초록 ▼

New thixotropic agents for the use in cross-linking systems, in particular one-component adhesives and sealants, are described. The thixotropic agents have the advantage that on the one hand they cause only a minor or no increase in viscosity, and on the other hand they do not cause any blead out or

New thixotropic agents for the use in cross-linking systems, in particular one-component adhesives and sealants, are described. The thixotropic agents have the advantage that on the one hand they cause only a minor or no increase in viscosity, and on the other hand they do not cause any blead out or migration, respectively. The thixotropic agents of the present invention are based on urea derivatives that usually are present in a concentration of 5 to 50 wt.-%, in particular of 15 to 30 wt.-%, in a preferably reactive carrier material. After the cross-linking of the system, the reactive carrier material is incorporated, preferably into the structure matrix, or interwoven with said structure matrix, respectively, such that it can not diffuse out of the cured material.

대표청구항 ▼

1. A thixotropic agent based on at least one urea compound in a carrier material, wherein said carrier material is a non-diffusing carrier material. 2. The thixotropic agent of claim 1, wherein said non-diffusing carrier material is a reactive carrier material. 3. The thixotropic agent of claim 1, w

1. A thixotropic agent based on at least one urea compound in a carrier material, wherein said carrier material is a non-diffusing carrier material. 2. The thixotropic agent of claim 1, wherein said non-diffusing carrier material is a reactive carrier material. 3. The thixotropic agent of claim 1, wherein said urea compound is the reaction product of an aromatic, monomeric diisocyanates with en aliphatic amine. 4. The thixotropic agent of claim 3, wherein said urea compound is the reaction product of 4,4'-diphenylmethylene diisocyante with butylamine. 5. The thixotropic agent of claim 1, wherein said urea compound is present in said carrier material in an amount of 5 to 50 wt-% based on the total weight of said urea compound end said carrier material. 6. The thixotropic agent of claim 5, wherein said urea compound is present in said carrier material in an amount of 16 to 30 wt.-% based on the total weight of said urea compound and said carrier material. 7. The thixotropic agent of claim 1, wherein said carrier material is a polyol with an OH-value of less than 28 mg KOH/g or a Mw per OH-group of greeter than 2000. 8. The thixotropic agent of claim 7, wherein said carrier material is a polyol with an OH-value of less than 10 mg KOH/g or a Mwper OH-group of greater than 6000. 9. The thixotropic agent of claim 7, wherein said polyol is liquid at a temperature of about 20° C. to about 25° C. 10. The thixotropic agent of claim 1, wherein said carrier material is a prepolymer terminated with isocyanate groups. 11. The thixotropic agent of claim 1, wherein said carrier material is a prepolymer terminated with blocked isocyanate groups. 12. The thixotropic agent of claim 1, wherein said carrier material is a prepolymer terminated with silane groups. 13. The thixotropic agent of claim 12, wherein said carrier material is a polyurethane hybrid prepolymer terminated with silane groups. 14. The thixotropic agent of claim 1, wherein said carrier material is a mixture of carrier materials with the same or different reactivity. 15. The thixotropic agent of claim 14, wherein said carrier material is a combination of a prepolymer comprising acrylate groups with a prepolymer on silane basis. 16. A viscous at least one curable binder comprising system containing a thixotropic agent of claim 1. 17. The system of claim 16 additionally comprising at least one substance selected from the group consisting of fillers, plasticizers, adhesion promoting agents, catalysts, UV-stabilizers, usual additives, and mixtures of two or more of said substances. 18. The system of claim 16 additionally comprising a curing component. 19. A method for the production of a thixotropic agent of claim 1, wherein a diisocyanate monomer in a carrier material, and an amine component in a carrier material are mixed and reacted. 20. The system of claim 18, wherein said curing component is a latent curing agent that can be activated by humidity and/or heat.