Dihydroxyalkyl substituted polygalactomannan, and methods for producing and using the same
AssigneeHercules Incorporated
InventorsMichael Albert Hermann Franzke, Xiaochun Zhang, Gijsbert Kroon
Life of this patent
Estimating the term…
Abstract
Disclosed are compositions including dihydroxyalkyl substituted polygalactomannan, and the optional further substitution of such with cationic and/or hydrophobic moieties. Method of making such compositions is also disclosed as well as the use of such compositions in industrial applications, fabric laundering, and personal and household care.
Claims18
A composition comprising a polygalactomannan substituted with at least one dihydroxyalkyl moiety and at least one cationic moiety, wherein the dihydroxyalkyl moiety comprises C2-C12 alkyl group and is selected from the group consisting of dihydroxyethyl, dihydroxypropyl, dihydroxybutyl, dihydroxypentyl, and dihyroxyhexy, wherein the composition comprises unsubstituted mannose, substituted mannose, unsubstituted galactose and substituted galactose, and wherein the molar ratio of the combined unsubstituted mannose and substituted mannose to the combined unsubstituted galactose and substituted galactose is at least about 2.0:1.
A method for making a non-hydrophobically modified dihydroxypropyl- and cationic-substituted-polygalactomannan comprising:
- a) combining an aqueous caustic solution with polygalactomannan comprising mannose and galactose at a molar ratio of mannose to galactose of at least about 2.0:1 to form a first mixture wherein at least a portion of the polygalactomannan is alkalized;
- b) adding a compound selected from the group consisting of 3-chloro-1,2-propanediol, 3-bromo-1,2-dihydroxypropanediol, 3-iodo-1,2-dihydroxypropanediol, 3-tosyl-1,2-dihydroxypropanediol, 3-chloro-2-hydroxypropyl phenyl/alkyl ether, 2,3-epoxy propyl phenyl ether, glycidol, and combinations thereof, to the first mixture to form a second mixture;
- c) heating the second mixture to a temperature of from about 40° C. to about 140° C. for a period of about 1 to about 4 hours to substitute at least one dihydroxypropyl moiety onto the polygalactomannan to form the dihydroxypropyl-substituted-polygalactomannan;
- d) cooling the second mixture to a temperature of from about 10° to about 60° C. and adjusting the pH of the second mixture to about 6.0 to 8.5;
- e) recovering the dihydroxypropyl-substituted-polygalactomannan from the second mixture;
- f) combining the dihydroxypropyl-substituted-polygalactomannan with a second aqueous caustic solution wherein at least a portion of the dihydroxypropyl-substituted-polygalactomannan is alkalized to form a third mixture;
- g) adding a cationic compound to the third mixture to form a fourth mixture;
- h) heating the fourth mixture to a temperature of from about 30° C. to about 100° C. for a period of about 1 to about 4 hours to substitute at least one cationic moiety onto the dihydroxypropyl-substituted-polygalactomannan to form a cation-and-dihydroxypropyl-substituted-polygalactomannan;
- i) cooling the fourth mixture to a temperature of from about 10° C. to about 50° C. and adjusting the pH of the fourth mixture to about 6.0 to 8.5;
- and
- j) recovering the cation-and-dihydroxypropyl-substituted-polygalactomannan from the fourth mixture.
Dependencies are inferred from the claim text.