Abstract: The invention provides a method of obtaining a cellulose material from corn fiber wherein the method comprises the steps of: (a) heating a mixture of corn fiber and a liquid; (b) contacting the mixture of step (a) with a protease enzyme, thereby providing a proteolyzed corn fiber and a liquid; (c) separating the liquid from the proteolyzed corn fiber; (d) contacting the proteolyzed corn fiber at least once with an alkaline extractant, thereby providing an insoluble cellulose material and a first liquid comprising arabinoxylan; (e) separating the insoluble cellulose material from the first liquid comprising arabinoxylan at a temperature of at or above about 60° C.; and (f) rinsing the insoluble cellulose material to remove essentially all alkali, thereby providing a cellulose material having a cellulose content of at least about 50% and consisting essentially of cellulose I. Cellulose esters and ethers are also prepared from the derivatizable cellulose prepared according to the methods herein.
Type:
Grant
Filed:
February 10, 2000
Date of Patent:
July 1, 2003
Assignee:
Eastman Chemical Company
Inventors:
Charles M. Buchanan, Norma L. Buchanan, John S. Debenham, Michael C. Shelton, Matthew D. Wood
Abstract: A gum base comprising at least one crosslinked branched aliphatic biodegradable polyester comprising repeat units formed from at least one polyol having three to four hydroxy groups, or ester thereof, at least one dibasic acid, or ester thereof, and at least one long chain monocarboxylic acid, or ester thereof. The process of producing a crosslinked branched aliphatic biodegradable polyester gum base by reactive extrusion is also included.
Type:
Grant
Filed:
April 26, 2000
Date of Patent:
August 27, 2002
Assignee:
Eastman Chemical Company
Inventors:
Phillip M. Cook, John M. Staples, Charles R. Tomlinson
Abstract: In one aspect, the invention provides methods of obtaining at least one monosaccharide from corn fiber the method comprises the steps of: (a) heating an aqueous mixture of corn fiber and a liquid; (b) contacting the mixture of step (a) with a protease enzyme, thereby providing a proteolyzed corn fiber and a liquid; (c) separating the liquid from the proteolyzed corn fiber; (d) contacting the proteolyzed corn fiber at least once with an alkaline extractant, thereby providing an insoluble cellulose material and a liquid comprising arabinoxylan; (e) separating the insoluble cellulose material from the liquid comprising arabinoxylan; (f) reducing the volume of the liquid comprising arabinoxylan by removing excess alkaline extractant, thereby providing a concentrated liquid comprising from about 10 to about 50% solids, wherein the solids comprise arabinoxylan; and (g) hydrolyzing the arabinoxylan from step (f) in the presence of a catalyst and a solvent, thereby providing a mixture comprising at least one monosacc
Type:
Grant
Filed:
February 10, 2000
Date of Patent:
March 5, 2002
Assignee:
Eastman Chemical Company
Inventors:
Charles M. Buchanan, Norma L. Buchanan, John S. Debenham, Michael C. Shelton, Matthew D. Wood, Michael J. Visneski, Bhaskar K. Arumugam, John K. Sanders, Larry R. Lingerfelt, Jr., Larry Blair
Abstract: The preparation of carbonyl compounds by oxidizing a nitro functional group of an organic compound is described. Oxidation is accomplished under catalyzed oxidative Nef reaction conditions.
Abstract: A die plate is shown suitable for extruding a viscous material into a convenient form for the preparation of small pellets or particles. The die plate includes solid support portions and perforated portions. Each perforated portion of the die plate includes a major portion of holes through the die plate spaced from each other by a first distance and a transition portion separating the major portion from the solid support portions, with the transition portions having holes spaced from each other by a distance that is greater than the first distances.
Type:
Grant
Filed:
February 26, 1999
Date of Patent:
February 27, 2001
Assignee:
Eastman Chemical Company
Inventors:
Amy E. Castle, Mark A. Thrasher, Shane K. Kirk
Abstract: The preparation of aromatic ketones substituted with a thioether group at the ortho position is accomplished by the initial reaction of an aromatic nucleus substituted with a halide and an ortho nitro group with a nitroalkane in the presence of a hydroxide base. The resulting ortho-nitroalkyl nitroarene compound is converted to the corresponding ortho-nitroaryl ketone by an oxidative Nef reaction. The aromatic nitro group of the ortho-nitroaryl ketone is replaced with a thioether group by reaction with a thiolate anion, most preferably under phase-transfer conditions. Aromatic ketones may be used to prepare various pharmaceutical and herbicidal compounds.