Abrasive product having binder comprising and aminoplast resin

B - Operations – Transporting – 24 – D

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57/13, 57/7

B24D 3/28 (2006.01) B24D 11/02 (2006.01) C08J 5/14 (2006.01) C09K 3/14 (2006.01)

Patent

CA 2001631

43531 CAN 9A ABSTRACT OF THE DISCLOSURE This invention relates to abrasive products having a resinous binder which holds and supports abrasive grains on a backing sheet or in a fibrous sheet. Generally, thermally curable binders provide coated abrasives having excellent properties, e.g., heat resistance. In order to obtain the proper coating viscosities, solvent is commonly added to these binders. When polyester backings are used, curing temperature is limited to about 130°C, resulting in long cure times. The long cure time along with solvent removal necessitate the use of festoon curing areas. Disadvantages of festoon curing areas include the formation of defects at the suspension rods, inconsistent cure due to temperature variations in the ovens, sagging of the binder, wrinkling of flexible webs, and shifting of abrasive grains. Although radiation curable resins solve the problems associated with thermally curable resins, with respect to festoon ovens, radiation curable resins are generally more expensive than thermally curable resins. This invention provides an abrasive product comprising abrasive grains bonded together or bonded to at least one major surface of a backing sheet, by a binder formed from a precursor comprising an aminoplast resin having on average at least 1.1 pendant .alpha.,.beta.-unsaturated carbonyl groups per molecule. The binder is formed by curing the precursor at the .alpha.,.beta.-unsaturated site of the carbonyl group, by radiation energy or by heat, in the presence of an appropriate initiator system. The aminoplast resin can also contain pendant amino or hydroxy functional qroups, which allow polymerization with condensation curable resins, such as phenolic, melamine, urea, urethane, and furfural resins. Polymerization at the unsaturated site of .alpha.,.beta.-unsaturated carbonyl group can be effected either by radiation energy or by heat, and curing at the sites of the amino or hydroxy functional group can be subsequently effected by heat.

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