Patent classifications
B01J2229/20
METAL TRAP FOR USE IN FLUID CATALYTIC CRACKING (FCC)
A metal trap for an FCC catalyst include pre-formed microspheres impregnated with an organic acid salt of a rare earth element.
Hybrid catalysts comprising a mixed metal oxide component for production of C2 and C3 hydrocarbons
A hybrid catalyst including a metal oxide catalyst component comprising chromium, zinc, and at least one additional metal selected from the group consisting of iron and manganese, and a microporous catalyst component that is a molecular sieve having 8-MR pore openings. The at least one additional metal is present in an amount from 5.0 at % to 20.0 at %.
LOW-TEMPERATURE NOx STORAGE CATALYST USED FOR AUTOMOBILE EXHAUST PURIFICATION AND PREPARATION METHOD THEREOF
A low-temperature NO.sub.x storage catalyst for automobile exhaust purification and a preparation method thereof. Loading a noble metal salt solution on molecular sieve by equal volume impregnation method, wherein the noble metal salt solution comprises palladium nitrate and platinum nitrate, and the molecular sieve comprises SSZ, SAPO and BETA, then drying at 60-120° C. for 2-6 h, roasting at 500-550° C. in air for 2-5 h, and further roasting at 750-850° C. in air for 2-5 h, and then mixing with aluminum sol, ball milling and pulping, and then coating the slurry on a carrier, wherein the loading on the coating is 100-250 g/L and the noble metal content is 10-150 g/ft.sup.3, drying at 60-120° C. for 2-6 h, then roasting at 500-550° C. in air for 2-5 h, and further continuing roasting at 750-850° C. in air for 2-5 h, to obtain the catalyst. Loading the noble metals Pt and Pd into a pore channel of a molecular sieve improves NO.sub.x storage capacity of a catalyst at low temperatures, and selecting a different type of molecular sieve as an NO.sub.x storage unit and increasing a roasting temperature of a molecular sieve material on which Pt and Pd are loaded significantly increases NO.sub.x storage capacity.
Catalytic conversion of alcohols and/or ethers to olefins
Processes for the catalytic conversion of alcohols and/or ethers to olefins over zeolite catalysts are described. ZSM-48 and metal containing variants, such as Zn ZSM-48, produce high yields of olefins, particularly ethylene or C3+ olefins, between 200 and 500° C.
Selective Hydroisomerization Catalyst
A catalyst is provided for hydrodeoxygenation and hydroisomerization of paraffins having higher activity. The catalyst contains a molecular sieve, such as SAPO-11, a metal component such as platinum and/or palladium or nickel tungsten sulfide or nickel molybdenum sulfide and a binder such as gamma alumina. The catalyst exhibits a high proportion of weak acid sites and a relatively equal distribution of the metal component on the molecular sieve and the binder.
ACIDIC AROMATIZATION CATALYSTS WITH IMPROVED ACTIVITY AND SELECTIVITY
Methods for producing supported catalysts containing a transition metal and a bound zeolite base are disclosed. These methods employ a step of impregnating the bound zeolite base with the transition metal, fluorine, and high loadings of chlorine. The resultant high chlorine content supported catalysts have improved catalyst activity in aromatization reactions.
COMBINED CATALYST AND PREPARATION METHOD THEREOF, AND METHOD FOR PREPARING XYLENE BY COUPLING CARBON DIOXIDE HYDROGENATION WITH TOLUENE ALKYLATION
The technical field of catalysts, in particular to a combined catalyst and a preparation method thereof, and a method for preparing xylene by coupling carbon dioxide hydrogenation with toluene alkylation. The combined catalyst of the present disclosure having a metal oxide and a zeolite. In the present disclosure, the metal oxide is mainly used to reduce carbon dioxide to methanol, and the zeolite is mainly used to react toluene with methanol to produce xylene. When the catalyst of the present disclosure is used to prepare xylene, carbon dioxide and hydrogen can be used as raw materials instead of methanol. Compared with the traditional alkylation of toluene with methanol, this method can avoid the side reaction of methanol to olefins caused by the improper methanol/toluene feeding ratio, and improve the production efficiency of xylene; meanwhile, it can inhibit xylene isomerization and increase p-xylene selectivity in the products.
Acidic aromatization catalyst with improved activity and stability
Methods for producing supported catalysts containing a transition metal and a bound zeolite base are disclosed. These methods employ a step of impregnating the bound zeolite base with the transition metal, fluorine, and high loadings of chlorine. The resultant high chlorine content supported catalysts have improved catalyst activity in aromatization reactions.
Olefin aromatization catalyst, preparation method and use thereof, and low-carbon olefin aromatization process
The present discloses an aromatization catalyst, preparation process and application thereof and a low-carbon olefin aromatization process. The aromatization catalyst comprises a microporous material, a binder and a modifier; the microporous material is a zeolite molecular sieve, the binder is alumina, the modifier is phosphorus, and the molar ratio of the aluminum element in the binder to the phosphorus element is more than or equal to 1 and less than 5; the ratio of the acidity of the strongly acidic sites to the acidity of the weakly acidic sites of the olefin aromatization catalyst is less than 1.
Manufacturing hydrocracking catalyst
A method including subjecting an ultra-stable Y-type zeolite having a low silica-to-alumina molar ratio (SAR), such as in a range of 3 to 6, to acid treatment and heteroatom incorporation contemporaneously to give a framework-modified ultra-stable Y-type zeolite.