Process for preparing polymethylols

Patent metadata

Field	Value
Publication number	US-8933277-B2
Application number	US-201013144124-A
Country	US
Kind code	B2
Filing date	Jan 7, 2010
Priority date	Jan 12, 2009
Publication date	Jan 13, 2015
Grant date	Jan 13, 2015

Abstract

A process is provided for recovering components from a low boiler mixture which is obtained in the distillation of hydrogenation effluents from the preparation of polymethylols, by multistage distillation of the low boiler mixture having a tertiary amine, water, methanol, a polymethylol, a methylolalkanal, an alcohol and an alkanal with a methylene group in the alpha position to the carbonyl group. A first distillation stage involves separating the low boiler mixture into a higher-boiling, predominantly water-rich fraction and into a lower-boiling aqueous organic fraction having the tertiary amine. A second distillation stage involves separating the aqueous organic fraction from the first distillation stage into a predominantly amine-containing fraction and a further amine-depleted fraction. The tertiary amine is trimethylamine or triethylamine and the bottom temperature in the second distillation stage is at least 110° C.

First claim

The invention claimed is:

1. A process for recovering components from a low boiler mixture which is obtained in distillation of hydrogenation effluents from preparation of polymethylols, wherein the low boiler mixture is prepared by
a) condensing an alkanal in an aldol reaction with formaldehyde in the presence of a tertiary amine as a catalyst to give a reaction mixture comprising a methylolalkanal of the formula (II)

b) distillatively separating the reaction mixture into a bottom discharge comprising predominately the methylolalkanal of the formula (II),
c) hydrogenating the bottom discharge, and
d) distilling the hydrogenated bottom discharge and removing the low boiler mixture

and wherein the process for recovering components from the low boiler mixture comprises
e) distilling the low boiler mixture comprising a tertiary amine, water, methanol, polymethylol of the formula (I)

the methylolalkanal of the formula (II)

an alcohol of the formula (III)

and an alkanal with a methylene group in the a position to the carbonyl group,
and in which each R is independently a further methylol group or an alkyl group having 1 to 22 carbon atoms or an aryl or aralkyl group having 6 to 22 carbon atoms,
in a multistage distillation by separating the low boiler mixture in a first distillation stage into a higher-boiling, predominantly water-rich fraction and into a lower-boiling aqueous organic fraction comprising the tertiary amine, and
f) separating the aqueous organic fraction from the first distillation stage in a second distillation stage into a predominantly amine-containing fraction and a further amine-depleted fraction,

wherein the tertiary amine is trimethylamine or triethylamine, and the bottom temperature in the second distillation stage is at least 110° C.

2. The process according to claim 1 , wherein a base is added to the low boiler mixture before introduction into the first distillation stage.

3. The process according to claim 1 , wherein the polymethylol of the formula (I) is neopentyl glycol, trimethylolpropane, pentaerythritol, trimethylolethane or trimethylolbutane.

4. The process according to claim 1 , wherein the tertiary amine is trimethylamine.

5. The process according to claim 1 , wherein the low boiler mixture comprises
1 to 20% by weight of methanol,
0.01 to 1% unconverted aldehyde,
0.5 to 5% by weight of alcohol (III),
0.5 to 5% by weight of tertiary amine,
0.01 to 1% by weight of methylolalkanal (II),
0 to 5% by weight of organic secondary compounds, and the remainder water.

6. The process according to claim 1 , wherein the bottom temperature in the second distillation stage is from 110 to 145° C.

7. The process according to claim 1 , wherein the residence time in the second distillation stage is from 5 to 45 minutes.

8. The process according to claim 1 , wherein the pressure in the second distillation stage is from 3 to 10 bar.

9. The process according to claim 1 , wherein the predominantly amine-containing fraction is worked up and used as a catalyst for condensing the alkanal with formaldehyde.

10. The process according to claim 1 , wherein the amine used is triethylamine and the predominantly amine-containing fraction from the second distillation stage is separated in a third distillation stage into a fraction which comprises predominantly tertiary amine and into a fraction which comprises predominantly water and/or methanol.

11. The process according to claim 1 , wherein the amine used is trimethylamine and the aqueous organic fraction from the second distillation stage is separated into a methanolic phase and an aqueous organic fraction.

12. The process according to claim 10 , wherein the second and the third distillation stages are performed together in one dividing wall column.

13. The process according to claim 10 , wherein the triethylamine from the third distillation stage is used as a catalyst for condensing the alkanal with formaldehyde.

14. The process according to claim 11 , wherein the trimethylamine from the second distillation stage is used as a catalyst for condensing the alkanal with formaldehyde.

15. The process according to claim 1 , wherein the low boiler mixture is obtained by a multistage hydrogenation process involving, in stage a), condensing alkanals with formaldehyde in the presence of tertiary amines as a catalyst to give methylolalkanals of the founula (II), and then, in stage b), distillatively separating the reaction mixture obtained from stage a) into bottoms comprising predominantly compounds of the formula (II), and a topstream comprising low boilers, and, in stage c), hydrogenating the bottom effluent from stage b) and then, in a stage d), distilling the effluent from stage c), the low boiler mixture being removed from stage d).

Assignees

• Schlitter Stephan
• Steiniger Michael
• Rittinger Stefan
• Sirch Tilman
• Maas Steffen
• Basf Se

Inventors

• Schlitter Stephan
• Steiniger Michael
• Rittinger Stefan
• Sirch Tilman
• Maas Steffen

Classifications

• C07C31/22

  Trihydroxylic alcohols, e.g. glycerol · CPC title

• C07C29/80 Primary

  by distillation · CPC title

• C07C45/75

  Reactions with formaldehyde · CPC title

• C07C29/141 Primary

  with hydrogen or hydrogen-containing gases · CPC title

• C07C47/19

  containing hydroxy groups (sugars C07H) · CPC title