IP Library Granted Patent US 9,115,000
Granted Patent B2
US 9,115,000 · App. 14/112,477 · Granted Aug 25, 2015

Process for producing carbonyl sulfide

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Quick Facts
Patent No.
US 9,115,000
App. No.
14/112,477
Granted
Aug 25, 2015
Kind
B2
Abstract

An efficient process is provided in which sulfur is reacted with carbon monoxide in a liquid phase to produce carbonyl sulfide. In the presence of a base catalyst, carbon monoxide is continuously introduced into a reactor in which a liquid reaction mixture obtained by dissolving or suspending sulfur in an organic solvent is held, and the sulfur is reacted with the carbon monoxide at a pressure of 0.2-3.0 MPa and a temperature of 40-120° C. to yield carbonyl sulfide. The gaseous-phase part is withdrawn from the reactor, and the withdrawn gaseous-phase part is cooled with a cooler to condense the carbonyl sulfide contained in the gaseous-phase part. The condensed carbonyl sulfide is continuously withdrawn, and the gas that has not been condensed with the cooler is returned to the reactor. Thus, carbonyl sulfide is continuously produced.

Claims (4)

1. A process for producing carbonyl sulfide, the process comprising continuously adding carbon monoxide into a reactor which contains sulfur dissolved or suspended in an organic solvent in the presence of a base catalyst; reacting the sulfur with the carbon monoxide at a pressure of 0.2-3.0 MPa and a temperature of 40-120° C. to form carbonyl sulfide; recovering a gas phase from the reactor; cooling the recovered gas phase using a condenser to condense the carbonyl sulfide in the gas phase; continuously recovering the condensed carbonyl sulfide; and returning the uncondensed gas to the reactor to continuously produce carbonyl sulfide,

wherein the base catalyst is a basic organic compound selected from the group consisting of amidine bases, guanidine bases, and phosphazene bases,

wherein the amidine bases are selected from the group consisting of 1,8-diazabicyclo[5.4.0]undec-7-ene and 1,5-diazabicyclo[4.3.0]non-5-ene, the guanidine bases are selected from the group consisting of 1,5,7-triazabicyclo[4.4.0]dec-5-ene and 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene, and the phosphazene bases are selected from the group consisting of alkylimino-tris(dimethylamino)phosphorane in which the alkyl is a C 1-8 alkyl group and alkylimino-tris(pyrrolidino)phosphorane in which the alkyl is a C 1-8 alkyl group.

2. The process for producing carbonyl sulfide according to claim 1 , the process further comprising continuously adding sulfur into the reactor.

Assignments (3)
CHANGE OF ADDRESS Recorded Feb 14, 2024
From: RESONAC CORPORATION
To: RESONAC CORPORATION
Reel/Frame 066599/0037 →
CHANGE OF NAME Recorded Jun 23, 2023
From: SHOWA DENKO K.K.
To: RESONAC CORPORATION
Reel/Frame 064082/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2013
From: OHNO, HIROMOTO; YOKOO, HIDEJIRO; IRIE, SHIHO
To: SHOWA DENKO K.K.
Reel/Frame 031444/0632 →