Patent classifications
B01J2523/48
PROCESS FOR MAKING CERIUM AND ZIRCONIUM CONTAINING COMPOSITIONS USING MESITYLENE AND COMPOSITION MADE BY SAME
Disclosed herein are catalyst compositions having improved mercury intrusion volume and surface areas and processes for making these compositions. The enhanced compositions disclosed herein contain zirconium, cerium, optionally yttrium, and optionally one or more rare earths other than cerium and yttrium. Further disclosed are processes of producing these compositions involving supercritical drying after addition of mesitylene. The compositions can be used as a catalyst and/or as part of a catalyst system in an automobile exhaust system.
PROCESS FOR MAKING CERIUM AND ZIRCONIUM CONTAINING COMPOSITIONS USING MESITYLENE AND COMPOSITION MADE BY SAME
Disclosed herein are catalyst compositions having improved mercury intrusion volume and surface areas and processes for making these compositions. The enhanced compositions disclosed herein contain zirconium, cerium, optionally yttrium, and optionally one or more rare earths other than cerium and yttrium. Further disclosed are processes of producing these compositions involving supercritical drying after addition of mesitylene. The compositions can be used as a catalyst and/or as part of a catalyst system in an automobile exhaust system.
Method of making mesoporous oxygen storage materials for exhaust gas treatment; said oxygen storage materials and their use
A method of making an oxygen storage material (OSM) with developed mesoporosity having a small fraction of pores <10 nm (fresh or aged), and resistance to thermal sintering is provided. This OSM is suitable for use as a catalyst and catalyst support. The method of making this oxygen storage material (OSM) includes the preparation of a solution containing pre-polymerized zirconium oligomers, cerium, rare earth and transition metal salts; the interaction of this solution with a complexing agent that has an affinity towards zirconium; the formation of a zirconium-based precursor; and the co-precipitation of all constituent metal hydroxide with abase.
Method of making mesoporous oxygen storage materials for exhaust gas treatment; said oxygen storage materials and their use
A method of making an oxygen storage material (OSM) with developed mesoporosity having a small fraction of pores <10 nm (fresh or aged), and resistance to thermal sintering is provided. This OSM is suitable for use as a catalyst and catalyst support. The method of making this oxygen storage material (OSM) includes the preparation of a solution containing pre-polymerized zirconium oligomers, cerium, rare earth and transition metal salts; the interaction of this solution with a complexing agent that has an affinity towards zirconium; the formation of a zirconium-based precursor; and the co-precipitation of all constituent metal hydroxide with abase.
Catalyst and process for thermo-neutral reforming of petroleum-based liquid hydrocarbons
A process for producing a hydrogen-rich gas stream from a liquid hydrocarbon stream, the process comprising the steps of introducing the liquid hydrocarbon stream to a dual catalytic zone, the liquid hydrocarbon stream comprises liquid hydrocarbons selected from the group consisting of liquid petroleum gas (LPG), light naphtha, heavy naphtha, gasoline, kerosene, diesel, and combinations of the same, the dual catalytic zone comprises: a combustion zone comprising a seven component catalyst, and a steam reforming zone, the steam reforming zone comprising a steam reforming catalyst; introducing steam to the dual catalytic zone, introducing an oxygen-rich gas to the dual catalytic zone; contacting the liquid hydrocarbon stream, steam, and oxygen-rich gas with the seven component catalyst to produce a combustion zone fluid; and contacting the combustion zone fluid with the steam reforming catalyst to produce the hydrogen-rich gas stream, wherein the hydrogen-rich gas stream comprises hydrogen.
Catalyst and process for thermo-neutral reforming of petroleum-based liquid hydrocarbons
A process for producing a hydrogen-rich gas stream from a liquid hydrocarbon stream, the process comprising the steps of introducing the liquid hydrocarbon stream to a dual catalytic zone, the liquid hydrocarbon stream comprises liquid hydrocarbons selected from the group consisting of liquid petroleum gas (LPG), light naphtha, heavy naphtha, gasoline, kerosene, diesel, and combinations of the same, the dual catalytic zone comprises: a combustion zone comprising a seven component catalyst, and a steam reforming zone, the steam reforming zone comprising a steam reforming catalyst; introducing steam to the dual catalytic zone, introducing an oxygen-rich gas to the dual catalytic zone; contacting the liquid hydrocarbon stream, steam, and oxygen-rich gas with the seven component catalyst to produce a combustion zone fluid; and contacting the combustion zone fluid with the steam reforming catalyst to produce the hydrogen-rich gas stream, wherein the hydrogen-rich gas stream comprises hydrogen.
CATALYTIC HYDROGENATION METHOD FOR CARBON NINE RESIN
The present invention discloses a catalytic hydrogenation method for carbon nine resin, comprising the following steps: 1) adding a Pt—W—Y/γ-Al.sub.2O.sub.3 catalyst in the first half of a fixed bed, adding a Pd—Zr—Nd/γ-Al.sub.2O.sub.3 catalyst in the second half of the fixed bed, and feeding hydrogen for reduction; and 2) catalytic hydrogenating the pretreated carbon nine resin in the fixed bed. In the present invention, different catalysts capable of reacting under the same catalytic conditions are added in the first and second halves of the fixed bed, and the two different catalysts play different roles, and can be active and complementary to each other under the same conditions. The synergistic effect of the two catalysts plays a good catalytic role. Moreover, the production process is simplified, and the production cost is saved.
CATALYTIC HYDROGENATION METHOD FOR CARBON NINE RESIN
The present invention discloses a catalytic hydrogenation method for carbon nine resin, comprising the following steps: 1) adding a Pt—W—Y/γ-Al.sub.2O.sub.3 catalyst in the first half of a fixed bed, adding a Pd—Zr—Nd/γ-Al.sub.2O.sub.3 catalyst in the second half of the fixed bed, and feeding hydrogen for reduction; and 2) catalytic hydrogenating the pretreated carbon nine resin in the fixed bed. In the present invention, different catalysts capable of reacting under the same catalytic conditions are added in the first and second halves of the fixed bed, and the two different catalysts play different roles, and can be active and complementary to each other under the same conditions. The synergistic effect of the two catalysts plays a good catalytic role. Moreover, the production process is simplified, and the production cost is saved.
POWDER OF COMPLEX OXIDE CONTAINING CERIUM AND ZIRCONIUM ELEMENTS, EXHAUST GAS PURIFICATION CATALYST COMPOSITION USING THE SAME, AND METHOD OF PRODUCING THE SAME
An object of the present invention is to provide a powder of a CeO.sub.2—ZrO.sub.2-based complex oxide which enables to achieve an improvement in the purification performance at a low to middle temperature of an exhaust gas purification catalyst, and, in order to achieve the above-mentioned object, the present invention provides a powder of a CeO.sub.2—ZrO.sub.2-based complex oxide, wherein a pore volume with from-10-to-100-nm diameters after a heat treatment performed at 1,000° C. for 3 hours in an air atmosphere, is 0.35 mL/g or more, and wherein an amount of carbon dioxide desorbed after the heat treatment, as measured by a temperature programmed desorption method, is 80 μmol/g or more.
POWDER OF COMPLEX OXIDE CONTAINING CERIUM AND ZIRCONIUM ELEMENTS, EXHAUST GAS PURIFICATION CATALYST COMPOSITION USING THE SAME, AND METHOD OF PRODUCING THE SAME
An object of the present invention is to provide a powder of a CeO.sub.2—ZrO.sub.2-based complex oxide which enables to achieve an improvement in the purification performance at a low to middle temperature of an exhaust gas purification catalyst, and, in order to achieve the above-mentioned object, the present invention provides a powder of a CeO.sub.2—ZrO.sub.2-based complex oxide, wherein a pore volume with from-10-to-100-nm diameters after a heat treatment performed at 1,000° C. for 3 hours in an air atmosphere, is 0.35 mL/g or more, and wherein an amount of carbon dioxide desorbed after the heat treatment, as measured by a temperature programmed desorption method, is 80 μmol/g or more.