摘要:
In a mixing structure with an injector 3 arranged 2 immediately after a bend 1a of an exhaust pipe 1, urea water 5 being injected by the injector 3 into the exhaust pipe 1 for mixing, a pipe diameter Dp downstream of the bend 1a of the exhaust pipe 1 is large relative to a pipe diameter De upstream of the bend.
摘要:
The present disclosure describes zero-platinum group metals (ZPGM) material compositions including binary Cu—Mn spinel oxide powders having stable reduction/oxidation (redox) reversibility useful for TWC and oxygen storage material applications. The behavior of Cu—Mn spinel oxide powder is analyzed under oxidation-reduction environments to determine redox reversibility, catalytic activity, and spinel structure stability. Characterization of spinel powder is performed employing X-ray diffraction analysis, hydrogen temperature-programmed reduction technique, transmission electron microscopy analysis, and X-ray photoelectron spectroscopy analysis. Test results confirm the phase and structural stability of the Cu—Mn spinel oxide during redox reaction, thereby indicating that the Cu—Mn spinel oxide can be employed in a plurality of TWC applications.
摘要:
The effect of firing (calcination) cycle on metallic substrates in ZPGM catalyst systems is disclosed. ZPGM catalyst samples with washcoat and overcoat are separately fired in a normal, slow and fast firing cycles to determine the optimal firing cycling that may provide an enhanced catalyst performance, as well as the minimal loss of washcoat adhesion from the samples.
摘要:
Provided are an exhaust gas purification catalyst comprising a nanocomposite material comprising CeO2 and NiO which are uniformly mixed; and a production method thereof. The uniform mixing satisfies at least one of following conditions: (a) when the nanocomposite material is analyzed using STEM-EDX, the number of Ni atoms is from 3 to 20 atomic % relative to the total number of Ni and Ce atoms at a majority of randomly selected 5 or more measurement points in which both Ce and Ni elements are detected; and (b) in the Fourier transform of EXAFS spectrum at Ni—K absorption edge regarding the nanocomposite material, the ratio of the peak intensity of Ni—O near an interatomic distance of 1.8 Å to the peak intensity of Ni—Ni near an interatomic distance of 2.6 Å is 1:at least 0.50 to less than 2.18.
摘要:
The present disclosure relates to selecting the layer of applying ZPGM active phase in washcoat, or applying ZPGM active phase in overcoat, for achieving optimized performance and enhanced thermal stability. Applying ZPGM active phase catalyst in overcoat shows improvements compare to applying ZPGM active phase in washcoat. The selected active phase material may include a chemical composition that is substantially free from PGM, including a formulation of stoichiometric Cu—Mn spinel structure active phase deposited on Niobium-Zirconium support oxide. The selected active phase layer applied in overcoat may include a washcoat of alumina coated on a suitable ceramic substrate. The disclosed active phase may be applied in overcoat to maximize efficiency of catalyst systems, which may exhibit enhanced catalytic activity properties, which may stable after aging and under steady state and oscillating condition, showing optimized performance purifying gases in TWC condition.
摘要:
Variations of bulk powder catalyst material including Cu—Co, Fe—Co, and Co—Mn spinel systems for ZPGM TWC applications are disclosed. The disclosed bulk powder catalyst samples include stoichiometric and non-stoichiometric Cu—Co, Fe—Co, and Co—Mn spinels on Pr6O11—ZrO2 support oxide, prepared using incipient wetness method. Activity measurements under isothermal steady state sweep test condition may be performed rich to lean condition. Catalytic activity of bulk powder samples may be compared to analyze the influence that different bimetallic spinel compositions may have on TWC performance, including ZPGM materials for a plurality of TWC applications. Stoichiometric Cu—Co, Fe—Co, and Co—Mn spinel systems exhibit higher catalytic activity than non-stoichiometric Cu—Co, Fe—Co, and Co—Mn spinel systems. The influence of stoichiometric Cu—Co, Fe—Co, and Co—Mn spinel systems may lead into cost effective manufacturing solutions for ZPGM TWC systems.
摘要:
Effect of the type of material composition employed within overcoat in conjunction with ZPGM composition in impregnation layer on thermal stability and TWC performance of ZPGM catalyst systems is disclosed. Effect of aging temperature on thermal stability of disclosed ZPGM catalyst systems is also described. Testing of ZPGM catalyst samples including isothermal steady state sweep test condition and isothermal oscillating TWC test on disclosed ZPGM catalyst systems show that ZPGM catalyst system that includes combination of Cu1Mn2O4 spinel and YMnO3 perovskite exhibit higher level of thermal stability at temperature higher than temperatures registered for under floor application of TWC.
摘要:
Variations of bulk powder catalyst material including Cu—Mn, Cu—Fe, and Fe—Mn spinel systems for ZPGM TWC applications are disclosed. The disclosed bulk powder catalyst samples include stoichiometric and non-stoichiometric Cu—Mn, Cu—Fe, and Fe—Mn spinels on Pr6O11—ZrO2 support oxide, prepared using incipient wetness method. Activity measurements under isothermal steady state sweep test condition may be performed under rich to lean condition. Catalytic activity of samples may be compared to analyze the influence that different binary spinel system bulk powders may have on TWC performance of ZPGM materials for a plurality of TWC applications. Stoichiometric Cu—Mn, Cu—Fe, and Fe—Mn spinel systems exhibit higher catalytic activity than non-stoichiometric Cu—Mn, Cu—Fe, and Fe—Mn spinel systems. The influence of prepared Cu—Mn, Cu—Fe, and Fe—Mn spinel systems may lead into cost effective manufacturing solutions for ZPGM TWC systems.
摘要:
Method for the preparation of a catalysed particulate filter and a particulate filter. The method comprises the steps of a) providing a catalyst wash coat with a first catalyst active in burning off of soot and a second catalyst active in selective catalytic reduction of nitrogen oxides; b) coating a particulate filter body with the catalyst wash coat on the dispersion side and the permeate side of the filter body and within partition walls of the filter body; and c) drying and heat treating the coated filter body to obtain the catalysed particulate filter.
摘要:
The present disclosure relates to selecting support oxide for ZPGM catalyst for optimal performance under TWC condition, for achieving enhanced catalyst activity, and improved thermal stability during aging. The selected active phase material may include a chemical composition that is substantially free from PGM, including a formulation of stoichiometric Cu—Mn spinel structure active phase with Niobium-Zirconium support oxide, which may include a washcoat of pure alumina coated on a suitable ceramic substrate. The disclosed Cu—Mn spinel structure active phase with Niobium-Zirconium support oxide may be applied in overcoat to maximize efficiency of ZPGM catalyst systems, which may exhibit enhanced catalytic activity properties that may increase with temperature, showing optimized performance purifying gases in TWC condition, and enhanced stability during aging.