Fabrication and characterization of hydroxyapatite/collagen bone-like nanocomposite through a self-assembly method

2012 ◽  
Vol 19 (2) ◽  
pp. 177-182 ◽  
Author(s):  
Zhenlin Wang ◽  
Yuhua Yan ◽  
Tao Wan

AbstractBased on a self-assembly mechanism, a co-precipitation method was utilized to fabricate bone-like biomimetic nanocomposite with a simplified preparation approach and accessible materials to investigate in depth some characteristics of hydroxyapatite/collagen(HAp/Col) nanocomposite for the elucidation of performances in some respects. The as-prepared composite was characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Fourier transformation infrared spectroscopy, and thermal analysis. The results show that HAp nanocrystals formed as preferentially oriented slender needles 50–100 nm in length on a felt-like Col matrix which is composed of large numbers of randomly oriented Col fibers and showed polycrystalline behavior. The as-prepared cellular composites are analogous in both composition and nanostructured architecture to native bone, longer aging time promotes the growth and purification of nano-HAp on Col, and characterization confirms that chemical interaction occurs and causes intimate bonding between HAp and Col.

2019 ◽  
Vol 17 (1) ◽  
pp. 865-873 ◽  
Author(s):  
Muhammad Ramzan Saeed Ashraf Janjua

AbstractThe nano aggregates of cobalt oxide (Co3O4) are synthesized successfully by adopting simple a co precipitation approach. The product obtained was further subjected to the calcination process that not only changed it morphology but also reduces the size of individual particles of aggregates. The prepared nano aggregates are subjected to different characterization techniques such as electron microscopies (scanning electron microscopy and transmission electron microscopy) and X-ray diffraction and results obtained by these instruments are analyzed by different software. The characterization results show that, although the arrangement of particles is compact, several intrinsic spaces and small holes/ pores can also be seen in any aggregate of the product. The as synthesized product is further tested for catalytic properties in thermal decomposition of ammonium perchlorate and proved to be an efficient catalyst.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
R. D. Ávila-Avilés ◽  
N. Torres-Gómez ◽  
M. A. Camacho-López ◽  
A. R. Vilchis-Nestor

Abstract Nature provides remarkable examples of mass-produced microscale particles with structures and chemistries optimized by evolution for particular functions. Synthetic chemical tailoring of such sustainable biogenic particles may be used to generate new multifunctional materials. Herein, we report a facile method for the synthesis of hybrid nano/microstructures Ag-Fe3O4 based on Dimorphotheca ecklonis pollen grains as bio-template. Silver nanoparticles was biosynthesized using pollen grains as a reduction and stabilization agent as well as a bio-template promoting the adhesion of silver nanoparticles to pollen surface. Fe3O4 nanoparticles were synthesized by co-precipitation method from FeSO4. Hybrid nano/microstructures Ag-Fe3O4 based on Dimorphotheca ecklonis pollen grains as bio-template were obtained and characterized using Scanning Electron Microscopy and Transmission Electron Microscopy to study the morphology and structure; Energy-Dispersive X-ray Spectroscopy to determine the chemical composition distribution; and Confocal Fluorescence Microscopy to demonstrate the fluorescence properties of hybrid nano-microstructures. Furthermore, these hybrid nano-microstructures have been studied by Surface-Enhanced Raman Scattering (SERS), using methylene blue as a target molecule; the hybrid nano-microstructures have shown 14 times signal amplification.


Materials ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 7673
Author(s):  
Ziyang You ◽  
Jing Xu

The usage of nanoscale calcium silicate hydrate (nano C-S-H) proved to have an excellent promotion effect on the early performance of concrete as nano C-S-H with ultra-fine particle size can act as seeding for cement hydration. Therefore, it is of importance to tune the particle size during the synthesis process of nano C-S-H. In this paper, the influence of several variables of the particle size distribution (PSD) of nano C-S-H synthesized by chemical co-precipitation method with the aid of polycarboxylate (PCE) was studied by orthogonal experimental design. In addition, the composition, microstructure, and morphology of the C-S-H/PCE nanocomposites were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Raman spectrum. The results showed that the concentration of reactants had a significant impact on the PSD of C-S-H/PCE nanocomposites, followed by the dosage of dispersant. Ultrasonic treatment was effective in breaking the C-S-H/PCE aggregates with unstable agglomeration structures. The change in synthetic variables had a negligible effect on the composition of the C-S-H/PCE nanocomposites but had a significant influence on the crystallinity and morphology of the composites.


2021 ◽  
Author(s):  
Waseem Raza ◽  
Ghulam Nabi ◽  
Asim Shahzad ◽  
Nafisa Malik ◽  
Nadeem Raza

Abstract Lanthanum cerium ferrite nanoparticles has been synthesized for the first time via hydrothermal and co-precipitation method. The structural and morphological study of the nanoparticles have been examined by using X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive x-ray spectroscopy (EDX). The electrochemical study of J1 and J2 electrodes have been examined using three electrode system in 6 M KOH electrolyte using cyclic voltammetry (CV), galvanostatic charging-discharging (GCD) and electrochemical impendence spectroscopy (EIS). The highest specific capacitance of 1195 F/g has been obtained at a scan rate of 10 mV/s from hydrothermal synthesis nanomaterial electrode (J2) and long cycling life 92.3% retention after 2000th cycles. Furthermore, the energy density and power density of the J2 electrode at a current density of 5 A/g was 59 Wh/kg and 9234 W/kg respectively. Hence, the fabricated J2 electrode is a favorable candidate for super-capacitor applications.


2007 ◽  
Vol 280-283 ◽  
pp. 521-524
Author(s):  
Li Qiong An ◽  
Jian Zhang ◽  
Min Liu ◽  
Sheng Wu Wang

Yb3+ and Ho3+ co-doped Lu2O3 nanocrystalline powders were synthesized by a reversestrike co-precipitation method. The as-prepared powders were examined by the X-ray diffraction and transmission electron microscopy. The phase composition of the powders was cubic and the particle size was in the range of 30~50 nm. Emission and excitation spectra of the powders were measured by a spectrofluorometer and the possible upconversion luminescence mechanism was also discussed.


2006 ◽  
Vol 972 ◽  
Author(s):  
Vincenzo Esposito ◽  
Marco Fronzi ◽  
Enrico Traversa

AbstractNanometric 20% molar Sm-doped ceria (SDC20) powders were synthesized by tetrametylethylen ammine (TMDA) co-precipitation method. SDC20 was sintered in several conditions to control the final microstructure. Fast firing and conventional sintering were performed. LiNO3was used as an additive to promote liquid phase sintering of ceria at low temperatures (900-1200°C). Powders and dense pellets were analysed using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM). Electrochemical impedance spectroscopy (EIS) measurements were performed on dense pellets in air to estimate the contribution of grain boundary and bulk to the electrical conductivity. Liquid phase sintering produced the densest samples with the highest conductivity.


2014 ◽  
Vol 879 ◽  
pp. 155-163 ◽  
Author(s):  
Rahizana Mohd Ibrahim ◽  
Markom Masturah ◽  
Huda Abdullah

Nanoparticles of Zn1-xFexS ( x=0.0,0.1,0.2 and 0.3) were prepared by chemical co-precipitation method from homogenous solution of zinc and ferum salt at room temperature with controlled parameter. These nanoparticles were sterically stabilized using Sodium Hexamethaphospate (SHMP). Here, a study of the effect of Fe doping on structure, morphological and optical properties of nanoparticles was undertaken. Elemental analysis, morphological and optical properties have been investigated by Fourier-Transform-Infrared spectroscopy (FT-IR), X-Ray Fluorescence (XRF), Field Emmision Scanning Electron Microscopy (FESEM), X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and UV-Visible Spectroscopy. FTIR measurement confirmed the presence of SHMP in the nanoparticles structure with the FESEM images depicting considerable less agglomeration of particles with the presence of SHMP. While XRF results confirm the presence of Fe2+ ion as prepared in the experiment. The particles sizes of the nanoparticles lay in the range of 2-10 nm obtained from the TEM image were in agreement with the XRD results. The absorption edge shifted to lower wavelengths with an increase in Fe concentration shown in the UV-Vis spectroscopy. The band gap energy value was in the range of 4.95 5.15 eV. The blueshift is attributed to the quantum confinement effect.


2021 ◽  
Vol 24 (12) ◽  
pp. 2147-2151
Author(s):  
Y.A. Dallatu ◽  
G.A. Shallangwa ◽  
S.N. Africa

The use of plant extracts has become an interesting ecofriendly method to synthesize and stabilize the different structures nanoparticles (NPs). This work investigated the effect of plant extract as a reducing and stabilizing agent on the growth and morphology of ZnO nanoparticles (ZnO-NPs). Green synthesis and growth of spherical ZnONPs was carried out by co-precipitation method using a Zinc acetate salt and various amounts of Azadirachta indica seed husk extract (20 ml and 40 ml). The synthesized ZnO-NPs were characterized by Fourier transform infrared (FTIR), scanning electron microscopy (SEM-EDX), and transmission electron microscopy (TEM). The FTIR analyses revealed the presence of Phenolic alcohol, amines and carboxylic acid groups and ZnO in synthesized NPs with more intense peaks at higher amount (40 ml) of A. indica extract. Also, structural morphology analyses using SEM revealed uniform spherical shaped particles with diameter from 25 to 60 nm (20 ml of extract) and 19 to 35 nm (40 ml of extract) for ZnO-NPs. The EDX spectral revealed that the required phase of Zn and O was present 69.54% (Zn) and 30.46% (O) at 20 ml of extract, also 73.71% (Zn), 26.26% (O) at 40 ml of extract respectively and confirmed high purity for the synthesized ZnO NPs. TEM revealed spherical shaped NPs with diameter ranging from 28 to 52 nm (20 ml of extract) and 8.2 to 11.9 nm (40 ml of extract) respectively, with a trend reduction in particle size of NPs at higher amount of A. indica seed extract (40 ml) and growth of more uniform particles with no agglomeration. The study showed successful growth of spherical ZnO-NPs with required properties at a higher amount of extract.


2011 ◽  
Vol 347-353 ◽  
pp. 1416-1419
Author(s):  
You Ning Xu ◽  
Hai Zhao ◽  
Duo Jiao Guan

Fe-Mn-Ce metal oxides nanosized particles have been prepared by co-precipitation approach using three kinds of precipitants NaOH, NH4OH and Na2CO3. The products were characterized by Powder X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and BET study. It was found that the samples prepared with NH4OH as a precipitator show higher surface areas and larger sulfur capacity at low calcinations temperature. At high reaction temperatures, the samples prepared with Na2CO3 as precipitator exhibited much better activities for SCR of nitric oxide with ammonia than catalysts prepared with NH4OH and NaOH as the precipitants.


2012 ◽  
Vol 271-272 ◽  
pp. 320-323
Author(s):  
Xiao Chun Ma ◽  
Lei Hao Cui ◽  
Guang Fei Xu

In this paper, the Fe3O4 magnetic nanometer particle was prepared by co-precipitation method. At the same time, the samples were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results show that the surface active agent (PEG4000) can be good for the dispersion performance of Fe3O4 magnetic nanometer particle; and the temperature of 80°C is the appropriate drying temperature to prepare the Fe3O4 magnetic nanometer particle.


Sign in / Sign up

Export Citation Format

Share Document