Patent classifications
C07C11/04
Removing acetylene from ethylene gas streams during polyethylene synthesis
Disclosed herein are methods for removing acetylene from an ethylene gas stream wherein a catalyst reacts with the acetylene to polymerize said acetylene forming an ethylene gas stream substantially free of acetylene.
Removing acetylene from ethylene gas streams during polyethylene synthesis
Disclosed herein are methods for removing acetylene from an ethylene gas stream wherein a catalyst reacts with the acetylene to polymerize said acetylene forming an ethylene gas stream substantially free of acetylene.
Solid-supported amino-diphosphine ligand catalysts for selective oligomerization of ethylene to form linear alpha-olefins
Ethylene oligomerization catalysts include a solid support having surface hydroxyl groups on a surface of the solid support. Functional groups attached to the solid support through at least one covalent bond and coordinated with at least one catalytically active transition metal. Individual functional groups are attached to the solid support as products of condensation reactions of at least one hydrolysable group of precursor ligands with a corresponding surface group of the solid support. The precursor ligands have a general formula (Ph.sub.2P).sub.2N—R.sup.1-A, where R.sup.1 is C.sub.1-C.sub.40 hydrocarbylene or C.sub.1-C.sub.40 heterohydrocarbylene; and A is a hydrolysable group selected from trialkoxysilyl, halosilyl, carboxylates, esters, phosphonates, amines, imines, thiols, thiocarboxylates, or halides.
Solid-supported amino-diphosphine ligand catalysts for selective oligomerization of ethylene to form linear alpha-olefins
Ethylene oligomerization catalysts include a solid support having surface hydroxyl groups on a surface of the solid support. Functional groups attached to the solid support through at least one covalent bond and coordinated with at least one catalytically active transition metal. Individual functional groups are attached to the solid support as products of condensation reactions of at least one hydrolysable group of precursor ligands with a corresponding surface group of the solid support. The precursor ligands have a general formula (Ph.sub.2P).sub.2N—R.sup.1-A, where R.sup.1 is C.sub.1-C.sub.40 hydrocarbylene or C.sub.1-C.sub.40 heterohydrocarbylene; and A is a hydrolysable group selected from trialkoxysilyl, halosilyl, carboxylates, esters, phosphonates, amines, imines, thiols, thiocarboxylates, or halides.
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.
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.
PROCESS FOR CONVERTING ONE OR MORE METHYL HALIDES INTO ETHYLENE AND PROPYLENE
The present disclosure concerns a process for converting methyl halides to ethylene and propylene, said process comprising the steps of (a) providing a feedstream comprising methyl halides; (b) providing a first and second catalyst composition, said second catalyst composition comprising a cracking catalyst; (c) contacting said feedstream with said first catalyst composition in a first reaction zone under first reaction conditions to provide a first product stream; and (d) subjecting at least a part of said first product stream to an Olefin Catalytic Cracking with said second catalyst composition in a second reaction zone under second reaction conditions to provide a second product steam. The process is remarkable in that said step (c) is performed under 400° C., and in that said first catalyst composition comprises molecular sieves with a Si/Al atomic between 2 and 18 and with a plurality of pores with a shape of an 8-membered ring or less.
PROCESS FOR CONVERTING ONE OR MORE METHYL HALIDES INTO ETHYLENE AND PROPYLENE
The present disclosure concerns a process for converting methyl halides to ethylene and propylene, said process comprising the steps of (a) providing a feedstream comprising methyl halides; (b) providing a first and second catalyst composition, said second catalyst composition comprising a cracking catalyst; (c) contacting said feedstream with said first catalyst composition in a first reaction zone under first reaction conditions to provide a first product stream; and (d) subjecting at least a part of said first product stream to an Olefin Catalytic Cracking with said second catalyst composition in a second reaction zone under second reaction conditions to provide a second product steam. The process is remarkable in that said step (c) is performed under 400° C., and in that said first catalyst composition comprises molecular sieves with a Si/Al atomic between 2 and 18 and with a plurality of pores with a shape of an 8-membered ring or less.
PROCESS FOR CONVERTING ONE OR MORE METHYL HALIDES INTO ETHYLENE AND PROPYLENE
The present disclosure concerns a process for converting methyl halides to ethylene and propylene, said process comprising the steps of (a) providing a feedstream comprising methyl halides; (b) providing a first and second catalyst composition, said second catalyst composition comprising a cracking catalyst; (c) contacting said feedstream with said first catalyst composition in a first reaction zone under first reaction conditions to provide a first product stream; and (d) subjecting at least a part of said first product stream to an Olefin Catalytic Cracking with said second catalyst composition in a second reaction zone under second reaction conditions to provide a second product steam. The process is remarkable in that said step (c) is performed under 400° C., and in that said first catalyst composition comprises molecular sieves with a Si/Al atomic between 2 and 18 and with a plurality of pores with a shape of an 8-membered ring or less.
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.