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The catalyst of the crystalline ceramics known as a perovskite-type oxide was designed and controlled at the atomic level in order to create a new function for self-regeneration of precious metals in a usage ambience without auxiliary treatment. We have already reported that a catalyst with Pd supported on the perovskite-type oxide has higher activity than a catalyst with Pd supported on alumina. It was also found that Pd supported on the perovskite catalyst is finely dispersed [1, 2 and 3] The object of this study was to investigate the mechanism of self-regeneration by using hyper-analytical facilities. XAFS analysis, at SPring-8 (8 GeV), revealed that Pd is in six-fold coordinations with oxygen in a perovskite crystal, which indicating that Pd occupies the B site of the unit formula of ABO3 in the perovskite crystal structure under oxidation atmosphere.

We have reported the innovation of “An Intelligent Catalyst” which has the function for self-regeneration of Pd realized through the solid solution and segregation of Pd in a perovskite crystal. In this study, we did further research on regeneration for three different precious metals (Rh, Pd and Pt) in two types of perovskite systems (LaCeFeO3 and LaCeCoO3). In perovskite catalysts loaded with precious metals, the durability of the perovskite structure in redox fluctuation at high temperature is indispensable to suppression of the grain growth of precious metals. The key technology for the development of intelligent catalysts is considered to be the affinity of precious metals to durable perovskite oxides. In the six kinds of perovskite catalysts investigated here, only the Pd loaded LaCeFeO3 catalyst was considered “intelligent”.

With emission regulations getting tighter and tighter, catalysts will need to be active at ever lower temperatures in order to meet future standards. To meet this need, automotive catalysts are being installed closer to the engine so as to be active immediately after start-up. In this location, catalysts must have high temperature durability. In this paper, we examined a heat-resistant support material, “hexa-aluminate”, for possible use in future automotive catalysts. Catalytic activity of hexa-aluminate was more better than La added γ - alumina after redox treatment in model gas and after engine aging. Since hexa-aluminate had the excellent thermal durability, and Pd, which are supported on it, maintains finer particles than those on La added γ-alumina. We suggest that hexa-aluminate is a effective support material for automotive catalysts. More specifically, hexa-aluminate is expected to be a key technology for meeting the stringent emission standards of the future.

We have already reported that a LaFeCoPdO3 perovskite catalyst has the function for self-regeneration of Pd [1, 2, 3, 4, 5 and 6]. But cobalt was recognized as an environmental burden. In order to prepare for its practical application, we examined the composition of perovskite without cobalt. In this paper, we have investigated the catalytic activity, the structural durability and the regenerative ability of Co-free perovskites LaFePdO3, in comparison with LaFeCoPdO3 and Pd/Al2O3. As a result, the structural durability of LaFePdO3 is high, and the light-off performance is excellent even after aging. “Co-free Intelligent Catalyst” is regarded as the next technology for practical use especially as it is efficient in the reduction of emissions at cold starting.

The catalytic performance and On-Board Diagnostics (OBD) of the manifold catalyst having high Oxygen Storage Capacity (OSC) are described in this paper. First of all, we compared the performance of three-way catalysts containing Cerium - Zirconium - Yttrium oxide with Cerium - Zirconium oxide. Three-way catalysts dispersed Pt, Rh and Pd on Cerium - Zirconium - Yttrium oxide showed excellent catalytic performance especially at cold starting and at transient states, after high temperature aging at 1050°C. The performance of these catalysts was studied using the Driving Mode Simulation Dynamometer, which was developed in-house, and oxygen storage and release responses were compared in actual gas. Then we investigated the possibility of on-board diagnostics of catalyst deactivation with high OSC in manifold and close-coupled positions, a diagnostic which is usually assumed to be difficult to attain with present conventional technology.