beads at lower sintering temperatures a limited amount of CC31 commercial-grade kaolin was used as a sintering additive (Al2O3:CC31 commercial-grade kaolin=14:1). Produced composite beads were heat treated at 1300°, 1400° and 1500°C for 1 hour to achieve partial densification of the beads. TG-DTA analysis of the CC31 commercial-grade kaolin showed that mullite phase formation took place approximately at 1000°C. However, XRD measurements revealed that there is only alumina phase in the sintered ceramic beads. Due to the low amount of CC31 commercial-grade kaolin, mullite formation was not detectable via XRD analysis. No significant grain growth was observed at the sintered samples depending on the increasing sintering temperature. However, when the sintering temperature was increased, densification ratio and mechanical properties of the produced beads were enhanced significantly. Microstructural investigations of the sintered beads shown that with the help of the liquid phase sintering process, a good chemical bonding was achieved between the alumina particles.

scholarly journals Synthesis and Optical Manifestation of NiO-Silica Nanocomposite

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
S. Chakrabarty ◽  
K. Chatterjee
Keyword(s):  
Sol Gel ◽  
Size Variation ◽  
Average Diameter ◽  
Xrd Analysis ◽  
Peak Position ◽  
Band Gap Energy ◽  
Strong Emission ◽  
Silica Nanocomposites ◽  
Composite Formation ◽  
Silica Nanocomposite

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.

scholarly journals Synthesis of Silica-Salen Derivative from Rice Husk Ash and its Use for Extraction of Divalent Metal Ions Co(II), Ni(II) and Cu(II)

2019 ◽  
Vol 20 (1) ◽  
pp. 16 ◽  
Author(s):  
Duha Hussien Attol ◽  
Hayder Hamied Mihsen
Keyword(s):  
Metal Ions ◽  
Rice Husk ◽  
Rice Husk Ash ◽  
Sol Gel ◽  
Xrd Analysis ◽  
Divalent Metal Ions ◽  
Prepared Compound ◽  
Absorption Bands ◽  
Pseudo Second Order ◽  
Ft Ir

Rice husk ash (RHA) was used to prepare sodium silicate, which in turn was functionalized with 3-(chloropropyl)triethoxysilane employing the sol-gel technique to form RHACCl. Chloro group in RHACCl was replaced with iodo group forming RHACI. Ethylenediamine was immobilized on RHACI in order to prepare it for the reaction with salicylaldehyde to form a silica derivative-salen. FT-IR analysis indicated the presence of secondary amine and –NH and C=N absorption bands. XRD analysis revealed the occurrence of the broad diffused peak with maximum intensity at 22–23° (2θ). BET measurements showed also that the surface area of the prepared compound is 274.55 m2/g. Elemental analysis proved the existence of nitrogen in the structure of the prepared compound. The silica derivative-salen showed high potential for extraction and removal of heavy contaminating metal ions Ni(II), Cu(II), and Co(II) from aqueous solutions. The kinetic study demonstrates that the adsorption of the metal ions follows the pseudo-second order.

scholarly journals Effect of Re and Tm-site on morphology structure and optical band gap of ReTmO3 (Re: La, Ce, Nd, Gd, Dy, Y and Tm: Fe, Cr) prepared by sol-gel method

2018 ◽  
Vol 64 (4) ◽  
pp. 381
Author(s):  
Muhammad Tufiq Jamil ◽  
Javed Ahmad ◽  
Syed Hamad Bukhari ◽  
Murtaza Saleem
Keyword(s):  
Band Gap ◽  
Sol Gel ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
X Ray ◽  
Average Grain Size ◽  
Auto Combustion ◽  
Uv Visible

Rare earth nano sized pollycrystalline orthoferrites and orthocromites ReT mO3 (Re = La, Nd, Gd, Dy, Y and T m = Fe, Cr) have been synthesized by sol-gel auto combustion citrate method. The samples have been characterized by means of X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDX), and UV-visible spectroscopy. The samples are single phase as confirmed by XRD analysis and correspond to the orthorhombic crystal symmetry with space group pbnm. Debye Scherer formula and Williamson Hall analysis have been used to calculate the average grain size which is consistent with that of determined from SEM analysis and varied between 25-75 nm. The elemental compositions of all samples have been checked by EDX analysis. Different crystallographic parameters are calculated with strong structural correlation among Re and Tm sites. The optical energy band gap has been calculated by using Tauc relation estimated to be in the range of 1.77 - 1.87 eV and 2.77 - 3.14 eV, for ReFeO3 and ReCrO3, respectively.

Sign in / Sign up

Export Citation Format

Share Document