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US3354032A - Production of paper of cellulose and polyamide fibers - Google Patents

Production of paper of cellulose and polyamide fibers Download PDF

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Publication number
US3354032A
US3354032A US364012A US36401264A US3354032A US 3354032 A US3354032 A US 3354032A US 364012 A US364012 A US 364012A US 36401264 A US36401264 A US 36401264A US 3354032 A US3354032 A US 3354032A
Authority
US
United States
Prior art keywords
paper
fibers
polyamide
cellulose
polyamide fibers
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.)
Expired - Lifetime
Application number
US364012A
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English (en)
Inventor
Sommer Erwin
Gerlach Klaus
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Glanzstoff AG
Vereinigte Glanzstoff Fabriken AG
Original Assignee
Glanzstoff AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Glanzstoff AG filed Critical Glanzstoff AG
Application granted granted Critical
Publication of US3354032A publication Critical patent/US3354032A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • D21H5/00Special paper or cardboard not otherwise provided for
    • D21H5/12Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials
    • D21H5/1254Special paper or cardboard not otherwise provided for characterised by the use of special fibrous materials of fibres which have been treated to improve their dispersion in the paper-making furnish
    • 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
    • D21H13/00Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
    • D21H13/10Organic non-cellulose fibres
    • D21H13/20Organic non-cellulose fibres from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H13/26Polyamides; Polyimides
    • 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
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds

Definitions

  • This invention relates to a sheet-like or paper-like product and the method by which it is produced. More particularly, this invention is concerned with the production of a sheet structure or paper product composed of at least about 50% by weight and preferably a major proportion of cellulose fibers in admixture with polyamide fibers by the conventional method of water-laying such materials from an aqueous fibrous slurry onto the screen or other foraminous supporting surface of a paper-making machine, and thereafter drying the water-laid web or nonwoven felt to form a flexible sheet structure.
  • the improvement of the present invention resides in a special pretreatment of the polyamide fibers prior to their combination with the cellulose fibers during the paper-making process.
  • Cellulose is most often used for the production of paper or paper-like sheet structures according to the well-known paper-making process in which staple lengths of the cellulose fibers are first dispersed in water and then transferred or flowed onto a moving screen or sieve for the removal of at least part of the water and formation of the fibrous web or fleece. Thereafter, the water-laid web is dried and pressed or otherwise treated to produce the final paper product.
  • the steps of making paper can be carried out commercially on a Fourdrinier machine or on a suitable cylinder machine for continuous production of the paper.
  • Paper products composed entirely of cellulose fibers have been produced by this process over a long period of time, but such cellulosic papers have a relatively 10W tearing strength, a low burst pressure and unsatisfactory crease resistance. Accordingly, many attempts have been made to improve these properties in the paper product without making substantial changes in the papermakiug process and without unduly increasing the cost of paper production.
  • a binder must be simultaneously added to the fibrous dispersion or else the water laid fibrous web must be treated with a binding resin during a subsequent stage of the process.
  • the binding agent must constitute at least by weight of the fibrous composition.
  • Gelatin is a common binding agent which is added to the fiber dispersion so as to adhere to the fibers during water-laying on the paper-making machine. Excess water is squeezed or pressed out of the water-laid fibrous web which is then dried to remove the remaining water.
  • Another technique of adding a binding agent consists in soaking or impregnating the water-laid web of cellulose and polyamide fibers with an aqueous dispersion of a synthetic resin, and then drying and hot-pressing the web to form the final paper product.
  • Cellulose-polyamide sheets produced in this manner generally require a large amount of the binding agent, and this high load of the binder causes the product to lose its paper-like texture. Moreover, the porosity of such products is very slight.
  • an improved cellulose-polyamide fibrous paper or sheet-like structure can be obtained in the con-- ventional process of water-laying the ceilulose and polyamide fibers from an aqueous dispersion as a fibrous web on a paper-making machine if the polyamide fibers are pretreated under an acid pH, prior to combination with the cellulose fibers in the aqueous dispersion, with an aqueous solution of the sodium salt of a styrene-maleic acid copolymer.
  • the pie-treatment with the copolymer solution should be carried out at an acid pH of about 1.8 to 2.5, and preferably about 2.0 to 2.2.
  • the pretreated or precoated polyamide fibers are mixed with the cellulose fibers in the preparation of the aqueous dispersion or fibrous slurry which is then water-laid on a formaminous supporting surface according to the conventional paper-making procedure.
  • the aqueous dispersion should contain at least about 50% up to about by weight of the cellulose fibers and from about 5 to 50%, preferably 10 to 25% by weight of the pretreated polyamide fibers.
  • the styrene-maleic acid copolymer employed as a precoating agent for the polyamide fibers can be prepared according to conventional methods.
  • the copolymer can be prepared by free radical polymerization of styrene and maleic acid anhydride as co-monomers in a molar ratio of about 0.5 :1 to 1:0.5, preferably in an approximately equimolar ratio of styrene to maleic acid anhydride. Subsequent treatment with sodium hydroxide renders the copolymer alkali-soluble.
  • the styrene and maleic acid anhydride are copolymerized in acetone in the presence of a free radical catalyst such as benzoyl peroxide, and the resultingproduct is reacted with normal NaOH at about 75 C. to give the water-soluble sodium salt of the copolymer.
  • the copolymer preferably has a molecular weight on the order of at least 10,000 up to about 250,000.
  • the polyamide fibers are those obtained from the usual fiber-forming high molecular weight polyamides such as polyhexamethylene adipamide or caprolactam, the fiberforming polymer being spun and then stretched as a monofilarnent and subsequently cut into a staple length suitable for felting or forming a water-laid web, for example staple lengths ofabout 2 to mm.
  • the methods of forming these polyamide filaments and their general use in the paper-making process are so well-known as to require no further elaboration here.
  • the precoating or pretreating of the polyamide filaments or fibers' can be easily accomplished in a single step by passing the polyamide filaments as a yarn or bundle through an aqueous solution of the styrene-maleic acid copolymer salt.
  • the treatment solution or bath is prepared by first dissolving the alkali-soluble copolymer salt in water, and it is essential that this solution be acidified in this one step procedure, preferably to a pH value just short of that at which the copolymer will recipides the free acid, this precipitation occurring at a pH value of about 1.8. It is also possible to apply the acidified copolymer salt solution to the polyamide fibers either before or after cutting the filaments into shorter or staple lengths.
  • the pretreatment can also be carried out as a two-bath process.
  • This two-bath process is accomplished, for example, by first drawing the polyamide filaments or yarn through a dilute acid bath, then squeezing or otherwise removing excess bath liquid from the filaments and thereafter conducting the filaments through a non-acidified aqueous solution of the copolymer salt.
  • the pH value of the non-acidified copolymer salt solutions should be maintained at a constant level by the continuous addition of an alkaline compound such as sodium hydroxide.
  • This two-bath technique substantially avoids any danger of copolymer recipitation which might be caused by an overadjustment of the pH in thesingle bath treatment.
  • the two-bath method avoids the careful adjustment of an acid pH value of the copolymer salt solution, but the preliminary dilute acid treatment does produce an acid condition at the surface of the filaments even though they are subsequently drawn through a neutral to alkaline solution of the copolymer salt.
  • any acid may be used in the process of the invention, i.e. all inorganic and organic acids are suitable, whether one employs the single bath method or the double bath method.
  • the pH value of the copolymer salt solution is simply adjusted to a value of :about 1.8 to 2.5, preferably 2.0 to 2.2, and this same condition is approximated when coating the filaments with dilute acid in the two-bath method.
  • the amount of acid to be supplied in any case can be readily determined by simple preliminary tests.
  • the precoated polyamide fibers can be readily dispersed and mixed together with the cellulose fibers in the head box of the paper-making machine. Thereafter, the slurry or pulp of precoated polyamide fibers and cellulose fibers is water-laid into a fibrous web and the web dried to form a paper sheet according to the conventional paper-making technique. It is not necessary to add additional binding agents to the fibrous web, and the drying of the web can take place with or without pressure at temperatures of 100 C. or at lower temperatures.
  • the aqueous solution of the styrenemaleic acid copolymer salt should have a copolymer concentration of about 0.1 to 1.0% by weight, preferably 0.3 to 0.7% by Weight.
  • the bath temperatures, whether single or double, can be maintained at a temperature of about 40 to 85 C., higher temperatures permitting shorter treatment periods.
  • the pretreated polyamide fibers should normally have an adherent coating of the styrene-maleic acid copolymer of about 0.5 to 3.0% by Weight, with the same content of the copolymer appearing in the final paper product. It will be understood that these amounts of the copolymer can be varied depending upon the particular quality and strength properties desired in the final product.
  • Example 1 A polyamide continuous filament yarn having a total denier of 86,000 and an individual denier of 1.4 was obtained by spinning and stretching from slit orifices having individual dimensions of 60 x 800g. This yarn was immersed in a 0.5% aqueous solution of the sodium salt of a copolymer of styrene and maleic acid anhydride combined in a molar ratio of 1:1. The copolymer had a molecular weight of about 100,000. The copolymer solution was previously acidified by addition of sulfuric acid in order to obtain a pH value of 2.2, and the polyamide yarn was immersed in this solution for a period of one minute at C.
  • Example 2 A polyamide filament yarn as described in Example 1 was dipped for one minute in 0.05 N sulfuric acid .at 80 C., squeezed between rollers to remove excess acid and finally treated with an aqueous and non-acidified solution of the styrene-maleic acid copolymer in the same manner as in Example 1, ie for one minute at 80 C. After cutting the pretreated polyamide filaments to the staple length of 6 mm., a fibrous slurry was again formed with cellulose fibers and water laid and dried as in Example 1 to provide paper sheets containing 20% by weight of the polyamide fibers. The properties of the paper products obtained by this two-bath method .are shown in the table below.
  • Example 3 For purposes of comparison and control, additional paper samples were prepared by the same paper-making procedure followed in the previous examples, but using cellulose fibers alone or in combination with 10% by weight and 20% by weight of untreated polyamide fibers. The results of these control tests are also shown in the 2.
  • the polyamide-cellulose fibrous paper product of the invention provides a substantial improvement in the product, even when using a smaller content of pretreated polyamide fibers when compared to the use of untreated polyamide fibers.
  • the quality and appearance of the paper product is maintained within desirable standards, and the crease resistance shows a very considerable improvement.
  • the pretreated polyamide fibers can be stored either in the dry state or in the moist state after application of the styrene-maleic acid copolymer salt.
  • the pretreated polyamide fibers do not stick together and can be subsequently dispersed without any difiiculty when forming the fibrous slurry in water together with cellulose fibers.
  • the paper manufacturer can thus obtain the pretreated polyamide fibers and admix them with cellulose fibers in any conventional papermaking process, .and it is unnecessary to use any special equipment or handle any chemicals such as solvents or the like during the paper-making process.
  • the precoating of the polyamide fibers can be accomplished in a relatively simple manner so that the improved results far outweigh any slight additional cost.
  • the paper products of this invention have a Wide range of utility wherever paper is used under conditions requiring high strength and good crease resistance. Specific applications of polyamide-cellulose papers are well known in the art.
  • a process for the production of a paper sheet from an aqueous dispersion of cellulose and polyamide fibers by water-laying said fibers as a fibrous web on a paper-making machine the improvement which comprises: pretreating said polyamide fibers under an acid pH, prior to combination with the cellulose fibers in said aqueous dispersion, with an aqueous solution of the sodium salt of a styrene-maleic acid copolymer.
  • polymer has a molar ratio of styrene to maleic acid of about 0.5:1 to 1:05.
  • a process for the production of a paper sheet having a fibrous content of about 50 to by weight of cellulose fibers and about 5 to 50% by weight of polyamide fibers which process comprises: precoating said polyamide fibers with a styrene-maleic acid copolymer by immersing the fibrous poly-amide in an aqueous solution maintained at a pH of about 1.8 to 2.5 of the sodium salt of said copolymer; mixing the precoated polyamide fibers with the cellulose fibers into a fibrous slurry; waterlaying the mixture of polyamide-cellulose fibers into a fibrous web; and drying the fibrous web to form a paper sheet.
  • a process for the production of a paper sheet having a fibrous content of about 50 to 95 by weight of cellulose fibers and about 5 to 50% by weight of polyamide fibers comprises: coating the fibrous polyamide with aqueous acid and removing excess liquid in a first stage; immersing the acidified fibrous polyamide in a non-acidified aqueous solution of the sodium salt of a styrene-maleic .acid copolymer in a second stage; mixing the resulting two-stage pretreated polyamide fibers with the cellulose fibers into a fibrous slurry; water-laying the mixture of polyamide-cellulose fibers into a fibrous web; and drying the fibrous web to form a paper sheet.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Paper (AREA)
US364012A 1963-05-02 1964-04-30 Production of paper of cellulose and polyamide fibers Expired - Lifetime US3354032A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEV24013A DE1240731B (de) 1963-05-02 1963-05-02 Verfahren zur Herstellung von Papier oder papieraehnlichen Flaechengebilden

Publications (1)

Publication Number Publication Date
US3354032A true US3354032A (en) 1967-11-21

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Family Applications (1)

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US364012A Expired - Lifetime US3354032A (en) 1963-05-02 1964-04-30 Production of paper of cellulose and polyamide fibers

Country Status (7)

Country Link
US (1) US3354032A (de)
AT (1) AT252722B (de)
BE (1) BE645911A (de)
CH (1) CH408634A (de)
DE (1) DE1240731B (de)
GB (1) GB1002019A (de)
NL (1) NL6404797A (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4164595A (en) * 1976-12-29 1979-08-14 American Can Company Premoistened flushable wiper
US4392861A (en) * 1980-10-14 1983-07-12 Johnson & Johnson Baby Products Company Two-ply fibrous facing material
US4425126A (en) 1979-12-28 1984-01-10 Johnson & Johnson Baby Products Company Fibrous material and method of making the same using thermoplastic synthetic wood pulp fibers
US9352607B1 (en) * 2013-01-23 2016-05-31 Abraham R. Albenda Wipeable writing surface

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT944921B (it) * 1970-11-16 1973-04-20 Gordon W Perfezionamento nella carta di sicurezza in particolare carta valuta e simili

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3095345A (en) * 1961-03-22 1963-06-25 Riegel Paper Corp Process for manufacturing paper from synthetic fibers
US3103462A (en) * 1960-04-18 1963-09-10 Eastman Kodak Co Method of improving the strength characteristics of paper prepared from partially acylated cellulose fibers

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3103462A (en) * 1960-04-18 1963-09-10 Eastman Kodak Co Method of improving the strength characteristics of paper prepared from partially acylated cellulose fibers
US3095345A (en) * 1961-03-22 1963-06-25 Riegel Paper Corp Process for manufacturing paper from synthetic fibers

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4164595A (en) * 1976-12-29 1979-08-14 American Can Company Premoistened flushable wiper
US4425126A (en) 1979-12-28 1984-01-10 Johnson & Johnson Baby Products Company Fibrous material and method of making the same using thermoplastic synthetic wood pulp fibers
US4392861A (en) * 1980-10-14 1983-07-12 Johnson & Johnson Baby Products Company Two-ply fibrous facing material
US9352607B1 (en) * 2013-01-23 2016-05-31 Abraham R. Albenda Wipeable writing surface
US9630445B2 (en) * 2013-01-23 2017-04-25 Abraham R. Albenda Wipeable writing surface

Also Published As

Publication number Publication date
CH408634A (de) 1966-02-28
DE1240731B (de) 1967-05-18
GB1002019A (en) 1965-08-18
NL6404797A (de) 1964-11-03
AT252722B (de) 1967-03-10
BE645911A (de) 1964-07-16

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