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Manufacture of cellulosic product

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US3096228A
US3096228A US8139361A US3096228A US 3096228 A US3096228 A US 3096228A US 8139361 A US8139361 A US 8139361A US 3096228 A US3096228 A US 3096228A
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Prior art keywords
web
wet
strength
moisture
glyoxal
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Winterton U Day
Harold F Donnelly
Henry L Rohs
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Kimberly-Clark Corp
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Kimberly-Clark Corp
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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
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/06Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
    • 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
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/18Reinforcing agents
    • D21H21/20Wet strength agents
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/17Glyoxal and polyaldehyde treatment of textiles

Description

July 2, 1963 W. U. DAY ETAL y 1963 w. u. DAY ETAL 3,096,228

MANUFACTURE OF CELLULOSIC PRODUCT Filed Jan. 9, 1961 3 Sheets-Sheet 2 July 2, 1963 w. 0. DAY ETAL MANUFACTURE OF CELLULOSIC PRODUCT 3 Sheets-Sheet 3 Filed Jan. 9, 1961 Nu ON a. Q 0. N. 9 0 Q v N Ii whom iwlo E.

United States Patent Ofiice 3,@-%,2Z8 Patented July 2, 1963 MANUFACT F CELLULOS1 PRQDUCT Winterton U. Day, Neenah, and Harold F. Donnelly, Ap-

pleton, Wis., and Henry L. Rolls, North Tonawanda,

N.Y., assignors to Kimberly-(Hark Corporation, Neenah, Wis, a corporation of Delaware Filed Jan. 9, 1%1, Ser. No. 81,393 6 Claims. (Cl. 162112) This invention relates to a method of treating absorbent paper webs to impart wet strength thereto. The invention is particularly directed to a method for imparting temporary wet strength to absorbent paper webs which are subsequently fabricated into disposable products such as toilet tissure, facial cleansing tissue, absorbent towels, and the like.

A major object of the invention is to provide a method of treating absorbent paper webs with a wet strength agent in a manner to impart temporary wet strength to the treated web, without loss of other desirable physical characteristics of the web.

An equally important object is to provide an improved facial tissue or the like which has the physical characteristic of resisting wet rupture for a short period of time after being wetted, but thereafter rapidly disintegrating to prevent clogging of sanitary disposal systems during passage therethrough.

Other objects and advantages will become readily apparent to persons skilled in the art upon examination of the description and drawings, as will various modifications, without departure from the inventive concepts as defined in the appended claims.

in the drawings:

FIG. 1 is a fragmentary schematic view illustrating a method for applying wet strength material to the paper Web, after the Web is creped off from the surface of the drier on a creped wadding paper machine.

FIG. 2 is another schematic view illustrating a method for applying wet strength material to a paper web in a converting operation separate from the paper machine.

FIG. 3 illustrates an alternate method of applying the wet strength material in a separate operation.

FIG. 4 illustrates still another method of applying the wet strength material to both sides of a multiply paper web in a converting operation separate from the paper machine.

FIG. 5 is a chart illustrating the effect of relative humidity conditions during aging on the development of the wet strength in treated papers.

While it is Well known that absorbent papers may be treated with various agents to impart permanent wet strength properties thereto, no satisfactory treatment has heretofore been developed which imparts relatively transient wet strength properties to the paper while retaining other desirable properties. Ideally, absorbent paper products such as toilet tissue, facial cleansing tissue, and toweling should have some degree of wet strength while retaining the desirable qualities of high absorptive ability and softness, but still must be readily disposable in conventional sanitary systems. Absorbent papers treated by prior art wet strength processes tend to lose some of their original softness and absorbent properties, and do not readily disintegrate in water after use without the aid of alkali or other chemicals. Thus, they often contribute to, or are the cause of, clogging in wet sanitary systems.

Wet strength generally is desirable in absorbent papers used for sanitary purposes to compensate for an inherent low tensile strength in the cross direction, i.e., transverse of the sheet, resulting from the limitations imposed by high speed forming and subsequent creping. Low cross direction tensile strength is the most common cause for failure when the papers are used in contact with moisture. Machine direction tensile strength in these papers is usually more than adequate, even for wet use. By increasing overall wet strength, the inherent deficiency in cross direction tensile strength is minimized and the potential usefulness of these papers greatly increased.

Thus, it is obvious that Wet strengthened papers, in general, have increased functional uses over papers with no Wet strength and can be employed where ordinary papers fail. However, when conventional wet strength treated papers are disposed of after use, care must be taken not to deposit them in toilets or other wet sanitary systems because they do not disintegrate readily. Domestic sanitary systems are thus constantly in danger of becoming clogged or stopped-up from careless disposition of wet strength papers. Such stoppages result in considerable inconvenience and expense to the user.

The present invention is directed to eliminating the disadvantages attendant the non-disintegration of ordinary wet strengthened papers after disposal, by treating the paper with a Wet strength agent in a manner to insure initial, but short-lived, resistance to wet rupture, without inhibiting subsequent rapid disintegration of the web when immersed in water. The above objective is accomplished by treating absorbent webs with an aqueous solution of glyoxal in a manner to control the amount of moisture added to the web during such treatment and thereafter aging the treated web at non-elevated room temperatures and under controlled humidity conditions to develop Wet strength. The wet strength developed in webs thus treated remains adequate to resist wet rupture for a period of about one minute after immersion in Water, but thereafter rapidly decays to a degree which permits disintegration of the web, and substantially disappears about 3 minutes after wetting. Thus, the paper treated in accordance with this invention disintegrates quickly in water, similar to absorbent paper products having no Wet strength treatment.

While it is known to use glyoxal per se as a wet strengthening agent for paper webs, and in the textile industry for modification of textile properties to improve crease resistance, the known treatments require the application of extrinsic heat, or cooperation with other chemicals, to develop wet strength properties. None of the prior art teachings recognize, however, that by applying aqueous solutions of glyoxal to absorbent papers under carefully controlled conditions of moisture addition and retention, it is possible to develop a highly fugitive wet strength, without employing extrinsic heat, which permits the treated papers to disintegrate rapidly after about one minute of immersion in water, while retaining wet strength properties when slightly moist as a result of use.

For example, it is known that wet strength may be significantly improved in absorbent paper by saturating a preformed sheet by immersion or spraying thereof with a dilute aqueouse solution containing glyoxal as its sole active ingredient and subsequently heating the treated sheet to a temperature of at least 212 F. for a limited period to react the glyoxal with the cellulose. While this known method results in a high degree of wet strength when employed in the manufacture :of heavier absorbent toweling, it has several disadvantages when employed in the manufacture of toilet paper, facial-type tissues, or light weight towels from creped cellulose wadding. Applying aqueous solutions of glyoxal to webs of the latter by saturation followed by drying with heat, as taught in the prior art, tends to embrittle the fibers and also causes an undesirable loss in tear strength of the web rendering subsequent converting steps difficult and expensive. Webs treated thus, break frequently when stretched as re quired during subsequent conversion, and if stretched to a lesser degree to avoid breaks, result in an undesirably harsh product.

The concept herein taught avoids the prior art disadvantages in part by applying an aqueous solution of glyoxal to a dry web in an amount such that the amount of moisture added to the web during such application is controlled relative to total moisture content, and in part by aging the glyoXal-treated web to develop wet strength at room temperatures and under controlled conditions of moisture content, instead of thereafter subjecting the treated web to elevated temperatures. The absorbent paper, thus treated, is characterized by an acceptable degree of temporary wet strength effective for normal use, while rapidly disintegrating within a few minutes after immersion in ordinary tap water, thus eliminating disposal problems.

Although this process is generally applicable to all types of absorbent paper, it is particularly applicable to creped cellulose wadding such as toilet tissue, facialtype tissue and light weight toweling. These webs are customarily made on Yankee cylinder or Fourdrinier machines, and creped off a Yankee drier at a moisture content of from about 3 to 7% based on the weight of the dry web. Drier basis weight of the web, i.e., basis weight before creping, usually is in the range of 7 to 20 pounds per 3000 square foot ream. The web is creped from the drier to a crepe ratio within the range between about 1.5 and 2.6. A crepe ratio of 1.5 means that one unit length of creped web will pull out to measure 1.5 unit lengths of substantially flat web. Pulps used for forming the web may include the usual bleached and unbleached commercial pulps, such as sulfite, kraft, soda and groundwood.

Generally, the process of the present invention comprises the following steps: A preformed Web of dry absorbent paper, i.e., having a moisture content of about 3 to 7% by weight based on the weight of the bone dry paper, is treated by applying thereto an aqueous solution of glyoxal in an amount such that the moisture added to the web by the applied solution brings the total moisture content of the Web to more than 4% and not more than 20% by weight. The treated web, without intermediate drying, may be wound into large storage rolls for transfer to further converting operations, or alternatively, may be converted and packaged directly after the glyoxal solution is applied. These converting operations usually include interfolding the treated web and inserting the interfolded packs in dispenser cartons, or rolling the treated web into small rolls and wrapping the rolls to obtain packages for commercial distribution. In either case, it is essential to maintain in the web a specified amount of the moisture, after the glyoxal application, in order for wet strength to develop. Usually, the sealed protection offered packaged items by the wrapper or carton under ordinary storage conditions serves to retain the moisture long enough for the full temporary wet strength to develop. In the case where unwrapped rolls are aged, or where abnormally dry conditions exist in storage, it is preferred that relative humidity be controlled at between 50% to 75%, to prevent excessive moisture loss, for at least 24 hours and preferably longer. If the treated web is allowed to dry out under ambient conditions without taking steps to control moisture content, wet strength development is inadequate and not of commercial significance.

The glyoxal used in the process may be any of the commercial or technical grades now available. It is preferred that the purer grades be used. Most commercial grades are supplied in a 30% solution and are strongly acid, having a pH range of l to 2. It is preferred to adjust the pH of the solution to between about 4 to 6 with a suitable alkali, such as soda ash, before application to the web. The glyoxal may be applied in the 30% concentration as commercially supplied, or further diluted. No matter what concentration is employed, the amount of moisture added to the web during application of the solution, must be controlled within the range specified.

The ultimate extent of wet strength developed is proportional to the amount of glyoxal present in the web. About 0.3% by weight, based on the bone dry weight of the web, appears to be a practical lower limit and about 5% by weight, an economically feasible upper limit. Amounts in excess of 5% produce additional wet strength but at disproportionate cost.

FIG. 1 illustrates the application of glyoxal to a web at the dry end of a Yankee Fourdrinier or cylinder creped wadding paper machine. The formed tissue web 2 is creped off Yankee drier 4 by doctor blade 6. An aqueous solution of glyoxal 12, in supply tray 11 is picked up by roll 10 and applied in a thin film to metering roll 8 which applies a controlled amount of glyoxal solution to the bottom surface of creped web '2. A pressure roll 7 is lightly pressed against the web 2 as it passes over metering roll '8 to aid penetration of the applied solution into the web. The treated web is then wound into roll 14 which may be stored under controlled humidity conditions, or immediately converted into consumer products. The amount of glyoxal applied is controlled by metering roll 8, which may be a plain rubber roll, a metal or rubber intaglio roll, or a metal or rubber roll with a textured or patterned surface.

In FIG. 2, web 24, is unwound from supply roll 22 and passes over patterned applicator roll 28 which dips directly into a glyoxal solution 30 in vat 25 and applies the solution to the underside of web 24. Applicator roll 28 may turn in either direction depending upon how much solution it is desired to apply to the web. When rotated in the same direction and speed as the moving web, less less solution is applied than when rotated counter tothe direction of web movement. Doctor blade 27, or 29, depending on direction of rotation of roll 28, wipes 0E excess solution leaving -a controlled amount to be transferred to the web by applicator roll 28. The treated web is rolled up into storage roll 26 and allowed to develop wet strength under conditions which substantially maintain in the web the amountof moisture added thereto during the application of the glyoxal solution.

In FIG. 3, web 34 is unwound from supply roll 32 and passes over transfer roll 31 which applies glyoxal solution to the underside of said web 34. The solution 38 is picked up from vat 37 by metering roll 33 which in this case is of the intaglio type. Excess solution is doctored off by blade 35 and the remaining amount transferred to roll 31 which applies the solution in a controlled amount to the underside of web 34. Rubber covered pressure roll 39 coacting with transfer roll 31 is optional, but is a useful means for accelerating penetration of the applied solution. The treated web then is maintained under controlled humidity conditions for a period suflicient to permit wet strength to develop in the presence of moisture added on during application of the glyox-al solution.

FIG. 4 shows an alternate method of spray application to a multiply paper web 44 supplied from roll 42. Spray nozzle 45a directs a fine patterned spray of minute drops of glyoxal solution onto the top surface of the upper p13 while spray nozzle 45b directs a similar spray of solution onto the underside of the lower ply. Interacting pressure rolls 46a and 46b aid in pressing the solution into the web. The treated web then proceeds directly to an interfolder or roll winder, not shown, for conversion into suitable end products, which are stored for at least 24 hours under controlled humidity conditions. It will be understood that other methods of controlled spray application, such as by a brush roll, may also be used. While this embodiment shows spraying the glyoxal solution onto both surfaces of the multiply web, adequate wet strength may be obtained by spraying, or otherwise applying, more solution on only one side thereof.

When the treated sheet is subsequently subjected to a converting operation which requires stretching and ironing, as is done to singly ply bulk rolls obtained from the paper machine, the preferred amount of moisture addon is about 2%, providing a total moisture content in the sheet of between 5 to 9%. At this rate of moisture addon, the treated sheet appears to be and feels dry, and tear strength and feel properties, or hand, are not adversely affected.

When the sheet to be treated has already been stretched and ironed, as is customary in the production of absorbent facial-type cleaning and toilet tissue, as much as 13% moisture may be added to the Web, but total moisture content in the treated web should not exceed 20%.

In the converting process, two or more plies of the creped tissue as received from the paper machine are supplied from a multi-roll backs tand to a conventional stretching and ironing apparatus. The juxtaposed plies are stretched until the crepe ratio is about 1.2 and then ironed between unheated rotating pressure rolls. This stretching and ironing operation contributes to the characteristic softness and cosmetic feel desired in tissues of this type. If total moisture in the treated web is allowed to exceed about 20% there are several undesirable results. Excess moisture tends to release the crepe and results in a weak, undesirably stiff sheet with poor drape characteristics. An excessively wet web also compacts easily, and such compaction adversely affects absorbent properties and desirable softness and feel characteristics. When total moisture is considerably in excess of 20%, the web is weakened in the area of moisture application to a point where frequent and costly breaks occur.

Applying the glyoxal in a manner to control the amount of water simutlaneously applied to the web, and aging at specific moisture content and non-elevated temperature are critical to the invention.

Non-elevated temperatures refer to room temperature, or temperatures normally maintained in manufacturing and storage areas, which may range from about 60 F. to about 80 F.

In the early stages of this development, attempts were made to apply rglyoxal to webs without saturation in order to retain softness and feel characteristics, followed immediately by heat treating, which, in accordance with prior art teachings, was believed essential to the development of wet strength. Surprisingly, although the amount of glyoxal retained in the sheet and the temperature used to cure the sheet were in the range taught in the prior art, it was found that little, if any, wet strength developed. It was only when the moisture content of the Web, during treatment with glyoxal solution, was controlled at between 4% and 20% by weight, followed by aging at nonelevated temperature while maintaining total moisture content as taught herein, that the desired fugitive wet strength was achieved.

Retention of the moisture added as a result of applying the glyoxal solution aids in uniform migration of the glyoxal throughout the sheet after application.

Cross CD Percent Direction Tensile, Wet (Wet/ Tensile, Wet, dryX) Dry 1. Heat Dried 355 44 12.4 2. Air Dried 868 59 16.0 3. Polyethylene wrapped 340 60 17. 7

(Tensile strength is given in grams per 3 inches of width. Samples were immersed between blotters in tap water and tested for wet tensile after 45 seconds of soaking.)

The samples in which substantially all of the moisture added during the glyoxal treatment was retained de veloped the best wet strength overnight while the heat dried sample developed least, and was, in fact, below the minimum cross direction wet tensile strength necessary for it to be classified as a wet strength facial tissue product.

FIG. 5 further demonstrates the effect which aging glyoxal treated webs at controlled humidity and moisture content has on wet strength development. Two-ply facial tisue having an initial moisture content of about 4% was sprayed with a 30% solution of glyoxal adjusted to a pH of about 4.0 with soda ash. Moisture added on :by the solution was about 2% by weight, bringing the total content to about 6%. Total glyoxal retained was about 0.65% by weight. Selected samples were aged in storage areas under conditions where relative humidity was controlled at 20%, 50%, and 75 respectively. The samples stored at 20% RH. (about 4% moisture in air) developed negligible wet strength. Those stored at 50% RH. (about 6% moisture) showed satisfactory development of about 18% wet strength, while those stored at 75% RH. (about 10% moisture) showed a more rapid and slightly higher development, leveling off at about 25% wet strength. In each case, the largest increment in wet strength developed in the first 24 hours.

At 20 %relative humidity, the total moisture content of the web dropped to about 4%, indicating that the total moisture content must be maintained in excess of 4% and preferably at 6% or over, but not exceeding 20%, to achieve satisfactory results.

Example A conventional two-ply facial tissue sheet had glyoxal applied as shown in PEG. 2. The starting web had a moisture content of about 5% and the moisture added during the glyoxal application amounted to about 5% by weight. An aqueous solution containing 30% glyoxal by weight( with pH adjusted to about 4, was used. Thus, the total amount of glyoxal added was about 1.5% by weight and total moisture content of the treated web was about 10%. The treated web was immediately interfolded, inserted in cartons, and aged for 24 hours under humidity conditions which maintained the total moisture content in the web at about 10%. Cross direction tensile strengths were then measured on four random samples with the following results:

(Tensile strength given in gm./ strip.)

Wet tensile of two-ply facial tissue, with no wet strength treatment, is almost negligible and difiicult to measure, however, it is estimated to be less than about 20 gum/3 strip, or less than 7% of the original dry tensile strength. Thus, the facial tissue treated in the manner taught herein shows an increase in initial wet strength, followed by a rapid decrease of wet strength 3 minutes after saturation with ordinary tap water. A tissue of this type is strong enough to be sneeze-proof or satisfactory for short time use in the presence of water, yet disintegrates readily when disposed of in a wet sanitary system.

Other methods and means of applying the principles of this invention may be used without departing from its spirit or scope as specifically pointed out and described in the above specification and the appended claims.

What is claimed is:

1. The process of producing an absorbent paper having temporary wet strength which comprises providing a substantially dry web of absorbent paper having an initial moisture content of about 3 to 7% by Weight, applying to said web an aqueous solution of glyoxal in an amount to obtain a total moisture content in said web after application of more than 4% and not more than 20% by weight of said web, and substantially maintaining said moisture content in said web while aging said web at room temperature to develop wet strength therein.

2. As a new article of manufacture, an improved absorbent paper having temporary wet strength and produced in accordance with the process of claim 1.

3. In a process of producing an absorbent paper having temporary wet strength, the steps of transferring to a substantially dry absorbent paper having an initial moisture content of about 3 to 7% by weight a metered amount least 24 hours under conditions wherein relative humidity is controlled at between to whereby said total moisture content is retained in said paper to develop wet strength therein.

4. The process of producing an absorbent paper having temporary wet strength which comprises forming, drying, and creping a web of absorbent cellulose wadding at a moisture content of from 3 to 7%, applying to said web an aqueous solution of glyoxal in an amount to obtain a total moisture content in said web of more than 4% and not more than 20% by weight, and substantially maintaining said moisture content while aging the treated web at about room temperature to develop wet strength therein.

5. The process of producing an absorbent paper having temporary wet strength which comprises providing a preformed creped web of substantially dry absorbent paper having a drier basis weight of between 7 and 20 pounds per 3000 square feet and an initial moisture content of from 3 to 7% by weight, transferring to said web a metered amount of a solution consisting essentially of glyoxaland water in a manner such that the glyoxal applied to said web amounts to from 0.3% to 5% based on the dry weight of said web while the water applied to said web from said solution provides a total moisture content in said web of more than 4% and not more than 20% by weight, and thereafter aging said web for at least 24 hours at room temperatures and under conditions which maintain said total moisture content in said web.

6. In a method of imparting water-dispersible wet strength to a two-ply web of absorbent facial-type tissue having an initial moisture content of 3 to 7% by Weight, the steps of applying to at least one surface of said twoply web an aqueous solution of glyoxal in an amount to deposit in said web from about 0.3% to 5% glyoxal by weight and enough moisture to bring the total moisture content of said two-ply web to more than 4% and less than 20% by weight, and thereafter aging the treated web for at least 24 hours at room temperature and under conditions which substantially maintain said total moisture content in said treated web.

References Cited in the file of this patent UNITED STATES PATENTS 1,119,816 Fogart-y Dec. 8, 1914 2,043,351 Fournes set al. June 9, 1936 2,622,960 Woods Dec. 23, 1952

Claims (1)

  1. 4. THE PROCESS OF PRODUCING AN ABSORBENT PAPER HAVING TEMPORARY WET STRENGTH WHICH COMPRISES FORMING, DRYING, AND CREPING A WEB OF ABSORBENT CELLULOSE WADDING AT A MOISTURE CONTENT OF FROM 3 TO 7%, APPLYING TO SAID WEB AN AQUEOUS SOLUTION OF GLYOXAL IN A AMOUNT TO OBTAIN A TOTAL MOISTURE CONTENT IN SAID WEB OF MORE THAN 4% AND NOT MORE THAN 20% BY WEIGHT, AND SUBSTANTIALLY MAINTAINING SAID MOISTURE CONTENT WHILE AGING THE TREATED WEB AT ABOUT ROOM TEMPERATURE TO DEVELOP WET STRENGTH THEREIN.
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Cited By (20)

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US3332835A (en) * 1964-01-29 1967-07-25 Union Carbide Corp Process of forming wood-fiber insulation board containing sulfine polymer, aldehyde and mineral acid and board thereof
US3484275A (en) * 1965-05-17 1969-12-16 Scott Paper Co Electrostatic deposition of compositions on sheet materials utilizing pre-existing friction induced electrostatic charges on said sheet materials
JPS57126896U (en) * 1981-02-04 1982-08-07
US4603176A (en) * 1985-06-25 1986-07-29 The Procter & Gamble Company Temporary wet strength resins
US4981557A (en) * 1988-07-05 1991-01-01 The Procter & Gamble Company Temporary wet strength resins with nitrogen heterocyclic nonnucleophilic functionalities and paper products containing same
US5008344A (en) * 1988-07-05 1991-04-16 The Procter & Gamble Company Temporary wet strength resins and paper products containing same
US5038997A (en) * 1990-02-26 1991-08-13 Brown & Williamson Tobacco Corporation Water resistant paperboard and method of making same
US5085736A (en) * 1988-07-05 1992-02-04 The Procter & Gamble Company Temporary wet strength resins and paper products containing same
US5138002A (en) * 1988-07-05 1992-08-11 The Procter & Gamble Company Temporary wet strength resins with nitrogen heterocyclic nonnucleophilic functionalities and paper products containing same
EP0672787A2 (en) * 1994-03-18 1995-09-20 James River Corporation Of Virginia Prewettable high-softness paper product having temporary wet strength
EP0768425A2 (en) * 1995-09-18 1997-04-16 James River Corporation Of Virginia Prewettable high softness paper product having temporary wet strength
US5695607A (en) * 1994-04-01 1997-12-09 James River Corporation Of Virginia Soft-single ply tissue having very low sidedness
EP0905318A2 (en) * 1997-09-26 1999-03-31 Fort James Corporation A soft chemi-mechanically embossed absorbent paper product and method of making same
US6319361B1 (en) 1996-03-28 2001-11-20 The Procter & Gamble Company Paper products having wet strength from aldehyde-functionalized cellulosic fibers and polymers
US20050045295A1 (en) * 2003-09-02 2005-03-03 Kimberly-Clark Worldwide, Inc. Low odor binders curable at room temperature
US20050247417A1 (en) * 2002-07-10 2005-11-10 Maurizio Tirimacco Multi-ply wiping products made according to a low temperature delamination process
US20060014884A1 (en) * 2004-07-15 2006-01-19 Kimberty-Clark Worldwide, Inc. Binders curable at room temperature with low blocking
US20060124261A1 (en) * 2003-09-02 2006-06-15 Lindsay Jeffrey D Method of making a clothlike pattern densified web
US20070051484A1 (en) * 2003-09-02 2007-03-08 Hermans Michael A Paper sheet having high absorbent capacity and delayed wet-out
US20070187056A1 (en) * 2003-09-02 2007-08-16 Goulet Mike T Low odor binders curable at room temperature

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US1119816A (en) * 1911-12-18 1914-12-08 John C Fogarty Process of and machine for making paper.
US2043351A (en) * 1935-06-01 1936-06-09 Int Cellucotton Products Method of making a tissue paper product
US2622960A (en) * 1948-03-16 1952-12-23 A P W Products Company Inc Glyoxal treatment of absorbent paper to improve wet strength

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US1119816A (en) * 1911-12-18 1914-12-08 John C Fogarty Process of and machine for making paper.
US2043351A (en) * 1935-06-01 1936-06-09 Int Cellucotton Products Method of making a tissue paper product
US2622960A (en) * 1948-03-16 1952-12-23 A P W Products Company Inc Glyoxal treatment of absorbent paper to improve wet strength

Cited By (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3332835A (en) * 1964-01-29 1967-07-25 Union Carbide Corp Process of forming wood-fiber insulation board containing sulfine polymer, aldehyde and mineral acid and board thereof
US3484275A (en) * 1965-05-17 1969-12-16 Scott Paper Co Electrostatic deposition of compositions on sheet materials utilizing pre-existing friction induced electrostatic charges on said sheet materials
JPS57126896U (en) * 1981-02-04 1982-08-07
US4603176A (en) * 1985-06-25 1986-07-29 The Procter & Gamble Company Temporary wet strength resins
US5008344A (en) * 1988-07-05 1991-04-16 The Procter & Gamble Company Temporary wet strength resins and paper products containing same
US5085736A (en) * 1988-07-05 1992-02-04 The Procter & Gamble Company Temporary wet strength resins and paper products containing same
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