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

• US 6,228,133 B1
• Filed: 05/01/1998
• Issued: 05/08/2001
• 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): MARCHESCHI, MICHAEL A
• Application Number:
  US09/071,263
• Time in Patent Office: 1,103 Days
• Field of Search: 51/295, 51/298, 51/293, 51/307, 51/309, 51/297
• US Class Current: 51/295
• 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 method of forming an abrasive article, comprising the steps of:

(a) incorporating a plurality of abrasive particles into a bond system to form a particulate mixture, wherein at least a portion of the bond system is derived from a solventless solid binder precursor, said binder precursor comprises a radiation curable component that is flowable at a temperature in the range of about 35°

C. to about 180°

C.;

(b) depositing the particulate mixture onto an underlying surface of the abrasive article;

(c) liquefying the binder precursor to form a melt layer on the underlying surface; and

(d) solidifying the melt layer to bond the abrasive particles to the underlying surface.

2. A method of forming an abrasive article comprising the steps of:

(a) depositing a bond system onto an underlying surface of the abrasive article, wherein at least a portion of the bond system is derived from a solventless solid binder precursor, said binder precursor comprising a radiation curable component that is flowable at a temperature in the range of about 35°

C. to about 180°

C.;

(b) liquefying the binder precursor to form a melt layer on the underlying surface;

(c) depositing a plurality of abrasive particles onto the melt layer; and

(d) solidifying the melt layer to bond the abrasive particles to the underlying surface.

3. The method of claim 2 further comprising the steps of:

(i) dry coating a fusible powder onto the abrasive layer, wherein at least a portion of the fusible powder is derived from a solventless binder precursor, said binder precursor comprising a radiation curable component that is flowable at a temperature in the range of about 35°

C. to about 180°

C.;

(ii) liquefying the fusible powder to form a size melt layer; and

(iii) solidifying the size melt layer to form a size coat.

4. The method of claim 3 further comprising the step of applying a supersize coating precursor over the size coat, wherein at least a portion of the supersize precursor is derived from a solventless binder precursor, said binder precursor comprising a radiation curable component that is flowable at a temperature in the range of about 35°

C. to about 180°

C.

21. The method of claim 2, wherein the bond system comprises a polymeric make coat binder, wherein at least a portion of the make coat binder is derived from the binder precursor.

22. The method of claim 2, wherein the liquefying step comprises heating the powder to a temperature in the range from about 40°

C. to about 140°

C.

23. The method of claim 2, wherein the radiation curable component comprises at least one compound having a backbone containing an aromatic or heterocyclic moiety.

24. The method of claim 2, 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.

25. The method of claim 2, wherein the radiation curable component comprises at least one polyfunctional, radiation curable monomer and at least one polyfunctional, radiation curable macromolecule selected from an oligomer, a polymer, or 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.

26. The method of claim 25, wherein at least one of the monomer or macromolecule is a solid at temperatures below about 35°

C.

27. The method of claim 25, wherein the monomer and macromolecule are both solids at temperatures below about 35°

C.

28. The method of claim 25, wherein the monomer is a solid at temperatures below about 35°

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

29. The method of claim 25, 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 or combinations thereof.

30. The method of claim 25, 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 bisphenol A epoxy oligomer functionalized with a plurality of radiation curable groups, an epoxy functional oligomer, a novolak oligomer functionalized with cyanate ester functionality and combinations thereof.

31. The method of claim 2, wherein the radiation curable component comprises a radiation curable, polyfunctional monomer and a radiation curable, polyfunctional 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 monomeric component to the oligomeric component is in the range from about 1;

10 to 10;

1.

32. The method of claim 2, 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.

33. The method of claim 2, 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.

34. The method of claim 2, wherein the radiation curable component comprises a monomer of the formula:

wherein X″

is a divalent linking group.

35. The method of claim 2, 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.

36. The method of claim 2, 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.

37. The method of claim 2, 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.

38. The method of claim 4, wherein the radiation curable component comprises a metal salt of a fatty acid.

5. An abrasive article comprising a plurality of abrasive particles incorporated into a bond system, wherein at least a portion of the bond system comprises a cured binder derived from a solventless, solid binder precursor, said binder precursor comprising a radiation curable component that is flowable at a temperature in the range from about 35°

C. to about 180°

C.

6. The abrasive article of claim 5, wherein the radiation curable component comprises at least one radiation curable binder precursor having a backbone containing an aromatic or heterocyclic moiety.

7. The abrasive article of claim 5, wherein the radiation curable component comprises at least one radiation curable binder precursor including a plurality of radiation curable groups and a plurality of OH groups.

8. The abrasive article of claim 5, wherein the radiation curable component comprises (i) at least one polyfunctional, radiation curable monomer, and (ii) at least one polyfunctional, radiation curable macromolecule selected from an oligomer, a polymer, or 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.

9. The abrasive article of claim 8, wherein at least one of the monomer or macromolecule is a solid at temperatures below about 35°

C.

10. The abrasive article of claim 8, wherein the monomer and macromolecule are both solids at temperatures below about 35°

C.

11. The abrasive article of claim 8, wherein the monomer is a solid at temperatures below about 35°

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

12. The abrasive article of claim 8, 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, or combinations thereof.

13. The abrasive article of claim 8, 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 bisphenol A epoxy oligomer functionalized with a plurality of radiation curable groups, an epoxy functional oligomer, a novolak oligomer functionalized with cyanate ester functionality and combinations thereof.

14. The abrasive article of claim 5, wherein the radiation curable component comprises a radiation curable, polyfunctional monomer and a radiation curable, polyfunctional 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 monomeric component to the oligomeric component is in the range from about 1;

10 to 10;

1.

15. The abrasive article of claim 5, 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.

16. The abrasive article of claim 5, 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.

17. The abrasive article of claim 5, wherein the radiation curable component comprises a monomer of the formula:

wherein X″

is a divalent linking group.

18. The abrasive article of claim 5, 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.

19. The abrasive article of claim 5, 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.

20. The abrasive article of claim 5, 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.

48. The abrasive article of claim 5, wherein the solventless solid binder precursor is a powder.

39. A method of forming a supersize coating on an underlying abrasive layer of an abrasive article, comprising:

(a) dry coating a fusible powder onto the abrasive layer, wherein the fusible powder comprises at least one metal salt of a fatty acid;

(b) liquefying the fusible powder to form a supersize melt layer; and

(c) solidifying the supersize melt layer, whereby the supersize coating is formed.

40. The method of claim 39, wherein the fusible powder further comprises 0 to 30 parts by weight of a radiation curable binder precursor per 100 parts by weight of the metal salt of a fatty acid.

41. The method of claim 39, wherein the fusible powder further comprises 0 to 30 parts by weight of a thermoplastic macromolecule per 100 parts by weight of the metal salt of a fatty acid.

42. The method of claim 39, wherein the fusible powder further comprises 0 to 30 parts by weight of a thermosetting macromolecule per 100 parts by weight of the metal salt of a fatty acid.

43. The method of claim 40, wherein step (b) comprises heating the fusible powder at a melt processing temperature in the range from about 35°

C. to about 140°

C.

44. The method of claim 40, wherein step (c) comprises irradiating the melt layer with radiation.

45. The method of claim 39, wherein the fusible powder comprises calcium stearate and zinc stearate, wherein the weight ratio of the calcium stearate to the zinc stearate is in the range from 1:

1 to 9;

1.

46. A method of forming a peripheral coating on an underlying abrasive layer of an abrasive article, comprising:

(a) dry coating a fusible powder onto the abrasive layer, wherein the fusible powder comprises at least one grinding aid;

(b) liquefying the fusible powder to form a peripheral melt layer; and

(c) solidifying the peripheral melt layer, whereby the peripheral coating is formed.

47. The method of claim 46 wherein the grinding aid is an organic halide, a halide salt, a metal, a metal alloy, or combinations thereof.