Synthesis and Characterization of CeO2-ZrO2-Al2O3 with High Thermal Stability and Oxygen Storage Capacity from Pseudoboehmite Precursor

2012 ◽  
Vol 463-464 ◽  
pp. 160-164
Author(s):  
Dong Zhang
Keyword(s):  
Thermal Stability ◽  
Storage Capacity ◽  
Oxygen Storage Capacity ◽  
Oxygen Storage ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Alumina Oxide ◽  
Composite Solid

The surface and structural properties, thermal stability and oxygen storage capability are inverstigated in ceria-zirconia-alumina oxide with deposition coprecipitation method using the Pseudoboehmite precursor. X-ray diffraction (XRD), Brunauer-Emmet Teller method (BET), Transmission electron microscopy (TEM) and oxygen pulsing technique are used to character the prepared materials. The prepared ceria-zirconia-alumina oxides are highly dispersed composite solid solution. After calcination at 650 °C and 1000 °C respectively, these compounds can still keep the structural and textural stability and hold excellent oxygen storage capability.

CO Oxidation over Pd Catalysts Supported on Different Supports: A Consideration of Oxygen Storage Capacity of Catalyst

2011 ◽  
Vol 347-353 ◽  
pp. 3298-3301
Author(s):  
Ye Xu ◽  
Jin Qiang Ma ◽  
Yuan Feng Xu ◽  
Hui Li ◽  
He Xing Li ◽  
...  
Keyword(s):  
Co Oxidation ◽  
Storage Capacity ◽  
Oxygen Storage Capacity ◽  
Oxygen Storage ◽  
X Ray Diffraction ◽  
Pd Catalysts ◽  
Transmission Electron ◽  
Pulse Experiment ◽  
Temperature Programmed

A series of Pd catalysts supported on different materials (SiO2, γ-Al2O3, CeO2, TiO2) were synthesized through precipitation reduction of palladium ions with H2. They exhibited different activity during catalytic oxidation of CO to CO2. With the characterization of N2 physisorption experiment, X-ray diffraction, transmission electron microscopy, temperature-programmed reduction, and CO and O2 multi-pulse experiment, the correlation of catalytic activity and oxygen storage capacity (OSC) of catalyst has been investigated. It was found that the reactivity is largely controlled by the OSC of the catalysts, and thus Pd/CeO2 and Pd/TiO2 were more active than Pd/SiO2 and Pd/Al2O3 for CO oxidation.

Synthesis and Characterization of Ce0.5Zr0.5O2 Nanocomposite and its Supported Pd-Only Catalysis Activity

2014 ◽  
Vol 633 ◽  
pp. 77-81
Author(s):  
Dong Xia Yang ◽  
Ping Ning ◽  
Jie Li He ◽  
Jing Fang Zhu ◽  
Ting Ting Zheng ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Storage Capacity ◽  
Oxygen Storage Capacity ◽  
Oxygen Storage ◽  
X Ray Diffraction ◽  
Fractional Precipitation ◽  
Temperature Programmed ◽  
Co Precipitation ◽  
Redox Ability

The Ce0.5Zr0.5O2 nanocomposites (CZ) were prepared by co-precipitation(CP), fractional precipitation (FP) and fractional precipitation with hydrothermal treatment (FP-HT). The samples were characterized by X-ray diffraction (XRD), Brunauer-Emmet Teller method (BET), H2-temperature programmed reduction (H2-TPR), and thermogravimetric analysis (TG) under H2-N2. XRD results displayed that all samples formed a single solid solution-like ceria-zirconia phase. BET results revealed CZ prepared by FP-HT (CZ-FP-HT) had the highest surface area. H2-TPR and TG analysis under H2-N2 showed CZ-FP-HT exhibited the strongest redox ability and oxygen storage capacity. Moreover, three-way catalysts of Pd-Rh supported on CZ -FP-HT and commercial CZ with same composites were prepared, and their three-way catalytic activity were also studied by engine evaluation. Pd-Rh/CZ-FP-HT showed a bit of higher oxygen storage capacity, catalytic activity and better thermal stability than Pd-Rh/CZ-commercial.

scholarly journals Effect of Sr on the properties of Ce-Zr-La mixed oxides

2006 ◽  
Vol 71 (3) ◽  
pp. 285-291 ◽  
Author(s):  
Richuan Rao ◽  
LI Lianyong ◽  
LI Fengyi
Keyword(s):  
Mixed Oxide ◽  
Storage Capacity ◽  
Mixed Oxides ◽  
Sol Gel ◽  
Oxygen Storage Capacity ◽  
Oxygen Storage ◽  
X Ray Diffraction ◽  
Pulse Technique ◽  
X Ray ◽  
Good Thermal Stability

Ce-Zr-La-Sr mixed oxides, with different Sr contents, were prepared by the sol-gel method. In a flow-system microreactor, the reduction properties and the oxygen storage capacity (OSC) of the Ce-Zr-La-Sr mixed oxides were investigated by a temperature programmed reduction (TPR) and a pulse technique. It was shown that the properties of the Ce-Zr-La mixed oxides depend on the Sr content and that the optimum Sr content in the Ce-Zr-La-Sr mixed oxide is 3 mol%. The Ce-Zr-La-Sr mixed oxides doped with 3 mol% Sr (Ce0.52Zr0.4La0.05Sr0.03O1.945) has the largest specific surface area and better reduction properties and oxygen storage capacity in comparison to the other investigated samples. The XRD results of the Ce-Zr-La-Sr mixed oxides showed that their X-ray diffraction patterns are well in agreement with that of fluorite-type CeO2 with Sr ions incorporated into the Ce-Zr-La mixed oxide structures. With increasing calcination temperature, the intensity of the X-ray diffraction peaks increased, but no new peaks were observed. All of these indicate that the synthesized samples had good thermal stability.

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.

Detonation Synthesis of Nano-Size Materials

1995 ◽  
Vol 418 ◽  
Author(s):  
J. Forbes ◽  
J. Davis ◽  
C. Wong
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Nucleation And Growth ◽  
Detonation Synthesis ◽  
X Ray Diffraction ◽  
Crystalline Materials ◽  
X Ray ◽  
Transmission Electron ◽  
Nano Size

AbstractThe detonation of explosives typically creates 100's of kbar pressures and 1000's K temperatures. These pressures and temperatures last for only a fraction of a microsecond as the products expand. Nucleation and growth of crystalline materials can occur under these conditions. Recovery of these materials is difficult but can occur in some circumstances. This paper describes the detonation synthesis facility, recovery of nano-size diamond, and plans to synthesize other nano-size materials by modifying the chemical composition of explosive compounds. The characterization of nano-size diamonds by transmission electron microscopy and electron diffraction, X-ray diffraction and Raman spectroscopy will also be reported.

Autothermal Reforming of Propane Over Ni Catalysts Supported on a Variety of Perovskites

2007 ◽  
Vol 7 (11) ◽  
pp. 4013-4016 ◽  
Author(s):  
SeungSoo Lim ◽  
DongJu Moon ◽  
JongHo Kim ◽  
YoungChul Kim ◽  
NamCook Park ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Storage Capacity ◽  
Flow Reactor ◽  
Oxygen Storage Capacity ◽  
Autothermal Reforming ◽  
Oxygen Storage ◽  
Hydrogen Yield ◽  
Impregnation Method ◽  
Ni Catalysts ◽  
Atmospheric Flow

Autothermal reforming of propane for hydrogen over Ni catalysts supported on a variety of perovskites was performed in an atmospheric flow reactor. Perovskite is known for its higher thermal stability and oxygen storage capacity, but catalytic activity of itself is low. A sites of the ABO3 structured perovskites were occupied by La while B sites by one of Fe, Co, Ni, and Al by citrate method. The composition of the reactant mixture was H2O/C/O2 = 8.96/1.0/1.1. The changes in the states of the catalysts after reaction were analyzed by XRD, TPD, and TGA. Ni/LaAlO3 catalyst maintained the perovskite structure after reaction. It showed higher hydrogen yield and thermal stability compared to those of the catalysts with Fe, Co, or Ni in B sites. Catalysts prepared by deposition-precipitation (DP) method showed higher activity than those prepared by impregnation method, presumably due to the smaller sizes of the NiO crystal particles.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

scholarly journals Characterization of ferrite nanoparticles for preparation of biocomposites

2017 ◽  
Vol 8 ◽  
pp. 1257-1265 ◽  
Author(s):  
Urszula Klekotka ◽  
Magdalena Rogowska ◽  
Dariusz Satuła ◽  
Beata Kalska-Szostko
Keyword(s):  
Chemical Method ◽  
Ferrite Nanoparticles ◽  
Chemical Activity ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Wet Chemical Method ◽  
X Ray ◽  
Transmission Electron ◽  
Wet Chemical

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).

Formation and Thermal Stability of Nd0.32Y0.68Si1.7 Layers Formed by Channeled Ion Beam Synthesis

1998 ◽  
Vol 514 ◽  
Author(s):  
M. F. Wu ◽  
A. Vantomne ◽  
S. Hogg ◽  
H. Pattyn ◽  
G. Langouche ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Ion Beam ◽  
Hexagonal Structure ◽  
Orthorhombic Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Good Crystalline Quality ◽  
Ion Beam Synthesis ◽  
Thermal Stability Of

ABSTRACTThe Nd-disilicide, which exists only in a tetragonal or an orthorhombic structure, cannot be grown epitaxially on a Si(111) substrate. However, by adding Y and using channeled ion beam synthesis, hexagonal Nd0.32Y0.68Si1.7 epilayers with lattice constant of aepi = 0.3915 nm and cepi = 0.4152 nm and with good crystalline quality (χmin of Nd and Y is 3.5% and 4.3 % respectively) are formed in a Si(111) substrate. This shows that the addition of Y to the Nd-Si system forces the latter into a hexagonal structure. The epilayer is stable up to 950 °C; annealing at 1000 °C results in partial transformation into other phases. The formation, the structure and the thermal stability of this ternary silicide have been studied using Rutherford backscattering/channeling, x-ray diffraction and transmission electron microscopy.

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