A kind of aminoethylated piperazine and its preparation method, carbon dioxide absorbent and its application
A technology of amine ethyl and piperazine, which is applied in the field of carbon dioxide capture, can solve the problems of poor thermal stability, unsatisfactory recycling performance, degradation and inactivation of alcohol amine absorbents, and achieve improved recycling rate and enhanced stability High performance, low energy consumption for desorption
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[0045] The present invention provides the preparation method of the amine ethylated piperazine described in the above technical scheme, (i) when the R 2 When it is a C1-C4 alkyl group, the preparation method comprises the following steps:
[0046] Compound 1, compound 2 and water are mixed to carry out substitution reaction to obtain amine ethylated piperazine;
[0047] where R 1 is C1-C4 alkyl;
[0048] (ii) when the R 2 for , the preparation method comprises the following steps:
[0049] Compound 3, compound 4 and water are mixed to carry out substitution reaction to obtain amine ethylated piperazine;
[0050] where R 1 , R 3 and R 4 independently C1-C4 alkyl.
[0051] In the present invention, unless otherwise specified, all raw material components are commercially available commodities well known to those skilled in the art.
[0052] When the R 2 When it is a C1-C4 alkyl group, the preparation method includes the following steps: mixing compound 1, compound...
Embodiment 1
[0088] Synthesis of N-(2-methylaminoethyl)-N'-methyl-piperazine
[0089]
[0090] Step 1: In a 500mL single-neck flask, dissolve 240mmol of triethanolamine in 350mL of dichloromethane, and stir for 10min at room temperature and 600r / min. Under ice-water bath cooling, 1200 mmol thionyl chloride was added dropwise to the solution at a constant speed with a constant pressure dropping funnel, and the dropwise addition was completed within 30 min. Immediately, the single-necked bottle was transferred to a 40° C. oil bath, and the reaction was refluxed for 12 h. Then the solvent dichloromethane and excess thionyl chloride were removed with a rotary evaporator to obtain the intermediate tris(2-chloroethyl)amine hydrochloride.
[0091] Step 2: Transfer all the tris(2-chloroethyl)amine hydrochloride obtained in step 1 into a 500 mL autoclave, add 260 mL of methylamine aqueous solution with a concentration of 40 wt %, seal it in an oil bath at 60 ° C, 800 r / The reaction was carrie...
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