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Publication numberUS3046079 A
Publication typeGrant
Publication dateJul 24, 1962
Filing dateMay 24, 1960
Priority dateMay 24, 1960
Publication numberUS 3046079 A, US 3046079A, US-A-3046079, US3046079 A, US3046079A
InventorsChance Leon H, Perkins Rita M, Reeves Wilson A
Original AssigneeChance Leon H, Perkins Rita M, Reeves Wilson A
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Process of reacting partially swollen cotton textiles with aqueous solutions of specific aldehydes containing acid catalysts to produce wet and dry crease resistance
US 3046079 A
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Description  (OCR text may contain errors)

United States Patent Office 3,046,079 Patented July 24, 1962 A non-exclusive, irrevocable, royalty-free license in the invention herein described, throughout the world for all purposes of the United States Government, with the power to grant sublicenses for suchpurposes, is hereby granted to the Government of the United States of America.

This invention relates to an improved process for the treatment of cotton textiles with formaldehyde.

The processes that have been known heretofore are not satisfactory for use on cotton textiles because of the great loss of strength that is brought about. An object of the present invention is to provide a process for reacting formaldehyde with cotton textiles without excessive reduction of the strength of the cotton fiber or fibrous product. Another object of the present invention is to provide an improved practical process for producing cotton textiles which are relatively non-shrinkable and which have a high degree of dry and wet wrinkle recovery, and which at the same time have good tearing and tensile strengths. Still another object of this invention is to produce crossliuked cotton textiles with the above named properties which have moisture regain values of about 7% or greater.

To achieve the object of this invention the cotton textiles is allowed to steep in .a solution containing water, a water-soluble organic liquid, formaldehyde, and a mineral acid catalyst under such conditions that the reaction of formaldehyde with the cotton textile reaches the desired stage. To stop the reaction at the desired stage the cotton textile is washed free of unreacted formaldehyde and acid or the acid is neutralized with a suitable base before drying it.

In carrying out the process of this invention the proportion of water to water-soluble organic liquid is the factor which determines to a large extent the final properties of the product. The proportion of water to watersoluble liquid must be such that the cotton cellulose is not in a fully swollen state, but in a partially swollen state. The proportion of water should range about from 8% to 40%, based on the weight of the solution. It is also very important that the cotton fiber is not in a completely dry condition at the time it is reacted with the formaldehyde. Therefore, itis necessary to have sufficient water-soluble organic liquid present to prevent the complete swelling which would be obtained if the system were entirely aqueous. The preferred proportion of water-soluble organic liquid lies in the range of about 50% to 90% based on the total weight of the solution, including water, water-soluble organic liquid, formaldehyde, and mineral acid.

The rate of reaction of formaldehyde with the cotton cellulose depends on the concentration of mineral acid and formaldehyde in the treating solution and upon temperature. The concentration of formaldehyde and mineral acid can be varied over a considerable range, but relatively low concentrations of mineral acid (1%- 17.2%) and formaldehyde (1%-10%) have been found to be adequate. The temperature at which the reaction is carried out will also affect the rate of reaction of formaldehyde with the cotton cellulose. The time required decreases rapidly with an increase in temperature.

' The reaction may be carried out at temperatures ranging from slightly above the freezing point of the solution to about 45 C. The preferable range is about 25 C. to 35 C. The strength of the modified cotton textile is greatly reduced at temperatures substantially above C. The time of reaction may be varied from about 3 minutes to several hours, the longer times generally being required at the lower temperatures.

After the reaction has been carried to the desired stage it is desirable to wash the product thoroughly to free it of unreacted formaldehyde and' acid. At some stage during the washing it is preferable to add in an alkaline substance such as sodium carbonate to the wash water to neutralize the acids.

The cotton textiles processed according to this invention may be in the form of loose fibers, yarns, or fabrics. The cotton textiles may be processed on existing textile machinery such as a jig or J-Box, or they may be processed by festooning. The type of equipment used for processing is not an important feature of this invention. The process using the jig is preferred for fabric. When the process is carried out at the higher temperatures the reaction proceeds at such a rate that a continuous process may be used. Yarn can be readily treated according to this invention in a package dye machine. Aldehydes other than formaldehyde which react with cellulose to crosslink it may be used in this process. Such aldehydes include glyoxal, glutaraldehyde, adipaldehyde, and 0&- hydroxy adipaldehyde, acetaldehyde and benzaldehyde. Aldehyde derivatives, such as dimethylol ethylene urea may also be used.

Water-soluble solvents useful in this invention are organic compounds which have relatively little (as compared to water) or no swelling action on cotton cellulose fibers. extent of at least 5%. Examples of useful water-soluble liquids are: acetone, dioxane, diethylene glycol, dimethyl ether, tetrahydrofurane, organic acids such as acetic, formic, propionic, and lactic acids. Mixtures of organic compounds such as benzene in acetic acid and xylene in tetrahydrofurane are useful liquids. With these mixtures it is important that water will dissolve in them to the extent of at least 5% of the weight of the mixture. Acetic acid is the preferred water soluble organic liquid for use in this invention.

Catalysts suitable for use in this invention include mineral acids of the group consisting of hydrochloric acid, sulfuric acid, and phosphoric acid. The reaction rate is greatest at a particular temperature and reagent concentration when hydrochloric acid is used.

The products obtained by the process described herein have excellent wet and dry crease resistance. Both of Water must be soluble in these liquids to the these qualities are necessary for a fabric if the fabric is to dry smooth and unwrinkled after Washing and tumble drying. When cotton fabrics or fibers are reacted with formaldehyde and an acid catalyst by the drying and curing process, they have good wet and dry crease recovery, but suffer a great loss in strength. In addition, the reproducibility of the process is diflicult and not practical. An advantage of the process of this invention is the greater tear and tensile strength retention of the product. This improved strength retention is made possible by allowing the reaction of formaldehyde with cotton to take place while the cellulosic material is Wet with the treating solution at a temperature not exceeding 45 C., and is in a partially swollen state. Temperatures much above 45 C. destroy the strength of the cotton. For example, at a temperature of 75 C., over 75% of the strength of cotton is lost in about 5 minutes, whereas the strength of regenerated cellulose is not greatly affected at the higher temperatures. Another advantage of the process is that various degrees of dry crease recovery can be obtained merely by changing the concentration of water in the solutions. At the lower concentrations of Water (8% to 30%) excellent dry crease recovery as well as excellent wet crease recovery can be obtained. As the water concentration is increased the dry crease recovery of fabric products show less improvement over the control, and finally with over about 50% water in the system no improvement at all is obtained in dry crease recovery, although the wet crease recovery is still very good. An object of this invention is to produce cotton fabrics with good wet and dry crease recovery. It is evident that properties of the final fabric product are dependent on the degree of fiber swelling at the time the reaction takes place, which in turn are determined by the amount of water present. For instance, cotton fabric soaked for 5 days in a solution containing 3.6% formaldehyde, 3.7% hydrochloric acid, and 92.7% water contained only 0.4% combined formaldehyde, and had no improvement in dry crease recovery. Bone dry cotton fabric soaked for 5 days in an anhydrous solution containing the same concentrations of formaldehyde and hydrogen chloride (the remainder being acetic acid) contained combined formaldehyde but was extremely degraded, the fabric retaining only about 15% of its original strength. On the other hand, cotton fabric soaked for only one hour in a solution containing 3.6% formaldehyde, 3.7% hydrochloric acid, 17.7% water, and 75% acetic acid contained 0.8l.0% combined formaldehyde and had excellent wet and dry crease recovery, and about 70% strength retention. This again illustrates the advantage of carrying out the reaction within specified limits of water concentration.

Softening agents such as silicones, polyethylene, polyacrylonitrile, or long chain fatty acid derivatives may be used to improve the strength, abrasion resistance and hand of the product. Up to 90% Elmendorf tearing strength retention has been obtained by this process by using a softener as an after treatment. The softeners may also be applied to the fabrics before treating with formaldehyde.

Cotton fabrics produced by this process have the quality of drying smooth after repeated laundering whether they are drip-dried, line-dried, or tumble-dried. Other properties such as fiber density, moisture regain, water of inhibition, and dyeability are affected by the treatment. For example, moisture regain of treated fabrics was generally greater than that of the untreated fabrics.

changed is again dependent on the degree of fiber swell- The extent to which these properties are ing at the time the reaction of formaldehyde with the cellulose takes place.

The following examples illustrate the methods of carrying out the invention but the invention is not restricted to these examples. Treated fabrics were tested by the standard methods of the American Society for Testing Materials, Philadelphia. Breaking strength was determined by the one inch strip method, tearing strength by the Elmendorf method, and dry crease recovery by the Monsanto method. Wet crease recovery was carried out by first thoroughly wetting the sample with water, blotting, and then measuring the crease recovery of the wet sample by the Monsanto method. The percentages are by weight.

EXAMPLE 1 A series of solutions was prepared containing varying amounts of formaldehyde, hydrochloric acid, water, and acetic acid. The composition of these solutions are shown in Table I.

Table I Calculated Amount of Acetic Acetic Solution No. Water in ECHO, H01, Acid, Anhy- Final Percent Percent Percent dride, Solution, Percent Percent 1 1 The amount of water indicated includes a small amount of methanol which was in the formaldehyde as a stabilizer.

2 The percent acetic acid here do s not include that formed from the reaction of Water and acetic anhydride.

The solutions were prepared by mixing glacial acetic acid, 36% aqueous formaldehyde, and 37% hydrochloric acid in the ratio required to give the desired concentrations. In some of the solutions containing a high concentration of water, it Was necessary to add water in addition to that present in the formaldehyde and hydrochloride acid to obtain the desired water concentration. In some of the solutions containing low concentrations of water, it was necessary to add enough acetic anhydride to react with a portion of the water in the formaldehyde and hydrochloric acid to obtain the desired Water concentration.

The water concentration in the series was varied from 92.7% (where no acetic acid was used) to 0.0% (where only acetic acid was used as the solvent). The concentration of formaldehyde was varied from 3.6% to 7.5%, and that of the hydrochloric acid from 3.7% to 17.2%.

Several samples of bleached unmercerized cotton print cloth were immersed in each solution. A sample was. removed from each solution at time intervals varying from 3 minutes to 6 hours in the more reactive solutions and up to 5 days in the less reactive solutions. All of the reactions were carried out by allowing the samples to steep in the solutions at room temperature (about 27 C.). After the samples of fabric had been removed from the reaction media, they were washed thoroughly with water to remove unreacted formaldehyde and acids. The amount of combined formaldehyde in the cotton was determined, as well as physical properties such as wet and dry crease recovery and tearing strength. The properties of some of these samples are shown in Table II.

Table II.-Physical Properties Formaldehyde Treated Bleached Cotton Print Cloth Physical Properties at various times and solution concentrations Reaction Time, Grease Recovery Hrs. Combined Tearing Angle Moisture ECHO, Strength (Warp Fill) Regain, Percent (Warp) Percent gnis.

Dry Wet SOLUTION NO. 2

SOLUTION NO. 5

SOLUTION NO. 7

SOLUTION NO. 8

SOLUTION NO. 9

CONTROL (UNTREATED PRINT CLOTH) The data shows that after two or three hours reaction time in solution No. 2 there is not much improvement in the dry crease recovery even at the higher formaldehyde and hydrochloric acid concentrations. This was due to the high degree of swelling in the completely aqueous system. The dry crease recovery began to increase as the water concentration was reduced. Good wet crease recovery was also obtained. Moisture regain values varied from about 7.0% to about 9.4%. The moisture regain of the untreated fabric was 6.7%. In this experiment optimum fabric properties were obtained when using solutions 5 through 8, at water concentrations of 30% to 12.6%. Print cloth reacted for two hours in solution No. 4, contained 1.84% combined formaldehyde and had dry crease recovery angle of 249 and a wet angle 360. Bone dry print cloth reacted for 3 days in solution No. 10 contained only 0.17% combined formaldehyde and had a dry crease recovery angle of only 156 and a wet crease recovery angle of only 180; the tearing strength was only 215 grams. The disadvantage of using a completely aqueous or completely anhydrous system is readily apparent if good wet and dry crease recovery and good strength are desired.

Print cloth was also reacted at time intervals of 3, 10, and minutes in the solutions of Table I. This cloth had formaldehyde contents varying from 0.25% to .75% and had wet and dry crease recovery.

EXAMPLE 2 A series of solutions were prepared containing 3.6% formaldehyde, 3.0% hydrochloric acid, 16.4% water,

and 77% acetic acid. Samples of bleached print cloth, bleached broadcloth, and mercen'zed bleached print cloth were steeped in these solutions at temperatures varying from about 20 C. to about 45 C. at time intervals varying from 5 minutes to 90 minutes. After the samples were allowed to react for the required length of time they were removed from the solut ons and washed thoroughly with water to remove unreacted formaldehyde and acids. The amount of combined formaldehyde was determined as well as tearing strength and wet and dry crease recovery angles. The results of some of these tests are shown in Table III. The advantage of using mercerized fabric is evident from the greater strength retained.

Table III.The Efiecr of Temperature and Time on Properties of Formaldehyde Treated Cotton Fabrics Wrinkle Recovery Tem- Time, Com- Tearing Angle Cotton Fabric, pera- Minbined Strength (Warp Type ture, utes H OH 0, (Warp), Fill) 0. Percent gms.

Dry Wet;

20 30 0. 57 465 210 232 20 90 1.10 315 257 290 35 5 0. 50 500 232 244 Bleached print 35 10 0. 68 490 244 274 cloth 35 30 1. 06 340 262 302 45 5 0. 84 360 258 278 45 10 1. 10 325 277 298 45 20 1. 36 255 280 303 0. 72 805 232 204 Mercerized print 25 6O 1. 02 670 249 288 cloth 10 0.71 760 228 287 35 30 1. 29 620 262 313 10 1. 26 655 265 209 Bleached broad- 35 10 0.72 360 248 302 cloth 45 5 0. 85 350 269 305 Untreated control, bleached print cloth 1,050 188 152 Mercerized control, print cloth... 1,150 195 199 Untreated control, bleached broadcloth 950 184 204 EXAMPLE 3 A pilot plant run was carried out as follows:

A solution was prepared containing 2,140 ml. of 37% aqueous formaldehyde, 2,380 m1. of 36% hydrochloric acid, and 17,780 ml. of glacial acetic acid. The solution contained about 3.7% formaldehyde, 3.6% hydrochloric acid, 12.1% water, and 80.6% acetic acid. A piece of broadcloth, print cloth, and mercerized print cloth were sewed together making a total of yards of 18" width fabric. The fabric was treated with the solution for one hour at room temperature (about 27 C.) using a jig. The reaction was stopped by first washing the fabric in water containing sodium carbonate, and then rinsing well with cold water, and finally with hot water and drying on a tenter. Best results were obtained on the mercerized print cloth, which had a formaldehyde content of 1.12%, a dry crease recovery angle of 250", a wet crease recovery angle of 300, and a tearing strength of 630 grams. The tearing strength was increased to 800 grams by applying 0.3 to 0.4% polyethylene softener to the treated fabric. This was a 75% strength retention based on the bleached control fabric and a strength retention based on the mercerized control fabric.

EXAMPLE 4 A pilot plant run was carried out as follows: A solution was prepared containing 2,132 ml. of 36% aqueous formaldehyde, 2,378 ml. of 37% hydrochloric acid, 13,742 ml. of acetic acid, and 3,138 ml. of acetic anhydride. The acetic anhydride reacted with a portion of the water to give a solution containing 3.6% formaldehyde, 3.7% hydrochloric acid, 10.0% water, and 82.7% acetic acid.

Fifty yards of fabric (consisting of 20 yards of bleached print cloth, 12 yards of mercerized print cloth, and bleached broadcloth) were treated with this solution in the same manner described in Example 3. Best results were obtained on the mercerized print cloth, which had a formaldehyde content of 0.96%, a dry crease recovery angle of 260, a wet crease recovery angle of 280, a tearing strength of 785 grams, and a breaking strength of 32 lbs. After 1% of a silicone softener was applied to the treated mercerized print cloth, it had tearing strength of 940 grams and a breaking strength of 36.3 lbs. This was a 95% tearing strength retention and a 70% breaking strength retention based on the unmercerized control. This also was an 87% tearing strength retention and a 64% breaking strength retention based on the mercerized control.

EXAMPLE A solution was prepared containing 3.6% formaldehyde, 9.4% sulfuric acid, 17.7% water and 69.3% acetic acid. A piece of bleached cotton print cloth was immersed in the solution for 1 hour at room temperature (about 27 C.). The fabric was then removed from the solution and washed free of unreacted formaldehyde and acids, and dried. The fabric contained 1.94% formaldehyde, and had a dry crease recovery angle of 275 and a wet crease recovery angle of 269.

EXAMPLE 6 A solution was prepared containing 3.6% formaldehyde, 2.9% hydrochloric acid, 16.9% water, and 76.6% acetic acid. A piec of mercerized cotton print cloth Was immersed in the solution for 1 hour and then removed and washed thoroughly with water. The fabric contained 0.94% formaldehyde, had a dry crease recovery of 244, a wet crease recovery of 288, and a breaking strength of 36.5 lbs. Th breaking strength of the mercerized control fabric was 52.4 lbs. The treated fabric retained 70% of its breaking strength. The treated fabric was subjected to home launderings using a detergent. The dry crease recovery was then 232, and the wet crease recovery was 273. The fabric lost only 5% of its crease recovery. The breaking strength after the 20 launderings was 40.4 lbs.a 77% strength retention based on the mercerized control fabric.

EXAMPLE 7 Each of four samples of mercerized cotton broadcloth was treated with a difierent softening and/ or water repelling agent. These agents were (1) a 1% aqueous solution of Saparnine WL (acid salt of a complex amino organic compound), (2) a 1% solution of Sapamine WL followed by the application of a 3% aqueous emulsion of Zelan AP, (3) a 1% aqueous emulsion of Primenit VS (N,N-octadecyl ethylene urea), (4) a 1% aqueous emulsion of a silicone. Each of these agents was applied to a sample of fabric by standard procedures. Then each softened or water repellent sample was immersed in a solution equivalent to solution No. 7 in Table I of Example I, and allowed to react for one hour at room temperature (27 C.). The samples were removed and washed free of excess formaldehyde and acid. The wet and dry crease recovery angles using the different softening and water repelling agents are shown in Table IV.

Silicone 324 288 We claim: 1. A process comprising steeping a cotton textile in a solution containing, based on the weight of the solution,

about from 50% to of an organic water-soluble liquid in which water is soluble to the extent of at least 5% and selected from the group consisting of acetone, dioxane, diethylene glycol, dimethyl ether, tetrahydrofurane, formic acid, acetic acid, propionic acid, lactic acid, a mixture of benzene in acetic acid, and a mixture of xylene in tctrahydrofurane, about from 1% to 10% of an aldehyde selected from the group consisting of formaldehyde, glyoxal, 'glutaraldehyde, adipaldehyde, a-hydroxy adipaldehyde, acetaldehyde, and benzaldehyde, about from 8% to 40% of water, and about from 1% to 17.2% of a mineral acid catalyst selected from the group consisting of hydrochloric acid, sulfuric acid, and phosphoric acid at a temperature not exceeding about 45 C. to partially swell and react the cotton cellulose with the aldehyde, and removing all steeping solution from the thus-treated cotton textile to obtain a modified cotton textile characterized in that it has a combined aldehyde content of at least 0.25% based on the weight of the textile, a moisture regain value of at least 7% based on the weight of the textile, a breaking strength of at least 50% of the original untreated textile, and possessing both wet and dry wrinkle recovery.

2. The process of claim 1 wherein the organic watersoluble liquid is acetic acid.

3. The process of claim 1 wherein the aldehyde is formaldehyde.

4. The process of claim 1 wherein the mineral acid catalyst is hydrochloric acid.

5. The process of claim 1 wherein the temperature ranges about from 20 C. to 45 C.

6. A process comprising steeping a cotton textile in a solution containing, based on the weight of the solution, about from 50% to 90% of acetic acid, about from 1% to 10% of formaldehyde, about from 8% to 40% of water, and about from 1% to 17.2% of hydrochloric acid at a temperature of about from 20 C. to 45 C. to partially swell and react the cotton cellulose with the formaldehyde, 'and washing the thus-steeped cotton textile free from the steeping solution with water to obtain a modified cotton textile characterized in that it has a combined formaldehyde content of at least 0.25% based on the weight of the textile, a moisture regain value of at least 7 based on the weight "of the textile, a breaking strength of at least 50% of the original untreated textile, and possessing both wet and dry wrinkle recovery.

References Cited in the file of this patent UNITED STATES PATENTS Schappel May 25, 1954 OTHER REFERENCES

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
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Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3113826 *Jan 11, 1961Dec 10, 1963Courtaulds LtdMethod of modifying cellulose with formaldehyde using lewis acid catalysts, solutions for use in such method, and products thereof
US3173751 *Apr 26, 1961Mar 16, 1965Courtaulds LtdTextile process and composition
US3216779 *Oct 6, 1960Nov 9, 1965Bradford Dyers Ass LtdTextile materials and process for manufacturing them
US3218119 *Feb 2, 1962Nov 16, 1965American Cyanamid CoMethod of applying cyclic urea resins to cellulosic textile materials
US3230108 *Nov 16, 1962Jan 18, 1966Schweizerische ViscoseStabilisation of paper and cardboard against dimensional change
US3265463 *Nov 17, 1961Aug 9, 1966Burlington Industries IncContinuous method of imparting wet and dry crease resistance to cellulosic materials through reaction with formaldehyde
US3371983 *Dec 4, 1961Mar 5, 1968Burlington Industries IncPrewetting cellulosic fabric before introduction to dehydrating solution of formaldehyde reactant in a continuous process
US3427121 *Jun 24, 1963Feb 11, 1969Us AgricultureWrinkle-resistant cotton fabrics with improved moisture absorption
US3505002 *Dec 21, 1965Apr 7, 1970Burlington Industries IncMethod for improving wet crease recovery
US3533728 *Jul 28, 1967Oct 13, 1970Gagliardi Research CorpInorganic and/or organic cellulose swelling agents used in conjunction with cross-linking agents in fabric modification process
US3645667 *May 22, 1970Feb 29, 1972Us AgricultureNonaqueous cross linking of cellulose with a methylolated urea in the absence of an acidic catalyst
US3660011 *May 3, 1967May 2, 1972Gagliardi Research CorpDimethyl sulfoxide used as a solvent for textile treating compositions
US3663974 *Mar 6, 1968May 23, 1972Toyo Spinning Co LtdTreatment of a cross-linking agent-impregnated cellulosic fabric with a gaseous acid catalyst
US3989457 *Mar 17, 1975Nov 2, 1976Heberlein & Co. AgFinishing processes for textile materials
US4033716 *Oct 15, 1974Jul 5, 1977Ciba-Geigy AgTransfer printing process for hydrophilic fibrous material
US4035147 *Apr 2, 1974Jul 12, 1977Centre Technique De L'industrie Des Papiers, Cartons Et CellulosesCellulosic materials capable of absorbing water of aqueous solutions, and their production
US4113936 *Oct 13, 1976Sep 12, 1978S. A. Beghin-SayCross-linking of cellulose fibers in gas suspension
US4182735 *May 25, 1978Jan 8, 1980International Paper CompanyProduction of high crimp, high strength, hollow rayon fibers
US4204054 *Sep 7, 1978May 20, 1980S. A. Beghin-SayPaper structures containing improved cross-linked cellulose fibers
US4204055 *Sep 7, 1978May 20, 1980S. A. Beghin-SayCross-linked cellulose fibers
US4242411 *Mar 26, 1979Dec 30, 1980International Paper CompanyHigh crimp, high strength, hollow rayon fibers
US4396390 *Sep 4, 1981Aug 2, 1983Springs Mills, Inc.Aqueous formaldehyde textile finishing process
US4822453 *Jun 27, 1986Apr 18, 1989The Procter & Gamble Cellulose CompanyAbsorbent structure containing individualized, crosslinked fibers
US4888093 *Feb 23, 1989Dec 19, 1989The Procter & Gamble Cellulose CompanyIndividualized crosslinked fibers and process for making said fibers
US4889595 *Mar 1, 1989Dec 26, 1989The Procter & Gamble Cellulose CompanyProcess for making individualized, crosslinked fibers having reduced residuals and fibers thereof
US4889596 *Jan 30, 1989Dec 26, 1989The Proter & Gamble Cellulose CompanyProcess for making individualized, crosslinked fibers and fibers thereof
US4889597 *Mar 1, 1989Dec 26, 1989The Procter & Gamble Cellulose CompanyProcess for making wet-laid structures containing individualized stiffened fibers
US4898642 *Feb 1, 1989Feb 6, 1990The Procter & Gamble Cellulose CompanyTwisted, chemically stiffened cellulosic fibers and absorbent structures made therefrom
US6544296Feb 7, 2001Apr 8, 2003The Proctor & Gamble CompanyEnhanced fabric comprising substrates and process to provide same
US6953485Feb 7, 2001Oct 11, 2005Strike Investments, LlcEnhanced fabric comprising substrates and process to provide same
Classifications
U.S. Classification8/116.4, 536/99, 8/120, 8/182, 8/195, 8/115.6, 8/185, 8/125
International ClassificationD06M13/12, D06M13/00
Cooperative ClassificationD06M13/12
European ClassificationD06M13/12