US3447956A - Process for strengthening swellable fibrous material with an amine oxide and the resulting material - Google Patents

Process for strengthening swellable fibrous material with an amine oxide and the resulting material Download PDF

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US3447956A
US3447956A US576853A US3447956DA US3447956A US 3447956 A US3447956 A US 3447956A US 576853 A US576853 A US 576853A US 3447956D A US3447956D A US 3447956DA US 3447956 A US3447956 A US 3447956A
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oxide
paper
amine oxide
fibrous material
fibers
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Dee Lynn Johnson
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Eastman Kodak Co
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    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
    • D21H11/16—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only modified by a particular after-treatment
    • D21H11/18—Highly hydrated, swollen or fibrillatable fibres
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/388—Amine oxides
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03—Non-macromolecular organic compounds
    • D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/07—Nitrogen-containing compounds
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H25/00—After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
    • D21H25/02—Chemical or biochemical treatment
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H5/00—Special paper or cardboard not otherwise provided for
    • D21H5/12—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials
    • D21H5/1272—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of fibres which can be physically or chemically modified during or after web formation
    • D21H5/1281—Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of fibres which can be physically or chemically modified during or after web formation by chemical treatment

Definitions

  • 117-154 20 Claims ABSTRACT OF THE DISCLOSURE Process for strengthening fibrous materials comprising imbibing an amine oxide into said fibrous material and exposing the imbibed fibrous material to a temperature at which said amine oxide will swell the fibers of said fibrous materials.
  • said amine oxide is a cyclic mono(N-methylamine-N-oxide) compound such as, for example, N-methylmorpholine- N-oxide, N methylpyrrolidine-N-oxide, N-methylazacycloheptane-N-oxide, nicotine-l-oxide, etc.
  • One aspect of this invention relates to articles of manufacture made by the above process.
  • This invention relates to a process for improving the Wet and dry strength of fibrous materials by treating them with certain amine oxides.
  • Fibrous materials such as papers, felts, and fabrics made from fibers are widely used, especially in such areas as packaging, clothing, and supports for photographic emulsions where strength is required, both when the materials are dry and when they are wet. It is beneficial to strengthen these materials by a quick, simple, and inexpensive process which does not unduly modify the normal desirable characteristics of these materials. This process should result in no degradation of the material, impart no color to it, and leave no potentially dangerous or unpleasant residue in the material. The strength imparted to the materials should be permanent or long-lasting and should not be affected by washing the material with water. These objectives are fulfilled when the fibrous materials are strengthened with certain amine oxides.
  • Another object is to provide strengthened fibrous materials.
  • a fibrous material may be strengthened by imbibing an amine oxide into the fibrous material and exposing the imbibed fibrous material to a temperature at which the amine oxide will swell the fibers.
  • the class of amine oxides useful in accordance with the invention for strengthening fibrous materials has the general formula:
  • each of R R and R represents a member selected from the group consisting of monovalent alkyl, cycloalkyl, aralkyl and heterocyclic radicals, and heterocyclic rings comprising two of said members and the N-atom of the formula.
  • a subclass of amine oxides, within the above formula, especially preferred for the invention are cyclic m0no(N- methylamine-N-oxide) compound having the formula wherein Z represents the atoms to complete a saturated heterocyclic ring.
  • Some preferred cyclic mono- (N-methylamine-N-oxide) compounds within this last formula include N-methylmorpholine-N-oxide, N-methylpiperidine- N-oxide, N methylpyrrolidone-N-oxide, N-methylazacycloheptane-N-oxide, nicotine-l-oxide, and the like.
  • a typical example of a useful amine oxide within the first formula above is triethyl amine-N-oxide.
  • the amine oxide may be imbibed into a fibrous material directly in liquid form, or it may be imbibed in solution, that is dissolved in a liquid solvent.
  • solvents one may use a volatile solvent which is easily removed by evaporation, or one may use a liquid solvent which will not evaporate. In the latter case, the solvent must be one that does not interfere with the strengthening action of the amine oxide.
  • the amine oxide While the amine oxide is imbibed in the fibrous material to be treated, it is necessary to attain a temperature adequately high to let the amine oxide act as a solvent or swelling agent on the fibers. This temperature will vary, depending on the particular amine oxide, particular fiber composition, etc. In cases where the amine oxide is imbibed pure or with a solvent that evaporates, the melting point of the amine oxide is the minimum required temperature. When a solvent not removed by evaporation is used, the minimum required temperature is simply the temperature required for the solution to cause the fibers to swell or begin to dissolve and will depend on the particular constituents of the solution and their concentrations.
  • Suitable volatile solvents for imbibing the amine oxides into the fibers include water, methanol, acetonitrile, and the like.
  • Useful solvents that are not removed by evaporation include dimethylsulfoxide, N-methylpyrrolidone, sulfolane, and the like.
  • the amine oxide After the amine oxide has acted on the fibrous material to effect hardening, it may be removed and a convenient way to do this is by washing with water or other selective solvent for the amine oxide.
  • fibrous material is used in describing my invention in a broad sense to comprise any woven or nonwoven fabric containing a substantial proportion of fibers that are soluble or swellable in the amine oxide, including natural cellulosic fibers such as wood pulp, cotton, linen and the like, animal fibers such as wool, fur and the like, and synthetic fibers such as nylon, rayon, polyester fibers, etc. and mixtures of such fibers.
  • fibers may be aggregate, as in papers of various kinds, felted and non-Woven fabrics and the like, or may be woven fabrics.
  • a particularly preferred embodiment of the invention is the strengthening of papers comprising cellulosic fibers, by means of amine oxides.
  • amine oxides strengthen fibrous materials can be explained by reference to cellulosic paper as an example.
  • the amine oxide partially dissolves or swells surface areas of the individual fibers of cellulose which make up the paper causing them to melt or fuse together forming a strong fiber lattice.
  • the paper Before treatment with the amine oxide, the paperconsists of fibers which are held together mainly by interfiber friction. After treatment, the fibers are actually physically locked together. This mechanism of the strengthening process has been observed in photomicrographs of a cellulosic paper monolayer made before, during, and after treatment with the amine oxides.
  • the invention avoids many disadvantages of the known methods of strengthening paper. Since the amine oxides used do not react with the fibers of the paper and the temperatures to which the paper must be heated are not extreme, there is no chemical degradation of the fibers.
  • the finished strengthened product need not contain any of the amine oxide, and, thus, the process does not discolor the product or require presence of any odorous or dangerous chemicals in the finished product.
  • Another advantage of the invention is that since the amine oxide agent does not react with the fiber and need not remain within the fabric, the amine oxide may be recovered and used again.
  • the process of this invention is relatively low in cost, simple and efiicient.
  • the strengthened material may be further treated without need for precautions to protect the strengthening agent.
  • Strengthened papers may be washed with water, aqueous acid, aqueous base, or organic solvents such as methanol or acetone and redried without losing the improved strength. If a strengthened paper is to be used as a support for coated layers, the coatings can be applied with solvents without affecting the strength of the support. Similarly, if a fabric which has been strengthened by the process of the invention is to be dyed, the dye solvents employed will not affect the improved strength of the fabric.
  • EXAMPLE 1 In a shallow tray thermostated at 110 C. was melted 20 grams of N-methylmorpholine-N-oxide. A strip of Whatman #4 paper was passed rapidly through the liquid and immediately washed with methanol (Water may be used instead of methanol) and dried. The paper had the A solution of grams of N-methylmorpholine-N- oxide in 20 ml. of dimethyl sulfoxide was heated in a shallow tray thermostated at 100 C. A strip of Whatman 4 #4 paper was passed through this solution at such a rate that both sides of the sheet were thoroughly wetted. The paper was then heated to 120 C., washed in methanol (water could also be used), and dried. The paper had the following wet and dry burst strengths (p.s.i.Minden):
  • Untreated Treated The strength of the treated paper was unaffected by washing in water, aqeous acid, or aqueous base. Samples of the N-methylmorpholine-N-oxide paper were stored in running water for 18 months with less than 5 percent loss in either wet or dry strength.
  • EXAMPLE 4 TABLE I Wet strength Amine oxide Dry strength None (untreated paper) 0 N-methylpyrrolidine-N-oxid N-methylpiperidineN-oxide. N-methylazaeycloheptane-N-oxide N-methylmorpholine-N-oxide Nieotine-l-oxide EXAMPLE 5 Table II shows a relationship of concentration of an amine oxide in the methanol solution used for strengthening a selected paper. The procedure described in Example 4 was employed except using varying concentrations of N-methylmorpholine-N-oxide in methanol in the respective treating solutions-as indicated in the table. The treated papers had the following wet and dry burst strengths (p.s.i.Minden):
  • the paper had the following wet and dry burst strengths (p.s.i.Minden) Untreated Treated Wet 0 42 Dry 12 78 EXAMPLE 7 A 20 percent methanolic solution of N-methylazacycloheptane-N-oxide was imbibed into a piece of a paper composed of 75 percent bleached sulfite pulp and 25 percent rayon fibers (30 denier, 1.5-inches long). The paper was heated to 120 C. for one minute, then washed with water and dried. The paper had the following burst strengths (p.s.i.Minden):
  • R R and R may be substituted or unsubstituted alkyl, cycloalkyl, aralkyl, or heterocyclic groups, and any two of the groups R R and R may be taken together to form a heterocyclic ring.
  • said fibrous material is a paper comprising cellulosic fibers.
  • a process for strengthening swellable fibrous materials comprising irnbibing a cyclic mono (N-methylamine- N-oxide) compound into said fibrous material and exposing the imbibed fibrous material to a temperature at which said amine oxide will swell said fibrous material.
  • nonvolatile liquid solvent is chosen from the group consisting of dimethyl sulfoxide, N-methylpyrrolidone, sulfolane, and mixtures thereof.
  • said volatile liquid solvent is chosen from the group consisting of methanol, water, acetonitrile, methanol-dioxane, methanol-acetone, and mixtures thereof.
  • said fibrous material is a paper comprising cellulosic fibers.
  • Z represents a saturated heterocyclic ring.
  • said fibrous material is a paper comprising cellulosic fibers.
  • a process for strengthening fibrous materials comprising imbibing an amine oxide into said fibrous material and exposing the imbided fibrous material to a heat source which will melt said amine oxide; wherein said amine oxide is N-methylmorpholine-N-oxide, N-methylpiperidine-N-oxide, N-methylpyrrolidone-N-oxide, N- methylazacycloheptane-N-oxide or nicotine-l-oxide.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Engineering & Computer Science (AREA)
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Description

United States Patent 3,447,956 PROCESS FOR STRENGTHENING SWELLABLE FIBROUS MATERIAL WITH AN AMINE OXIDE AND THE RESULTING MATERIAL Dee Lynn Johnson, Rochester, N.Y., assignor to Eastman Kodak Company, Rochester, N.Y., a corporation of New Jersey No Drawing. Filed Sept. 2, 1966, Ser. No. 576,853 Int. Cl. D06m 13/38; D2111 3/12 U.S. Cl. 117-154 20 Claims ABSTRACT OF THE DISCLOSURE Process for strengthening fibrous materials comprising imbibing an amine oxide into said fibrous material and exposing the imbibed fibrous material to a temperature at which said amine oxide will swell the fibers of said fibrous materials. In a highly preferred embodiment, said amine oxide is a cyclic mono(N-methylamine-N-oxide) compound such as, for example, N-methylmorpholine- N-oxide, N methylpyrrolidine-N-oxide, N-methylazacycloheptane-N-oxide, nicotine-l-oxide, etc. One aspect of this invention relates to articles of manufacture made by the above process.
This invention relates to a process for improving the Wet and dry strength of fibrous materials by treating them with certain amine oxides.
Fibrous materials such as papers, felts, and fabrics made from fibers are widely used, especially in such areas as packaging, clothing, and supports for photographic emulsions where strength is required, both when the materials are dry and when they are wet. It is beneficial to strengthen these materials by a quick, simple, and inexpensive process which does not unduly modify the normal desirable characteristics of these materials. This process should result in no degradation of the material, impart no color to it, and leave no potentially dangerous or unpleasant residue in the material. The strength imparted to the materials should be permanent or long-lasting and should not be affected by washing the material with water. These objectives are fulfilled when the fibrous materials are strengthened with certain amine oxides.
It is an object of this invention to provide a process for improving the wet and dry strength of fibrous materials.
Another object is to provide strengthened fibrous materials.
Still further objects will become apparent from the following specification and claims.
According to my invention, it has been found that a fibrous material may be strengthened by imbibing an amine oxide into the fibrous material and exposing the imbibed fibrous material to a temperature at which the amine oxide will swell the fibers.
The class of amine oxides useful in accordance with the invention for strengthening fibrous materials has the general formula:
wherein each of R R and R represents a member selected from the group consisting of monovalent alkyl, cycloalkyl, aralkyl and heterocyclic radicals, and heterocyclic rings comprising two of said members and the N-atom of the formula.
A subclass of amine oxides, within the above formula, especially preferred for the invention are cyclic m0no(N- methylamine-N-oxide) compound having the formula wherein Z represents the atoms to complete a saturated heterocyclic ring. Some preferred cyclic mono- (N-methylamine-N-oxide) compounds within this last formula include N-methylmorpholine-N-oxide, N-methylpiperidine- N-oxide, N methylpyrrolidone-N-oxide, N-methylazacycloheptane-N-oxide, nicotine-l-oxide, and the like. A typical example of a useful amine oxide within the first formula above is triethyl amine-N-oxide.
The amine oxide may be imbibed into a fibrous material directly in liquid form, or it may be imbibed in solution, that is dissolved in a liquid solvent. When solvents are used, one may use a volatile solvent which is easily removed by evaporation, or one may use a liquid solvent which will not evaporate. In the latter case, the solvent must be one that does not interfere with the strengthening action of the amine oxide.
While the amine oxide is imbibed in the fibrous material to be treated, it is necessary to attain a temperature suficiently high to let the amine oxide act as a solvent or swelling agent on the fibers. This temperature will vary, depending on the particular amine oxide, particular fiber composition, etc. In cases where the amine oxide is imbibed pure or with a solvent that evaporates, the melting point of the amine oxide is the minimum required temperature. When a solvent not removed by evaporation is used, the minimum required temperature is simply the temperature required for the solution to cause the fibers to swell or begin to dissolve and will depend on the particular constituents of the solution and their concentrations.
Suitable volatile solvents for imbibing the amine oxides into the fibers include water, methanol, acetonitrile, and the like. Useful solvents that are not removed by evaporation include dimethylsulfoxide, N-methylpyrrolidone, sulfolane, and the like.
After the amine oxide has acted on the fibrous material to effect hardening, it may be removed and a convenient way to do this is by washing with water or other selective solvent for the amine oxide.
The term fibrous material is used in describing my invention in a broad sense to comprise any woven or nonwoven fabric containing a substantial proportion of fibers that are soluble or swellable in the amine oxide, including natural cellulosic fibers such as wood pulp, cotton, linen and the like, animal fibers such as wool, fur and the like, and synthetic fibers such as nylon, rayon, polyester fibers, etc. and mixtures of such fibers. These fibers may be aggregate, as in papers of various kinds, felted and non-Woven fabrics and the like, or may be woven fabrics. A particularly preferred embodiment of the invention is the strengthening of papers comprising cellulosic fibers, by means of amine oxides.
A possible mechanism by which the amine oxides strengthen fibrous materials can be explained by reference to cellulosic paper as an example. In strengthening paper, apparently the amine oxide partially dissolves or swells surface areas of the individual fibers of cellulose which make up the paper causing them to melt or fuse together forming a strong fiber lattice. Before treatment with the amine oxide, the paperconsists of fibers which are held together mainly by interfiber friction. After treatment, the fibers are actually physically locked together. This mechanism of the strengthening process has been observed in photomicrographs of a cellulosic paper monolayer made before, during, and after treatment with the amine oxides. It also appears that during treatment, loose fines in the 3 paper are melted and fused into the cellulose fibers, becoming an integral part of the paper, thus reducing the dusting characteristics of the paper. By the same mechanism scaling is reduced in scaly fibers such as wool. In strengthening woven fabrics, the amine oxides function by the same mechanism to fuse the warp threads to the woof threads, as Well as to strengthen the individual threads by fusing the fibers in the thread, resulting in a stronger physical connection of the fibers and threads than by mere interfiber friction.
Most methods of improving wet and dry strength of papers known in the prior art involve coating of a material onto the surface of the paper or imbibing a material into the body of the paper. This material may then chemically react with the paper to strengthen it, and may remain a part of the treated paper. Such treatments may degrade the paper or may leave harmful or undesirable chemicals in the paper. Paper has also been strengthened by coating with a material which forms a strengthening continuous phase within the body of, or on the surface of, the paper. This type of strengthening is usually costly and may give stiff or brittle paper. The amine oxides used in this invention do not react chemically with the paper, or with other fibrous materials which may be treated, nor is it necessary that they remain a part of the strengthened product.
The invention avoids many disadvantages of the known methods of strengthening paper. Since the amine oxides used do not react with the fibers of the paper and the temperatures to which the paper must be heated are not extreme, there is no chemical degradation of the fibers. The finished strengthened product need not contain any of the amine oxide, and, thus, the process does not discolor the product or require presence of any odorous or dangerous chemicals in the finished product.
Another advantage of the invention is that since the amine oxide agent does not react with the fiber and need not remain within the fabric, the amine oxide may be recovered and used again. Thus, the process of this invention is relatively low in cost, simple and efiicient.
Since the improvement in wet and dry strength imparted to fibrous materials does not depend on presence of any strengthening agent in the finished material, the strengthened material may be further treated without need for precautions to protect the strengthening agent. Strengthened papers may be washed with water, aqueous acid, aqueous base, or organic solvents such as methanol or acetone and redried without losing the improved strength. If a strengthened paper is to be used as a support for coated layers, the coatings can be applied with solvents without affecting the strength of the support. Similarly, if a fabric which has been strengthened by the process of the invention is to be dyed, the dye solvents employed will not affect the improved strength of the fabric.
To illustrate the invention and to demonstrate a most preferred mode of carrying out the invention we refer to the following specific examples embodying the invention.
EXAMPLE 1 In a shallow tray thermostated at 110 C. was melted 20 grams of N-methylmorpholine-N-oxide. A strip of Whatman #4 paper was passed rapidly through the liquid and immediately washed with methanol (Water may be used instead of methanol) and dried. The paper had the A solution of grams of N-methylmorpholine-N- oxide in 20 ml. of dimethyl sulfoxide was heated in a shallow tray thermostated at 100 C. A strip of Whatman 4 #4 paper was passed through this solution at such a rate that both sides of the sheet were thoroughly wetted. The paper was then heated to 120 C., washed in methanol (water could also be used), and dried. The paper had the following wet and dry burst strengths (p.s.i.Minden):
Untreated Wet 0 Dry 12 Treated EXAMPLE 3 A 25 percent methanolic solution of N-methylmorpholine-N-oxide was imbibed into a piece of Whatman #1 filter paper. The paper was heated to 120 C. for one minute, then washed in water and dried. The paper had the following wet and dry burst strengths (p.s.i.- Minden):
Untreated Treated The strength of the treated paper was unaffected by washing in water, aqeous acid, or aqueous base. Samples of the N-methylmorpholine-N-oxide paper were stored in running water for 18 months with less than 5 percent loss in either wet or dry strength.
EXAMPLE 4 TABLE I Wet strength Amine oxide Dry strength None (untreated paper) 0 N-methylpyrrolidine-N-oxid N-methylpiperidineN-oxide. N-methylazaeycloheptane-N-oxide N-methylmorpholine-N-oxide Nieotine-l-oxide EXAMPLE 5 Table II shows a relationship of concentration of an amine oxide in the methanol solution used for strengthening a selected paper. The procedure described in Example 4 was employed except using varying concentrations of N-methylmorpholine-N-oxide in methanol in the respective treating solutions-as indicated in the table. The treated papers had the following wet and dry burst strengths (p.s.i.Minden):
. TABLE II Cone. of N-methylmorpholine N'oxide, percent Wet strength Dry strength None (untreated paper) 0 1 9 EXAMPLE 6 A 20 percent solution of N-methylmorpholine-N-oxide in methanol was imbibed into a piece of a paper composed of percent bleached sulfite pulp and 15 percent polyethylene terephthalate fibers. The paper was heated to 120 C. for one minute, then washed in water and dried. The paper had the following wet and dry burst strengths (p.s.i.Minden) Untreated Treated Wet 0 42 Dry 12 78 EXAMPLE 7 A 20 percent methanolic solution of N-methylazacycloheptane-N-oxide was imbibed into a piece of a paper composed of 75 percent bleached sulfite pulp and 25 percent rayon fibers (30 denier, 1.5-inches long). The paper was heated to 120 C. for one minute, then washed with water and dried. The paper had the following burst strengths (p.s.i.Minden):
Untreated Treated Wet 1 37 Dry 9 98 wherein R R and R may be substituted or unsubstituted alkyl, cycloalkyl, aralkyl, or heterocyclic groups, and any two of the groups R R and R may be taken together to form a heterocyclic ring.
2. The process of claim 1 wherein said fibrous material is a paper comprising cellulosic fibers.
3. A process for strengthening swellable fibrous materials comprising irnbibing a cyclic mono (N-methylamine- N-oxide) compound into said fibrous material and exposing the imbibed fibrous material to a temperature at which said amine oxide will swell said fibrous material.
4. The process of claim 3 wherein said amine oxide is N-methylmorpholine-N-oxide.
5. The process of claim 3 wherein said amine oxide is N-methylpiperidine-N-oxide.
6. The process of claim 3 wherein said amine oxide is N-methylpyrrolidine-N-oxide.
7. The process of claim 3 wherein said amine Oxide is N-methylazacycloheptane-N-oxide.
8. The process of claim 3 wherein said amine oxide is nicotine-l-oxide.
9. The process of claim 3 wherein a solution of said amine oxide is made in a nonvolatile liquid solvent, and the amine oxide is imbibed in said solution into said fibrous material.
10. The process of claim 9 wherein said nonvolatile liquid solvent is chosen from the group consisting of dimethyl sulfoxide, N-methylpyrrolidone, sulfolane, and mixtures thereof.
11. The process of claim 3 wherein a solution of said amine oxide is made in a volatile liquid solvent, said solution is imbibed into said fibrous material, and said volatile liquid solvent is removed from said fibrous material prior to exposing said imbibed fibrous material to a temperature at which said amine oxide will swell the fibers of said fibrous material.
12. The process of claim 11 wherein said volatile liquid solvent is chosen from the group consisting of methanol, water, acetonitrile, methanol-dioxane, methanol-acetone, and mixtures thereof.
13. The process of claim 3 wherein said amine oxide is removed from said fibrous material subsequent to exposing said imbibed fibrous material to a temperature at which said amine oxide will swell the fibers of said fibrous material.
14. An article of manufacture comprising a fibrous material which has been strengthened by the process described in claim 3.
15. The article of manufacture of claim 14 wherein said fibrous material is a paper comprising cellulosic fibers.
16. A process according to claim 3 wherein said cyclic mono(N-methylamine-N-oxide) compound is a compound of the formula:
wherein Z represents a saturated heterocyclic ring.
17. A process according to claim 3 wherein said imbibed fibrous material is heated to at least the melting point temperature of said cyclic mono(N-methylamine-N- oxide) compound.
18. A process according to claim 3 wherein said fibrous material is a paper comprising cellulosic fibers.
19. A process for strengthening fibrous materials comprising imbibing an amine oxide into said fibrous material and exposing the imbided fibrous material to a heat source which will melt said amine oxide; wherein said amine oxide is N-methylmorpholine-N-oxide, N-methylpiperidine-N-oxide, N-methylpyrrolidone-N-oxide, N- methylazacycloheptane-N-oxide or nicotine-l-oxide.
20. An article of manufacture comprising a fibrous material which has been strengthened by the process of claim 19.
References Cited UNITED STATES PATENTS 1,158,400 10/1915 Cohoe 106127 1,943,176 1/1934 Graenacher 106-163 2,027,682 1/ 1936 Eichman 106-163 2,060,568 11/1936 Graenacher et al. 260-293 2,482,631 9/1949 Morris et al. 252-364 2,757,148 7/1956 Heritage 26017.4 3,047,579 7/1962 Witman 260-289 3,236,669 2/ 1966 Williams 106163 WILLIAM D. MARTIN, Primary Examiner. THEODORE G. DAVIS, Assistant Examiner.
U.S. Cl. X.R.
8-l30.l; ll7-2l, 138.8, 141, 143
Patent No. 3,L1 Li7,956 Dated June 3, 9 9
lnventorba) Dee Lvnn Johnson It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
r- Column 2, line 12, "N1rr1ethylpyrr'olidone-N--oxicle should read ---N-methylpyrrolidine-NoXide--.
Column 6, line L O, "N-methylpyrrolidone-N-0Xide" should read --N-methylpyrr*o1idine-N-oxide---.
Signed and sealed this 2nd day of November 1 971 (SEAL) Attest:
EDWARD M.FLETCHER,JR. ROBERT GOTTSCHALK Attesting Officer Acting Commissioner of Patents
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Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3508941A (en) * 1966-09-02 1970-04-28 Eastman Kodak Co Method of preparing polymers from a mixture of cyclic amine oxides and polymers
FR2398758A1 (en) * 1977-07-26 1979-02-23 Akzona Inc PROCESS FOR PREPARING AN IMPREGNATED SOLID RAW MATERIAL USING ITSELF IN THE PREPARATION OF A CELLULOSE SOLUTION AND PRODUCT OBTAINED
US4142913A (en) * 1977-07-26 1979-03-06 Akzona Incorporated Process for making a precursor of a solution of cellulose
US4246221A (en) * 1979-03-02 1981-01-20 Akzona Incorporated Process for shaped cellulose article prepared from a solution containing cellulose dissolved in a tertiary amine N-oxide solvent
US5409532A (en) * 1992-01-23 1995-04-25 Lenzing Aktiengesellschaft Amine-oxides
US5556452A (en) * 1993-09-14 1996-09-17 Lenzing Aktiengesellschaft Moulding materials and spinning materials containing cellulose
US5601767A (en) * 1994-09-05 1997-02-11 Lenzing Aktiengesellschaft Process for the production of a cellulose moulded body
US5626810A (en) * 1993-10-19 1997-05-06 Lenzing Aktiengesellschaft Process for the preparation of cellulose solutions
US5788939A (en) * 1995-09-19 1998-08-04 Lenzing Aktiengesellschaft Process for the production of a cellulose moulded body
WO1998038373A1 (en) * 1997-02-25 1998-09-03 Lenzing Aktiengesellschaft Method for producing a reinforced fiber composite
US6042890A (en) * 1997-02-25 2000-03-28 Lenzing Aktiengesellschaft Process for producing a strengthened fiber assembly
US6117378A (en) * 1995-10-13 2000-09-12 Lenzing Aktiengesellschaft Process for producing cellulose fibres
US6241927B1 (en) 1997-06-17 2001-06-05 Lenzing Aktiengesellschaft Method of producing cellulose fibers
US6245837B1 (en) 1996-08-27 2001-06-12 Akzo Nobel Surface Chemistry Ab Use of a linear synthetic polymer to improve the properties of a cellulose shaped body derived from a tertiary amine oxide process
US6500215B1 (en) 2000-07-11 2002-12-31 Sybron Chemicals, Inc. Utility of selected amine oxides in textile technology
US20050083466A1 (en) * 2003-10-16 2005-04-21 Yun-Bok Lee Array substrate for in-plane switching mode liquid crystal display device and method of fabricating the same
US20050230860A1 (en) * 2004-04-16 2005-10-20 Birla Research Institute For Applied Science Process for the preparation of a cellulose solution for spinning of fibres, filaments or films therefrom
US10011931B2 (en) 2014-10-06 2018-07-03 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing dyed and welded substrates
WO2018234638A1 (en) 2017-06-22 2018-12-27 Helsingin Yliopisto METHOD FOR ASSEMBLING POLYMERIC BIOMATERIALS
US10982381B2 (en) 2014-10-06 2021-04-20 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates
US11085133B2 (en) 2016-05-03 2021-08-10 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing dyed and welded substrates
US11766835B2 (en) 2016-03-25 2023-09-26 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates
US12060679B2 (en) 2016-02-09 2024-08-13 Bradley University Lignocellulosic composites prepared with aqueous alkaline and urea solutions in cold temperatures systems
US12338574B2 (en) 2017-11-11 2025-06-24 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates

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US2027682A (en) * 1932-09-10 1936-01-14 Eichmann Friedrich Process for making transparent films, foils, or skins
US2060568A (en) * 1934-06-23 1936-11-10 Soc Of Chemical Ind Assisting agents for the textile industry
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US2757148A (en) * 1955-10-21 1956-07-31 Weyerhaeuser Timber Co Manufacture of thermosetting cellulosic particle compositions
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Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3508941A (en) * 1966-09-02 1970-04-28 Eastman Kodak Co Method of preparing polymers from a mixture of cyclic amine oxides and polymers
FR2398758A1 (en) * 1977-07-26 1979-02-23 Akzona Inc PROCESS FOR PREPARING AN IMPREGNATED SOLID RAW MATERIAL USING ITSELF IN THE PREPARATION OF A CELLULOSE SOLUTION AND PRODUCT OBTAINED
US4142913A (en) * 1977-07-26 1979-03-06 Akzona Incorporated Process for making a precursor of a solution of cellulose
US4246221A (en) * 1979-03-02 1981-01-20 Akzona Incorporated Process for shaped cellulose article prepared from a solution containing cellulose dissolved in a tertiary amine N-oxide solvent
US5409532A (en) * 1992-01-23 1995-04-25 Lenzing Aktiengesellschaft Amine-oxides
US5556452A (en) * 1993-09-14 1996-09-17 Lenzing Aktiengesellschaft Moulding materials and spinning materials containing cellulose
US5679146A (en) * 1993-09-14 1997-10-21 Lenzing Aktiengesellschaft Moulding materials and spinning materials containing cellulose
US5626810A (en) * 1993-10-19 1997-05-06 Lenzing Aktiengesellschaft Process for the preparation of cellulose solutions
US5601767A (en) * 1994-09-05 1997-02-11 Lenzing Aktiengesellschaft Process for the production of a cellulose moulded body
US5788939A (en) * 1995-09-19 1998-08-04 Lenzing Aktiengesellschaft Process for the production of a cellulose moulded body
US6117378A (en) * 1995-10-13 2000-09-12 Lenzing Aktiengesellschaft Process for producing cellulose fibres
US6245837B1 (en) 1996-08-27 2001-06-12 Akzo Nobel Surface Chemistry Ab Use of a linear synthetic polymer to improve the properties of a cellulose shaped body derived from a tertiary amine oxide process
US6042890A (en) * 1997-02-25 2000-03-28 Lenzing Aktiengesellschaft Process for producing a strengthened fiber assembly
AT404368B (en) * 1997-02-25 1998-11-25 Chemiefaser Lenzing Ag METHOD FOR PRODUCING A FASTENED FIBER COMPOSITE
AU727252B2 (en) * 1997-02-25 2000-12-07 Lenzing Aktiengesellschaft Process for producing a strengthened fiber assembly
WO1998038373A1 (en) * 1997-02-25 1998-09-03 Lenzing Aktiengesellschaft Method for producing a reinforced fiber composite
CN1105798C (en) * 1997-02-25 2003-04-16 连津格股份公司 Method for producing reinforced fiber composition
US6241927B1 (en) 1997-06-17 2001-06-05 Lenzing Aktiengesellschaft Method of producing cellulose fibers
US6500215B1 (en) 2000-07-11 2002-12-31 Sybron Chemicals, Inc. Utility of selected amine oxides in textile technology
US20050083466A1 (en) * 2003-10-16 2005-04-21 Yun-Bok Lee Array substrate for in-plane switching mode liquid crystal display device and method of fabricating the same
US20090127750A1 (en) * 2004-04-16 2009-05-21 Birla Research Institute For Applied Science Process for making cellulose fibre, filaments or films
US7459015B2 (en) * 2004-04-16 2008-12-02 Birla Research Institute For Applied Sciences Process for the preparation of a cellulose solution for spinning of fibres, filaments or films therefrom
US20050230860A1 (en) * 2004-04-16 2005-10-20 Birla Research Institute For Applied Science Process for the preparation of a cellulose solution for spinning of fibres, filaments or films therefrom
US7938993B2 (en) 2004-04-16 2011-05-10 Birla Research Institute For Applied Sciences Process for making cellulose fibre, filaments or films
US10011931B2 (en) 2014-10-06 2018-07-03 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing dyed and welded substrates
US12091815B2 (en) 2014-10-06 2024-09-17 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates
US10982381B2 (en) 2014-10-06 2021-04-20 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates
US11555263B2 (en) 2014-10-06 2023-01-17 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing dyed and welded substrates
US12060679B2 (en) 2016-02-09 2024-08-13 Bradley University Lignocellulosic composites prepared with aqueous alkaline and urea solutions in cold temperatures systems
US11766835B2 (en) 2016-03-25 2023-09-26 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates
US11920263B2 (en) 2016-05-03 2024-03-05 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing dyed and welded substrates
US11085133B2 (en) 2016-05-03 2021-08-10 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing dyed and welded substrates
US11753565B2 (en) 2017-06-22 2023-09-12 Teknologian Tutkimuskeskus Vtt Oy Method of joining polymeric biomaterials
WO2018234638A1 (en) 2017-06-22 2018-12-27 Helsingin Yliopisto METHOD FOR ASSEMBLING POLYMERIC BIOMATERIALS
US12338574B2 (en) 2017-11-11 2025-06-24 Natural Fiber Welding, Inc. Methods, processes, and apparatuses for producing welded substrates

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BE703202A (en) 1968-01-15
DE1619013A1 (en) 1970-09-24

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