US4414189A — Modification of catalytic activity of synthetic z…

Claim 1

Independent Claim 191 words

A method for altering catalytic activity of a synthetic crystalline zeolite characterized as having a crystal structure which provides constrained access to and egress from the intracrystalline free space by virtue of having a pore dimension greater than about 5 Angstroms and pore windows of about a size as would be provided by 10-membered rings of oxygen atoms which comprises the sequential steps of synthesizing said zeolite from a reaction mixture containing a source of bulky organic cations, contacting the synthesized zeolite with an aqueous hydrogen fluoride solution of from about 0.005 Normal to about 0.5 Normal at a temperature of from about ambient to about 100° C. and a pressure of from about atmospheric to about 40 psig for a contact time of from about 1 hour to about 10 hours, calcining the hydrogen fluoride solution contacted zeolite at a temperature of from about 200° C. to about 600° C., contacting the calcined zeolite with an ammonium exchange solution at a temperature of from about ambient to about 100° C., and calcining the ammonium exchange solution contacted zeolite at a temperature of from about 200° C. to about 600° C.

Claim 2

Independent Claim 191 words

A method for altering catalytic activity of a synthetic crystalline zeolite characterized as having a crystal structure which provides constrained access to and egress from the intracrystalline free space by virtue of having a pore dimension greater than about 5 Angstroms and pore windows of about a size as would be provided by 10-membered rings of oxygen atoms which comprises the sequential steps of synthesizing said zeolite from a reaction mixture containing a source of bulky organic cations, contacting the synthesized zeolite with an aqueous hydrogen fluoride solution of from about 0.005 Normal to about 0.5 Normal at a temperature of from about ambient to about 100° C. and a pressure of from about atmospheric to about 40 psig for a contact time of from about 1 hour to about 10 hours, calcining the hydrogen fluoride solution contacted zeolite at a temperature of from about 200° C. to about 600° C., contacting the calcined zeolite with an ammonium exchange solution at a temperature of from about ambient to about 100° C., and calcining the ammonium exchange solution contacted zeolite at a temperature of from about 200° C. to about 600° C.

Claim 3

Dependent Claim 20 words

The method of claim 1 wherein said crystalline zeolite is characterized by a silica/aluminum mole ratio of at least 12.

Claim 4

Dependent Claim 24 words

The method of claim 2 wherein said crystalline zeolite is selected from the group consisting of ZSM-5, ZSM-11, ZSM-12, ZSM-23 ZSM-35, ZSM-38 and ZSM-48.

Claim 5

Dependent Claim 11 words

The method of claim 3 wherein said crystalline zeolite is ZSM-5.

Claim 6

Dependent Claim 37 words

The method of claim 1 wherein said source of bulky organic cations is selected from the group consisting of trialkylamines, wherein alkyl is from 1 to 20 carbon atoms, onium compounds and compounds containing multiple cationic centers.

Claim 7

Dependent Claim 81 words

The method of claim 5 wherein said source of bulky organic cations is onium compounds having the formula R.sub.4 M.sup.+ X.sup.- wherein R is alkyl of from 1 to 20 carbon atoms, heteroalkyl of from 1 to 20 carbon atoms, aryl, heteroaryl, cycloalkyl of from 3 to 6 carbon atoms, cycloheteroalkyl of from 3 to 6 carbon atoms, or combinations thereof; M is a quadricoordinate element or a heteroatom in an alicyclic, heteroalicyclic or heteroaromatic structure; and X is an anion.

Claim 8

Dependent Claim 142 words

The method of claim 5 wherein said source of bulky organic cations is compounds containing multiple cationic centers having the formula ((R).sub.3 M.sup.+ (Z).sub.n M.sup.+ (R).sub.3)(X.sup.-).sub.2 wherein R is alkyl of from 1 to 20 carbon atoms, heteroalkyl of from 1 to 20 carbon atoms, aryl, heteroaryl, cycloalkyl of from 3 to 6 carbon atoms, cycloheteroalkyl of from 3 to 6 carbon atoms, or combinations thereof; M is a quadricoordinate element or a heteroatom in an alicyclic, heteroalicyclic or heteroaromatic structure; X is an anion; Z is a bridging member selected from the group consisting of alkyl of from 1 to 20 carbon atoms, alkenyl of from 2 to 20 carbon atoms, aryl, heteroalkyl of from 1 to 20 carbon atoms, heteroalkenyl of from 2 to 20 carbon atoms and heteroaryl; and n is a number of from 1 to about 50.

Claim 9

Dependent Claim 24 words

The method of claim 5 wherein said source of bulky organic cations is a trialkylamine wherein alkyl is from 1 to 20 carbon atoms.

Claim 10

Dependent Claim 21 words

The method of claim 1 wherein said ammonium exchange solution is an aqueous solution of an ammonium salt or ammonium hydroxide.

Claim 11

Dependent Claim 17 words

The method of claim 9 wherein said ammonium salt is ammonium nitrate, ammonium sulfate or ammonium chloride.

Claim 12

Independent Claim 164 words

A method for altering catalytic activity of a synthetic crystalline zeolite having a constraint index of from about 1 to about 12 and a silica/alumina mole ratio of at least 12 which comprises the sequential steps of synthesizing said zeolite from a reaction mixture containing a source of bulky organic cations, contacting the synthesized zeolite with an aqueous hydrogen fluoride solution of from about 0.005 Normal to about 0.5 Normal at a temperature of from about ambient to about 100° C. and a pressure of from about atmospheric to about 40 psig for a contact time of from about 1 hour to about 10 hours, calcining the hydrogen fluoride solution contacted zeolite at a temperature of from about 200° C. to about 600° C., contacting the calcined zeolite with an ammonium exchange solution at a temperature of from about ambient to about 100° C., and calcining the ammonium exchange solution contacted zeolite at a temperature of from about 200° C. to about 600° C.

Claim 13

Independent Claim 164 words

A method for altering catalytic activity of a synthetic crystalline zeolite having a constraint index of from about 1 to about 12 and a silica/alumina mole ratio of at least 12 which comprises the sequential steps of synthesizing said zeolite from a reaction mixture containing a source of bulky organic cations, contacting the synthesized zeolite with an aqueous hydrogen fluoride solution of from about 0.005 Normal to about 0.5 Normal at a temperature of from about ambient to about 100° C. and a pressure of from about atmospheric to about 40 psig for a contact time of from about 1 hour to about 10 hours, calcining the hydrogen fluoride solution contacted zeolite at a temperature of from about 200° C. to about 600° C., contacting the calcined zeolite with an ammonium exchange solution at a temperature of from about ambient to about 100° C., and calcining the ammonium exchange solution contacted zeolite at a temperature of from about 200° C. to about 600° C.

Claim 14

Dependent Claim 37 words

The method of claim 11 wherein said source of bulky organic cations is selected from the group consisting of trialkylamines, wherein alkyl is from 1 to 20 carbon atoms, onium compounds and compounds containing multiple cationic centers.

Claim 15

Dependent Claim 81 words

The method of claim 12 wherein said source of bulky organic cations is onium compounds having the formula R.sub.4 M.sup.+ X.sup.- wherein R is alkyl of from 1 to 20 carbon atoms, heteroalkyl of from 1 to 20 carbon atoms, aryl, heteroaryl, cycloalkyl of from 3 to 6 carbon atoms, cycloheteroalkyl of from 3 to 6 carbon atoms, or combinations thereof; M is a quadricoordinate element or a heteroatom in an alicyclic, heteroalicyclic or heteroaromatic structure; and X is an anion.

Claim 16

Dependent Claim 141 words

The method of claim 12 wherein said source of bulky organic cations is compounds containing multiple centers having the formula ((R).sub.3 M.sup.+ (Z).sub.n M.sup.+ (R).sub.3)(X.sup.-).sub.2 wherein R is alkyl of from 1 to 20 carbon atoms, heteroalkyl of from 1 to 20 carbon atoms, aryl, heteroaryl, cycloalkyl of from 3 to 6 carbon atoms, cycloheteroalkyl of from 3 to 6 carbon atoms, or combinations thereof; M is a quadricoordinate element or a heteroatom in an alicyclic, heteroalicyclic or heteroaromatic structure; X is an anion; Z is a bridging member selected from the group consisting of alkyl of from 1 to 20 carbon atoms, alkenyl of from 2 to 20 carbon atoms, aryl, heteroalkyl of from 1 to 20 carbon atoms, heteroalkenyl of from 2 to 20 carbon atoms and heteroaryl; and n is a number of from 1 to about 50.

Claim 17

Dependent Claim 24 words

The method of claim 12 wherein said source of bulky organic cations is a trialkylamine wherein alkyl is from 1 to 20 carbon atoms.

Claim 18

Independent Claim 150 words

A method for altering catalytic activity of a synthetic crystalline zeolite having the structure of zeolite ZSM-5 which comprises the sequential steps of synthesizing said zeolite from a reaction mixture containing a source of bulky organic cations, contacting the synthesized zeolite with an aqueous hydrogen fluoride solution of from about 0.005 Normal to about 0.5 Normal at a temperature of from about ambient to about 100° C. and a pressure of from about atmospheric to about 40 psig for a contact time of from about 1 hour to about 10 hours, calcining the hydrogen fluoride solution contacted zeolite at a temperature of from about 200° C. to about 600° C., contacting the calcined zeolite with an ammonium exchange solution at a temperature of from about ambient to about 100° C., and calcining the ammonium exchange solution contacted zeolite at a temperature of from about 200° C. to about 600° C.

Claim 19

Independent Claim 150 words

A method for altering catalytic activity of a synthetic crystalline zeolite having the structure of zeolite ZSM-5 which comprises the sequential steps of synthesizing said zeolite from a reaction mixture containing a source of bulky organic cations, contacting the synthesized zeolite with an aqueous hydrogen fluoride solution of from about 0.005 Normal to about 0.5 Normal at a temperature of from about ambient to about 100° C. and a pressure of from about atmospheric to about 40 psig for a contact time of from about 1 hour to about 10 hours, calcining the hydrogen fluoride solution contacted zeolite at a temperature of from about 200° C. to about 600° C., contacting the calcined zeolite with an ammonium exchange solution at a temperature of from about ambient to about 100° C., and calcining the ammonium exchange solution contacted zeolite at a temperature of from about 200° C. to about 600° C.

Annuity Stage	Window Opens	Payment Deadline	Surcharge Period Until	Estimated Fee	Status
3.5 Years (Year 4)	1986-11-07	1987-05-09	1987-11-08	$2000.00	Window Closed / Lapsed
7.5 Years (Year 8)	1990-11-07	1991-05-09	1991-11-08	$3760.00	Window Closed / Lapsed
11.5 Years (Year 12)	1994-11-07	1995-05-09	1995-11-08	$7700.00	Window Closed / Lapsed

Modification of catalytic activity of synthetic zeolites

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