ChemInform Abstract: FORMATION AND CATALYTIC PROPERTIES OF NICKEL METAL PARTICLES SUPPORTED ON ZEOLITE

1981 ◽  
Vol 12 (20) ◽  
Author(s):  
D. DELAFOSSE
2000 ◽  
Vol 35 (1) ◽  
pp. 143-148 ◽  
Author(s):  
S Kapoor ◽  
H.G Salunke ◽  
A.K Tripathi ◽  
S.K Kulshreshtha ◽  
J.P Mittal

Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2445
Author(s):  
Tianyu Cao ◽  
Ohhun Kwon ◽  
Raymond J. Gorte ◽  
John M. Vohs

Exsolution is a novel technology for attaching metal catalyst particles onto ceramic anodes in the solid oxide fuel cells (SOFCs). The exsolved metal particles in the anode exhibit unique properties for reaction and have demonstrated remarkable stabilities under conditions that normally lead to coking. Despite extensive investigations, the underlying principles behind exsolution are still under investigation. In this review, the present status of exsolution materials for SOFC applications is reported, including a description of the fundamental concepts behind metal incorporation in oxide lattices, a listing of proposed mechanisms and thermodynamics of the exsolution process and a discussion on the catalytic properties of the resulting materials. Prospects and opportunities to use materials produced by exsolution for SOFC are discussed.


1987 ◽  
Vol 66 (2) ◽  
pp. 376-378 ◽  
Author(s):  
L. Ganapathi ◽  
G.N. Subbanna ◽  
K.S. Nanjundaswamy ◽  
C.N.R. Rao

1986 ◽  
Vol 83 ◽  
Author(s):  
E. I. Altman ◽  
R. J. Gorte

ABSTRACTIndustrial metal catalysts are usually in the form of small metal particles supported on a porous oxide. The typical size of these metal particles ranges between 1.0 and 10.0 nm and it is well known that the particle size and the oxide substrate can affect the catalytic properties of the metal for some important reactions[1]. Previous work with adsorption on small particles has indicated that desorption temperatures[2–4] and the ability to dissociate CO[5,6] can also be affected by the particle size. To further investigate these size and substrate effects, we have examined the adsorption properties of several simple gases on small Pt particles supported on alumina using temperature programmed desorption (TPD). We will show that the desorption curves for CO, H2, and NO on these particles are very similar to curves measured on single crystals.


1999 ◽  
Vol 28 (7) ◽  
pp. 607-608 ◽  
Author(s):  
Yuji Wada ◽  
Hiromitsu Kuramoto ◽  
Takao Sakata ◽  
Hirotaro Mori ◽  
Takayuki Sumida ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 2890 ◽  
Author(s):  
Zachary Daniels ◽  
Wilson Rydalch ◽  
Troy Y. Ansell ◽  
Claudia C. Luhrs ◽  
Jonathan Phillips

Described herein is a novel method, Reduction Expansion Synthesis-Sintered Metal (RES-SM), to create a sintered metal body of a designed shape at ambient pressure, hundreds of degrees below the metal melting temperature. The precursor to the metal part is a mixture of metal oxide particles and activated metal particles, and in this study specifically nickel oxide and activated nickel metal particles. It is postulated that the metal oxide component is reduced via exposure to chemical radical species produced via thermal decomposition of urea or other organic compounds. In the study performed, the highest temperature required was 950 °C, the longest duration of high temperature treatment was 1200 s, and in all cases, the atmosphere was inert gas at ambient pressure. As discovered using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and x-ray diffraction (XRD), the metal that forms via the RES process presents necks of completely reduced metal between existing metal particles. The ‘as produced’ parts are similar in properties to ‘brown’ metal parts created using more standard methods and require ‘post processing’ to full densify. Parts treated by hot isostatic pressing show fully self-supporting, robust structures, with hardness values like others reported in literature for traditional fabrication methods. This novel method uses affordable and environmentally friendly precursors to join metallic parts at moderate temperatures, produces fully reduced metals in a very short time and has potential to make many parts simultaneously in a standard laboratory furnace.


In Part I hereof it was established that the rate of cathodic combustion of electrolytic gas is proportional to the current traversing the cathode zone. Subsequent investigations (III to IV) have shown that sputtered metal particles play an important rôle in the cathodic combustion of carbonic oxide, and that the nature of the cathode materials employed in the experiments described in (I) was therefore such as to render difficult a full interpretation of the results set forth therein; because, from the point of view of cathodic sputtering, copper occupies a position intermediate between the non-sputtering and freely sputtering classes of metals. Also, the results of recent experiments on the catalytic properties of sputtered platinum films, an account of which it is hoped will shortly be submitted to the Society, have shown that even at room temperature sputtered platinum is sometimes capable of powerfully catalysing the union of hydrogen and oxygen. These considerations clearly indicated the need for extending the study of the cathodic combustion of electrolytic gas to that occurring at electrodes such as gold, silver, tantalum and tungsten. Furthermore, with the object previously outlined in (VII), i. e. the elucidation of the mechanism of the combustion of hydrogen by oxygen and the rôle played by hydrogen in promoting the combustion of carbonic oxide, the scope of the present investigation was extended in order to study the effect of such diluents as oxygen, hydrogen and steam upon the cathodic combustion of electrolytic gas. The results of our experiments, of which an account is given in what follows, have shown, inter alia , that the rate of combustion of electrolytic gas at a non-sputtering cathode increases rapidly on dilution with hydrogen; whereas, at a freely sputtering cathode, this effect is far less pronounced.


Author(s):  
Ming-Hui Yao

The chemisorption ability and catalytic properties of metal particles supported on reducible oxides are often altered by high temperature reduction(HTR) in a process known as strong metal-support interaction(SMSI). Different models have been proposed to explain the SMSI mechanism. In recent years, experimental evidences have favored the "decoration model", which suggests that SMSI is due to the encapsulation of the metal particles by oxide overlayer species dial have migrated from the support. HREM profile imaging was the most useful tool to directly relate these surface decorations to the SMSI effects. The profile imaging can provide atomic-scale information about supported particles and Uieir surfaces without image being obscured by overlapping contrast from the support.In the present work, the SMSI effect in Pt/TiO2 and Pt/CeO2 model catalysts have been studied using HREM profile imaging and multislice simulations. HREM observations were made with a JEM-4000EX microscope, operated at 400 kV. Fig. 1(a) shows a typical profile image of TiO2 after HTR in H2 at 923K.


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