Process for preparing polysaccharides with alkyl-aryl hydrophobes and latex compositions containing same
AssigneeUnion Carbide Corporation
InventorsEmmett Malone Partain, III, George Lewis Brode, II, Richard Charles Hoy
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Abstract
Polysaccharides, including hydroxyethyl cellulose, having alkyl-aryl hydrophobic substitution, provide latex compositions, such as paints, with improved rheology and stability. Improved processes for producing such polysaccharides are also provided.
Claims14
A process for producing a water-soluble cellulose ether substituted with an alkyl-aryl hydrophobe which comprises reacting a cellulose ether with an alkyl-aryl hydrophobe-containing glycidyl ether compound, said alkyl-aryl hydrophobe having one aryl ring and a total of from about 10 to 24 carbon atoms.
A process for preparing an alkyl-aryl hydrophobically modified hydroxyethyl cellulose with a hydroxyethyl MS of 3 to 5 which comprises the steps of:
- (a) reacting hydroxyethyl cellulose or a hydroxyethyl cellulose precursor with a molecular weight of 15,000 to 1,200,000 under alkaline conditions with from 0.09 to 2.74% by weight of an alkyl-aryl glycidyl ether having one aryl ring and a total of from about 10 to about 24 carbon atoms at a temperature between 20° C. to 125° C. for about 0.5 hour to about 12 hours in the presence of an aqueous diluent;
- (b) cooling the reaction mixture;
- (c) neutralizing the reaction mixture;
- (d) slurrying the reaction mixture in acetone;
- and
- (e) recovering a purified alkyl-aryl hydrophobically modified hydroxyethyl cellulose.
A process for producing an alkyl-aryl hydrophobically modified hydroxyethyl cellulose having improved leveling properties within an aqueous protective coating composition which comprises the steps of:
- (a) adding a t-butyl alcohol solution of an alkyl-aryl glycidyl ether selected from the group of consisting nonylphenyl glycidyl ether and dodecylphenyl glycidyl ether to an alkalized cellulose having a molecular weight of 15,000 to 1,200,000 to prepare a reaction mixture;
- (b) heating the reaction mixture to between 20° C. to 125° C. and allowing the glycidyl ether to react with the slurry of alkalized cellulose for about 1 to 6 hours;
- (c) cooling the reaction mixture;
- (d) neutralizing the reaction mixture;
- (e) slurrying the reaction mixture in aqueous acetone;
- (f) reslurrying the reaction mixture in acetone;
- (g) recovering an alkyl-aryl hydrophobically modified hydroxyethyl cellulose.
Dependencies are inferred from the claim text.