Process For The Treatment Of Liquefied Hydrocarbons Using 3-(Piperazine-1-YL)Propane-1,2-Diol Compounds
US-2015126793-A1 · May 7, 2015 · US
US9732298B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9732298-B2 |
| Application number | US-201314399783-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 11, 2013 |
| Priority date | Jun 15, 2012 |
| Publication date | Aug 15, 2017 |
| Grant date | Aug 15, 2017 |
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A method for treating liquefied hydrocarbons including acid gases to remove said acid gases while minimizing loss of amine species, said method comprising the steps of contacting the liquefied hydrocarbons with an absorbent aqueous solution of a first amine compound, the first amine compound having the structure: wherein R 1 is propane-2,3-diol; R 2 is hydrogen, methyl ethyl, 2-hydroxyethyl, or propane-2,3-diol; and R 3 is hydrogen, methyl, ethyl, 2-hydroxyethyl or propane-2,3-diol.
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The claimed invention is: 1. A method for treating liquefied hydrocarbons comprising acid gases to remove said acid gases while minimizing loss of amine species, said method comprising the step of contacting said liquefied hydrocarbons with an absorbent aqueous solution of a first amine compound, said first amine compound having the structure: wherein R 1 is propane-2,3-diol; R 2 is hydrogen, methyl, ethyl, 2-hydroxyethyl, or propane-2,3-diol; and R 3 is hydrogen, methyl, ethyl, 2-hydroxyethyl or propane-2,3-diol. 2. The method of claim 1 , wherein said absorbent aqueous solution comprises from about 0.1 wt. % to 90 wt. % of said first amine compound and additionally comprising from about 1 wt. % to 90 wt. % of a second amine compound. 3. The method of claim 1 , wherein said absorbent aqueous solution comprises from about 0.1 wt. % to 50 wt. % of said first amine compound and additionally comprising from about 5 wt. % to 50 wt. % of a second amine compound. 4. The method of claim 1 , wherein R 1 is propane-2,3-diol; R 2 is 2-hydroxyethyl and R 3 is methyl. 5. The method of claim 1 , wherein R 1 and R 2 are propane-2,3-diol and R 3 is methyl. 6. The method of claim 1 , wherein said acid gases comprise one or more gas selected from the group consisting of CO 2 , H 2 S, a mercaptan compound, COS, CS 2 , and mixtures thereof. 7. The method of claim 1 , wherein said aqueous solution comprises a second amine compound comprising a piperazine compound selected from the group consisting of piperazine, 2-methylpiperazine, 1-hydroxyethylpiperazine, 3-(piperazin-1-yl)propane-1,2-diol, 3,3′-(piperazin-1,4-diyl)bis(propane-1,2-diol) and mixtures thereof. 8. The method of claim 1 , wherein said absorbent aqueous solution comprises a second amine compound selected from the group consisting of triethanolamine, diethanolamine, methyldiethanloamine, diisopropanolamine, 2-amino-2-(hydroxymethyl)propane-1,3-diol, 2-methylamino-2(hydroxymethyl) propane-1,3-diol, 2-dimethylalmino-2-(hydroxymethyl)propane-1,3-diol and mixtures thereof. 9. The method of claim 1 , wherein said absorbent aqueous solution additionally comprises an acid, said acid selected from the group consisting of boric acid, hydrochloric acid, sulfuric acid, phosphoric acid and mixtures thereof.
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