IP Library Granted Patent US 9,840,453
Granted Patent B2
US 9,840,453 · App. 15/322,492 · Granted Dec 12, 2017

Method for producing isobutylene, method for producing methacrylic acid, and method for producing methyl methacrylate

Inventors: Shuji Akihara (Sapporo, JP); Tatsuya Suzuki (Otake, JP); Toshiya Yasukawa (Otake, JP); Akio Takeda (Otake, JP); Kenichi Miyaki (Otake, JP); Ken Ooyachi (Otake, JP)
Assignee: Mitsubishi Chemical Corporation
C07C67/08C07C1/24C07C29/172C07C51/21C07C51/23C07C51/235C07C51/252C07C2521/04
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Quick Facts
Patent No.
US 9,840,453
App. No.
15/322,492
Granted
Dec 12, 2017
Kind
B2
Abstract

Provided is a method for producing isobutylene with a high selectivity by a dehydration reaction of isobutanol. There are provided a method for producing isobutylene by dehydration of isobutanol, in which the dehydration of isobutanol is performed in a state where at least one of an organic acid and an organic acid ester is present in a reaction system, and methods for producing methacrylic acid and methyl methacrylate from the obtained isobutylene.

Claims (32)

1. A method for producing isobutylene, the method comprising dehydrating isobutanol in a reactor to obtain isobutylene, wherein the dehydrating occurs in the presence of at least one of an organic acid and an organic acid ester, and wherein the content of the organic acid, the organic acid ester, or both the organic acid and the organic acid ester, is 0.005 to 10% by mass with respect to a total of the mass of the isobutanol, the mass of the organic acid, and the mass of the organic acid ester.

2. The method according to claim 1 , wherein the content of the organic acid, the organic acid ester, or both the organic acid and the organic acid ester, is 0.02 to 5% by mass with respect to a total of the mass of the isobutanol, the mass of the organic acid, and the mass of the organic acid ester.

3. The method according to claim 1 , wherein the organic acid is a carboxylic acid and the organic acid ester is a carboxylate ester.

4. The method according to claim 3 , wherein the dehydrating occurs in the presence of at least one carboxylic acid selected from the group consisting of acetic acid. propionic acid, butyric acid, Valerie, acid, and methacrylic acid.

5. The method according to claim 3 , wherein the dehydrating occurs in the presence of at least one carboxylate ester selected from the group consisting of an acetate ester, a propionate ester, a butyrate ester, a valerate ester and a methacrylate ester.

6. The method according to claim 1 , wherein the dehydrating is performed in the presence of both the organic acid and the organic acid ester.

7. A method for producing methacrylic acid, the method comprising:

producing isobutylene by the method of claim 1 ; and

subjecting the isobutylene to vapor phase catalytic oxidation with molecular oxygen to obtain methacrylic acid.

8. A method for producing methacrylic acid, the method comprising:

producing isobutylene by the method of claim 1 ;

subjecting the isobutylene to hydration in the presence of an acid catalyst to obtain tert-butyl alcohol; and

subjecting the tent-butyl alcohol to vapor phase catalytic oxidation with molecular oxygen to obtain methacrylic acid.

9. A method for producing methyl methacrylate, the method comprising:

producing methacrylic acid by the method of claim 7 ; and

subjecting the methacrylic acid to an esterification reaction with methanol in the presence of an acid catalyst to obtain methyl methacrylate.

10. A method for producing methyl methacrylate, the method comprising:

producing methacrylic acid by the method of claim 8 ; and

subjecting the methacrylic acid to an esterification reaction with methanol in the presence of an acid catalyst to obtain methyl methacrylate.

11. The method according to claim 1 , wherein said dehydrating is performed in the gas phase.

12. The method according to claim 11 , wherein said reactor is a fixed bed reactor comprising a catalyst.

13. The method according to claim 11 , wherein said reactor is a fluidized bed reactor comprising a catalyst.

14. The method according to claim 12 , wherein the temperature of the catalyst during the dehydrating is 108 to 500° C.

15. The method according to claim 12 , wherein the temperature of the catalyst during the dehydrating is 150 to 400° C.

16. The method according to claim 13 , wherein the temperature of the catalyst during the dehydrating is 108 to 500° C.

17. The method according to claim 13 , wherein the temperature of the catalyst during the dehydrating is 150 to 400° C.

18. The method according to claim 15 , wherein the dehydrating occurs

in the presence of at least one carboxylic acid selected from the group consisting of acetic acid, propionic acid, butyric acid, valeric acid, and methacrylic acid, or

in the presence of at least one carboxy late ester selected from the group consisting of an acetate ester, a propionate ester, a butyrate ester, valerate ester and a methacrylate ester.

19. The method according to claim 17 , wherein the dehydrating occurs

in the presence of at least one carboxylic acid selected from the group consisting of acetic acid, propionic acid, butyric acid, valeric acid, and methacrylic acid, or

in the presence of at least one carboxylate ester selected from the group consisting of an acetate ester, a propionate ester, a butyrate ester, a valerate ester and a methacrylate ester.

Assignments (2)
CHANGE OF NAME Recorded Jun 28, 2017
From: MITSUBISHI RAYON CO., LTD.
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 043028/0747 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2016
From: AKIHARA, SHUJI; SUZUKI, TATSUYA; YASUKAWA, TOSHIYA; TAKEDA, AKIO; MIYAKI, KENICHI; OOYACHI, KEN
To: MITSUBISHI RAYON CO., LTD.
Reel/Frame 040781/0023 →
Priority Claims (1)
JP 2014-136712 · Jul 2, 2014 · national
Continuity (1)
Related Publication 20170129844A1 · May 11, 2017