High charge density metallophosphate molecular sieves

Patent metadata

Field	Value
Publication number	US-11033887-B2
Application number	US-201916594144-A
Country	US
Kind code	B2
Filing date	Oct 7, 2019
Priority date	May 25, 2016
Publication date	Jun 15, 2021
Grant date	Jun 15, 2021

Abstract

A new family of highly charged crystalline microporous metallophosphate molecular sieves has been synthesized. These metallophosphates are represented by the empirical formula of:

R p+ r A + m M 2+ x E y PO z

where A is an alkali metal cation, R is at least one quaternary organoammonium cation, M is a divalent metal such as zinc and E is a trivalent framework element such as aluminum or gallium. This family of high charge density metallophosphate materials are among the first metalloalumino(gallo)phosphate-type molecular sieves to be stabilized by combinations of alkali and quaternary organoammonium cations, enabling unique compositions. This family of high charge density metallophosphate molecular sieves has catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

First claim

The invention claimed is:

1. A process for preparing a microporous crystalline metallophosphate material having a three-dimensional framework of [M 2+ O 4/2 ] 2− , [EO 4/2 ] − and [PO 4/2 ] + tetetrahedral units and an empirical composition in the as synthesized form and on an anhydrous basis expressed by an empirical formula of:
R p+ r A + m M 2+ x E y PO z
where R is at least one of any quaternary ammonium cation, diquaternary ammonium cation triquaternary ammonium cation, quatroquaternary ammonium cation and mixtures thereof, “r” is the mole ratio of R to P and has a value of about 0.04 to about 1.0, “p” is the weighted average valence of R and varies from 1 to 4, A is an alkali metal selected from the group consisting of Li + , Na + , K + , Rb + and Cs + and mixtures thereof, “m” is the mole ratio of A to P and varies from 0.1 to 1.0, M is a divalent element selected from the group of Zn, Mg, Co, Mn and mixtures thereof, “x” is the mole ratio of M to P and varies from 0.2 to about 0.9, E is a trivalent element selected from the group consisting of aluminum and gallium and mixtures thereof, “y” is the mole ratio of E to P and varies from 0.1 to about 0.8 and “z” is the mole ratio of O to P and has a value determined by the equation:
z =( m+p·r+ 2 ·x+ 3 ·y+ 5)/2

 and is characterized by a specific x-ray diffraction pattern, the process comprising forming a reaction mixture containing reactive sources of R, A, E, M and P, and heating the reaction mixture at a temperature of about 60° C. to about 200° C. for a time sufficient to form the metallophosphate molecular sieve, the reaction mixture having a composition expressed in terms of mole ratios of the oxides of:
a R 2/p O: b A 2 O: c MO:E 2 O 3 :d P 2 O 5 :e H 2 O

 where “a” has a value of about 2.1 to about 100, “b” has a value of about 0.1 to about 8.0, “c” has a value of about 0.25 to about 8, “d” has a value of about 1.69 to about 25, and “e” has a value from 30 to 5000.

2. The process of claim 1 where the initial reaction mixture is a clear solution before digestion.

3. The process of claim 1 where A is selected from the group consisting of Li + , Na + , K + , Rb + and Cs + and mixtures thereof and the source of A is selected from the group consisting of halide salts, nitrate salts, acetate salts, sulfate salts, hydroxide salts and mixtures thereof.

4. The process of claim 1 where M is selected from the group consisting of Zn 2+ , Mg 2+ , Co 2+ and Mg 2+ and mixtures thereof and the source of M is selected from the group consisting of halide salts, nitrate salts, acetate salts, sulfate salts and mixtures thereof.

5. The process of claim 1 where the source of E is selected from the group consisting of aluminum isopropoxide, aluminum sec-butoxide, precipitated alumina, Al(OH) 3 , alkali aluminate salts, aluminum metal, aluminum halide salts, aluminum sulfate salts, aluminum nitrate salts, precipitated gallium oxyhydroxide, gallium nitrate, gallium sulfate and mixtures thereof.

6. The process of claim 1 where the reaction mixture is reacted at a temperature of about 85° C. to about 185° C. for a time of about 1 day to about 14 days.

7. The process of claim 1 where R is at least one quaternary ammonium cation selected from the group of quaternary ammonium cations consisting of tetramethylammonium (TMA + ), ethyltrimethylammonium (ETMA + ), propyltrimethylammonium (PTMA + ), isopropyltrimethylammonium, diethyldimethylammonium (DEDMA + ), trimethylbutylammonium (TMBA + ), methyltriethylammonium (MTEA + ), propylethyldimethylammonium (PEDMA + ), N,N-dimethylpiperidinium, N,N-dimethyl-3,5-dimethylpiperidinium, dipropyldimethylammonium (DPDMA + ), diethylmethylpropylammonium, trimethylpentylammonium (TMPA + ), dimethyldiisopropylammonium, tetraethylammonium (TEA + ), hexyltrimethylammonium (HTMA + ), methylethyldipropylammonium, triethylpropylammonium, dibutyldimethylammonium, benzyltrimethylammonium (BzTMA + ), diethyldipropylammonium, octyltrimethylammonium, tetrapropylammonium (TPA + ), decyltrimethylammonium, adamantyltrimethylammonium, methyltributylammonium, dodecyltrimethylammonium, hexadecyltrimethylammonium, tetrabutylammonium (TBA + ), methylene-bis-(trimethylammonium), bis-1,2-(trimethylammonium)ethylene, bis-1,3(trimethylammonium)propane, bis-1,3-(trimethylammonium)-2-propanol, bis-1,4-(trimethylammonium)butane, bis-1,5-(trimethylammonium)pentane (i.e., pentamethonium), bis-1,6-(trimethylammonium)hexane (i.e., hexamethonium, HM 2+ ), bis-1,8-(trimethylammonium)octane, bis-1,10-(trimethylammonium)decane, bis-1,5-(triethylammonium)pentane (i.e., pentaethonium), bis-1,6-(triethylammonium)hexane (i.e., hexaethonium), bis-α,α′-(dimethylethylammonium)-p-xylene, bis-α,α′-(dimethylethylammonium)-m-xylene, bis-α,α′-(dimethylethylammonium)-o-xylene, bis-1,5-(N-methylpiperidinum)pentane and bis-1,6-(N-methylpiperidinum)hexane, N,N,N′,N′-tetramethyl-N,N′-p-xyleno-1,6-hexanediammonium, N,N,N′,N′-tetramethyl-N,N′-butano-1,6-hexanediammonium, N,N,N′,N′-tetrmaethyl-N,N′-hexano-1,6-hexanediammonium, N,N,N′,N′-tetraethyl-N,N′-hexano-1,5-pentanediammonium, N,N,N′,N′-tetramethyl-N,N′-m-xyleno-1,6-hexanediammonium, N,N,N′,N′-tetramethyl-N,N′-o-xyleno-1,2-ethylenediammonium, N,N,N′,N′-tetramethyl-N,N′-butano-1,2-ethylenediammonium, N,N,N′,N′-tetramethyl-N,N′-hexano-1,2-ethylenediammonium, tris-1,3,5-(triethylammoniomethyl)benzene, tris-1,3,5-(trimethylammoniomethyl)benzene, tris-1,3,5-(dimethylethylammoniomethyl)benzene, [(C 6 H 5 CH 2 )(Me 2 )N(—CH 2 CH(OH)CH 2 N(Me 2 )-) 3 CH 2 C 6 H 5 ] 4+ (i.e., dibenzylquatroquat), tetrakis-1,2,4,5-(trimethylammoniomethyl)benzene, tetrakis-1,2,4,5-(triethylammoniomethyl)benzene, tetrakis-1,2,4,5-(dimethylethylammoniomethyl)benzene and mixtures thereof.

8. The process of claim 1 further comprising adding seeds of an as-synthesized metallophosphate material to the reaction mixture.

9. The process of claim 1 further comprising modifying the microporous crystalline metallophosphate material by subjecting said microporous crystalline metallophosphate material to calcination, ion-exchange, steaming, ammonium hexafluorosilicate treatment, or any combination thereof.

10. A hydrocarbon conversion process comprising contacting a hydrocarbon stream with a catalyst at hydrocarbon conversion conditions to generate at least one converted product, wherein the catalyst is selected from the group consisting of a crystalline microporous high charge density metallophosphate material, a modified crystalline microporous high charge density metallophosphate material and mixtures thereof, where the high charge density metallophosphate material is a crystalline microporous metallophosphate having a three-dimensional framework of [M 2+ O 4/2 ] 2− , [EO 4/2 ] − and [PO 4/2 ] + tetrahedral units and an empirical composition in the as synthesized form and on an anhydrous basis expressed by an empirical formula of:
R p+ r A + m M 2+ x E y PO z
where R is at least one of any quaternary ammonium cation, diquaternary ammonium cation triquaternary ammonium cation, quatroquaternary ammonium cation and mixtures thereof, “r” is the mole ratio of R to P and has a value of about 0.04 to about 1.0, “p” is the weighted average valence of R and varies from 1 to 4, A is an alkali metal selected from the group consisting of Li + , Na + , K + , Rb + and Cs + and mixtures thereof, “m” is the mole ratio of A to P and varies from 0.1 to 1.0, M is a divalent element selected from the group of Zn, Mg, Co, Mn and mixtures thereof, “x” is the mole ratio of M to P and varies from 0.2 to about 0.9, E is a trivalent element selected from the group consisting of aluminum and gallium and mixtures thereof, “y” is the mole ratio of E to P and varies from 0.1 t

Assignees

• Uop Llc

Inventors

• Lewis Gregory J
• Moscoso Jaime G
• Knight Lisa M
• Seo Seungwan
• Nicholas Christopher P
• Lee Junghwan
• Hong Suk Bong

Classifications

• C01P2002/74

  by peak-intensities or a ratio thereof only · CPC title

• B01D2255/50

  Zeolites · CPC title

• B01J29/84 Primary

  Aluminophosphates containing other elements, e.g. metals, boron · CPC title

• Y02P30/20

  using bio-feedstock · CPC title

• Y02P30/40

  Ethylene production · CPC title