Method for the production of ethyleneamines
US-2020131111-A1 · Apr 30, 2020 · US
US11021434B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11021434-B2 |
| Application number | US-201816759348-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 17, 2018 |
| Priority date | Oct 27, 2017 |
| Publication date | Jun 1, 2021 |
| Grant date | Jun 1, 2021 |
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The present invention relates to a process for preparing ethyleneamines and/or alkanolamines, comprising the following steps: 1) reacting MEG with ammonia in the presence of hydrogen and an amination catalyst; 2) removing hydrogen and ammonia from the reaction output from stage 1 , wherein the removal of hydrogen and ammonia in stage 2 comprises the following steps: 2-1) separating the reaction output from stage 1 into a gaseous phase comprising ammonia and hydrogen, and a liquid phase comprising ethyleneamines and/or alkanolamines, 2-2) passing the gaseous phase from stage 2 - 1 ) through one or more condensers to obtain one or more liquid phases in which ammonia has been enriched, and a gaseous phase in which hydrogen has been enriched, 2-3) contacting the gaseous phase from stage 2 - 2 ) with MEG so as to obtain a liquid phase comprising MEG and ammonia and a gaseous phase comprising hydrogen and optionally ammonia.
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The invention claimed is: 1. A process for preparing ethyleneamines and/or alkanolamines, comprising the following steps: 1) reacting monoethylene glycol with ammonia in the presence of hydrogen and an amination catalyst; 2) removing hydrogen and ammonia from the reaction output from stage 1 , wherein the removal of hydrogen and ammonia in stage 2 comprises the following steps: 2-1) separating the reaction output from stage 1 into a gaseous phase comprising ammonia and hydrogen, and a liquid phase comprising ethyleneamines and/or alkanolamines, 2-2) passing the gaseous phase from stage 2 - 1 ) through one or more condensers to obtain one or more liquid phases in which ammonia has been enriched, and a gaseous phase in which hydrogen has been enriched, 2-3) contacting the gaseous phase from stage 2 - 2 ) with monoethylene glycol so as to obtain a liquid phase comprising monoethylene glycol and ammonia and a gaseous phase comprising hydrogen and optionally ammonia. 2. The process according to claim 1 , wherein the monoethylene glycol before being contacted with the gaseous phase from 2 - 2 ) is at a temperature in the range from 20 to 80° C. 3. The process according to claim 1 , wherein the monoethylene glycol which is used in stage 2 - 3 comprises a sulfur content of less than 100 ppm. 4. The process according to claim 1 , wherein the liquid phase from stage 2 - 3 is passed into stage 1 ). 5. The process according to claim 1 , wherein stage 2 - 1 is effected at a pressure in the range from 20 to 80 bar. 6. The process according to claim 1 , wherein stage 2 - 2 ) consists of one condenser. 7. The process according to claim 1 , wherein stage 2 - 2 ) consists of two condensers. 8. The process according to claim 1 , wherein the one or more condensers in stage 2 - 2 ) are designed such that the temperature of the gaseous phase from stage 2 - 2 ) which is introduced into stage 2 - 3 ) is in the range from 25 to 75° C. 9. The process according to claim 1 , wherein the liquid phases from stage 2 - 2 ) are recycled separately or together into stage 1 ). 10. The process according to claim 1 , wherein the gaseous phase from stage 2 - 3 ) is compressed and recycled into stage 1 ). 11. The process according to claim 1 , wherein stage 1 ) is conducted at a pressure in the range from 50 to 500 bar. 12. The process according to claim 1 , wherein stage 1 ) is conducted at a temperature in the range from 50 to 350° C. 13. The process according to claim 1 , wherein stage 1 ) is conducted at a temperature in the range from 50 to 350° C.
by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups · CPC title
with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings · CPC title
with only one hydroxy group and one amino group bound to the carbon skeleton · CPC title
containing at least two amino groups bound to the carbon skeleton · CPC title
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