Process for producing taurine from alkali taurinates
The present invention discloses a process and catalysts for producing taurine by catalytic ammonolysis of alkali ditaurinate, alkali tritaurinate, and their mixture. Useful catalysts are the ammonium and alkali salts of sulfate, bisulfate, sulfite, bisulfite, carbonate, bicarbonate, nitrate, phosphate, and organic carboxylic acids.
1. A process for producing taurine from alkali ditaurinate, alkali tritaurinate, or their mixture, comprising,
(a) adding one or a combination of two or more catalysts and an excess amount of ammonia to a solution of alkali ditaurinate, alkali tritaurinate, or their mixture;
(b) subjecting the solution of (a) to ammonolysis reaction;
(c) removing excess ammonia and neutralizing with an acid to obtain a crystalline suspension of taurine; and
(d) recovering taurine by solid-liquid separation.
2. The process according to claim 1 , wherein the catalysts are selected from the group consisting of the ammonium and alkali salts of hydroxide, sulfate, bisulfate, carbonate, bicarbonate, sulfite, bisulfate, phosphate, nitrate, and organic carboxylic acids.
3. The process according to claim 1 , wherein the amount of catalyst in molar ratio relative to ditaurine, tritaurine, or their mixture is from 0.01 to 10.
4. The process according to claim 2 , wherein the alkali are selected from the group consisting of lithium, sodium, potassium, and cesium.
5. The process according to claim 2 , wherein the organic carboxylic acids are selected from the group consisting of C 1 -C 12 monocarboxylic acid, dibasic carboxylic acid, aromatic acid, and hydroxy carboxylic acids.
6. The process according to claim 5 , wherein the organic carboxylic acids are selected from the group consisting of formic acid, acetic acid, propionic acid, butyric acid, glycolic acid, malic acid, tartaric acid, oxalic acid, succinic acid, adipic acid, citric acid, and benzoic acid.
7. The process according to claim 1 , wherein the acid is selected from the group consisting of hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, and organic carboxylic acids.
8. The process according to claim 1 , wherein the ammonolysis reaction is carried out at a temperature from 160° C. to 260° C. under the pressure from autogenous to 260 bars.
9. The process of claim 1 further comprising after step (d):
(e) returning the mother liquor to (a) for further ammonolysis.