Abrasive articles having abrasive layer bond system derived from solid, dry-coated binder precursor particles having a fusible, radiation curable component

• US 6,441,058 B2
• Filed: 01/16/2001
• Issued: 08/27/2002
• Est. Priority Date: 05/01/1998
• Status: Active Grant

• Current Assignee: 3M Innovative Properties Company (3M Company)
• Original Assignee: 3M Innovative Properties Company (3M Company)
• Inventors: Larson, Eric G., DeVoe, Robert J., Dahlke, Gregg D., Thurber, Ernest L., Kirk, Alan R., Stubbs, Roy, Meierotto, Mark R.
• Primary Examiner(s): Berman, Susan W.
• Application Number:
  US09/761,371
• Publication Number:
  US 20010011108A1
• Time in Patent Office: 588 Days
• Field of Search: 522/103, 522/182, 522/173, 522/174, 522/175, 522/181, 522/179, 522/107, 522/96
• US Class Current: 522/96
• CPC Class Codes: B24D 11/001 Manufacture of flexible abrasive materials
• CPC Class Codes: B24D 11/005 Making abrasive webs
• CPC Class Codes: B24D 3/28 Resins or natural or synthetic macromolecular compounds B24D3/22 takes precedence
• CPC Class Codes: B24D 3/344 the bonding agent being organic
• CPC Class Codes: Y10T 428/24372 Particulate matter
• CPC Class Codes: Y10T 428/24413 Metal or metal compound

Abstract

The present invention involves the use of powder coating methods to form coated abrasives. In one embodiment, the powder is in the form of a multiplicity of binder precursor particles comprising a radiation curable component. In other embodiments, the powder comprises at least one metal salt of a fatty acid and optionally an organic component that may be a thermoplastic macromolecule, a radiation curable component, and/or a thermally curable macromolecule. In either embodiment, the powder exists as a solid under the desired dry coating conditions, but is easily melted at relatively low temperatures and then solidified also at reasonably low processing temperatures. The principles of the present invention can be applied to form make coats, size coats, and/or supersize coats, as desired.

Claims

1. A powder comprising a radiation curable component that is flowable at a temperature in the range from about 35°

C. to about 180°

C. containing at least one polyfunctional, radiation curable monomer and at least one polyfunctional, radiation curable macromolecule selected from an oligomer, a polymer, and a combination of at least one oligomer and at least one polymer, wherein the weight ratio of the monomer to the macromolecule is in the range from about 1;

10 to about 10;

1.

2. The powder of claim 1, wherein the radiation curable component comprises at least one radiation curable macromolecule including a plurality of radiation curable groups and a plurality of OH groups.

3. The powder of claim 1, wherein the radiation curable component comprises at least one radiation curable compound having a backbone containing an aromatic or heterocyclic moiety.

4. The powder of claim 1, wherein at least one of the monomer and macromolecule is a solid at temperatures below about 35°

C.

5. The powder of claim 1, wherein the monomer and macromolecule are both solids at temperatures below about 35°

C.

6. The powder of claim 1, wherein the monomer is a solid at temperatures below about 35°

C. and the macromolecule is a liquid at least under ambient conditions.

7. The powder of claim 1, wherein the monomer is selected from a reaction product of a dicarboxylic acid and a reactant comprising hydroxy and radiation curable functionality, a reaction product of a hydroxyl functional isocyanurate and a carboxylic acid, a reaction product of a diisocyanate and a reactant comprising hydroxy and radiation curable functionality, a cyanate ester, a vinyl ether, and combinations thereof.

8. The powder of claim 1, wherein the oligomer is selected from the group consisting of a novolak phenolic oligomer functionalized with a plurality of radiation curable groups, a chain-extended bishenol A epoxy oligomer functionalized with a plurality of radiation curable groups, an epoxy functional oligomer, a novolak oligomer having cyanate ester functionality and combinations thereof.

9. The powder of claim 1, wherein the binder precursor comprises a radiation curable, monomer and a radiation curable, oligomer, wherein each of said monomer and oligomer independently has a melting point such that a blend of the monomer and oligomer is a solid at a temperature below about 35 C. and such that said blend is a melt at a temperature above about 35 C., wherein the weight ratio of the monomer to the oligomer is in the range from about 1:

10 to 10;

1.

10. The powder of claim 1, wherein the radiation curable component comprises a monomer of the formula:

wherein W is a divalent aromatic moiety, X is divalent linking group, and R is selected from hydrogen or a lower alkyl group of 1 to 4 carbon atoms.

11. The powder of claim 1, wherein the radiation curable component comprises a monomer of the formula:

wherein W′

is a divalent, aromatic moiety, Z′

is a divalent linking group, and R is hydrogen or a lower alkyl group of 1 to 4 carbon atoms.

12. The powder of claim 1, wherein the radiation curable component comprises a monomer of the formula:

wherein X″

is a divalent linking group.

13. The powder of claim 1, wherein the radiation curable component comprises an oligomer of the formula:

wherein n has an average value in the range from about 3 to about 20.

14. The powder of claim 1, wherein the radiation curable component comprises an oligomer of the formula:

wherein n has an average value in the range from about 3 to about 20.

15. The powder of claim 1, wherein the radiation curable component comprises an oligomer of the formula:

wherein n has a value such that the oligomer has a number average molecular weight in the range from about 800 to about 5000.

16. A powder, comprising a radiation curable component that is a solid at temperatures below about 35°

C. and is fluidly flowable at a temperature in the range from about 35°

C. to about 180°

C. and containing at least one monomer selected from the group consisting of (meth)acrylamide functional polyesters, (meth)acrylate-functional esters of aromatic dicarboxylic acids, (meth)acrylate-functional amides of aromatic dicarboxylic acids, and cyanate esters, and at least one macromolecule selected from the group consisting of cyanate ester oligomers, mixtures of cyanate esters and epoxy resins, and acrylamidomethyl novolaks.