IP Library Patent Application 19016084
Patent Application
App. No. 19/016,084

METHOD FOR REPULPING WET STRENGTH FIBER

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Patent No.
US None
App. No.
19/016,084
Abstract

The present disclosure is directed to a method for repulping lignocellulosic fibers having at least one wet strength resin disposed thereon, the method comprising: a) preparing an aqueous slurry comprising (1) the lignocellulosic fiber, (2) the resin, and (3) an enzymatic agent present in an amount of from about 0.01 to about 1 wt. %, based on the dry weight of the lignocellulosic fiber, wherein the enzymatic agent comprises: i) at least one hemicellulase; and, ii) at least one cellulase; and, b) agitating the slurry.

Claims (30)

1 . A method for repulping lignocellulosic fibers having at least one wet strength resin disposed thereon, the method comprising:

a) preparing an aqueous slurry of (1) the lignocellulosic fibers, (2) the resin, and (3) an enzymatic agent present in an amount of from about 0.01 to about 1 wt. %, based on the dry weight of the lignocellulosic fiber, wherein the enzymatic agent comprises:

i) at least one hemicellulase; and,

ii) at least one cellulase; and,

b) agitating the slurry.

2 . The method according to claim 1 , wherein at least a portion of the lignocellulosic fibers are provided from paper broke.

3 . The method according to claim 1 , wherein the lignocellulosic fibers comprise or consist of wet strength secondary fiber.

4 . The method according to claim 1 , wherein the wet strength resin is covalently bound to the lignocellulosic fibers.

5 . The method according to claim 1 , wherein the wet strength resin is a polyamine-epichlorohydrin resin.

6 . The method according to claim 1 , wherein the step of preparing comprises:

i) adding the lignocellulosic fiber to an aqueous liquid under agitation; and,

ii) dispersing the enzymatic agent into the agitated aqueous liquid to form the aqueous slurry.

7 . The method according to claim 1 , wherein the at least one hemicellulase is chosen from: xylanase; α-L-arabinofuranosidase; acetyl xylan esterase; α-d-glucuronidase; α-d-galactosidase; mannanase; endo-polygalacturonase; endoarabinase; exoarabinase; exo-β-1,3-galactanase; xyloglucan-specific exo-beta-1,4-glucanase ferulic acid esterase; galactomannanase; and, combinations thereof.

8 . The method according to claim 1 , wherein the at least one hemicellulase comprises or consists of at least one xylanase.

9 . The method according to claim 8 , wherein the xylanase is chosen from: endoxylanases; exoxylanases; D3-xylosidases; and, combinations thereof.

10 . The method according to claim 1 , wherein the at least one cellulase is chosen from: cellobiohydrolase (CBH); endoglucanase (EG); beta-glucosidase (BG); and, combinations thereof.

11 . The method according to claim 1 , wherein the ratio by weight of hemicellulase to cellulase in the enzymatic agent is from 10:1 to 1:10.

12 . The method according to claim 1 , wherein the enzymatic agent further comprises at least one de-inking enzyme chosen from lipases, pectinases, ligninolytic enzymes and combinations thereof.

13 . The method according to claim 1 , wherein the enzymatic agent comprises or consists of, based on the weight of the enzymatic agent:

from 30 to 100 wt. % of the sum of the i) at least one hemicellulase and ii) at least one cellulase;

from 0 to 30 wt. % of iii) at least one proteolytic enzyme;

from 0 to 30 wt. % of iv) at least one esterase which does not have hemicellulase or cellulase activity; and,

from 0 to 30 wt. % of v) at least one amylase chosen from α-amylase, β-amylase, γ-amylase and combinations thereof.

14 . The method according to claim 13 , wherein the enzymatic agent comprises the at least one proteolytic enzyme.

15 . The method according to claim 14 , wherein the enzymatic agent comprises at least one protease chosen from: pronase; trypsin; chymotrypsin; bromelain; pepsin; collagenase; papain; and, combinations thereof.

16 . The method according to claim 13 , wherein the enzymatic agent comprises the at least one esterase which does not have hemicellulase or cellulase activity.

17 . The method according to claim 13 , wherein the enzymatic agent comprises the at least one amylase chosen from α-amylase, β-amylase, γ-amylase and combinations thereof.

18 . The method of claim 1 , wherein the step of agitating is performed for a duration of from 5 to 75 minutes.

19 . The method according to claim 1 , wherein the aqueous slurry comprises less than 1000 ppm by weight of oxidizing agents.

20 . The method according to claim 1 , wherein the aqueous slurry comprises less than 1000 ppm by weight of hypochlorite salts.

Assignments (5)
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 073564/0584 →
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 073564/0656 →
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073570/0838 →
SECURITY AGREEMENT (NOTES) Recorded Oct 10, 2025
From: DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073061/0885 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2025
From: WHITLEY, FRANK; THEUT, TIMOTHY N.; RAMSEYER, TYLER G.; PETTY, ANTHONY, II
To: SOLENIS TECHNOLOGIES, L.P
Reel/Frame 069813/0360 →