scholarly journals Synthesis of Colloidal Ruthenium Nanocatalyst by Chemical Reduction Method

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
R. G. Patharkar ◽  
S. U. Nandanwar ◽  
M. Chakraborty

Colloidal ruthenium nanoparticles were prepared by chemical reduction of ruthenium trichloride (RuCl3) using sodium borohydrate (NaBH4) as reducing agent and sodium dodecyl sulfate (SDS) as a stabilizer. Size and size distribution of synthesized colloidal Ru nanoparticles were studied by varying different parameters such as molar ratio (MR) of SDS/RuCl3, NaBH4/RuCl3, effects of different stabilizers, and reducing agents. Prepared nanoparticles were characterized by transmission electron microscope (TEM) and dynamic light scattering (DLS). Stability of colloidal nanoparticles was detected by Turbiscan. Stable Ru nanoparticles were dispersed onγ-Al2O3to prepare Ru/γ-Al2O3catalyst. This catalyst was characterized by X-ray Diffraction (XRD) and transmission electron microscope (TEM).

2013 ◽  
Vol 328 ◽  
pp. 674-678
Author(s):  
Xiao Juan Jiang ◽  
Guo Qiang Luo ◽  
Mei Juan Li ◽  
Qiang Shen ◽  
Lian Meng Zhang

The RGO/Ag nanocomposite with a homogeneous dispersion of Ag on the surface of RGO has been successfully prepared via situ chemical reduction method using DMF (dimethylformamide) as solvent and reducing agent. The RGO/Ag nanocomposite was characterized by X-ray diffractometer (XRD), Fourier transform-infrared (FTIR) spectra, Fieldemission scanning electron microscope (FESEM) and transmission electron microscope (TEM). It is suggested that in the presence of the PVP (polyvinylpyrrolidone), the electrostatic attraction of Ag+ions with negative GO sheets lead to the decoration of Ag nanoparticles on the surface of RGO sheets in RGO/Ag nanocomposite.


2014 ◽  
Vol 1024 ◽  
pp. 44-47 ◽  
Author(s):  
Nur Syafinaz Ridhuan ◽  
Nabil Iman Muzzafaruddin ◽  
Abdul Razak Khairunisak ◽  
K.C. Aw

This work describes the formation of platinum nanodendrites (PtNDs) using the chemical reduction method. The PtNDs were formed with varying concentration of K2PtCl4 precursor (5-20 mM) and growth duration (8-16 min). The optimum concentration of K2PtCl4 was 15 mM whereby high crystalline nanodendrites with an average size of 118 nm were produced. Aggregation of nanodendrites occurred when the growth duration was prolonged to more than 12 minutes. The morphology and size of PtNDs were characterized by using a transmission electron microscope (TEM), high resolution transmission electron microscope (HRTEM) and X-ray diffractometer (XRD). Additionally, the memory characteristics of PtNDs embedded in polymethylsilsesquioxanes (PMSSQ)/Si with gold electrodes were studied in this work. PtNDs played a role as charge-trapped sites and showed good memory effect when embedded in PMSSQ. Optimum memory properties of PMSSQ-embedded PtNDs were obtained for PtNDs synthesized with 15 mM K2PtCl4 concentration at 12 min of growth duration with 170 electrons trapped per PtNDs and Vth of 2.8 V.


2021 ◽  
Author(s):  
Yan Chen ◽  
Yuemei Lan ◽  
Dong Wang ◽  
Guoxing Zhang ◽  
Wenlong Peng ◽  
...  

A series of Gd2-xMoO6:xEu3+(x=0.18-0.38) nanophosphors were synthesized by the solvothermal method. The properties of this nanophosphor were characterized by x-ray diffraction (XRD), transmission electron microscope (TEM), fluorescence spectra and diffuse...


2011 ◽  
Vol 80-81 ◽  
pp. 217-220 ◽  
Author(s):  
Xue Qing Yue ◽  
Hai Jun Fu ◽  
Da Jun Li

Graphite encapsulated nickel nanoparticles were prepared by ball milling andsubsequently annealing a mixture of expanded graphite with nickel powders. The products were characterized by transmission electron microscope and X-ray diffraction. The formation mechanism of the products was discussed. Results show that the products have a size range of 20-150 nm. The graphite and nickel in the products all exhibit a high crystallinity.


2011 ◽  
Vol 311-313 ◽  
pp. 1713-1716 ◽  
Author(s):  
Yan Rong Sun ◽  
Tao Fan ◽  
Chang An Wang ◽  
Li Guo Ma ◽  
Feng Liu

Nano-hydroxyapatite with different morphology was synthesized by the co-precipitation method coupled with biomineralization using Ca(NO3)2•4H2O and (NH4)2HPO4 as reagents, adding chondroitin sulfate, agarose and aspartic acid as template. The structure and morphology of the prepared powders were characterized by X-ray diffraction (XRD) and transmission electron microscope (TEM).


Nanopages ◽  
2019 ◽  
pp. 1-11
Author(s):  
G. M. Taha ◽  
M. N. Rashed ◽  
M. S. El-Sadek ◽  
M. A. Moghazy

Abstract BiFeO3 (BFO) nanopowder was synthesized in a pure form via a sol- gel method based on glycol gel reaction. Effect of drying and preheating temperature on preventing other phases was studied. Many parameters were studied as calcination temperature and time & stirring temperature as well. The prepared powder was characterized by X-Ray Diffraction of powder (XRD) and Transmission Electron Microscope (TEM). High pure BiFeO3 was obtained by preheated process at 400 °C for 0.5 h and calcination at 600 °C for 0.5 h without any impurities compared to dry at110 °C.


2006 ◽  
Vol 71 (11) ◽  
pp. 1153-1160 ◽  
Author(s):  
Chang Hu-Yuan ◽  
Feng Li ◽  
Li. Hua ◽  
Bin Zhang

As prepared carbon nanotubes were pretreated with nitric acid (CNTs-HNO3) or ammonia (CNTs-NH3). Fourier transform infrared spectroscopy (FTIR) measurements showed that the surface of the nanotubes was functionalized with carboxylic and hydroxyl functional groups after the acid treatment and that basic groups containing nitrogen, such as N-H and C-N, were introduced to the surface of the nanotubes after the ammonia treatment. X-Ray diffraction analysis implied that the nickel residue in the CNTs was effectively removed by acid treatment. However, the nickel residue was only partially eliminated by ammonia pretreatment. NiB amorphous catalysts supported on CNTs-HNO3 and CNTs-NH3 were prepared by the impregnation-chemical reduction method and characterized by transmission electron microscopy (TEM), as well as inductively coupled plasma (ICP) spectroscopy and studied in the selective hydrogenation of acetylene. TEM measurements showed that a high density NiB particles of about 9 nm were homogeneously dispersed on the CNTs-NH3. However, NiB particles (13-23 nm)with amean size of 16 nm were scattered on the CNTs-HNO3.As a result, the activity and selectivity of NiB/CNTs-NH3 were higher than those of NiB/CNTs-HNO3 in the selective hydrogenation of acetylene.


2009 ◽  
Vol 79-82 ◽  
pp. 1719-1722
Author(s):  
Zhi Hong Zhang ◽  
Shao Yu Zhang ◽  
Xue Dong Liu

Attapulgite clay(ATP) from Xuyi county of China was purified by a wet method then treated with NaOH and 1.0 mol/L, 2.0 mol/L and 3.0 mol/L solutions of HCl. Transmission electron microscope(TEM) and X-ray diffraction (XRD) were used to characterize treated ATP. Results showed that wet purification could remove most of impurities. Treatment by alkaline and HCl of 1.0 mol/L and 2.0 mol/L could increase purity while treatment of 3.0 mol/L hydrochloric acid could dissolve some element of ATP so much as form SiO2 and destroy fiber structure to clips. Adsorption experiments of Fe3+ and Ni2+ from aqueous solutions were done using original ATP, purified ATP and treated ATP as absorbents. Results showed that Attapulgite could adsorb metal cations in significant amounts. Sodium hydroxide activation had little influence on adsorption capacity. Influences of acid treatments to ATP on adsorption capacity varied on different concentration solutions.


2010 ◽  
Vol 63 ◽  
pp. 392-395
Author(s):  
Yoshifumi Aoi ◽  
Satoru Furuhata ◽  
Hiromi Nakano

ZrN/TiN multi-layers were synthesized by ion beam sputtering technique. Microstructure and mechanical property of the ZrN/TiN multi-layers were characterized and the relationships between microstructure and hardness of the ZrN/TiN multi-layers with various bilayer thicknesses and thickness ratios were investigated. The microstructure of multi-layers have been investigated using transmission electron microscope (TEM) and X-ray diffraction (XRD).


2010 ◽  
Vol 177 ◽  
pp. 32-36 ◽  
Author(s):  
An Rong Wang ◽  
Jian Li ◽  
Qing Mei Zhang ◽  
Hua Miao

Weak magnetic ZnFe2O4 nanoparticles were prepared by coprecipitation and treated with different concentrations of Fe(NO3)3 solution. Untreated and treated particles were studied using a vibrating sample magnetometer, transmission electron microscope, by X-ray diffraction, X-ray energy dispersive spectroscopy and X photoelectron spectroscopy. The results showed that, after treatment, the ZnFe2O4/γ-Fe2O3 forms disphase nanoparticles, with enlarged size, enhanced magnetic properties and with a surface parceled with Fe(NO3)3. The size of the particles and their magnetic properties are related to the concentration of the treatment solution. The particle size and magnetic properties could be controlled by controlling the concentration of treating solution, therefore nanoparticles can be more widely used.


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