IP Library Granted Patent US 8,858,893
Granted Patent B2
US 8,858,893 · App. 13/591,982 · Granted Oct 14, 2014

Process for the preparation of an alkylene carbonate and an alkylene glycol

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Quick Facts
Patent No.
US 8,858,893
App. No.
13/591,982
Granted
Oct 14, 2014
Kind
B2
Abstract

The invention provides a reaction system for the production of an alkylene carbonate comprising: an epoxidation zone containing an epoxidation catalyst located within an epoxidation reactor; a carboxylation zone containing an bromide-containing carboxylation catalyst located within an alkylene oxide absorber; and one or more purification zones containing a purification absorbent capable of reducing the quantity of bromide-containing impurities in a feed comprising a recycle gas, which purification zones are located upstream from the epoxidation zone; and a process for the production of an alkylene carbonate and an alkylene glycol.

Claims (13)

1. A reaction system for the production of an alkylene carbonate and/or alkylene glycol comprising:

an epoxidation zone containing an epoxidation catalyst located within an epoxidation reactor;

a carboxylation zone containing an bromide-containing carboxylation catalyst located within an alkylene oxide absorber; and

a purification zone containing a purification absorbent capable of reducing the quantity of bromide-containing impurities in a feed comprising a recycle gas, which purification zone is located upstream from the epoxidation zone.

2. The reaction system of claim 1 wherein the epoxidation reactor is a shell-and-tube heat exchanger comprising a plurality of reactor tubes positioned substantially parallel to the central longitudinal axis of the epoxidation reactor; wherein the upper ends of the reactor tubes are connected to a substantially horizontal upper tube plate and the lower ends of the reactor tubes are connected to a substantially horizontal lower tube plate; and wherein the epoxidation catalyst is in the form of a packed bed positioned within the reactor tubes.

3. The reaction system of claim 2 wherein the purification zone is located within the reactor tubes.

4. The reaction system of claim 2 wherein the purification zone is located within the epoxidation reactor upstream from the reactor tubes.

5. The reaction system of claim 1 wherein the purification zone comprises a separate purification vessel located upstream from the epoxidation zone which comprises a separate epoxidation reactor.

6. The reaction system of claim 1 wherein the purification absorbent comprises a metal having an atomic number of 22 through 44 or 82.

7. The reaction system of claim 1 wherein the purification absorbent comprises silver.

8. The reaction system of claim 1 wherein the purification absorbent comprises silver, an alkali or alkaline earth metal component, and a support material having a surface area of more than 20 m 2 /g.

9. The reaction system of claim 1 wherein the purification absorbent is a spent epoxidation catalyst which has produced more olefin oxide than the epoxidation catalyst.

10. The reaction system of claim 1 wherein the purification absorbent comprises a basic zeolite.

Assignments (2)
CHANGE OF NAME Recorded Mar 7, 2022
From: SHELL OIL COMPANY
To: SHELL USA, INC.
Reel/Frame 059694/0819 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2012
From: EVANS, WAYNE ERROL; HESS, MARTIN LYSLE; MATUSZ, MAREK; VAN KRUCHTEN, EUGENE MARIE GODFRIED ANDRE
To: SHELL OIL COMPANY
Reel/Frame 028830/0784 →