Patent classifications
B01J35/396
CATALYST FOR SELECTIVE HYDRODESULPHURIZATION OF CRACKED NAPHTHA STREAMS, METHOD OF PREPARATION THEREOF, AND PROCESS FOR SELECTIVE HYDRODESULPHURIZATION OF CRACKED NAPHTHA
The present invention relates to a catalyst for selective hydrodesulphurization of cracked naphtha streams in the form of an extrudate, which comprises a support based on an inorganic oxide and an outer layer bound to the support, wherein the outer layer comprises desulphurization metals dispersed therein forming a crown, the desulphurization metals being cobalt and molybdenum. The present invention also relates to the preparation of said catalyst by the incipient wetness impregnation method and to the process for selective hydrodesulphurization of cracked naphtha employing same.
Process for preparing hydrocracking catalyst
The invention relates to a process for preparing a hydrocracking catalyst, comprising (i) contacting a shaped body comprising a zeolite and a binder with an aqueous solution of a hydrogenation metal compound which is a complex or a salt of a hydrogenation metal to deposit the hydrogenation metal onto the shaped body, wherein the aqueous solution comprises an ammonium salt and (ii) calcining the shaped body obtained by step (i).
COMPOSITION FOR EXHAUST GAS PURIFICATION, EXHAUST GAS PURIFYING CATALYST CONTAINING SAME, AND EXHAUST GAS PURIFYING CATALYST STRUCTURE
A composition for exhaust gas purification including first alumina including alumina containing lanthanum and second alumina including alumina containing lanthanum. The first alumina has a higher lanthanum content than the second alumina. The second alumina has a larger particle size than the first alumina. The lanthanum content of the first alumina is preferably 2 to 12 mass %, in terms of oxide, based on the total mass of alumina and lanthanum oxide of the first alumina. The lanthanum content of the second alumina is preferably 9 mass % or less, in terms of oxide, based on the total mass of alumina and lanthanum oxide of the second alumina.
Systems and methods for scale-up synthesis multi-layered Pt-skin nanoparticle catalysts
A method for scaled-up synthesis of PtNi nanoparticles. Synthesizing a Pt nanoparticle catalyst comprises the steps of: synthesizing PtNi nanoparticles, isolating PtNi/substrate nanoparticles, acid leaching the PtNi/substrate, and annealing the leached PtNi/substrate nanoparticles, and forming a Pt-skin on the PtNi/substrate nanoparticles.
Zeolite catalyst containing metals
Provided is catalyst material useful for the selective catalytic reduction of NOx in lean burn exhaust gas, wherein the catalyst material is a hydrothermally stable, low SAR aluminosilicate zeolite loaded with a synergistic combination of one or more transition metals, such as copper, and one or more alkali or alkaline earth metals, such as calcium or potassium.
AMMONIA FACILITATED CATION LOADING OF ZEOLITE CATALYSTS
The present disclosure features a high metal cation content zeolite-based binary catalyst (e.g., a high copper and/or iron content zeolite-based binary catalyst, where the zeolite can be a chabazite) for NO.sub.x reduction, having relatively low N.sub.2O make, and having low corresponding metal oxide content; where the metal in the metal oxide corresponds to the metal of the metal cation. The present disclosure also describes the synthesis of the zeolite-based binary catalyst having high metal cation content.
Transition-metal-supporting intermetallic compound, supported metallic catalyst, and ammonia producing method
An electride, which is more stable and can be more easily obtained, is provided or is made available, and as a result, a catalyst particularly useful for chemical synthesis, in which the electride is particularly used, is provided. A transition metal-supporting intermetallic compound having a transition metal supported on an intermetallic compound represented by the following formula (1): A.sub.5X.sub.3 . . . (1) wherein A represents a rare earth element, and X represents Si or Ge.
NICKEL-COBALT-BASED CATALYSTS FOR CO AND NO OXIDATION; THEIR ACTIVATION
A catalyst obtainable by exsolving particles of Ni, Co and/or a mixture of Ni and Co from a perovskite metal oxide of formula (I) (M.sup.1.sub.aM.sup.2.sub.b)(CO.sub.xNi.sub.yM.sup.3.sub.z)O.sub.3, wherein M.sup.1 and M.sup.2 are each independently an alkali earth metal or a rare earth metal, M.sup.3 is Ti or Cr, 0a1, 0b1, 0<a+b1, 0x<1, 0y<1, 0z<1, x+y+z=1 and where at least one of x and y>0. The invention includes methods of converting this catalyst into one or more catalytically active forms. The catalysts and the activated forms of same are useful in the catalysing CO oxidation and/or NO oxidation.
Three-way catalyst for purifying gasoline engine exhaust gas
A three-way catalyst for purifying exhaust including noble metal components, enables sintering of the noble metal to be suppressed even at high temperature, enables carbon monoxide (CO), hydrocarbons (HC), and nitrogen oxides (NOx) to be removed and a method for purifying exhaust gas. A carrier having a honeycomb structure is coated with two or more layers of the catalyst compositions, an upper layer including a heat resistant inorganic oxide supporting Pd and a La-containing oxide, a lower layer including a heat resistant inorganic oxide supporting Rh. The content of La in terms of La.sub.2O.sub.3 is 9.6 g/L to 23 g/L, the content of Ce in terms of CeO.sub.2 is 5 g/L to 20 g/L, and the content of Ba in terms of BaO is 1.2 g/L or less per unit volume of the honeycomb structure.
EXHAUST GAS PURIFICATION CATALYST
Provided is an exhaust gas purification catalyst that allows enhancing purification performance on exhaust gas. The exhaust gas purification catalyst according to the present invention has a substrate 10 of wall flow structure having a porous partition wall 16 which partitions inlet cells 12 and outlet cells 14, a first catalyst layer 20 formed on the surface of the partition wall 16, on the side facing the inlet cells 12, and a second catalyst layer 30 formed in the interior of the partition wall 16, at least in a region facing the outlet cells 14.