IP Library › Granted Patent US 12,606,952
Granted Patent B2
US 12,606,952 · App. 17/051,065 · Granted Apr 21, 2026

Method for producing modified cellulose fiber, and modified cellulose fiber

Inventors: Yutaka Yoshida (Wakayama, JP); Shotaro Shibata (Wakayama, JP); Haruka Nakagawa (Wakayama, JP); Yoshiaki Kumamoto (Wakayama, JP); Norihiro Ito (Wakayama, JP); Yusaku Asai (Wakayama, JP)
Assignee: KAO CORPORATION
D06M13/11C08K7/02C08L1/02D06M13/08
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Quick Facts
Patent No.
US 12,606,952
App. No.
17/051,065
Granted
Apr 21, 2026
Kind
B2
Abstract

The present invention relates to a method for producing modified cellulose fibers having cellulose I crystal structure, comprising: step A: introducing Substituent Group A to cellulose fibers via an ether bond in a solvent comprising water in the presence of a base, and step B: introducing Substituent Group B to cellulose fibers via an ether bond in a solvent comprising water in the presence of a base, wherein the method includes the steps A and B concurrently, or in the order of the step A and then the step B. The cellulose fibers of the present invention obtained by the method for production of the present invention have favorable dispersibility in a hydrophobic medium and a controlled increase in viscosity.

Claims (11)

1 . A method for producing modified cellulose fibers having cellulose I crystal structure, comprising:

step A: introducing at least one of propylene oxide, butylene oxide, allyl glycidyl ether, and iodoethane

to cellulose fibers via an ether bond in a solvent comprising water in the presence of a base wherein the proportion which is occupied by water in the solvent comprising water is 99% by mass or more; and

step B: introducing at least one of 2-ethylhexyl glycidyl ether, dodecyl glycidyl ether, isostearyl glycidyl ether,

1-iodododecane, 1,2-epoxydodecane, stearyl glycidyl ether, and 1-iodooctadecane

to cellulose fibers via an ether bond in a solvent comprising water in the presence of a base,

wherein the cellulose raw materials are subjected to the step A and the step B in the order of the step A and then the step B and wherein step A and step B are performed at a temperature of 40° C. to 90° C. for a period of 10 hours to 36 hours.

2 . The method for production according to claim 1 , wherein the solvent comprising water in the step A is water, or a mixture comprising water and one or more solvents selected from the group consisting of ethanol, isopropanol, t-butanol, ethylene glycol, propylene glycol, 1,2-butanediol, 1,3-butanediol, N-methylpyrrolidone, dimethyl formamide, dimethyl sulfoxide, dimethyl acetamide, 1,3-dimethyl-2-imidazolidinone, acetone, methyl ethyl ketone, methyl isobutyl ketone, tetrahydrofuran, and 1,4-dioxane.

3 . The method for production according to claim 1 , wherein the solvent comprising water in the step B is water, or a mixture comprising water and one or more solvents selected from the group consisting of ethanol, isopropanol, t-butanol, ethylene glycol, propylene glycol, 1,2-butanediol, 1,3-butanediol, N-methylpyrrolidone, dimethyl formamide, dimethyl sulfoxide, dimethyl acetamide, 1,3-dimethyl-2-imidazolidinone, acetone, methyl ethyl ketone, methyl isobutyl ketone, tetrahydrofuran, and 1,4-dioxane.

4 . The method for production according to claim 1 , wherein a washing treatment step is not carried out between the step A and the step B.

5 . The method for production according to claim 1 , wherein the solvent comprising water in the step B comprises water in an amount of 3% by mass or more.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2020
From: YOSHIDA, YUTAKA; SHIBATA, SHOTARO; NAKAGAWA, HARUKA; KUMAMOTO, YOSHIAKI; ITO, NORIHIRO; ASAI, YUSAKU
To: KAO CORPORATION
Reel/Frame 054196/0286 →
Priority Claims (2)
JP 2018-112238 · Jun 12, 2018 · national
JP 2018-112239 · Jun 12, 2018 · national
Continuity (1)
Related Publication 20210230795A1 · Jul 29, 2021
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