IP Library Granted Patent US 8,206,782
Granted Patent B2
US 8,206,782 · App. 10/570,194 · Granted Jun 26, 2012

Method for surface hardening substances by application of particularly transparent polymethacrylate layers

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Quick Facts
Patent No.
US 8,206,782
App. No.
10/570,194
Granted
Jun 26, 2012
Kind
B2
Abstract

The present invention describes a process for the surface finishing of materials via application of specific polymethacrylate layers. The polymethacrylate layers are composed of blends of at least two (co)polymers of polymethacrylates, and specific “reactive monomers” are present here in a polymerized mixture which forms the polymethacrylate layer. At the application temperature established, these form a chemical and, where appropriate, also a physical bond to the substrate, and therefore have adhesion-promoting action.

Claims (56)

1. A process for the surface finishing of a material, comprising:

applying at least one thermoplastic polymethacrylate layer to the material at temperatures which permit chemical bonding of the polymethacrylate layer to the material to obtain a surface finished composite material;

wherein said polymethacrylate layer is transparent;

wherein the at least one thermoplastic polymethacrylate layer is obtained by:

mixing at least one polymer based on polymerized monomer mixture a. and at least one polymer based on polymerized monomer mixture b.,

wherein the polymerized mixture a. is present in the polymethacrylate-based surface finish in an amount of 50 to 99% by weight and a corresponding amount of the polymerized mixture b. is present in the polymethacrylate-based surface finish to give a total amount of the sum of a. and b. of 100% by weight;

wherein monomer mixture a. comprises:

wherein a. comprises:

A) from 20 to 100% by weight of methyl methacrylate,

B) from 0 to 80% by weight of a (meth)acrylate of the formula I, other than methyl methacrylate,

wherein R 1 is a hydrogen or a methyl, and R 2 is a linear or branched alkyl radical or cycloalkyl radical having from 1 to 18 carbon atoms or is phenyl or naphthyl,

C) from 0 to 40% by weight of a further unsaturated monomer other than a.A) and a.B), but copolymerizable with these, wherein (a.A) to (a.C) together give 100% by weight of the copolymerizable constituents of a., and from 0 to 80 parts by weight of further polymers, and also amounts of from 0 to 150 parts by weight of conventional additives, are added to 100 parts by weight of this polymerized mixture;

and monomer mixture b. comprises:

A) from 20 to 99% by weight of a methyl (meth)acrylate of the formula I wherein

R 1 is a hydrogen or a methyl and

R 2 is a linear or branched alkyl radical or cycloalkyl radical having from 1 to 18 carbon atoms, or is phenyl or naphthyl,

B) from 1 to 80% by weight of one or more ethylenically unsaturated “reactive monomers” other than b.A) but copolymerizable with (b.A), wherein (b.A) and (b.B) together give 100% by weight of the copolymerizable constituents of b., and

from 0 to 80 parts by weight of further polymers, and also amounts of from 0 to 150 parts by weight of conventional additives, are added to 100 parts by weight of this polymerized mixture;

wherein component b.B) has a functional group which can interact with the material to be coated;

wherein said functional group is an amino group, a (cyclic) amide group, an imide group, a hydroxy group, an (ep)oxy group, a carboxy group, or an (iso)cyano group;

wherein component b.B) is selected from the group consisting of i) a nitrogen-containing vinyl heterocycle having 5-membered rings alongside 6-membered rings, ii) vinylimidazoles, iii) vinyllactams, iv) vinylcarbazoles, v) vinylpyridines, vi) glycidyl methacrylate, vii) maleic acid, viii) maleic anhydride, ix) methylmaleic anhydride, x) maleimide,xi) methylmaleimide, xii) maleamides, xiii) phenylmaleimide, xiv) cyclohexylmaleimide, xv) fumaric acid derivatives, xvi) methacrylic anhydride, and xvii) acrylic anhydride.

2. The process according to claim 1 , wherein the further polymer used comprises those selected from the group consisting of polyvinylidene difluoride, PVC, polyethylene, polyester, and polyamides.

3. The process according to claim 1 , wherein the surface-finishing method applies a melt by means of coextrusion coating or melt coating.

4. The process according to claim 1 , wherein the surface-finishing method applies a film by colamination, extrusion lamination, adhesive bonding, coil coating, sheathing or high-pressure lamination.

5. The process according to claim 1 , wherein the material is treated with an adhesive prior to application of the surface finish.

6. The process according to claim 1 , wherein no multilayer system or adhesive is used.

7. The process according to claim 1 , wherein chemical crosslinking between the polymethacrylate layer and the material is developed via an elevated temperature during a finishing process.

8. The process according to claim 1 , wherein interpenetration between material and polymethacrylate layer occurs.

9. The process according to claim 1 , wherein component a.B) is butyl methacrylate, 2-ethylhexyl methacrylate, cyclohexyl methacrylate, phenyl methacrylate, or naphthyl methacrylate.

10. The process according to claim 1 , wherein said additive is calcium carbonate, titanium dioxide, calcium oxide, perlite, precipitated chalk, coated chalk, or fumed silica.

11. The process according to claim 1 , wherein component b.B) is capable of free-radical polymerization.

12. The process according to claim 1 , wherein the material is in the form of a film or sheet, or cut-to-size film or sheet.

13. The process according to claim 1 , wherein the material is a polyethylene textile.

14. A process for the surface finishing of a material, comprising:

applying at least one thermoplastic polymethacrylate layer to the material at temperatures which permit chemical bonding of the polymethacrylate layer to the material to obtain a surface finished composite material having simultaneously good adhesion of the finishing layer, transparency and weathering resistance;

wherein no adhesive is used;

wherein chemical crosslinking between the polymethacrylate layer and the material is developed via an elevated temperature during the process of obtaining the surface finished composite material;

wherein said polymethacrylate layer is transparent;

wherein the at least one thermoplastic polymethacrylate layer is obtained by:

mixing at least one polymer based on polymerized monomer mixture a. and at least one polymer based on polymerized monomer mixture b.,

wherein the polymerized mixture a. is present in the polymethacrylate-based surface finish in an amount of 50 to 99% by weight and a corresponding amount of the polymerized mixture b. is present in the polymethacrylate-based surface finish to give a total amount of the sum of a. and b. of 100% by weight;

wherein monomer mixture a. comprises:

A) from 20 to 100% by weight of methyl methacrylate,

B) from 0 to 80% by weight of a (meth)acrylate of the formula I, other than methyl methacrylate,

wherein R 1 is a hydrogen or a methyl, and R 2 is a linear or branched alkyl radical or cycloalkyl radical having from 1 to 18 carbon atoms or is phenyl or naphthyl,

C) from 0 to 40% by weight of a further unsaturated monomer other than a.A) and a.B), but copolymerizable with these, wherein component C) is styrene, a styrene derivative, a vinyl esters, vinyl chloride, vinyl fluoride or an olefin;

wherein (a.A) to (a.C) together give 100% by weight of the copolymerizable constituents of a., and from 0 to 80 parts by weight of further polymers, and also amounts of from 0 to 150 parts by weight of conventional additives, are added to 100 parts by weight of this polymerized mixture; and monomer mixture b. comprises:

A) from 20 to 99% by weight of a (meth)acrylate of the formula I wherein

R 1 is a hydrogen or a methyl and

R 2 is a linear or branched alkyl radical or cycloalkyl radical having from 1 to 18 carbon atoms, or is phenyl or naphthyl,

B) from 1 to 80% by weight of one or more ethylenically unsaturated “reactive monomers” other than b.A) but copolymerizable with (b.A), wherein (b.A) and (b.B) together give 100% by weight of the copolymerizable constituents of b., and

from 0 to 80 parts by weight of further polymers, and also amounts of from 0 to 150 parts by weight of conventional additives, are added to 100 parts by weight of this polymerized mixture;

wherein component b.B) has a functional group which can interact with the material to be coated;

wherein said functional group is an amino group, a (cyclic) amide group, an imide group, a hydroxy group, an (ep)oxy group, a carboxy group, or an (iso)cyano group;

wherein component b.B) is selected from the group consisting of i) a nitrogen-containing vinyl heterocycle having 5-membered rings alongside 6 -membered rings, ii) vinylimidazoles, iii) vinyllactams, iv) vinylcarbazoles, v) vinylpyridines, vi) glycidyl methacrylate, vii) maleic acid, viii) maleic anhydride, ix) methylmaleic anhydride, x) maleimide,xi) methylmaleimide, xii) maleamides, xiii) phenylmaleimide, xiv) cyclohexylmaleimide, xv) fumaric acid derivatives, xvi) methacrylic anhydride, and xvii) acrylic anhydride.

15. The process according to claim 14 , wherein interpenetration between material and polymethacrylate layer occurs.

Assignments (5)
CORPORATE ADDRESS CHANGE Recorded Jul 31, 2020
From: ROEHM GMBH
To: ROEHM GMBH
Reel/Frame 053837/0501 →
CHANGE OF NAME Recorded Sep 30, 2019
From: EVONIK RÖHM GMBH
To: RÖHM GMBH
Reel/Frame 050587/0022 →
CHANGE OF ENTITY Recorded Feb 25, 2010
From: ROHM GMBH & CO. KG
To: ROHM GMBH
Reel/Frame 023998/0760 →
CHANGE OF NAME Recorded Feb 25, 2010
From: ROHM GMBH
To: EVONIK ROHM GMBH
Reel/Frame 023998/0789 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 7, 2008
From: NUMRICH, UWE; WICKER, MICHAEL; NEUHAEUSER, ACHIM; KROHMER, CHRISTOPH; DICKHAUT-BAYER, GUENTHER
To: ROEHM GMBH & CO. KG
Reel/Frame 021356/0049 →