Preparation and Characterization of Fibrous Hydroxyapatite/Chitosan Nanocomposites with High Hydroxyapatite Dosage

2012 ◽  
Vol 457-458 ◽  
pp. 365-371 ◽  
Author(s):  
Cai Yun Zhang ◽  
Dai Yin Peng ◽  
Chuan Hua Lu ◽  
Xian Ping Wang ◽  
Qian Feng Fang
Keyword(s):  
Morphological Properties ◽  
In Vitro Tests ◽  
X Ray Diffraction ◽  
Permeable Membrane ◽  
X Ray ◽  
Chitosan Matrix ◽  
Transmission Electron

In this paper the hydroxyapatite fibers reinforced chitosan nanocomposites with high hydroxyapatite dosage (70~90 wt%) were synthesized by in-situ hybridization. The semi-permeable membrane was used to control the process of hybridization and morphology of hydroxyapatite. The compositional and morphological properties of nanocomposites were investigated by FTIR spectroscopy, X-ray diffraction, and transmission electron microscopy. The results showed that the hydroxyapatite were carbonated nanometer crystalline fibers with high aspect ratio (about 25) and dispersed uniformly in the nanocomposites. The high-resolution image indicated that the growth of nano-hydroxyapatite crystallites in the chitosan matrix preferred in the c-axis. The mechanical properties of these nanocomposites were enhanced dramatically and the compressive strength increases almost to 170MPa when the hydroxyapatite content is 70 wt%. The in vitro tests indicated that the composites have high bioactivity and degradation. These properties illustrated the potential application of this kind of nanocomposites for bone tissue engineering.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

scholarly journals Engineering of Chitosan-Hydroxyapatite-Magnetite Hierarchical Scaffolds for Guided Bone Growth

Materials ◽  
2019 ◽  
Vol 12 (14) ◽  
pp. 2321 ◽  
Author(s):  
Pistone ◽  
Celesti ◽  
Piperopoulos ◽  
Ashok ◽  
Cembran ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Bone Growth ◽  
Cell Attachment ◽  
X Ray Diffraction ◽  
Culture Studies ◽  
X Ray ◽  
Support Cell ◽  
Chitosan Matrix

Bioabsorbable materials have received increasing attention as innovative systems for the development of osteoconductive biomaterials for bone tissue engineering. In this paper, chitosan-based composites were synthesized adding hydroxyapatite and/or magnetite in a chitosan matrix by in situ precipitation technique. Composites were characterized by optical and electron microscopy, thermogravimetric analyses (TGA), x-ray diffraction (XRD), and in vitro cell culture studies. Hydroxyapatite and magnetite were found to be homogeneously dispersed in the chitosan matrix and the composites showed superior biocompatibility and the ability to support cell attachment and proliferation; in particular, the chitosan/hydroxyapatite/magnetite composite (CS/HA/MGN) demonstrated superior bioactivity with respect to pure chitosan (CS) and to the chitosan/hydroxyapatite (CS/HA) scaffolds

Mechanical, microstructural properties and cell adhesion of Sr/Se-hydroxyapatite/graphene/polycaprolactone nanofibers

2020 ◽  
pp. 089270572091278 ◽  
Author(s):  
Reem Al-Wafi ◽  
SF Mansour ◽  
MK Ahmed
Keyword(s):  
Electron Microscopy ◽  
Tensile Strength ◽  
Microstructural Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nanofibrous Scaffolds ◽  
Transmission Electron ◽  
Fesem Micrographs

Electrospun nanofibrous scaffolds containing co-dopant of Sr/Se into carbonated hydroxyapatite has been synthesized in situ with graphene (G) nanosheets and carried on polycaprolactone at different contributions of G. The powder and the nanofibrous samples were investigated using X-ray diffraction, transmission electron microscopy, and field emission scanning electron microscopy (FESEM). The FESEM micrographs show that the highest content of G (0.2 G) was formed in non-oriented/rough/cracked fibers with diameters around 0.3–0.4 µm at the maximum. The tensile strength of nanofibrous scaffolds was improved with the addition of G nanosheets and the maximum tensile strength of 0.2 G was around 6.39 ± 0.24 MPa, while the minimum cell viability ratio was about 94.4 ± 3.2% for the free G nanofibers. The in vitro attachment of HFB4 cell lines was investigated and it showed that nanofibrous scaffolds have induced cells to be proliferated and spread on the nanofibrous scaffolds’ surface. This behavior of cells growth encourages more investigations for these nanofibrous scaffolds to be promoted for clinical applications.

Synthesis and characterization of organic–inorganic poly(3,4-ethylenedioxythiophene)/MoS2 nanocomposite via in situ oxidative polymerization

2006 ◽  
Vol 21 (1) ◽  
pp. 112-118 ◽  
Author(s):  
A. Vadivel Murugan ◽  
Mathieu Quintin ◽  
Marie-Helene Delville ◽  
Guy Campet ◽  
Annamraju Kasi Viswanath ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxidative Polymerization ◽  
X Ray Diffraction ◽  
Rechargeable Lithium Batteries ◽  
X Ray ◽  
Transmission Electron ◽  
Basal Distance ◽  
New Type

Here we demonstrate the synthesis of a new type of layered poly(3,4-ethylenedioxy- thiophene) (PEDOT)/MoS2 nanocomposite via flocculation of delaminated MoS2 with subsequent in situ oxidative polymerization of 3,4-ethylenedioxythiophene. The resulting nanocomposite was characterized by Fourier transform infrared spectroscopy, powder x-ray diffraction, x-ray photoelectron spectroscopy, thermal analysis, transmission electron microscopy, and four-probe electrical conductivity measurements with respect to temperature. X-ray diffraction results indicated that the exfoliated MoS2 and PEDOT are restacked to produce a novel nanoscale composite material containing alternate nanoribbons of PEDOT in between MoS2 with a basal distance of ∼1.38 nm. The nanocomposite, which could be used as a cathode material for small power rechargeable lithium batteries, has also been demonstrated by the electrochemical insertion of lithium into the PEDOT/MoS2 nanocomposite, where a significant enhancement in the discharge capacity is observed, compared to that of respective pristine molybdenum disulfide.

Microstructural Characterization of In Situ Reaction TiB2/Zn-30Al-1Cu Composites Prepared by Spray Deposition Process

2014 ◽  
Vol 1015 ◽  
pp. 688-691 ◽  
Author(s):  
Feng Wang ◽  
Qiang Zhang ◽  
Bai Qing Xiong ◽  
Yong An Zhang ◽  
Hong Wei Liu ◽  
...  
Keyword(s):  
Spray Deposition ◽  
Microstructural Characterization ◽  
Deposition Process ◽  
Deposition Technique ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

An innovative spray deposition technique has been applied to produce in situ TiB2/Zn-30Al-1Cu composites. The microstructures of the spray-deposited composite were studied using scanning electron microscopy, transmission electron microscope and X-ray diffraction. The results have shown that the TiB2particulates are formed in the microstructure. It was found that the TiB2particles were distributed in Zn-30Al-1Cu matrix uniformly, and the TiB2particles are about 2μm in size.

scholarly journals Preparation and Characterization of Biomimetic Hydroxyapatite Nanocrystals by Using Partially Hydrolyzed Keratin as Template Agent

Nanomaterials ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 241 ◽  
Author(s):  
Chunxia Gao ◽  
Ke Zhao ◽  
Liwei Lin ◽  
Jinyu Wang ◽  
Yang Liu ◽  
...  
Keyword(s):  
Tissue Repair ◽  
X Ray Diffraction ◽  
Natural Structure ◽  
X Ray ◽  
Tissue Repair And Regeneration ◽  
Transmission Electron ◽  
Biomimetic Hydroxyapatite ◽  
Hydroxyapatite Nanocrystals

Hydroxyapatite (HA), a typical inorganic component of bone, is a widely utilized biomaterial for bone tissue repair and regeneration due to its excellent properties. Inspired by the recent findings on the important roles of protein in biomineralization and natural structure of fish scales, keratin was chosen as a template for modulating the assembly of HA nanocrystals. A series of HA nanocrystals with different sizes were synthesized by adjusting the concentration of partially hydrolyzed keratin. The structure and compositions of the prepared HA were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectrum, and Transmission electron microscopy (TEM). Results revealed that the size of the synthesized HA nanocrystals can be controlled by adjusting the concentration of partially hydrolyzed keratin. Specifically, the size of synthesized HA decreased from 63 ± 1.5 nm to 27 ± 0.9 nm with the increasing concentration of partially hydrolyzed keratin from 0 to 0.6g. In addition, in vitro cytocompatibility of synthesized HA nanocrystals were evaluated using the MG-63 cells.

Synthesis and Characterization of Nanocrystalline SnO2 Powder

2011 ◽  
Vol 675-677 ◽  
pp. 267-270
Author(s):  
Shi Min Liu ◽  
Wan Yu Ding ◽  
Wei Wei Jiang ◽  
Wei Ping Chai
Keyword(s):  
Morphological Properties ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Direct Precipitation ◽  
Transmission Electron ◽  
Crystal Structural ◽  
Sno2 Powder ◽  
Direct Precipitation Method

Nanocrystalline SnO2 powder has been synthesized via direct precipitation method starting from Sn, HNO3, HCl, and NH4OH. Thermal properties, crystal structural and morphological properties of the precursor and SnO2 powder were investigated using simultaneous thermogravimetry-differential thermal analysis, X-ray diffraction and transmission electron microscopy. The results indicated that the precursor was SnO2 rather than Sn(OH)2 or Sn(OH)4. On the basis of the precursor, well crystallized SnO2 powder with 4-5 nm in diameter was obtained, after calcined at 350 °C for 2 h.

scholarly journals Characterization of Highly Dispersed Rod- and Particle-Shaped CuFe19Ox Catalysts and Their Shape Effects on WGS

Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 635
Author(s):  
Lingjuan Ma ◽  
Dawei Han ◽  
Hongbin Ma ◽  
Longgang Liu ◽  
Huichao Guo
Keyword(s):  
X Ray Diffraction ◽  
X Ray ◽  
In Situ Xrd ◽  
Transmission Electron ◽  
Highly Dispersed ◽  
Shape Effects ◽  
Temperature Programmed ◽  
Water Gas

Highly dispersed CuFe19Ox catalysts with different shapes were prepared and further characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), H2 temperature-programmed reduction (H2-TPR), and in-situ XRD. XRD and TEM results showed that the synthesized CuFe19Ox nanoparticles consisted of CuO and Fe2O3, while CuFe19Ox nanorods consisted of CuFe2O4 and Fe2O3. The reduction properties of CuFe19Ox samples were finely studied by H2-TPR, and the phase composition was identified by in-situ XPS, HR-TEM, and surface TPR (s-TPR). In-situ X-ray photoelectroscopy (XPS) indicated that the metallic Cu and Fe3O4 were the main species after reduction. Moreover, s-TPR studies showed that the reduction performance of copper was significantly affected by the shapes of the Fe3O4 supports. Low-temperature water gas shift (LT-WGS) was chosen to characterize the Cu species on the surface. It was found that reduced CuFe19Ox nanorods had no activity. On the contrary, reduced CuFe19Ox particles showed higher initial WGS activity, where the active Cu0 should originate from the reduction of Cu2O at lower temperatures, as confirmed by the s-TPR profiles.

Preparation and characterization of poly(2-hydroxyethyl methacrylate)/ Na-montmorillonite intercalated nanocomposites

2013 ◽  
Vol 33 (1) ◽  
pp. 27-32 ◽  
Author(s):  
Zafer Koç ◽  
Meltem Çelik ◽  
Müşerref Önal ◽  
Yüksel Sarıkaya ◽  
Yesim Mogulkoc
Keyword(s):  
Interlayer Spacing ◽  
Hydroxyethyl Methacrylate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Monomer Content ◽  
Diffraction Patterns ◽  
Thermal Stability Of

Abstract A series of intercalated nanocomposites were prepared via in situ polymerization of 2-hydroxyethyl methacrylate (HEMA) between the interlayer spacing of hydrous Na-montmorillonite (Na-MMT) using benzoyl peroxide (Bz2O2) as a radical initiator. X-ray diffraction patterns showed the absence of any intercalation up to 61.7 mass% of HEMA, but anhydrous Na-MMT formed by the hydrophilic effect of HEMA. The interlayer spacing (d001) values of hydrous and anhydrous Na-MMT were calculated as 1.19 and 1.03 nm, respectively. At higher monomer contents, the increase in the value of d001 from 1.19 to 2.01 nm indicated intercalation of polymer in the interlayer spacing of Na-MMT. Besides, transmission electron microscopy results supported the formation of the intercalated nanocomposites. Thermogravimetric analysis showed that the thermal stability of the nanocomposites increased considerably by intercalation of pure poly-HEMA. Specific surface area and specific nanopore volume of the nanocomposites decreased with the increasing of the monomer content taken by the preparations. The decrease is due to the nonporous nature of the polymer matrix.

Photoluminescence Enhancement of CdS Nanocrystals Fabricated on Dithiocarbamate Functionalized PET Substrates

2012 ◽  
Vol 512-515 ◽  
pp. 1511-1515
Author(s):  
Chun Lin Zhao ◽  
Li Xing ◽  
Xiao Hong Liang ◽  
Jun Hui Xiang ◽  
Fu Shi Zhang ◽  
...  
Keyword(s):  
Room Temperature ◽  
Hexagonal Structure ◽  
Diffraction Measurement ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
X Ray ◽  
Cds Nanocrystals ◽  
Morphological Studies ◽  
Transmission Electron

Cadmium sulfide (CdS) nanocrystals (NCs) were self-assembled and in-situ immobilized on the dithiocarbamate (DTCs)-functionalized polyethylene glycol terephthalate (PET) substrates between the organic (carbon disulfide diffused in n-hexane) –aqueous (ethylenediamine and Cd2+ dissolved in water) interface at room temperature. Powder X-ray diffraction measurement revealed the hexagonal structure of CdS nanocrystals. Morphological studies performed by scanning electron microscopy (SEM) and high-resolution transmission electron microscope (HRTEM) showed the island-like structure of CdS nanocrystals on PET substrates, as well as energy-dispersive X-ray spectroscopy (EDS) confirmed the stoichiometries of CdS nanocrystals. The optical properties of DTCs modified CdS nanocrystals were thoroughly investigated by ultraviolet-visible absorption spectroscopy (UV-vis) and fluorescence spectroscopy. The as-prepared DTCs present intrinsic hydrophobicity and strong affinity for CdS nanocrystals.

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