Eastman Chemical Company

Eastman-kodak Company

Basf Corporation

Chung M Kuo

Paul Lee Lucas

Larry Gerald Curtis

Phillip Michael Cook

Kevin J Edgar

I Daniel Sand

Richard T Bogan

Anna M Budde

C Rhea Dunn, Jr

Alan R Dunn

The present invention relates to a process for preparing a substituted cellulose acetoacetate alkanoate without using a carboxamide/lithium chloride solvent system. The process involves contacting cellulose in a carboxylic acid diluent with an acetylating compound selected from the group consisting of a carboxylic acid anhydride and an acid chloride, an acetoacetylating compound selected from the group consisting of diketene, an alkyl acetoacetate and 2,2,6-trimethyl-4H-1,3-dioxin-4-one, and a mineral acid catalyst under conditions and in a molar ratio sufficient to cause the cellulose, acetylating compound and acetoacetylating compound to react to produce a substituted cellulose acetoacetate alkanoate.

Process for preparing a cellllose acetoacetate alkanoates

The specification discloses a process for the manufacture of cellulose acetate. The process reacts, at a temperature suitable for acetylation, an acetic acid activated pretreated cellulose raw material containing 100 parts cellulose by dry weight, and 0.5 to 40 parts of a bisulfate catalyst by dry weight of the cellulose. The bisulfate catalyst is selected from lithium bisulfate, sodium bisulfate, and potassium bisulfate. To enhance mixing with the activated and pretreated cellulose, the catalyst may be mixed with 2 to 4 parts of acetic anhydride by dry weight of the cellulose, and 4 to 6 parts of acetic acid by dry weight of the cellulose. In a further embodiment, 0.05 to 10 parts of a strong Bronsted acid by weight of the dry cellulose may be added as a co-catalyst.

Process for the manufacture of cellulose acetate

A stable aqueous dispersion and process for making the dispersion are provided containing hydrolyzed cellulose ester, organic solvent, water and acrylic resin having free acid functionalities that are at least partially neutralized. The dispersion is useful in coatings and can also contain surfactant and cross-linking agent.

Aqueous dispersion useful in coatings containing hydrolyzed cellulose

Novel coating compositions containing modified cellulose esters are disclosed. The modified cellulose esters contain acid functionality, permitting their dispersion in aqueous systems. The modified cellulose esters are particularly useful as rheology control agents in coatings which are applied as waterborne dispersions. The novel coating compositions are used to produce coated substrates with desirable appearance characteristics.

Cellulose esters moidified with anhydrides of dicarboxylic acids and

Modified starch ester-urethanes prepared by reacting a starch ester containing residual hydroxyl groups with an ethylenically unsaturated isocyanate. The grafted starch ester is a urethane-containing product having pendent groups such as alphamethylstyrene and/or methacrylate moieties. The starch ester-urethane is capable of undergoing crosslinking reactions on exposure to ultraviolet radiation in the presence of a photoinitiator, and optionally ethylenically unsaturated monomers or oligomers. The ethylenically unsaturated starch ester-urethanes of this invention are useful for protective coatings for wood, metal, and plastics.

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Kingsport, TN, United States of America

Chung M Kuo