Process for conversion of acyclic C5 compounds to cyclic C5 compounds and catalyst composition for use therein

Patent metadata

Field	Value
Publication number	US-9856187-B2
Application number	US-201615288452-A
Country	US
Kind code	B2
Filing date	Oct 7, 2016
Priority date	Nov 4, 2015
Publication date	Jan 2, 2018
Grant date	Jan 2, 2018

Abstract

Disclosed is a process for the conversion of acyclic C 5 feedstock to a product comprising cyclic C 5 compounds, such as for example, cyclopentadiene, and catalyst compositions for use in such process. The process comprising the steps of contacting said feedstock and, optionally, hydrogen under acyclic C 5 conversion conditions in the presence of a catalyst composition to form said product. The catalyst composition comprising a microporous crystalline ferrosilicate, a Group 10 metal, and, optionally, a Group 11 metal, in combination with an optional Group 1 alkali metal and/or an optional Group 2 alkaline earth metal.

First claim

What is claimed is:

1. A process for conversion of an acyclic C 5 feedstock to a product comprising cyclic C 5 compounds including cyclopentadiene, said process comprising the steps of contacting said feedstock and, optionally, hydrogen under acyclic C 5 conversion conditions in the presence of a catalyst composition to form said product, wherein said catalyst composition comprises a microporous crystalline ferrosilicate, a Group 10 metal, and, optionally, a Group 11 metal, in combination with an optional Group 1 alkali metal and/or an optional Group 2 alkaline earth metal.

2. A process for conversion of an acyclic C 5 feedstock to a product comprising cyclic C 5 compounds, said process comprising the steps of contacting said feedstock and, optionally, hydrogen under acyclic C 5 conversion conditions in the presence of a catalyst composition to form said product, wherein said catalyst composition is made by the method comprising the steps of:
(a) providing a microporous crystalline ferrosilicate comprising a Group 1 alkali metal and/or a Group 2 alkaline earth metal;
(b) heating said microporous crystalline ferrosilicate in one or more steps to a first temperature of 450° C. or above in an atmosphere which comprises an inert gas;
(c) adding oxygen to said atmosphere until the oxygen concentration in said atmosphere is up to 20% and then cooling said microporous crystalline ferrosilicate; and
(d) contacting said cooled microporous crystalline ferrosilicate of step (c) with a source of a Group 10 metal, and, optionally, a Group 11 metal, to form said catalyst composition, whereby said catalyst composition having said Group 10 metal and/or said Group 11 metal deposited thereon.

3. The process of claim 1 , wherein said catalyst composition has a Group 10 metal content in the range from 0.005 wt % to 10 wt %, based on the weight of the catalyst composition.

4. The process of claim 1 , wherein said Group 10 metal is platinum, and said Group 11 metal is copper or silver.

5. The process of claim 2 , wherein said Group 10 metal is platinum and said source of platinum is selected from the group consisting of platinum nitrate, chloroplatinic acid, platinous chloride, platinum amine compounds, platinum acetylacetonate, tetraamine platinum hydroxide, and mixtures of two or more thereof, and/or said optional Group 11 metal is copper and said source of copper is selected from the group consisting of copper nitrate, copper nitrite, copper acetate, copper hydroxide, copper acetylacetonate, copper carbonate, copper lactate, copper sulfate, copper phosphate, copper chloride, and mixtures of two or more thereof, and/or said Group 11 metal is silver, and/or said source of silver is selected from the group consisting of silver nitrate, silver nitrite, silver acetate, silver hydroxide, silver acetylacetonate, silver carbonate, silver lactate, silver sulfate, silver phosphate, and mixtures of two or more thereof.

6. The process of claim 1 , wherein said Group 1 alkali metal and/or said Group 2 alkaline earth metal is present as an oxide.

7. The process of claim 1 , wherein said Group 1 alkali metal is selected from the group consisting of lithium, sodium, potassium, rubidium, cesium, and mixtures of two or more thereof, and/or said Group 2 alkaline earth metal is selected from the group consisting of beryllium, magnesium, calcium, strontium, barium, and mixtures of two or more thereof.

8. The process of claim 1 , wherein said microporous crystalline ferrosilicate has a constraint index of less than 12.

9. The process of claim 1 , wherein said microporous crystalline ferrosilicate has a framework type selected from the group consisting of MWW, MFI, LTL, MOR, BEA, TON, MTW, MTT, FER, MRE, MFS, MEL, DDR, EUO, FAU, and mixtures of two or more thereof.

10. The process of claim 1 , wherein said microporous crystalline ferrosilicate has a Si/Fe molar ratio in the range from 50 to 1200.

11. The process of claim 1 , wherein said catalyst composition has an Alpha Value (as measured prior to the addition of said Group 10 metal, and/or prior to the addition of said optional Group 11 metal) of less than 25.

12. The process of claim 1 , wherein the molar ratio of said Group 1 alkali metal to Al plus Fe is at least 0.1, and/or the molar ratio of said Group 2 alkaline earth metal to Al plus Fe is at least 0.1.

13. The process of claim 1 , wherein said catalyst composition provides a conversion of at least about 40% of an n-pentane feedstock with equimolar H 2 under acyclic C 5 conversion conditions of a temperature in the range of 550° C. to 600° C., an n-pentane partial pressure between 3 psia and 30 psia at the reactor inlet (21 to 207 kPa-a), and an n-pentane weight hourly space velocity between 5 and 20 hr −1 .

14. The process of claim 1 , wherein said catalyst composition provides a carbon selectivity to cyclopentadiene of at least 30% of an n-pentane feedstock with equimolar H 2 under acyclic C 5 conversion conditions of a temperature in the range of 550° C. to 600° C., an n-pentane partial pressure between 3 psia and 30 psia at the reactor inlet (21 to 207 kPa-a), and an n-pentane weight hourly space velocity between 5 and 20 hr −1 .

15. The process of claim 1 , wherein said acyclic C 5 feedstock comprises pentane, pentene, pentadiene, or mixtures of two or more thereof.

16. The process of claim 1 , wherein said cyclic C 5 compounds comprise cyclopentane, cyclopentene, cyclopentadiene, or mixtures of two or more thereof.

17. The process of claim 1 , wherein said acyclic C 5 feedstock comprises at least 75 wt % n-pentane.

18. The process of claim 1 , wherein said cyclic C 5 compounds comprise at least 20 wt % cyclopentadiene.

19. The process of claim 1 , wherein said acyclic C 5 conversion conditions include at least a temperature of 450° C. to 650° C., the molar ratio of said optional hydrogen co-feed to the acyclic C 5 feedstock is in the range of 0.01 to 3, said acyclic C 5 feedstock has a partial pressure in the range of 3 psia to 100 psia (21 to 689 kPa-a), and said acyclic C 5 feedstock has a weight hourly space velocity in the range from 1 hr −1 to 50 hr −1 .

Assignees

• Exxonmobil Chemical Patents Inc

Inventors

• Iaccino Larry L
• Bedard Jeremy W
• Lai Wenyih F
• Evans Christopher M
• Cheng Jane C

Classifications

• B01J29/46 Primary

  Iron group metals or copper · CPC title

• C07C5/373 Primary

  with simultaneous isomerisation · CPC title

• C07C2529/46

  Iron group metals or copper · CPC title

• C07C2601/10

  the ring being unsaturated · CPC title

• C07C2529/62

  Noble metals · CPC title