Study on Synthesis of Calcium Phosphate Biomaterials Containing SMB

2007 ◽  
Vol 330-332 ◽  
pp. 1033-1036 ◽  
Author(s):  
M.H. Li ◽  
Shu Xin Qu ◽  
R. Shen ◽  
N. Yao ◽  
P.D. Ren ◽  
...  

Calcium phosphate (CaP) biomaterials containing Chinese medicine, Danshen (Salvia Miltiorrhiza Bunge, SMB), have been synthesized in our previous study via the wet chemical method. However, CaP biomaterials were generally synthesized in the alkaline solution. The purpose of the present study was to investigate the effect of pH on SMB and the influence of SMB on the synthesis of CaP biomaterials. The SMB solutions of different pH from 5.0 to 10.0, were scanned with the UV-VIS spectrophotometer (UV-VIS) in the wavelength ranged from 200.00 to 400.00 nm. CaP biomaterials containing SMB were synthesized from (NH4)2HPO4, Ca(NO3)2, NH4OH and SMB. The filtrates of the wet synthesis of CaP biomaterials containing SMB were measured by UV-VIS. The synthesized CaP biomaterials containing SMB were characterized by the X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR). The results showed that the maximum absorption peak appeared at 281.00 nm for solutions of pH 5.0, 6.0 and 7.0. Although there were a new absorption peaks as the pH were 8.0 and 9.0, the absorption curves of SMB became similar to that of SMB as pH at 7.0 after the pH were readjusted to 7.0. The absorption peak appeared an Einstein shift to 347.00 nm at pH 10.0, which did not return to 281.00 nm when the pH of SMB solution was readjusted to 7.0. The absorption peak of filtrates containing SMB of CaP biomaterials reaction system was still at 281.00 nm when their pH was 7.0 and 8.0. Moreover, SMB had no obvious effect on the phase component and functional groups of products. Hence, it could be predicted that calcium phosphate biomaterials containing SMB, such as DCPD and TCP containing SMB, which could be prepared at the pH ranged from 5.0 to 9.0.

2017 ◽  
Vol 8 ◽  
pp. 1257-1265 ◽  
Author(s):  
Urszula Klekotka ◽  
Magdalena Rogowska ◽  
Dariusz Satuła ◽  
Beata Kalska-Szostko

Ferrite nanoparticles with nominal composition Me0.5Fe2.5O4 (Me = Co, Fe, Ni or Mn) have been successfully prepared by the wet chemical method. The obtained particles have a mean diameter of 11–16 ± 2 nm and were modified to improve their magnetic properties and chemical activity. The surface of the pristine nanoparticles was functionalized afterwards with –COOH and –NH2 groups to obtain a bioactive layer. To achieve our goal, two different modification approaches were realized. In the first one, glutaraldehyde was attached to the nanoparticles as a linker. In the second one, direct bonding of such nanoparticles with a bioparticle was studied. In subsequent steps, the nanoparticles were immobilized with enzymes such as albumin, glucose oxidase, lipase and trypsin as a test bioparticles. The characterization of the nanoparticles was acheived by transmission electron microscopy, X-ray diffraction, energy dispersive X-ray and Mössbauer spectroscopy. The effect of the obtained biocomposites was monitored by Fourier transform infrared spectroscopy. The obtained results show that in some cases the use of glutaraldehyde was crucial (albumin).


2013 ◽  
Vol 1506 ◽  
Author(s):  
L. Wang ◽  
B. K. Rai ◽  
S. R. Mishra

AbstractNanostructured Al3+ doped Ni0.75Zn0.25Fe2-xAlxO4 (x = 0.0,0.2,0.4,0.6,0.8, and 1.0) ferrites were synthesized via wet chemical method. X-ray diffraction, transmission electron microscopy, and magnetization measurements have been used to investigate the structural and magnetic properties of spinel ferrites calcined at 950 °C .With the doping of Al3+, the particle size of Ni0.75Zn0.25Fe2-xAlxO4 first increased to 47 nm at x = 0.4 and then decreased down to 37 nm at x = 1. Saturation magnetization decreased linearly with Al3+ due to magnetic dilution. The coercive field showed an inverse dependence on the particle size of ferrites.


Author(s):  
Nguyen Ca ◽  
N. D Vinh ◽  
Phan Van Do ◽  
N. T. Hien ◽  
Xuan Hoa Vu ◽  
...  

Tb3+-doped ZnSe quantum dots (QDs) with Tb content in the range of 0.5 - 7% were successfully synthesized by a wet chemical method. X-ray diffraction (XRD) and transmission electron microscopy...


2018 ◽  
Vol 24 (8) ◽  
pp. 5519-5522
Author(s):  
Israr Ul Hassan ◽  
Liji John ◽  
R. Selwin Joseyphus ◽  
I. Hubert Joe ◽  
R. S Amritha ◽  
...  

Synthesis of nanocrystalline cadmium oxide particles were explored by the reaction of inorganic precursor (cadmium chloride) and alkali (sodium hydroxide) via modified wet-chemical method followed by annealing at various temperatures (250, 500 and 750 °C). The structural, optical and morphological studies of cadmium oxide samples were carried out by X-ray diffraction, infrared, ultraviolet-visible, and scanning electron microscope techniques. From X-ray diffraction analysis, it was confirmed that cadmium oxide particles furnish a face centred cubic phase structure and revealing a grain size of around 59 nm. The scanning electron microscope micrographs admit that cadmium oxide samples are agglomerated and have spherical shapes. The bonding deformation and stretching frequency results of cadmium oxide samples were obtained from infrared spectra. The corresponding increase in calcination temperatures has shown an increase in particle size while as no change was found in band gape. These results attribute that the variation in annealing temperature has a significant role on the crystalline nature, grain size and its optical properties. Furthermore, the synthesized cadmium oxide samples were examined for bioactivity analysis.


2014 ◽  
Vol 875-877 ◽  
pp. 232-236
Author(s):  
Ming Tao Zhou ◽  
Peng Xi Zhu ◽  
Yue Zhao ◽  
Yi Ni Min ◽  
Xiang Peng ◽  
...  

A simple, two-step fabrication technique was presented to prepare the Ag/ZnO hybrid nanostructures using silver nitrate and zinc nitrate. Silver particles were synthesized by chemical reduction method and the ZnO layer was coated on the surface of silver using wet chemical method. The microstructure, the composition and the optical properties of the obtained materials were further characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM) and fluorescence (FL) spectroscopy. The results showed that the silver and zinc oxide composite had been successful prepared. The intensity of fluorescence showed an enhancement of R6G (dye) indicate that ZnO shell had an improvement on the silver metal enhance fluorescence.


2010 ◽  
Vol 25 (10) ◽  
pp. 2042-2046
Author(s):  
R.M. Catchings ◽  
A.N. Thorpe ◽  
J.R. Grant ◽  
R. Douglas ◽  
C. Viragh ◽  
...  

Bismuth telluride (Bi2Te3) systems containing 2%, 4%, and 8% of iron were prepared using a low temperature wet chemical method. Iron oxide nanoparticles were formed when the samples were heated in hydrogen at 250 °C for at least six hours. The samples were characterized by x-ray diffraction, magnetization, magnetic susceptibility, x-ray photoelectron spectroscopy, Mössbauer spectroscopy, and wet chemical analysis measurements. The nanoparticles of iron oxide were identified as γ-Fe2O3 with a particle size of ˜5 nm.


2015 ◽  
Vol 24 (04) ◽  
pp. 1550050 ◽  
Author(s):  
Kieu Loan Phan Thi ◽  
Lam Thanh Nguyen ◽  
Anh Tuan Dao ◽  
Nguyen Huu Ke ◽  
Vu Tuan Hung Le

In this paper, ZnO nanorods were grown by wet chemical method on p-Si (100) substrate to form n-ZnO nanorods/p-Si (100) heterojunction. The optical, electrical, structural properties of n-ZnO nanorods/p-Si(100) heterojunction were analyzed by the photoluminescence (PL) spectroscopy, [Formula: see text]–[Formula: see text] measurement, X-ray diffraction (XRD) and scanning electron microscope (SEM), respectively. The room temperature PL spectra reveal the good optical property of the heterojunction with strong UV peak at 385[Formula: see text]nm. The ZnO nanorods were vertically well-aligned on p-Si (100) and had an average height of about 1.6[Formula: see text][Formula: see text]m. The n-ZnO nanorods/p-Si (100) heterojunction also exhibits diode-like-rectifying-behavior.


RSC Advances ◽  
2016 ◽  
Vol 6 (93) ◽  
pp. 90559-90570 ◽  
Author(s):  
K. Manikandan ◽  
S. Dhanuskodi ◽  
Anitta Rose Thomas ◽  
N. Maheswari ◽  
G. Muralidharan ◽  
...  

SnO2 nanoparticles (NPs) were prepared by a wet chemical method and characterized by X-ray diffraction (XRD) (rutile tetragonal), Fourier transform infrared spectroscopy (FTIR) (Sn–O, 657 cm−1) and micro Raman spectroscopy (Sn–O, 635 cm−1).


2016 ◽  
Vol 17 (4) ◽  
pp. 281 ◽  
Author(s):  
J. Li ◽  
J.W. Ko ◽  
W.B. Ko

<p>BaTiO<sub>3</sub>-TiO<sub>2</sub> nanoparticles were fabricated by a wet-chemical method using barium chloride dihydrate (BaCl<sub>2</sub>·2H<sub>2</sub>O), titanium dioxide (TiO<sub>2</sub>), and oxalic acid (C<sub>2</sub>H<sub>2</sub>O<sub>4</sub>) as precursors. BaTiO<sub>3</sub>-TiO<sub>2</sub>-graphene nanocomposites were obtained by heating the BaTiO<sub>3</sub>-TiO<sub>2</sub> nanoparticles with graphene in an electric furnace at 700 °C for 2 h. X-ray diffraction analysis revealed that the resulting products were BaTiO<sub>3</sub>-TiO<sub>2</sub>-graphene nanocomposites. Scanning electron microscopy revealed the morphologyof the nanocomposites. UV-vis spectrophotometry was used to analyze the photocatalytic degradation of several organic dyes using the BaTiO<sub>3</sub>-TiO<sub>2</sub>-graphene nanocomposites as a photocatalyst under ultraviolet irradiation at 254 nm.</p>


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