Patent classifications
B01J2229/16
Alkyl halides conversion into acyclic C3-C6 olefins
The present disclosure relates to a process for converting one or more alkyl halides to acyclic C3-C6 olefins, said process comprising the steps of (a) providing a feedstream comprising one or more alkyl halides; (b) providing a catalyst composition; and (c) contacting said feedstream with said catalyst composition under reaction conditions. The process is remarkable in that said process further comprises a step of steaming said catalyst composition before the step (c) and in that said catalyst composition comprises one or more zeolites and a binder, wherein said one or more zeolites comprise at least one 10-membered ring channel. The present disclosure further relates to the use of a catalyst composition in said process, said catalyst composition comprising one or more zeolites and a binder, wherein said catalyst composition is steamed before use.
CATALYST COMPOSITION FOR FLUID CATALYTIC CRACKING, AND USE THEREOF
In accordance with the present subject matter there is provided a catalyst composition including 70-98% of a non-zeolitic material; and 2-30% of at least one zeolite material, the percentage being based on weight of the catalyst composition. The subject matter also relates to a method for preparation of the catalyst composition. The subject matter further relates to a process for the fluid catalytic cracking of a hydrocarbon feedstock.
CATALYST AND ITS USE IN ETHYLBENZENE DEALKYLATION
An ethylbenzene dealkylation catalyst composition comprising a ZSM-5 type zeolite as a carrier component, wherein said zeolite has been synthesized from an aqueous reaction mixture comprising one or more alumina sources, one or more silica sources, one or more alkali sources, and one or more primary and/or secondary amines and wherein the ZSM-5 type zeolite has a number average crystallite size in the range of from 1 to 10 μm and a molar silica-to-alumina ratio (SAR) in the range of from 30 to 70; a method for reducing xylene losses in an ethylbenzene dealkylation process, said method comprising conducting the ethylbenzene dealklylation process in the presence of the afore-mentioned catalyst composition; and a process for the dealkylation of ethylbenzene, which process comprises contacting, in the presence of hydrogen, a feedstock which comprises ethylbenzene with said catalyst composition.
ALKYLAROMATIC CONVERSION CATALYST SYSTEM
An alkylaromatic conversion catalyst system having (a) a first catalyst composition having (i) a carrier which includes a binder composition prepared from a mixture having one or more oligomerized alkoxy silicates and one or more hydrolyzing agents; and a ZSM-5 zeolite; (ii) one or more metals chosen from the group consisting of Groups 6, 9, 10 and 11; and optionally, (iii) a Group 14 metal; and (b) a second catalyst composition having (i) a carrier which includes a refractory oxide binder and a zeolite selected from one or more of ZSM-5, ferrierite, ZSM-11, ZSM-12 and EU-1; (ii) one or more metals chosen from the group consisting of Groups 6, 9, 10 and 11; and optionally, (iii) a Group 14 metal.
Process for making modified small-crystal mordenite, transalkylation process using same, and modified small-crystal mordenite
A modified UZM-14 zeolite is described. The modified UZM-14 zeolite has a Modification Factor of 6 or more. The modified UZM-14 zeolite may have one or more of: a Si/Al.sub.2 ratio of 14 to 30; a total pore volume in a range of 0.5 to 1.0 cc/g; at least 5% of a total pore volume being mesopores having a diameter of 10 nm of less; a cumulative pore volume of micropores and mesopores having a diameter of 100 Å or less of 0.25 cc/g or more; or a Collidine IR Bronsted acid site distribution greater than or equal to an area of 3/mg for a peak in a range of 1575 to 1700 cm.sup.−1 after desorption at 150° C. Processes of making the modified UZM-14 zeolite and transalkylation processes using the modified UZM-14 zeolite are also described.
Phosphorus-containing molecular sieve, its preparation and application thereof
A phosphorus-containing molecular sieve has a phosphorus content of about 0.3-5 wt %, a pore volume of about 0.2-0.95 ml/g, and a ratio of B acid content to L acid content of about 2-10. The molecular sieve has a specific combination of characteristics, including a high ratio of B acid content to L acid content, thereby exhibiting higher hydrocracking activity and ring-opening selectivity when used in the preparation of a hydrocracking catalyst.
NaY molecular sieve with an aluminum-rich surface and a process of preparing same
A NaY molecular sieve with an aluminum-rich surface is prepared using a process that includes the steps of: a. mixing a directing agent and a first silicon source to obtain a first mixture, wherein the directing agent has a molar composition of Na.sub.2O:Al.sub.2O.sub.3:SiO.sub.2:H.sub.2O=(6-25):1:(6-25):(200-400); b. mixing the first mixture obtained in the step a with a second silicon source, an aluminum source and water to obtain a second mixture; c. carrying out hydrothermal crystallization on the second mixture obtained in the step b, and collecting a solid product. Calculated as SiO.sub.2, the weight ratio of the first silicon source to the second silicon source is 1:(0.01-12). The NaY molecular sieve has larger aluminum distribution gradient from the surface to the center of the particle than the conventional molecular sieve.
Modified Y-type molecular sieve, catalytic cracking catalyst comprising the same, its preparation and application thereof
A modified Y-type molecular sieve has a modifying metal content of about 0.5-6.3 wt % calculated on the basis of an oxide of the modifying metal and a sodium content of no more than about 0.5 wt % calculated on the basis of sodium oxide. The modifying metal is magnesium and/or calcium. The modified Y-type molecular sieve has a proportion of non-framework aluminum content to the total aluminum content of no more than about 20%, a total pore volume of about 0.33-0.39 ml/g, a proportion of the pore volume of secondary pores having a pore size of 2-100 nm to the total pore volume of about 10-25%, a lattice constant of about 2.440-2.455 nm, a lattice collapse temperature of not lower than about 1040° C., and a ratio of B acid to L acid in the total acid content of no less than about 2.30.
Modified Y-type molecular sieve, catalytic cracking catalyst comprising the same, their preparation and application thereof
A modified Y-type molecular sieve has a rare earth content of about 4% to about 11% by weight on the basis of the oxide, a phosphorus content of about 0.05% to about 10% by weight on the basis of P.sub.2O.sub.5, a sodium content of no more than about 0.5% by weight on the basis of sodium oxide, and an active element content of about 0.1% to about 5% by weight on the basis of the oxide, with the active element being gallium and/or boron. The modified Y-type molecular sieve has a total pore volume of about 0.36 mL/g to about 0.48 mL/g, a percentage of the pore volume of secondary pores having a pore size of 2-100 nm of about 20% to about 40%; a lattice constant of about 2.440 nm to about 2.455 nm, and a lattice collapse temperature of not lower than about 1060° C.
Modified Y-type molecular sieve, catalytic cracking catalyst comprising the same, its preparation and application thereof
A modified Y-type molecular sieve having a calcium content of about 0.3-4 wt % calculated on the basis of calcium oxide, a rare earth content of about 2-7 wt % calculated on the basis of rare earth oxide, and a sodium content of no more than about 0.5 wt % calculated on the basis of sodium oxide. The modified Y-type molecular sieve has a total pore volume of about 0.33-0.39 ml/g, a proportion of the pore volume of secondary pores having a pore size of 2-100 nm to the total pore volume of about 10-25%, a lattice constant of about 2.440-2.455 nm, a proportion of non-framework aluminum content to the total aluminum content of no more than about 20%, a lattice collapse temperature of not lower than about 1050° C., and a ratio of B acid to L acid in the total acid content of no less than about 2.30.