Method for the 3D printing of two-component polyurethane compositions

Patent metadata

Field	Value
Publication number	US-12234366-B2
Application number	US-201917291174-A
Country	US
Kind code	B2
Filing date	Dec 18, 2019
Priority date	Dec 21, 2018
Publication date	Feb 25, 2025
Grant date	Feb 25, 2025

Abstract

A method applying a two-component polyurethane composition by means of 3D printing, including steps providing pumpable first component A including at least one polyol having OH functionality in range from 1.5-4 and average molecular weight Mn in range from 250 to 15 000 g/mol, and at least one diol having two hydroxyl groups joined via a C2-C9 carbon chain, and at least one compound T having at least one thiol group; feeding pumpable second component B into continuous mixer's mixing region, where second component B includes at least one polyisocyanate; wherein one of components A and B additionally includes at least one metal catalyst for reaction of hydroxyl groups and isocyanate groups that is able to form thio complexes, and molar ratio of all thiol groups in at least one compound T to all metal atoms in at least one metal catalyst K is between 1:1 and 250:1.

First claim

The invention claimed is:

1. A method of applying a two-component polyurethane composition by means of 3D printing, comprising the steps of
providing a pumpable first component A comprising
at least one polyol A1 having an OH functionality in a range from 1.5 to 4 and an average molecular weight (number average) Mn in a range from 250 to 15 000 g/mol, and
at least one diol A2 having two hydroxyl groups joined via a C2 to C9 carbon chain, and
at least one compound T having at least one thiol group;
feeding the first component A to a continuous mixer comprising
an inlet,
a mixing region having at least one static or dynamic mixing element connected to the inlet,
an outlet into which the mixing region opens,

wherein the first component A is conveyed through the at least one inlet into the mixing region;
feeding a pumpable second component B into the mixing region of the continuous mixer, where the second component B comprises at least one polyisocyanate I;
mixing the first component A with the second component B in the mixing region of the continuous mixer to give a mixed curable polyurethane composition;
conveying the mixed curable polyurethane composition to the outlet; and
applying the mixed curable polyurethane composition in a 3D printing layer-by-layer manner under computer control according to a defined mass or shape;
wherein one of the two components A and B additionally includes at least one metal catalyst K for reaction of hydroxyl groups and isocyanate groups that is able to form thio complexes, and
a molar ratio of all the thiol groups in the at least one compound T to all metal atoms in the at least one metal catalyst K is between 1:1 and 250:1.

2. The method as claimed in claim 1 , wherein the metal catalyst K comprises a bismuth (III) compound.

3. The method as claimed in claim 2 , wherein the bismuth (III) compound additionally contains an 8-hydroxyquinoline ligand or a 1,3-ketoamide ligand.

4. The method as claimed in claim 1 , wherein the diol A2 is selected from the group consisting of butane-1,3-diol, butane-2,3-diol, butane-1,4-diol, 2-methylpropane-1,3-diol, pentane-1,2-diol, pentane-1,5-diol, pentane-2,4-diol, 2-methylbutane-1,4-diol, 2,2-dimethylpropane-1,3-diol, hexane-1,2-diol, hexane-1,6-diol, 3-methylpentane-1,5-diol, octane-1,2-diol, octane-3,6-diol, nonane-1,9-diol, 2-ethylhexane-1,3-diol, 2,2,4-trimethylpentane-1,3-diol, 2-butyl-2-ethylpropane-1,3-diol, 2,7-dimethyloctane-3,6-diol, cyclohexane-1,4-diol, cyclohexane-1,3-dimethanol and cyclohexane-1,4-dimethanol.

5. The method as claimed in claim 1 , wherein the at least one compound T comprises a polythiol compound having 2 to 6 thiol groups, or a mercaptosilane.

6. The method as claimed in claim 5 , wherein the at least one compound T is selected from the group consisting of ethylene glycol di (3-mercaptopropionate), ethylene glycol dimercaptoacetate, dipentaerythritol hexa (3-mercaptopropionate), and 3-mercaptopropyltrimethoxysilane.

7. The method as claimed in claim 1 , wherein the molar ratio of all the thiol groups in the at least one compound T to all metal atoms in the at least one metal catalyst K is between 5:1 and 100:1.

8. The method as claimed in claim 1 , wherein the metal catalyst K is present in the first component A.

9. The method as claimed in claim 1 , wherein the polyol A1 comprises a polyether polyol.

10. The method as claimed in claim 1 , wherein the polyisocyanate I is a form of diphenylmethane 4,4′-, 2,4′- or 2,2′-diisocyanate that is liquid at room temperature and any mixtures of these isomers (MDI) in the form of polymeric MDI or MDI containing proportions of oligomers or derivatives.

11. The method as claimed in claim 1 , wherein the second component B comprises a polyurethane polymer containing isocyanate groups.

12. The method as claimed in claim 1 , wherein the composition comprises less than 0.5% by weight of carboxylic acids, based on a total weight of the composition.

13. The method as claimed in claim 1 , wherein the two components A and B each have a viscosity, measured at 20° C. on a plate-plate viscometer with plate separation 1 mm and plate diameter 25 mm, of less than 75 Pas at a shear rate of 10 s −1 .

14. The method as claimed in claim 1 , wherein the static or dynamic mixer is mounted on a moving printhead.

15. The method as claimed in claim 1 , wherein an individual layer formed in the applying step has a height of 0.5 mm to 1 cm.

16. The method as claimed in claim 1 , wherein the step of applying the mixed curable polyurethane composition in a 3D printing layer-by-layer manner forms a shaped body having a total height of 1 cm to 50 cm.

Assignees

• Sika Tech Ag

Inventors

• Lootens Didier
• Liard Maxime
• Bernardini Nicolas
• Chaignon-Lesetre Fleur
• Corsaro Antonio

Classifications

• C08G18/7671

  containing only one alkylene bisphenyl group · CPC title

• C08G18/6674

  with compounds of group C08G18/3203 · CPC title

• C08G18/4829

  Polyethers containing at least three hydroxy groups (C08G18/4833 - C08G18/5096 take precedence) · CPC title

• C08G18/3876

  containing mercapto groups · CPC title

• C08G18/3206

  aliphatic · CPC title