Isocyanate polymerization catalyst, preparation method thereof, and method for preparing polyisocyanate by using same

Patent metadata

Field	Value
Publication number	US-11111332-B2
Application number	US-201616320794-A
Country	US
Kind code	B2
Filing date	Aug 16, 2016
Priority date	Aug 12, 2016
Publication date	Sep 7, 2021
Grant date	Sep 7, 2021

Abstract

An isocyanate polymerization catalyst, a preparation method thereof and a method for preparing polyisocyanates comprising isocyanurate groups by using the same. The catalyst is a carboxylic acid salt containing a di-quaternary ammonium ion. The structure of the catalyst contains hydroxyl-containing aromatic heterocyclic residues. The catalyst is highly active. Only a small quantity of the catalyst is required for the polymerization of isocyanates. The prepared polyisocyanates have color values lower than 25 Hazen, monomer contents of less than 0.5% by weight, high contents of isocyanurates and low viscosities.

First claim

The invention claimed is:

1. A catalyst for the polymerization of isocyanates, wherein the catalyst has a structural formula represented by formula I:

wherein, Y is a residue of a hydroxyl-containing aromatic heterocyclic compound;
wherein, R 1 , R 2 and R 3 are independently selected from alkyls having 1-20 carbon atoms, cycloalkyls having 4-15 carbon atoms, aralkyls having 7-15 carbon atoms, aryls having 6-15 carbon atoms, or R 1 and R 2 together form a ring structure having 4-6 carbon atoms, the ring structure formed by R 1 and R 2 optionally contains a N heteroatom and/or a 0 heteroatom in the ring structure; and R is selected from hydrogen or alkyls having 1-10 carbon atoms.

2. The catalyst according to claim 1 , wherein the catalyst is selected from the compounds of formulas II, III, IV and V:

3. The catalyst according to claim 1 , wherein the catalyst is selected from the compounds of the following structural formulas:

4. A preparation method for the catalyst having the structural formula represented by formula I according to claim 1 , comprising the following steps:
(1) adding a secondary amine, formaldehyde and a hydroxyl-containing aromatic heterocyclic compound, then adding an aqueous HCl solution dropwise, then conducting a reaction at a temperature of 70-100° C.; after the completion of the reaction, allowing the system of the reaction to stand still, and to be stratified and separated to obtain an organic phase; then adding an alkyl halide to the organic phase, mixing and stirring the newly obtained mixture comprising the alkyl halide at a reaction temperature of 40-50° C. to obtain a halide containing a di-quaternary ammonium ion after the completion of the reaction;
(2) reacting a carboxylic acid with the halide containing the di-quaternary ammonium ion obtained in step (1) to obtain a carboxylic acid salt containing the di-quaternary ammonium ion.

5. The preparation method according to claim 4 , wherein in step (1), the secondary amine, formaldehyde and hydroxyl-containing aromatic heterocyclic compound are fed in a molar ratio of (2-2.1): (2-2.1):1; the formaldehyde is used as an aqueous formaldehyde solution having a concentration of 20%-50% by weight.

6. The preparation method according to claim 4 , wherein the molar content of HCl in the aqueous HCl solution used in step (1) is 5%-15% of the molar amount of the hydroxyl-containing aromatic heterocyclic compound, and the concentration of the aqueous HCl solution is 20%-50% by weight, the molar ratio of the alkyl halide to the secondary amine is (1-1.2):1.

7. The preparation method according to claim 4 , wherein the molar amount of the carboxylic acid used in step (2) is 2-2.5 times, of the molar amount of the hydroxyl-containing aromatic heterocyclic compound in step (1).

8. The preparation method according to claim 4 , wherein the temperature of the reaction of step (2) is 100-120° C.

9. The preparation method according to claim 4 , wherein the secondary amine has a structural formula represented by NHR 1 R 2 , wherein R 1 and R 2 are independently selected from alkyls having 1-20 carbon atoms, cycloalkyls having 4-15 carbon atoms, aralkyls having 7-15 carbon atoms, aryls having 6-15 carbon atoms, or R 1 and R 2 together form a ring structure having 4-6 carbon atoms, and the ring structure formed by R 1 and R 2 optionally contains a N heteroatom and/or a 0 heteroatom.

10. The preparation method according to claim 4 , wherein the alkyl halide has a structure represented by R 3 X, wherein R 3 is selected from alkyls having 1-20 carbon atoms, cycloalkyls having 4-15 carbon atoms, aralkyls having 7-15 carbon atoms, and aryls having 6-15 carbon atoms, and wherein X is chlorine, bromine or iodine atom.

11. The preparation method according to claim 4 , wherein the

carboxylic acid has a structural formula represented by wherein R is selected from hydrogen or alkyls having 1-10 carbon atoms.

12. The preparation method according to claim 4 , wherein the hydroxyl-containing aromatic heterocyclic compound is a hydroxyl-substituted aromatic heterocyclic compound containing one or two nitrogen atoms.

13. A method for preparing polyisocyanates comprising isocyanurate groups using the catalyst according to claim 1 , comprising the steps as follows:
under the protection of an inert gas, reacting an isocyanate starting material under the catalysis of the catalyst at a reaction temperature of 10-100° C.

14. The method according to claim 13 , wherein the catalyst is used in an amount of 5-300 ppm based on the mass of the isocyanate starting material.

15. The method according to claim 13 , wherein the isocyanate starting material is treated with an adsorbent before conducting a polymerization reaction.

16. The method according to claim 15 , wherein the isocyanate starting material is treated with the adsorbent at 25-30° C. for 5-24 hours; the adsorbent is used in an amount of 1-5 g adsorbent per 100 g isocyanate starting material; the adsorbent is selected from the group consisting of molecular sieves, activated carbon, silica gel and adsorbent resins, and a mixture of more thereof, and the adsorbent has a particle size of 0.1-2 mm and a moisture content of <0.05% by weight.

17. The preparation method according to claim 4 , wherein the molar content of HCl in the aqueous HCl solution used in step (1) is 5%-15% of the molar amount of the hydroxyl-containing aromatic heterocyclic compound, and the concentration of the aqueous HCl solution is 20%-50% by weight, the molar ratio of the alkyl halide to the secondary amine is (1-1.05):1; and the molar amount of the carboxylic acid used in step (2) is 2 times of the molar amount of the hydroxyl-containing aromatic heterocyclic compound in step (1).

18. The preparation method according to claim 4 , wherein the secondary amine has a structural formula represented by NHR 1 R 2 , wherein R 1 and R 2 are independently selected from methyl, ethyl, propyl, butyl, octyl, dodecyl, benzyl and phenyl; the secondary amine is dimethylamine, diethylamine, methylethylamine, dipropylamine, methylbenzylamine, dibutylamine, methylbutylamine, ethylpropylamine, ethyloctylamine, methyldodecylamine or methylphenylamine;
wherein the alkyl halide is selected from methyl chloride, ethyl chloride, n-butyl chloride, propyl chloride, isobutyl chloride, isopropyl chloride, n-octyl chloride, n-butyl iodide and methyl bromide;
wherein the carboxylic acid is selected from formic acid, acetic acid, propionic acid, n-butyric acid, isobutyric acid, n-hexanoic acid, n-octanoic acid and isooctanoic acid; and
the hydroxyl-containing aromatic heterocyclic compound is selected from the compounds having the following structural formulas:

19. The preparation method according to claim 4 , wherein the hydroxyl-containing aromatic heterocyclic compound is selected from the compounds having the following structural formulas:

20.

Assignees

• Wanhua Chemical Group Co Ltd

Inventors

• Liu Wei
• Shang Yonghua
• Shi Bin
• Wang Yuqi
• Sun Lidong
• Li Yuan
• Hua Weiqi

Classifications

• C07D213/64 Primary

  attached in position 2 or 6 · CPC title

• C08G18/2018

  having one nitrogen atom in the ring · CPC title

• C07D239/36

  as doubly bound oxygen atom or as unsubstituted hydroxy radical · CPC title

• C08G18/2063 Primary

  having two nitrogen atoms in the condensed ring system · CPC title

• C08G18/022

  the polymeric products containing isocyanurate groups · CPC title