US2536285A - Process of making high wet strength paper - Google Patents

Process of making high wet strength paper Download PDF

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US2536285A
US2536285A US686125A US68612546A US2536285A US 2536285 A US2536285 A US 2536285A US 686125 A US686125 A US 686125A US 68612546 A US68612546 A US 68612546A US 2536285 A US2536285 A US 2536285A
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paper
nitrogen peroxide
wet
strength
wet strength
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Herman C N Heckel
Arthur C Salisbury
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Champion Paper and Fibre Co
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63Inorganic compounds

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  • This invention relates to high wet strength paper and to a method of manufacturing it.
  • Wet strength paper is ordinarily regarded as paper which retains 40 to 50% or more of its strength when it becomes thoroughly Wet. This high wet strength paper has assumed a place of considerable importance in the manufacture of bags and other wrappings for wet foods, construction papers, map and blueprint paper, toweling, paper fabrics, twine, etc.
  • Wet strength may be imparted to paper by parchmentizing with sulfuric acid, zinc chloride or the like; but such processes also impart a stiffness and harshness, reduce the porosity and otherwise profoundly change the physical properties of the paper.
  • Certain resin-forming materials may be incorporated with the papermaking fibers in the beater or may be used to impregnate the paper web, the resinous properties being subsequently developed in the paper by the aid of heat and of a suitable catalyst.
  • Such materials are relatively expensive, and if the necessary conditions of temperature, time, concentration, etc. are not strictly controlled, curing of the resin is likely to be more or less incomplete, resulting in variations in the degree of wet strength in the iinished paper. In methods where the resin-producing materials are added to the beater, adequate retention of the resin in the sheet is an additional problem.
  • One object of the present invention is to produce a paper which when wet has high tensile strength, high bursting strength, and good abrasion resistance. Another object is to produce a paper of high wet strength properties without serious impairment of its flexibility, porosity, softness. absorptlve capacity or other physical properties. A further object is to impart high wet strength properties to paper economically. Another object is to produce high wet strength papers which are uniform in quality and substantially free from variations due to processes which depend upon curing operations. Another object is to produce high wet strength paper in which the bonding agents is formed from the cellulose fibers of the sheet. Other objects of the invenltion will be apparent from the hereinafter describedprocess.
  • the fibers become more or less bonded together with a water-resistant cement to produce a paper having high wet strength properties.
  • 'Ihis amounts to a cementing of the fibers in situ in the sheet; consequently the desired results are obtained only with a formed web of interlaced cellulose bres such as is found in a sheet of paper.
  • cellulose pulp as such is treated with nitrogen peroxide it can subsequently be formed into a sheet of paper only with great difliculty and the sheets made therefrom do not possess wet strength characteristics;
  • the action of nitrogen peroxide on the cellulose bers in the paper sheet according to the present invention appears in some respects to be similar to a controlled or selective parchmentizing, but is limited to the surface of the bers.
  • the exact mechanism of the reaction is not clearly understood it may be that the nitrogen peroxide reacts with absorbed moisture of the fibers to form nitric acid, with subsequent formation of a solution of nitrogen peroxide in nitric acid and this may act upon the fibers, probably forming a plastic gel-like material on the surface which is precipitated when the sheet of paper is treated with water to form a water resistant adhesive.
  • the web of paper is improved in wet strength and wet abrasion resistance with no further processing such as heating or drying or curing.
  • the paper may contain chemical wood pulp, groundwood, cotton, or other cellulosic bers. In the case of papers of abnormally high moisture content, there may be sufficient acid developed in theL paper to producey a deleterious parchmentizing effect.
  • the temperature has little effect on the rate of production of wet strength but high temperatures are conducive to the secondarv reaction wherein oxidation to carboxvl groups takes place. Room temperature is satisfactory for most purposes.
  • the nitrogen peroxide mav contain other gases inert to itself and cellulose but in such cases the rate of action is reduced.
  • the maior portion of the wet Istrength is imparted during the first minute.
  • a sheet of paper contacted by liouid nitrogen peroxide at about '70 l"4 for 1 minute, followed by immediate removal of free nitrogen peroxide and then immersion in water developed a wet bursting strength as determined bv the Mullen tester of 24 points: a similar sheet contacted for 2 minutes developed a wet bursting strength of 25 points.
  • a third sheet contacted for minutes developed a wet bursting strength of 30 points while a fourth sheet contacted for 60 minutes developed a wet bursting strength of 39. points.
  • the Solvent must be capable of forming solutions of sufficient strength to bring about the reouired effect on the paper within a reasonable time but should be substantiallv inert. i. e.. unaffected bv nitrogen peroxide, and should itself have no detrimental effect on the paper.
  • the wet strength continues to increase as the interval of contact is increased and then levels oil or decreases.
  • the time of contact can convenientlv be varied to obtain varying degrees of wet strengthywbere only a partial development ofthe wet strength properties of a paper mav be required it can be produced by a shorter interval of peroxide contact. For example, paper which has been dipped in and removed from a water.
  • tbe paper should be well freed of mechanically held or adsorbed nitrogen peroxide by any suitable means before treatment with Where gaseous nitrogen peroxide has been employed this is not so important. butjwbere the paper has been saturated with licluid nitrogen peroxide or with a nitrogen peroxide solution. the liquid should be removed by drainage, suction, evaporation or the like before the water treatment as otherwise an overall parchmentizingv eilect is obtained which renders the paper stiff and bard. For some. purposes this stiilness may not be. objectionable and it mav even be desired, but if the excess. mechanically held nitrogen peroxide is removed before applying water to the sheet, the paper will retain in a very large measure practically all of its original softness and exibilitv while acquiring improved wet strength properties.
  • the step of treating the paper with water following tbe nitrogen peroxide treatment produces a two fold result: the inter-uber wet-strength bonding material is precipitated. regenerated. or in some manner developed, and the action of the nitrogen peroxide present in the paper is terminated.
  • the paper is immersed in a stream of water or is passed through a series of water baths.
  • the paper is Washed with copioutquantities of water until substantially free of acid to prevent any acidic deterioration.
  • Papers made from well bleached p'ulns in addition to developing wet strength properties are improved in color by the nitrogen peroxide treatment. Sized and unsized paper may be processed equally well but in some cases the sizing effect is somewhat adversely affected by the nitrogen peroxide. T
  • Example 1 A sheet of bleached kraft paper was placed in a large glass chamber, the air was displaced with substantially dry nitrogen peroxide gas, and ad dltional nitrogen peroxide was introduced in a slow stream. After the paper had remained in contact with the gas at room temperature for about 20 minutes it was removed and washed in water until free of acid by passing it through 3 tanks of running water. The paper was then dried. The product had a wet tensile strength of 6.9 pounds per inch While the wet tensile strength of the untreated vpaper was 1.0 pound per inch. The dry tensile strength -of the product was 20.1 pounds per inch as compared to 13 pounds per inch for the untreated paper.
  • the wet bursting strength of the product was 18 points Mullen and the dry value was 36 points while the untreated paper had a Wet Mullen too low to be measured and a dry Mullen of 24.5 points. 'I'he general appearance, flexibility, feel, porosity, and absorptiveness were unimpaired.
  • the treated paper withstood severe abrasion while wet without disturbance of the surface fibers. Scotch tape firmly pressed against the dried treated paper and stripped therefrom failed to lift any fibers from the sheet.
  • Example 2 A sheet of 55-pound paper, 25 x 38-500 basis weight, made from bleached chemical wood pulp was immersed in liquid nitrogen peroxide for 1 minute at a temperature just below its boiling point, e. g. about 70% F. The paper was removed from the bath and allowed to' drain momentarily, then air was drawn throughthe paper for about 2 minutes until substantially all the mechanically held nitrogen peroxide was evaporated; the paper was then immersed in running water until free of acid, and dried. The treated paper had a wet bursting strength of 25 points Mullen and a dry bursting strength of 63 points. Corresponding values for the untreated paper were 6 points wet and 39 points dry. Wet and dry tensile were markedly increased, and the sheet remained soft, porous, and unchanged in appearance from its original condition.
  • Example 3 oughlyin water and dried.
  • the product had a wet Mullen test of 21 points and a dry Mullen of 40 points as compared to 3 points wet and 42 points dry for the untreated paper.
  • a transparent, greaseproof, glassine-like sheet may be obtained.
  • paper is saturated with liquid nitrogen peroxide, and while in this condition it is subjected to pressure, such as by passing it through the nip of two press rolls, following which it is freed of excess nitrogen peroxide by a stream of air and is then washed with water.
  • the resulting sheet is more or less vtransparent depending largely upon the degree of pressure exerted and in addition to having wet strength has marked greaseprooi' properties.
  • the process of our invention also improves the dry strength of paper in some respects. This is particularly true in and moderately beaten pulps.
  • the dry tensile strength of the sheet which was made from a lightly beaten kraft pulp was 13 pounds per inch, whereas the dry tensile of the same paper after it was treated was 20.1 pounds per inch.
  • the dry bursting strength of a treated lightly-beaten sheet is from 40% to 100% higher than that of a similar but untreated sheet.
  • a sheet made from unbeaten cellulosic fibers and having little strength can be transformed by this process into a sheet showing considerable toughness, both when dry and when wet.
  • commercially dry paper is contacted with substan tially dry nitrogen peroxide for a time sufficient to yield improved wet strength properties but insuflicient to deleteriously alter the dry properties, then is freed of substantially all the unreacted that is, mechanically held nitrogen peroxide, and finally is washed with water until free of acid. Little or no acid parchmentizing takes place and the sheet is substantially unaltered in'softness; flexibility, porosity, and absorptiveness.
  • the Wet strength papers of this invention are similar to cloth and can be used in water, dried, and reused several times without disintegrating.
  • wet strength developing agent can be applied in gaseous or liauid form affords a wide range oi' operating conditions.
  • interval of contact of the paper with the nitrogen peroxide is specified in the claims, it is understood to mean that time which the paper is within the gas chamber or .peroxide bath; it does not include, for example, an interval during which a roll of nitrogen peroxide treated paper is allowed to stand before it is treated with f water.
  • Process of imparting wet strength properties to paper which comprises exposing a web or sheet -oi? paper to nitrogen peroxide and then treating the paper with an excess of water to produce partial gelatinization of the surface of the fibers and limiting the time of exposure of the paper to the nitrogen peroxide in relation to the concentration ⁇ of nitrogen peroxide used, to a degree such that the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulosel is less than 0.2%.
  • the time of exposure of the paper to the nitrogen peroxide is less than one hour.
  • Process of imparting wet strength properties topaper without materially decreasing the dry strength, porosity or softness of the paper which comprises exposing a web or sheet of paper to nitrogen peroxide, removing mechanically-held nitrogen peroxide from the paper, immersing the paper inwater and limiting the time of exposure papers made from lightly of the paper to the nitrogen peroxide in relation to the concentration of nitrogen peroxide used, to a degree such that the carboxy content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%
  • Process of improving the wet strength of paper which comprises contacting paper in web or sheet form with an atmosphere containing substantial proportions of gaseous nitrogen peroxide for an interval from 15 minutes to 4 hours, treating said paper with an excess of water and limiting the time of exposure of the paper to the nitrogen peroxide ln relation to the concentration of nitrogen peroxide in the said atmosphere to a degree such that the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%.
  • Process of improving the wet strength of paper without materially impairing its softness, porosity or dry strength properties which comprises contacting paper in web or sheet form with gaseous nitrogen peroxide for from 5 to 60 minutes, and treating said paper with an excess of water whereby the cellulose in the paper has a carboxyl content of less than 1% and a nitrogen content of less than 0.2%.
  • Process of improving the wet strength of paper without materially impairing its softness, porosity, or dry strength properties which comprises contacting paper in web or sheet form with liquid nitrogen peroxide for about one minute, removing the mechanically held nitrogen vperoxide from said paper, and treating said paper with an excess of Water, whereby the cellulose in the paper has a carboxyl content of less than 1% and a nitrogen content of less than 0.2%
  • Process of imparting wet strength and greaseproof properties to paper which comprises immersing paper in liquid nitrogen peroxide, subjecting said paper to pressure while still saturated with liquid nitrogen peroxide, removing mechanically held nitrogen peroxide, treating said paper with water and limiting the time of exposure to nitrogen peroxide to a degree suchthat the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%.
  • Paper having improved wet strength properties and substantially unchanged softness, porosity and absorptiveness said Wet strength properties produced by exposing paper to nitrogen peroxide and then treating the paper with an excess of water and limiting the time of exposure of the paper to the nitrogen peroxide in relation to the concentration of nitrogen peroxide used, to a degree such that the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%.

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Description

Jan.
H. C. N. HECKEL ET AL PROCESS Oll MAKING HIGH WET STRENGTH PAPER Filed July 25, 1946 Patented Jan. 2, 1951 PROCESS F MAKING HIGH WET STRENGTH PAPER Herman C. N. Heckel, Oxford, and Arthur C. Salisbury, Hamilton, Ohio, assignors to The Champion Paper and Fibre Company, Hamilton, Ohio, a corporation of Ohio Application July 25, 1946, Serial No. 686,125
This invention relates to high wet strength paper and to a method of manufacturing it.
Paper as normally manufactured, unlike fabrics, loses practically all its strength when it becomes thoroughly wet; accordingly, for many purposes it is desirable to impart "Wet strength to paper. Wet strength paper is ordinarily regarded as paper which retains 40 to 50% or more of its strength when it becomes thoroughly Wet. This high wet strength paper has assumed a place of considerable importance in the manufacture of bags and other wrappings for wet foods, construction papers, map and blueprint paper, toweling, paper fabrics, twine, etc.
Wet strength may be imparted to paper by parchmentizing with sulfuric acid, zinc chloride or the like; but such processes also impart a stiffness and harshness, reduce the porosity and otherwise profoundly change the physical properties of the paper. Certain resin-forming materials may be incorporated with the papermaking fibers in the beater or may be used to impregnate the paper web, the resinous properties being subsequently developed in the paper by the aid of heat and of a suitable catalyst. Such materials are relatively expensive, and if the necessary conditions of temperature, time, concentration, etc. are not strictly controlled, curing of the resin is likely to be more or less incomplete, resulting in variations in the degree of wet strength in the iinished paper. In methods where the resin-producing materials are added to the beater, adequate retention of the resin in the sheet is an additional problem.
One object of the present invention is to produce a paper which when wet has high tensile strength, high bursting strength, and good abrasion resistance. Another object is to produce a paper of high wet strength properties without serious impairment of its flexibility, porosity, softness. absorptlve capacity or other physical properties. A further object is to impart high wet strength properties to paper economically. Another object is to produce high wet strength papers which are uniform in quality and substantially free from variations due to processes which depend upon curing operations. Another object is to produce high wet strength paper in which the bonding agents is formed from the cellulose fibers of the sheet. Other objects of the invenltion will be apparent from the hereinafter describedprocess.
We have discovered that when a formed webl .9 Claims. (Cl. 8-116) or sheet of paper is treated ilrst with nitrogen l y trogen peroxide is from 5 to 60 minutes.
with water, the fibers become more or less bonded together with a water-resistant cement to produce a paper having high wet strength properties. 'Ihis amounts to a cementing of the fibers in situ in the sheet; consequently the desired results are obtained only with a formed web of interlaced cellulose bres such as is found in a sheet of paper. On the contrary, if cellulose pulp as such is treated with nitrogen peroxide it can subsequently be formed into a sheet of paper only with great difliculty and the sheets made therefrom do not possess wet strength characteristics;
We have further discovered that by controlling the time and intensity of the treatment, it is possible to impart the above mentioned wet strength properties Without materially altering flexibility, porosity, softness, and other desirable properties of the paper.
The action of nitrogen peroxide on the cellulose bers in the paper sheet according to the present invention appears in some respects to be similar to a controlled or selective parchmentizing, but is limited to the surface of the bers. Although the exact mechanism of the reaction is not clearly understood it may be that the nitrogen peroxide reacts with absorbed moisture of the fibers to form nitric acid, with subsequent formation of a solution of nitrogen peroxide in nitric acid and this may act upon the fibers, probably forming a plastic gel-like material on the surface which is precipitated when the sheet of paper is treated with water to form a water resistant adhesive. Whatever the explanation may be the web of paper is improved in wet strength and wet abrasion resistance with no further processing such as heating or drying or curing.
Neither the kind of paper nor its moisture content appears to be critical in carrying out the invention; the paper may contain chemical wood pulp, groundwood, cotton, or other cellulosic bers. In the case of papers of abnormally high moisture content, there may be sufficient acid developed in theL paper to producey a deleterious parchmentizing effect.
The time of treatment necessary for the development of wet strength depends upon the concentration of nitrogen peroxidev employed. In treating paper with gaseous nitrogen peroxide, the greater part of the Wet strength results from the ilrst 15 to 20 minutes of exposure; thereafter the wet strength increases slowly and after from about l to 4 hours starts to decrease. Advantageously the exposure of the paper to gaseous ni- This is illustrated in the accompanying drawing, Figure 1 of which is a graph showing the increase in dry and wet bursting strength, as measured by the Mullen tester, of a paper made from lightly beaten bleached kraft pulp when treated with gaseous nitrogen peroxide for various intervals and then with water. The increase in bursting strength is expressed in terms of percentage dry bursting strength of the untreated sheet. The temperature has little effect on the rate of production of wet strength but high temperatures are conducive to the secondarv reaction wherein oxidation to carboxvl groups takes place. Room temperature is satisfactory for most purposes. The nitrogen peroxide mav contain other gases inert to itself and cellulose but in such cases the rate of action is reduced.
In the case where liouid nitrogen peroxide is employed, the maior portion of the wet Istrength is imparted during the first minute. For instance, a sheet of paper contacted by liouid nitrogen peroxide at about '70 l"4 for 1 minute, followed by immediate removal of free nitrogen peroxide and then immersion in water developed a wet bursting strength as determined bv the Mullen tester of 24 points: a similar sheet contacted for 2 minutes developed a wet bursting strength of 25 points. a third sheet contacted for minutes developed a wet bursting strength of 30 points while a fourth sheet contacted for 60 minutes developed a wet bursting strength of 39. points. In comparison the untreated paper had a wet bursting strength of about 5 points and a dry bursting strength oi 40 points. The rate of increase of wet bursting strength fwhen treated with liouid nitrogen peroxide is shown in Figure 3 in terms of percentage drv bursting strength of the untreated sheet. A lower treating temthe undiluted gas.
Where a solution of nitrogen peroxide is employed in treating the paper. the Solvent must be capable of forming solutions of sufficient strength to bring about the reouired effect on the paper within a reasonable time but should be substantiallv inert. i. e.. unaffected bv nitrogen peroxide, and should itself have no detrimental effect on the paper.
In general. a 20 minute interval of contact with the paper when undiluted gaseoivs nitrogen neroxide or a 30% solution of nitrogen peroxide in carbon tetrachloride is used, and a 1 minute ini terval when liquid nitrogen peroxide is used. is
sufficient to obtain a high degree of wet strength, of the order of at least 50 to 60"/n of the. dry strength of the untreated paper. As indicated by the previous data and the aceomnanving drawing the wet strength continues to increase as the interval of contact is increased and then levels oil or decreases. Thus the time of contact can convenientlv be varied to obtain varying degrees of wet strengthywbere only a partial development ofthe wet strength properties of a paper mav be required it can be produced by a shorter interval of peroxide contact. For example, paper which has been dipped in and removed from a water.
bath of liquid nitrogen peroxide as quickly as possible. then immediately passed over a suction box and treated with water has increased wet strength.
Ordinarily exposures of beyond 1 hour are unnecessary regardless of whether the nitrogen peroxide be liquid, gaseous or in solution. The softness, exibility, porosity, and tear strength do decrease with length of treatment with the nitrogen peroxide but become signicant only over a protracted time of exposure, of the order of several hours where gaseous nitrogen peroxide is employed; therefore long periods of contact with the nitrogen peroxide are preferably avoided. Papers having a high alpha cellulose content show the least decrease in softness.
Neither oxidation nor nitration appears to bev a primary reaction in imparting wet'strength to paper with nitrogen peroxide. Papers produced according to the herein described process in the preferred form where the interval of contact is of the order of about 20 minutes for gaseous nitrogen peroxide and about 1 minute for liquid nitrogen peroxide are found to have a carboxyl content on the cellulose of less than 1% and only a negligible amount of nitrogen (less than 0.2% N). On long exposure of the paper to nitrogen peroxide, asfor example, 2 or 3 hours contact with the gas, a noticeable increase in carboxyl content is obtained but with little or no effect on the wet strength although as noted above, there may be a decrease in softness and flexibility. Advantageously a relatively short peroxide -treatment is employed whereby the optimum increase in wet strength for the least amount of deleterious oxidation is obtained.
At the conclusion of the nitrogen peroxide treatment, tbe paper should be well freed of mechanically held or adsorbed nitrogen peroxide by any suitable means before treatment with Where gaseous nitrogen peroxide has been employed this is not so important. butjwbere the paper has been saturated with licluid nitrogen peroxide or with a nitrogen peroxide solution. the liquid should be removed by drainage, suction, evaporation or the like before the water treatment as otherwise an overall parchmentizingv eilect is obtained which renders the paper stiff and bard. For some. purposes this stiilness may not be. objectionable and it mav even be desired, but if the excess. mechanically held nitrogen peroxide is removed before applying water to the sheet, the paper will retain in a very large measure practically all of its original softness and exibilitv while acquiring improved wet strength properties.
The step of treating the paper with water following tbe nitrogen peroxide treatment produces a two fold result: the inter-uber wet-strength bonding material is precipitated. regenerated. or in some manner developed, and the action of the nitrogen peroxide present in the paper is terminated. Usuallv the paper is immersed in a stream of water or is passed through a series of water baths. Preferably the paper is Washed with copioutquantities of water until substantially free of acid to prevent any acidic deterioration.
Papers made from well bleached p'ulns in addition to developing wet strength properties are improved in color by the nitrogen peroxide treatment. Sized and unsized paper may be processed equally well but in some cases the sizing effect is somewhat adversely affected by the nitrogen peroxide. T
The following examples are givento illustrate the invention:
Example 1 A sheet of bleached kraft paper was placed in a large glass chamber, the air was displaced with substantially dry nitrogen peroxide gas, and ad dltional nitrogen peroxide was introduced in a slow stream. After the paper had remained in contact with the gas at room temperature for about 20 minutes it was removed and washed in water until free of acid by passing it through 3 tanks of running water. The paper was then dried. The product had a wet tensile strength of 6.9 pounds per inch While the wet tensile strength of the untreated vpaper was 1.0 pound per inch. The dry tensile strength -of the product was 20.1 pounds per inch as compared to 13 pounds per inch for the untreated paper. The wet bursting strength of the product was 18 points Mullen and the dry value was 36 points while the untreated paper had a Wet Mullen too low to be measured and a dry Mullen of 24.5 points. 'I'he general appearance, flexibility, feel, porosity, and absorptiveness were unimpaired. The treated paper withstood severe abrasion while wet without disturbance of the surface fibers. Scotch tape firmly pressed against the dried treated paper and stripped therefrom failed to lift any fibers from the sheet.
In a modified process a sheet of the same paper was left in the gas chamber for only minutes, and then allowed to stand in the room for an interval of minutesbefore it was washed. An' increase in wet Mullen and tensile properties not quite as large as the above was obtained.
Example 2 A sheet of 55-pound paper, 25 x 38-500 basis weight, made from bleached chemical wood pulp was immersed in liquid nitrogen peroxide for 1 minute at a temperature just below its boiling point, e. g. about 70% F. The paper was removed from the bath and allowed to' drain momentarily, then air was drawn throughthe paper for about 2 minutes until substantially all the mechanically held nitrogen peroxide was evaporated; the paper was then immersed in running water until free of acid, and dried. The treated paper had a wet bursting strength of 25 points Mullen and a dry bursting strength of 63 points. Corresponding values for the untreated paper were 6 points wet and 39 points dry. Wet and dry tensile were markedly increased, and the sheet remained soft, porous, and unchanged in appearance from its original condition.
Example 3 oughlyin water and dried. The product had a wet Mullen test of 21 points and a dry Mullen of 40 points as compared to 3 points wet and 42 points dry for the untreated paper.
According to another modification of the invention a transparent, greaseproof, glassine-like sheet may be obtained. In this case paper is saturated with liquid nitrogen peroxide, and while in this condition it is subjected to pressure, such as by passing it through the nip of two press rolls, following which it is freed of excess nitrogen peroxide by a stream of air and is then washed with water. The resulting sheet is more or less vtransparent depending largely upon the degree of pressure exerted and in addition to having wet strength has marked greaseprooi' properties.
In addition to improving wet strength properties, the process of our invention also improves the dry strength of paper in some respects. This is particularly true in and moderately beaten pulps. Thus in Example 1, the dry tensile strength of the sheet which was made from a lightly beaten kraft pulp, was 13 pounds per inch, whereas the dry tensile of the same paper after it was treated was 20.1 pounds per inch. The dry bursting strength of a treated lightly-beaten sheet is from 40% to 100% higher than that of a similar but untreated sheet. A sheet made from unbeaten cellulosic fibers and having little strength can be transformed by this process into a sheet showing considerable toughness, both when dry and when wet.
In the preferred form of our invention commercially dry paper is contacted with substan tially dry nitrogen peroxide for a time sufficient to yield improved wet strength properties but insuflicient to deleteriously alter the dry properties, then is freed of substantially all the unreacted that is, mechanically held nitrogen peroxide, and finally is washed with water until free of acid. Little or no acid parchmentizing takes place and the sheet is substantially unaltered in'softness; flexibility, porosity, and absorptiveness.
The Wet strength papers of this invention are similar to cloth and can be used in water, dried, and reused several times without disintegrating.
They are useful as toweling, drapery substitutes,
filtering material, twisting paper, disposable sheet material, impregnating papers, etc. The fact that the wet strength developing agent can be applied in gaseous or liauid form affords a wide range oi' operating conditions.
Where an interval of contact of the paper with the nitrogen peroxide is specified in the claims, it is understood to mean that time which the paper is within the gas chamber or .peroxide bath; it does not include, for example, an interval during which a roll of nitrogen peroxide treated paper is allowed to stand before it is treated with f water.
We claim: i
1. Process of imparting wet strength properties to paper which comprises exposing a web or sheet -oi? paper to nitrogen peroxide and then treating the paper with an excess of water to produce partial gelatinization of the surface of the fibers and limiting the time of exposure of the paper to the nitrogen peroxide in relation to the concentration `of nitrogen peroxide used, to a degree such that the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulosel is less than 0.2%.
2. Process of claim 1 wherein the paper has not materially lost dry strength. porosity, or softness,
and the time of exposure of the paper to the nitrogen peroxide is less than one hour.
3. Process of imparting wet strength properties topaper without materially decreasing the dry strength, porosity or softness of the paper, which comprises exposing a web or sheet of paper to nitrogen peroxide, removing mechanically-held nitrogen peroxide from the paper, immersing the paper inwater and limiting the time of exposure papers made from lightly of the paper to the nitrogen peroxide in relation to the concentration of nitrogen peroxide used, to a degree such that the carboxy content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%
4. Process of improving the wet strength of paper which comprises contacting paper in web or sheet form with an atmosphere containing substantial proportions of gaseous nitrogen peroxide for an interval from 15 minutes to 4 hours, treating said paper with an excess of water and limiting the time of exposure of the paper to the nitrogen peroxide ln relation to the concentration of nitrogen peroxide in the said atmosphere to a degree such that the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%.
5. Process of improving the wet strength of paper without materially impairing its softness, porosity or dry strength properties which comprises contacting paper in web or sheet form with gaseous nitrogen peroxide for from 5 to 60 minutes, and treating said paper with an excess of water whereby the cellulose in the paper has a carboxyl content of less than 1% and a nitrogen content of less than 0.2%.
6. Process of improving the wet strength of paper without materially impairing its softness, porosity, or dry strength properties which comprises contacting paper in web or sheet form with liquid nitrogen peroxide for about one minute, removing the mechanically held nitrogen vperoxide from said paper, and treating said paper with an excess of Water, whereby the cellulose in the paper has a carboxyl content of less than 1% and a nitrogen content of less than 0.2%
7. Process for increasing the wet strength of paper which comprises treating paper with a'solution of nitrogen peroxide in an inert solvent,
8. Process of imparting wet strength and greaseproof properties to paper which comprises immersing paper in liquid nitrogen peroxide, subjecting said paper to pressure while still saturated with liquid nitrogen peroxide, removing mechanically held nitrogen peroxide, treating said paper with water and limiting the time of exposure to nitrogen peroxide to a degree suchthat the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%.
9. Paper having improved wet strength properties and substantially unchanged softness, porosity and absorptiveness, said Wet strength properties produced by exposing paper to nitrogen peroxide and then treating the paper with an excess of water and limiting the time of exposure of the paper to the nitrogen peroxide in relation to the concentration of nitrogen peroxide used, to a degree such that the carboxyl content of the cellulose in the paper is less than 1% and the nitrogen content of the cellulose is less than 0.2%.
HERMAN C. N. HECKEL. ARTHUR C. SALISBURY.
REFERENCES CITED The following references are of record in the le of this patent:
UNITED STATES PATENTS Number Name Date 1,699,779 Cochran Jan. 22, 1929 1,850,808 Redd Mar. 22, 1932 1,917,400 Staud et al July 11, 1933 1,934,956 Wait Nov. 14, 1933 2,018,244 Alm Oct. 22, 1935 2,232,990 Yackel et al Feb. 25, 1941 2,338,587 Kenyon et al Jan. 4, 1944 2,423,707 Kenyon et al July 8, 1947 2,448,892 Kenyon et al Sept. 7, 1948 f OTHER REFERENCES Frantz, Absorbable Cotton, Paper and Gauze," Annals of Surgery, July 1943, pages 116, 117, 125, 126.

Claims (1)

1. PROCESS OF IMPARTING WET STRENGTH PROPERTIES TO PAPER WHICH COMPRISES EXPOSING A WEB OR SHEET OF PAPER TO NITROGEN PEROXIDE AND THEN TREATING THE PAPER WITH AN EXCESS OF WATER TO PRODUCE PARTIAL GELATINIZATION OF THE SURFACE OF THE FIBERS AND LIMITING THE TIME OF EXPOSURE OF THE
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE967144C (en) * 1953-04-19 1957-10-10 Harry Pauling Dipl Ing Process for the oxidation of cellulose by treatment with nitrogen dioxide
US3608560A (en) * 1968-11-07 1971-09-28 Sutton Res Corp Smokable product of oxidized cellulosic material
US4365059A (en) * 1981-08-03 1982-12-21 The United States Of America As Represented By The Secretary Of The Army Nitration of cellulose

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US1699779A (en) * 1927-07-15 1929-01-22 Westinghouse Electric & Mfg Co Process for improving tensile strength of fabric materials
US1850808A (en) * 1931-12-03 1932-03-22 Nat Paper Napkin Mfg Company Method of treating and seasoning paper
US1917400A (en) * 1930-12-31 1933-07-11 Eastman Kodak Co Nitration of cellulose with a nitrogen oxide
US1934956A (en) * 1928-12-19 1933-11-14 Justin F Wait Process for dyeing goods
US2018244A (en) * 1931-10-07 1935-10-22 Dennison Mfg Co Paper product and method of making
US2232990A (en) * 1938-07-15 1941-02-25 Eastman Kodak Co Preparation of oxycellulose
US2338587A (en) * 1941-02-24 1944-01-04 Eastman Kodak Co Method of treating cellulose esters
US2423707A (en) * 1945-03-02 1947-07-08 Eastman Kodak Co Fabric or gauze of uniformly oxidized cellulose
US2448892A (en) * 1945-01-01 1948-09-07 Eastman Kodak Co Oxidation of cellulose

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1699779A (en) * 1927-07-15 1929-01-22 Westinghouse Electric & Mfg Co Process for improving tensile strength of fabric materials
US1934956A (en) * 1928-12-19 1933-11-14 Justin F Wait Process for dyeing goods
US1917400A (en) * 1930-12-31 1933-07-11 Eastman Kodak Co Nitration of cellulose with a nitrogen oxide
US2018244A (en) * 1931-10-07 1935-10-22 Dennison Mfg Co Paper product and method of making
US1850808A (en) * 1931-12-03 1932-03-22 Nat Paper Napkin Mfg Company Method of treating and seasoning paper
US2232990A (en) * 1938-07-15 1941-02-25 Eastman Kodak Co Preparation of oxycellulose
US2338587A (en) * 1941-02-24 1944-01-04 Eastman Kodak Co Method of treating cellulose esters
US2448892A (en) * 1945-01-01 1948-09-07 Eastman Kodak Co Oxidation of cellulose
US2423707A (en) * 1945-03-02 1947-07-08 Eastman Kodak Co Fabric or gauze of uniformly oxidized cellulose

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE967144C (en) * 1953-04-19 1957-10-10 Harry Pauling Dipl Ing Process for the oxidation of cellulose by treatment with nitrogen dioxide
US3608560A (en) * 1968-11-07 1971-09-28 Sutton Res Corp Smokable product of oxidized cellulosic material
US4365059A (en) * 1981-08-03 1982-12-21 The United States Of America As Represented By The Secretary Of The Army Nitration of cellulose

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