Patent classifications
C08B11/12
Carboxymethylated microfibrillated cellulose fibers and composition thereof
Provided is a carboxymethylated microfibrillated cellulose fiber having a Canada standard freeness of less than 200 mL and an average fiber diameter of not less than 500 nm. Said fiber provides a composition having excellent water retention ability.
Carboxymethylated microfibrillated cellulose fibers and composition thereof
Provided is a carboxymethylated microfibrillated cellulose fiber having a Canada standard freeness of less than 200 mL and an average fiber diameter of not less than 500 nm. Said fiber provides a composition having excellent water retention ability.
PRIMARY AMINE COMPOUND OR SECONDARY AMINE COMPOUND-ACIDIC POLYSACCHARIDE CONJUGATE AND PRODUCTION METHOD THEREFOR
Provided is a novel conjugate of a primary or secondary amine compound with an acidic polysaccharide, which is a compound represented by Formula (I) or a pharmaceutically acceptable salt thereof, where in Formula (I), D, R.sup.1, R.sup.2, A, and Poly are as defined in the specification.
MANUFACTURING METHOD OF CARBOXYMETHYL CELLULOSE SALT FOR ELECTRODE OF NONAQUEOUS ELECTROLYTE SECONDARY BATTERY, ELECTRODE FOR NONAQUEOUS ELECTROLYTE SECONDARY BATTERY, AND NONAQUEOUS ELECTROLYTE SECONDARY BATTERY
A manufacturing method which includes: (1) an alkali cellulose reaction step wherein a mixed solvent having a mixing ratio (a mass ratio) of an alcohol having a carbon number of 3 or less and water of 75:25 to 95:5 is used, and the concentration of the base to the water is 25 to 40 mass %; (2) an etherification reaction step wherein a reaction is carried out under an excess base of 0.2 to 0.5 moles per unit of an anhydroglucose of the cellulose; (3) a neutralization step wherein acid is added to adjust the pH of the reaction mixture to 6.0 to 8.0; and (4) a heating step wherein the mixed solvent is removed, and a base is added to adjust the pH of the reaction mixture to 8.0 to 9.0, and then a heat treatment is performed at 40 to 70° C. for 30 to 120 minutes.
MANUFACTURING METHOD OF CARBOXYMETHYL CELLULOSE SALT FOR ELECTRODE OF NONAQUEOUS ELECTROLYTE SECONDARY BATTERY, ELECTRODE FOR NONAQUEOUS ELECTROLYTE SECONDARY BATTERY, AND NONAQUEOUS ELECTROLYTE SECONDARY BATTERY
A manufacturing method which includes: (1) an alkali cellulose reaction step wherein a mixed solvent having a mixing ratio (a mass ratio) of an alcohol having a carbon number of 3 or less and water of 75:25 to 95:5 is used, and the concentration of the base to the water is 25 to 40 mass %; (2) an etherification reaction step wherein a reaction is carried out under an excess base of 0.2 to 0.5 moles per unit of an anhydroglucose of the cellulose; (3) a neutralization step wherein acid is added to adjust the pH of the reaction mixture to 6.0 to 8.0; and (4) a heating step wherein the mixed solvent is removed, and a base is added to adjust the pH of the reaction mixture to 8.0 to 9.0, and then a heat treatment is performed at 40 to 70° C. for 30 to 120 minutes.
MONOLITHIC COMPOSITION FOR DUAL-RATE RELEASE WITH HIGH DRUG LOADING
The present document describes a process for the preparation of a low functionalization polysaccharide having carboxyl groups, comprising a) swelling of a polysaccharide granule in boiling water or a water/polyol mixture, to obtain a swollen polysaccharide; b) partial gelatinization of said swollen polysaccharide in an alkaline solvent mixture of water and alcohol and/or polyol, to obtain a partially gelatinized polysaccharide; and c) partial functionalization of said partially gelatinized polysaccharide with a functionalizing agent, to obtain the low functionalization polysaccharide.
MONOLITHIC COMPOSITION FOR DUAL-RATE RELEASE WITH HIGH DRUG LOADING
The present document describes a process for the preparation of a low functionalization polysaccharide having carboxyl groups, comprising a) swelling of a polysaccharide granule in boiling water or a water/polyol mixture, to obtain a swollen polysaccharide; b) partial gelatinization of said swollen polysaccharide in an alkaline solvent mixture of water and alcohol and/or polyol, to obtain a partially gelatinized polysaccharide; and c) partial functionalization of said partially gelatinized polysaccharide with a functionalizing agent, to obtain the low functionalization polysaccharide.
Crosslinked pulps, cellulose ether products made therefrom; and related methods of making pulps and cellulose ether products
Pulps, cellulose ether products, and methods of making pulps are described.
FIBRILLATED CHEMICALLY MODIFIED CELLULOSE FIBER
Provided is a fibrillated chemically modified cellulose fiber, which has a type-I cellulose crystallinity of at least 50%, an anionic charge density of 0.10-2.00 meq/g, and an average fiber diameter of greater than 500 nm. Also, provided is a fibrillated chemically modified cellulose fiber, wherein the value (A/B) obtained by dividing the viscosity A measured at a shear rate of 0.01/sec by the viscosity B measured at a shear rate of 1000/sec in an aqueous dispersion having a solid content of 1 mass % is at least 100. These fibers have high water retention and high thixotropy.
FIBRILLATED CHEMICALLY MODIFIED CELLULOSE FIBER
Provided is a fibrillated chemically modified cellulose fiber, which has a type-I cellulose crystallinity of at least 50%, an anionic charge density of 0.10-2.00 meq/g, and an average fiber diameter of greater than 500 nm. Also, provided is a fibrillated chemically modified cellulose fiber, wherein the value (A/B) obtained by dividing the viscosity A measured at a shear rate of 0.01/sec by the viscosity B measured at a shear rate of 1000/sec in an aqueous dispersion having a solid content of 1 mass % is at least 100. These fibers have high water retention and high thixotropy.