Urea synthesis method

Patent metadata

Field	Value
Publication number	US-9890114-B2
Application number	US-201514950325-A
Country	US
Kind code	B2
Filing date	Nov 24, 2015
Priority date	May 28, 2013
Publication date	Feb 13, 2018
Grant date	Feb 13, 2018

Abstract

There is provided a urea synthesis method having excellent reliability and productivity with the amount of oxygen used as a corrosion-resistant agent minimized without using special duplex stainless steel. In a urea synthesis apparatus having a synthesis tower, a stripper, and a condenser, general-purpose austenitic-ferritic duplex stainless steel with Cr content: 21 to 26 wt %, Ni content: 4.5 to 7.5 wt %, Mo content: 2.5 to 3.5 wt %, N content: 0.08 to 0.30 wt %, C content: 0.03 wt % or less, Si content: 1.0 wt % or less, Mn content: 2.0 wt % or less, P content: 0.04 wt % or less, and S content: 0.03 wt % is used as a urea synthesis apparatus material in at least some of parts where the urea synthesis apparatus comes into contact with a fluid having corrosiveness, and oxygen feed concentration with respect to carbon dioxide is 100 to 2,000 ppm.

First claim

The invention claimed is:

1. A urea synthesis method using only oxygen previously mixed with raw material carbon dioxide as a corrosion-resistant agent forming a passivation film on a stainless steel surface in which:
ammonia and the raw material carbon dioxide are reacted at a urea synthesis temperature and pressure in a urea synthesis tower in a urea synthesis apparatus to produce a urea synthesis liquid comprising at least urea, unreacted ammonia, unreacted carbon dioxide, and water;
contacting the urea synthesis liquid with at least some of the raw material carbon dioxide under heating at a pressure substantially equal to the urea synthesis pressure in a stripper to separate the unreacted ammonia and the unreacted carbon dioxide as a mixed gas of ammonia, carbon dioxide, and water;
further treating the urea synthesis liquid obtained in the stripper containing unseparated unreacted ammonia and unreacted carbon dioxide to obtain urea;
introducing the mixed gas separated in the stripper into a bottom of a condenser to bring the mixed gas into contact with an absorbing medium under cooling to condense the mixed gas; and
circulating the mixed gas condensate to the urea synthesis tower,
wherein a majority of the raw material carbon dioxide is fed into the stripper, and wherein a remaining portion of the raw material carbon dioxide is fed into the urea synthesis tower, and
wherein a molar ratio of ammonia (including ammonia converted to ammonium carbamate and urea) to carbon dioxide (including carbon dioxide converted to ammonium carbamate and urea) in the condenser is 2.5 to 3.5, and
wherein an oxygen concentration of the raw material carbon dioxide fed into both the stripper and the urea synthesis tower is 200 to 2,000 ppm, and
wherein general-purpose austenitic-ferritic duplex stainless steel comprising Cr content: 21 to 26 wt %, Ni content: 4.5 to 7.5 wt %, Mo content: 2.5 to 3.5 wt %, N content: 0.08 to 0.30 wt %, C content: 0.03 wt % or less, Si content: 1.0 wt % or less, Mn content: 2.0 wt % or less, P content: 0.04 wt % or less, and S content: 0.03 wt % or less is used as the apparatus material in at least one of the synthesis tower, the stripper, the condenser, or a piping, wherein the piping connects at least two of the synthesis tower, the stripper, and the condenser with each other.

2. The urea synthesis method according to claim 1 , wherein austenitic-stainless steel is used as the apparatus material of the synthesis tower, the condenser, the piping, and valves, wherein the piping connects the synthesis tower and the condenser with each other.

3. The urea synthesis method according to claim 2 , wherein the general-purpose austenitic-ferritic duplex stainless steel is either S31803 or S31260, and the austenitic-stainless steel is S31603.

4. A urea synthesis method using only oxygen previously mixed with raw material carbon dioxide as a corrosion-resistant agent forming a passivation film on a stainless steel surface in which:
ammonia and the raw material carbon dioxide are reacted at a urea synthesis temperature and pressure in a urea synthesis tower in a urea synthesis apparatus to produce a urea synthesis liquid comprising at least urea, unreacted ammonia, unreacted carbon dioxide, and water;
contacting the urea synthesis liquid with at least some of the raw material carbon dioxide under heating at a pressure substantially equal to the urea synthesis pressure in a stripper to separate the unreacted ammonia and the unreacted carbon dioxide as a mixed gas of ammonia, carbon dioxide, and water;
further treating the urea synthesis liquid obtained in the stripper containing unseparated unreacted ammonia and unreacted carbon dioxide to obtain urea;
introducing the mixed gas separated in the stripper into a bottom of a condenser to bring the mixed gas into contact with an absorbing medium under cooling to condense the mixed gas; and
circulating the mixed gas condensate to the urea synthesis tower,
wherein a majority of the raw material carbon dioxide is fed into the stripper, and wherein a remaining portion of the raw material carbon dioxide is fed into the urea synthesis tower, and
wherein a molar ratio of ammonia (including ammonia converted to ammonium carbamate and urea) to carbon dioxide (including carbon dioxide converted to ammonium carbamate and urea) in the condenser is 2.5 to 3.5, and
wherein an oxygen concentration of the raw material carbon dioxide fed into both the stripper and the urea synthesis tower is 100 to 500 ppm, and
wherein specific austenitic-ferritic duplex stainless steel comprising Cr content: 26 to 35 wt %, Ni content: 3 to 10 wt %, Mo content: 0.2 to 4.0 wt %, N content: 0.2 to 0.6 wt %, is used as the apparatus material of the stripper, and
wherein general purpose austenitic-ferritic duplex stainless steel comprising Cr content: 21 to 26 wt %, Ni content: 4.5 to 7.5 wt %, Mo content: 2.5 to 3.5 wt %, and N content: 0. 08 to 0.3 wt %, C content: 0.03 wt % or less, Si content: 1.0 wt % or less, Mn content: 2.0 wt % or less, P content: 0.04 wt % or less, and S content: 0.03 wt % or less is used as the apparatus material in at least one of the synthesis tower, the condenser, a piping, or valves, and wherein the piping connects the synthesis tower and the condenser with each other.

5. The urea synthesis method according to claim 4 , wherein the specific austenitic-ferritic duplex stainless steel material is either S32707 or S32808 and the general-purpose austenitic-ferritic duplex stainless steel is either S31803 or S31260.

Assignees

• Toyo Engineering Corp

Inventors

• Takahashi Masashi
• Nagashima Eiki

Classifications

• B01J2219/0236

  Metal based · CPC title

• B01J19/02

  Apparatus characterised by being constructed of material selected for its chemically-resistant properties · CPC title

• C07C273/04 Primary

  from carbon dioxide and ammonia · CPC title

• C22C38/00

  Ferrous alloys, e.g. steel alloys (cast-iron alloys C22C37/00) · CPC title

• C07C275/00

  Derivatives of urea, i.e. compounds containing any of the groups [IMAGE cpc-sch-C07C-0967.gif], the nitrogen atoms not being part of nitro or nitroso groups · CPC title