Synthesis of cobalt nanoparticles from [bis(2-hydroxyacetophenato)cobalt(II)] by thermal decomposition

Polyhedron ◽  
2009 ◽  
Vol 28 (6) ◽  
pp. 1065-1068 ◽  
Author(s):  
Masoud Salavati-Niasari ◽  
Zeinab Fereshteh ◽  
Fatemeh Davar
2011 ◽  
Vol 127 ◽  
pp. 85-88 ◽  
Author(s):  
Xiao Ming Fu

Metallic cobalt nanoparticles are successfully obtained by the pyrolytic decomposition of CoC2O4. 2H2O in the argon gas. The pyrolysates of CoC2O4. 2H2O were investigated by TG-DSC and SEM. The results showed that there are two stages in the process of the pyrolytic decomposition of CoC2O4. 2H2O in the argon gas. The crystal water in CoC2O4. 2H2O was lost from 150 °C to 275 °C. CoC2O4was pyrolysized into metallic cobalt powder from 300 °C to 500 °C. At the same time, the pattern of pyolysate of CoC2O4. 2H2O was fined at 347.7 °C for 10 min. But, the particles of pyolysate of CoC2O4. 2H2O were sintered into cobalt blocks at 500.0 °C for 10 min. Therefore, the conditions of pyrolytic decomposition of CoC2O4. 2H2O were controlled if single cobalt powder was obtained at 500.0 °C..


2006 ◽  
Vol 99 (8) ◽  
pp. 08N702 ◽  
Author(s):  
Huiping Shao ◽  
Yuqiang Huang ◽  
HyoSook Lee ◽  
Yong Jae Suh ◽  
ChongOh Kim

2006 ◽  
Vol 304 (1) ◽  
pp. e28-e30 ◽  
Author(s):  
Huiping Shao ◽  
Yuqiang Huang ◽  
HyoSook Lee ◽  
Yong Jae Suh ◽  
Chong Oh Kim

2011 ◽  
Vol 2012 (2) ◽  
pp. 198-202 ◽  
Author(s):  
Axel Dreyer ◽  
Michael Peter ◽  
Jochen Mattay ◽  
Katrin Eckstädt ◽  
Andreas Hütten ◽  
...  

2008 ◽  
Vol 320 (3-4) ◽  
pp. 575-578 ◽  
Author(s):  
Masoud Salavati-Niasari ◽  
Fatemeh Davar ◽  
Mehdi Mazaheri ◽  
Maryam Shaterian

2006 ◽  
Vol 6 ◽  
pp. e195-e197 ◽  
Author(s):  
Huiping Shao ◽  
Yuqiang Huang ◽  
HyoSook Lee ◽  
Yong Jae Suh ◽  
Chong Oh Kim

2016 ◽  
Vol 6 (10) ◽  
pp. 3443-3448 ◽  
Author(s):  
Haixia Wang ◽  
Yaran Zhao ◽  
Fangyi Cheng ◽  
Zhanliang Tao ◽  
Jun Chen

Cobalt nanoparticles uniformly embedded in porous N-doped carbon prepared through the thermal decomposition of Co(salen) are promising catalysts for hydrolysis of ammonia borane.


Author(s):  
William J. Baxter

In this form of electron microscopy, photoelectrons emitted from a metal by ultraviolet radiation are accelerated and imaged onto a fluorescent screen by conventional electron optics. image contrast is determined by spatial variations in the intensity of the photoemission. The dominant source of contrast is due to changes in the photoelectric work function, between surfaces of different crystalline orientation, or different chemical composition. Topographical variations produce a relatively weak contrast due to shadowing and edge effects.Since the photoelectrons originate from the surface layers (e.g. ∼5-10 nm for metals), photoelectron microscopy is surface sensitive. Thus to see the microstructure of a metal the thin layer (∼3 nm) of surface oxide must be removed, either by ion bombardment or by thermal decomposition in the vacuum of the microscope.


Author(s):  
A. Legrouri

The industrial importance of metal catalysts supported on reducible oxides has stimulated considerable interest during the last few years. This presentation reports on the study of the physicochemical properties of metallic rhodium supported on vanadium pentoxide (Rh/V2O5). Electron optical methods, in conjunction with other techniques, were used to characterise the catalyst before its use in the hydrogenolysis of butane; a reaction for which Rh metal is known to be among the most active catalysts.V2O5 powder was prepared by thermal decomposition of high purity ammonium metavanadate in air at 400 °C for 2 hours. Previous studies of the microstructure of this compound, by HREM, SEM and gas adsorption, showed it to be non— porous with a very low surface area of 6m2/g3. The metal loading of the catalyst used was lwt%Rh on V2Q5. It was prepared by wet impregnating the support with an aqueous solution of RhCI3.3H2O.


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