Catalyzed bulk process for producing cyclic ester-modified acrylic polymers

• US 4,988,763 A
• Filed: 04/26/1988
• Issued: 01/29/1991
• Est. Priority Date: 04/26/1988
• Status: Expired due to Fees

• Current Assignee: SC Johnson & Son Incorporated
• Original Assignee: SC Johnson & Son Incorporated
• Inventors: Stackman, Robert W., Kessler, Lisa M., Scholsky, Kevin M.
• Primary Examiner(s): Lipman, Bernard
• Application Number:
  US07/186,515
• Time in Patent Office: 1,008 Days
• Field of Search: 525/328.8, 525/386, 525/61
• US Class Current: 525/61
• CPC Class Codes: C08F 20/00 Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
• CPC Class Codes: C08F 8/14 Esterification
• CPC Class Codes: C08F 8/30 Introducing nitrogen atoms or nitrogen-containing groups
• CPC Class Codes: C08G 18/6233 the monomers or polymers being esterified with carboxylic acids or lactones

Abstract

A bulk process for the formation of hydroxyl-containing polymeric compositions comprising the reaction in the presence of a Lewis acid catalyst of a hydroxyl group containing ethylenic polymer with a cyclic ester in the absence of a solvent is described. The compositions have enhanced film-forming characteristics including flexibility, resistance to corrosion, and the like.

Claims

1. Bulk process for reacting at a temperature of from 100°

-300°

C. for a period of from less than one minute to six hours in the presence of a Lewis acid catalyst selected from the group consisting of BF₃.etherate, tetrabutyl-titanate, zinc chloride, stannous chloride, aluminum isoproperoxide, zinc acetate and mixtures thereof, a polymer component which is a member of the group consisting of a polyacrylate containing hydroxyl alkyl moieties, a poly(vinyl alcohol) containing reactive hydroxyl groups and mixtures thereof, with a cyclic ester component having the formula ##STR3## wherein n is at least one, at least n+1R are hydrogen, and the remainder of the R'"'"'s are hydrogen, alkyl, cycloalkyl, alkoxy or single ring aromatic hydrocarbon radicals;

said cyclic ester component being present in an amount of from 0.1 to 10 moles per mole of hydroxyl group on said polymer component and being selected to be substantially miscible with the polymer component at the conditions of the reaction, said process being carried out without use of a solvent.

2. The process according to claim 1 wherein the lactone is epsilon-caprolactone.

3. The process according to claim 1 wherein the cyclic ester is delta-valerolactone.

4. The process according to claim 1 wherein the cyclic ester is beta-butyrolactone.

5. The process according to claim 1 wherein the cyclic ester is pivalolactone.

6. The process according to claim 1 wherein the temperature of reaction is from about 210°

-250°

C.

7. The process according to claim 1 wherein the cyclic ester is present at from 0.5-5 moles per mole of hydroxyl group on the polymer component.