Selective production of para-aromatics

Claim 2

A process for the selective para-alkylation of mon-substituted aromatic compounds comprising reacting the aromatic compound with an effective amount of an alkylating agent at effective alkylating conditions in the presence of a catalyst comprising an effective amount of at least one NZMS containing at least three framework elements as tetrahedral oxides and characterized in its active catalytic form by an adsorption of isobutane of at least 2 percent by weight at a partial pressure of 500 torr and a temperature of 20° C. and also characterized in its active catalytic form by an absorption of triethylamine less than 5 percent by weight at a pressure of 2.6 torr and a temperature of 22° C.

Claim 3

The process of claim 1 wherein said NZMS is characterized in its calcined form by an adsorption of isobutane of at least 4 percent by weight at a pressure of 500 torr and a temperature of 20° C.

Claim 4

The process of claim 1 wherein said NZMS is further characterized in its calcined form by an adsorption of triethylamine less than 3 percent by weight at a pressure of 2.6 torr and a temperature of 22° C.

Claim 5

The process of claim 1 or claim 2 wherein said effective process conditions include a temperature between about 50° C. and about 500° C.

Claim 6

The process of claim 4 wherein said effective process conditions include a temperature between about 30 ° C. and about 450° C.

Claim 7

The process of claim 1 wherein said catalyst comprises an inorganic oxide component in an amount between about 5 and about 95 percent by weight, based on the total weight of said catalyst.

Claim 8

The process of claim 1 or claim 2 wherein said NZMS has at least part of its cations as H + or hydrogen forming species.

Claim 9

The process of claim 7 wherein said hydrogen forming species is NH 4 + or H + .

Claim 10

The process of claim 1 or claim 2 wherein the process is carried out at an effective temperature between about 100° C. and about 500° C., effective pressure between zero psig and about 1000 psig, a WHSV of between about 0.1 and about 100 and a molar ratio of alkylating agent to mono-substituted aromatic compounds of between 1:50 and 50:1.

Claim 11

The process of 6 wherein said inorganic oxide matrix component is selected from the group consisting of clays, silicas, aluminas, and mixtures thereof.

Claim 12

The process of 6 wherein said inorganic oxide matrix component is selected from the group consisting of clays, silicas, aluminas, and mixtures thereof.

Claim 13

The process of claim 1 or claim 2 or claim 3 wherein said NZMS is selected from the group consisting of CoAPSOs, FeAPSOs, MgAPSOs, MnAPSOs, TiAPSOs, ZnAPSOs, CoMgAPSOs, CoMnMgAPSOs, MeAPOs, TiAPOs, FeAPOs, FCAPOs and mixture thereof.

Claim 14

The process of claim 1 or claim 2 wherein said NZMS is selected from the group consisting of CoAPSOs, FeAPSOs, MgAPSOs, MnAPSOs, TiAPSOs, ZnAPSOs, CoMgAPSOs, CoMnMgAPSOs and mixtures thereof.

Claim 15

The process of claim 1 or claim 2 or claim 3 wherein said NZMS is selected from the group consisting of ELAPSO-11, ELAPSO-31, ELAPSO-41, and mixtures thereof.

Claim 16

The process of claim 13 wherein said NZMS is selected from the group consisting of SAPO-11, SAPO-31, SAPO-41, CoAPSO-11, CoAPSO-31, CoAPSO-41, FeAPSO-11, FeAPS-31, FeAPSO-41, MgAPSO-11, MgAPSO-31, MgAPSO041, MnAPSO-11, MnAPSO-31, MnAPSO-41, TiAPSO-11, TiAPSO-31, TiAPSO-41, ZnAPSO-11, ZnAPSO-31, ZnAPSO-41, CoMgAPSO-11, CoMgAPSO-31, CoMgAPSO-41, CoMnMgAPSO-11, CoMnMgAPSO-31, CoMnMgAPSO-41 and mixtures thereof.

Claim 17

The process of claim 1 or claim 2 or claim 3 wherein said NZMS is selected from the group consisting of MeAPO011, MeAPO-31, MeAPO-41, TiAPO-11, TiAPO-31, TiAPO-41, FeAPO-11, FeAPO-31, FeAPO-41, FCAPO-11, FCAPO-31, FCAPO-41 and mixtures thereof.

Claim 18

The process of claim 15 wherein "Me" is selected from the group consisting of cobalt magnesium, manganese, zinc and mixtures thereof.

Claim 19

The process of claim 15 wherein "Me" is selected from the group consisting of magnesium, manganese and mixtures thereof.

Claim 20

The process according to claim 1 wherein said mono-substituted aromatic is at least one selected from the group consisting of mono-alkylbenzenes, chlorobenzene, fluorobenzene, bromobenzene and said alkylating agent is at least one selected from the group consisting of olefins and compounds of the formula "RX" wherein "R" is an alkyl or substitued alkyl containing from 1 to 30 carbon atoms and "X" is halide, hydroxyl carbonate, carbonyl, alkoxyl, alkylsulfide.

Claim 21

In a process for the selective production of para-xylene by the reaction of toluene with a methylating agent under effective methylation conditions in the presence of a methylation catalyst, the improvement which comprises reacting toluene and said methylating agent in the presence of a methylation catalyst containing at least one NZMS containing at least three framework elements as tetrahedral oxides and characterized in its active catalytic form by an adsorption of isobutane of at least 2 percent by weight at a partial pressure of 500 torr and a temperature of 20° C. and also characterized in its active catalytic form by an adsorption of triethylamine less than 5 percent by weight at a pressure of 2.6 torr and a temperature of 22° C.

Claim 22

In a process for the selective production of para-xylene by the reaction of toluene with a methylating agent under effective methylation conditions in the presence of a methylation catalyst, the improvement which comprises reacting toluene and said methylating agent in the presence of a methylation catalyst containing at least one NZMS containing at least three framework elements as tetrahedral oxides and characterized in its active catalytic form by an adsorption of isobutane of at least 2 percent by weight at a partial pressure of 500 torr and a temperature of 20° C. and also characterized in its active catalytic form by an adsorption of triethylamine less than 5 percent by weight at a pressure of 2.6 torr and a temperature of 22° C.