EP0540541A1

EP0540541A1 - Method of preparing polyether polyamines

Info

Publication number: EP0540541A1
Application number: EP91912421A
Authority: EP
Inventors: Ralf Bohlander; Günter Uphues; Uwe Ploog
Original assignee: Henkel AG and Co KGaA
Current assignee: Henkel AG and Co KGaA
Priority date: 1990-07-26
Filing date: 1991-07-17
Publication date: 1993-05-12
Also published as: WO1992001729A1; US5371119A; JPH0488019A

Abstract

La présente invention se rapporte à un procédé pour la fabrication de polyamines de polyéther, caractérisé en ce que l'on ajoute de l'hydroxyde alcalin aux éthers de bischlorydrine, obtenus par réaction d'un polyol avec un épihalogènehydrine, avant leur réaction avec de l'ammoniaque et/ou des amines, et que l'on procède ensuite à une distillation et à une filtration.The present invention relates to a process for the manufacture of polyether polyamines, characterized in that alkali metal hydroxide is added to the bischlorohydrin ethers, obtained by reaction of a polyol with an epihalogenhydrin, before their reaction with ammonia and/or amines, followed by distillation and filtration.

Description

"Process for the Production of Polyether Polyamines"

The invention relates to a process for the preparation of polyether polyamines.

Polyether polyaines are known compounds which are used, for example, as hair treatment agents or according to DE 16 19082 and DE 2246434 as textile auxiliaries. Polyether polyamines are usually prepared in two stages by reacting a polyol with epichlorohydrin in the presence of a catalyst and then converting the bishlorohydrin ether obtained in the presence of solvents with amine compounds with addition of alkali metal hydroxide to the corresponding polyether polyamine.

The polyether polyamines produced by this process contain decomposition products of the catalyst, which lead to turbidity or crystalline deposits in the polyether polyamine, as well as the toxicologically and ecologically questionable substances dioxane and epichlorohydrin.

The object on which the invention was based was to produce polyether polyamines which contain no catalyst decomposition products and are free from dioxane and epichlorohydrin.

The invention accordingly relates to a process for the preparation of polyether polyamines by reacting a polyol with an epihalohydrin in the presence of a catalyst and subsequent reaction with ammonia and / or aliphatic mono-di- and / or polyamines, which is characterized in that m after the reaction with epihalohydrin and before the reaction m ammonia and / or amines the reaction mixture, based on the amount of catalyst used, is at least equimolar Add a lot of alkali hydroxide in the form of an aqueous solution, then remove the volatile constituents from the reaction mixture by distillation at a temperature below 150 ° C. and a pressure below 1.33 × 10 ^ Pa and then filter at 80 to 100 ° C.

The volatile constituents are preferably removed by distillation at temperatures between 110 and 130 ° C. and a pressure below 0.67 × 10 ⁴ Pa. Distillation is particularly preferably carried out in the presence of water. For this purpose, 0.2 to 10% by weight of water, preferably 0.5 to 5% by weight of water, based in each case on the weight of the reaction mixture, is added to the reaction mixture during the distillation.

It may also be advantageous to add monoamines to the reaction mixture after the addition of alkali hydroxide.

The reaction of a polyol with an epihalohydrin, preferably with epichlorohydrin, is carried out in a known manner at temperatures between 60 and 90 ° C., preferably between 65 and 75 ° C. in the presence of a catalyst, for example boron trifluoride-diacetic acid, BF3 [0 (C2Hs) 2] 2f Aluminum trichloride or tin tetrachloride. Epichlorohydrin is used, based on an OH function, in quantities of preferably 0.9 to 1.3 mol. Particularly suitable polyols are polyethylene glycols with an average molecular weight between 200 and 2000, alone or in combination with polypropylene glycols with average molecular weights between 400 and 1000. After the removal of volatile constituents by distillation and after the removal of decomposition products of the catalyst used, for example a3ßθ3 or Na fSn (0H) 6], by filtration, the bishlorohydrin ether obtained in a manner known per se at temperatures between 40 and 100 ° C., preferably between 6 and 90 ° C with ammonia and / or amine compounds in the presence of alkali catalysts, for example alkali metal hydroxides, reacted to polyethene polyamines. The reaction is ended by adding acids, for example acetic acid, lactic acid and / or hydrochloric acid. Examples of suitable aliphatic mono-, di- and / or polyamines are dodecylamine, 2-ethylhexylamine, coconut amine, tallow amine, stearylamine, ethylene diamine, propylene diamine, hexamethylene diamine, diethylene triamine, dipropylene triamine, dihexaethylene triamine, 1,2-dihydroxyethyl diaminoethane, piperazine, polyethylene diamine with average molecular weights between 200 and 10,000, bis- [3,3-aminopropyl] methylamine N, N-dimethylaminopropylamine, N-stearylpropylenediamine and / or N-Acy amidoamines which can be prepared by aminolysis of natural fats and / or oils or by amidation of fatty acids in each case with di and / or polyamines, for example reaction products of beef valley with tetraethylene pentamine or stearic acid with diethylenetriamine or aminoethylethanolamine.

The polyether polyamines which can be prepared by the process according to the invention are notable for the fact that they have practically no dioxane and epichlorohydrin and no decomposition products of the catalysts used. Example

A. Preparation of Bischlorhvdrinethern

AI. A mixture of 1500 kg (2.5 k ol) of polyethylene glycol with an average molecular weight of 600 and 36 kg (0.19 kmol) of boron trifluoride-diacetic acid as catalyst with 460 was placed in an evacuable and heatable 2m3 enamel container with stirrer and condensation attachment kg (5 kmol) of epichlorohydrin reacted within 2 hours at 75 ° C. After stirring for 30 minutes, the bischlorohydrin ether Al was obtained.

A2. The bischlorohydrin ether A2 was prepared under the conditions specified in AI. Instead of 36 kg of boron trifluoride-diacetic acid, 36 kg (0.14 kmol) of tin tetrachloride were used.

B. Removal of the volatile constituents from the bischlorohydrin ethers prepared according to A. and subsequent filtration.

Bl. In an evacuable and heatable 500 1 reactor with stirrer and condensation attachment, 345 kg of bischlorohydrin ether Al were mixed with 11.9 kg of 50% strength by weight sodium hydroxide solution and then the volatile constituents at a temperature of 120 ° C. and a pressure of 4 x 10 ^ Pa removed by distillation in two hours. During the distillation, 8 kg of water were introduced into the bischlorohydrin ether via a dip tube.

B2. The product obtained according to B1 was filtered through a suction filter which was covered with filter paper (2 μ) at 90 ° C. 7 kg of white filtration residue were separated off.

B3. In an evacuable and heatable 500 1 reactor with stirrer and- condensation attachment 340 kg of bischlorohydrin ether Al were successively mixed with 17.5 kg of 50% by weight sodium hydroxide solution and 18.2 kg (0.07 kmol) of stearylamine. The volatile constituents were then removed by distillation analogously to B1 in three hours. It was then filtered in accordance with B2, 16 kg of filtration residue being separated off.

B4. In an evacuable and heatable 5001 reactor with stirrer and condensation attachment, 345 kg of bischlorohydrin ether A2 were mixed with 7.5 kg of 50% by weight sodium hydroxide solution and then the volatile constituents at a temperature of 120 ° C. and a pressure of 4 × 10 ^ Pa removed by distillation in two hours.

B5. Sodium hydroxide solution was added to bischlorohydrin ether A2 under the conditions specified in B4, and the volatile constituents were then removed by distillation. During the distillation, 8 kg of water were passed into the bischlorohydrin ether via a dip tube. After the distillation had ended, the mixture was filtered under the conditions given in B2.

B6. Under the conditions specified in B3 was 340 kg

Bischlorohydrin ether A2 with 13 kg of 50 wt .-% sodium hydroxide solution and 18.2 kg of stearylamine. The volatile constituents were then removed by distillation at a temperature of 120 ° C. and a pressure of 4 × 10 * 3 Pa.

B7. The bishlorohydrin ether obtained according to B6 was filtered under the conditions described in B2.

C. Implementation with anrines

Cl. 330 kg of the bischlorohydrin ether distilled and filtered according to B2 were at 80 ° C. in a 1 m ** stainless steel reactor 18.2 kg of melted stearylamine, 14.5 kg of diethylene triamine (1.41 kmol) and a mixture of 28 kg of 50% strength by weight sodium hydroxide solution in 470 kg of water were added in succession at a 10-minute interval. After stirring for three hours, the viscosity had increased significantly. The addition was terminated by adding 30 kg of glacial acetic acid. A yellow, 40% by weight polyether polyamine solution was obtained.

C2. Under the conditions described in Cl, 338 kg of the Na B3 distilled and filtered bischlorohydrin ether were mixed with 14.5 kg of diethylenetriamine and a mixture of 22 50% strength by weight sodium hydroxide solution in 475 kg of water. A polyether polyamine was obtained in the form of a clear, yellow,% by weight solution.

C3. Under the conditions described in C2, 338 kg of the Na B6 distilled bischlorohydrin ether were mixed with diethylene triamine and sodium hydroxide solution. As a result of the precipitation of tin, an opaque-clouded, 40% by weight polyether polyamine solution was obtained.

C4. Instead of the distilled bischlorohydrin ether used in C3, the bischlorohydrin ether distilled and filtered according to B7 was used. A clear,% by weight polyether polyamine solution was obtained.

Table 1 shows the dioxane content, the epichlorohydrin content and the catalyst residue content in the bischlorohydrin ethers and polyether polyamines prepared. Table 1

Claims

- 8-patent claims

1. A process for the preparation of polyether polyamines by reacting a polyol with an epihalohydrin in the presence of a catalyst and subsequent reaction with ammonia and / or aliphatic mono-, di- and / or polyamines, characterized in that after the reaction with epihalohydrins and before the reaction with ammonia and / or amines de reaction mixture, based on the amount of catalyst used, adds an at least equi olar amount of alkali metal hydroxide in the form of an aqueous solution, then at a temperature below 150 ° C. and a pressure below 1.33 × 10 ⁴ P the volatile constituents are removed from the reaction mixture by distillation and then filtered at 80 to 100.degree.

2. The method according to claim 1, characterized in that the volatile constituents are removed at a temperature between 110 and 130 ° C and a pressure below 0.67 x 10 ⁴ Pa distillati.

3. The method according to one or both of claims 1 to 2, characterized in that during the distillative removal of volatile components from 0.2 to 10 wt .-%, preferably 0.5 to 5 wt .-% water - each based on the weight of the reaction mixture - added.

4. The method according to one or more of claims 1 to 3, characterized in that monoamines are added before the volatile constituents are removed by distillation.