Methods and systems for producing olefins and aromatics are provided. Methods can include removing silica from the coker naphtha feedstock to produce a first effluent, hydrogenating the first effluent to produce a second effluent, reacting the second effluent to produce a third effluent comprising aromatics, a fourth effluent comprising olefins, and a fifth effluent, separating the fourth effluent to produce a propylene product stream, an ethylene product stream, and a sixth effluent, recycling the sixth effluent by combining it with the second effluent.

Methods and systems for producing olefins and aromatics are provided. Methods can include removing silica from the coker naphtha feedstock to produce a first effluent, hydrogenating the first effluent to produce a second effluent, reacting the second effluent to produce a third effluent comprising aromatics, a fourth effluent comprising olefins, and a fifth effluent, separating the fourth effluent to produce a propylene product stream, an ethylene product stream, and a sixth effluent, recycling the sixth effluent by combining it with the second effluent.

A hydrocarbon conversion catalyst composition which comprises ZSM-48 and/or EU-2 zeolite particles and refractory oxide binder essentially free of alumina in which the average aluminium concentration of the ZSM-48 and/or EU-2 zeolite particles is at least 1.3 times the aluminium concentration at the surface of the particles, processes for preparing such catalyst compositions and processes for converting hydrocarbon feedstock with the help of such compositions.

The invention relates to a process for the catalytic cracking of a gasoline feedstock for the production of light olefins, in which said gasoline feedstock is brought into contact with a catalyst comprising at least one zeolite NU-86, alone or in a mixture with at least one other zeolite, at a temperature comprised between 500 and 700 C., at an absolute pressure comprised between 10 and 60 MPa, and with a contact time of the feedstock on said catalyst comprised between 10 milliseconds and 100 seconds.

The present invention provides catalyst comprising metal modified zeolite, particularly Group IIIA or Group IIB metal modified zeolite, or a Group IIIA metal and Group IIB metal modified zeolite for reforming of heart cut naphtha stream. The present disclosure also relates to a process for synthesis of the catalyst. The present disclosure further relates to a process for reforming of heart cut naphtha stream, with high selectivity towards aromatics and good activity using the catalytic system, in the absence of hydrogen.

The present disclosure relates to a reforming catalyst composition comprising a spherical gamma AI.sub.2O.sub.3 support; at least one Group VB metal oxide sheet coated on to the AI.sub.2O.sub.3 support; and at least one active metal and at least one promoter metal impregnated on the AI.sub.2O.sub.3 coated support. The reforming catalyst composition of the present disclosure has improved activity, better selectivity for total aromatics during naphtha reforming and results in less coke formation. The reforming catalyst composition has improved catalyst performance with simultaneous modification of acidic sites as well as metallic sites through metal support interaction. The acid site cracking activity of the catalyst is inhibited because of the use of chloride free alumina support modified with solid acid such as Group VB metal oxide and impregnated with active metals. The present disclosure provides a process for naphtha reforming in the presence of the reforming catalyst composition of the present disclosure to obtain reformates of naphtha.

The present disclosure relates to a reforming catalyst composition comprising a spherical gamma AI.sub.2O.sub.3 support; at least one Group VB metal oxide sheet coated on to the AI.sub.2O.sub.3 support; and at least one active metal and at least one promoter metal impregnated on the AI.sub.2O.sub.3 coated support. The reforming catalyst composition of the present disclosure has improved activity, better selectivity for total aromatics during naphtha reforming and results in less coke formation. The reforming catalyst composition has improved catalyst performance with simultaneous modification of acidic sites as well as metallic sites through metal support interaction. The acid site cracking activity of the catalyst is inhibited because of the use of chloride free alumina support modified with solid acid such as Group VB metal oxide and impregnated with active metals. The present disclosure provides a process for naphtha reforming in the presence of the reforming catalyst composition of the present disclosure to obtain reformates of naphtha.

Methods for fabricating a membrane with an organosilica material which is a polymer comprising independent units of Formula [Z.sup.3Z.sup.4SiCH.sub.2].sub.3 (I), wherein each Z.sup.3 represents a hydroxyl group, a C.sub.1-C.sub.4 alkoxy group or an oxygen atom bonded to a silicon atom of another unit or an active site on the support and each Z.sup.4 represents a hydroxyl group, a C.sub.1-C.sub.4 alkoxy group, a C.sub.1-C.sub.4 alkyl group, an oxygen atom bonded to a silicon atom of another unit or an active site on the support are provided. Methods of removing a contaminant from a hydrocarbon stream are also provided.

Methods for fabricating a membrane with an organosilica material which is a polymer comprising independent units of Formula [Z.sup.3Z.sup.4SiCH.sub.2].sub.3 (I), wherein each Z.sup.3 represents a hydroxyl group, a C.sub.1-C.sub.4 alkoxy group or an oxygen atom bonded to a silicon atom of another unit or an active site on the support and each Z.sup.4 represents a hydroxyl group, a C.sub.1-C.sub.4 alkoxy group, a C.sub.1-C.sub.4 alkyl group, an oxygen atom bonded to a silicon atom of another unit or an active site on the support are provided. Methods of removing a contaminant from a hydrocarbon stream are also provided.

A family of highly charged crystalline microporous metallophosphate molecular sieves designated PST-17 has been synthesized. These metallophosphates are represented by the empirical formula of:
R.sup.p+.sub.rA.sub.m.sup.+M.sub.xE.sub.yPO.sub.z
where A is an alkali metal such as potassium, R is a quaternary ammonium cation such as ethyltrimethylammonium, M is a divalent metal such as zinc and E is a trivalent framework element such as aluminum or gallium. The PST-17 family of molecular sieves are stabilized by combinations of alkali and organoammonium cations, enabling unique metalloalumino(gallo)phosphate compositions and exhibit the BPH topology. The PST-17 family of molecular sieves has catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.