US3739782A - Absorbent fibers of phosphorylated cellulose with ion exchange properties and catamenial tampons made therefrom - Google Patents

Abstract

Absorbent dressings, such as tampons, made from highly absorbent cellulose fibers with ion exchange properties. These fibers are obtained by phosphorylating cellulose fibers, hydrolyzing the fiber walls with acid, converting the phosphorylated fibers to the sodium salt form, mechanically refining these fibers to rupture the primary fiber wall and permit subsequent swelling or ballooning, acidifying the refined fibers to reconvert the phosphorylated cellulose into the acid form, and drying the fibers in a manner to substantially avoid appreciable hydrogen bonding.

Description

0 United States Patent 1 [111 3,739,782 Bernardin June 19, 1973 ABSORBENT FIBERS OF 3,052,593 9/1962 Battista 260/212 PHOSPHORYLATED CELLULOSE WITH 3,067,745 12/1962 Burgeni et al. 128/285 ION EXCHANGE PROPERTIES AND CATAMENIAL TAMPONS MADE THEREFROM Inventor: Leo J. Bernardin, Appleton, Wis.

Assignee: Kimberly-Clark Corporation,

Neenah, Wis.

Filed: Nov. 1, 1971 Appl, No.: 194,748

Related US. Application Data Division of Ser. No. 34,878, May 5, 1970, Pat. No, 3,691,154.

References Cited UNITED STATES PATENTS 3/1948 Manning 128/285 Rrimqry Examiner-Charles F. Rosenbaum Attorney-Daniel .l. l-lanlon, Jr., William D. Hern'ck and Raymond J. Miller [5 7 ABSTRACT Absorbent dressings, such as tampons, made from highly absorbent cellulose fibers with ion exchange properties. These fibers are obtained by phosphorylating cellulose fibers, hydrolyzing the fiber walls with acid, converting the phosphorylated fibers to the sodium salt form, mechanically refining these fibers to rupture the primary fiber wall and permit subsequent swelling or ballooning, acidifying the refined fibers to reconvert the phosphorylated cellulose into the acid form, and drying the fibers in a manner to substantially avoid appreciable hydrogen bonding.

3 Claims, No Drawings ABSORBENT FIBERS OF PHOSPHORYLATED CELLULOSE WITH ION EXCHANGE PROPERTIES AND CATAMENIAL TAMPONS MADE THEREFROM CROSS REFERENCE TO RELATED APPLICATIONS This application is a division of copending application Ser. No. 34,878 filed May 5, 1970 and now U.S. Pat. No. 3,691,154. A related application is copending application of Leo J. Bernardin, Ser. No. 30,81 1, filed April 22, 1970 and now U.S. Pat. No. 3,658,790.

BACKGROUND OF THE INVENTION lt is well know that the normal healthy vagina is acidic, having a pH in the neighborhood of about 3.8 to 4.5. At that pl-l, numerous species of microorganisms are present which play a beneficial role in providing protection and resistance to infection. During menstruation, however, a slightly alkaline pH is frequently established. Under such conditions growth of favorable microflora is inhibited while undesirable types thrive. This causes the vagina to be more susceptible to infection and inflammation during menses.

Various attempts have been made to control this condition by providing catamenial devices which act to lower the alkaline pH during menstruation to the desired pH of 4.5 or less while simultaneously absorbing discharged menstrual fluids. One of these may be found in U.S. Pat. No. 3,091,241 to Kellett which employs glyceryl triacetate in an absorbent tampon as a physiological biostat or automatic pl-l controller.

In another U.S. Pat. No. 3,187,747 to Burgeni et al., catamenial tampons are made from multicomponent alloy fibers in which one of the components is absorbent, such as regenerated cellulose, while the other is an acidifying polymer, such as carboxymethyl cellulose in hydrogen form.

in each of the above patents, the tampon structure required at least two components, one performing the necessary absorbency function, while the other acts as the pH controller.

The present invention is directed to a cellulose fiber product which combines the pH control and the absorbency function in one fiber, without requiring chemical adjuvants or alloys.

in the copending Bernardin application, referenced above, phosphorylated cellulose fibers in sodium salt form were found to have a markedly increased absorbency over unmodified cellulose. The product was obtained by chemically substituting phosphate groups for hydroxyls on the cellulose, hydrolyzing the fiber walls with acid, then converting the substituted and hydrolyzed fibers to the salt form by ion exchange, and solvent drying or otherwise drying the fibers in a manner to substantially avoid appreciable hydrogen bonding. It was found that the phosphorylated fibers in their acid form, before conversion to salt form, and whether solvent dried or not, showed no improvement in absorbency over unmodified cellulose, while the salt form was found to be up to 5 times as absorbent. These results appeared to confirm the belief, at that time, that in order for substituted celluloses to have a sufficient increase in absorbency to warrant commercial use, it was necessary for the cellulose to be in an alkaline salt form. Prior art developments involving carboxymethyl cellulose having particular degrees of substitution also supported this belief.

However, as work continued it was found that even greater absorbency could be developed in the phosphorylated cellulose in salt form if the fibers were refined for at least one minute before drying. Such refining increased absorbent properties almost threefold over the unrefined fibers. It was then found, rather unexpectedly, that if these refined fibers were reconverted to the acid form, they retained much of the increased absorbency developed by refining and exhibited by the salt form fibers. This finding seemed to contradict the earlier conclusion that the acid form of phosphorylated cellulose shows no increase in absorbency over unmodified pulp. This unexpected result immediately opened up a number of possibilities for use of the product in areas where absorbency and ion exchange complement one another.

SUMMARY OF THE INVENTION Phosphorylated fibers in acid form with improved absorbency characteristics combined with high ion exchange capacity are produced by first saturating cellulose pulp sheets in a phosphorylating bath; drying and reacting the saturated sheets at elevated temperature; dispersing the reacted sheets in water, which preferably is deionized, and washing the reactant therefrom; converting the washed phosphorylated fibers to the acid form by treatment with acid; converting the acidified fibers to sodium salt form; mechanically refining the fibers in aqueous dispersion; reconverting the refined fibers to acid form; and finally drying the fibers in a manner to substantially avoid appreciable hydrogen bonding of the fibers to each other during the water removal process. When formed into mats the resulting fibers exhibit high ion exchange capacity and much higher capillary suction pressure and absorbent capacity than unmodified cellulose fibers.

These fibers are markedly superior in absorbent capacity to phosphorylated fibers in the acid form which have not been refined. They are also superior in absor bency to fibers which have been refined while in acid form. Accordingly, in order to obtain this improved absorbency in the acid-form fibers of this invention, it is necessary to first refine the fibers in salt form and then reconvert the refined fibers to acid form.

The preferred method of phosphorylating is the urea phosphate method, wherein the fibers are reacted at a temperature of from about to C for about 5 to over 30 minutes in a solution of urea and phosphoric acid. Other known but less satisfactory methods of phosphorylation may be used including treatment with phosphorous oxychloride and pyridine; phosphorous oxychloride and phosphoric acid; phosphorous oxychloride and dioxane; phosphorous oxychloride alone, and alkali metal salts of phosphoric acid.

When convertingthe washed phosphorylated fibers to acid form immediately after phosphorylation, cold acid may be used, but it is preferred to use hot acid because the latter more readily hydrolyzes the fiber walls which is highly desirable in developing the improved capillary suction pressures described herein.

In converting the phosphorylated fibers to salt form the alkali preferably employed is a dilute solution of sodium hydroxide. However, other solutions of basic salts such as sodium carbonates, phosphates and the like may be used.

In order to dry the fibers in a manner to avoid hydrogen bonding, conventional solvents such as acetone, alcohol, alcohol followed by hexane, and the like may be used.

Freeze drying may also be used since such a drying method also substantially avoids hydrogen bonding.

It is the primary object of this invention to provide chemically modified cellulose fibers which in their acid form have markedly improved fluid absorbency characteristics.

Another object is to provide absorbent pads from fibers which have high absorbency combined with high ion exchange capacity.

Other features, objects and advantages of the invention will become apparent by reference to the following specification.

DESCRIPTION OF THE PREFERRED EMBODIMENTS In a preferred embodiment, four sheets of unbeaten, bleached, northern softwood, kraft pulp weighing about 14 grams each were immersed for about 30 minutes in a bath consisting of 50 percent urea, 18 percent orthophosphoric acid, and 32 percent water by weight. The saturated pulp sheets were drained to a consistency of 1 part fiber to 3 parts by weight of solution. The moist sheets were dried and reacted or cured in an oven for 20 minutes at 160C. The cured sheets were dispersed in deionized water and the resulting slurry washed free of the treating solution by several rinses with deionized water using a suction filter.

The filtered material which is believed to be comprised of cellulose monoammonium monohydrogen phosphate was dispersed in a 3 percent solution of hot hydrochloric acid and soaked at a temperature of between 60 and 70C for one-half hour. The acid form of phosphorylated fiber thus obtained was washed free of excess acid and separated into two portions. One portion was refined in a conventional PFI laboratory refiner for 2% minutes at 10 percent consistency and solvent dried from acetone, the other portion was converted to salt form by soaking in a 5 percent solution of Na cO for one-half hour. The fiber was washed again and then refined at percent consistency in a conventional PFl laboratory refiner for 2% minutes. The refined pulp was reconverted to acid form, i.e., a pH of 3, with hydrochloric acid, washed free of excess acid, and then solvent dried from acetone.

Absorbency characteristics in terms of capillary suction pressure of the two kinds of phosphorylated cellulose in acid form obtained by the above described process were then compared to each other and to an unmodified cellulose which was also refined for 2% minutes and solvent dried.

Results were as follows:

WATER CONTENT IN GRAMS OF H O PER GRAM OF FIBER Phosphorylated Pulp in Acid Form Absorption of liquid water as a function of capillary suction pressure on airlaid mats of fiber is measured by means of a known capillary tension cell apparatus of the type described in an article from the Textile Research Journal, Vol. 37, No. 5, May, 1967, pp. 356-366, A. A. Burgeni and C. Kapur, Capillary Sorption Equilibria in Fiber Masses. Absorption capabilities for a fiber mass are cited in the number of grams of water per gram of fiber which a mat of fibers will absorb under the specified capillary suction head or pressure indicated.

The results indicate that when phosphorylated pulp is merely converted to acid form and then refined, it shows no measurable improvement over unmodified pulp.

The results also show very clearly that when the phosphorylated pulp is refined in its salt form before converting back to acid form there is a dramatic increase in its absorbent properties.

It became apparent that the refining of the fibers in salt form and converting to acid form has a different effect on the fibers than when they are originally refined while in acid form.

Microscopic examination of the fibers, before and after refining, indicated that, before refining, the fibers of the phosphorylated pulp in acid form look very much like ordinary wood pulp fibers when wet with the fiber walls substantially intact, while the walls of the phosphorylated pulp in salt form showed signs of rupture of fraying with some ballooning of the internal structure in a number of places. Refined unmodified pulp and phosphorylated pulp in acid form also appeared quite similar, showing some fraying of the fiber wall, but little ballooning or swelling. The refined phosphorylated fibers in salt form, on the other hand, exhibited considerable ballooning and swelling, as the internal structure expanded down the length of the fiber with only a few confining rings appearing where the primary fiber wall remained unruptured and intact. The ballooned and swelled form of the main internal body of the fiber structure was retained when these fibers in salt form were converted back to acid form.

Refining phosphorylated fibers in the salt form prior to reconversion to the acid form is therefore considered to be a necessary step in the preparation of the highly absorbent fibers in the acid form of this invention. Without such refining the acid form of phosphorylated fibers show no improvement in absorbency. In structure therefore, the acid form of phosphorylated fibers must be substantially stripped or denuded of the primary fiber wall in order to obtain the demonstrated improvement in absorbency.

In considering this improved acid form of phosphorylated cellulose fiber for tampon useage it was also determined that ion exchange capacity is significant. Accordingly, ion exchange capacity was tested by potentiometric titration with 0.1N sodium hydroxide. As indicated in the Burgeni et al. US. Pat. No. 3,187,747, the acidifying capacity of a tampon in vivo can be approximated in terms of the volume of 0.1N sodium hydroxide consumed by the fibers in an environment of 0.8 percent NaCl solution at pH values up to about 4.5. It is also indicated that in distilled water, less sodium hydroxide would be required for equivalent capacity because NaCl tends to aid in the liberation of hydrogen ions. Accordingly the ion exchange capacity exhibited under actual use would be higher than the capacity indicated by titration in distilled water.

A number of samples of the acid form of phosphorylated cellulose fibers refined in salt form as described above were titrated in distilled water with 0.1N NaOH to determine ion exchange capacities. One gram of fiber was found to consume about 12.5 ml of 0.1N sodium hydroxide in reaching a pH of about 4.5. Accordingly a normal tampon weight of about 3 grams would have adequate capacity for maintaining an acid pH in the vagina under even the most severe conditions of use. Since such a tampon acts to maintain the menstrual fluids at an acid pH, the surrounding skin surface is also maintained slightly acid whereby the environment for the useful microflora stays favorable.

In view of this high ion exchange capacity it is not necessary to make the entire absorption device of the phosphorylated fibers of this invention. They may be admixed with ordinary wood pulp fibers, with phosphorylated fibers in salt form, with other absorptive fibers, or with resilient fibers as set forth in the prior art to provide better expansion properties when used in compressed form.

While the improved pulp fibers are indicated as being of particular use in catamenial tampons, they may also be employed where the dual characteristics of high absorbency and high ion exchange capacity are required.

The invention is particularly applicable to fibers converted from wood pulp because of their low cost and ready availability. However, other fibers normal to the papermaking art may also be employed such as hemp, jute, esparto, cereal straws, flax, bagasse, bamboo, reeds, cotton linters, kenaf and the like.

What is claimed is:

1. An improved absorbent dressing for absorbing and simultaneously acidifying body fluids in contact therewith, comprising a fibrous mat of phosphorylated cellulose fibers in acid form, said fibers being characterized by a structure in which a major portion of the primary wall of each of said fibers is broken away leaving the main internal body of each of said fibers substantially unconfined by said primary wall, said internal body structure being in a swelled and ballooned condition, whereby said fiber mat provides improved capacity for absorbing aqueous fluids.

2. The dressing of claim 1 in which said mat is in the form of a tampon suitable for internal deployment in body cavities.

3. The dressing of claim 1 in which said mat has other absorbent fibers admixed therewith.

Claims (2)

1. 2. The dressing of claim 1 in which said mat is in the form of a tampon suitable for internal deployment in body cavities.
2. 3. The dressing of claim 1 in which said mat has other absorbent fibers admixed therewith.