Blends of polymers as wet strengthening agents for paper
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
D21H-017/57
D21H-017/55
D21H-021/20
D21H-017/56
출원번호
US-0679417
(2015-04-06)
등록번호
US-9506196
(2016-11-29)
발명자
/ 주소
Hagiopol, Cornel
Townsend, David F.
Ringold, Clay E.
Johnston, James W.
McDonald, Robert
Simpson, Metric M.
Potter, Frederick S.
출원인 / 주소
Georgia-Pacific Chemicals LLC
대리인 / 주소
Sabnis, Ram W.
인용정보
피인용 횟수 :
2인용 특허 :
35
초록▼
Resin systems and methods for making and using same are provided. The method for making a paper product can include contacting a plurality of pulp fibers with a resin system. The resin system can include a first polyamidoamine-epihalohydrin resin and a second resin that can include a second polyamid
Resin systems and methods for making and using same are provided. The method for making a paper product can include contacting a plurality of pulp fibers with a resin system. The resin system can include a first polyamidoamine-epihalohydrin resin and a second resin that can include a second polyamidoamine-epihalohydrin resin, a urea-formaldehyde resin, or a mixture thereof to produce a paper product. The first resin and the second resin can be sequentially or simultaneously contacted with the plurality of pulp fibers. The period for sequential addition between the first resin and the second resin is about 1 second to about 1 hour.
대표청구항▼
1. A method for making a paper product, comprising: contacting a plurality of pulp fibers with a resin system comprising a polyamidoamine-epihalohydrin resin and a urea-formaldehyde resin to produce a mixture, wherein the resin system comprises greater than 30 wt % to about 80 wt % of the urea-forma
1. A method for making a paper product, comprising: contacting a plurality of pulp fibers with a resin system comprising a polyamidoamine-epihalohydrin resin and a urea-formaldehyde resin to produce a mixture, wherein the resin system comprises greater than 30 wt % to about 80 wt % of the urea-formaldehyde resin, based on a combined solids weight of the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin, andat least partially curing the resin system in the mixture to produce a paper product. 2. The method of claim 1, wherein the plurality of pulp fibers is contacted with the urea-formaldehyde resin about 1 second to about 1 hour after the plurality of pulp fibers is contacted with the polyamidoamine-epihalohydrin resin. 3. The method of claim 1, wherein the plurality of pulp fibers is contacted with the urea-formaldehyde resin about 1 minute to about 15 minutes after the plurality of pulp fibers is contacted with the polyamidoamine-epihalohydrin resin. 4. The method of claim 1, wherein a synthesis of the polyamidoamine-epihalohydrin resin comprises reacting a polyamine with a functionally-symmetric cross-linker, and wherein the functionally-symmetric cross-linker comprises a di-acrylate compound, a bis(acrylamide) compound, a di-epoxide compound, a polyazetidinium compound, N,N′-methylene-bis-methacrylamide, a poly(alkylene glycol) diglycidyl ether, or any mixture thereof. 5. The method of claim 1, wherein the polyamidoamine-epihalohydrin resin has a charge density of about 2.5 mEq/g of solids to about 3.2 mEq/g of solids, and wherein the resin system comprises about 40 wt % to about 80 wt % of the urea-formaldehyde resin, based on the combined solids weight of the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin. 6. The method of claim 1, wherein the plurality of pulp fibers is contacted with the resin system in an amount of about 5 lbs/ton of the plurality of pulp fibers to about 10 lbs/ton of the plurality of pulp fibers. 7. The method of claim 1, wherein the polyamidoamine-epihalohydrin resin is made by reacting a polyamine with a functionally-symmetric cross-linker to produce a partially cross-linked polyamine, reacting an epihalohydrin with the partially cross-linked polyamine to produce a halohydrin-functionalized polymer, and cyclizing the halohydrin-functionalized polymer to produce the polyamidoamine-epihalohydrin resin, wherein the polyamidoamine-epihalohydrin resin has azetidium moieties, and wherein the functionally-symmetric cross-linker selected from the group consisting of a di-acrylate compound, a bis(acrylamide) compound, N,N′-methylene-bis-methacrylamide, a di-epoxide compound, a polyazetidinium compound, or any mixture thereof. 8. The method of claim 1, wherein the polyamidoamine-epihalohydrin resin is made by reacting a polyamine with a functionally-symmetric cross-linker to produce a partially cross-linked polyamine, reacting an epihalohydrin with the partially cross-linked polyamine to produce a halohydrin-functionalized polymer, and cyclizing the halohydrin-functionalized polymer to produce the polyamidoamine-epihalohydrin resin, wherein the polyamidoamine-epihalohydrin resin has azetidium moieties, and wherein the functionally-symmetric cross-linker selected from the group consisting of N,N′-methylene-bis-acrylamide, N,N′-methylene-bis-methacrylamide, a poly(ethylene glycol) diglycidyl ether, a poly(propylene glycol) diglycidyl ether, a polyethylene glycol diacrylate, or any mixture thereof. 9. The method of claim 1, wherein the resin system further comprises a second polyamidoamine-epihalohydrin resin, and wherein the polyamidoamine-epihalohydrin resin and the second polyamidoamine-epihalohydrin resin have a different molecular weight, a different chemical structure, or a different molecular weight and a different chemical structure with respect to one another. 10. The method of claim 1, wherein the paper product has a repulpability of 98% or more. 11. The method of claim 1, wherein the polyamidoamine-epihalohydrin resin has a charge density of about 2 mEq/g of solids to about 4 mEq/g of solids. 12. The method of claim 1, wherein the polyamidoamine-epihalohydrin resin has a ratio of azetidinium moieties to amide residues of about 0.6 to about 1. 13. The method of claim 1, wherein the polyamidoamine-epihalohydrin resin has a charge density of about 2 mEq/g of solids to about 4 mEq/g of solids and a ratio of azetidinium moieties to amide residues of about 0.6 to about 1. 14. A method for making a paper product, comprising contacting a plurality of pulp fibers with: (1) a first resin system comprising a polyamidoamine-epihalohydrin resin having a pH of about 2 to about 4.5, a charge density of about 2 mEq/g of solids to about 4 mEq/g of solids, and a ratio of azetidinium moieties to amide residues of about 0.6 to about 1, and(2) a second resin system comprising a urea-formaldehyde resin or a polyamidoamine-epihalohydrin resin having a different molecular weight or a different chemical structure than the polyamidoamine-epihalohydrin resin in the first resin system. 15. The method of claim 14, wherein the second resin system comprises greater than 30 wt % to about 80 wt % of the urea-formaldehyde resin, based on a combined solids weight of the polyamidoamine-epihalohydrin resin in the first resin system and the urea-formaldehyde resin in the second resin system. 16. The method of claim 14, wherein the second resin system comprises a urea-formaldehyde resin and a polyamidoamine-epihalohydrin resin having a different molecular weight or a different chemical structure than the polyamidoamine-epihalohydrin resin in the first resin system. 17. The method of claim 14, wherein the polyamidoamine-epihalohydrin resin of the second resin system has a different molecular weight and a different chemical structure than that of the polyamidoamine-epihalohydrin resin in the first resin system. 18. A method for making a paper product, comprising contacting a plurality of pulp fibers with: (1) a first resin system comprising a polyamidoamine-epihalohydrin resin comprising azetidinium ions and at least one polyamine that is partially crosslinked with a bridging moiety, wherein the bridging moiety is derived from a functionally-symmetric cross-linker selected from the group consisting of a di-acrylate compound, a bis(acrylamide) compound, a di-epoxide compound, a polyazetidinium compound, N,N′-methylene-bis-methacrylamide, a poly(alkylene glycol) diglycidyl ether, or any mixture thereof, and(2) a second resin system comprising a urea-formaldehyde resin or a polyamidoamine-epihalohydrin resin having a different molecular weight or a different chemical structure than the polyamidoamine-epihalohydrin resin in the first resin system. 19. The method of claim 18, wherein the second resin system comprises greater than 30 wt % to about 80 wt % of the urea-formaldehyde resin, based on a combined solids weight of the polyamidoamine-epihalohydrin resin in the first resin system and the urea-formaldehyde resin in the second resin system. 20. The method of claim 18, wherein the second resin system comprises a urea-formaldehyde resin and a polyamidoamine-epihalohydrin resin having a different molecular weight or a different chemical structure than the polyamidoamine-epihalohydrin resin in the first resin system. 21. The method of claim 18, wherein the polyamidoamine-epihalohydrin resin of the second resin system has a different molecular weight and a different chemical structure than that of the polyamidoamine-epihalohydrin resin in the first resin system. 22. A method for making a paper product, comprising: contacting a plurality of pulp fibers with a polyamidoamine-epihalohydrin resin to produce a first mixture;contacting the first mixture with a urea-formaldehyde resin to produce a second mixture, wherein the second mixture comprises greater than 30 wt % to about 80 wt % of the urea-formaldehyde resin, based on a combined solids weight of the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin; andat least partially curing the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin to produce a paper product. 23. The method of claim 22, wherein the polyamidoamine-epihalohydrin resin has a charge density of about 2 mEq/g of solids to about 4 mEq/g of solids, and wherein the second mixture comprises about 40 wt % to about 80 wt % of the urea-formaldehyde resin, based on the combined solids weight of the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin. 24. The method of claim 22 wherein the polyamidoamine-epihalohydrin resin has a pH of about 2.5 to about 3.7, a charge density of about 2.4 mEq/g of solids to about 3.2 mEq/g of solids, and a ratio of azetidinium moieties to amide residues of about 0.6 to about 1, and wherein the paper product has a repulpability of 98% or more. 25. A method for making a paper product, comprising contacting a plurality of pulp fibers with a resin system comprising a polyamidoamine-epihalohydrin resin and a urea-formaldehyde resin to produce a paper product, wherein the resin system comprises greater than 30 wt % to about 80 wt % of the urea-formaldehyde resin, based on a combined solids weight of the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin. 26. The method of claim 25, wherein: the polyamidoamine-epihalohydrin resin has a pH of about 2.5 to about 3.7, a charge density of about 2.4 mEq/g of solids to about 3.2 mEq/g of solids, and a ratio of azetidinium moieties to amide residues of about 0.6 to about 1,the resin system comprises about 40 wt % to about 80 wt % of the urea-formaldehyde resin, based on the combined solids weight of the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin,the urea-formaldehyde resin has a molar ratio of formaldehyde to urea of about 1.5 to about 2.5 and a weight average molecular weight of about 14,000 to about 500,000,the plurality of pulp fibers is sequentially contacted with the polyamidoamine-epihalohydrin resin followed by the urea-formaldehyde resin, andthe period for sequential addition between the polyamidoamine-epihalohydrin resin and the urea-formaldehyde resin is about 1 second to about 1 hour. 27. The method of claim 25, wherein the polyamidoamine-epihalohydrin resin is made by reacting a polyamine with a functionally-symmetric cross-linker to produce a partially cross-linked polyamine, reacting an epihalohydrin with the partially cross-linked polyamine to produce a halohydrin-functionalized polymer, and cyclizing the halohydrin-functionalized polymer to produce the polyamidoamine-epihalohydrin resin, wherein the polyamidoamine-epihalohydrin resin has azetidium moieties, and wherein the functionally-symmetric cross-linker selected from the group consisting of a di-acrylate compound, a bis(acrylamide) compound, N,N′-methylene-bis-methacrylamide, a di-epoxide compound, poly(ethylene glycol) diglycidyl ether, a poly(propylene glycol) diglycidyl ether, a polyazetidinium compound, or any mixture thereof. 28. The method of claim 25, wherein the polyamidoamine-epihalohydrin resin comprises azetidinium ions and at least one polyamine that is partially crosslinked with a bridging moiety, and wherein the bridging moiety is derived from a functionally-symmetric cross-linker selected from the group consisting of a di-acrylate compound, a bis(acrylamide) compound, a di-epoxide compound, a polyazetidinium compound, N,N′-methylene-bis-methacrylamide, a poly(ethylene glycol) diglycidyl ether, a poly(propylene glycol) diglycidyl ether, or any mixture thereof. 29. The method of claim 25, wherein the polyamidoamine-epihalohydrin resin has a pH of about 2 to about 4.5, a charge density of about 2 mEq/g of solids to about 4 mEq/g of solids, and a ratio of azetidinium moieties to amide residues of about 0.6 to about 1.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (35)
Thornton, Jeffrey Wilson; Van Brussel-Verraest, Dorine Lisa; Besemer, Arie; Sandberg, Sussan, Aldehyde-containing polymers as wet strength additives.
Hagiopol, Cornel; Luo, Yuping; Townsend, David F.; Johnston, James W.; Ringold, Clay E.; Favors, Karla D., Blends of glyoxalated polyacrylamides and paper strengthening agents.
Hagiopol,Cornel; Luo,Yuping; Townsend,David F.; Johnston,James W.; Ringold,Clay E.; Favors,Karla D., Blends of glyoxalated polyacrylamides and paper strengthening agents.
Hagiopol, Cornel; Townsend, David F.; Ringold, Clay E.; Johnston, James W.; McDonald, Robert; Simpson, Metric M.; Potter, Frederick S., Blends of polymers as wet strengthening agents for paper.
Pudney Ian A. (Corringham GBX) Stubbs Brian M. (Sidcup GB2) Welch Malcolm J. (Barneveld NLX), Cationic compounds useful as drainage aids and stabilizers for rosin-based sizing agents.
Grigoriev, Vladimir A.; Furman, Gary S.; Archer, Sammy Lee; Su, Winston; Kaley, Christopher D.; Wei, Mingli, Creping adhesives comprising blends of polyaminoamide epihalolhydrin resins and polyamides.
Schroeder Wen Zyo ; Clarahan Daniel Arthur ; Goulet Mike Thomas ; Shannon Thomas Gerard, Modified condensation polymers having azetidinium groups and containing polysiloxane moieties.
Hagiopol, Cornel; Townsend, David F.; Ringold, Clay E.; Johnston, James W.; McDonald, Robert; Simpson, Metric M.; Potter, Frederick S., Paper products containing a polymeric wet strengthening agent.
Lu, Chen; Grigoriev, Vladimir; Nguyen, Danny; Rosencrance, Scott, Polyamine polyamidoamine epihaloohydrin compositions and processes for preparing and using the same.
Dulany Margaret A. (Decatur GA) Garvey Chad E. (Ball Ground GA) Ringold Clay E. (Decatur GA) Srinivasan Ramji (Duluth GA), Repulpable wet strength resins for paper and paperboard.
Kokko Bruce Jerome ; Post Elroy Wayne, Wet strength thermosetting resin formulations and polyaminamide polymers suitable for use in the manufacture of paper products.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.