EP0057212A1 - Method for producing a high quality, water absorbent, cellulosic sheet having high surface-perceived softness - Google Patents

Method for producing a high quality, water absorbent, cellulosic sheet having high surface-perceived softness

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Publication number
EP0057212A1
EP0057212A1 EP19810902213 EP81902213A EP0057212A1 EP 0057212 A1 EP0057212 A1 EP 0057212A1 EP 19810902213 EP19810902213 EP 19810902213 EP 81902213 A EP81902213 A EP 81902213A EP 0057212 A1 EP0057212 A1 EP 0057212A1
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EP
European Patent Office
Prior art keywords
web
sheet
treated
level
treatment step
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP19810902213
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German (de)
French (fr)
Inventor
Yong Woon Lim
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Individual
Original Assignee
Individual
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Filing date
Publication date
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Publication of EP0057212A1 publication Critical patent/EP0057212A1/en
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • D21H25/00After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
    • D21H25/005Mechanical treatment
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21FPAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
    • D21F11/00Processes for making continuous lengths of paper, or of cardboard, or of wet web for fibre board production, on paper-making machines
    • D21F11/14Making cellulose wadding, filter or blotting paper
    • 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
    • D21H17/14Carboxylic acids; Derivatives thereof

Definitions

  • This invention is directed to a method for producing a highly absorbent cellulosic sheet having excellent over-all quality and a high level of surface- perceived softness, respectively, which is capable of being employed in high softness grades of tissue and towel.
  • U. S. 3,844,880 to Meisel et al.; and U. S. 3,903,342 to Roberts et al., respectively, describe the addition of materials such as the above mentioned debonding agents to an aqueous slurry of cellulosic fibers to minimize hydrogen bonding in an attempt to increase softness.
  • the above chemical debonding agents comprise surfactants such as those described in the Hervey et al. U. S. patents, Nos . 3,554,862; 3,554,863; and 3,395,708.
  • the subject invention contemplates treating the cellulose fibers in the formed web with a chemical bonding inhibitor having an acidic pH. More specifically, the cellulosic web immediately after formation preferably has an initial pH of not less than about 6.0, and preferably not less than about 6.5, and more preferably not less than about 7.0. At least one surface of the web is treated with the chemical bonding inhibitor, and the pH of the treated web immediately after the treatment step is not more than about 5.0, and preferably not more than about 4.5, and more preferably not more than about 4..0, and most preferably not more than about 3.0.
  • a method for producing a highly absorbent, cellulosic sheet which exhibits excellent over-all quality and a high degree of surface-perceived softness.
  • a schematic drawing depicting a process configuration is set forth in FIGURE 1.
  • an aqueous furnish including cellulose papermaking fibers is initially formed.
  • the cellulosic fibers have undergone some degree of lignin modification, such as at least partial chemical treatment, to produce materials such as chemimechanical pulp, semichemical pulp, chemical pulp, or mixtures thereof.
  • lignin modification such as at least partial chemical treatment
  • Suitable materials from which the above cellulose fibers can be derived include the usual species of coniferous and deciduous pulpwood, the cellulosic components being preferably produced from coniferous pulpwood because of its greater fiber length.
  • the aqueous furnish is transported to a headbox 2 at a level sufficient to permit the formation of a substantially dry sheet upon completion of the hereinafter described dewatering and thermal drying steps , respectively, without requiring further drying thereof subsequent to creping.
  • the consistency of the aqueous furnish used in forming the subject wet web is desirably maintained at a level of from about 0.05% by weight, and more preferably from about 0.1% by weight, based on the total weight of cellulosic fibers in the aqueous furnish, up to a pre- ferred consistency of about 1.0% by weight, and more 5 preferably up to about 0.75% by weight.
  • a wet web 1 is then formed by deposition of the aqueous furnish onto a web forming means 3 , typically a conventional papermaking system including a foraminous conveying means 4 such as a Fourdrinier wire, Stevens former, or the like.
  • a foraminous conveying means 4 such as a Fourdrinier wire, Stevens former, or the like.
  • Dewatering of the wet web is then provided prior to the thermal drying operation typically employing a nonthermal dewatering means 5.
  • the nonthermal dewatering step is usually accomplished by various means for imparting mechanical compaction to the web 1 such as vacuum boxes, slot boxes, coacting press rolls, or combinations thereof.
  • the wet web 1 is de watered by subjecting same to a series of vacuum boxes and/or slot boxes, as shown in FIGURE 1. Thereafter, the web is further dewatered by subjecting same to the compressive forces exerted by nonthermal dewatering means such as, for example, a pair of rolls, followed by a pressure roll coacting with a thermal drying means .
  • the wet web 1 is carried by the foraminous conveying means 4 through the nonthermal dewatering means 5, where it is dewatered to a consistency of at least about 5%, preferably at least 10%, and more preferably at least 15%, up to a consistency of preferably about 50%, and more preferably up to about 45%, and most preferably up to about 35%.
  • the cellulosic web formed, as described above preferably has an initial pH of at least about 6 in order to minimize corrosion problems which can occur with respect to the foraminous conveying means, as well as other portions of the papermaking equipment if the pH per se is too low. More preferably, the initial pH of the web is maintained at a level, as previously described.
  • the wet web 1 prior to the thermal drying step is treated with an acidic chemical material 6 , which inhibits the formation of papermaking bonds between adjacent cellulosic fibers.
  • an acidic chemical material 6 which inhibits the formation of papermaking bonds between adjacent cellulosic fibers.
  • this chemical bonding inhibitor per se is a "chemical debonding agent" .
  • these materials are well-known in the prior art, and are preferably substantially cationic in nature. Examples of suitable chemical bonding inhibitor materials include Quaker 2001 (Quaker Chemical) , Ceranine HCS (Sandoz) , Leomin KP (Hoechst AG) , and Amasoft-PM (American Color and Chemical) .
  • the bonding inhibitor 6 employed for treatment of the web is provided at a treatment level which is sufficient to minimize the formation of the above described hydrogen bonds, but less than an amount which would cause significant runnability and sheet strength problems in the final commercial product.
  • the amount of acid chemical bonding inhibitor 6 employed, on a 100% active basis is preferably from about 0.5 pound per ton (1 kg/tonne) of cellulose pulp, up to about 15 pounds per ton (30 kg/tonne) of cellulose pulp. However, a more preferred addition of from about 1 pound (2 kg) , up to about 10 pounds (20 kg) , of chemical bonding inhibitor per ton (tonne) of cellulose pulp can be employed.
  • Treatment of the wet web with the bonding inhibitor material can be accomplished by various means.
  • the treatment step can comprise spraying, applying with a direct contact applicator means or by employing an applicator felt.
  • the preferred method of application is by spraying the web such as by employing spray header 6a, at various points prior to thermal drying means 8 (see FIGURE 1) .
  • the adjustment of the pH of the web is localized at a given point of treatment, as opposed to having the web adjusted to the desired acidic pH level in the headbox.
  • the pH of the chemical bonding inhibitor 6 is adjusted to a pH level, prior to treatment therewith, which will facilitate the requisite minimum pH of the treated web at a level within the previously set forth pH limits.
  • the pH of the web is first adjusted to a prescribed level and thereafter the sheet is treated with the chemical bonding inhibitor.
  • the acidity level of the bonding inhibitor material 6 can be adjusted employing numerous materials capable of performing that function. However, organic acids such as formic acid, acetic acid, propionic acid and benzoic acid, and inorganic acids such as hydro- chloric acid, sulfuric acid, phosphoric acid and nitric acid, or salts thereof, are preferred. Of the above acidic materials, however, sulfuric acid is the most preferred.
  • the surface treated web la is then applied to the surface 7 of the.rmal drying means 8, preferably a thermal drying cylinder such as a Yankee drying cylinder, employing preferably an adhesive to supplement the adhesion process.
  • a thermal drying cylinder such as a Yankee drying cylinder
  • typical adhesive compounds which may be used include carboxymethyl cellulose, polyvinyl alcohol, anionic starch, various soluble natural polymers such as gums and the like, and synthetic resins such as polyamide resins, and the like.
  • Adhesion of the treated web la to the cylinder surface 7 is preferably facilitated by the mechanical compressive action exerted thereon, generally using one or more press rolls 9 , which form a nip in combination with the.rmal drying means 8 and which brings the web into more uniform contact with the thermal drying surface 7.
  • the web is then dried on the thermal drying surface preferably to a consistency of at least abour 92%, and more preferably to a consistency of at least about 97%.
  • the creping means 11 then removes the dried, creped sheet 20 from the thermal drying surface, the creping action disrupting bonds between respective fibers and causing a softening effect to be imparted to the sheet.
  • the creping means is a doctor blade which crepes and removes the sheet from the thermal drying surface.
  • Sheet 20 has a high degree of bulk softness .
  • "Bulk softness” is measured by conducting a Handle-O-Meter test (HOM) according to TAPPI T-498.
  • HOM Handle-O-Meter test
  • the bulk softness (reciprocal of stiffness) of a given sheet is then calculated by dividing the HOM value by the square of the caliper of a given single sheet being tested, the quotient thereof being multiplied by 10 .
  • HOM/ (Caliper) 2 x 10 5 is preferably not more than about 1.0, and more preferably not more than about 0.8, and most preferably not more than about 0.6.
  • the basis weight of a given sheet is determined according to TAPPI test number T-410.
  • the basis weight of the sheet produced by the subject method can, in general, range from about 5 pounds per 3,000 square feet (118.8 kg/3000 2 ) , and preferably from about 8 pounds per 3,000 square feet (190.1 kg per 3000 2 ), up to about 50 pounds per 3,000 square feet (1180 kg/3000 2 ) , and preferably up to about 40 pounds per 3,000 square feet (950.4 kg per 3000 2 ).
  • Each sheet must have enough structural integrity so that it will be capable of being manufactured without being damaged.
  • a measure of the structural integrity of a sheet is breaking length. This procedure is run according to TAPPI T-222, except that in stead of a 15-millimeter-wide sample strip, a one-inch
  • the BL avg of a sheet is then calculated after the tensile strength of the sample in the machine direction (MD) and cross-machine direction (CMD) , respectively, is determined, using the following equation:
  • MD machine direction
  • CMD cross-machine direction
  • the BL aVg of preferably at least about 150 meters, and more preferably at least about 250 meters is provided.
  • the creped sheet has too high a BLavg value, it will be too harsh to the feel and, therefore, unacceptable to the consumer.
  • the BL avg be not more than about 450 meters, and more preferably not greater than about 400 meters.
  • the water absorbency parameter is expressed as the number of seconds it takes for a single sheet (4.5 inches by 4.5 inches) (11.43 cm by 11.43 cm) to absorb 0.1 cc of water, the test being described in TAPPI T-432.
  • an unexpected increase in the absorben-cy will result.
  • an increase in water absorbency of at least about 50% , and more preferably at least 100%, and most preferably at least 150% can be provided.
  • EXAMPLE 1 A series of three experiments (A-C) was conducted, employing a paper machine having a configuration set out in FIGURE 1.
  • a chemical bonding inhibitor material namely, Quaker 2001, a cationic quaternary ammonium compound produced by Quaker Chemical Company, at a pH of 5.48 was sprayed on the formed web at a consistency of about 10%.
  • Experiments 3 and C 25 and 50 ml of a 10% solution of sulfuric acid was added to 4 gallons
  • the over-all quality and surface-perceived softness, respectively, of a cellulose sheet are subjectively determined to a great extent by the hand feel as discerned by the ultimate consumer. Objective testing of the sheets in question are a measure of these properties and cannot totally act as a substitute for such a subjective determination. Therefore, the over-all quality and surface-perceived softness of sheets such as those produced by the method of this invention can best be subjectively determined by polling randomly selected respondents who have compared cellulosic sheets prepared by various methods, including the subject method. More specifically, four sheets prepared in substantially the same manner, except for pH of the chemical bonding inhibitor employed, were compared.
  • Each of the four sheets was then rated by a group of ten respondents with respect to over-all quality and surface-perceived softness .
  • An average over-all quality and surface-perceived softness for each of the sheets tested was then determined by adding the total points received for each of the sheets tested from a given respondent and dividing that total by ten, i.e., the total number of respondents.
  • An over-all quality factor and surface-perceived scftness factor for sheets produced by the subject invention were then determined by dividing the average over-all quality, or the average surface-perceived softness, for the subject sheet by the comparable average value of the sheet, using a chemical bonding inhibitor per se.
  • a series of four experimental sheets, including the three cellulosic sheet products described in Example 1 (Nos. A-C) were tested, and an average overall quality factor and an average surface-perceived softness factor for each were determined.
  • the sheets produced by the method of this invention have an over-all quality factor and a surface-perceived softness factor of preferably at least about 1.5, and more preferably at least about 2.0, and most preferably at least about 2.5.

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Paper (AREA)

Abstract

Procede de production d'une feuille de cellulose (20) pouvant etre utilisee dans des mouchoirs et des serviettes de haute qualite et ayant d'excellentes proprietes d'absorption de l'eau et tres douce en surface. Le procede comprend les etapes de formation d'une bande de cellulose (1), le traitement de cette bande avec un inhibiteur de liaison chimique (6) pour que le pH de la bande, apres traitement, ne depasse pas 5,0 environ, puis le crepage et le sechage de la bande traitee. La feuille (20) produite par cette methode possede un facteur de qualite et un facteur de douceur sensible en surface, respectivement, d'au moins 1,5 environ.Method for producing a cellulose sheet (20) which can be used in high quality handkerchiefs and towels and which has excellent water absorption properties and is very soft on the surface. The method comprises the steps of forming a cellulose band (1), treating this band with a chemical binding inhibitor (6) so that the pH of the band, after treatment, does not exceed about 5.0, then creping and drying of the treated strip. The sheet (20) produced by this method has a quality factor and a surface softness factor, respectively, of at least about 1.5.

Description

METHOD FOR PRODUCING A HIGH QUALITY, WATER ABSORBENT, CELLULOSIC SHEET HAVING HIGH SURFACE-PERCEIVED SOFTNESS
TECHNICAL FTELD
This invention is directed to a method for producing a highly absorbent cellulosic sheet having excellent over-all quality and a high level of surface- perceived softness, respectively, which is capable of being employed in high softness grades of tissue and towel.
BACKGROUND ART In the production of standard grades of paper on a conventional paper machine, cellulosic fibers and water are combined in a headbox to form an aqueous fiber slurry having a fiber consistency of from about 0.05% to 0.2% by weight, based on the total weight of that slurry. The wet web from the headbox is formed on a papermaking wire at a consistency of at least about 5% for purposes of mechanically removing water therefrom. This mechanical dewatering step increases the consistency of the web up to a level of about 45-50%. As the water is mechanically displaced, the fibers are moved into close proximity one with the other, and chemical bonds, generally described as "hydrogen bonds", are formed between the adjacent cellulosic fiber surfaces. The formation of these hydrogen bonds serves to strengthen the web, as measured, for example, by a substantial increase in physical properties such as an increase in the breaking length of the web.
The uncontroled formation of substantial members of hydrogen bonds between the surfaces of adjacent fibers is detrimental to certain paper pro perties such as softness and absorbency. Specifically, various types of paper products such as certain grades of tissue and towel in which the sheet must be absorbent and soft to the touch cannot tolerate the unlimited formation of hydrogen bonds . These high softness and absorbency properties are not present in paper products made by the above described conventional papermaking techniques.
In an attempt to produce a sheet having the above described requisite degree of softness and absorbency, certain prior art methods incorporate a chemical "debonding agent" into the aqueous fiber slurry to inhibit the formation of hydrogen bonds. The incorporation of the debonder must, however, be accomplished without destroying the integrity of the web since it is necessary to form a sheet having the requisite strength properties for its intended use as a finished product of commerce, i.e., to produce a sheet having a high, over-all quality. U. S. Patent 3,812,000 to Salvucci et al.;
U. S. 3,844,880 to Meisel et al.; and U. S. 3,903,342 to Roberts et al., respectively, describe the addition of materials such as the above mentioned debonding agents to an aqueous slurry of cellulosic fibers to minimize hydrogen bonding in an attempt to increase softness. Typically, the above chemical debonding agents comprise surfactants such as those described in the Hervey et al. U. S. patents, Nos . 3,554,862; 3,554,863; and 3,395,708. The addition of a chemical debonding agent to the fiber slurry promotes the overall treatment of all fibers without regard to whether the treated fibers are located at the web surface, where hand-feel properties are measured, or in the interstices of the sheet. Therefore, certain patents such as U. S. 3,556,931 to Champaigne; U. S. 2,756,647 to Thompson; and U. S. 4,158,594 to Becker et al., disclose adding a debonding agent to a cellulosic web after web formation, but prior to drying. These latter patents describe softening the web to a certain extent, but do not provide a sheet having the requisite quality, absorbency, and surface-perceived softness level, as hereinafter defined.
DISCLOSURE OF INVENTION In order to overcome the previously described problems associated with the prior art resulting from the addition to the headbox of chemical debonding agents , the subject invention contemplates treating the cellulose fibers in the formed web with a chemical bonding inhibitor having an acidic pH. More specifically, the cellulosic web immediately after formation preferably has an initial pH of not less than about 6.0, and preferably not less than about 6.5, and more preferably not less than about 7.0. At least one surface of the web is treated with the chemical bonding inhibitor, and the pH of the treated web immediately after the treatment step is not more than about 5.0, and preferably not more than about 4.5, and more preferably not more than about 4..0, and most preferably not more than about 3.0. The result of treating the web with a chemical bonding inhibitor under the pH conditions described above is an unexpected, dramatic improvement in quality, absorbency, and surface-perceived softness of the sheet products. The treatment of the cellulosic fibers with the acidic chemical bonding inhibitors does not occur until the consistency of the web, as measured immediately after the treatment step, is at least about 5% by weight, up to about 50% by weight. BRIEF DESCRIPTION OF THE DRAWING FIGURE 1 is a schematic representation of a preferred method within the scope of this invention.
MODES FOR CARRYING OUT THE INVENTION
In accordance with the present invention, a method is provided for producing a highly absorbent, cellulosic sheet which exhibits excellent over-all quality and a high degree of surface-perceived softness. A schematic drawing depicting a process configuration is set forth in FIGURE 1.
In the method of the present invention, an aqueous furnish including cellulose papermaking fibers is initially formed. The cellulosic fibers have undergone some degree of lignin modification, such as at least partial chemical treatment, to produce materials such as chemimechanical pulp, semichemical pulp, chemical pulp, or mixtures thereof. Suitable materials from which the above cellulose fibers can be derived include the usual species of coniferous and deciduous pulpwood, the cellulosic components being preferably produced from coniferous pulpwood because of its greater fiber length.
The aqueous furnish is transported to a headbox 2 at a level sufficient to permit the formation of a substantially dry sheet upon completion of the hereinafter described dewatering and thermal drying steps , respectively, without requiring further drying thereof subsequent to creping. As a practical matter, however, the consistency of the aqueous furnish used in forming the subject wet web is desirably maintained at a level of from about 0.05% by weight, and more preferably from about 0.1% by weight, based on the total weight of cellulosic fibers in the aqueous furnish, up to a pre- ferred consistency of about 1.0% by weight, and more 5 preferably up to about 0.75% by weight.
A wet web 1 is then formed by deposition of the aqueous furnish onto a web forming means 3 , typically a conventional papermaking system including a foraminous conveying means 4 such as a Fourdrinier wire, Stevens former, or the like.
Dewatering of the wet web is then provided prior to the thermal drying operation typically employing a nonthermal dewatering means 5. The nonthermal dewatering step is usually accomplished by various means for imparting mechanical compaction to the web 1 such as vacuum boxes, slot boxes, coacting press rolls, or combinations thereof. For purposes of illustration of the method of this invention, the wet web 1 is de watered by subjecting same to a series of vacuum boxes and/or slot boxes, as shown in FIGURE 1. Thereafter, the web is further dewatered by subjecting same to the compressive forces exerted by nonthermal dewatering means such as, for example, a pair of rolls, followed by a pressure roll coacting with a thermal drying means .
The wet web 1 is carried by the foraminous conveying means 4 through the nonthermal dewatering means 5, where it is dewatered to a consistency of at least about 5%, preferably at least 10%, and more preferably at least 15%, up to a consistency of preferably about 50%, and more preferably up to about 45%, and most preferably up to about 35%. The cellulosic web formed, as described above, preferably has an initial pH of at least about 6 in order to minimize corrosion problems which can occur with respect to the foraminous conveying means, as well as other portions of the papermaking equipment if the pH per se is too low. More preferably, the initial pH of the web is maintained at a level, as previously described. The wet web 1 prior to the thermal drying step is treated with an acidic chemical material 6 , which inhibits the formation of papermaking bonds between adjacent cellulosic fibers. By treating the web 1 in this manner, a sheet 20 having the hereinafter defined, unexpected properties can be produced. The pH of web immediately after the treatment step, denoted "la", is not more than about 5.0, and is preferably not more than about 4.5, and is more preferably not more than about 4.0, and is most preferably not more than about 3.0.
The consistency of the web immediately after the treatment step is preferably within the previously defined consistency parameters. Preferably, this chemical bonding inhibitor per se is a "chemical debonding agent" . These materials are well-known in the prior art, and are preferably substantially cationic in nature. Examples of suitable chemical bonding inhibitor materials include Quaker 2001 (Quaker Chemical) , Ceranine HCS (Sandoz) , Leomin KP (Hoechst AG) , and Amasoft-PM (American Color and Chemical) .
The bonding inhibitor 6 employed for treatment of the web is provided at a treatment level which is sufficient to minimize the formation of the above described hydrogen bonds, but less than an amount which would cause significant runnability and sheet strength problems in the final commercial product. The amount of acid chemical bonding inhibitor 6 employed, on a 100% active basis, is preferably from about 0.5 pound per ton (1 kg/tonne) of cellulose pulp, up to about 15 pounds per ton (30 kg/tonne) of cellulose pulp. However, a more preferred addition of from about 1 pound (2 kg) , up to about 10 pounds (20 kg) , of chemical bonding inhibitor per ton (tonne) of cellulose pulp can be employed. Treatment of the wet web with the bonding inhibitor material can be accomplished by various means. For instance, the treatment step can comprise spraying, applying with a direct contact applicator means or by employing an applicator felt. However, the preferred method of application is by spraying the web such as by employing spray header 6a, at various points prior to thermal drying means 8 (see FIGURE 1) . The adjustment of the pH of the web is localized at a given point of treatment, as opposed to having the web adjusted to the desired acidic pH level in the headbox. In a preferred method, the pH of the chemical bonding inhibitor 6 is adjusted to a pH level, prior to treatment therewith, which will facilitate the requisite minimum pH of the treated web at a level within the previously set forth pH limits. In a further preferred method, the pH of the web is first adjusted to a prescribed level and thereafter the sheet is treated with the chemical bonding inhibitor. The acidity level of the bonding inhibitor material 6 can be adjusted employing numerous materials capable of performing that function. However, organic acids such as formic acid, acetic acid, propionic acid and benzoic acid, and inorganic acids such as hydro- chloric acid, sulfuric acid, phosphoric acid and nitric acid, or salts thereof, are preferred. Of the above acidic materials, however, sulfuric acid is the most preferred.
The surface treated web la is then applied to the surface 7 of the.rmal drying means 8, preferably a thermal drying cylinder such as a Yankee drying cylinder, employing preferably an adhesive to supplement the adhesion process. Examples of typical adhesive compounds which may be used include carboxymethyl cellulose, polyvinyl alcohol, anionic starch, various soluble natural polymers such as gums and the like, and synthetic resins such as polyamide resins, and the like. Adhesion of the treated web la to the cylinder surface 7 is preferably facilitated by the mechanical compressive action exerted thereon, generally using one or more press rolls 9 , which form a nip in combination with the.rmal drying means 8 and which brings the web into more uniform contact with the thermal drying surface 7. The web is then dried on the thermal drying surface preferably to a consistency of at least abour 92%, and more preferably to a consistency of at least about 97%.
The creping means 11 then removes the dried, creped sheet 20 from the thermal drying surface, the creping action disrupting bonds between respective fibers and causing a softening effect to be imparted to the sheet. In general, the creping means is a doctor blade which crepes and removes the sheet from the thermal drying surface.
Sheet 20 has a high degree of bulk softness . "Bulk softness" is measured by conducting a Handle-O-Meter test (HOM) according to TAPPI T-498. The bulk softness (reciprocal of stiffness) of a given sheet is then calculated by dividing the HOM value by the square of the caliper of a given single sheet being tested, the quotient thereof being multiplied by 10 . For example, in single-ply tissue and towel applications, depending on the type of furnish employed, bulk softness, expressed as HOM/ (Caliper)2 x 105 is preferably not more than about 1.0, and more preferably not more than about 0.8, and most preferably not more than about 0.6.
An important aspect of this invention is the ability of the subject method to produce sheets in an extremely broad basis weight range. The basis weight of a given sheet is determined according to TAPPI test number T-410. The basis weight of the sheet produced by the subject method can, in general, range from about 5 pounds per 3,000 square feet (118.8 kg/30002) , and preferably from about 8 pounds per 3,000 square feet (190.1 kg per 30002), up to about 50 pounds per 3,000 square feet (1180 kg/30002) , and preferably up to about 40 pounds per 3,000 square feet (950.4 kg per 30002). Each sheet must have enough structural integrity so that it will be capable of being manufactured without being damaged. A measure of the structural integrity of a sheet is breaking length. This procedure is run according to TAPPI T-222, except that in stead of a 15-millimeter-wide sample strip, a one-inch
(25.4 mm) wide strip is used. Average breaking length
(BLavg) of a sheet is then calculated after the tensile strength of the sample in the machine direction (MD) and cross-machine direction (CMD) , respectively, is determined, using the following equation: In order to insure runnability of a web on papermaking equipment, the BLaVg of preferably at least about 150 meters, and more preferably at least about 250 meters is provided. Furthermore, if the creped sheet has too high a BLavg value, it will be too harsh to the feel and, therefore, unacceptable to the consumer. Thus , it is preferred that the BLavg be not more than about 450 meters, and more preferably not greater than about 400 meters.
Another important sheet property is its ability to absorb water. The water absorbency parameter is expressed as the number of seconds it takes for a single sheet (4.5 inches by 4.5 inches) (11.43 cm by 11.43 cm) to absorb 0.1 cc of water, the test being described in TAPPI T-432.
If the method of the present invention is employed in a wet treatment step, as opposed to the prior art methods in which chemical bonding inhibitor per se is employed, an unexpected increase in the absorben-cy will result. Preferably, an increase in water absorbency of at least about 50% , and more preferably at least 100%, and most preferably at least 150% can be provided.
EXAMPLE 1 A series of three experiments (A-C) was conducted, employing a paper machine having a configuration set out in FIGURE 1. In the first experiment, 0.25% of a chemical bonding inhibitor material, namely, Quaker 2001, a cationic quaternary ammonium compound produced by Quaker Chemical Company, at a pH of 5.48 was sprayed on the formed web at a consistency of about 10%. In Experiments 3 and C, 25 and 50 ml of a 10% solution of sulfuric acid was added to 4 gallons
(15.2 liters) of bonding inhibitor solution prior to spraying same on the wet web. This produced a pH of 2.78 and 2.48, respectively, immediately after treatment of the wet web in Experiments B and C. Sheets produced in Experiments A-C were tested, and the results re water absorbency and bulk softness are summarized in Table I.
The effect of employing an acidic bonding inhibitor treatment solution is clearly demonstrated by the above experimental comparison. Specifically, the stiffness of the subject sheets (B and C) have been substantially reduced (softness increased) by employing the method of the subject invention to about one- half that of the sheet (A) employing a chemical bond ing inhibitor per se. At the same time, the water absorbency of sheets B and C is dramatically increased, as compared to its higher pH counterpart, so that the sheets produced in Experiments B and C are 324% and 260%, respectively, more absorbent than the sheet pro duced in Experiment A.
The over-all quality and surface-perceived softness, respectively, of a cellulose sheet are subjectively determined to a great extent by the hand feel as discerned by the ultimate consumer. Objective testing of the sheets in question are a measure of these properties and cannot totally act as a substitute for such a subjective determination. Therefore, the over-all quality and surface-perceived softness of sheets such as those produced by the method of this invention can best be subjectively determined by polling randomly selected respondents who have compared cellulosic sheets prepared by various methods, including the subject method. More specifically, four sheets prepared in substantially the same manner, except for pH of the chemical bonding inhibitor employed, were compared. Each of the four sheets was then rated by a group of ten respondents with respect to over-all quality and surface-perceived softness . An average over-all quality and surface-perceived softness for each of the sheets tested was then determined by adding the total points received for each of the sheets tested from a given respondent and dividing that total by ten, i.e., the total number of respondents. An over-all quality factor and surface-perceived scftness factor for sheets produced by the subject invention were then determined by dividing the average over-all quality, or the average surface-perceived softness, for the subject sheet by the comparable average value of the sheet, using a chemical bonding inhibitor per se. For example, a series of four experimental sheets, including the three cellulosic sheet products described in Example 1 (Nos. A-C) , were tested, and an average overall quality factor and an average surface-perceived softness factor for each were determined.
Accordingly, the sheets produced by the method of this invention have an over-all quality factor and a surface-perceived softness factor of preferably at least about 1.5, and more preferably at least about 2.0, and most preferably at least about 2.5.

Claims

1. A method for producing a highly absorbent, cellulosic sheet having excellent quality and a high level of surface-perceived softness, respectively, which comprises a) forming a web of cellulosic fibers ; b) treating the web with an acidic chemi cal material for inhibiting the formation of papermaking bonds between said cellulose fibers and said web, the consistency of the treated web immediately after said treatment step being from about 5% by weight, up to about 50% by weight, and the pH of the treated web immediately after the treatment step being not more than about 5.0; c) adhering the treated web to a thermal drying means , and drying said treated web thereon; and d) creping the dried web, the dried web having an over-all quality factor and a surface perceived softness factor, respectively, of at least about 1.5.
2.
The method of claim 1, wherein at least one surface of the web is treated with the acidic chemical bonding inhibitor.
3. The method of claim 1, wherein the initial pH of the web prior to treatment is not less than about 6.0.
4. The method of claim 3, wherein the initial pH is not more than about 6.5.
5. The method of claim 4, wherein the initial pH is not less than about 7.0.
6. The method of claim 1, wherein the pH immediately after the treatment step is not more than about 4.0.
7. The method of claim 6 , wherein the pH is not more than about 3.0.
8. The method of claim 1, wherein the acidity level is adjusted in the treatment step by employing an inorganic acid.
9. The method of claim 1, wherein the pH of the wet web is first adjusted to the prescribed level and, thereafter, the sheet is treated with a chemical bonding inhibitor material.
10. The method of claim 1, wherein the pH of the chemical bonding inhibitor is adjusted to a level which will facilitate the requisite minimum pH level of the treated web at a pH of not greater than 5.0.
11. The method of claim 1, wherein the acidity level is adjusted with an organic acid.
12. The method of claim 1, wherein the respective over-all quality and surface-perceived softness factors of the sheet are at least about 2.0.
13.
The method of claim 1, wherein the treatment step comprises spraying said chemical bonding inhibitor onto the wet web.
EP19810902213 1980-08-07 1981-08-03 Method for producing a high quality, water absorbent, cellulosic sheet having high surface-perceived softness Withdrawn EP0057212A1 (en)

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US17622580A 1980-08-07 1980-08-07
US176225 1980-08-07

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EP0184603A1 (en) * 1984-12-07 1986-06-18 Korsnäs-Marma Ab Process for preparing a fluff pulp
US4795530A (en) * 1985-11-05 1989-01-03 Kimberly-Clark Corporation Process for making soft, strong cellulosic sheet and products made thereby
US5059282A (en) * 1988-06-14 1991-10-22 The Procter & Gamble Company Soft tissue paper
US5164046A (en) * 1989-01-19 1992-11-17 The Procter & Gamble Company Method for making soft tissue paper using polysiloxane compound
US5227242A (en) * 1989-02-24 1993-07-13 Kimberly-Clark Corporation Multifunctional facial tissue
US4992140A (en) * 1989-04-06 1991-02-12 Scott Paper Company Method for creping a paper web and product produced thereby
US5399241A (en) * 1993-10-01 1995-03-21 James River Corporation Of Virginia Soft strong towel and tissue paper
US5730839A (en) * 1995-07-21 1998-03-24 Kimberly-Clark Worldwide, Inc. Method of creping tissue webs containing a softener using a closed creping pocket

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US2032645A (en) * 1933-08-18 1936-03-03 Northern Paper Mills Absorbent paper product and process of producing the same
US1986291A (en) * 1933-11-23 1935-01-01 Brown Co Manufacture of absorbent waterlaid webs of felted fiber
US2683088A (en) * 1952-06-10 1954-07-06 American Cyanamid Co Soft bibulous sheet
US2940890A (en) * 1956-06-25 1960-06-14 Kimberly Clark Co Treatment of cellulosic pulps
GB852678A (en) * 1958-03-18 1960-10-26 Canadian Aniline And Extract C Pulp production using non-ionic surface active agents
DE2314060A1 (en) * 1973-03-21 1974-10-10 Honshu Paper Co Ltd SURFACE-ACTIVE SUBSTANCE

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WO1982000485A1 (en) 1982-02-18

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